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15 pages, 291 KiB  
Article
Self-Perceived Health, Mood, and Substance Use Among Adolescents: An Analysis to Enhance Family, Community, and Mental Health Care
by José Antonio Zafra-Agea, Cristina García-Salido, Estel·la Ramírez-Baraldes, Mireia Vilafranca-Cartagena, Ester Colillas-Malet, Anna Portabella-Serra and Daniel García-Gutiérrez
Healthcare 2024, 12(22), 2304; https://doi.org/10.3390/healthcare12222304 - 18 Nov 2024
Viewed by 537
Abstract
Background: Adolescence is a critical period for developing self-perception, emotional well-being, and health behaviors. Mental health disorders represent a substantial burden for adolescents worldwide. This study examines self-perceived health, mood, and substance use among adolescents, identifying associated risk factors. Method: A cross-sectional study [...] Read more.
Background: Adolescence is a critical period for developing self-perception, emotional well-being, and health behaviors. Mental health disorders represent a substantial burden for adolescents worldwide. This study examines self-perceived health, mood, and substance use among adolescents, identifying associated risk factors. Method: A cross-sectional study was conducted with 121 adolescents aged from 14 to 18 from a secondary school in Baix Llobregat, Catalonia. Data were collected through questionnaires, and descriptive and comparative analyses were performed. Results: Poor self-perceived health and negative mood were associated with higher alcohol and tobacco use. Girls exhibited better emotional regulation than boys. Conclusions: Poor health perception and negative mood are linked to increased substance use. Early intervention should focus on emotional well-being and prevention, involving both families and schools. Full article
13 pages, 2892 KiB  
Article
Analysis of In Vivo Plant Volatiles Using Active Sampling and TD-GC×GC-TOFMS
by Sheri A. Schmidt, Ewenet Yemane Mesfin, Chaminda De Silva Weeraddana, A. Paulina de la Mata, Alejandro C. Costamagna and James J. Harynuk
Metabolites 2024, 14(11), 623; https://doi.org/10.3390/metabo14110623 - 14 Nov 2024
Viewed by 482
Abstract
Background: Plants constantly produce primary and secondary metabolites, and a significant fraction of these are volatile organic compounds (VOCs). Factors including the life stage of the plant, temperature, environment, and stress influence the abundance and types of VOCs emitted. The analysis of VOCs [...] Read more.
Background: Plants constantly produce primary and secondary metabolites, and a significant fraction of these are volatile organic compounds (VOCs). Factors including the life stage of the plant, temperature, environment, and stress influence the abundance and types of VOCs emitted. The analysis of VOCs released by plants during different stages or with different conditions provides insight into plant metabolism and stress responses. Collecting the VOC profiles of plants in vivo makes it possible to obtain a representative sample of the entire plant volatilome under controlled conditions with minimal invasiveness. In addition, in vivo sampling can also be used to compare the impacts of different environmental conditions or stressors on plants, i.e., the presence/absence of a pest or amount of nitrogen in soil. Methods: In this study, an in vivo plant sampling technique is introduced and validated using active sampling and thermal desorption (TD) tubes with comprehensive two-dimensional gas chromatography coupled to a time-of-flight mass spectrometer (TD-GC×GC-TOFMS). The purpose of this work is to highlight a novel technique to analyze headspace secondary plant metabolites with a minimal invasiveness. Results: It was concluded that in vivo active sampling onto TD tubes provides a wider global coverage of compounds and larger peak areas when compared to extraction by solid-phase microextraction (SPME). Additionally, the Horwitz ratio of active sampling onto TD tubes was 0.893, demonstrating this technique to be a reliable and reproducible method. Lastly, a variety of plants were sampled to assess the versatility of this technique across various plant species with different sizes and volatile profiles. Hundreds of compounds were measured with this analysis, including terpenes, aldehydes, ketones, terpenoids, and alcohols. Conclusions: This novel in vivo active sampling method provides an additional technique for extracting and analyzing volatile secondary plant metabolites. Full article
(This article belongs to the Special Issue Method Development in Metabolomics and Exposomics)
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<p>GC×GC-TOFMS TIC contour plots obtained from Little Napoli tomato plant. (<b>A</b>) SPME extraction. (<b>B</b>) Active sampling onto a TD tube extraction.</p>
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<p>GC×GC-TOFMS TIC contour plots of four plant species using active sampling onto a TD tube. (<b>A</b>) = Little Napoli tomato, (<b>B</b>) = Sugar Rush tomato, (<b>C</b>) = Patriot blueberry bush, (<b>D</b>) = Mojito mint.</p>
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<p>GC×GC-TOFMS TIC contour plots of four plant species using active sampling onto a TD tube. (<b>A</b>) = Little Napoli tomato, (<b>B</b>) = Sugar Rush tomato, (<b>C</b>) = Patriot blueberry bush, (<b>D</b>) = Mojito mint.</p>
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18 pages, 5510 KiB  
Article
Metabolomic Analysis of Specific Metabolites in Codonopsis pilosula Soil Under Different Stubble Conditions
by Fengbin Xu, Daiyu Qiu, Yurong Hu, Xianxian Chen, Zhonghu Li and Qian Li
Molecules 2024, 29(22), 5333; https://doi.org/10.3390/molecules29225333 - 13 Nov 2024
Viewed by 369
Abstract
To investigate the soil-specific metabolites of Codonopsis pilosula under different stubble management practices, this study analyzed differentially abundant metabolites in the rhizosphere soils of rotational (DS) and continuous (LS) cropping systems via liquid chromatography–tandem mass spectrometry (LC–MS/MS)-based metabolomic approaches. The results revealed that [...] Read more.
To investigate the soil-specific metabolites of Codonopsis pilosula under different stubble management practices, this study analyzed differentially abundant metabolites in the rhizosphere soils of rotational (DS) and continuous (LS) cropping systems via liquid chromatography–tandem mass spectrometry (LC–MS/MS)-based metabolomic approaches. The results revealed that 66 metabolites, including amino acids and their derivatives, nucleic acids, alcohols, organic acids, amines, fatty acids, purines, and sugars, were significantly different (p < 0.05) between the DS and LS groups. Under continuous cropping, the levels of amines, fatty acids, organic acids, and sugars in the rhizosphere soil were significantly greater (p < 0.05) than those under rotational cropping, whereas the levels of amino acids and their derivatives, nucleic acids, and purines and pyrimidines were significantly lower (p < 0.05). KEGG pathway enrichment analysis revealed that these differentially abundant metabolites were enriched in metabolic pathways such as amino acid metabolism (e.g., alanine, aspartate, and glutamate metabolism), carbon metabolism, the cAMP signaling pathway, ABC transporter proteins, phenylalanine metabolism, and the biosynthesis of plant secondary metabolites. These metabolic pathways were involved in osmoregulation, energy supply, and resilience in plants. In conclusion, inter-root soil metabolites in rotational and continuous cropping of Codonopsis pilosula were able to influence soil physicochemical properties and microbial populations by participating in various biological processes. Full article
(This article belongs to the Special Issue Analytical Chemistry in Agriculture Application: 2nd Edition)
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<p>Multivariate analysis of the interroot soil metabolomic data of Radix et Rhizoma ginseng via LC–MS. (<b>a</b>,<b>b</b>): Principal component analysis (PCA) of the metabolomes of six continuous soil samples, six rotational crop samples, and quality control (QC) samples in positive (+) and negative (−) ion modes. (<b>c</b>,<b>d</b>): Partial least squares discriminant analysis (PLS-DA) in positive (+) and negative (−) ion modes, respectively. (<b>e</b>,<b>f</b>): Results of the permutation test for the PLS-DA model in positive (+) and negative (−) ion modes, respectively.</p>
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<p>(<b>a</b>) Top 10 compounds with significantly upregulated differentially abundant metabolites. (<b>b</b>) Top 10 compounds with significantly downregulated differentially abundant metabolites. (<b>c</b>) Z-score plot. (<b>d</b>) Base peak chromatogram of typical soil samples in positive ion mode. (<b>e</b>) Base peak chromatogram of typical soil samples in negative ion mode. When <span class="html-italic">p</span> value &lt; 0.05 and <span class="html-italic">p</span> value &gt; 0.01, it is displayed as *; when <span class="html-italic">p</span> value &lt; 0.01 and <span class="html-italic">p</span> value &gt; 0.001, it is displayed as **.</p>
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<p>(<b>a</b>) Top 10 compounds with significantly upregulated differentially abundant metabolites. (<b>b</b>) Top 10 compounds with significantly downregulated differentially abundant metabolites. (<b>c</b>) Z-score plot. (<b>d</b>) Base peak chromatogram of typical soil samples in positive ion mode. (<b>e</b>) Base peak chromatogram of typical soil samples in negative ion mode. When <span class="html-italic">p</span> value &lt; 0.05 and <span class="html-italic">p</span> value &gt; 0.01, it is displayed as *; when <span class="html-italic">p</span> value &lt; 0.01 and <span class="html-italic">p</span> value &gt; 0.001, it is displayed as **.</p>
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<p>(<b>a</b>) Top 10 compounds with significantly upregulated differentially abundant metabolites. (<b>b</b>) Top 10 compounds with significantly downregulated differentially abundant metabolites. (<b>c</b>) Z-score plot. (<b>d</b>) Base peak chromatogram of typical soil samples in positive ion mode. (<b>e</b>) Base peak chromatogram of typical soil samples in negative ion mode. When <span class="html-italic">p</span> value &lt; 0.05 and <span class="html-italic">p</span> value &gt; 0.01, it is displayed as *; when <span class="html-italic">p</span> value &lt; 0.01 and <span class="html-italic">p</span> value &gt; 0.001, it is displayed as **.</p>
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<p>Heatmap of cluster analysis of differentially abundant metabolites in two interrooted soil samples of <span class="html-italic">Codonopsis pilosula</span> (rotational cropping (DS) and continuous cropping (LS)).</p>
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<p>Metabolite–metabolite correlation analysis. Positive correlations are shown in red; negative correlations are shown in blue.</p>
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<p>Top 30 enriched KEGG pathways from differentially accumulated metabolites (DAMs) identified between DS and LS.</p>
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19 pages, 2336 KiB  
Article
Prenatal Opioid and Alcohol Exposures: Association with Altered Placental Serotonin Transporter Structure and/or Expression
by Nune Darbinian, Nana Merabova, Gabriel Tatevosian, Sandra Adele, Armine Darbinyan, Mary F. Morrison, C. Lindsay DeVane, Sammanda Ramamoorthy, Laura Goetzl and Michael E. Selzer
Int. J. Mol. Sci. 2024, 25(21), 11570; https://doi.org/10.3390/ijms252111570 - 28 Oct 2024
Viewed by 598
Abstract
Fetal exposures to many drugs of abuse, e.g., opioids and alcohol (EtOH), are associated with adverse neurodevelopmental problems in early childhood, including abnormalities in activity of the serotonin (5HT) transporter (SERT), which transports 5HT across the placenta. Little is known about the effects [...] Read more.
Fetal exposures to many drugs of abuse, e.g., opioids and alcohol (EtOH), are associated with adverse neurodevelopmental problems in early childhood, including abnormalities in activity of the serotonin (5HT) transporter (SERT), which transports 5HT across the placenta. Little is known about the effects of these drugs on SERT expression. Pregnant women who used EtOH or opioids were compared to gestational age-matched controls using a structured questionnaire to determine prenatal substance exposure. Following elective pregnancy termination, placental membranous vesicles and exosomes were prepared from first and second trimester human placentas. Changes in EtOH- or opioid-exposed placental SERT expression and modifications were assessed by quantitative western blot. Novel SERT isoforms were sequenced and analyzed. Opioid-exposed but not EtOH-exposed maternal placentas showed SERT cleavage and formation of new SERT fragments (isoforms). Alcohol-exposed cases showed reduced SERT levels. Antibodies to the N-terminal SERT region did not recognize either of the two cleavage products, while antibodies to the central and C-terminal regions recognized both bands. The secondary band seen in the opioid group may represent a hypophosphorylated SERT fragment. These changes in SERT modifications and expression may result in altered fetal brain serotonergic neurotransmission, which could have neurodevelopmental implications. Full article
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<p><b>Effect of <span class="html-italic">in utero</span> opioid exposure on SERT and ABCB1 expression in human placental membranous vesicles.</b> (<b>A</b>) Downregulation of SERT levels in qWestern blot analysis of protein lysates, comparing 20 first and second trimester opioid-exposed human placentas with 20 unexposed controls individually matched for fetal sex, GA, and maternal age. (<b>B</b>) Reduced levels of the drug transporter ABCB1 in opioid-exposed placentas. Inside out placental brush border membrane vesicles were used to measure and quantify the ABCB1 expression. In both (<b>A</b>,<b>B</b>), Grb2 served as a loading control. Data are presented as fold change (* for <span class="html-italic">p</span> &lt; 0.05, *** for <span class="html-italic">p</span> &lt; 0.001).</p>
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<p><b>SERT is modified by maternal opioid exposure.</b> (<b>A</b>) Immunoblot detection of SERT in placental vesicles of first and second trimester fetuses, using a rabbit polyclonal anti-serotonin transporter antibody specific for 70 kDa SERT. Grb2 served as a loading control. Subjects who admitted to chronic opioid use were compared to fetal sex-, GA-, and maternal age-matched controls. <b>Left panel</b>, lanes 1–4 are unexposed controls. Lanes 5–8 are subjects not exposed to opioids or EtOH but who were being treated for depression with SSRIs. <b>Right panel</b>, 12 opiod-exposed cases not exposed to other drugs. (<b>B</b>) Alteration of the SERT protein band pattern is seen only in opioid-exposed cases (lanes 4–10), not with other drug exposures—Adderall (lanes 1–3) and Keppra (lanes 11–12). The cleaved forms of SERT were observed only in opiate cases (lanes 4–10, top panel). (<b>C</b>) The smaller of the double-bands between 34 and 32 kDA representing cleaved forms of SERT (clSERT) in the opioid-exposed cases may represent a hypo-phosphorylated SERT fragment (see <a href="#ijms-25-11570-f003" class="html-fig">Figure 3</a>).</p>
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<p><b>Cleaved SERT isoforms in opioid-exposed cases are within the central domain</b>. (<b>A</b>) The immunoblot used for <a href="#ijms-25-11570-f003" class="html-fig">Figure 3</a> was used for detection of the central domain and C-terminal of SERT in placental vesicles from first and second trimester human pregnancies. Western immunoblots demonstrate expression of SERT isoforms in vesicles from 12-opioid exposed placentas at two GAs. Post-translational modification of SERT was studied by treatment with phosphatase inhibitors (Lane 5 vs. 6). This resulted in enhancement of the lower of the opioid-induced bands at 32–34 kDa, suggesting that most of this smaller clSERT is unphosphorylated. Antibodies to the N-terminal of SERT did not recognize either of the smaller (32 and 34 kDa) bands, while an antibody to the C-terminal region of SERT recognized both bands (upper panel), identical to the bands identified by antibodies to the central region of SERT (lower panel). SDS-PAGE stained with Coomassie blue was used to assure equal protein loading. The actin band (42 kDa) is labeled. (<b>B</b>) An antibody specific for the macrophage marker CD163 was used as a negative control, in combination with an antibody to GAPDH as a positive control, to confirm the purity of placental vesicles, the lack of contamination by other sources of SERT, and the specificity of the SERT double bands in panels (<b>A</b>,<b>B</b>) Note the absence of a band at 70 kDa.</p>
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<p><b>SERT sequencing in opioid cases.</b> The Edman degradation experiment was performed to get the N-terminal sequence of truncated SERT protein double-band versions in opioid-exposed placental vesicles. Two SERT fragments were present in the opioid samples. The sequences were compared with two 5HT transporter isoforms downloaded from Unipro. Sequence alignment was performed using ClustalW2 on two isoforms of SERT fragments on SLC6A4 (Synonyms:HTT, SERT; Organism Homo sapiens (Human), Taxonomic identifier9606 [NCBI]). The first four amino acids of the Central region of SERT were detected in two potential truncated bands corresponding to the sequence of SERT. In combination with the western blot results, we confirm the presence of a truncated SERT protein. Truncated proteins were located using the sequence alignment tool. Version 1 (the upper band) encompasses the amino acids 183–227 (out of 672) of human SERT. Truncated Version 2 (lower band) encompasses amino acids 224–276 of human SERT, which includes the phosphorylation site Thr276.</p>
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<p><b>Prenatal alcohol exposure-associated downregulation of SERT and ABCB1 in placenta vesicles, placenta-derived exosomes, and fetal brain-derived exosomes.</b> (<b>A</b>) EtOH exposure is associated with downregulation of total SERT in right side out (brush border membranous) placental vesicles (IOV) and placenta-derived exosomes from maternal blood (PE; bars 3–4) from human placenta tissues (n = 20) obtained from first and second trimester pregnancies. Analysis was completed by ELISA using a SERT ELISA kit, and results were obtained in picograms/microliters according to SERT standards. Bars represent fold changes between SERT levels in vesicles from EtOH-exposed cases compared to unexposed controls. (<b>B</b>) A similar reduction in expression of ABCB1 was seen in inside-out vesicles IOV. (<b>C</b>) Downregulation of SERT in fetal brain-derived exosomes. All assays were completed in triplicate (catalog #HS0096, detection range is within 0, 0.5, 1.0, 2.5, 5.0, 10 ng/mL, or picogram/microliter, and sensitivity is 0.1 ng/mL). ( *** for <span class="html-italic">p</span> &lt; 0.001).</p>
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31 pages, 5963 KiB  
Review
Dilated Cardiomyopathy: A Genetic Journey from Past to Future
by Noah A. Newman and Michael A. Burke
Int. J. Mol. Sci. 2024, 25(21), 11460; https://doi.org/10.3390/ijms252111460 - 25 Oct 2024
Viewed by 1014
Abstract
Dilated cardiomyopathy (DCM) is characterized by reduced systolic function and cardiac dilation. Cases without an identified secondary cause are classified as idiopathic dilated cardiomyopathy (IDC). Over the last 35 years, many cases of IDC have increasingly been recognized to be genetic in etiology [...] Read more.
Dilated cardiomyopathy (DCM) is characterized by reduced systolic function and cardiac dilation. Cases without an identified secondary cause are classified as idiopathic dilated cardiomyopathy (IDC). Over the last 35 years, many cases of IDC have increasingly been recognized to be genetic in etiology with a core set of definitively causal genes in up to 40% of cases. While over 200 genes have been associated with DCM, the evidence supporting pathogenicity for most remains limited. Further, rapid advances in sequencing and bioinformatics have recently revealed a complex genetic spectrum ranging from monogenic to polygenic in DCM. These advances have also led to the discovery of causal and modifier genetic variants in secondary forms of DCM (e.g., alcohol-induced cardiomyopathy). Current guidelines recommend genetic counseling and screening, as well as endorsing a handful of genotype-specific therapies (e.g., device placement in LMNA cardiomyopathy). The future of genetics in DCM will likely involve polygenic risk scores, direct-to-consumer testing, and pharmacogenetics, requiring providers to have a thorough understanding of this rapidly developing field. Herein we outline three decades of genetics in DCM, summarize recent advances, and project possible future avenues for the field. Full article
(This article belongs to the Special Issue Genetic Insights into Cardiovascular Diseases)
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<p>Visual illustration of the breadth of gene ontologies in dilated cardiomyopathy. Summarized are genes involved in (<b>A</b>) cell junctions, (<b>B</b>) the sarcomere, (<b>C</b>) mitochondria, (<b>D</b>) nuclear architecture and protein trafficking, and (<b>E</b>) cytoskeletal architecture (bold font—definitively pathogenic genes; standard font—putatively pathogenic genes).</p>
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<p>Summary of the genetic underpinnings of the various cardiomyopathy syndromes. Genes that produce channelopathies, ACM, LVNC, and mitochondrial disease can also produce a DCM phenotype. Similarly, genes implicated in RCM and mitochondrial disease can also produce an HCM phenotype. ACM arrhythmogenic cardiomyopathy, ARVC arrhythmogenic right ventricular cardiomyopathy, ALVC arrhythmogenic left ventricular cardiomyopathy, BiV biventricular, DCM dilated cardiomyopathy, HCM hypertrophic cardiomyopathy, LVNC left ventricular non-compaction, and RCM restrictive cardiomyopathy.</p>
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<p>The relationship between variant effect size and its frequency in a population. Effect size refers to the magnitude of influence the variant has on a phenotype, whereas allele frequency describes the prevalence of the variant in a population. DCM is an example of a complex genetic disorder with a causal genetic basis ranging from monogenic, whereby very rare variants in specific genes have a marked effect on cardiac phenotype, to polygenic, where more prevalent minor variants, which individually have little effect on phenotype, can in aggregate result in the disease.</p>
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<p>Summary of major guidelines recommendations to genetics screening in DCM. (<b>Left panel</b>) demonstrates steps provider should take for proband (index) patient. (<b>Right panel</b>) demonstrates algorithmic approach to first-degree relatives [<a href="#B4-ijms-25-11460" class="html-bibr">4</a>,<a href="#B34-ijms-25-11460" class="html-bibr">34</a>,<a href="#B259-ijms-25-11460" class="html-bibr">259</a>].</p>
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<p>A 60-year history of advances in cardiomyopathy genetics. Our understanding of the genetic basis of the cardiomyopathies has paralleled major advances in genetics research tools. HCM hypertrophic cardiomyopathy; RFLP restriction fragment length polymorphism; MD muscular dystrophy; DCM dilated cardiomyopathy; ARVC arrhythmogenic right ventricular cardiomyopathy; NGS next-generation sequencing; GWAS genome-wide association study; ESP the NHLBI Exome Sequencing Project; ExAC exome aggregation consortium; gnomAD genome aggregation database consortium; TOPmed the NHLBI Trans-omics for precision medicine study. References in the figure include [<a href="#B2-ijms-25-11460" class="html-bibr">2</a>,<a href="#B3-ijms-25-11460" class="html-bibr">3</a>,<a href="#B36-ijms-25-11460" class="html-bibr">36</a>,<a href="#B43-ijms-25-11460" class="html-bibr">43</a>,<a href="#B53-ijms-25-11460" class="html-bibr">53</a>,<a href="#B54-ijms-25-11460" class="html-bibr">54</a>,<a href="#B56-ijms-25-11460" class="html-bibr">56</a>,<a href="#B81-ijms-25-11460" class="html-bibr">81</a>,<a href="#B95-ijms-25-11460" class="html-bibr">95</a>,<a href="#B105-ijms-25-11460" class="html-bibr">105</a>,<a href="#B133-ijms-25-11460" class="html-bibr">133</a>,<a href="#B266-ijms-25-11460" class="html-bibr">266</a>,<a href="#B267-ijms-25-11460" class="html-bibr">267</a>,<a href="#B268-ijms-25-11460" class="html-bibr">268</a>,<a href="#B269-ijms-25-11460" class="html-bibr">269</a>,<a href="#B270-ijms-25-11460" class="html-bibr">270</a>,<a href="#B271-ijms-25-11460" class="html-bibr">271</a>,<a href="#B272-ijms-25-11460" class="html-bibr">272</a>,<a href="#B273-ijms-25-11460" class="html-bibr">273</a>,<a href="#B274-ijms-25-11460" class="html-bibr">274</a>,<a href="#B275-ijms-25-11460" class="html-bibr">275</a>,<a href="#B276-ijms-25-11460" class="html-bibr">276</a>,<a href="#B277-ijms-25-11460" class="html-bibr">277</a>,<a href="#B278-ijms-25-11460" class="html-bibr">278</a>,<a href="#B279-ijms-25-11460" class="html-bibr">279</a>].</p>
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19 pages, 1281 KiB  
Article
Music-Based Therapy for the Treatment of Perioperative Anxiety and Pain—A Randomized, Prospective Clinical Trial
by Shiv K. Goel, Valdemir Kim, Jeremy Kearns, Daniel Sabo, Lynsie Zoeller, Coleen Conboy, Nicole Kelm, Ann E. Jackovich and Jacques E. Chelly
J. Clin. Med. 2024, 13(20), 6139; https://doi.org/10.3390/jcm13206139 - 15 Oct 2024
Viewed by 915
Abstract
Background: Music-based intervention has been advocated as a nonpharmacologic approach for the perioperative control of pain and anxiety in surgical patients. However, its impact on patients with preoperative anxiety has not been clearly established. Our study aimed to examine the impact of [...] Read more.
Background: Music-based intervention has been advocated as a nonpharmacologic approach for the perioperative control of pain and anxiety in surgical patients. However, its impact on patients with preoperative anxiety has not been clearly established. Our study aimed to examine the impact of music-based intervention administered before, during, and after surgery on postoperative opioid consumption and pain levels, as well as preoperative anxiety, depression, and pain catastrophizing. We hypothesized that, compared to a control group, music-based intervention would be effective in reducing opioid requirements and mood disorders. Methods: This study was a single-center, prospective, single-blinded, randomized controlled trial. Inclusion criteria isame-day or observation surgery. Exclusion criteria included American Society of Anesthesiologists physical status IV, use of spinal anesthesia, PROMIS Anxiety T-scores ≤ 57.4 and ≥74.1, preoperative chronic opioid use, transgender surgery, and history of drug or alcohol abuse. Music-based intervention was developed by a certified music therapist. Each patient was randomized to receive standard of care (SC) or SC plus music-based intervention before, during, and after surgery. The primary end point was postoperative oral morphine equivalents (OMEs) over 5 days following surgery using the area under the curve (AUC)Secondary end points were PROMIS Anxiety, PROMIS Depression scores Pain Catastrophizing Scale scores, postoperative nausea and vomiting, time of hospital discharge, and patient satisfaction (0 = totally unsatisfied to 10 = completely satisfied). Results: A total of 75 patients were randomized to a music-based intervention (n = 33) or control (n = 42) group. Patients in the music-based intervention group consumed 56.7% less opioids than those in the control group (AUC was 2.8 in the music-based intervention group vs. 6.4 in the control group, absolute standardized mean difference (aSMD) = 0.34 (−0.17, 0.85)). No difference in pain scores was recorded between groups. Music-based intervention also reduced anxiety on postoperative day (POD)2 (aSMD = 0.38 (−0.16, 0.91)), depression on POD2 (aSMD = 0.31 (−0.23, 0.84)) and POD4 (aSMD = 0.24 (−0.29, 0.77)), and pain catastrophizing on POD1 (aSMD = 0.24 (−0.3, 0.77)). Conclusions: Our data support the use of music-based intervention to reduce postoperative opioid requirements. Music-based intervention may also reduce anxiety, depression, and pain catastrophizing. Full article
(This article belongs to the Special Issue Non-pharmacological Approach to the Perioperative Management of Pain)
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<p>CONSORT flow diagram.</p>
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<p>aSMD love plot for OME and pain in the intervention music therapy group vs. the control group. aSMD—absolute standardized mean difference; OME—oral morphine equivalent; POD—postoperative day. The blue line represents a reference for aSMD = 0.2.</p>
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<p>aSMD love plot for PROMIS and PCS scores in the intervention music therapy group vs. the control group. aSMD—absolute standardized mean difference; POD—postoperative day; PCS—Pain Catastrophizing Scale. The blue line represents a reference for aSMD = 0.2.</p>
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18 pages, 633 KiB  
Article
Differences in the Rates of Diagnoses of Mental and Behavioral Disorders Due to Psychoactive Substance Use by Sex and Age during Pre-Pandemic and COVID-19 Pandemic Periods in Kazakhstan
by Kamila Akkuzinova, Ken Inoue, Elaman Toleuov, Timur Moldagaliyev, Nursultan Seksenbayev, Ulzhan Jamedinova, Nargul Ospanova and Altay Dyussupov
Healthcare 2024, 12(20), 2012; https://doi.org/10.3390/healthcare12202012 - 10 Oct 2024
Viewed by 660
Abstract
Background: The COVID-19 pandemic had profound impacts worldwide on individuals with mental and behavioral disorders, including disorders due to psychoactive substance use. We investigated how the COVID-19 pandemic affected the trends in these disorders in the Republic of Kazakhstan. Methods: We researched and [...] Read more.
Background: The COVID-19 pandemic had profound impacts worldwide on individuals with mental and behavioral disorders, including disorders due to psychoactive substance use. We investigated how the COVID-19 pandemic affected the trends in these disorders in the Republic of Kazakhstan. Methods: We researched and compared ICD-10 data on mental and behavioral disorders due to substance use in Kazakhstan that were diagnosed in 2018–2019 (pre-pandemic) versus 2020–2021 (the pandemic period). Results: The data for the pandemic period were significantly different from those of the pre-pandemic in that (i) ‘other stimulant-related disorders (F15)’ and ‘other psychoactive substance-related disorders (F19)’ were increased in the younger age groups, (ii) the risk of ‘opioid-related disorders (F11)’ was decreased in the 30-year-old group in both males and females, and (iii) the risk of ‘alcohol-related disorders (F10)’ was increased in the 30-year-old group and decreased in the 20- and 50-year-old groups. In only the males, (iv) the risk of ‘other psychoactive substance-related disorders (F19)’ was increased in almost all of the age groups, and (v) the risk of ‘cannabis-related disorders (F12)’ was increased in the ≥50-year-olds. The pre-pandemic and pandemic periods thus involved changes due to COVID-19 in both males and females that were especially notable in males. Conclusions: These results indicate that further measures designed to prevent mental and behavioral disorders due to psychoactive substances are necessary at the primary, secondary, and tertiary levels, and personnel in medicine/nursing, the government, private organizations, and the public need to collaborate to devise such measures. Full article
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<p>The number of new diagnoses of mental and behavioral disorders due to substance use in Kazakhstan during the pre-pandemic period (2018–2019) and the COVID-19 pandemic (2020–2021) in the overall population, males, and females.</p>
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21 pages, 3110 KiB  
Article
Comparative Analysis of Microbial Diversity and Metabolic Profiles during the Spontaneous Fermentation of Jerusalem Artichoke (Helianthus tuberosus L.) Juice
by Tiandi Zhu, Zhongwang Li, Xinxing Liu, Chen Chen and Yuwen Mu
Plants 2024, 13(19), 2782; https://doi.org/10.3390/plants13192782 - 4 Oct 2024
Viewed by 640
Abstract
Jerusalem artichoke juice is valued for its nutritional content and health benefits. Spontaneous fermentation enhances its flavor, quality, and functional components through microbial metabolic activities. This study used high-throughput sequencing to analyze microbial community changes, and LC–MS and GC–MS to detect secondary metabolites [...] Read more.
Jerusalem artichoke juice is valued for its nutritional content and health benefits. Spontaneous fermentation enhances its flavor, quality, and functional components through microbial metabolic activities. This study used high-throughput sequencing to analyze microbial community changes, and LC–MS and GC–MS to detect secondary metabolites and flavor compounds during fermentation. During natural fermentation, beneficial bacteria like Lactobacillus and Pediococcus increased, promoting lactic acid production and inhibiting harmful bacteria, while environmental bacteria decreased. Similarly, fungi shifted from environmental types like Geosmithia and Alternaria to fermentation-associated Pichia and Penicillium. A total of 1666 secondary metabolites were identified, with 595 upregulated and 497 downregulated. Key metabolic pathways included phenylpropanoid biosynthesis, with significant increases in phenylalanine, tryptophan, and related metabolites. Lipid and nucleotide metabolism also showed significant changes. Flavor compounds, including 134 identified alcohols, esters, acids, and ketones, mostly increased in content after fermentation. Notable increases were seen in Phenylethyl Alcohol, Ethyl Benzenepropanoate, 3-Methylbutyl Butanoate, Ethyl 4-Methylpentanoate, 5-Ethyl-3-Hydroxy-4-Methyl-2(5H)-Furanone, Ethyl Decanoate, Hexanoic Acid, and 1-Octanol. γ-aminobutyric acid (GABA) and other functional components enhanced the health value of the juice. This study provides insights into microbial and metabolic changes during fermentation, aiding in optimizing processes and improving the quality of fermented Jerusalem artichoke juice for functional food development. Full article
(This article belongs to the Special Issue Application of Plant Extracts in the Food Industry)
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<p>Composition and diversity of bacterial communities during spontaneous fermentation. α-diversity index analysis of bacteria (<b>A</b>). Heatmap of genus-level species composition for co-clustering (<b>B</b>). Species diversity and abundance of bacteria at the phylum and genus levels (<b>C</b>). Statistical significance is indicated by ** (<span class="html-italic">p</span> &lt; 0.01).</p>
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<p>Composition and diversity of bacterial communities during spontaneous fermentation. α-diversity index analysis of bacteria (<b>A</b>). Heatmap of genus-level species composition for co-clustering (<b>B</b>). Species diversity and abundance of bacteria at the phylum and genus levels (<b>C</b>). Statistical significance is indicated by ** (<span class="html-italic">p</span> &lt; 0.01).</p>
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<p>Composition and diversity of fungal communities during spontaneous fermentation. α-diversity index analysis of fungi (<b>A</b>). Heatmap of genus-level species composition for co-clustering (<b>B</b>). Species diversity and abundance of fungi at the phylum and genus levels (<b>C</b>). Statistical significance is indicated by ** (<span class="html-italic">p</span> &lt; 0.01).</p>
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<p>Composition and diversity of fungal communities during spontaneous fermentation. α-diversity index analysis of fungi (<b>A</b>). Heatmap of genus-level species composition for co-clustering (<b>B</b>). Species diversity and abundance of fungi at the phylum and genus levels (<b>C</b>). Statistical significance is indicated by ** (<span class="html-italic">p</span> &lt; 0.01).</p>
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<p>Dynamic changes in secondary metabolites during fermentation. Volcano plot (<b>A</b>). The OPLS–DA S−plot (<b>B</b>). Heatmap of the differential secondary metabolites (<b>C</b>). Enrichment of the differential secondary metabolites (<b>D</b>).</p>
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<p>Dynamic changes in secondary metabolites during fermentation. Volcano plot (<b>A</b>). The OPLS–DA S−plot (<b>B</b>). Heatmap of the differential secondary metabolites (<b>C</b>). Enrichment of the differential secondary metabolites (<b>D</b>).</p>
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<p>Dynamic changes in secondary metabolites during fermentation. Volcano plot (<b>A</b>). The OPLS–DA S−plot (<b>B</b>). Heatmap of the differential secondary metabolites (<b>C</b>). Enrichment of the differential secondary metabolites (<b>D</b>).</p>
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26 pages, 2379 KiB  
Review
When to Intervene in Acute Necrotizing Pancreatitis: A Narrative Review of the Optimal Timing for Intervention Strategies
by Daniel Paramythiotis, Eleni Karlafti, Dimitrios Tsavdaris, Alexandros Giakoustidis, Stavros Panidis, Aristeidis Ioannidis, Panos Prassopoulos and Antonios Michalopoulos
Medicina 2024, 60(10), 1592; https://doi.org/10.3390/medicina60101592 - 27 Sep 2024
Viewed by 853
Abstract
Introduction: Acute necrotizing pancreatitis (ANP) is the acute inflammation of pancreatic parenchyma, most commonly due to alcohol abuse or cholelithiasis. The treatment can be either conservative or invasive, including a variety of techniques; however, it has not yet been established if the [...] Read more.
Introduction: Acute necrotizing pancreatitis (ANP) is the acute inflammation of pancreatic parenchyma, most commonly due to alcohol abuse or cholelithiasis. The treatment can be either conservative or invasive, including a variety of techniques; however, it has not yet been established if the intervention should be early or if it should be delayed. The aim of this review is to investigate the optimal time for intervention in ANP. Methods: A literature search was conducted in PubMed and Scopus from inception until September 2024 for studies reporting the comparison between early and late intervention. Results: Early intervention, within 4 weeks of symptom onset, often involves drainage via percutaneous, endoscopic, or combined methods. Delayed intervention occurs after 4 weeks of symptom onset. This can be conducted either surgically or via minimally invasive means. The results of this review reveal that the time of intervention for ANP plays an important role in the prognosis and the course of the disease. In particular, early intervention is associated with higher mortality, which is also the primary clinical outcome. Delayed intervention is also superior regarding secondary clinical outcomes, specifically the complications associated with the intervention. Thus, it is accompanied by fewer episodes of new-onset organ failure, bleeding, gastrointestinal fistula, pancreatic fistula, wound infection, endocrine pancreatic insufficiency, and other complications. Finally, delayed intervention results in shorter stays, both in hospitals and the ICU. Conclusions: Delayed intervention is clearly more effective than early intervention and should be preferred. However, early intervention appears to be both safe and effective, and it is feasible. Full article
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<p>A comprehensive overview of acute pancreatitis. The figure was created using <a href="http://Canva.com" target="_blank">Canva.com</a>.</p>
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<p>This figure demonstrates the superior benefits of minimally invasive approaches over traditional surgery in the management of acute pancreatitis. The figure was created using <a href="http://Canva.com" target="_blank">Canva.com</a>.</p>
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<p>Advantages of endoscopic drainage. The figure was created using <a href="http://Canva.com" target="_blank">Canva.com</a>.</p>
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<p>Comprehensive overview of acute pancreatitis risk factors. The figure was created using <a href="http://Canva.com" target="_blank">Canva.com</a>.</p>
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<p>Comparative of early vs. delayed intervention in acute pancreatitis. The figure was created using <a href="http://Canva.com" target="_blank">Canva.com</a>.</p>
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17 pages, 1781 KiB  
Article
Microbiological Bioreduction of Bulky–Bulky Pyrimidine Derivatives as an Alternative to Asymmetric Chemical Synthesis
by Renata Kołodziejska, Hanna Pawluk, Agnieszka Tafelska-Kaczmarek, Szymon Baumgart, Renata Studzińska, Agnieszka Kosinska and Marcin Kwit
Catalysts 2024, 14(10), 667; https://doi.org/10.3390/catal14100667 - 27 Sep 2024
Viewed by 494
Abstract
Heterocyclic scaffolds are often present in many natural and non-natural products with important biological activity, such as synthetic intermediates used to synthesise many drugs. Among others, heterocycles based on a pyrimidine ring may have antioxidant, antibacterial, antiviral, antifungal, antituberculosis, and anti-inflammatory properties. The [...] Read more.
Heterocyclic scaffolds are often present in many natural and non-natural products with important biological activity, such as synthetic intermediates used to synthesise many drugs. Among others, heterocycles based on a pyrimidine ring may have antioxidant, antibacterial, antiviral, antifungal, antituberculosis, and anti-inflammatory properties. The present study investigated commercially available microbial biocatalysts in the enzymatic desymmetrization reaction of bulky–bulky ketones derived from pyrimidine bases. The influence of some parameters on the efficiency of biocatalysis, i.e., the substrate concentration and pH of the reaction medium, was evaluated. In the one-step bioreduction catalysed by Saccharomyces cerevisiae, secondary alcohols with a defined absolute configuration were obtained with high enantiomeric excess up to 99% ee and moderate conversion. Biocatalysis offers economic and environmental benefits as an alternative to conventional methods, becoming a powerful tool in the synthesis of crowded alcohols. Full article
(This article belongs to the Section Biocatalysis)
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<p>Structures of the lowest energy conformers of the alcohols <b>1a′</b>, <b>1b′</b>, <b>2a′</b>, and <b>2b′</b>, optimized at the B3LYP/6-311++G(d,p) level. The broken lines indicate possible attractive interactions. The percentage populations of a given species in conformational equilibrium are given in parentheses.</p>
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<p>Examples of ECD spectra of alcohols <b>1a′</b> (<b>left</b>) and <b>2a′</b> (<b>right</b>) measured in cyclohexane (black lines) and calculated at the TD-M06-2X/6-311++G(2d,2p) level and Boltzmann-averaged based on ΔΔG values (blue lines). The inserts show the comparison between the ECD spectra calculated for the lowest energy conformer of a given compound (dashed blue lines) and the ΔΔG-based and Boltzmann-averaged (solid blue lines).</p>
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<p>Therapeutic potential of heterocyclic pyrimidine scaffolds.</p>
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<p>Synthesis of <b>1a</b>, <b>1b</b>, <b>2a</b>, and <b>2b</b>.</p>
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<p>EED of prochiral pyrimidine derivatives.</p>
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19 pages, 3489 KiB  
Article
Rhododendron luteum Sweet Flower Supercritical CO2 Extracts: Terpenes Composition, Pro-Inflammatory Enzymes Inhibition and Antioxidant Activity
by Lena Łyko, Marta Olech, Urszula Gawlik, Agnieszka Krajewska, Danuta Kalemba, Katarzyna Tyśkiewicz, Narcyz Piórecki, Andriy Prokopiv and Renata Nowak
Int. J. Mol. Sci. 2024, 25(18), 9952; https://doi.org/10.3390/ijms25189952 - 15 Sep 2024
Viewed by 994
Abstract
Terpenes are plant secondary metabolites known for their anti-inflammatory and antioxidant activities. According to ethnobotanical knowledge, Rhododendron luteum Sweet was used in traditional medicine against inflammation. The present study was conducted to determine the triterpene profile and antioxidant and anti-inflammatory activity of supercritical [...] Read more.
Terpenes are plant secondary metabolites known for their anti-inflammatory and antioxidant activities. According to ethnobotanical knowledge, Rhododendron luteum Sweet was used in traditional medicine against inflammation. The present study was conducted to determine the triterpene profile and antioxidant and anti-inflammatory activity of supercritical CO2 (SC-CO2) extracts of Rhododendron luteum Sweet flower (RLF). An LC-APCI-MS/MS analysis showed the presence of eight pentacyclic triterpenes and one phytosterol in the extracts obtained with pure CO2 as well as CO2 with the addition of aqueous ethanol as a co-solvent. Among the compounds detected, oleanolic/ursolic acid, β-sitosterol and 3β-taraxerol were the most abundant. The extract obtained with pure SC-CO2 was additionally subjected to HS-SPME-GC-FID-MS, which revealed more than 100 volatiles, mainly eugenol, β-phenylethanol, dodecane, β-caryophyllene, estragole and (Z)- and (E)-cinnamyl alcohol, followed by δ-cadinene. The extracts demonstrated significant hyaluronidase inhibition and exhibited varying modes of lipoxygenase and xanthine oxidase inhibitory activities. The studies of RLF have shown that their SC-CO2 extracts can be a rich source of triterpenes with anti-inflammatory potential. Full article
(This article belongs to the Special Issue Bioactive Compounds and Their Antioxidant Role)
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<p>The scheme of the SC-CO<sub>2</sub> extraction of <span class="html-italic">Rhododendron luteum</span> Sweet flowers. In the brackets, the extraction efficiency of specific steps are given. Abbreviations: SFE—Supercritical fluid extraction; RLF-CO<sub>2</sub>—extract obtained with pure CO<sub>2</sub>, RLF-CO<sub>2</sub> + 30%EtOH—extract obtained with the addition of 30% aqueous ethanol.</p>
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<p>LC-APCI-MS/MS chromatograms obtained in the multiple reaction monitoring (MRM) mode of triterpenes and sterols detected in <span class="html-italic">Rhododendron luteum</span> Sweet flowers: (<b>a</b>) euscaphic acid; (<b>b<sub>I</sub></b>) maslinic acid; (<b>b<sub>II</sub></b>) corosolic acid; (<b>c</b>) ursolic acid; (<b>d</b>) oleanolic acid; (<b>e</b>) erythrodiol; (<b>f</b>) uvaol; (<b>g</b>) lupeol; (<b>h</b>) 3<span class="html-italic">β</span>-taraxerol; (<b>i</b>) <span class="html-italic">α</span>-amyrin; (<b>j</b>) <span class="html-italic">β</span>-sitosterol.</p>
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<p>Chromatographic profile of volatile constituents in <span class="html-italic">Rhododendron luteum</span> Sweet SFE extract.</p>
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<p>Mode of lipoxygenase (LOX) inhibition by <span class="html-italic">Rhododendron luteum</span> flower samples: RLF-CO<sub>2</sub> (<b>A</b>), RLF-CO<sub>2</sub> + 30%EtOH (<b>B</b>) and OA (<b>C</b>). Abbreviations are presented as in <a href="#ijms-25-09952-t001" class="html-table">Table 1</a>.</p>
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<p>Mode of xanthine oxidase (XO) inhibition by <span class="html-italic">Rhododendron luteum</span> flower samples: RLF-CO<sub>2</sub> (<b>A</b>), RLF-CO<sub>2</sub> + 30%EtOH (<b>B</b>) and OA (<b>C</b>). Abbreviations are presented as in <a href="#ijms-25-09952-t001" class="html-table">Table 1</a>.</p>
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14 pages, 3843 KiB  
Article
Comparative Metabolomic Responses of Three Rhododendron Cultivars to the Azalea Lace Bug (Stephanitis pyrioides)
by Bei He, Yuan Zhou, Yu Peng, Dongyun Xu, Jun Tong, Yanfang Dong, Linchuan Fang and Jing Mao
Plants 2024, 13(18), 2569; https://doi.org/10.3390/plants13182569 - 13 Sep 2024
Viewed by 559
Abstract
Rhododendron, with its high ornamental value and ecological benefits, is severely impacted by the azalea lace bug (Stephanitis pyrioides), one of its primary pests. This study utilized three Rhododendron cultivars, ‘Zihe’, ‘Yanzhimi’, and ‘Taile’, to conduct a non-targeted metabolomic analysis of [...] Read more.
Rhododendron, with its high ornamental value and ecological benefits, is severely impacted by the azalea lace bug (Stephanitis pyrioides), one of its primary pests. This study utilized three Rhododendron cultivars, ‘Zihe’, ‘Yanzhimi’, and ‘Taile’, to conduct a non-targeted metabolomic analysis of leaf samples before and after azalea lace bug stress using headspace solid-phase microextraction combined with gas chromatography–mass spectrometry (HS-SPME/GCMS) and liquid chromatography–mass spectrometry (LCMS). A total of 81 volatile metabolites across 11 categories and 448 nonvolatile metabolites across 55 categories were detected. Significant differences in metabolic profiles were observed among the different cultivars after pest stress. A total of 47 volatile compounds and 49 nonvolatile metabolites were upregulated in the most susceptible cultivar ‘Zihe’, including terpenes, alcohols, nucleotides, amino acids, and carbohydrates, which are involved in energy production and secondary metabolism. Conversely, ‘Yanzhimi’ showed a downtrend in both the differential volatiles and metabolites related to purine metabolism and zeatin biosynthesis under pest stress. The resistant cultivar ‘Taile’ exhibited moderate changes, with 17 volatile compounds and 17 nonvolatile compounds being upregulated and enriched in the biosynthesis of amino acids, pentose, glucuronate interconversions, carbon metabolism, etc. The phenylalanine metabolic pathway played an important role in the pest resistance of different susceptible cultivars, and relevant metabolites such as phenylethyl alcohol, methyl salicylate, and apigenin may be involved in the plant’s resistance response. The results of this study provide a new perspective on the metabolomics of Rhododendron–insect interactions and offer references for the development of pest control strategies. Full article
(This article belongs to the Collection Feature Papers in Plant Protection)
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<p>The susceptibility of different Rhododendron cultivars to ALB (azalea lace bug, <span class="html-italic">Stephanitis pyrioides</span>). (<b>A</b>) The average number of ALBs on the leaves of different Rhododendron cultivars in the field; (<b>B</b>) the feeding selection of the ALBs between ‘Zihe’ and ‘Taile’; (<b>C</b>) the feeding selection of the ALBs between ‘Yanzhimi’ and ‘Taile’; (<b>D</b>) the feeding selection of the ALBs between ‘Zihe’ and ‘Yanzhimi’. Note: different letters indicate statistically significant differences according to Tukey’s test, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The susceptibility of different Rhododendron cultivars to ALB (azalea lace bug, <span class="html-italic">Stephanitis pyrioides</span>). (<b>A</b>) The average number of ALBs on the leaves of different Rhododendron cultivars in the field; (<b>B</b>) the feeding selection of the ALBs between ‘Zihe’ and ‘Taile’; (<b>C</b>) the feeding selection of the ALBs between ‘Yanzhimi’ and ‘Taile’; (<b>D</b>) the feeding selection of the ALBs between ‘Zihe’ and ‘Yanzhimi’. Note: different letters indicate statistically significant differences according to Tukey’s test, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Numbers of all volatile (<b>A</b>) and nonvolatile (<b>B</b>) metabolites identified in Rhododendron leaf samples.</p>
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<p>Volatile DAMs (differentially accumulated metabolites) in three Rhododendron cultivars. (<b>A</b>) The number of upregulated and downregulated DAMs in 3 cultivars infected by the ALBs (azalea lace bugs); (<b>B</b>) the types of DAMs upregulated in‘Zihe’(ZH) and ‘Taile’ (TL); (<b>C</b>) Venn diagram of volatile DAMs in 3 cultivars after pest infestation; (<b>D</b>) regulation pattern of the overlapped DAMs between ZH and TL. Note: YZM-SH—‘Yanzhimi’ after ALB stress; YZM-CK—‘Yanzhimi’ with no ALB infestation; ZH-SH—‘Zihe’ after ALB stress; ZH-CK—‘Zihe’ with no ALB infestation; TL-SH—‘Taile’ after ALB stress; TL-CK—‘Taile’ with no ALB infestation (below are the same).</p>
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<p>Volatile DAMs (differentially accumulated metabolites) in three Rhododendron cultivars. (<b>A</b>) The number of upregulated and downregulated DAMs in 3 cultivars infected by the ALBs (azalea lace bugs); (<b>B</b>) the types of DAMs upregulated in‘Zihe’(ZH) and ‘Taile’ (TL); (<b>C</b>) Venn diagram of volatile DAMs in 3 cultivars after pest infestation; (<b>D</b>) regulation pattern of the overlapped DAMs between ZH and TL. Note: YZM-SH—‘Yanzhimi’ after ALB stress; YZM-CK—‘Yanzhimi’ with no ALB infestation; ZH-SH—‘Zihe’ after ALB stress; ZH-CK—‘Zihe’ with no ALB infestation; TL-SH—‘Taile’ after ALB stress; TL-CK—‘Taile’ with no ALB infestation (below are the same).</p>
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<p>Nonvolatile DAMs (differentially accumulated metabolites) in three Rhododendron cultivars. (<b>A</b>) The number of upregulated and downregulated DAMs in three Rhododendron cultivars infected by ALBs; (<b>B</b>) Venn diagram of DAMs in three cultivars after pest infestation; (<b>C</b>) cluster heatmap of nonvolatile DAMs in ZH(‘Zihe’); (<b>D</b>) cluster heatmap of nonvolatile DAMs in TL (‘Taile’); (<b>E</b>) cluster heatmap of nonvolatile DAMs in YZM (‘Yanzhimi’).</p>
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<p>Differential metabolites involved in the phenylalanine metabolism pathway. Note: AADC—aromatic amino acid decarboxylase; MAO—monoamine oxidase; PAR—2-phenylacet aldehyde reductase; PAL—phenylalanine ammonialyase; C4H—cinnamate 4-hydroxylase; 4CL—4-coumarate:CoA ligase; BALD—benzaldehyde dehydrogenase; B2L/BA2H—benzoic acid 2-hydroxylase; SABP2—salicylic acid binding protein 2; SAMT—salicylic acid carboxyl methyltransferase; CHS—chalcone synthase; CHI—chalcone isomerase; FNS—flavone synthase. Asterisks indicate significantly (*, <span class="html-italic">p</span> &lt; 0.05) and extremely significantly (**, <span class="html-italic">p</span> &lt; 0.01) upregulated differential metabolites.</p>
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10 pages, 727 KiB  
Article
Continuous Primary Beer Fermentation with Yeast Immobilized in Alginate–Chitosan Microcapsules with a Liquid Core
by Vesela Shopska, Mina Dzhivoderova-Zarcheva and Georgi Kostov
Beverages 2024, 10(3), 87; https://doi.org/10.3390/beverages10030087 - 11 Sep 2024
Viewed by 784
Abstract
The application of continuous fermentation with immobilized cells in brewing is a challenge because of problems with carrier selection and reactor design, which have economic impacts on the beer produced. Moreover, immobilization alters yeast physiology, which significantly affects beer flavor and aroma. Therefore, [...] Read more.
The application of continuous fermentation with immobilized cells in brewing is a challenge because of problems with carrier selection and reactor design, which have economic impacts on the beer produced. Moreover, immobilization alters yeast physiology, which significantly affects beer flavor and aroma. Therefore, the aim of this study was to investigate the feasibility of a continuous fermentation system, consisting of a packed bed column bioreactor, containing lager brewing yeast, immobilized in alginate–chitosan microcapsules with a liquid core, in the primary beer fermentation. The results showed that the system entered in a stationary mode on the 3rd day and worked stably in this mode for 6 days. The “green” beer was taken at every 24 h at the output of the reactor and used for secondary fermentation with the yeast cells leaked from the capsules during the primary fermentation. The extract consumption, ethanol production, and pH change during primary and secondary fermentation were investigated. Some of the secondary yeast metabolites such as vicinal diketones, higher alcohols, esters, and aldehydes in “green” and final beers were determined and it was found that the flavor profile of the final beer was comparable to two industrially produced Bulgarian beers. Full article
(This article belongs to the Section Malting, Brewing and Beer)
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<p>Immobilized cell system for continuous main fermentation: 1—wort tank; 2—peristaltic pump; 3—pipes; 4—water bath; 5—packed bed; 6—column; 7—overflow; 8—pressure control connection; 9—“green” beer tank; 10—grid [<a href="#B9-beverages-10-00087" class="html-bibr">9</a>].</p>
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<p>Changes in extract, alcohol, and pH during continuous primary fermentation.</p>
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<p>Basic beer parameters in the final beers, produced by continuous primary fermentation with immobilized cells and batch secondary fermentation with free cells.</p>
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9 pages, 1641 KiB  
Systematic Review
Dexmedetomidine as Adjunctive Therapy for the Treatment of Alcohol Withdrawal Syndrome: A Systematic Review and Meta-Analysis
by Marco Fiore, Aniello Alfieri, Giacomo Torretta, Maria Beatrice Passavanti, Pasquale Sansone, Vincenzo Pota, Vittorio Simeon, Paolo Chiodini, Antonio Corrente and Maria Caterina Pace
Pharmaceuticals 2024, 17(9), 1125; https://doi.org/10.3390/ph17091125 - 26 Aug 2024
Viewed by 975
Abstract
Alcohol withdrawal syndrome (AWS) is defined as the cessation or reduction in heavy and prolonged alcohol use within several hours to a few days of cessation. The recommended first-line therapy for AWS ranging from mild to severe or complicated remains benzodiazepines; in cases [...] Read more.
Alcohol withdrawal syndrome (AWS) is defined as the cessation or reduction in heavy and prolonged alcohol use within several hours to a few days of cessation. The recommended first-line therapy for AWS ranging from mild to severe or complicated remains benzodiazepines; in cases where benzodiazepines are not adequate in controlling persistent autonomic hyperactivity or anxiety, dexmedetomidine could be utilized. The possible advantage of dexmedetomidine compared to benzodiazepines is that it does not cause respiratory depression, thus reducing the risk of intubation and hospitalization in the ICUs, with the potential reduction in healthcare costs. The purpose of this systematic review and meta-analysis (PROSPERO CRD42018084370) is to evaluate the effectiveness and safety of dexmedetomidine as adjunctive therapy to the standard of care for the treatment of AWS. We retrieved literature from PubMed, EMBASE, and CENTRAL until 10 January 2024. Eligible studies were both randomized trials and nonrandomised studies with a control group, published in the English language and peer-reviewed journals. The primary outcome was tracheal intubation; secondary outcomes were (i) bradycardia and (ii) hypotension. A total of 3585 papers were retrieved: 2635 from EMBASE, 930 from Medline, and 20 from CENTRAL. After eliminating duplicates, 2960 papers were screened by title and abstract; 75 out of the 2960 papers were read in full text. The qualitative synthesis included nine of all manuscripts read in full text. The quantitative synthesis included eight studies for the primary outcome (tracheal intubation), seven for the secondary outcome bradycardia, and six for the secondary outcome hypotension. The meta-analysis showed that Dexmedetomidine, as adjunctive therapy, is not more effective than standard therapy in reducing the risk of tracheal intubation in AWS [RR: 0.57, 95% CI: 0.25–1.3, p = 0.15]. It also appears to be less safe than sedative therapy as it significantly increases the risk of bradycardia [RR: 2.68, 95% CI: 1.79–4.16, p = 0.0016]. Hypotension was not significantly different in patients who received dexmedetomidine [RR: 1.5, 95% CI: 0.69–3.49, p = 0.21]. Full article
(This article belongs to the Section Pharmacology)
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<p>PRISMA 2020 flow diagram for new systematic reviews, which included searches of databases and registers only.</p>
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<p>Forest Plot Intubation [<a href="#B9-pharmaceuticals-17-01125" class="html-bibr">9</a>,<a href="#B10-pharmaceuticals-17-01125" class="html-bibr">10</a>,<a href="#B11-pharmaceuticals-17-01125" class="html-bibr">11</a>,<a href="#B12-pharmaceuticals-17-01125" class="html-bibr">12</a>,<a href="#B13-pharmaceuticals-17-01125" class="html-bibr">13</a>,<a href="#B14-pharmaceuticals-17-01125" class="html-bibr">14</a>,<a href="#B16-pharmaceuticals-17-01125" class="html-bibr">16</a>,<a href="#B17-pharmaceuticals-17-01125" class="html-bibr">17</a>].</p>
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<p>Forest Plot Bradycardia [<a href="#B9-pharmaceuticals-17-01125" class="html-bibr">9</a>,<a href="#B10-pharmaceuticals-17-01125" class="html-bibr">10</a>,<a href="#B11-pharmaceuticals-17-01125" class="html-bibr">11</a>,<a href="#B12-pharmaceuticals-17-01125" class="html-bibr">12</a>,<a href="#B13-pharmaceuticals-17-01125" class="html-bibr">13</a>,<a href="#B14-pharmaceuticals-17-01125" class="html-bibr">14</a>].</p>
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<p>Forest Plot Hypotension [<a href="#B9-pharmaceuticals-17-01125" class="html-bibr">9</a>,<a href="#B10-pharmaceuticals-17-01125" class="html-bibr">10</a>,<a href="#B11-pharmaceuticals-17-01125" class="html-bibr">11</a>,<a href="#B12-pharmaceuticals-17-01125" class="html-bibr">12</a>,<a href="#B13-pharmaceuticals-17-01125" class="html-bibr">13</a>,<a href="#B15-pharmaceuticals-17-01125" class="html-bibr">15</a>].</p>
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14 pages, 3399 KiB  
Article
Metal-Nitrate-Catalyzed Levulinic Acid Esterification with Alkyl Alcohols: A Simple Route to Produce Bioadditives
by Márcio José da Silva and Mariana Teixeira Cordeiro
Processes 2024, 12(9), 1802; https://doi.org/10.3390/pr12091802 - 24 Aug 2024
Viewed by 1068
Abstract
This work developed an efficient route to produce fuel bioadditive alkyl levulinates. Special attention was paid to butyl levulinate, which is a bioadditive with an adequate carbon chain size to be blended with liquid fuels such as diesel or gasoline. In this process, [...] Read more.
This work developed an efficient route to produce fuel bioadditive alkyl levulinates. Special attention was paid to butyl levulinate, which is a bioadditive with an adequate carbon chain size to be blended with liquid fuels such as diesel or gasoline. In this process, levulinic acid was esterified with butyl alcohol using cheap and commercially affordable metal nitrates as catalysts, producing bioadditives at more competitive costs. Iron (III) nitrate was the most active and selective catalyst toward butyl levulinate among the salts evaluated. In solvent-free conditions, with a low molar ratio and catalyst load (1:6 acid to alcohol, 3 mol% of Fe (NO3)3), conversion and selectivity greater than 90% after an 8 h reaction was achieved. A comparison of the iron (III) nitrate with other metal salts demonstrated that its superior performance can be assigned to the highest Lewis acidity of Fe3+ cations. Measurements of pH allow the conclusion that a cation with high Lewis acidity led to a greater H+ release, which results in a higher conversion. Butyl levulinate and pseudobuty levulinate were always the primary and secondary products, respectively. The consecutive character of reactions between butyl alcohol and levulinic acid (formation of the pseudobutyl levulinate and its conversion to butyl levulinate) was verified by assessing the reactions at different temperatures and conversion rates. A variation in Fe(NO3)3 catalyst load impacted the conversion much more than reaction selectivity. The same effect was verified when the reactions were carried out at different temperatures. The reactivity of alcohols with different structures depended more on steric hindrance on the hydroxyl group than the size of the carbon chain. A positive aspect of this work is the use of a commercial iron nitrate salt as the catalyst, which has advantages over traditional mineral acids such as sulfuric and hydrochloric acids. This solid catalyst is not corrosive and avoids neutralization steps after reactions, minimizing the generation of residues and effluents. Full article
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Graphical abstract

Graphical abstract
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<p>Effect of catalyst nature on levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), metal nitrate catalyst (3.0 mol%); temperature (333 K), volume (10 mL).</p>
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<p>Effect of catalyst nature on conversion and selectivity of levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), metal nitrate catalyst (3.0 mol%); temperature (333 K), volume (10 mL).</p>
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<p>Effect of iron salt nature on kinetic curves of levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), iron cation catalyst (3.0 mol%); temperature (333 K), reaction time (8 h), volume (10 mL).</p>
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<p>Effect of iron catalyst on conversion and selectivity of levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), metal nitrate catalyst (3.0 mol%); temperature (333 K), volume (10 mL).</p>
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<p>Variation in reaction selectivity of levulinic acid esterification butyl alcohol at different conversions: (<b>a</b>) 30%, (<b>b</b>) 92%, and (<b>c</b>) 40% <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), catalyst (3.0 mol%), volume (10 mL).</p>
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<p>Effect of catalyst concentration on the kinetic curves of Fe(NO<sub>3</sub>)<sub>3</sub>-catalyzed levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), Fe(NO<sub>3</sub>)<sub>3</sub> catalyst (variable); temperature (333 K), volume (10 mL).</p>
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<p>Impact of catalyst concentration on conversion and selectivity of levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), Fe(NO<sub>3</sub>)<sub>3</sub> catalyst (variable); temperature (333 K), reaction time (8 h); volume (10 mL).</p>
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<p>Effect of temperature on kinetic curves of levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> Reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), Fe(NO<sub>3</sub>)<sub>3</sub> catalyst (3.0 mol%); temperature (variable), reaction time (8 h); volume (10 mL).</p>
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<p>Impact of temperature on conversion and selectivity of levulinic acid esterification with butyl alcohol <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), butyl alcohol (91.8 mmol), Fe(NO<sub>3</sub>)<sub>3</sub> catalyst (3.0 mol%); temperature (333 K), reaction time (8 h); volume (10 mL).</p>
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<p>Kinetic curves of Fe(NO<sub>3</sub>)<sub>3</sub>-catalyzed levulinic acid esterification reactions with alkyl alcohols <sup>a</sup>, <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), alkyl alcohol (91.8 mmol), Fe(NO<sub>3</sub>)<sub>3</sub> catalyst (3.0 mol%); temperature (333 K), reaction time (8 h); volume (10 mL).</p>
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<p>Conversion and selectivity of Fe(NO<sub>3</sub>)<sub>3</sub>-catalyzed levulinic acid esterification reactions with alkyl alcohols <sup>a</sup>; <sup>a</sup> reaction conditions: levulinic acid (15.3 mmol), alkyl alcohol (91.8 mmol), Fe(NO<sub>3</sub>)<sub>3</sub> catalyst (3.0 mol%); temperature (333 K), reaction time (8 h); volume (10 mL).</p>
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<p>Mechanism proposal of levulinic acid esterification with butyl alcohol catalyzed by H<sup>+</sup> cations generated in the hydrolysis of metal nitrates.</p>
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<p>Mechanism proposal for the esterification of levulinic acid with butyl alcohol catalyzed by M<sup>+</sup> cations generated in the dissociation of metal nitrates.</p>
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<p>Products of levulinic acid esterification with butyl alcohol.</p>
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<p>Proposed mechanism for the conversion of levulinic acid to pseudobutyl levulinate.</p>
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