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Search Results (3)

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Keywords = Malus hupehensis (Pamp.) Rehd.

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12 pages, 1043 KiB  
Article
Nine New Glycosylated Compounds from the Leaves of the Medicinal Plant Malus hupehensis
by Lin-Lin Yuan, Yi Wang, Guo-Kai Wang and Ji-Kai Liu
Molecules 2024, 29(22), 5269; https://doi.org/10.3390/molecules29225269 - 7 Nov 2024
Viewed by 477
Abstract
Nine new compounds (19), including four dihydrochalcone glycosides, two dibenzofuran glycosides, and two biphenyl glycosides, were isolated from the leaves of the medicinal plant Malus hupehensis collected in Shennongjia Forestry District (Hubei, China). Their structures were elucidated by comprehensive [...] Read more.
Nine new compounds (19), including four dihydrochalcone glycosides, two dibenzofuran glycosides, and two biphenyl glycosides, were isolated from the leaves of the medicinal plant Malus hupehensis collected in Shennongjia Forestry District (Hubei, China). Their structures were elucidated by comprehensive spectroscopic techniques, including HRESIMS and NMR spectra. All compounds were tested by preliminary biological evaluation for their α-glucosidase inhibitory and NO production activities. Compound 4 was found to show significant inhibitory activity against NO production in LPS-activated RAW 264.7 macrophage cells with an IC50 value of 29.60 μM, and compounds 3 and 4 were found to exhibit potent α-glucosidase inhibition with IC50 values of 44.17 and 60.15 μM, respectively. This work represents the first report of the diverse glycosides from the plant Malus hupehensis. It expands our understanding of the secondary metabolites of this medicinal plant and lays the foundation for the study of the bioactive principles of the ethnic hypoglycemic medicinal plant. Full article
(This article belongs to the Section Bioorganic Chemistry)
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Figure 1

Figure 1
<p>Key HMBC, <sup>1</sup>H-<sup>1</sup>H COSY, and ROESY correlations of <b>1</b>–<b>9</b>.</p>
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<p>Structures of compounds <b>1</b>–<b>9</b>.</p>
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<p>Molecular docking of <b>3</b> and <b>4</b> and α-glucosidase. The 3D structure of α-glucosidase is shown in blue slate color, ligands are shown in cyan, side chain amino acids are shown in violet, and distances (Angstrom) are shown in black; (<b>A</b>) interactions of <b>3</b>; (<b>B</b>) interactions of <b>4</b>.</p>
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15 pages, 737 KiB  
Article
Effect of Aged Cherry Orchard Soil on the Potted Seedling Growth of Malus hupehensis (Pamp.) Rehd
by Lei Qin, Xiaoxuan Li, Weitao Jiang, Yusong Liu, Chengmiao Yin and Zhiquan Mao
Horticulturae 2024, 10(3), 223; https://doi.org/10.3390/horticulturae10030223 - 26 Feb 2024
Viewed by 1141
Abstract
Due to the aging of trees, aged apple and cherry orchards need to be rebuilt urgently. However, due to the limitation of land resources, it is inevitable to rebuild the apple orchard by taking the aged cherry orchard as a replacement, which will [...] Read more.
Due to the aging of trees, aged apple and cherry orchards need to be rebuilt urgently. However, due to the limitation of land resources, it is inevitable to rebuild the apple orchard by taking the aged cherry orchard as a replacement, which will lead to replant disease and seriously affect the sustainable development of the horticulture industry. This study investigated the effect of aged cherry orchard soil on the growth of M. hupehensis seedlings grown in pots, and it was further verified that allelochemicals in soil were one of the reasons for this effect. Three treatments were implemented: aged apple orchard soil (ppl), aged cherry orchard soil (pyl), and aged cherry orchard soil after fumigation with methyl bromide (pyz). Compared with pyz, pyl treatment significantly decreased the biomass, root growth, and antioxidant enzyme activity of M. hupehensis seedlings, and increased the content of MDA. Compared with ppl, pyl contains a smaller number of fungi and bacteria, but the abundance of the four disease-causing Fusarium remained high. In addition, the levels of allelochemicals found in the soil of aged cherry orchards can inhibit the normal growth and development of M. hupehensis seedlings. Amygdalin most strongly inhibited these seedlings. In summary, directly planting M. hupehensis seedlings in the soil of the aged cherry orchards still inhibits their normal growth and development, although the seedlings grow better than in aged apple orchard soil. Therefore, it is not feasible to directly plant M. hupehensis seedlings in the soil of aged cherry orchards, and measures should be taken to eliminate allelochemicals such as amygdalin and harmful microorganisms. Full article
(This article belongs to the Section Protected Culture)
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<p>Effects of different treatments on the soil microbial communities. (<b>A</b>) Changes in the gene copy number of four apple pathogens under different soil treatments. (<b>B</b>) Analysis of the common and endemic communities of soil fungi after different treatments. (<b>C</b>) Effects of different treatments on the soil fungal community composition. (<b>D</b>) Principal coordinate analysis (PCoA) of the soil fungal community in different treatments. Lowercase letters indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). ppl, replant soil from a 32-year-aged apple orchard; pyl, replant soil from a 20-year-aged cherry orchard; pyz, replant soil from a 20-year-aged cherry orchard after methyl bromide fumigation.</p>
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17 pages, 3766 KiB  
Article
Evaluation of In Vitro Bio-Activities Effects of WST (Wushanshencha)
by Chong Li, Chaomin Liu, Jing Zhang, Honggang Li, Yan Zhou, Yidong Li, Xin Zhao and Weiwei Liu
Appl. Sci. 2019, 9(7), 1325; https://doi.org/10.3390/app9071325 - 29 Mar 2019
Cited by 7 | Viewed by 2443
Abstract
As a traditional Chinese drink, tea is favored for its rich flavor and its medicinal functionality. In this study, the in vitro bioactivities of Wushanshencha (WST; a local tea from Chongqing, China), which is processed mainly from the leaves of the wild Malus [...] Read more.
As a traditional Chinese drink, tea is favored for its rich flavor and its medicinal functionality. In this study, the in vitro bioactivities of Wushanshencha (WST; a local tea from Chongqing, China), which is processed mainly from the leaves of the wild Malus hupehensis (Pamp.) Rehd.). We assessed the scavenging capacity of tea extracts on 1, 1-diphenyl-2-picrylhydrazyl (DPPH); 2, 2′-azino-bis (3-ethylbenzthiazoline-6- sulphonic acid) diammonium salt (ABTS); and hydroxyl (OH) free radicals, and demonstrate the high antioxidant activity and dose-dependent relationship of these extracts. We also detail the anti-mutagenic effect of these tea extracts against the Salmonella typhimurium TA98 strain induced by the 2, 7-diaminofluorene (2, 7-AF) mutagen and the TA100 strain induced by the N-methyl-N′-nitro- N- nitrosoguanidine (MNNG) mutagen at concentrations of 1.25 and 2.50 mg/plate, respectively, with the high-dose groups showing better results. We investigated the anticancer mechanisms of WST extracts (40, 100, and 160 μg/mL) in HepG2 human hepatoma cells via 3-(4, 5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide (MTT) assay and quantitative real-time reverse transcription-polymerase chain reaction (RT-qPCR). The results showed that the proliferation of HepG2 cells was significantly inhibited in a dose-dependent manner by the tea extracts. Moreover, apoptosis in HepG2 cells was induced via upregulation of Caspase-3, Caspase-7, Caspase-8, Caspase-9, p21, p53, and Bax as well as downregulation of Bcl-2 apoptosis-associated factors, as assessed via mRNA expression levels after treating with WST extracts. The expression of inflammation-related factors, e.g., NF-κB, and Cox-2, was significantly downregulated by the WST extracts, demonstrating its inflammatory properties. Together, these observations indicated that WST extracts have anti-inflammatory and anti-cancer properties. In addition, high-performance liquid chromatography (HPLC) analysis showed that WST extracts contained chlorogenic acid, 4-hydroxycinnamic acid, isoquercitrin, taxifolin, quercitrin, rosmarinic acid, myricetin, baicalin, neosperidin dihydrochalcone, and quercetin. As such, WST appears to be an effectively functional drink, due to its rich functional components and anti-cancer activity. Full article
(This article belongs to the Section Applied Biosciences and Bioengineering)
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<p>Scavenging activity of Wushanshencha (WST) extracts towards 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH), hydroxyl radicals (OH), and 2, 2’-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) diammonium salt radicals (ABTS). (<b>A</b>): DPPH radical; (<b>B</b>): OH radical; (<b>C</b>): ABTS radical. Ascorbic acid was used as positive control in anti-oxidant experiments. <sup>a–d</sup> Mean values with different letters in the same bar graph are significantly different (<span class="html-italic">p</span> &lt; 0.05) according to Duncan’s multiple range test.</p>
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<p>Growth inhibition of human hepatoma HepG2 cells treated with WST extract as evaluated using MTT assays. <sup>a–j</sup> Mean values with different letters in the same bar graph are significantly different (<span class="html-italic">p</span> &lt; 0.05) according to Duncan’s multiple range test.</p>
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<p>Effects of WST extracts on the gene expression of Capase-3 (<b>A</b>), -7 (<b>B</b>), -8 (<b>C</b>), and -9 (<b>D</b>) in human hepatoma HepG2 cells. The fold increase of Capases-3 (<b>A</b>), -7 (<b>B</b>), -8 (<b>C</b>), and -9 (<b>D</b>) mRNA expression relative to the control. The calculation formula is as follows: gene expression/GAPDH × control numerical value (control fold ratio: 1). <sup>a–d</sup> Mean values with different letters in the same bar graph are significantly different (<span class="html-italic">p</span> &lt; 0.05) according to Duncan’s multiple range test.</p>
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<p>Effects of WST extracts on the gene expression of p21 (<b>A</b>) and p53 (<b>B</b>) in human hepatoma HepG2 cells. Fold ratio of p21 (<b>A</b>) and p53 (<b>B</b>) mRNA expression over the control. The calculation formula is as follows: gene expression/GAPDH × control numerical value (control fold ratio: 1). <sup>a–d</sup> Mean values with different letters in the same bar graph are significantly different (<span class="html-italic">p</span>&lt; 0.05) according to Duncan’s multiple range test.</p>
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<p>Effects of WST extracts on the gene expression of Bax (<b>A</b>) and Bcl-2 (<b>B</b>) in human hepatoma HepG2 cells. Fold ratio of Bax (<b>A</b>) and Bcl-2 (<b>B</b>) mRNA expression over the control. The calculation formula is as follows: gene expression/GAPDH × control numerical value (control fold ratio: 1). <sup>a–d</sup> Mean values with different letters in the same bar graph are significantly different (<span class="html-italic">p</span>&lt; 0.05) according to Duncan’s multiple range test.</p>
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<p>Effects of WST extracts on the gene expression of NF-κB (<b>A</b>) and Cox-2 (<b>B</b>) in human hepatoma HepG2 cells. Fold ratio of NF-κB (<b>A</b>) and Cox-2 (<b>B</b>) mRNA expression over the control. The calculation formula is as follows: gene expression/GAPDH × control numerical value (control fold ratio: 1). <sup>a–d</sup> Mean values with different letters in the same bar graph are significantly different (<span class="html-italic">p</span> &lt; 0.05) according to Duncan’s multiple range test.</p>
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<p>Analysis of the constituents of WST extracts via HPLC assay. (<b>A</b>): WST chromatogram; (<b>B</b>): standard chromatograms.</p>
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