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9 pages, 1139 KiB  
Article
The Test–Retest Reliability of a Belt-Fixated Dynamometer for Assessing Maximal Knee Strength, Inter-Limb Asymmetries, and Hamstring–Quadriceps Ratios
by Nenad Nedović, Stevan Jovanović, Danilo Vujičić, Chris Bishop and Žiga Kozinc
Symmetry 2024, 16(11), 1541; https://doi.org/10.3390/sym16111541 - 18 Nov 2024
Abstract
Evaluating maximal strength, inter-limb asymmetries, and the hamstring-to-quadriceps (HQ) ratio is essential for identifying strength deficits in athletes. This cross-sectional study assessed the test–retest (inter-visit) reliability of the EasyForce dynamometer for knee extension and flexion strength in 21 young healthy participants (11 women [...] Read more.
Evaluating maximal strength, inter-limb asymmetries, and the hamstring-to-quadriceps (HQ) ratio is essential for identifying strength deficits in athletes. This cross-sectional study assessed the test–retest (inter-visit) reliability of the EasyForce dynamometer for knee extension and flexion strength in 21 young healthy participants (11 women and 10 men; age = 19.4 ± 0.7 years). The dynamometer demonstrated excellent relative reliability, with ICC values of 0.99 for knee extension and 0.95–0.98 for knee flexion. Absolute reliability was also acceptable (typical error = 5.63–16.44 N; coefficient of variation = 3.94–6.80%). Reliability for inter-limb asymmetries (ICC = 0.90) and HQ ratios (ICC = 0.91–0.92) was good to excellent. Agreement for inter-limb asymmetry direction between visits was excellent for knee extension (κ = 0.90) and substantial for knee flexion (κ = 0.71). These findings suggest that EasyForce is reliable for assessing muscle strength, inter-limb asymmetries, and HQ ratios in physically active adults. Future research should explore the broader applicability of EasyForce in muscle strength assessment, particularly for professional athletes and during rehabilitation. Full article
(This article belongs to the Special Issue Application of Symmetry in Biomechanics)
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<p>Participant position and dynamometer fixation for knee extension (<b>A</b>) and knee flexion (<b>B</b>) strength measurements.</p>
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<p>Inter-limb asymmetry values, shown separately for each participant for each visit for knee extensors (<b>A</b>) and knee flexors (<b>B</b>).</p>
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20 pages, 4386 KiB  
Article
Effect of Dietary Concentrate-to-Forage Ratios During the Cold Season on Slaughter Performance, Meat Quality, Rumen Fermentation and Gut Microbiota of Tibetan Sheep
by Shijia Wang, Wenhui Tang, Ting Jiang, Ru Wang, Ruoxi Zhang, Jingyu Ou, Qiangjun Wang, Xiao Cheng, Chunhuan Ren, Jiahong Chen, Yafeng Huang and Zijun Zhang
Animals 2024, 14(22), 3305; https://doi.org/10.3390/ani14223305 (registering DOI) - 17 Nov 2024
Viewed by 214
Abstract
This study aimed to investigate the effects of different dietary concentrate-to-forage ratios on slaughter performance, meat quality, rumen fermentation, rumen microbiota and fecal microbiota in Tibetan sheep. A total of sixty male Tibetan sheep were equally allocated into three dietary groups based on [...] Read more.
This study aimed to investigate the effects of different dietary concentrate-to-forage ratios on slaughter performance, meat quality, rumen fermentation, rumen microbiota and fecal microbiota in Tibetan sheep. A total of sixty male Tibetan sheep were equally allocated into three dietary groups based on concentrate-to-forage ratios, i.e., 30:70 (C30), 50:50 (C50), and 70:30 (C70). Compared with the C30 group, sheep fed the C70 diet resulted in a higher (p < 0.05) slaughter live weight (SLW), hot carcass weight (HCW), dressing percentage (DP), eye muscle area, average daily gain (ADG), and ruminal total volatile fatty acids concentration and propionate molar proportion and lower (p < 0.05) shear force and cooking loss of meat, and ruminal acetate molar proportion and acetate:propionate ratio. Sheep in the C50 group exhibited a higher (p < 0.05) SLW, HCW, ADG, and ruminal propionate molar proportion and lower (p < 0.05) shear force and cooking loss of meat, and ruminal acetate molar proportion and acetate: propionate ratio compared with the C30 group. In rumen fluid, the relative abundance of Butyrivibrio was lower (p = 0.031) in the C30 group, and that of Ruminococcus was higher (p = 0.003) in the C70 group compared with the C50 group. In feces, genus Monoglobus and UCG_002 were the most abundant in the C30 group (p < 0.05), and the relative abundance of Prevotella was significantly higher in the C70 group than in other groups (p = 0.013). Correlation analysis revealed possible links between slaughter performance and meat quality and altered microbiota composition in the rumen and feces of Tibetan sheep. Overall, feeding a C70 diet resulted in superior carcass characteristics and meat quality in Tibetan sheep, thus laying a theoretical basis for the application of short-term remote feeding during the cold season. Full article
(This article belongs to the Section Animal Nutrition)
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<p>Effect of dietary concentrate-to-forage ratios on the Venn analysis of operational taxonomic units from the ruminal (<b>a</b>) and fecal (<b>b</b>) microbiota of Tibetan sheep (5 animals in each group). Abbreviations: C30 = 30:70 concentrate: forage; C50 = 50:50 concentrate: forage; C70 = 70:30 concentrate: forage.</p>
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<p>Effect of dietary concentrate-to-forage ratios on principal coordinate (PCoA) analysis of the microorganisms of the rumen (<b>a</b>) and feces (<b>b</b>) of Tibetan sheep (5 animals in each group). Abbreviations: C30 = 30:70 concentrate: forage; C50 = 50:50 concentrate: forage; C70 = 70:30 concentrate: forage.</p>
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<p>Effect of dietary concentrate-to-forage ratios on relative abundance of ruminal (<b>a</b>,<b>b</b>) and fecal (<b>c</b>,<b>d</b>) microbiome at the phylum level of Tibetan sheep (5 animals in each group). Abbreviations: C30 = 30:70 concentrate: forage; C50 = 50:50 concentrate: forage; C70 = 70:30 concentrate: forage; * 0.01 &lt; <span class="html-italic">p</span> &lt; 0.05, ** 0.001 &lt; <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Effect of dietary concentrate-to-forage ratios on relative abundance of ruminal (<b>a</b>,<b>b</b>) and fecal (<b>c</b>,<b>d</b>) microbiome at the genus levels of Tibetan sheep (5 animals in each group). Abbreviations: C30 = 30:70 concentrate: forage; C50 = 50:50 concentrate: forage; C70 = 70:30 concentrate: forage; * 0.01 &lt; <span class="html-italic">p</span> &lt; 0.05, ** 0.001 &lt; <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Effect of dietary concentrate-to-forage ratios on ruminal (<b>a</b>) and fecal (<b>b</b>) microbial composition using the linear discriminant analysis effect size analysis (LDA &gt; 3 and <span class="html-italic">p</span> &lt; 0.05) in Tibetan sheep (5 animals in each group). Abbreviations: C30 = 30:70 concentrate: forage; C50 = 50:50 concentrate: forage; C70 = 70:30 concentrate: forage.</p>
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<p>Pearson correlation coefficients between ruminal (<b>a</b>) and fecal (<b>b</b>) microbiota composition at the genus level and slaughter performance and meat quality (<span class="html-italic">n</span> = 15) of Tibetan sheep. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, ****** <span class="html-italic">p</span> &lt; 0.000001.</p>
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14 pages, 15084 KiB  
Article
Study of the Impact on Zygomatic Bone Using Numerical Simulation
by Gonzalo Ruiz-de-León, María Baus-Domínguez, Maribel González-Martín, Aida Gutiérrez-Corrales, Eusebio Torres-Carranza, Álvaro-José Martínez-González, Daniel Torres-Lagares, José-Manuel López-Millan and Jesús Ambrosiani-Fernández
Biomimetics 2024, 9(11), 696; https://doi.org/10.3390/biomimetics9110696 - 14 Nov 2024
Viewed by 328
Abstract
The zygomatic bone, a fundamental structure in facial anatomy, is exposed to fractures in impact situations, such as traffic accidents or contact sports. The installation of zygomatic implants can also alter the distribution of forces in this region, increasing the risk of fractures. [...] Read more.
The zygomatic bone, a fundamental structure in facial anatomy, is exposed to fractures in impact situations, such as traffic accidents or contact sports. The installation of zygomatic implants can also alter the distribution of forces in this region, increasing the risk of fractures. To evaluate this situation, the first step is to develop a complex anatomical model from the stomatognathic point of view so that simulations in this sense can be validated. This study uses numerical simulation using a finite-element method (FEM) to analyze the behavior of the zygomatic bone under impacts of different velocities, offering a more realistic approach than previous studies by including the mandible, cervical spine, and masticatory muscles. Methods: An FEM model was developed based on 3D scans of actual bones, and simulations were performed using Abaqus Explicit 2023 software (Dassault Systemes, Vélizy-Villacoublay, France). The impact was evaluated using a steel cylinder (200 mm length, 40 mm diameter, 2 kg weight) impacted at speeds of 5, 10, 15, and 20 km/h. Zygomatic, maxillary, and mandibular bone properties were based on dynamic stiffness parameters, and bone damage was analyzed using ductile fracture and fracture energy criteria. Results: The results show that at impact velocities of 15 and 20 km/h, the zygomatic bone suffered crush fractures, with impact forces up to 400 kg. At 10 km/h, a combination of crushing and bending was observed, while at 5 km/h, only local damage without complete fracture was detected. The maximum stresses were concentrated at the zygoma–jaw junction, with values above 100 MPa at some critical points. Conclusion: The FEM model developed offers a detailed representation of the mechanical behavior, integrating the main structures of the stomatognathic apparatus of the zygomatic bone under impact, providing valuable information to, for example, advance injury prevention and zygomatic implant design. Higher impact velocities result in severe fractures, underscoring the need for protective measures in clinical and sports settings. Full article
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<p>Cortical bone. True stress–strain curves.</p>
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<p>Cancellous bone. True stress–strain curves.</p>
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<p>Impactor position.</p>
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<p>FEM model: (<b>a</b>) FEM model with detailed dentition; (<b>b</b>) FEM model with simplified dentition. The red lines refer to the masticatory muscles represented and integrated in the model.</p>
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<p>FEM model of bite analysis with intact dentition. Detail—lateral view. The grey lines refer to the masticatory muscles represented and integrated in the model.</p>
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<p>FEM model of bite analysis with intact dentition. Temporomandibular joint: (<b>Left</b>), an anatomical model with solid bone. (<b>Right</b>), an anatomical model with a transparent bone to better observe the internal structures.</p>
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<p>Impactor–bone contact law.</p>
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<p>Dynamic FEM model: (<b>a</b>) frontal flexion. 3.26 Hz; (<b>b</b>) second frontal flexion. 14.96 Hz; (<b>c</b>) second lateral flexion. 3.39 Hz; (<b>d</b>) lateral flexion. 20.22 Hz; (<b>e</b>) torsion. 4.35 Hz; (<b>f</b>) axial flexion. 29.11 Hz.</p>
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<p>Total contact force: (<b>a</b>) unfiltered impact forces; (<b>b</b>) impact forces filtered with SAE180 standard in Abaqus CAE.</p>
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<p>Evolution of zygomatic bone damage for 20 km/h impact. The entire middle third of the face is highlighted in blue. The red field indicates the initiation of bone damage.</p>
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<p>Lines of rupture and initiation of zygomatic bone damage. The entire middle third of the face is highlighted in blue. The red field indicates the initiation of bone damage: (<b>a</b>) impact at 20 km/h; (<b>b</b>) impact at 15 km/h; (<b>c</b>) impact at 10 km/h; (<b>d</b>) impact at 5 km/h.</p>
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<p>Von Mises stresses [N/mm<sup>2</sup>] zygomatic bone. Impact 15 km/h.</p>
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<p>Von Mises stresses [N/mm<sup>2</sup>] zygomatic bone. Impact 15 km/h.</p>
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21 pages, 1551 KiB  
Article
Beef Carcasses Aged at Mild Temperature to Improve Sustainability of Meat Production
by André Ndereyimana, Michela Contò, Antonella Chiariotti, Gianluca Renzi and Sebastiana Failla
Sustainability 2024, 16(22), 9907; https://doi.org/10.3390/su16229907 - 13 Nov 2024
Viewed by 404
Abstract
Beef carcass aging, which enhances tenderness and flavor through proteolysis, is traditionally costly and slow, requiring long-term storage at temperatures near 0 °C. To reduce energy consumption, a new technique using moderate cooling room temperatures was tested. Six carcasses of Holstein bulls were [...] Read more.
Beef carcass aging, which enhances tenderness and flavor through proteolysis, is traditionally costly and slow, requiring long-term storage at temperatures near 0 °C. To reduce energy consumption, a new technique using moderate cooling room temperatures was tested. Six carcasses of Holstein bulls were used. From each carcass, two shoulders were processed in different ways: one was refrigerated at 8 °C (W), and after spraying with a solution with calcium chloride and sodium chloride, was coated with sodium alginate. The other shoulder was stored at 2 ± 1 °C as a cold control (C). After five days of aging, the shoulders were dissected, and two muscles (Caput longum triceps brachii and Supraspinatus) were subjected to physico-chemical analysis, microbiological safety assessment, and sensory testing. The remaining samples of both muscles were stored in domestic conditions for an additional 5 days at various temperatures (2, 4, 8 °C), where the same physic-chemical and sensory tests were conducted. The results showed that moderate aging temperature improved meat quality, significantly reducing the shear force (p = 0.001) and increasing sarcomere length, the myofibrillar fragmentation index, and sensory tenderness (p = 0.042, p = 0.039, and p = 0.027, respectively). However, domestic storage post-dissection should not exceed 4 °C to prevent rapid lipid oxidation, as observed at 8 °C for both muscles (p < 0.001). Mild aging temperature maintained legal safety standards, enhanced certain meat qualities, and promoted enzymatic activity similar to traditional dry aging while reducing high energy consumption. Full article
(This article belongs to the Section Sustainable Food)
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<p>Experimental diagram.</p>
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<p>Myofibrillar fragmentation index (MFI) on muscles in domestic storage. MFI = myofibrillar fragmentation index; C-CL = cold shoulder, muscle <span class="html-italic">Caput longum triceps brachii</span>, domestic storage at temperatures of 2°, 4°, 8 °C; C-SS = cold shoulder, muscle <span class="html-italic">Supraspinatus</span> domestic storage at temperatures of 2°, 4°, 8 °C; W-CL = warm shoulder, muscle <span class="html-italic">Caput longum triceps brachii</span>, domestic storage at temperatures of 2°, 4°, 8 °C; W-SS = warm shoulder, muscle <span class="html-italic">Supraspinatus</span> domestic storage at temperatures of 2°, 4°, 8 °C. Vertical bar shows the deviation standard. Different letters mean significant differences for <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>TBArs on muscles in domestic storage. TBArs = substance of lipid oxidation that reacts with thiobarbituric acid expressed in mg MDA/kg (MDA = malondialdehyde); C-CL = cold shoulder, muscle <span class="html-italic">Caput longum triceps brachii</span>, domestic storage at temperatures of 2°, 4°, 8 °C; C-SS = cold shoulder, muscle <span class="html-italic">Supraspinatus</span> domestic storage at temperatures of 2°, 4°, 8 °C; W-CL = warm shoulder, muscle <span class="html-italic">Caput longum triceps brachii</span>, domestic storage at temperatures of 2°, 4°, 8 °C; W-SS = warm shoulder, muscle <span class="html-italic">Supraspinatus</span> domestic storage at temperatures of 2°, 4°, 8 °C. Vertical bar shows the deviation standard. Different letters mean significant differences for <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Radar chart of sensory data on muscles in domestic storage. C-2 °C, C-4 °C, C-8 °C = cold shoulder; W-2 °C, W-4 °C, W-8 °C = warm shoulder; CL = <span class="html-italic">Caput longum triceps brachii</span>; SS = <span class="html-italic">Supraspinatus</span>.</p>
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18 pages, 1689 KiB  
Article
Effects of Flavonoids in Fructus Aurantii Immaturus on Carcass Traits, Meat Quality and Antioxidant Capacity in Finishing Pigs
by Zekun Yang, Qiuping Guo, Xiangfeng Kong, Yixing Li and Fengna Li
Antioxidants 2024, 13(11), 1385; https://doi.org/10.3390/antiox13111385 - 13 Nov 2024
Viewed by 508
Abstract
This experiment aimed to explore the effects of flavonoids in Fructus Aurantii Immaturus (FFAI) on carcass traits, meat quality, and the antioxidant capacity of finishing pigs. The results indicated that the addition of an appropriate amount of FFAI into their diet could significantly [...] Read more.
This experiment aimed to explore the effects of flavonoids in Fructus Aurantii Immaturus (FFAI) on carcass traits, meat quality, and the antioxidant capacity of finishing pigs. The results indicated that the addition of an appropriate amount of FFAI into their diet could significantly reduce the backfat thickness and perirenal fat percentage of finishing pigs, as well as the drip loss, water-holding capacity, shear force, and the levels of lactate, glucose-6-phosphate, glucose, ATP, phosphofructokinase, and pyruvate in the longissimus dorsi (LD) muscle. It also elevated the levels of flavor amino acids such as glutamate, serine, and threonine, and enriched the composition of flavor substances, including benzene and octanal, which significantly contributed to the enhancement of pork flavor. Furthermore, it enhanced the expression levels of MyHC I and MyHC IIa. In summary, the appropriate addition of FFAI to the diet could improve the carcass traits, meat quality, and antioxidant capacity of finishing pigs. The optimal level of FFAI supplementation is 0.12%. Full article
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<p>Analysis of flavor substances in LD muscle. (<b>A</b>) Electronic nose PCA diagram; (<b>B</b>) radar diagram of odor response values; (<b>C</b>) Cluster heat map of differential flavor substances in LD muscle. Values are the mean ± SEM (<span class="html-italic">n</span> = 8), Significance was expressed as ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Effects of dietary FFAI supplementation on the antioxidant capacity in serum and LD muscle (<b>A</b>), glycolytic potential (<b>B</b>), and muscle fiber types in LD muscle (<b>C</b>) of finishing pigs. CAT, catalase; T-AOC, total antioxidant capacity; GSH-Px, glutathione peroxidase; SOD, superoxide Dismutase; MDA, malondialdehyde, ATP, Adenosine Triphosphate; PFK, Phosphofructokinase; LDH, Lactate Dehydrogenase. Different groups with different lower case letters above the bar graphs indicate significant differences between groups (<span class="html-italic">p</span> &lt; 0.05). Values are the mean ± SEM (<span class="html-italic">n</span> = 8).</p>
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<p>Correlation analysis between antioxidant capacity, meat quality, glycolysis, and muscle fiber type in finishing pigs based on the Mantel-test at 45min; the redness values of the LD muscle at 45 min; the redness values of the LD muscle at 24 h; LDH, Lactate Dehydrogenase; PFK, Phosphofructokinase. Interaction of antioxidant capacity with meat quality, glycolysis, and muscle fiber type in finishing pigs. Significance was expressed as * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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23 pages, 6338 KiB  
Article
Inclusion of Muscle Forces Affects Finite Element Prediction of Compression Screw Pullout but Not Fatigue Failure in a Custom Pelvic Implant
by Yuhui Zhu, Ata Babazadeh-Naseri, Matthew R. W. Brake, John E. Akin, Geng Li, Valerae O. Lewis and Benjamin J. Fregly
Appl. Sci. 2024, 14(22), 10396; https://doi.org/10.3390/app142210396 - 12 Nov 2024
Viewed by 381
Abstract
Custom implants used for pelvic reconstruction in pelvic sarcoma surgery face a high complication rate due to mechanical failures of fixation screws. Consequently, patient-specific finite element (FE) models have been employed to analyze custom pelvic implant durability. However, muscle forces have often been [...] Read more.
Custom implants used for pelvic reconstruction in pelvic sarcoma surgery face a high complication rate due to mechanical failures of fixation screws. Consequently, patient-specific finite element (FE) models have been employed to analyze custom pelvic implant durability. However, muscle forces have often been omitted from FE studies of the post-operative pelvis with a custom implant, despite the lack of evidence that this omission has minimal impact on predicted bone, implant, and fixation screw stress distributions. This study investigated the influence of muscle forces on FE predictions of fixation screw pullout and fatigue failure in a custom pelvic implant. Specifically, FE analyses were conducted using a patient-specific FE model loaded with seven sets of personalized muscle and hip joint contact force loading conditions estimated using a personalized neuromusculoskeletal (NMS) model. Predictions of fixation screw pullout and fatigue failure—quantified by simulated screw axial forces and von Mises stresses, respectively—were compared between analyses with and without personalized muscle forces. The study found that muscle forces had a considerable influence on predicted screw pullout but not fatigue failure. However, it remains unclear whether including or excluding muscle forces would yield more conservative predictions of screw failures. Furthermore, while the effect of muscle forces on predicted screw failures was location-dependent for cortical screws, no clear location dependency was observed for cancellous screws. These findings support the combined use of patient-specific FE and NMS models, including loading from muscle forces, when predicting screw pullout but not fatigue failure in custom pelvic implants. Full article
(This article belongs to the Section Applied Biosciences and Bioengineering)
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<p>Post-operative assembly of the ipsilesional hemipelvis. (<b>a</b>) Geometric model of the post-operative pelvis assembly showing the layout of the nine screws securing the implant to the remaining bone. (<b>b</b>) Finite element (FE) model of the ipsilesional hemipelvis post-surgery. (<b>c</b>) Attachment areas of the muscle–tendon units retained after surgery and used in the model.</p>
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<p>Hip joint contact forces for the seven load cases used in the FE analyses. <b>Upper left</b>: Gait; <b>Upper right</b>: Squatting down and up; <b>Lower left</b>: Stairs up; <b>Lower right</b>: Stairs down. The second half of the stairs down plot is grayed out due to the absence of experimental data for that portion of the motion. The x-, y-, and z-components of each load case were represented in the pelvic coordinate system, where x, y, and z indicate anterior–posterior, superior–inferior, and medial–lateral directions, respectively. <span class="html-italic">F<span class="html-small-caps">res</span></span> indicates the magnitude of the resultant force.</p>
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<p>Flowchart summarizing the process used to construct the FE model and conduct the subsequent fixation screw durability analyses.</p>
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<p>Illustrations depicting the fixation screw models used in the present study. (<b>a</b>) Illustration showing the boundary conditions used to construct the screw model. (<b>b</b>) Illustration explaining key elements of the screw core. The free zone refers to the portion of the screw that begins at the beginning of the screw core and ends where the screw becomes partially embedded in the bone. The axial force within the free zone was consistently evaluated at the end of the free zone.</p>
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<p>Predicted axial force in the free zone of each screw normalized by the respective pullout failure threshold under different loading conditions.</p>
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<p>Predicted peak von Mises stress of each screw under different loading conditions.</p>
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<p>Von Mises stress distribution in Cancellous screw 3 under different loading conditions. Due to the compressive forces applied within the pretension region, the stress distributions within the screw head and screw shank were discarded and considered non-physical.</p>
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<p>Predicted axial force normalized by pullout failure threshold (<b>top</b>) and peak von Mises stress (<b>bottom</b>) of each screw weighted by annual load cycles from all activities.</p>
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<p>Muscle contributions to hip joint contact forces throughout a gait cycle. The red dashed lines correspond to GAIT 1 and GAIT 2.</p>
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<p>Muscle contributions to hip joint contact forces throughout a squat cycle. The red dashed lines correspond to SQDN and SQUP.</p>
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<p>Muscle contributions to hip joint contact forces throughout a stair-up cycle. The red dashed lines correspond to STUP 1 and STUP 2.</p>
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<p>Muscle contributions to hip joint contact forces throughout a stair-down cycle. The red dashed line corresponds to STDN.</p>
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14 pages, 1875 KiB  
Article
Effects of Heat Stress on the Muscle Meat Quality of Rainbow Trout
by Yalan Li, Changqing Zhou, Yong Zhang and Xingxu Zhao
Fishes 2024, 9(11), 459; https://doi.org/10.3390/fishes9110459 - 11 Nov 2024
Viewed by 524
Abstract
The effects of heat stress on aquatic animals are increasingly being discerned, but little is known about the effects of heat stress on muscle meat quality or the flavor of muscle. This study aimed to evaluate the effects of heat stress on the [...] Read more.
The effects of heat stress on aquatic animals are increasingly being discerned, but little is known about the effects of heat stress on muscle meat quality or the flavor of muscle. This study aimed to evaluate the effects of heat stress on the muscle antioxidant properties, structural and physical properties (e.g., pH, muscle color, shear force, and expressible moisture), chemical composition (e.g., nucleotides, organic acids, amino acids, and minerals), and volatile substances of rainbow trout. We observed that the antioxidant capacity of muscle decreased after stress experiments at 22.5 °C for 24 h. The content of inflammatory factors notably increased (p < 0.05), the pH value and red value of muscle decreased (p < 0.05), the interfiber space increased, and several muscle fibers were broken. Heat stress changed the contents of nucleotides, organic acids, minerals, and amino acids in muscle. The contents of IMP and AMP, which play an important role in the flavor of muscle, decreased (p < 0.05). The contents of two amino acids that provide a sweet taste decreased; those of five amino acids that provide a bitter taste increased (p < 0.05). Heat stress also affected the amount and type of volatile substances in muscle, which affected muscle odor. These results suggest that heat stress may exert adverse effects on the oxidative stability, structure, meat quality, and flavor of muscle, requiring attention and prevention. Full article
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<p>Effects of heat stress on muscle histology (<b>A</b>,<b>B</b>) muscle transection; (<b>C</b>,<b>D</b>) longitudinal sectioning of muscle; (<b>A</b>,<b>C</b>) control group; (<b>B</b>,<b>D</b>) heat stress group; ▲: rupture of muscle fibers).</p>
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<p>Effects of heat stress on volatile substance content in muscle of rainbow trout. (<b>A</b>) Relative volatile substance content in the control group (%); (<b>B</b>) relative volatile substance content in the heat stress group (%).</p>
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16 pages, 1603 KiB  
Article
Nerve Signal Transferring Mechanism and Mathematical Modeling of Artificial Biological System Design
by Jeongseop Park, Sehwan Yoo and Taikyeong Jeong
Fractal Fract. 2024, 8(11), 648; https://doi.org/10.3390/fractalfract8110648 - 7 Nov 2024
Viewed by 412
Abstract
Our investigation demonstrates the necessity of mathematical modeling and design methodologies for nerve signals in the creation of artificial arms. Nerve impulses vary widely in speed; for example, unmyelinated nerves transmit impulses at around one mile per hour, while myelinated nerves conduct impulses [...] Read more.
Our investigation demonstrates the necessity of mathematical modeling and design methodologies for nerve signals in the creation of artificial arms. Nerve impulses vary widely in speed; for example, unmyelinated nerves transmit impulses at around one mile per hour, while myelinated nerves conduct impulses at around 200 miles per hour. The electrical signals originating from the brain, such as those measured by electroencephalography, are translated into chemical reactions in each organ to produce energy. In this paper, we describe the mechanism by which nerve signals are transferred to various organs, not just the brain or spinal cord, as these signals account for the measured amounts of physical force—i.e., energy—as nerve signals. Since these frequency signals follow no fixed pattern, we consider wavelength and amplitude over a particular time frame. Our simulation results begin with the mechanical distinction that occurs throughout the entire process of nerve signal transmission in the artificial arm as an artificial biological system, and show numerical approaches and algebraic equations as a matrix in mathematical modeling. As a result, the mathematical modeling of nerve signals accurately reflects actual human nerve signals. These chemical changes, involving K (potassium), Na (sodium), and Cl (chloride), are linked to muscle states as they are converted into electrical signals. Investigating and identifying the neurotransmitter signal transmission system through theoretical approaches, mechanical analysis, and mathematical modeling reveals a strong relationship between mathematical simulation and algebraic matrix analysis. Full article
(This article belongs to the Section Numerical and Computational Methods)
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<p>Overall structure of human bone, anterior view of <span class="html-italic">x</span>-axis and <span class="html-italic">z</span>-axis.</p>
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<p>(<b>a</b>) The forces acting on the arm and (<b>b</b>) the free-body diagram of the arm. (A) Humerus, (B) radius, (C) ulna. a, b, and c are distances from point O.</p>
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<p>Design method for mathematical three-dimensional modeling. (A) Humerus, (B) radius, (C) ulna ●. In this figure, node (<b>a</b>) subdivides the bones into the bar of elements and nodes. (<b>b</b>) The two nodes use brick elements in three-dimensional modeling. (<b>c</b>) The global coordinates system and vector.</p>
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<p>Human nerve signal transmission simulation results which include amplitude 0 to 90 degrees and wavelength 0 to 90 degrees angle, respectively. (a) Pink-colored amplitude 0 to 90 degrees, (b) Blue-colored wavelength 0 to 90 degrees in the <span class="html-italic">x</span>-axis (time) and <span class="html-italic">y</span>-axis (frequency signal).</p>
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<p>Divergence and convergence in neurotransmitter (<b>a</b>) divergence stage, (<b>b</b>) convergence stage, (<b>c</b>) integrated divergence and convergence stage.</p>
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14 pages, 9484 KiB  
Article
A Gain-of-Function Mutation in the Ca2+ Channel ORAI1 Causes Stormorken Syndrome with Tubular Aggregates in Mice
by Laura Pérez-Guàrdia, Emma Lafabrie, Nadège Diedhiou, Coralie Spiegelhalter, Jocelyn Laporte and Johann Böhm
Cells 2024, 13(22), 1829; https://doi.org/10.3390/cells13221829 - 6 Nov 2024
Viewed by 539
Abstract
Store-operated Ca2+ entry (SOCE) controls Ca2+ homeostasis and mediates multiple Ca2+-dependent signaling pathways and cellular processes. It relies on the concerted activity of the reticular Ca2+ sensor STIM1 and the plasma membrane Ca2+ channel ORAI1. STIM1 and [...] Read more.
Store-operated Ca2+ entry (SOCE) controls Ca2+ homeostasis and mediates multiple Ca2+-dependent signaling pathways and cellular processes. It relies on the concerted activity of the reticular Ca2+ sensor STIM1 and the plasma membrane Ca2+ channel ORAI1. STIM1 and ORAI1 gain-of-function (GoF) mutations induce SOCE overactivity and excessive Ca2+ influx, leading to tubular aggregate myopathy (TAM) and Stormorken syndrome (STRMK), two overlapping disorders characterized by muscle weakness and a variable occurrence of multi-systemic anomalies affecting spleen, skin, and platelets. To date, different STIM1 mouse models exist, but only a single ORAI1 mouse model with muscle-specific TAM/STRMK phenotype has been described, precluding a comparative analysis of the physiopathology in all affected tissues. Here, we generated and characterized mice harboring a prevalent ORAI1 TAM/STRMK mutation and we provide phenotypic, physiological, biochemical, and functional data. Examination of Orai1V109M/+ mice revealed smaller size, spleen enlargement, reduced muscle force, and decreased platelet numbers. Morphological analyses of muscle sections evidenced the presence of tubular aggregates, the histopathological hallmark on biopsies from TAM/STRMK patients absent in all reported STIM1 models. Overall, Orai1V109M/+ mice reliably recapitulate the human disorder and highlight the primary physiological defects caused by ORAI1 gain-of-function mutations. They also provide the possibility to investigate the formation of tubular aggregates and to develop a common therapy for different TAM/STRMK forms. Full article
(This article belongs to the Section Cellular Pathology)
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<p>SOCE (store-operated Ca<sup>2+</sup> entry) and ORAI1 domains. (<b>A</b>) In normal conditions, reticular Ca<sup>2+</sup> store depletion induces STIM1 unfolding, oligomerization, and interaction with ORAI1 to trigger extracellular Ca<sup>2+</sup> entry (<b>left</b>). In TAM/STRMK, ORAI1 gain-of-function (GoF) mutations generate a leaky channel and induce excessive Ca<sup>2+</sup> influx independently of the reticular Ca<sup>2+</sup> load and STIM1 binding, resulting in elevated Ca<sup>2+</sup> levels in the cytosol and the reticulum (<b>right</b>) [<a href="#B9-cells-13-01829" class="html-bibr">9</a>]. (<b>B</b>) Schematic representation of the ORAI1 protein domains with position of the described GoF mutations (<b>above</b>). ORAI possesses 4 transmembrane domains (TM1–TM4). G97C, G98S, and V107M affect conserved amino acids in TM1, forming the channel pore (<b>below</b>). R = arginine-rich, P = proline-rich, CAD = CRAC channel activating domain; R/K = arginine/lysine-rich.</p>
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<p>Generation of <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice and postnatal follow-up. (<b>A</b>) The ORAI1 V109M mutation was introduced into murine C57BL/6N ES cells using a single-strand DNA (ssDNA) and CRISPR/Cas9 technology. (<b>B</b>) Sanger sequencing confirmed the heterozygous GTC&gt;ATG codon change (arrowheads) and the introduction of a <span class="html-italic">Tse</span>I restriction site (GCWGC) in <span class="html-italic">Orai1</span> exon 2. (<b>C</b>) <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice were born with Mendelian ratio. (<b>D</b>,<b>E</b>) Western blot on muscle samples and quantification of signal intensities revealed similar ORAI1 protein levels in WT and <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice. (<b>F</b>) Postnatal weight gain was comparable in WT and <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice from 4 to 16 weeks. (<b>G</b>) At 4 months, <span class="html-italic">Orai1<sup>V109M/+</sup></span> males were smaller than WT littermates. Significant differences are indicated as ** <span class="html-italic">p</span> &lt; 0.01. (<b>H</b>) Moderate or severe kyphosis was noted in the majority of <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice at 4 months and was absent in WT littermates. (<b>I</b>) Representative images showing kyphosis (arrowheads) in <span class="html-italic">Orai1<sup>V109M/+</sup></span> males.</p>
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<p>Spleen anomalies and abnormal blood parameters in <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice. (<b>A</b>) <span class="html-italic">Orai1<sup>V109M/+</sup></span> female mice exhibited a higher spleen/body mass ratio compared with female WT littermates. (<b>B</b>) Representative images illustrating spleen enlargement in an <span class="html-italic">Orai1<sup>V109M/+</sup></span> female mouse. (<b>C</b>) Megakaryocyte numbers were increased in <span class="html-italic">Orai1<sup>V109M/+</sup></span> spleen from males and females compared with WT controls. (<b>D</b>) Representative images of WT and <span class="html-italic">Orai1<sup>V109M/+</sup></span> spleen sections; megakaryocytes are indicated by arrowheads. (<b>E</b>) Compared with WT controls, platelet numbers were significantly decreased in <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice. (<b>F</b>,<b>G</b>) Biochemical blood analyses revealed hypocalcemia and elevated serum creatine kinase (CK) levels in <span class="html-italic">Orai1<sup>V109M/+</sup></span> males, while <span class="html-italic">Orai1<sup>V109M/+</sup></span> females showed a tendency of CK elevation. Significant differences are indicated as * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Abnormal muscle function in <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice. (<b>A</b>) Force transduction experiments disclosed reduced maximal force of <span class="html-italic">Orai1<sup>V109M/+</sup></span> tibialis anterior compared with WT. (<b>B</b>) Increasing stimulation frequencies evidenced normal submaximal force in <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice but reduced maximal force compared with WT littermates. (<b>C</b>) <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice showed abnormal fatigue curves with absence of muscle force increase in <span class="html-italic">Orai1<sup>V109M/+</sup></span> males after 10 stimulations and a similar tendency in <span class="html-italic">Orai1<sup>V109M/+</sup></span> females (insets). (<b>D</b>) Ratiometric analyses revealed increased resting Ca<sup>2+</sup> levels in isolated <span class="html-italic">Orai1<sup>V109M/+</sup></span> myoblasts compared with WT controls. Significant differences are indicated as * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, and **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>Abnormal muscle structure in <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice. (<b>A</b>) Representative images of transverse sections of WT and <span class="html-italic">Orai1<sup>V109M/+</sup></span> tibialis anterior stained with hematoxylin and eosin and Alizarin red. Arrowheads indicate internal nuclei and Ca<sup>2+</sup> deposits/Ca<sup>2+</sup>-rich myofibers. (<b>B</b>,<b>C</b>) <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice exhibited a higher ratio of smaller muscle fibers and internal nuclei compared with WT littermates. (<b>D</b>) <span class="html-italic">Orai1<sup>V109M/+</sup></span> muscle sections showed a significantly higher ratio of Ca<sup>2+</sup>-rich fibers compared with controls. (<b>E</b>) Toluidine blue-stained semithin sections and electron microscopy evidenced the presence of tubular aggregates (arrowheads) in longitudinal and transversal <span class="html-italic">Orai1<sup>V109M/+</sup></span> muscle sections (<b>top right</b>), while no tubular aggregates were detected in WT animals (<b>top left</b>). The lower panel shows tubular aggregates on semithin and EM sections from <span class="html-italic">Orai1<sup>V109M/+</sup></span> mice with increasing magnification. Significant differences are indicated as * <span class="html-italic">p</span> &lt; 0.05, **<sup>/##</sup> <span class="html-italic">p</span> &lt; 0.01, and ****<sup>/####</sup> <span class="html-italic">p</span> &lt; 0.0001.</p>
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15 pages, 709 KiB  
Article
Dynamic Analysis of Upper- and Lower-Extremity Performance During Take-Offs and Landings in High-Wall Climbing: Effects of a Plyometric and Strength Training Intervention
by Wen-Lung Shih, Ming-Lang Yeh, Ming-Hsi Chuang and Cheng-En Wu
Appl. Sci. 2024, 14(22), 10137; https://doi.org/10.3390/app142210137 - 5 Nov 2024
Viewed by 490
Abstract
This study used a 12-week plyometric and strength training program as an intervention to improve upper- and lower-extremity muscle strength for jumping and landing when climbing high walls. Sixty general non-athlete male college students were openly recruited and divided into an experimental group [...] Read more.
This study used a 12-week plyometric and strength training program as an intervention to improve upper- and lower-extremity muscle strength for jumping and landing when climbing high walls. Sixty general non-athlete male college students were openly recruited and divided into an experimental group and a control group. The experimental group underwent a plyometric and strength training program twice a week for 12 weeks (24 sessions). The intervention was divided into three phases, each lasting four weeks, with the training intensity gradually increasing in each phase. A hand grip dynamometer was used to measure grip strength, and a PASCO double-track force plate was used to assess upper-extremity push-up force and lower-extremity take-off and landing strength. The results of the 12-week intervention showed that the experimental group experienced significant increases in grip strength (both hands), hand-ground reaction force, and upper-extremity hang time. Additionally, the time of upper-extremity action on the force plate decreased. Lower-extremity take-off strength improved, as reflected in increased ground reaction force, rate of force development, and passage time. Upon landing, ground reaction force decreased by 3.2%, and cushioning time shortened by 52.7%. This study concludes that plyometric and strength training have promising effects in enhancing upper- and lower-extremity strength, particularly in climbing and landing tasks. Full article
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<p>Q-Q plots of participants’ age, height, and weight.</p>
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<p>Pre- and post-test of GRF when landing instantly and landing buffer time. Note: The left side was the average GRF of each group at the moment of landing, and the right side was the buffer time of each group when landing.</p>
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17 pages, 1967 KiB  
Article
Consumption of a Branched-Chain Amino Acids-Containing Sports Beverage During 21 km of Running Reduces Dehydration, Lowers Muscle Damage, and Prevents a Decline in Lower Limb Strength
by Zhuoying Liang, Yiheng Liang, Chengnan Zhang, Xueyuan Zhao and Junqiang Qiu
Nutrients 2024, 16(22), 3799; https://doi.org/10.3390/nu16223799 - 5 Nov 2024
Viewed by 955
Abstract
Objectives: The purpose of this study was to examine the acute effects of branched-chain amino acids (BCAAs)-containing electrolyte beverage (AE) on water–electrolyte balance, muscle damage, time to finish the final 5 km, and muscle strength compared to a standard commercially available carbohydrate–electrolyte sports [...] Read more.
Objectives: The purpose of this study was to examine the acute effects of branched-chain amino acids (BCAAs)-containing electrolyte beverage (AE) on water–electrolyte balance, muscle damage, time to finish the final 5 km, and muscle strength compared to a standard commercially available carbohydrate–electrolyte sports beverage (CE), pure water (W), and no rehydration (N). Methods: Fourteen trained male participants (20 ± 2 years old) completed four randomized 21 km running trials. The participants were instructed to consume their drink (150 mL W, 150 mL CE, or 150 mL AE) or no rehydration (N) at 5 km, 10 km, and 15 km. Body mass and muscle strength were assessed, and blood samples were collected before and after exercise. Perceptual scales were administered during and after running. Blood electrolyte levels (sodium, potassium, and chloride) and creatine kinase (CK) concentration were analyzed. Results: The change in plasma volume with AE was significantly smaller than that with N (p < 0.05). Consuming AE maintained the best potassium balance (p < 0.05). Twenty-four hours after exercise, serum CK concentrations significantly elevated in N, W, and CE (p < 0.05), but did not reach statistical significance in the AE group (p > 0.05). Compared to N, consuming AE resulted in significantly less soreness 24 h after exercise (p < 0.05). There was no difference in time to finish the final 5 km (p > 0.05). Maximal voluntary isometric force output was significantly lower after exercise with N and W (p < 0.05) but not with CE or AE (p > 0.05). Conclusions: Consuming a BCAAs-containing sports beverage during a 21 km run can help reduce dehydration, maintain potassium balance, lower muscle damage, and prevent the decline in lower limb strength after 21 km running. Full article
(This article belongs to the Section Sports Nutrition)
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<p>Study design. Abbreviations: USG, urine specific gravity; N, no rehydration during running; W, consuming pure water during running; CE, consuming a standard carbohydrate–electrolyte sports beverage during running; AE, consuming a branched-chain amino acids (BCAAs)-containing electrolyte beverage during running.</p>
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<p>Hydration status of the participants: (<b>A</b>) percentage of nude body mass lost after 21 km running; (<b>B</b>) plasma volume changes; (<b>C</b>) plasma osmolality changes. Significance symbols: <sup>#</sup>, significantly different from N, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Analysis of serum electrolyte concentration before and after the exercise protocol for the four conditions evaluated: (<b>A</b>) serum sodium concentration; (<b>B</b>) serum potassium concentration; (<b>C</b>) serum chlorine concentration. Significance symbols: <sup>#</sup>, significantly different from N, <span class="html-italic">p</span> &lt; 0.05; *, significantly different from pre-exercise, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Analysis of muscle damage markers and muscle soreness after exercise: (<b>A</b>) serum creatine kinase concentration; (<b>B</b>) perceived muscle soreness ratings. Significance symbols: <sup>#</sup>, significantly different from N, <span class="html-italic">p</span> &lt; 0.05; *, significantly different from pre-exercise, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>A 5 km time trial performance and muscle strength: (<b>A</b>) 5 km time trial performance; (<b>B</b>) maximal vertical jump height; (<b>C</b>) maximal voluntary isometric contraction output of quadriceps muscles (newton meters). Significance symbols: *, significantly different from pre-exercise, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Perceptual responses during the experimental trials: (<b>A</b>) rating of perceived exertion; (<b>B</b>) rating of thirst; (<b>C</b>) rating of gastrointestinal comfort.</p>
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15 pages, 6362 KiB  
Article
Impact of a 20-Week Resistance Training Program on the Force–Velocity Profile in Novice Lifters Using Isokinetic Two-Point Testing
by Joffrey Drigny, Nicolas Pamart, Hélène Azambourg, Marion Remilly, Emmanuel Reboursière, Antoine Gauthier and Amir Hodzic
J. Funct. Morphol. Kinesiol. 2024, 9(4), 222; https://doi.org/10.3390/jfmk9040222 - 5 Nov 2024
Viewed by 570
Abstract
Objectives: This study aimed to assess the impact of a 20-week resistance training program on force–velocity (F-V) parameters using an isokinetic two-point method and comparing one-repetition maximum (1-RM) methods in novice lifters. Methods: Previously untrained individuals completed a supervised, three-session weekly [...] Read more.
Objectives: This study aimed to assess the impact of a 20-week resistance training program on force–velocity (F-V) parameters using an isokinetic two-point method and comparing one-repetition maximum (1-RM) methods in novice lifters. Methods: Previously untrained individuals completed a supervised, three-session weekly resistance training program involving concentric, eccentric, and isometric phases, repeated every 2 to 4 weeks. Isokinetic dynamometry measured the strength of elbow flexors/extensors at 60°/s and 150°/s, and knee flexors/extensors at 60°/s and 240°/s at Baseline, 3 months, and 5 months. F-V parameters, including maximal theoretical force (F0) and the F-V slope, were calculated. Participants also performed 1-RM tests for the upper and lower limbs. Repeated measures ANOVA with effect size (η2 > 0.14 as large) was used to analyze changes in F-V parameters and repeated measures correlation was used to test their association with 1-RM outcomes. Results: Eighteen male participants (22.0 ± 3.4 years) were analyzed. F0 significantly increased for all muscle groups (η2 = 0.423 to 0.883) except elbow flexors. F-V slope significantly decreased (steeper) for knee extensors and flexors (η2 = 0.348 to 0.695). Knee extensors showed greater F0 gains and steeper F-V slopes than flexors (η2 = 0.398 to 0.686). F0 gains were associated with 1-RM changes (r = 0.38 to 0.83), while F-V slope changes correlated only with lower limb 1-RM (r = −0.37 to −0.68). Conclusions: The 20-week resistance training program significantly increased F0 and shifted the F-V profile towards a more “force-oriented” state in knee muscles. These changes correlated with improved 1-RM performance. Future studies should include longer follow-ups and control groups. Full article
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<p>Chronological overview of the 20-week resistance training program with 1-RM assessment.</p>
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<p>Setup and positioning for knee and elbow flexion/extension testing.</p>
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<p>Example of the linear regression models obtained from the force and velocity data during the knee extension using data measured at 60°/s and 240°/s (data were obtained from one participant and assessed at Baseline).</p>
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<p>Force–velocity parameter changes illustrated through linear regression models of force and velocity data during (<b>a</b>) elbow extension and flexion and (<b>b</b>) knee extension and flexion isokinetic tasks with repeated measures ANOVA. ext: extensors.</p>
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<p>Force–velocity parameter changes illustrated through linear regression models of force and velocity data during (<b>a</b>) elbow extension and flexion and (<b>b</b>) knee extension and flexion isokinetic tasks with repeated measures ANOVA. ext: extensors.</p>
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10 pages, 663 KiB  
Article
Effects of Foot Position-Based Gait Training on Muscle Activity, Gait Parameters, and Balance in Subacute Stroke Patients
by Yubin Lee, Yeongjae Pyo and Chaegil Lim
Healthcare 2024, 12(22), 2206; https://doi.org/10.3390/healthcare12222206 - 5 Nov 2024
Viewed by 431
Abstract
Background: the effects of gait training based on the positioning of affected foot muscle activity, gait parameters, and balance ability were investigated in patients with subacute stroke. Material and Methods: Forty-five patients with subacute stroke were randomly assigned to three groups: straight gait [...] Read more.
Background: the effects of gait training based on the positioning of affected foot muscle activity, gait parameters, and balance ability were investigated in patients with subacute stroke. Material and Methods: Forty-five patients with subacute stroke were randomly assigned to three groups: straight gait training (SGT) group (n = 15), outward curved gait training group (OCGT) with the paretic foot positioned laterally (n = 15), or inward curved gait training (ICGT) group with the paretic foot positioned medially (n = 15). All groups received 30 min interventions, comprising 15 min of gait training, five times per week for four weeks. Outcomes were measured in terms of muscle activation of the gluteus maximus (GM), vastus medialis, and vastus lateralis; five gait parameters (step length, stance phase, swing phase, velocity, and maximum force); and balance ability assessed using the timed up and go (TUG) test. Results: All groups exhibited significant improvements in all variables after the four-week intervention period (p < 0.05). Specifically, the overall muscle activation and gait parameters for each group increased as follows: the SGT showed increases of 38.8% and 5.7%, respectively; the OCGT exhibited improvements of 38.9% and 7.4%; and the ICGT demonstrated enhancements of 59.8% and 9.2%. However, except for comparisons between the SGT and ICGT groups in terms of GM muscle activity and TUG, no significant differences were observed between the groups for the other variables (p > 0.05). Conclusions: although patients with subacute stroke can improve their overall physical function regardless of the gait training method, ICGT may be more effective in enhancing muscle activity and balance ability. Full article
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<p>Flow chart.</p>
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<p>Curved walking path: ① large circle; ② small circle.</p>
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14 pages, 4946 KiB  
Article
The Asymmetries in Straight Jumps on the Trampoline Under Different Sensory Conditions
by Matjaž Pezdirc, Igor Pušnik, Maja Pajek, Ivan Čuk and Karmen Šibanc
Symmetry 2024, 16(11), 1472; https://doi.org/10.3390/sym16111472 - 5 Nov 2024
Viewed by 491
Abstract
The trampoline is a popular piece of sports equipment both for recreational use and for Olympic trampolining as a competitive sport. Maintaining body position during jumps is influenced by sensory inputs (visual, auditory, and somatosensory) and symmetrical muscle activity that help athletes to [...] Read more.
The trampoline is a popular piece of sports equipment both for recreational use and for Olympic trampolining as a competitive sport. Maintaining body position during jumps is influenced by sensory inputs (visual, auditory, and somatosensory) and symmetrical muscle activity that help athletes to perform consecutive jumps as vertically as possible. To evaluate the effects of these inputs, 15 male and 15 female students (with an average age of 24.4 years, height of 174.3 cm, and average weight of 69.7 kg) performed 10 consecutive straight jumps under four sensory conditions: (1) looking at the edge of the trampoline, (2) without sight, (3) without hearing, and (4) without hearing or sight. Using insoles with integrated pressure sensors (Pedar®, novel GmbH, Munich, Germany), the contact forces on the trampoline during the jump were measured separately for the left and right feet. The results showed that the lack of visual input significantly shortened flight times and increased the asymmetry of ground reaction forces between the left and right legs. For example, in the second series without vision, the average normalized force difference between the legs increased by 0.33 G compared to the control condition. An ANOVA revealed significant differences in the ground reaction forces between sensory conditions, with vision playing a key role in maintaining body control. These results provide practical insights for coaches looking to improve jumping performance and address asymmetries during training by focusing on sensory feedback strategies. Full article
(This article belongs to the Section Life Sciences)
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<p>Pressure sensors used in a study (<b>left</b>) and socks with rubber bottoms (<b>right</b>).</p>
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<p>Straight jumps in the series. Note: 1–looking down at the edge of the trampoline, 2–without seeing, 3–looking at the edge of the trampoline without hearing, and 4–without hearing or seeing.</p>
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<p>Variables during one take-off in a straight jump. Note: <span class="html-italic">F</span><sub>T</sub> = total ground reaction force; <span class="html-italic">F</span><sub>L</sub> = ground reaction force for the left leg; <span class="html-italic">F</span><sub>R</sub> = ground reaction force for the right leg; <span class="html-italic">F</span><sub>D</sub> = difference in ground reaction forces between left and right; <span class="html-italic">t</span><sub>D</sub> = time difference in maximum ground reaction force for left and right leg; <span class="html-italic">t</span><sub>f</sub> = time of flight.</p>
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<p>Raw ground reaction forces during the straight jump (1st series of jumps) for one person. Note: <span class="html-italic">F</span><sub>L</sub> + <span class="html-italic">F</span><sub>R</sub> = <span class="html-italic">F</span><sub>T</sub> = total ground reaction force (green); <span class="html-italic">F</span><sub>L</sub> = ground reaction force for the left leg (blue); <span class="html-italic">F</span><sub>R</sub> = ground reaction force for the right leg (orange); <span class="html-italic">t</span><sub>f3</sub> and <span class="html-italic">t</span><sub>f4</sub> = flight time after 3rd and 4th jump in one series.</p>
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<p>Raw ground reaction forces without seeing (2nd series of jumps) for one person. Note: <span class="html-italic">F</span><sub>L</sub> + <span class="html-italic">F</span><sub>R</sub> = <span class="html-italic">F</span><sub>T</sub> = total ground reaction force (green); <span class="html-italic">F</span><sub>L</sub> = ground reaction force for the left leg (blue); <span class="html-italic">F</span><sub>R</sub> = ground reaction force for the right leg (orange).</p>
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<p>Raw ground reaction forces without hearing (3rd series of jumps) for one person. Note: <span class="html-italic">F</span><sub>L</sub> + <span class="html-italic">F</span><sub>R</sub> = <span class="html-italic">F</span><sub>T</sub> = total ground reaction force (green); <span class="html-italic">F</span><sub>L</sub> = ground reaction force for the left leg (blue); <span class="html-italic">F</span><sub>R</sub> = ground reaction force for the right leg (orange).</p>
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<p>Raw ground reaction forces without seeing or hearing (4th series of jumps) for one person. Note: <span class="html-italic">F</span><sub>L</sub> + <span class="html-italic">F</span><sub>R</sub> = <span class="html-italic">F</span><sub>T</sub> = total ground reaction force (green); F<sub>L</sub> = ground reaction force for the left leg (blue); <span class="html-italic">F</span><sub>R</sub> = ground reaction force for the right leg (orange).</p>
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<p>The sum of differences in ground reaction forces between the left and right leg for all four jump series. Note: <span class="html-italic">F</span><sub>Dsum</sub>/<span class="html-italic">F</span><sub>g</sub> = the sum of the difference in ground reaction forces between the left and right leg; 1–4 = number of series; 1 = 1st series of jumps; 2 = 2nd series of jumps without vision; 3 = 3rd series of jumps without hearing; 4 = 4th series of jumps without vision or hearing.</p>
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9 pages, 1012 KiB  
Article
Efficacy of Warmup Using a Flexible Bar to Increase Countermovement Jump
by Benjamin J. Snyder, Anthony Caterisano, Evan P. DiMaggio and Jackson D. King
Sports 2024, 12(11), 298; https://doi.org/10.3390/sports12110298 - 1 Nov 2024
Viewed by 353
Abstract
Preparation of athletes to begin a competition or enter mid-competition with the ability to reach peak performance immediately may be partly dependent on the efficacy of the warmup protocol. Previous research on flexible barbells reported significant differences in muscle activation when compared to [...] Read more.
Preparation of athletes to begin a competition or enter mid-competition with the ability to reach peak performance immediately may be partly dependent on the efficacy of the warmup protocol. Previous research on flexible barbells reported significant differences in muscle activation when compared to steel barbells. The manufacturers of handheld flexible bars with a combined weight of 3.63 kg claim that using them immediately before competition helps increase power and jump height. The purpose of the study was to determine the effects of maximal jumping with handheld flexible bars on maximal jump parameters in Division-I American collegiate football players. Participants completed 10 warmup jumps with no weight, flexible barbells, or similarly weighted dumbbells and immediately completed a maximal countermovement jump. When comparing the effects of different high-velocity warmup (HVW) protocols, there were no differences in any jump parameters as measured by a portable force plate. Likewise, the use of flexible bars during the warmup did not result in enhanced muscle activity when executing a maximal jump in comparison to control conditions. Based on these results there is no evidence to support the use of flexible bars during a warmup just prior to entry into a competition to enhance jumping power. Full article
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Figure 1

Figure 1
<p>(<b>A</b>) Resting position (<b>B</b>) downward and (<b>C</b>) upward oscillatory bending of the bar during jumping. Source: authors.</p>
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<p>Conceptual map of project.</p>
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