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Many studies have proven that autophagy plays a pivotal role in the development of depression and it also affects the expression of GLUT4 in the hypothalamus. Xiaoyaosan has been shown to exert antidepressant effects in a variety of ways, but its underlying mechanism by which Xiaoyaosan regulates autophagy as well as GLUT4 in the hypothalamus remains unclear. Thus, in this study, we established a mouse model of depression induced by chronic unpredictable mild stress (CUMS), and set up autophagy blockade as a control to explore whether Xiaoyaosan exerts antidepressant effect by affecting autophagy. We examined the effects of Xiaoyaosan on behaviors exhibited during the open field test, tail suspension test and sucrose preference test, and the changes in autophagy in hypothalamic neurons as well as changes in GLUT4 and the related indicators of glucose metabolism in CUMS-induced depressive mouse model. We found that CUMS- and 3-MA-induced mice exhibited depressive-like behavioral changes, with decreased LC3 expression and increased p62 expression, suggesting decreased levels of autophagy in the mouse hypothalamus. The expression of GLUT4 was also decreased, and it was closely related to the level of autophagy through Rab8 and Rab10. Nevertheless, after the intervention of Xiaoyaosan, the above changes were effectively reversed. These results show that Xiaoyaosan can regulate the autophagy in hypothalamic neurons and the expression of GLUT4 in depressed mice.
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http://dx.doi.org/10.3389/fphar.2022.873646 | DOI Listing |
Int J Vitam Nutr Res
August 2025
Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Dhaka, 1000 Dhaka, Bangladesh.
Diabetes mellitus (DM) is a chronic metabolic disorder characterized by persistent hyperglycemia and associated with severe complications, including cardiovascular diseases, neuropathy, nephropathy, and retinopathy. Although synthetic antidiabetic drugs are available, the side effects and limited long-term effectiveness of these medications highlight the urgent need for safer, more potent alternative therapies. L.
View Article and Find Full Text PDFFitoterapia
August 2025
Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Mysuru 570 015, Karnataka, India. Electronic address:
From past to the present, plants and trees have benefited humans in many ways. As technology advanced the biological properties of plants are much more explored especially by the pharma industry. Rosemary plant has gained attention as a phytoconstituent-rich herb that may help to manage diabetes mellitus (DM), however, exact mechanism of action is still unknown.
View Article and Find Full Text PDFEnviron Res
August 2025
Department of Environmental Engineering, Seoul National University of Science and Technology, Seoul, 01811, Republic of Korea. Electronic address:
Perfluorooctane sulfonamide (PFOSA) is an indirect source of perfluorooctane sulfonic acid (PFOS) in the environment as a precursor; however, toxicological study of PFOSA is limited. This study aimed to investigate the effects of PFOSA on glucose and lipid metabolism in 3T3-L1 adipocytes and in zebrafish larvae. 3T3-L1 adipocytes were treated with PFOSA, PFOS, and rosiglitazone (RSG) for 48 h, and assessed for cell viability, adipogenesis, glucose uptake, and regarding molecular mechanisms.
View Article and Find Full Text PDFInt J Mol Sci
August 2025
Department of Biochemistry, Federal University of Technology, P.M.B. 704, Akure 340252, Nigeria.
Studies utilizing cell-based systems to investigate plant-based diets for diabetes management are gaining attention due to the adverse effects associated with commercially available drugs. However, the molecular mechanisms underlying the anti-diabetic effects of specific plant-derived products remain inadequately explored. The major aim of our study was to elucidate the molecular mechanisms by which bioactive compounds in the fruit of spp.
View Article and Find Full Text PDFAm J Physiol Cell Physiol
August 2025
Division of Pharmacology and Toxicology, College of Pharmacy, The University of Texas at Austin, Austin, Texas, United States of America.
Uncoupling protein 3 (UCP3), a member of the mitochondrial solute carrier family, shares high homology with both UCP1 and UCP2. Its exact functional role has been elusive since its discovery, with previous studies primarily focusing on studying UCP3 function in differentiated skeletal muscle myotubes or whole animal models because basal levels of UCP3 protein are low in undifferentiated myoblasts. In the present study, we demonstrate that UCP3 plays a role in modulating energy and redox stress related pathways in undifferentiated muscle myoblasts.
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