A novel phenolic formulation for treating hepatic and peripheral insulin resistance by regulating GLUT4-mediated glucose uptake
Journal of Traditional and Complementary Medicine, ISSN: 2225-4110, Vol: 12, Issue: 2, Page: 195-205
2022
- 12Citations
- 27Usage
- 24Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations12
- Citation Indexes12
- 12
- Usage27
- Abstract Views24
- Downloads3
- Captures24
- Readers24
- 24
Article Description
Chronic insulin resistance suppresses muscle and liver response to insulin, which is partially due to impaired vesicle trafficking. We report here that a formula consisting of resveratrol, ferulic acid and epigallocatechin-3- O -gallate is more effective in ameliorating muscle and hepatic insulin resistance than the anti-diabetic drugs, metformin and AICAR. The formula enhanced glucose transporter-4 (GLUT4) translocation to the plasma membrane in the insulin-resistant muscle cells by regulating both insulin-independent (calcium and AMPK) and insulin-dependent (PI3K) signaling molecules. Particularly, it regulated the subcellular location of GLUT4 through endosomes to increase glucose uptake under insulin-resistant condition. Meanwhile, this phytochemicals combination increased glycogen synthesis and decreased glucose production in the insulin-resistant liver cells. On the other hand, this formula also showed anti-diabetic potential by the reduction of lipid content in the myotubes, hepatocytes, and adipocytes. This study demonstrated that the three phenolic compounds in the formula could work in distinct mechanisms and enhance both insulin-dependent and independent vesicles trafficking and glucose transport mechanisms to improve carbohydrate and lipid metabolism.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2225411021000961; http://dx.doi.org/10.1016/j.jtcme.2021.08.004; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85112549688&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/35528476; https://linkinghub.elsevier.com/retrieve/pii/S2225411021000961; https://www.airitilibrary.com/Article/Detail/P20190807002-202203-202203100006-202203100006-195-205; https://dx.doi.org/10.1016/j.jtcme.2021.08.004
Elsevier BV
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