Supplementation of scopoletin improves insulin sensitivity by attenuating the derangements of insulin signaling through AMPK
Autor: | Chandrasekaran Sathiya Priya, Nanda Dipti, Carani Venkatraman Anuradha, Kalaivanan Kalpana, Ramachandran Vidhya |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
medicine.medical_specialty medicine.medical_treatment Clinical Biochemistry Enzyme Activators AMP-Activated Protein Kinases Carbohydrate metabolism 03 medical and health sciences 0302 clinical medicine Insulin resistance Cell Line Tumor Internal medicine otorhinolaryngologic diseases medicine Animals Molecular Biology Protein kinase B Scopoletin biology Chemistry Insulin AMPK Cell Biology General Medicine medicine.disease Dietary Fats Rats IRS1 Insulin receptor 030104 developmental biology Endocrinology Diabetes Mellitus Type 2 Lipotoxicity 030220 oncology & carcinogenesis biology.protein sense organs Insulin Resistance Signal Transduction |
Zdroj: | Molecular and Cellular Biochemistry. 453:65-78 |
ISSN: | 1573-4919 0300-8177 |
DOI: | 10.1007/s11010-018-3432-7 |
Popis: | Scopoletin (SPL), a phenolic coumarin, is reported to regulate glucose metabolism. This study is initiated to substantiate the action of SPL on the regulation of insulin signaling in insulin resistant RIN5f cells and high fat, high fructose diet (HFFD)-fed rat model. Adult male Sprague Dawley rats were fed HFFD for 45 days to induce type 2 diabetes and then treated or untreated with SPL for the next 45 days. The levels of glucose, insulin, lipid profile, oxidative stress markers along with insulin signaling and AMPK protein expressions were examined at the end of 90 days. SPL lowered the levels of plasma glucose, insulin, and lipids which were increased in HFFD-fed rats. HFFD intake suppressed the activities of antioxidant enzymes such as superoxide dismutase, catalase, and glutathione peroxidase; however, they were reversed by SPL supplementation, which reduced TBARS, lipid hydroperoxide, and protein carbonyl levels both in plasma and pancreas. SPL supplementation significantly activated insulin receptor substrate 1 (IRS1), phosphatidyl inositol 3-kinase (PI3K), and protein kinase B (Akt) phosphorylation which was suppressed in HFFD rats due to lipotoxicity. Moreover, SPL significantly activated AMPK and enhanced the association of IRS1-PI3K-Akt compared to the control group. The results revealed that SPL alleviated T2D induced by HFFD by escalating the antioxidant levels and through insulin signaling regulation. We conclude that SPL can improve insulin signaling through AMPK, thereby confirming the role of SPL as an AMPK activator. |
Databáze: | OpenAIRE |
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