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Does Resveratrol Improve Insulin Signalling in HepG2 Cells?
Marjan Norouzzadeh1, Fatemehsadat Amiri2, Ali Akbar Saboor-Yaraghi1
1Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetic, Tehran University of Medical Sciences, Tehran, Iran.
Objectives:
Diabetes mellitus is a common metabolic disorder with high global prevalence. It is characterized by a decrease in insulin secretion or a decrease in insulin sensitivity or both. The aim of the present study was to investigate the effects of resveratrol treatment on the expression of the genes involved in insulin signalling cascade, such as Forkhead box protein O1 (FoxO1), 3-phosphoinositide-dependent protein kinase 1 (PDPK1) and mammalian target of rapamycin (mTOR).
Methods:
HepG2 cells were cultured in serum-free medium with high concentrations of glucose and insulin and then were treated with resveratrol (5, 10 and 20 µM) for 24 and 48 hours. Complementary deoxyribonucleic acids (cDNAs) were synthesized followed by RNA extraction. Real-time quantitative reverse transcription polymerase chain reaction was used to analyze the expression of FoxO1, PDPK1 and mTOR.
Results:
Resveratrol increased the expression of PDPK1, mTOR and FoxO1. No significant difference was seen among differing dosages of resveratrol, but treatments for 48 hours exerted the greatest effectiveness.
Conclusions:
Our results were consistent with other studies showing the beneficial effects of resveratrol on diabetes. However, considering the effects of resveratrol in increasing FoxO1 and gluconeogenic gene expression, long-term usage of resveratrol should be investigated in greater depth in future studies.
Insights
Resveratrol treatment increased the expression of key insulin signaling genes, including Forkhead box protein O1 (FoxO1), 3-phosphoinositide-dependent protein kinase 1 (PDPK1), and mammalian target of rapamycin (mTOR) in liver cells. Longer treatment durations showed greater effectiveness for managing diabetes.
Area of Science:
- Metabolic disorders
- Molecular biology
- Diabetes mellitus research
Background:
- Diabetes mellitus is a prevalent metabolic disorder characterized by impaired insulin secretion or sensitivity.
- Understanding the molecular mechanisms underlying insulin signaling is crucial for developing effective diabetes treatments.
Purpose of the Study:
- To investigate the impact of resveratrol on the expression of genes within the insulin signaling pathway.
- Specifically examining the effects on Forkhead box protein O1 (FoxO1), 3-phosphoinositide-dependent protein kinase 1 (PDPK1), and mammalian target of rapamycin (mTOR).
Main Methods:
- HepG2 cells were cultured under high glucose and insulin conditions.
- Cells were treated with varying concentrations of resveratrol (5, 10, 20 µM) for 24 and 48 hours.
- Gene expression analysis of FoxO1, PDPK1, and mTOR was performed using real-time quantitative reverse transcription polymerase chain reaction.
Main Results:
- Resveratrol treatment led to increased expression of PDPK1, mTOR, and FoxO1.
- No significant dose-dependent effect was observed across resveratrol concentrations.
- A 48-hour treatment duration demonstrated the most significant impact on gene expression.
Conclusions:
- Resveratrol exhibits beneficial effects relevant to diabetes management, as indicated by its influence on insulin signaling genes.
- The study highlights the potential of resveratrol in modulating key components of the insulin cascade.
- Further research is warranted to explore the long-term effects of resveratrol, particularly concerning its impact on FoxO1 and gluconeogenic gene expression.
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