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Aida Moeini , Sirous Farsi , Mehrzad Moghaddasi ,
Volume 22, Issue 2 (6-2019)
Abstract

Background and Aim: Curcumin is one of the most important nutritional polyphenols that is included in daily supplements diet highly and plays a role in moderating some of the intracellular messenger pathways associated with the regulation of pathologic hypertrophy. The purpose of the present study is to survey the effect of curcumin supplementation on the expression of some genes regulators of the pathological processes of the heart muscle in rats.
Materials and Methods: In this eight-week experimental study, 12 male Sprague Dawley rats were divided into two groups: obesity control (n=6) and curcumin supplement (n=6). Curcumin supplementation was conducted for eight weeks. 24 hours after the completion of the curcumin supplement protocol, the rats were dissected and their heart muscle was removed. The expression of the genes (AMPK, mTOR, S6K, 4EBP, COL1, COL3, and Ang) was performed using Real-Time PCR technique. The expression of the genes was calculated by the 2-∆∆CT method. One way ANOVA was applied to determine the significance of the variables among the study groups.
Ethical Considerations: This study with research ethics code IR.SUMS.REC.1396.S446 has been approved by research ethics committee at Shiraz University of Medical Sciences.
Findings:The results has showed that supplement group of curcumin reduced the expression of mTOR (p < 0.001), S6K (p < 0.011), 4EBP (p > 0.005) collagen 1 (p > 0.002), Collagen 3 (p < 0.001) and Ang (p < 0.003) compared to the placebo group. There was also an increase in the expression of AMPK gene (p < 0.001) which was statistically significant.
Conclusion: it seems that the supplementation of 10 mg curcumin moderate the pathological pathway of cardiac muscle hypertrophy by reducing or keeping up the expression of mTOR gene in obese rats and increasing the expression of AMPK gene. Moreover, this supplement can affect on reducing the pathological hypertrophy during the consumption of curcumin supplementation

Dr. Maryam Arabloei Sani, Dr. Zahra Hajebrahimi, Dr. Parichehreh Yaghmaei, Dr. Nasim Hayati Roodbari,
Volume 26, Issue 5 (12-2023)
Abstract

Background and Aim: Diabetes is a type of metabolic disease and one of the most common endocrine diseases. Oxidative stress and inflammation play an important role in the development and progression of diabetes. mTOR signaling pathway play an important role in glucose homeostasis and proliferation of pancreatic beta cells. In the present study, the therapeutic effects of p-cymene on oxidative stress markers and expression of the mTOR gene in diabetic male Wistar rats were investigated.
Materials and Methods: Diabetes was induced by injecting 55 mg/kg body weight of streptozotocin. Biochemical analyses of pancreatic tissue and real-time PCR were done to investigate the effects of metformin (55 mg/kg body weight) and p-cymene (25, 50, and 100 mg/kg body weight) on the activities of catalase and glutathione peroxidase enzymes and mTOR gene expression.
Findings: Streptozotocin decreased catalase and glutathione peroxidase enzymes and decreased the expression of the mTOR gene in pancreatic tissue. Treatment with metformin or p-cymene improved the activities of catalase and glutathione peroxidase enzymes and the expression of the mTOR gene in a dose-independent manner.
Conclusion: Results indicate that p-cymene has antioxidant properties and can regulate the mTOR signaling pathway. Therefore, p-cymene may be effective for the treatment of diabetes alone or in combination with metformin.

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