Effect of growth factors present in serum on insulin resistance and endothelial dysfunction in endothelial cells

Q3 Biochemistry, Genetics and Molecular Biology Journal of Advanced Biotechnology and Experimental Therapeutics Pub Date : 2022-01-01 DOI:10.5455/jabet.2022.d141
Harika Maganti, Prabu Thandapani, Ragulprasath Kailasam, Adithi Pisapati, Akshaya Bala, A. Mendonça, S. Sundaresan
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Abstract

Insulin Resistance is a pathophysiological function of Type II Diabetes Mellitus which can be comprehended by quantifying the parameters critical in the insulin signaling pathway. Serum has a profound role in evaluating cellular growth and metabolism in vitro. The growth factors present in serum such as IGF, EGF, FGF affects the regulatory components of insulin signaling pathway that leads to insulin resistance. This study explores the effect of growth factors present in Fetal Bovine Serum (FBS) in insulin signaling and endothelium regulation in endothelial cells (Ea. hyp926). The dose-dependent and time-dependent treatment of FBS on the cells displayed changes that were detected by MTT and 2-NBDG assays for assessing cell viability and glucose uptake. Spectrophotometric analysis of nitric oxide (NO) and lactate dehydrogenase (LDH) determined vascular homeostasis and no cytotoxic effects of serum, respectively, in endothelial cells. These findings indicate that FBS at higher levels could possibly lead to loss of NO activity which in turn could impair endothelium-mediated dilation. The inhibition of enzymatic activity of eNOS may activate the release of LDH in endothelial cells. In conclusion, our findings indicate a specific concentration of serum enhances insulin signaling and endothelium cell regulation by modulating glucose uptake and NO production.
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血清生长因子对内皮细胞胰岛素抵抗和内皮功能障碍的影响
胰岛素抵抗是II型糖尿病的一种病理生理功能,可以通过量化胰岛素信号通路中的关键参数来理解。血清在体外评价细胞生长和代谢方面具有重要作用。血清中存在的生长因子如IGF、EGF、FGF影响胰岛素信号通路的调控成分,导致胰岛素抵抗。本研究探讨了胎牛血清(FBS)中存在的生长因子在内皮细胞胰岛素信号传导和内皮调节中的作用(Ea. hyp926)。通过MTT和2-NBDG检测,FBS对细胞的剂量依赖性和时间依赖性显示出变化,以评估细胞活力和葡萄糖摄取。分光光度法分析一氧化氮(NO)和乳酸脱氢酶(LDH)分别测定内皮细胞血管稳态和血清无细胞毒性作用。这些发现表明,高水平的FBS可能导致NO活性丧失,从而损害内皮介导的舒张。eNOS酶活性的抑制可能会激活内皮细胞中LDH的释放。总之,我们的研究结果表明,特定浓度的血清通过调节葡萄糖摄取和NO产生来增强胰岛素信号传导和内皮细胞调节。
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来源期刊
Journal of Advanced Biotechnology and Experimental Therapeutics
Journal of Advanced Biotechnology and Experimental Therapeutics Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
1.90
自引率
0.00%
发文量
41
审稿时长
8 weeks
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