Bredemolic acid restores glucose utilization and attenuates oxidative stress in palmitic acid-induced insulin-resistant C2C12 cells

Q3 Medicine
Karabo R Matee, A. Akinnuga, Angezwa Siboto, P. Ngubane, A. Khathi
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引用次数: 2

Abstract

Abstract Objective. Due to insulin resistance and oxidative stress that are associated with type 2 diabetes mellitus (T2DM), T2DM has become a prevalent metabolic disorder that presents various side effects. However, alternative antidiabetic treatment has commonly been used in treating diabetes mellitus in diabetic patients. In our previous studies, bredemolic acid has been reported as an antidiabetic agent that improves glucose uptake, ameliorates insulin resistance, and oxidative stress in the liver, heart, kidney, and skeletal muscle of prediabetic rats. However, these effects have not been validated in vitro. Therefore, this study was aimed to investigate the effects of bredemolic acid on insulin-mediated glucose utilization, lipid peroxidation, and the total antioxidant capacity (TOAC) in palmitic acid-induced insulin-resistant C2C12 skeletal muscle cells in vitro. Methods. Insulin resistance was induced in the skeletal muscle cells after 4 h of exposure to palmitic acid (0.5 mmol/l). Different cell groups were incubated in culture media DMEM supplemented with fetal calf serum (10%), penicillin/streptomycin (1%), and L-glutamine (1%) and then treated with either insulin (4 µg/ml) or bredemolic acid (12.5 mmol/l) or with both. Thereafter, the cells were seeded in 24- or 96-well plates for determination of the cell viability, glucose utilization, glycogen formation, and antioxidant capacity. Results. The results showed that bredemolic acid significantly improved TOAC and promoted glucose utilization via attenuation of lipid peroxidation and increased glycogen formation in the insulin-resistant cells, respectively. Conclusion. This study showed that bredemolic acid restored the insulin resistance through improved glucose utilization, glycogen formation, and TOAC in the skeletal muscle cells.
在棕榈酸诱导的胰岛素抵抗的C2C12细胞中,丁二酸恢复葡萄糖利用并减轻氧化应激
摘要目的。由于与2型糖尿病(T2DM)相关的胰岛素抵抗和氧化应激,T2DM已成为一种常见的代谢紊乱,具有多种副作用。然而,糖尿病患者的糖尿病治疗通常采用替代降糖治疗。在我们之前的研究中,已经报道了一种抗糖尿病药物,可以改善糖尿病前期大鼠的葡萄糖摄取,改善胰岛素抵抗和肝脏、心脏、肾脏和骨骼肌的氧化应激。然而,这些效果尚未在体外得到验证。因此,本研究旨在探讨苦参酸对棕榈酸诱导的胰岛素抵抗型C2C12骨骼肌细胞胰岛素介导的葡萄糖利用、脂质过氧化和总抗氧化能力(TOAC)的影响。方法。暴露于0.5 mmol/l棕榈酸4 h后,骨骼肌细胞产生胰岛素抵抗。不同细胞组在添加胎牛血清(10%)、青霉素/链霉素(1%)和l -谷氨酰胺(1%)的DMEM培养基中孵育,然后用胰岛素(4µg/ml)或牛黄酸(12.5 mmol/l)或两者同时处理。之后,将细胞接种于24孔或96孔板中,测定细胞活力、葡萄糖利用、糖原形成和抗氧化能力。结果。结果表明,在胰岛素抵抗细胞中,苦参酸通过抑制脂质过氧化作用和增加糖原形成,显著改善TOAC和促进葡萄糖利用。结论。本研究表明,菊醛酸通过改善骨骼肌细胞的葡萄糖利用、糖原形成和TOAC来恢复胰岛素抵抗。
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来源期刊
Endocrine regulations
Endocrine regulations Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.70
自引率
0.00%
发文量
33
审稿时长
8 weeks
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