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核黄素对2型糖尿病小鼠高血糖、氧化应激和DNA损伤的改善作用:作用机制与治疗策略

Ameliorative effect of riboflavin on hyperglycemia, oxidative stress and DNA damage in type-2 diabetic mice: Mechanistic and therapeutic strategies.

作者信息

Alam Md Maroof, Iqbal Sarah, Naseem Imrana

机构信息

Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, U.P., India.

Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, U.P., India.

出版信息

Arch Biochem Biophys. 2015 Oct 15;584:10-9. doi: 10.1016/j.abb.2015.08.013. Epub 2015 Aug 28.

Abstract

Increasing evidence in both experimental and clinical studies suggests that oxidative stress play a major role in the pathogenesis of type-2 diabetes mellitus (T2DM). Abnormally high levels of free radicals and the simultaneous decline of antioxidant defence mechanisms can lead to damage of cellular organelles and enzymes. Riboflavin constitutes an essential nutrient for humans and is also an important food additive for animals. It is a precursor of flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which serves as a coenzyme for several enzymes. The aim of this study was to observe the effects of illuminated and non-illuminated riboflavin in a diabetic mice model. The protocol included treatment of diabetic mice with illuminated RF and a control set without light. To our surprise, group receiving RF without light gave better results in a dose dependent manner. Significant amelioration of oxidative stress was observed with an increased glucose uptake in skeletal muscles and white adipose tissue. Histological studies showed recovery in the liver and kidney tissue injury. Cellular DNA damage was also recovered. Therefore, it is suggested that supplementation with dietary riboflavin might help in the reduction of diabetic complications. A possible mechanism of action is also proposed.

摘要

越来越多的实验和临床研究证据表明,氧化应激在2型糖尿病(T2DM)的发病机制中起主要作用。自由基水平异常升高以及抗氧化防御机制同时下降会导致细胞器和酶的损伤。核黄素是人类必需的营养素,也是动物重要的食品添加剂。它是黄素单核苷酸(FMN)和黄素腺嘌呤二核苷酸(FAD)的前体,而FMN和FAD作为几种酶的辅酶。本研究的目的是观察光照和未光照的核黄素对糖尿病小鼠模型的影响。实验方案包括用光照的核黄素治疗糖尿病小鼠以及设置无光照的对照组。令我们惊讶的是,未光照核黄素组以剂量依赖的方式取得了更好的结果。观察到氧化应激显著改善,骨骼肌和白色脂肪组织中的葡萄糖摄取增加。组织学研究显示肝脏和肾脏组织损伤得到恢复。细胞DNA损伤也得到了恢复。因此,建议补充膳食核黄素可能有助于减少糖尿病并发症。还提出了一种可能的作用机制。

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