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二甲双胍、格列美脲和西他列汀对高脂饮食/链脲佐菌素诱导的糖尿病大鼠脂肪细胞因子生成及血清游离脂肪酸水平的调节作用

Modulation of Adipocytokines Production and Serum NEFA Level by Metformin, Glimepiride, and Sitagliptin in HFD/STZ Diabetic Rats.

作者信息

Saad Mohamed I, Kamel Maher A, Hanafi Mervat Y

机构信息

Biochemistry Department, Medical Research Institute, Alexandria University, 165 Elhorreya Avenue, P.O. Box 21561, Alexandria, Egypt.

出版信息

Biochem Res Int. 2015;2015:138134. doi: 10.1155/2015/138134. Epub 2015 Mar 1.

Abstract

Type 2 diabetes mellitus (T2DM) is a group of metabolic disorders characterized by hyperglycemia owing to insulin resistance and/or insulin deficiency. Current theories of T2DM pathophysiology include a decline in β-cells function, a defect in insulin signaling pathways, and a dysregulation of secretory function of adipocytes. This study aimed to investigate the effect of different antidiabetic drugs on serum levels of certain adipocytokines and nonesterified fatty acids (NEFA) in high-fat diet (HFD)/streptozotocin- (STZ-) induced diabetic rats. All treatments significantly decreased serum NEFA level. Metformin and sitagliptin increased serum adiponectin level, whereas they decreased serum leptin level. Glimepiride showed significant decline in serum levels of both adiponectin and leptin. All treatments remarkably ameliorated insulin resistance, suggested by an improvement of glycemic control, a significant reduction in homeostasis model assessment of insulin resistance (HOMA-IR), and a correction in lipid profile. Modulation of adipocytokines production (i.e., increased serum adiponectin and decreased serum leptin) may also underlie the improvement of insulin resistance and could be a possible mechanism for the beneficial cardiovascular effects of metformin and sitagliptin.

摘要

2型糖尿病(T2DM)是一组代谢紊乱疾病,其特征为由于胰岛素抵抗和/或胰岛素缺乏导致的高血糖。目前关于T2DM病理生理学的理论包括β细胞功能下降、胰岛素信号通路缺陷以及脂肪细胞分泌功能失调。本研究旨在探讨不同抗糖尿病药物对高脂饮食(HFD)/链脲佐菌素(STZ)诱导的糖尿病大鼠血清中某些脂肪细胞因子和非酯化脂肪酸(NEFA)水平的影响。所有治疗均显著降低了血清NEFA水平。二甲双胍和西他列汀提高了血清脂联素水平,而降低了血清瘦素水平。格列美脲使血清脂联素和瘦素水平均显著下降。所有治疗均显著改善了胰岛素抵抗,表现为血糖控制改善、胰岛素抵抗稳态模型评估(HOMA-IR)显著降低以及血脂谱得到纠正。脂肪细胞因子产生的调节(即血清脂联素增加和血清瘦素减少)也可能是胰岛素抵抗改善的基础,并且可能是二甲双胍和西他列汀产生有益心血管作用的一种可能机制。

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