Endocrine Physiology Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Endocrine Physiology Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Biomed J. 2022 Apr;45(2):387-395. doi: 10.1016/j.bj.2021.04.004. Epub 2021 Apr 20.
Nitrite stimulates insulin secretion from pancreatic β-cells; however, the underlying mechanisms have not been completely addressed. The aim of this study is to determine effect of nitrite on gene expression of SNARE proteins involved in insulin secretion from isolated pancreatic islets in Type 2 diabetic Wistar rats.
Three groups of rats were studied (n = 10/group): Control, diabetes, and diabetes + nitrite, which treated with sodium nitrite (50 mg/L) for 8 weeks. Type 2 diabetes was induced using a low-dose of streptozotocin (25 mg/kg) combined with high-fat diet. At the end of the study, pancreatic islets were isolated and mRNA expressions of interested genes were measured; in addition, protein expression of proinsulin and C-peptide in pancreatic tissue was assessed using immunofluorescence staining.
Compared with controls, in the isolated pancreatic islets of Type 2 diabetic rats, mRNA expression of glucokinase (59%), syntaxin1A (49%), SNAP25 (70%), Munc18b (48%), insulin1 (56%), and insulin2 (52%) as well as protein expression of proinsulin and C-peptide were lower. In diabetic rats, nitrite administration significantly increased gene expression of glucokinase, synaptotagmin III, syntaxin1A, SNAP25, Munc18b, and insulin genes as well as increased protein expression of proinsulin and C-peptide.
Stimulatory effect of nitrite on insulin secretion in Type 2 diabetic rats is at least in part due to increased gene expression of molecules involved in glucose sensing (glucokinase), calcium sensing (synaptotagmin III), and exocytosis of insulin vesicles (syntaxin1A, SNAP25, and Munc18b) as well as increased expression of insulin genes.
亚硝酸盐刺激胰岛β细胞分泌胰岛素,但作用机制尚未完全阐明。本研究旨在确定亚硝酸盐对 2 型糖尿病 Wistar 大鼠胰岛中参与胰岛素分泌的 SNARE 蛋白基因表达的影响。
研究了三组大鼠(每组 n=10):对照组、糖尿病组和糖尿病+亚硝酸盐组,后者用亚硝酸钠(50mg/L)治疗 8 周。2 型糖尿病采用小剂量链脲佐菌素(25mg/kg)联合高脂肪饮食诱导。研究结束时,分离胰岛,测量感兴趣基因的 mRNA 表达;此外,还通过免疫荧光染色评估胰腺组织中胰岛素原和 C 肽的蛋白表达。
与对照组相比,2 型糖尿病大鼠胰岛中葡萄糖激酶(59%)、突触融合蛋白 1A(49%)、SNAP25(70%)、Munc18b(48%)、胰岛素 1(56%)和胰岛素 2(52%)的 mRNA 表达以及胰岛素原和 C 肽的蛋白表达均降低。在糖尿病大鼠中,亚硝酸盐给药可显著增加葡萄糖激酶、突触融合蛋白 III、突触融合蛋白 1A、SNAP25、Munc18b 和胰岛素基因的表达,并增加胰岛素原和 C 肽的蛋白表达。
亚硝酸盐对 2 型糖尿病大鼠胰岛素分泌的刺激作用至少部分是由于参与葡萄糖感应(葡萄糖激酶)、钙感应(突触融合蛋白 III)和胰岛素囊泡出胞(突触融合蛋白 1A、SNAP25 和 Munc18b)的分子的基因表达增加以及胰岛素基因表达增加所致。