Lotfy Mohamed, Singh Jaipaul, Rashed Hameed, Tariq Saeed, Zilahi Erika, Adeghate Ernest
Department of Biology, College of Science, United Arab Emirates University, P.O. Box 17666, Al Ain, United Arab Emirates.
Cell Tissue Res. 2014 Nov;358(2):343-58. doi: 10.1007/s00441-014-1959-9. Epub 2014 Aug 13.
Incretins, such as glucagon-like peptide-1 (GLP)-1, have been shown to elevate plasma insulin concentration. The purpose of this study is to investigate the cellular and molecular basis of the beneficial effects of GLP-1. Normal and diabetic male Wistar rats were treated with GLP-1 (50 ng/kg body weight) for 10 weeks. At the end of the experiment, pancreatic tissues were taken for immunohistochemistry, immunoelectron microscopy and real-time polymerase chain reaction studies. Samples of blood were retrieved from the animals for the measurement of enzymes and insulin. The results show that treatment of diabetic rats with GLP-1 caused significant (P < 0.05) reduction in body weight gain and blood glucose level. GLP-1 (10(-12)-10(-6) M) induced significant (P < 0.01) dose-dependent increases in insulin release from the pancreas of normal and diabetic rats compared to basal. Diabetes-induced abnormal liver (aspartate aminotransferase and alanine aminotransferase) and kidney (blood urea nitrogen and uric acid) parameters were corrected in GLP-1-treated rats compared to controls. GLP-1 treatment induced significant (P < 0.05) elevation in the expression of pancreatic duodenal homeobox-1, heat shock protein-70, glutathione peroxidase, insulin receptor and GLP-1-receptor genes in diabetic animals compared to controls. GLP-1 is present in pancreatic beta cells and significantly (P < 0.05) increased the number of insulin-, glutathione reductase- and catalase-immunoreactive islet cells. The results of this study show that GLP-1 is co-localized with insulin and seems to exert its beneficial effects by increasing cellular concentrations of endogenous antioxidant genes and other genes involved in the maintenance of pancreatic beta cell structure and function.
肠促胰岛素,如胰高血糖素样肽-1(GLP-1),已被证明可提高血浆胰岛素浓度。本研究的目的是探讨GLP-1有益作用的细胞和分子基础。将正常和糖尿病雄性Wistar大鼠用GLP-1(50 ng/kg体重)治疗10周。实验结束时,取胰腺组织进行免疫组织化学、免疫电子显微镜和实时聚合酶链反应研究。从动物身上采集血样以测量酶和胰岛素。结果表明,用GLP-1治疗糖尿病大鼠可使体重增加和血糖水平显著降低(P<0.05)。与基础值相比,GLP-1(10^(-12)-10^(-6) M)可使正常和糖尿病大鼠胰腺胰岛素释放显著增加(P<0.01),呈剂量依赖性。与对照组相比,GLP-1治疗的大鼠纠正了糖尿病诱导的肝脏(天冬氨酸转氨酶和丙氨酸转氨酶)和肾脏(血尿素氮和尿酸)参数异常。与对照组相比,GLP-1治疗可使糖尿病动物胰腺十二指肠同源盒-1、热休克蛋白-70、谷胱甘肽过氧化物酶、胰岛素受体和GLP-1受体基因的表达显著升高(P<0.05)。GLP-1存在于胰腺β细胞中,可使胰岛素、谷胱甘肽还原酶和过氧化氢酶免疫反应性胰岛细胞数量显著增加(P<0.05)。本研究结果表明,GLP-1与胰岛素共定位,似乎通过增加内源性抗氧化基因和其他参与维持胰腺β细胞结构和功能的基因的细胞浓度发挥其有益作用。