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Effects of bezafibrate on beta-cell function of rat pancreatic islets.

机译:苯扎贝特对大鼠胰岛β细胞功能的影响。

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摘要

Bezafibrate is an activator of peroxisome proliferator-activated receptors (PPAR) alpha. The present study was performed to investigate the effects of bezafibrate and the PPAR alpha activator, 4-Cholro-6-(2.3-xylidino)-2-pyrimidin-ylthio acetic acid (WY14643), on the beta-cell function of rat pancreatic islets in vitro. In islets cultured with 300 microM bezafibrate or WY14643 for 8 h, a low glucose concentration induced insulin release and increased the levels of mRNA for PPAR alpha, acyl CoA oxidase, carnitine palmitoyl transferase-1, pyruvate dehydrogenase E1 alpha or pyruvate carboxylase. In contrast, after a 48-h culture period, a high glucose concentration induced insulin release and islet insulin content, but decreased the levels of mRNA for glucose transporter-2 (GLUT-2), preproinsulin or pancreatic/duodenal homeobox-1. Diazoxide, the KATP channel opener, restored these responses. We conclude that bezafibrate enhances insulin release through the activation of PPAR alpha gene expression during a short culture period, whereas it may contribute to beta-cell dysfunction through the mechanism of "excessive stimulation" during longer culture periods.
机译:苯扎贝特是过氧化物酶体增殖物激活受体(PPAR)α的激活剂。进行本研究以研究苯扎贝特和PPARα激活剂4-Cholro-6-(2.3-xylidino)-2-pyrimidin-ylthio乙酸(WY14643)对大鼠胰岛β细胞功能的影响体外。在用300 microM苯甲酸酯或WY14643培养8小时的胰岛中,低葡萄糖浓度会诱导胰岛素释放,并增加PPARα,酰基辅酶A氧化酶,肉碱棕榈酰转移酶-1,丙酮酸脱氢酶E1α或丙酮酸羧化酶的mRNA水平。相反,在培养48小时后,高浓度的葡萄糖诱导了胰岛素的释放和胰岛胰岛素的含量,但降低了葡萄糖转运蛋白2(GLUT-2),胰岛素原或胰腺/十二指肠同源盒1的mRNA水平。 KATP通道开放剂二氮嗪恢复了这些反应。我们得出的结论是,苯扎贝特通过在短培养期间激活PPARα基因表达来增强胰岛素释放,而它可能通过长培养期间的“过度刺激”机制导致β细胞功能障碍。

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