Luo X, Li K, Zhang C, Yang G, Yang M, Jia Y, Zhang L, Ma Z A, Boden G, Li L
The Key Laboratory of Laboratory Medical Diagnostics in the Ministry of Education and Department of Clinical Biochemistry, College of Laboratory Medicine, Chongqing Medical University, Chongqing, China.
Department of Endocrinology, Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
Int J Obes (Lond). 2016 Jun;40(6):947-54. doi: 10.1038/ijo.2016.24. Epub 2016 Feb 12.
To investigate the effects of vaspin signaling conveyed by the brain on liver glucose fluxes in rats.
To determine the effects and underlying mechanisms of central vaspin signaling, normal-chow-diet- and high-fat-diet (HFD)-fed rats with or without hepatic branch vagotomy (HBV) received acute infusion of vaspin to the third cerebral ventricle or MK801, a dorsal vagal complex (DVC) N-methyl-D-aspartate (NMDA) receptor inhibitor, to the DVC during the pancreatic euglycemic clamp.
Central administration of vaspin in HFD-fed rats significantly increased glucose infusion required to maintain euglycemia owing to an inhibition of glucose production during the clamps. These changes were accompanied by decreased hepatic phosphoenolpyruatecarboxykinase and G6Pase expression levels and increased hepatic insulin receptor, insulin receptor substrate-1, Akt kinase and the forkhead box-containing protein of the O subfamily-1 phosphorylation, suggesting improving hepatic insulin sensitivity in these animals. Conversely, selective HBV or DVC MK-801 infusion in HFD-fed rats blocked the effect of central vaspin on glucose production and hepatic insulin sensitivity.
Our findings suggest that brain vaspin inhibited hepatic glucose production and improved insulin sensitivity via DVC to the hepatic branch of the vagus nerve in insulin resistance rats induced by HFD.
研究大脑传递的内脂素信号对大鼠肝脏葡萄糖通量的影响。
为了确定中枢内脂素信号的作用及潜在机制,在正常饮食和高脂饮食(HFD)喂养的大鼠中,无论是否进行肝支迷走神经切断术(HBV),在胰腺正常血糖钳夹期间,向第三脑室急性输注内脂素或向背侧迷走神经复合体(DVC)输注MK801(一种DVC N-甲基-D-天冬氨酸(NMDA)受体抑制剂)。
在高脂饮食喂养的大鼠中,中枢给予内脂素显著增加了维持正常血糖所需的葡萄糖输注量,这是由于钳夹期间葡萄糖生成受到抑制。这些变化伴随着肝脏磷酸烯醇式丙酮酸羧激酶和葡萄糖-6-磷酸酶表达水平降低,以及肝脏胰岛素受体、胰岛素受体底物-1、Akt激酶和O亚家族-1含叉头框蛋白磷酸化增加,表明这些动物的肝脏胰岛素敏感性得到改善。相反,在高脂饮食喂养的大鼠中选择性输注HBV或DVC MK-801可阻断中枢内脂素对葡萄糖生成和肝脏胰岛素敏感性的影响。
我们的研究结果表明,在高脂饮食诱导的胰岛素抵抗大鼠中,大脑内脂素通过DVC至迷走神经肝支抑制肝脏葡萄糖生成并改善胰岛素敏感性。