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连接蛋白32间隙连接增强胰高血糖素和去甲肾上腺素对小鼠肝脏葡萄糖输出的刺激作用。

Connexin 32 gap junctions enhance stimulation of glucose output by glucagon and noradrenaline in mouse liver.

作者信息

Stümpel F, Ott T, Willecke K, Jungermann K

机构信息

Institut für Biochemie und Molekulare Zellbiologie, Georg-August-Universität Göttingen, Göttingen, Germany.

出版信息

Hepatology. 1998 Dec;28(6):1616-20. doi: 10.1002/hep.510280622.

Abstract

Gap junctions connect neighboring cells via intercellular channels composed of connexins (Cx). Connexin 32 (Cx32) is the main connexin in hepatocytes. Gap junctions propagate a signal from periportal to perivenous hepatocytes generated by electrical stimulation of sympathetic liver nerves. Therefore, it was the aim of this study to examine the involvement of hepatocellular gap junctions in hormonal regulation. In perfused livers from wild-type mice and Cx32-deficient mice, the stimulation of glucose release by varying noradrenaline and glucagon concentrations was investigated. At saturating hormone concentrations, glucose release was the same in wild-type and Cx32-deficient livers. However, glucose output was significantly smaller in Cx32-deficient than wild-type livers at half-maximally effective hormone concentrations. Because the two hormones circulate at less than half-saturating concentrations and because they are degraded during passage of blood through the liver, they lose efficiency from the periportal to the perivenous zone. In wild-type livers, this decrease in efficiency can be partially compensated by intercellular signal propagation through gap junctions, resulting in higher hormone actions than in Cx32-deficient livers. It is concluded that gap junctions are not only involved in intercellular propagation of nervous, but also of hormonal signals from periportal to perivenous hepatocytes.

摘要

缝隙连接通过由连接蛋白(Cx)组成的细胞间通道连接相邻细胞。连接蛋白32(Cx32)是肝细胞中的主要连接蛋白。缝隙连接将交感肝神经电刺激产生的信号从门静脉周围肝细胞传播到肝静脉周围肝细胞。因此,本研究的目的是研究肝细胞缝隙连接在激素调节中的作用。在野生型小鼠和Cx32缺陷型小鼠的灌注肝脏中,研究了通过改变去甲肾上腺素和胰高血糖素浓度来刺激葡萄糖释放的情况。在激素浓度饱和时,野生型和Cx32缺陷型肝脏中的葡萄糖释放量相同。然而,在激素浓度达到半数最大效应时,Cx32缺陷型肝脏中的葡萄糖输出量明显低于野生型肝脏。由于这两种激素在血液循环中的浓度低于半数饱和浓度,并且在血液流经肝脏的过程中会被降解,它们从门静脉周围区域到肝静脉周围区域的效率会降低。在野生型肝脏中,这种效率的降低可以通过缝隙连接进行的细胞间信号传播得到部分补偿,从而导致激素作用比Cx32缺陷型肝脏更高。结论是,缝隙连接不仅参与神经信号的细胞间传播,也参与从门静脉周围肝细胞到肝静脉周围肝细胞的激素信号传播。

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