Jungermann K
Z Gastroenterol. 1987 Apr;25 Suppl 1:44-54.
The liver is innervated by sympathetic and parasympathetic nerves. The effects and mechanisms of actions of hepatic nerves were studied in the isolated rat, guinea pig and Tupaia liver perfused in a non-recirculating manner either via the portal vein or via both the hepatic artery and the portal vein. The arterial plexus was stimulated at the common hepatic artery, the portal plexus at the mesenteric vein or both plexus jointly at the artery and the portal vein in the liver hilus (1-20 Hz, 2 ms, 20 V, 0.5-5 min). Upon nerve stimulation sympathetic effects clearly predominated; parasympathetic actions could only be demonstrated in the presence of alpha- and beta-antagonists. Sympathetic stimulation increased glucose output, shifted lactate uptake to output, decreased ketone body, urea and glutamine formation as well as ammonia uptake, lowered oxygen uptake, reduced perfusion flow combined with an intrahepatic redistribution and perfusate mobilization, and caused an overflow of noradrenaline into the hepatic vein. All effects were mediated predominantly via alpha-receptors; they were dependent on extracellular calcium. Some effects were modulated by hormones: the glucagon-mediated increase of glucose output was further enhanced but that of lactate uptake was decreased by nerve stimulation; in the presence of insulin glucose output was increased only slightly. Parasympathetic stimulation had no effect on basal metabolism or hemodynamics. Yet, it antagonized the glucagon-stimulated glucose release and enhanced the slight, insulin-dependent increase of glucose utilization. The sympathetic nerves may act directly at the parenchymal cells or indirectly via an overflow of neurotransmitter from the vasculature or via hemodynamic changes. Experiments with the vessel relaxant sodium nitroprusside and with retrograde perfusion indicate that neither hemodynamic alterations nor noradrenaline overflow from the vasculature play a major role in the sympathetic alterations in glucose and lactate metabolism; rather the nerves appear to act directly within the parenchyma. Comparative studies with rat, guinea pig and tupaia livers corroborate the view that the sympathetic nerves act in the rat via contacts to only a few periportal hepatocytes with signal propagation through gap junctions, while they act in the guinea pig and tupaia via contacts to almost all parenchymal cells. Sympathetic nerve stimulation caused an increase in the activity of glycogen phosphorylase and a decrease of glycogen synthase; it left the activity of pyruvate kinase and the levels of fructose 2.6-bisphosphate and cyclic AMP unaltered.(ABSTRACT TRUNCATED AT 400 WORDS)
肝脏受交感神经和副交感神经支配。通过对经门静脉或经肝动脉和门静脉以非循环方式灌注的离体大鼠、豚鼠和树鼩肝脏进行研究,探讨了肝神经的作用及其作用机制。在肝总动脉刺激动脉丛,在肠系膜静脉刺激门静脉丛,或在肝门处联合刺激动脉和门静脉丛(1 - 20Hz,2ms,20V,0.5 - 5分钟)。神经刺激后,交感效应明显占主导;只有在存在α和β拮抗剂的情况下才能显示出副交感作用。交感神经刺激增加葡萄糖输出,使乳酸摄取转变为输出,减少酮体、尿素和谷氨酰胺的生成以及氨摄取,降低氧摄取,减少灌注流量并伴有肝内再分布和灌注液动员,还导致去甲肾上腺素溢入肝静脉。所有这些效应主要通过α受体介导;它们依赖于细胞外钙。一些效应受激素调节:胰高血糖素介导的葡萄糖输出增加在神经刺激下进一步增强,但乳酸摄取的增加则减少;在胰岛素存在的情况下,葡萄糖输出仅略有增加。副交感神经刺激对基础代谢或血流动力学无影响。然而,它拮抗胰高血糖素刺激的葡萄糖释放,并增强胰岛素依赖性的轻微葡萄糖利用增加。交感神经可能直接作用于实质细胞,或通过血管系统中神经递质的溢出或血流动力学变化间接起作用。使用血管舒张剂硝普钠和逆行灌注的实验表明,血流动力学改变和血管系统中去甲肾上腺素的溢出在交感神经对葡萄糖和乳酸代谢的改变中均不起主要作用;相反,神经似乎直接在实质内起作用。对大鼠、豚鼠和树鼩肝脏的比较研究证实了这样一种观点,即交感神经在大鼠中仅通过与少数门静脉周围肝细胞接触并通过缝隙连接进行信号传播来发挥作用,而在豚鼠和树鼩中则通过与几乎所有实质细胞接触来发挥作用。交感神经刺激导致糖原磷酸化酶活性增加,糖原合酶活性降低;丙酮酸激酶活性、果糖2,6 - 二磷酸水平和环磷酸腺苷水平未发生改变。(摘要截短至400字)