Gardemann A, Jungermann K
Biol Chem Hoppe Seyler. 1986 Jul;367(7):559-66. doi: 10.1515/bchm3.1986.367.2.559.
Electrical stimulation of the nerve bundles around the hepatic artery and the portal vein activates both the sympathetic and parasympathetic liver nerves; the sympathetic effects clearly predominate. Parasympathetic effects were therefore studied in the rat liver perfused in situ by perivascular nerve stimulation in the presence of both an alpha- and a beta-blocker. In the presence of the alpha-blocker phentolamine and the beta-blocker propranolol all sympathetic nerve effects were prevented; the remaining parasympathetic stimulation had no influence on the basal glucose and lactate metabolism nor on the hemodynamics. Insulin alone, with both alpha- and beta-blockade, provoked a small, parasympathetic nerve stimulation in the presence of insulin a more pronounced enhancement of glucose utilization. In the presence of an alpha- and beta-blocker perivascular nerve stimulation antagonized the glucagon stimulated glucose release, but did not affect lactate exchange. The nerve effect was abolished by the parasympathetic antagonist atropine. Acetylcholine or insulin, with both an alpha- and beta-blocker present, mimicked the effects of nerve stimulation antagonizing the glucagon-stimulated glucose release. Nerve stimulation in the presence of insulin was more effective than either stimulus alone. The present results show that in rat liver stimulation of the parasympathetic hepatic nerves has direct effects on glucose metabolism synergistic with insulin and antagonistic to glucagon.
对肝动脉和门静脉周围神经束进行电刺激会激活肝脏的交感神经和副交感神经;其中交感神经的作用明显占主导。因此,在同时使用α受体阻滞剂和β受体阻滞剂的情况下,通过对大鼠原位灌注肝脏的血管周围神经进行刺激来研究副交感神经的作用。在使用α受体阻滞剂酚妥拉明和β受体阻滞剂普萘洛尔时,所有交感神经的作用均被阻断;剩余的副交感神经刺激对基础葡萄糖和乳酸代谢以及血流动力学均无影响。单独使用胰岛素时,在α受体和β受体均被阻断的情况下,会引发轻微的副交感神经刺激,而在有胰岛素存在时,葡萄糖利用会有更明显的增强。在同时存在α受体阻滞剂和β受体阻滞剂的情况下,血管周围神经刺激会拮抗胰高血糖素刺激的葡萄糖释放,但不影响乳酸交换。副交感神经拮抗剂阿托品可消除神经效应。在同时存在α受体阻滞剂和β受体阻滞剂的情况下,乙酰胆碱或胰岛素可模拟神经刺激的作用,拮抗胰高血糖素刺激的葡萄糖释放。在有胰岛素存在的情况下,神经刺激比单独任何一种刺激都更有效。目前的结果表明,在大鼠肝脏中,刺激副交感肝神经对葡萄糖代谢有直接作用,与胰岛素协同,拮抗胰高血糖素。