Lin W C, Yano S, Watanabe K
Department of Drug Evaluation and Toxicological Sciences, Faculty of Pharmaceutical Sciences, Chiba University, Japan.
Jpn J Pharmacol. 1989 Feb;49(2):267-74. doi: 10.1254/jjp.49.267.
Effect of intravenous administration of GABA antagonists on gastric acid secretion in perfused stomachs was studied in rats anesthetized with urethane. Bethanechol (BeCh)-stimulated acid secretion was definitely inhibited by bicuculline, a GABA antagonist, and strychnine, a glycine antagonist, but not by picrotoxin and pentylenetetrazol, GABA antagonists. The inhibitory effect of bicuculline and strychnine was accompanied by vigorous convulsions. Only the bicuculline-induced inhibition was still seen in d-tubocurarine paralyzed rats, and it was abolished in spinal rats. 2-Deoxy-D-glucose (2-DG)-stimulated acid secretion was apparently depressed by all the GABA antagonists of bicuculline, picrotoxin and pentylenetetrazol. The inhibitory effect of picrotoxin, but not bicuculline, on the 2-DG stimulation was still elicited in spinal rats. Inhibition of acid secretion stimulated by pentobarbital, a centrally acting secretagogue, was produced by picrotoxin and pentylenetetrazol in spinal rats. These findings suggest that bicuculline acts centrally to inhibit acid secretion stimulated both peripherally by BeCh and centrally by 2-DG, besides nonspecific mechanisms due to convulsions, and the action would be directed to centers which are implicated in stimulation of the sympatho-adrenomedullary system; picrotoxin and pentylenetetrazol also act centrally to inhibit 2-DG- or pentobarbital-stimulated acid secretion through depression of the central vagal tone which leads to inhibition of gastric acid secretion.
在用氨基甲酸乙酯麻醉的大鼠中,研究了静脉注射γ-氨基丁酸(GABA)拮抗剂对灌流胃胃酸分泌的影响。毒蕈碱(BeCh)刺激的胃酸分泌被GABA拮抗剂荷包牡丹碱和甘氨酸拮抗剂士的宁明确抑制,但未被GABA拮抗剂苦味毒和戊四氮抑制。荷包牡丹碱和士的宁的抑制作用伴随着剧烈惊厥。在筒箭毒碱麻痹的大鼠中仍可见荷包牡丹碱诱导的抑制作用,而在脊髓大鼠中则消失。2-脱氧-D-葡萄糖(2-DG)刺激的胃酸分泌明显受到荷包牡丹碱、苦味毒和戊四氮等所有GABA拮抗剂的抑制。苦味毒而非荷包牡丹碱对2-DG刺激的抑制作用在脊髓大鼠中仍可引发。在脊髓大鼠中,苦味毒和戊四氮可抑制由中枢作用的促分泌剂戊巴比妥刺激的胃酸分泌。这些发现表明,荷包牡丹碱除了通过惊厥产生的非特异性机制外,还通过中枢作用抑制由BeCh外周刺激和2-DG中枢刺激的胃酸分泌,其作用将针对与交感-肾上腺髓质系统刺激有关的中枢;苦味毒和戊四氮也通过中枢作用抑制2-DG或戊巴比妥刺激的胃酸分泌,其机制是通过降低中枢迷走神经张力从而抑制胃酸分泌。