Yamasaki K, Goto Y
Department of Pharmacology, Tokushima Bunri University, Japan.
Nihon Yakurigaku Zasshi. 1990 Jul;96(1):11-21. doi: 10.1254/fpj.96.1_11.
The effects of 2-(p-chlorophenyl)-GABA (PCPGABA), thyrotropin releasing hormone (TRH), insulin and 2-deoxy-D-glucose (2DG) on gastric acid secretion, vagal nerve efferent activity and blood glucose level were examined in anesthetized rats. The latencies of onset of hypersecretion were 10 min for TRH (1 microgram/rat, i.c.), 20 min for PCPGABA (4 mg/kg, s.c.), 60 min for 2DG (200 mg/kg, i.v.) and 90 min for insulin (2 U/kg, i.v.), respectively. The secretagogue actions of PCPGABA and TRH were more potent than those of 2DG and insulin. All these secretagogues caused the efferent activation of the cervical vagal transmission, and the latencies for these vagal activation were shorter than those seen in gastric acid hypersecretion. Atropine and vagotomy completely abolished the secretagogue actions of these stimulants. PCPGABA and TRH were ineffective on the blood glucose level, unlike insulin and 2DG. These results suggest that PCPGABA, TRH, 2DG and insulin stimulate gastric acid secretion via central vagal cholinergic pathways, even though the precise mechanisms for each stimulant seem to be different.
在麻醉大鼠中研究了2-(对氯苯基)-γ-氨基丁酸(PCPGABA)、促甲状腺激素释放激素(TRH)、胰岛素和2-脱氧-D-葡萄糖(2DG)对胃酸分泌、迷走神经传出活动和血糖水平的影响。TRH(1微克/大鼠,腹腔注射)引起胃酸分泌亢进的潜伏期为10分钟,PCPGABA(4毫克/千克,皮下注射)为20分钟,2DG(200毫克/千克,静脉注射)为60分钟,胰岛素(2单位/千克,静脉注射)为90分钟。PCPGABA和TRH的促分泌作用比2DG和胰岛素更强。所有这些促分泌剂均引起颈迷走神经传递的传出激活,且这些迷走神经激活的潜伏期短于胃酸分泌亢进时的潜伏期。阿托品和迷走神经切断术完全消除了这些刺激剂的促分泌作用。与胰岛素和2DG不同,PCPGABA和TRH对血糖水平无影响。这些结果表明,PCPGABA、TRH、2DG和胰岛素通过中枢迷走胆碱能途径刺激胃酸分泌,尽管每种刺激剂的确切机制似乎有所不同。