Yokotani K, Fujiwara M
J Pharmacol Exp Ther. 1985 Mar;232(3):826-30.
Effects of substance P (SP) on gastric acid secretion and mucosal blood flow (MBF) were examined in anesthetized Wistar rats. Intravenous infusion of graded doses of SP (5 and 10 nmol/kg/min) had no effects on either the basal gastric acid secretion or on the MBF. When gastric acid secretion was increased by giving a supramaximal dose of bethanechol (10 micrograms/kg/min), a muscarinic parasympathetic stimulant, SP had no effect on the gastric acid secretion but did decrease the MBF. On the other hand, when gastric acid secretion was increased by left cervical vagus nerve stimulation (0.5 mA, 3 Hz, 0.5 msec duration), SP inhibited both acid secretion and MBF, in a dose-dependent manner. The inhibitory effects of SP on the vagally stimulated gastric responses were not affected by pretreatment with phentolamine (5 mg/kg i.m.), propranolol (10 mg/kg i.m.), mepyramine (20 mg/kg i.m.) or indomethacin (30 mg/kg i.v., followed by 4 mg/kg/hr). These findings suggest that SP acts directly on the gastric vascular system and decreases gastric MBF, and that this substance also acts on the parasympathetic neurons in the gastric wall and inhibits the vagally stimulated gastric acid secretion. The inhibitory effects of SP on the gastric acid secretion do not appear to be mediated by adrenergic or by histamine H-1 receptor-, prostaglandin-involved mechanisms.
在麻醉的Wistar大鼠中研究了P物质(SP)对胃酸分泌和黏膜血流量(MBF)的影响。静脉输注不同剂量的SP(5和10 nmol/kg/min)对基础胃酸分泌和MBF均无影响。当给予超大剂量的毒蕈碱型副交感神经兴奋剂氨甲酰甲胆碱(10微克/千克/分钟)使胃酸分泌增加时,SP对胃酸分泌无影响,但可降低MBF。另一方面,当通过左颈迷走神经刺激(0.5 mA,3 Hz,0.5毫秒持续时间)使胃酸分泌增加时,SP以剂量依赖的方式抑制胃酸分泌和MBF。SP对迷走神经刺激的胃反应的抑制作用不受酚妥拉明(5毫克/千克,肌肉注射)、普萘洛尔(10毫克/千克,肌肉注射)、美吡拉敏(20毫克/千克,肌肉注射)或吲哚美辛(30毫克/千克,静脉注射,随后4毫克/千克/小时)预处理的影响。这些发现表明,SP直接作用于胃血管系统并降低胃MBF,并且该物质还作用于胃壁中的副交感神经元并抑制迷走神经刺激的胃酸分泌。SP对胃酸分泌的抑制作用似乎不是由肾上腺素能或组胺H-1受体、前列腺素参与的机制介导的。