Sim S S, Yoon S H, Hahn S J, Jo Y H, Kim C C, Kim M S
Dept. of Physiology, Catholic University Medical College, Seoul, Korea.
Scand J Gastroenterol. 1989 Oct;24(8):961-8. doi: 10.3109/00365528909089241.
The effect of histamine on contractile and electric activity was studied in the isolated stomach muscle strips of 138 cats. Histamine dose-dependently produced tonic and phasic contractions of the muscle preparations from the fundus and the corpus but only phasic contraction of the antral muscle preparations. The frequency of gastric slow waves (SWs) was also increased dose-dependently by histamine. The responses of muscle contractions and gastric SW frequency to histamine were completely blocked by pretreatment with pyrilamine (10(-6) M) and were significantly inhibited by atropine (10(-5) M) but not by cimetidine (10(-5) M), hexamethonium (10(-5) M), phentolamine (10(-5) M), or propranolol (10(-5) M). The inhibition by pyrilamine was competitive. Although atropine inhibited the effect of histamine significantly, it could not completely block the effect of histamine even at a high concentration (3 x 10(-5) M). It is concluded that histamine may participate in the regulation of gastric motility in the cat by acting on the H1 receptor to cause the release of acetylcholine and also other contractile substance(s).
在138只猫的离体胃肌条上研究了组胺对收缩和电活动的影响。组胺剂量依赖性地引起胃底和胃体肌条的强直性和相性收缩,但仅引起胃窦肌条的相性收缩。组胺还剂量依赖性地增加胃慢波(SWs)的频率。用吡苄明(10^(-6) M)预处理可完全阻断肌肉收缩和胃SW频率对组胺的反应,阿托品(10^(-5) M)可显著抑制该反应,但西咪替丁(10^(-5) M)、六甲铵(10^(-5) M)、酚妥拉明(10^(-5) M)或普萘洛尔(10^(-5) M)则无此作用。吡苄明的抑制作用具有竞争性。虽然阿托品显著抑制组胺的作用,但即使在高浓度(3×10^(-5) M)下也不能完全阻断组胺的作用。结论是,组胺可能通过作用于H1受体导致乙酰胆碱及其他收缩物质的释放,从而参与猫胃动力的调节。