Kishibayashi N, Karasawa A
Department of Pharmacology, Kyowa Hakko Kogyo Co., Ltd., Shizuoka, Japan.
Jpn J Pharmacol. 1995 Nov;69(3):269-72. doi: 10.1254/jjp.69.269.
We examined the effects of KW-5092 ((1-[2-[[[5-(piperidinomethyl)-2-furanyl]methyl]-amino]ethyl]- 2-imidazolidinylidene) propanedinitrile fumarate), a novel gastroprokinetic agent, on gastric mucosal blood flow (GMBF) in anesthetized rats. Intravenous infusion of KW-5092 (0.1 mg/kg/min for 30 min), which did not affect the basal GMBF, reversed the norepinephrine (1 microgram/kg/min, i.v. infusion for 30 min)-induced decline of GMBF in the corpus and the antrum. The improvement by KW-5092 of the GMBF was abolished by atropine (0.1 mg/kg/min, i.v. infusion for 30 min). These results suggest that KW-5092, via cholinergic activation, could counteract the decline of GMBF induced by adrenergic activation.
我们研究了新型促胃动力药KW - 5092(富马酸(1 - [2 - [[[5 - (哌啶甲基) - 2 - 呋喃基]甲基] - 氨基]乙基] - 2 - 咪唑烷叉)丙二腈)对麻醉大鼠胃黏膜血流量(GMBF)的影响。静脉输注KW - 5092(0.1毫克/千克/分钟,持续30分钟),这并未影响基础GMBF,却逆转了去甲肾上腺素(1微克/千克/分钟,静脉输注30分钟)诱导的胃体和胃窦GMBF下降。KW - 5092对GMBF的改善作用被阿托品(0.1毫克/千克/分钟,静脉输注30分钟)消除。这些结果表明,KW - 5092可通过胆碱能激活来抵消肾上腺素能激活诱导的GMBF下降。