Scarpignato C, Capovilla T, Bertaccini G
Arch Int Pharmacodyn Ther. 1980 Aug;246(2):286-94.
Caerulein was shown to delay gastric emptying in conscious rats in a dose-dependent fashion. The threshold dose was about 0.05 mug/kg by the intraperitoneal route. Maximum effect was obtained with 5 mug/kg. Neutralization of acidity or reduction of gastric juice by mean of NaHCO3 or cimetidine, respectively, did not modify the effect of the peptide. Chlorpheniramine was similarly ineffective. The effect of caerulein on gastric emptying was most probably connected with a strong contraction of the gastroduodenal junction previously observed in different experimental conditions and was not affected by H1- or H2-histamine antagonists. The C-terminal heptapeptide of cholecystokinin behaved quite similarly to caerulein. The present study emphasizes the close parallelism between results obtained in the in situ stomach preparation of anaesthetized rats and gastric emptying in conscious animals.
已证明蛙皮素能以剂量依赖方式延缓清醒大鼠的胃排空。腹腔注射途径的阈剂量约为0.05微克/千克。5微克/千克时可获得最大效应。分别用碳酸氢钠或西咪替丁中和酸度或减少胃液分泌,均未改变该肽的作用。氯苯那敏同样无效。蛙皮素对胃排空的作用很可能与先前在不同实验条件下观察到的胃十二指肠连接处的强烈收缩有关,且不受H1或H2组胺拮抗剂的影响。胆囊收缩素的C末端七肽的表现与蛙皮素非常相似。本研究强调了在麻醉大鼠原位胃制备中获得的结果与清醒动物胃排空之间的密切平行关系。