Masliński S, Sewing K F
Digestion. 1977 Feb;15(2):121-8. doi: 10.1159/000197993.
In conscious rats and in anaesthetized gastric fistula rats, the effects of low and high doses of the histamine H2-receptor antagonist cimetidine was studied on gastric mucosal histamine concentration and histidine decarboxylase activity with or without concomitant administration of pentagastrin. In conscious animals a singleinjection of pentagastrin reduced gastric mucosal histamine concentration and elevated histidine decarboxylase activity. This effect was not antagonized by low doses of cimetidine. High doses of cimetidine, like pentagastrin, reduced the histamine concentration and elevated the histidine decarboxylase activity. In anaesthetized rats low doses of cimetidine and reduced gastric acid secretion. The effects of cimetidine on gastric mucosal histamine and histidine decarboxylase were less pronounced than in conscious animals. The histidine decarboxylase stimulating activity of high doses of cimetidine was not abolished by gastric perfusion with acid suggesting that endogenously released gastrin is not involved. A feedback relationship between the blockade of the target organ and increased histamine biosynthesis is discussed.
在清醒大鼠和麻醉的胃瘘大鼠中,研究了低剂量和高剂量组胺H2受体拮抗剂西咪替丁对胃黏膜组胺浓度和组氨酸脱羧酶活性的影响,实验中伴有或不伴有五肽胃泌素的给药。在清醒动物中,单次注射五肽胃泌素可降低胃黏膜组胺浓度并提高组氨酸脱羧酶活性。低剂量西咪替丁并未拮抗此作用。高剂量西咪替丁与五肽胃泌素一样,可降低组胺浓度并提高组氨酸脱羧酶活性。在麻醉大鼠中,低剂量西咪替丁可减少胃酸分泌。西咪替丁对胃黏膜组胺和组氨酸脱羧酶的作用不如在清醒动物中明显。高剂量西咪替丁的组氨酸脱羧酶刺激活性不会因胃酸灌注而被消除,这表明内源性释放的胃泌素未参与其中。文中讨论了靶器官阻断与组胺生物合成增加之间的反馈关系。