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3-N-(3-[3-(1-哌啶甲基)苯氧基]丙基)氨基-4-氨基-1,2,5-噻二唑-1-氧化物(L-643,441)明显的不可逆H2受体阻断作用及延长的胃抗分泌活性

Apparent irreversible H2-receptor blocking and prolonged gastric antisecretory activities of 3-N-(3-[3-(1-piperidinomethyl)phenoxy]propyl) amino-4-amino-1,2,5-thiadiazole-1-oxide (L-643, 441).

作者信息

Torchiana M L, Pendleton R G, Cook P G, Hanson C A, Clineschmidt B V

出版信息

J Pharmacol Exp Ther. 1983 Mar;224(3):514-9.

PMID:6131118
Abstract

L-643,441 is a highly potent histamine H2-receptor antagonist in guinea-pig atria, acting via a unique mechanism. Unlike ranitidine, the onset of action of this compound was slow and its inhibitory action persisted after repeated washing of the tissues. Preincubation of atria with ranitidine, however, protected the H2-receptor from the apparently irreversible antagonism of L-643,441. H2-receptor antagonism produced by L-643,441 was not surmountable by increasing the concentration of dimaprit. The compound did not alter the response of this tissue to isoproterenol or affect basal atrial rate under conditions in which maximal H2-receptor blockade was achieved. In dogs, L-643,441 was effective both orally and i.v. in inhibiting gastric acid secretion evoked by histamine, gastrin, 2-deoxy-D-glucose and food. Orally, it was equipotent with ranitidine against histamine-induced secretion, but the duration of action of L-643,441 was substantially longer.

摘要

L-643,441是一种在豚鼠心房中具有高效能的组胺H2受体拮抗剂,其作用机制独特。与雷尼替丁不同,该化合物的起效缓慢,且在组织反复冲洗后其抑制作用仍持续存在。然而,心房预先用雷尼替丁孵育可保护H2受体免受L-643,441明显不可逆的拮抗作用。增加二甲双胍的浓度并不能克服L-643,441产生的H2受体拮抗作用。在达到最大H2受体阻断的条件下,该化合物不会改变该组织对异丙肾上腺素的反应,也不会影响基础心房率。在犬类中,L-643,441口服和静脉注射均能有效抑制组胺、胃泌素、2-脱氧-D-葡萄糖和食物引起的胃酸分泌。口服时,它在抑制组胺诱导的分泌方面与雷尼替丁等效,但L-643,441的作用持续时间长得多。

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