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S 16118(对胍基苯甲酰基-[Hyp3,Thi5,D-Tic7,Oic8]缓激肽)在体外和体内都是一种强效且长效的缓激肽B2受体拮抗剂。

S 16118 (p-guanidobenzoyl-[Hyp3,Thi5,D-Tic7,Oic8]bradykinin) is a potent and long-acting bradykinin B2 receptor antagonist, in vitro and in vivo.

作者信息

Félétou M, Robineau P, Lonchampt M, Bonnardel E, Thurieau C, Fauchère J L, Widdowson P, Mahieu J P, Serkiz B, Volland J P

机构信息

Division de Pneumologie, Institut de Recherches Servier, Suresnes, France.

出版信息

J Pharmacol Exp Ther. 1995 Jun;273(3):1071-7.

PMID:7791077
Abstract

The in vitro and in vivo effects of S 16118 [p-guanidobenzoyl-[Hyp3, Thi5,D-Tic7,Oic8]bradykinin (BK)], a new BK receptor antagonist, were studied. S 16118 inhibited the contraction produced by BK in the rabbit jugular vein, but was ineffective in the rabbit aorta, indicating the BK B2 receptor specificity of the compound. In isolated organs from various species including humans, S 16118 was a potent antagonist (Ki, pA2 or pKB value from 9.58-7.37). The effect of S 16118 was specific as it did not show any affinity for a number of other receptors or channels and did not possess residual agonistic properties in most of the tissues studied. Furthermore, S 16118 is a poor secretagogue agent either in the rat or human mast cells and is resistant to degradation with an in vitro half-life in blood from different species, including humans, of more than 24 hr. In vivo, in the rabbit, i.v. injection of S 16118 inhibited the hypotension induced by BK up to 4 hr after administration. In the guinea pig, it was also effective in inhibiting the bronchoconstriction induced by BK, although when administered i.v. it had a shorter duration than in the rabbit. However, in the same species, when aerosolized, S 16118 was effective and long-acting against BK-induced bronchoconstriction. Changes in permeability induced by BK injection in the guinea pig trachea and bronchus, and by BK superfusion in the hamster cheek pouch, were abolished by i.v. pretreatment with S 16118.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了新型缓激肽(BK)受体拮抗剂S 16118 [对胍基苯甲酰基-[Hyp3, Thi5,D-Tic7,Oic8]缓激肽]的体外和体内效应。S 16118抑制BK在兔颈静脉引起的收缩,但对兔主动脉无效,表明该化合物具有BK B2受体特异性。在包括人类在内的各种物种的离体器官中,S 16118是一种强效拮抗剂(Ki、pA2或pKB值为9.58 - 7.37)。S 16118的作用具有特异性,因为它对许多其他受体或通道没有任何亲和力,并且在大多数研究的组织中不具有残留激动特性。此外,S 16118在大鼠或人类肥大细胞中是一种较弱的促分泌剂,并且在包括人类在内的不同物种的血液中具有抗降解能力,体外半衰期超过24小时。在体内,在兔中,静脉注射S 16118可在给药后长达4小时内抑制BK诱导的低血压。在豚鼠中,它也能有效抑制BK诱导的支气管收缩,尽管静脉注射时其作用持续时间比在兔中短。然而,在同一物种中,雾化给药时,S 16118对BK诱导的支气管收缩有效且作用持久。豚鼠气管和支气管中BK注射以及仓鼠颊囊中BK灌流引起的通透性变化,在静脉注射S 16118预处理后被消除。(摘要截短于250字)

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