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卢帕他定,一种新型强效的组胺和血小板活化因子(PAF)口服活性双重拮抗剂。

Rupatadine, a new potent, orally active dual antagonist of histamine and platelet-activating factor (PAF).

作者信息

Merlos M, Giral M, Balsa D, Ferrando R, Queralt M, Puigdemont A, García-Rafanell J, Forn J

机构信息

Department of Pharmacology, Research Center, J. Uriach & Cía, Barcelona, Spain.

出版信息

J Pharmacol Exp Ther. 1997 Jan;280(1):114-21.

PMID:8996188
Abstract

Rupatadine (UR-12592, 8-chloro-6, 11-dihydro-11-[1-[(5-methyl3-pyridinyl) methyl]-4-piperidinylidene]-5H-benzo[5,6]-cyclohepta[1,2b]pyridine ) is a novel compound that inhibits both platelet-activating factor (PAF) and histamine (H1) effects through its interaction with specific receptors (Ki(app) values against [3H]WEB-2086 binding to rabbit platelet membranes and [3H]-pyrilamine binding to guinea pig cerebellum membranes were 0.55 and 0.10 microM, respectively). Rupatadine competitively inhibited histamine-induced guinea pig ileum contraction (pA2 = 9.29 +/- 0.06) without affecting contraction induced by ACh, serotonin or leukotriene D4 (LTD4). It also competitively inhibited PAF-induced platelet aggregation in washed rabbit platelets (WRP) (pA2 = 6.68 +/- 0.08) and in human platelet-rich plasma (HPRP) (IC50 = 0.68 microM), while not affecting ADP- or arachidonic acid-induced platelet aggregation. Rupatadine blocked histamine- and PAF-induced effects in vivo, such as hypotension in rats (ID50 = 1.4 and 0.44 mg/kg i.v., respectively) and bronchoconstriction in guinea pigs (ID50 = 113 and 9.6 micrograms/kg i.v.). Moreover, it potently inhibited PAF-induced mortality in mice (ID50 = 0.31 and 3.0 mg/kg i.v. and p.o., respectively) and endotoxin-induced mortality in mice and rats (ID50 = 1.6 and 0.66 mg/kg i.v.). Rupatadine's duration of action was long, as assessed by the histamine- and PAF-induced increase in vascular permeability test in dogs (42 and 34% inhibition at 26 h after 1 mg/kg p.o.). Rupatadine at a dose of 100 mg/kg p.o. neither modified spontaneous motor activity nor prolonged barbiturate-sleeping time in mice, which indicates a lack of sedative effects. Overall, rupatadine combines histamine and PAF antagonist activities in vivo with high potency, the antihistamine properties being similar to or higher than those of loratadine, whereas rupatadine's PAF antagonist effects were near those of WEB-2066. Rupatadine is therefore a good candidate for further development in the treatment of allergic and inflammatory conditions in which both PAF and histamine are implicated.

摘要

卢帕他定(UR - 12592,8 - 氯 - 6,11 - 二氢 - 11 - [1 - [(5 - 甲基 - 3 - 吡啶基)甲基] - 4 - 哌啶亚基] - 5H - 苯并[5,6] - 环庚[1,2 - b]吡啶)是一种新型化合物,它通过与特定受体相互作用来抑制血小板活化因子(PAF)和组胺(H1)的作用(针对[3H] - WEB - 2086与兔血小板膜结合以及[3H] - 吡苄明与豚鼠小脑膜结合的Ki(app)值分别为0.55和0.10微摩尔)。卢帕他定竞争性抑制组胺诱导的豚鼠回肠收缩(pA2 = 9.29±0.06),而不影响乙酰胆碱、5 - 羟色胺或白三烯D4(LTD4)诱导的收缩。它还竞争性抑制PAF诱导的洗涤兔血小板(WRP)聚集(pA2 = 6.68±0.08)以及人富血小板血浆(HPRP)中的聚集(IC50 = 0.68微摩尔),同时不影响ADP或花生四烯酸诱导的血小板聚集。卢帕他定在体内可阻断组胺和PAF诱导的效应,如大鼠的低血压(静脉注射的ID50分别为1.4和0.44毫克/千克)以及豚鼠的支气管收缩(静脉注射的ID50分别为113和9.6微克/千克))。此外,它能有效抑制PAF诱导的小鼠死亡(静脉注射和口服的ID50分别为0.31和3.0毫克/千克)以及内毒素诱导的小鼠和大鼠死亡(静脉注射的ID50分别为1.6和0.66毫克/千克)。通过组胺和PAF诱导的犬血管通透性增加试验评估,卢帕他定的作用持续时间较长(口服1毫克/千克后26小时抑制率分别为42%和34%)。口服剂量为100毫克/千克的卢帕他定既不改变小鼠的自发运动活性,也不延长巴比妥类药物诱导的睡眠时间,这表明它没有镇静作用。总体而言,卢帕他定在体内结合了高效的组胺和PAF拮抗剂活性,其抗组胺特性与氯雷他定相似或更高,而卢帕他定的PAF拮抗剂作用与WEB - 2066相近。因此,卢帕他定是治疗涉及PAF和组胺的过敏性和炎症性疾病进一步开发的良好候选药物。

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