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组胺受体在吗啡诱导的小鼠纳洛酮效力增强中的作用。

The involvement of histamine receptors in morphine-induced increased naloxone potency in mice.

作者信息

Wong C L

出版信息

Methods Find Exp Clin Pharmacol. 1985 Feb;7(2):69-74.

PMID:3990446
Abstract

In the present study, the effect of histamine agonists and antagonists on morphine antinociception and naloxone antagonism were studied. The antinociceptive effect of morphine and the antagonistic effect of naloxone were measured by the acetic acid-induced abdominal constriction test in mice. It was found that pretreatment with 2-methylhistamine, a histamine H1-receptor agonist, altered neither the antinociceptive effect of morphine nor the antagonistic effect of naloxone. When 2-methylhistamine was given together with morphine as pretreatment, the naloxone potency was enhanced compared with pretreatment by morphine alone. Pretreatment with 2-pyridylethylamine, another histamine H1-receptor agonist, alone or in combination with morphine, altered neither the antinociceptive activity of morphine nor the antagonistic potency of naloxone. Pretreatment with 4-methylhistamine, a histamine H2-receptor agonist, did not alter the antinociceptive activity of morphine or the antagonistic effect of naloxone. However, when given together with morphine as the pretreatment, the antinociceptive effect of morphine as well as the antagonistic activity of naloxone were enhanced. Similar effects were observed with dimaprit, another histamine H2-receptor agonist. Pretreatment with diphenhydramine, a histamine H1-receptor antagonist, alone or in combination with morphine, altered neither the antinociceptive effect of morphine nor the antagonistic activity of naloxone. Pretreatment with cimetidine, a histamine H2-receptor antagonist, did not affect the antinociceptive effect of morphine and the antagonistic potency of naloxone. However, when given together with morphine as pretreatment, it suppressed the ability of morphine in inducing an increase in naloxone potency. Similar effects were observed with ranitidine, another histamine H2-receptor blocker.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,研究了组胺激动剂和拮抗剂对吗啡镇痛及纳洛酮拮抗作用的影响。通过小鼠醋酸诱导扭体试验测定吗啡的镇痛作用和纳洛酮的拮抗作用。结果发现,组胺H1受体激动剂2-甲基组胺预处理既不改变吗啡的镇痛作用,也不改变纳洛酮的拮抗作用。当2-甲基组胺与吗啡一起作为预处理给药时,与单独用吗啡预处理相比,纳洛酮的效能增强。另一种组胺H1受体激动剂2-吡啶乙胺单独或与吗啡联合预处理,既不改变吗啡的镇痛活性,也不改变纳洛酮的拮抗效能。组胺H2受体激动剂4-甲基组胺预处理不改变吗啡的镇痛活性或纳洛酮的拮抗作用。然而,当与吗啡一起作为预处理给药时,吗啡的镇痛作用以及纳洛酮的拮抗活性均增强。另一种组胺H2受体激动剂二甲双胍也观察到类似的效果。组胺H1受体拮抗剂苯海拉明单独或与吗啡联合预处理,既不改变吗啡的镇痛作用,也不改变纳洛酮的拮抗活性。组胺H2受体拮抗剂西咪替丁预处理不影响吗啡的镇痛作用和纳洛酮的拮抗效能。然而,当与吗啡一起作为预处理给药时,它抑制了吗啡诱导纳洛酮效能增加的能力。另一种组胺H2受体阻滞剂雷尼替丁也观察到类似的效果。(摘要截短至250字)

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