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组胺受体拮抗剂与丙咪嗪联合给药后大鼠脑β-肾上腺素能受体亚敏感性的加速

Acceleration of rat brain beta-adrenoceptor subsensitivity following the coadministration of histamine receptor antagonists with imipramine.

作者信息

Alhaider A A, Mustafa A A

机构信息

Department of Medical Pharmacology College of Medicine, King Saud University, Riyadh.

出版信息

Agents Actions. 1989 Nov;28(3-4):153-8. doi: 10.1007/BF01967394.

Abstract

Systemic administration of isoprenaline to rats produced a dose-dependent increase in water drinking which was effectively blocked by propranolol. This dipsogenic effect was significantly inhibited by the subacute (4 days) administration of imipramine (18.1 mg/kg/day) together with either the H1-histamine receptor antagonist, chlorpheniramine (0.1 or 1.32 mg/kg/day), or the H2-histamine antagonist, cimetidine (1.91 mg/kg/day) or ranitidine (0.60 or 1.51 mg/kg/day). The oral subacute administration of imipramine alone had no significant effect on this behavior. However, chronic ingestion of imipramine alone (21 days) caused a significant reduction in the isoprenaline-induced behavior. It is concluded that the desensitization of central beta-adrenoceptors, as evidenced by inhibition of isoprenaline-induced drinking, can be accelerated following the oral subacute co-administration of imipramine with either H1- or H2-histamine receptor antagonists. It is also seems the central histamine receptors may partially contribute towards the mechanism of antidepressant effect of imipramine.

摘要

给大鼠全身注射异丙肾上腺素会导致饮水呈剂量依赖性增加,而普萘洛尔可有效阻断这种增加。亚急性(4天)给予丙咪嗪(18.1毫克/千克/天),同时给予H1组胺受体拮抗剂氯苯那敏(0.1或1.32毫克/千克/天)、H2组胺拮抗剂西咪替丁(1.91毫克/千克/天)或雷尼替丁(0.60或1.51毫克/千克/天),这种致渴作用会受到显著抑制。单独口服亚急性给予丙咪嗪对这种行为没有显著影响。然而,单独长期摄入丙咪嗪(21天)会导致异丙肾上腺素诱导的行为显著减少。得出的结论是,口服亚急性联合给予丙咪嗪与H1或H2组胺受体拮抗剂后,可加速中枢β-肾上腺素能受体脱敏,这可通过抑制异丙肾上腺素诱导的饮水来证明。似乎中枢组胺受体也可能部分参与丙咪嗪抗抑郁作用的机制。

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