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二氢吡啶对L型钙离子通道的调节增强了κ-阿片受体激动剂诱导的急性镇痛作用,并抑制大鼠耐受性的发展。

L-type Ca2+ channel modulation by dihydropyridines potentiates kappa-opioid receptor agonist induced acute analgesia and inhibits development of tolerance in rats.

作者信息

Gullapalli S, Ramarao P

机构信息

Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Phase - X, Sector 67, S.A.S.Nagar (Mohali) - 160 062, Punjab, India.

出版信息

Neuropharmacology. 2002 Mar;42(4):467-75. doi: 10.1016/s0028-3908(01)00200-3.

Abstract

The effect of 1,4-dihydropyridine (DHP) calcium channel blockers (CCBs), nimodipine (NIM) and lercanidipine (LDP) on the analgesic response of selective kappa-opioid receptor agonists, U50,488H, PD117,302 and U69,593 was determined in male Sprague-Dawley rats using the tail-flick test. The effect of NIM on development of tolerance to U50,488H-induced analgesia and the status of brain DHP-sensitive Ca(2+) channel (L-type) binding sites in both U50,488H-naive and tolerant rats was determined using the highly selective DHP radioligand, [(3)H]PN200-110. Tolerance was induced by injecting U50,488H (25 mg/kg, i.p.) twice daily for 4 days. Intraperitoneal (i.p.) injection of kappa-opioid receptor agonists produced a dose-dependent acute analgesic response. NIM (1 mg/kg; i.p.) and LDP (0.3 mg/kg; i.p.) used in the study produced no tail-flick analgesia. Administration of NIM and LDP (15 min prior) significantly potentiated the analgesia produced by three kappa-opioid receptor agonists. Tolerance developed completely to the analgesic effect induced by U50,488H (25 mg/kg, i.p.) administered on the 5th day. NIM (1 mg/kg, i.p.) twice daily for 4 days not only completely inhibited the development of tolerance to analgesic response but also significantly potentiated it (supersensitivity). There was a significant up-regulation of DHP binding sites (B(max): +41%) in whole brain membranes of tolerant rats when compared to vehicle treated naive rats, implicating increased influx of Ca(2+) through L-type channels in kappa-opioid tolerance. U50,488H (25 mg/kg, i.p.) and NIM (1 mg/kg, i.p.) twice daily for 4 days also resulted in an equivalent up-regulation of DHP binding sites (+36%) as that of U50,488H alone. These results strongly suggest a functional role of L-type Ca(2+) channels in the regulation of pain sensitivity, mechanism of kappa-opioid analgesia and expression of tolerance.

摘要

在雄性斯普拉格 - 道利大鼠中,采用甩尾试验测定了1,4 - 二氢吡啶(DHP)类钙通道阻滞剂(CCB)尼莫地平(NIM)和乐卡地平(LDP)对选择性κ - 阿片受体激动剂U50,488H、PD117,302和U69,593镇痛反应的影响。使用高选择性DHP放射性配体[³H]PN200 - 110,测定了NIM对U50,488H诱导镇痛耐受性发展的影响以及U50,488H未用药和耐受大鼠脑内DHP敏感钙(Ca²⁺)通道(L型)结合位点的状态。通过每天两次腹腔注射(i.p.)U50,488H(25 mg/kg),持续4天诱导耐受性。腹腔注射κ - 阿片受体激动剂产生剂量依赖性急性镇痛反应。本研究中使用的NIM(1 mg/kg;i.p.)和LDP(0.3 mg/kg;i.p.)未产生甩尾镇痛作用。预先15分钟给予NIM和LDP可显著增强三种κ - 阿片受体激动剂产生的镇痛作用。对第5天腹腔注射U50,488H(25 mg/kg)诱导的镇痛作用完全产生了耐受性。每天两次腹腔注射NIM(1 mg/kg),持续4天,不仅完全抑制了镇痛反应耐受性的发展,还显著增强了该反应(超敏反应)。与溶剂处理的未用药大鼠相比,耐受大鼠全脑膜中DHP结合位点显著上调(Bmax:+41%),这表明κ - 阿片耐受性中通过L型通道的Ca²⁺内流增加。每天两次腹腔注射U50,488H(25 mg/kg)和NIM(1 mg/kg),持续4天,也导致DHP结合位点上调(+36%),与单独使用U50,488H时相当。这些结果强烈表明L型Ca²⁺通道在疼痛敏感性调节、κ - 阿片镇痛机制和耐受性表达中具有功能性作用。

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