The antinociceptive effect of moclobemide in mice is mediated by noradrenergic pathways

被引:26
作者
Schreiber, S
Getslev, V
Weizman, A [1 ]
Pick, CG
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Anat & Anthropol, IL-69978 Tel Aviv, Israel
[2] Chaim Sheba Med Ctr, Dept Psychiat C, IL-52621 Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[4] Geha Psychiat Hosp, Petah Tiqwa, Israel
[5] Felsenstein Med Res Ctr, Rabin Med Ctr, Petah Tiqwa, Israel
关键词
moclobemide; monoamine oxidase A; antinociception; opioid receptor subtypes; serotonin; noradrenaline;
D O I
10.1016/S0304-3940(98)00638-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Moclobemide is an antidepressant which affects the monoaminergic neurotransmitter system through a reversible inhibition of monoamine oxidase (MAO), preferentially type A. We examined the antinociceptive effects of moclobemide alone and in conjunction with specific opioid, adrenergic and serotonergic antagonists, using the mouse-tail flick test. Intraperitoneal moclobemide produced a dose-dependent antinociceptive effect with an ED50 Of 69.1 mg/kg. Tests with selective antagonists yielded positive results only for yohimbine (P < 0.001), implying a noradrenergic mechanism of action in the moclobemide antinociceptive effect. This was confirmed by the coadministration of moclobemide with inactive doses of prototype agonists of the opioid, adrenergic and serotonergic systems. Only clonidine, an alpha 2 agonist, significantly shifted (8-fold) the dose response curve of moclobemide. We conclude that there is a selective involvement of the alpha 2 adrenergic pathways in the moclobemide-induced antinociceptive effect and a lesser involvement (if any) of the opioid, serotonergic and alpha 1 adrenergic mechanisms. More research is needed to establish a possible role for moclobemide in pain management. (C) 1998 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:183 / 186
页数:4
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