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抗抑郁药给药后大鼠中枢肾上腺素能受体信号传递的评估。

Evaluation of central adrenergic receptor signal transmissions after an antidepressant administration to the rat.

作者信息

Sapena R, Morin D, Zini R, Tillement J P

机构信息

Département de Pharmacologie, Faculté de Médicine de Paris XII, Créteil, France.

出版信息

Biochem Pharmacol. 1992 Sep 25;44(6):1067-72. doi: 10.1016/0006-2952(92)90369-t.

Abstract

The effects of several antidepressants, amitriptyline, citalopram, desipramine, fluoxetine, maprotiline, mianserin, nialamide, nomifensine, tranylcypromine and viloxazine, on the accumulation of cyclic AMP and inositol monophosphates were studied in rat cerebral cortical slices. The two enzymatic systems were stimulated either by adrenergic agonists or by forskolin. Cyclic AMP and inositol monophosphates (IPs) formed were determined by a double label method. In vitro all drugs, except inhibitors of monoamine oxidase, nialamide and tranylcypromine, inhibited alpha 1-agonist-mediated production but did not modify the cyclic AMP accumulation. Otherwise, chronic desipramine but not citalopram administration decreased the accumulation of cyclic AMP (-39%) elicited by beta-adrenoceptor agonists; no change was observed in inositol phosphate metabolism after administration of these two drugs. These data support previous investigations showing a decrease in cyclic AMP production after chronic treatment with norepinephrine uptake blockers but do not confirm the hypothesis of a modification of alpha 1-adrenoceptor-stimulated inositol phosphate metabolism.

摘要

研究了几种抗抑郁药(阿米替林、西酞普兰、地昔帕明、氟西汀、马普替林、米安色林、尼亚酰胺、诺米芬辛、反苯环丙胺和维洛沙嗪)对大鼠大脑皮质切片中环磷酸腺苷(cAMP)和肌醇单磷酸积累的影响。这两种酶系统分别由肾上腺素能激动剂或福司可林刺激。通过双标记法测定形成的cAMP和肌醇单磷酸(IPs)。在体外,除单胺氧化酶抑制剂尼亚酰胺和反苯环丙胺外,所有药物均抑制α1-激动剂介导的生成,但不改变cAMP的积累。此外,长期给予地昔帕明而非西酞普兰可降低β-肾上腺素受体激动剂引起的cAMP积累(-39%);给予这两种药物后,肌醇磷酸代谢未观察到变化。这些数据支持了先前的研究结果,即去甲肾上腺素摄取阻滞剂长期治疗后cAMP生成减少,但未证实α1-肾上腺素受体刺激的肌醇磷酸代谢改变这一假说。

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