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氟哌啶醇对大鼠肾上腺鸟氨酸脱羧酶活性的影响。

Effect of haloperidol on adrenal ornithine decarboxylase activity of the rat.

作者信息

Almazan G, Sourkes T L

出版信息

Eur J Pharmacol. 1981 Oct 22;75(2-3):131-6. doi: 10.1016/0014-2999(81)90072-8.

Abstract

The administration of the dopamine antagonist haloperidol (HLP) to rats produced a temporary increase in adrenomedullary and cortical ornithine decarboxylase (ODC) activity. The time-course of stimulation of ODC activity by HLP showed different patterns in both structures. Medullary ODC activity was highest at 2.5 h, decreasing at later times; cortical ODC activity was not affected by the drug at 2.5 h, but then increased up to at least 6.5 h. The medullary increase observed at 2.5 h was dose-related and could be prevented by splanchnicotomy. Hypophysectomized rats, on the contrary, showed an enhanced response to HLP. The results suggest that haloperidol-induced increase of adrenomedullary ODC activity is caused by a reflex increase in preganglionic nerve activity, and that the pituitary gland can modulate this response. Cortical ODC response to HLP, as previously demonstrated, is mediated entirely by the hypophysis.

摘要

给大鼠注射多巴胺拮抗剂氟哌啶醇(HLP)会使肾上腺髓质和皮质的鸟氨酸脱羧酶(ODC)活性暂时增加。HLP刺激ODC活性的时间进程在这两个结构中呈现出不同的模式。髓质ODC活性在2.5小时时最高,随后逐渐下降;皮质ODC活性在2.5小时时不受药物影响,但随后至少增加到6.5小时。在2.5小时观察到的髓质增加与剂量相关,并且可以通过内脏神经切断术来预防。相反,垂体切除的大鼠对HLP的反应增强。结果表明,氟哌啶醇诱导的肾上腺髓质ODC活性增加是由节前神经活动的反射性增加引起的,并且垂体可以调节这种反应。如先前所示,皮质对HLP的ODC反应完全由垂体介导。

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