Almazan G, Sourkes T L
Eur J Pharmacol. 1981 Oct 22;75(2-3):131-6. doi: 10.1016/0014-2999(81)90072-8.
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.
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。