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β-肾上腺素能受体激动剂对中枢5-羟色胺代谢率的刺激作用。

Stimulation of central serotonin turnover by beta-adrenoceptor agonists.

作者信息

Waldmeier P C

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):115-9. doi: 10.1007/BF00500065.

Abstract

The beta 2-stimulators salbutamol (0.3--30 mg/kg i.v.) and clenbuterol (0.3 and 1 mg/kg i.v.), and, to a lesser extent, the beta 1-stimulators dobutamine (30 mg/kg i.v.) and prenalterol (30 mg/kg i.v.) increased serotonin metabolism in several rat brain areas, as indicated by increased concentrations of 5-hydroxyindoleacetic acid (5-HIAA) or increased tryptophan hydroxylation in vivo. With salbutamol, increases in 5-HIAA in c. striatum and brainstem, but not in cortex, were observed after intraventricular administration of relatively low doses (3--30 micrograms). Direct application of the compound into the dorsal raphe nucleus at doses of 100 ng and 1 microgram were without effect, and only minimal 5-HIAA increases occurred after the high dose of 10 micrograms. The effects of salbutamol on the concentrations of 5-HIAA were antagonized by both propranolol and WB4101, indicating an involvement not only of beta-receptors but also of postsynaptic alpha-receptors. The evidence for an against a central site of action of beta-agonists with respect to their effect on serotonergic systems is discussed.

摘要

β2 激动剂沙丁胺醇(静脉注射剂量为 0.3 - 30 毫克/千克)和克伦特罗(静脉注射剂量为 0.3 和 1 毫克/千克),以及在较小程度上,β1 激动剂多巴酚丁胺(静脉注射剂量为 30 毫克/千克)和普瑞特罗(静脉注射剂量为 30 毫克/千克)可增加大鼠多个脑区的 5-羟色胺代谢,这表现为 5-羟吲哚乙酸(5-HIAA)浓度升高或体内色氨酸羟化增加。使用沙丁胺醇时,脑室内注射相对低剂量(3 - 30 微克)后,在尾状核和脑干中观察到 5-HIAA 增加,但在皮质中未观察到。以 100 纳克和 1 微克的剂量将该化合物直接注入中缝背核无效,而在 10 微克的高剂量后仅出现最小程度的 5-HIAA 增加。普萘洛尔和 WB4101 均能拮抗沙丁胺醇对 5-HIAA 浓度的影响,这表明不仅β受体参与其中,突触后α受体也参与其中。文中讨论了支持和反对β激动剂对血清素能系统作用的中枢作用位点的证据。

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