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右旋苯丙胺和钾对大鼠大脑皮质组织中5-羟色胺释放及代谢的影响。

The effects of d-amphetamine and potassium on serotonin release and metabolism in rat cerebral cortex tissue.

作者信息

Homan H D, Ziance R J

出版信息

Res Commun Chem Pathol Pharmacol. 1981 Feb;31(2):223-40.

PMID:6164082
Abstract

Chopped rat cerebral cortex tissue released tritiated serotonin (3H-5HT) when exposed to d-amphetamine (d-A) (10(-5)-10(-3)M) or potassium ion (K) (24-60mM). The d-A-induced release was not dependent upon calcium, whereas, K-induced release was dependent upon calcium. Potassium caused a significant increase in the percentage of 3H-5-hydroxyindoleacetic acid (3H-5HIAA) released from the tissue. The increased metabolite was formed totally by oxidative deamination as shown by inhibition of the formation and release of 3H-5HIAA following inhibition of monoamine oxidase with clorgyline. The increased deamination as a result of incubation with K apparently occurred prior to release of 5HT from the nerve terminal, since incubation of the tissue with fluoxetine, a selective 5HT uptake inhibitor, did not alter the increased 3H-5IAA formation in response to K. These findings indicate that d-A and K apparently release 3H-5HT by different mechanisms and emphasize the importance of measuring metabolite formation in studies examining the effects of drugs on the release of 5HT in vitro.

摘要

切碎的大鼠大脑皮层组织在暴露于d-苯丙胺(d-A)(10^(-5)-10^(-3)M)或钾离子(K)(24-60mM)时会释放出氚标记的血清素(3H-5HT)。d-A诱导的释放不依赖于钙,而K诱导的释放依赖于钙。钾导致从组织中释放的3H-5-羟吲哚乙酸(3H-5HIAA)的百分比显著增加。增加的代谢产物完全是通过氧化脱氨形成的,如用氯吉兰抑制单胺氧化酶后3H-5HIAA的形成和释放受到抑制所表明的那样。由于与K孵育导致的脱氨增加显然发生在5HT从神经末梢释放之前,因为用选择性5HT摄取抑制剂氟西汀孵育组织并没有改变对K反应时增加的3H-5IAA形成。这些发现表明d-A和K显然通过不同机制释放3H-5HT,并强调在研究药物对体外5HT释放的影响时测量代谢产物形成的重要性。

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