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吗啡、毒扁豆碱及中缝核刺激对猫大脑皮层5-羟色胺释放的影响。

Effects of morphine, physostigmine and raphe nuclei stimulation on 5-hydroxytryptamine release from the cerebral cortex of the cat.

作者信息

Aiello-Malmberg P, Bartolini A, Bartolini R, Galli A

出版信息

Br J Pharmacol. 1979 Apr;65(4):547-55. doi: 10.1111/j.1476-5381.1979.tb07863.x.

Abstract
  1. The release of 5-hydroxytryptamine (5-HT) from the cerebral cortex and caudate nucleus of brainstem-transected cats and from the cerebral cortex of rats anaesthetized with urethane was determined by radioenzymatic and biological assay. 2. The stimulation of nucleus linearis intermedius of raphe doubles the basal 5-HT release in the caudate nucleus and increases it 3 fold in the cerebral cortex. The effects of the electrical stimulation of the raphe are potentiated by chlorimipramine. 3. Brain 5-HT release is greatly increased by morphine hydrochloride (6 mg/kg i.v.) and by physostigmine (100 microgram/kg i.v.), but not by DL-DOPA (50 mg/kg i.v.). 4. It is suggested that the 5-HT releasing action of physostigmine can contribute to some of its pharmacological effects such as the analgesic effect so far attributed exclusively to its indirect cholinomimetic activity. 5. The 5-HT releasing action of physostigmine seems unrelated to its anticholinesterase activity.
摘要
  1. 通过放射酶法和生物测定法测定了脑干横断猫的大脑皮层和尾状核以及氨基甲酸乙酯麻醉大鼠大脑皮层中5-羟色胺(5-HT)的释放量。2. 刺激中缝中间线性核可使尾状核中的基础5-HT释放量增加一倍,并使大脑皮层中的释放量增加两倍。氯米帕明可增强对中缝的电刺激效果。3. 盐酸吗啡(静脉注射6毫克/千克)和毒扁豆碱(静脉注射100微克/千克)可使脑内5-HT释放量大幅增加,但左旋多巴(静脉注射50毫克/千克)则无此作用。4. 有人提出,毒扁豆碱的5-HT释放作用可能有助于其某些药理作用,例如迄今为止仅归因于其间接拟胆碱活性的镇痛作用。5. 毒扁豆碱的5-HT释放作用似乎与其抗胆碱酯酶活性无关。

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A sensitive method for the assay of 5-hydroxytryptamine.一种测定5-羟色胺的灵敏方法。
Br J Pharmacol Chemother. 1957 Sep;12(3):344-9. doi: 10.1111/j.1476-5381.1957.tb00146.x.
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Morphine tolerance, physical dependence, and synthesis of brain 5-hydroxytryptamine.
Science. 1968 Dec 13;162(3859):1290-2. doi: 10.1126/science.162.3859.1290.
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Inhibition of morphine tolerance and physical dependence development and brain serotonin synthesis by cycloheximide.
Biochem Pharmacol. 1969 Oct;18(10):2711-21. doi: 10.1016/0006-2952(69)90179-8.

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