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埃托啡对脑单胺选择性耗竭大鼠的镇痛作用。

Analgesic effect of etorphine in rats with selective depletions of brain monoamines.

作者信息

Miranda F, Candelaresi G, Samanin R

出版信息

Psychopharmacology (Berl). 1978 Jun 15;58(1):105-9. doi: 10.1007/BF00426798.

Abstract

The analgesic effect of etorphine was compared with that of morphine in rats with electrolytic lesions of the nucleus medianus raphe or injected intraventricularly with 6-hydroxydopamine. The effect of both compounds was markedly reduced in animals with raphe lesions, but not significantly modified in those receiving 6-hydroxydopamine. Etorphine and morphine significantly increased the forebrain levels of 5-hydroxyindolacetic acid when administered subcutaneously at doses of 5mg/kg and 2 microgram/kg, respectively. Neither drug significantly affected the forebrain levels of monoamines. It is concluded that, as for morphine the integrity of the serotoninergic system in the brain is important for the full analgesic effect of etorphine.

摘要

将埃托啡的镇痛作用与吗啡在中缝正中核电解损伤或脑室内注射6-羟基多巴胺的大鼠中的镇痛作用进行了比较。在中缝损伤的动物中,两种化合物的作用均显著降低,但在接受6-羟基多巴胺的动物中未发生显著改变。当分别以5mg/kg和2μg/kg的剂量皮下给药时,埃托啡和吗啡显著提高了前脑5-羟吲哚乙酸水平。两种药物均未显著影响前脑单胺水平。结论是,与吗啡一样,大脑中5-羟色胺能系统的完整性对于埃托啡的完全镇痛作用很重要。

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