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(D-青霉胺2,D-青霉胺5)脑啡肽对大鼠脑内内源性锌水平的部分消耗

Partial depletion of endogenous zinc level by (D-Pen2, D-Pen5)enkephalin in the rat brain.

作者信息

Gulya K, Kovács G L, Kása P

机构信息

Central Research Laboratory, Albert Szent-Györgyi Medical University, Szeged, Hungary.

出版信息

Life Sci. 1991;48(12):PL57-62. doi: 10.1016/0024-3205(91)90462-k.

Abstract

The effects of the potent delta opioid agonist (D-Pen2, D-Pen5)enkephalin (DPDPE) were studied on the endogenous levels and regional distribution of Zn2+ in rat central nervous system by means of flame atomic absorption spectrophotometry. The olfactory bulb exhibited the highest Zn2+ level, followed by the frontal and parietal cortices, striatum and hippocampus; the lowest ion levels were found in the medulla and thoracic spinal cord. Intracerebroventricular administration of DPDPE resulted in significant, time- and dose-dependent decreases in endogenous Zn2+ contents in the parietal cortex, hippocampus and striatum. The action of DPDPE was antagonized by a 30 min naloxone pretreatment. Naloxone alone was without effect in eliciting these responses. Thus, delta opioid receptors may regulate or modulate endogenous Zn2+ levels in the rat brain.

摘要

采用火焰原子吸收分光光度法,研究了强效δ阿片受体激动剂(D-青霉胺2,D-青霉胺5)脑啡肽(DPDPE)对大鼠中枢神经系统内源性锌离子水平及其区域分布的影响。嗅球的锌离子水平最高,其次是额叶和顶叶皮质、纹状体和海马体;延髓和胸段脊髓中的离子水平最低。脑室内注射DPDPE导致顶叶皮质、海马体和纹状体内源性锌离子含量显著降低,且呈时间和剂量依赖性。纳洛酮预处理30分钟可拮抗DPDPE的作用。单独使用纳洛酮不会引发这些反应。因此,δ阿片受体可能调节大鼠脑内的内源性锌离子水平。

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