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4'-[3H]氯地西泮(Ro 5-4864)与苯二氮䓬“外周”位点结合的内源性抑制剂。

Endogenous inhibitors of 4'-[3H]chlorodiazepam (Ro 5-4864) binding to 'peripheral' sites for benzodiazepines.

作者信息

Mantione C R, Weissman B A, Goldman M E, Paul S M, Skolnick P

出版信息

FEBS Lett. 1984 Oct 15;176(1):69-74. doi: 10.1016/0014-5793(84)80913-8.

Abstract

'Peripheral' binding sites for benzodiazepines are under neural or homonal control in the pineal gland, olfactory bulb, and kidney. These observations prompted a search for an endogenous substance which could modulate these sites under physiological conditions. Acidified methanol extracts from several tissues (e.g. stomach, kidney, lung) were found to inhibit the binding of [3H]Ro 5-4864 to 'peripheral' binding sites, but did not significantly affect the binding of [3H]diazepam to 'brain' benzodiazepine receptors. Fractionation of a crude extract prepared from antral stomach by either ultrafiltration or gel filtration chromatography yielded high (Mr greater than 10 000) and low (Mr less than 1000) Mr fractions which competitively inhibited [3H]Ro 5-4864 binding to 'peripheral' sites. These observations suggest the presence of endogenous substances in several rat tissues which may represent physiologically important ligands for 'peripheral' binding sites for benzodiazepines.

摘要

苯二氮䓬类药物的“外周”结合位点在松果体、嗅球和肾脏中受神经或激素控制。这些观察结果促使人们寻找一种内源性物质,该物质在生理条件下可以调节这些位点。研究发现,来自几种组织(如胃、肾脏、肺)的酸化甲醇提取物可抑制[3H]Ro 5-4864与“外周”结合位点的结合,但对[3H]地西泮与“脑”苯二氮䓬受体的结合没有显著影响。通过超滤或凝胶过滤色谱法对从胃窦制备的粗提物进行分级分离,得到了高分子量(Mr大于10000)和低分子量(Mr小于1000)的组分,它们竞争性抑制[3H]Ro 5-4864与“外周”位点的结合。这些观察结果表明,在几种大鼠组织中存在内源性物质,这些物质可能是苯二氮䓬类药物“外周”结合位点的生理重要配体。

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