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首页> 外文期刊>FEBS Letters >Endogenous inhibitors of 4'‐[3H]chlorodiazepam (Ro 5‐4864) binding to ‘peripheral’ sites for benzodiazepines
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Endogenous inhibitors of 4'‐[3H]chlorodiazepam (Ro 5‐4864) binding to ‘peripheral’ sites for benzodiazepines

机译:内源性4′-[3H]氯二氮杂胺抑制剂(Ro 5-4864)与苯并二氮杂卓的“外围”位点结合

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摘要

>‘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 (M r 10000) and low (M r 1000) M r 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.
机译:苯二氮卓类药物的“外围”结合位点在松果体,嗅球和肾脏中处于神经或同源控制之下。这些发现促使人们寻找一种可以在生理条件下调节这些部位的内源性物质。发现来自多个组织(例如胃,肾,肺)的酸化甲醇提取物可以抑制[ 3 H] Ro 5-4864与“外围”结合位点的结合,但不会显着影响结合[ 3 H]二氮杂to对“脑”苯并二氮杂receptor受体的影响。通过超滤或凝胶过滤色谱分离从胃窦胃中提取的粗提取物,分离出的高( M r M < sub> r <1000) M r 组分,竞争性抑制[ 3 H] Ro 5-4864与'peripheral'的结合网站。这些观察结果表明,一些大鼠组织中存在内源性物质,这些物质可能代表了苯并二氮杂卓“外围”结合位点的重要生理配体。

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