Mantione C R, Goldman M E, Weissman B A, Paul S M, Skolnick P
Prog Clin Biol Res. 1985;192:167-73.
Recent observations have shown that "peripheral-type" binding sites for benzodiazepines (PBS) are under neural and/or hormonal control in the pineal gland, olfactory bulb, and kidney. These studies resulted in a search for endogenous substances which might physiologically subserve PBS. Acidified methanol or trichloroacetic acid extraction of both peripheral tissues and brain followed by ultrafiltration and/or gel filtration and high performance liquid chromatography revealed the presence of both high (Mr greater than 10,000) and low (Mr less than 500) molecular weight substances which inhibit the binding of [3H] Ro 5-4864 to PBS while only slightly inhibiting the binding of [3H] diazepam to classical "brain-type" benzodiazepine receptors.
最近的观察结果表明,苯二氮䓬类药物的“外周型”结合位点(PBS)在松果体、嗅球和肾脏中受神经和/或激素控制。这些研究促使人们寻找可能在生理上作用于PBS的内源性物质。用酸化甲醇或三氯乙酸对外周组织和大脑进行提取,然后进行超滤和/或凝胶过滤以及高效液相色谱分析,结果显示存在高分子量(Mr大于10,000)和低分子量(Mr小于500)的物质,它们能抑制[3H] Ro 5-4864与PBS的结合,而对[3H]地西泮与经典“脑型”苯二氮䓬受体的结合仅有轻微抑制作用。