Eichinger A, Sieghart W
J Neurochem. 1986 Jan;46(1):173-80. doi: 10.1111/j.1471-4159.1986.tb12941.x.
The postnatal development of several proteins irreversibly labeled by [3H]flunitrazepam in membranes from rat cerebral cortex was investigated. It was demonstrated that in the early postnatal days proteins with apparent molecular weights 55,000 and 59,000 were predominantly labeled whereas irreversible labeling of a protein with apparent molecular weight 51,000 started to predominate only in the second postnatal week. Irreversible labeling of another protein with apparent molecular weight 62,000 was weak throughout development. All these proteins seem to be associated with central benzodiazepine receptors. Irreversible labeling at various time points after birth seems to parallel the postnatal development of these proteins, and the different time course of development and different binding properties of the individual proteins support the hypothesis that these proteins are associated with separate and distinct benzodiazepine receptor subtypes. The pharmacological properties of the individual receptor subtypes seem to be fully developed in the early postnatal days, and therefore newborn animals seem to be a good model system for the investigation of properties and function of these various benzodiazepine receptor subtypes.
研究了用[3H]氟硝西泮不可逆标记的几种蛋白质在大鼠大脑皮质膜中的产后发育情况。结果表明,在出生后的早期,表观分子量为55,000和59,000的蛋白质被大量标记,而表观分子量为51,000的蛋白质的不可逆标记仅在出生后的第二周才开始占主导地位。另一种表观分子量为62,000的蛋白质的不可逆标记在整个发育过程中都很弱。所有这些蛋白质似乎都与中枢苯二氮䓬受体有关。出生后不同时间点的不可逆标记似乎与这些蛋白质的产后发育平行,并且各个蛋白质不同的发育时间进程和结合特性支持了这些蛋白质与不同且独特的苯二氮䓬受体亚型相关的假说。各个受体亚型的药理学特性似乎在出生后的早期就已完全发育,因此新生动物似乎是研究这些不同苯二氮䓬受体亚型的特性和功能的良好模型系统。