Zheng J, Ali A, Ramirez V D
Neuroscience Program, University of Illinois, Urbana 61801, USA.
J Psychiatry Neurosci. 1996 May;21(3):187-97.
Our laboratory has pioneered the use of bovine serum albumin (BSA) linked to different positions of the ring structure of progesterone to investigate steroid-membrane interactions. The complex can be radioiodinated to demonstrate the existence of specific membrane progesterone binding sites in the rat brain. Not only are these progesterone complexes specific ligands, but they also elicit functional responses in the central nervous system (CNS), particularly in the corpus striatum (CS) where progesterone-BSA conjugates linked at C-3 and C-11 positions (P-3-BSA and P-11-BSA) alter amphetamine-evoked dopamine release. In this communication we will report our current studies that use radioiodinated progesterone-BSA conjugates (P-3-125I-BSA, P-6-125I-BSA, and P-11-125I-BSA) and estradiol-BSA conjugates linked at C-6 position (17 beta-E-6-125I-BSA and 17-E-6-BSA) to demonstrate the existence of specific membrane binding sites for progesterone and estrogen in several regions of the rat brain. In addition, initial studies to isolate and purify these membrane binding sites from digitonin-solubilized P2-membrane fractions by affinity chromatography are reported. The data indicate that these sites are part of a complex membrane receptor for either estrogen or progesterone, the so-called membrane estrogen receptor (mER) and the membrane progesterone receptor (mPR), respectively.
我们的实验室率先使用与孕酮环结构不同位置相连的牛血清白蛋白(BSA)来研究类固醇与膜的相互作用。该复合物可进行放射性碘化,以证明大鼠脑中存在特定的膜孕酮结合位点。这些孕酮复合物不仅是特异性配体,还能在中枢神经系统(CNS)引发功能性反应,特别是在纹状体(CS)中,与C-3和C-11位置相连的孕酮-BSA缀合物(P-3-BSA和P-11-BSA)会改变苯丙胺诱发的多巴胺释放。在本通讯中,我们将报告我们目前的研究,该研究使用放射性碘化的孕酮-BSA缀合物(P-3-125I-BSA、P-6-125I-BSA和P-11-125I-BSA)以及与C-6位置相连的雌二醇-BSA缀合物(17β-E-6-125I-BSA和17-E-6-BSA)来证明大鼠脑几个区域中存在孕酮和雌激素的特定膜结合位点。此外,还报告了通过亲和色谱从洋地黄皂苷溶解的P2膜组分中分离和纯化这些膜结合位点的初步研究。数据表明,这些位点分别是雌激素或孕酮复合膜受体的一部分,即所谓的膜雌激素受体(mER)和膜孕酮受体(mPR)。