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大鼠视网膜和脑不同区域中D1多巴胺受体的不同周转率。

Differential turnover rates of D1 dopamine receptors in the retina and in distinct areas of the rat brain.

作者信息

Giorgi O, Pibiri M G, Biggio G

机构信息

Department of Experimental Biology, University of Cagliari, Italy.

出版信息

J Neurochem. 1991 Sep;57(3):754-9. doi: 10.1111/j.1471-4159.1991.tb08216.x.

Abstract

The present study was designed to examine the steady-state density and the turnover rates of D1 dopamine (DA) receptors in the striatum, nucleus accumbens, substantia nigra, and retina of the rat. The turnover rates were measured by monitoring the repopulation kinetics of D1 DA receptors labelled with [3H]SCH 23390 after the irreversible inactivation induced by a single dose of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (10 mg/kg s.c.). The repopulation of D1 DA receptors could be described adequately in all the neural tissues investigated by a theoretical model that assumes a constant rate of receptor production (i.e., zero order) and a rate of degradation that is dependent on the receptor density at any time (i.e., first order). The quantitative analysis of the experimental data using this theoretical model revealed significant regional differences in the rates of receptor production and degradation. Thus, the receptor production rates determined in the nucleus accumbens and striatum (8.03 and 9.96 fmol/mg of protein/h, respectively) were four- to sixfold larger than those measured in the substantia nigra (1.80 fmol/mg of protein/h) and retina (1.50 fmol/mg of protein/h). On the other hand, the receptor degradation rates in the striatum, nucleus accumbens, and retina (0.0093 h-1, 0.0110 h-1, and 0.0123 h-1, respectively) were 2.6-3.5-fold larger than the receptor degradation rate in the substantia nigra (0.0035 h-1).

摘要

本研究旨在检测大鼠纹状体、伏隔核、黑质和视网膜中D1多巴胺(DA)受体的稳态密度和周转率。通过监测单剂量N - 乙氧基羰基 - 2 - 乙氧基 - 1,2 - 二氢喹啉(10 mg/kg皮下注射)诱导不可逆失活后,用[3H]SCH 23390标记的D1 DA受体的再填充动力学来测量周转率。在所有研究的神经组织中,D1 DA受体的再填充可以用一个理论模型充分描述,该模型假设受体产生速率恒定(即零级),降解速率取决于任何时刻的受体密度(即一级)。使用该理论模型对实验数据进行定量分析,结果显示受体产生和降解速率存在显著的区域差异。因此,伏隔核和纹状体中测定的受体产生速率(分别为8.03和9.96 fmol/mg蛋白质/h)比黑质(1.80 fmol/mg蛋白质/h)和视网膜(1.50 fmol/mg蛋白质/h)中测量的速率大四至六倍。另一方面,纹状体、伏隔核和视网膜中的受体降解速率(分别为0.0093 h-1、0.0110 h-1和0.0123 h-1)比黑质中的受体降解速率(0.0035 h-1)大2.6至3.5倍。

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