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小牛脑和视网膜中的α2A肾上腺素能受体及非肾上腺素能咪唑克生结合位点与人脑的不同。

Alpha 2A adrenoceptors and non-adrenergic idazoxan binding sites in calf brain and retina are distinct from those in human brain.

作者信息

Van Liefde I, Vauquelin G, De Keyser J, De Backer J P, De Vos H

机构信息

Department of Protein Chemistry, Vrije Universiteit Brussel, St. Genesius-Rode, Belgium.

出版信息

Neurochem Int. 1993 May;22(5):501-9. doi: 10.1016/0197-0186(93)90046-8.

Abstract

alpha 2 Adrenoceptors in membrane preparations of human and calf frontal cortex and of calf retina can be labelled by the antagonists [3H]idazoxan, [3H]rauwolscine and [3H]RX 821002. Present and previous data indicate that [3H]idazoxan possesses the highest affinity for the alpha 2 adrenoceptors in the calf tissues, whereas [3H]rauwolscine displays the highest affinity for those in the human frontal cortex. Competition binding experiments with adrenergic and serotonergic drugs further support the notion that the alpha 2 adrenoceptors in calf frontal cortex and retina are similar, but distinct from the receptors in human frontal cortex. The alpha 2 adrenoceptors in the three investigated tissues display low affinity for the antagonist prazosin, which suggests that they all belong to the alpha 2A subclass. The competition binding curves of the alpha 2A adrenoceptor subtype-selective agonist oxymetazoline are shallow, but undergo a rightward shift and steepening in the presence of GTP. The shallow curves can therefore be attributed to the coupling of the alpha 2 adrenoceptors to G proteins. The different binding characteristics of the alpha 2A adrenoceptors from the investigated human and bovine tissues are likely to reflect species-related differences in protein structure. [3H]Idazoxan binds also to non-adrenergic sites in membrane preparations from the three tissues. However, the affinity of [3H]idazoxan for these sites in calf cortex and retina is appreciably lower than for those in human cortex. The species-related differences of the non-adrenergic idazoxan binding sites may be due to differences in protein structure or even to differences in gene-product.

摘要

人类和小牛额叶皮质以及小牛视网膜膜制剂中的α2肾上腺素能受体可用拮抗剂[3H]咪唑克生、[3H]育亨宾和[3H]RX 821002进行标记。目前和先前的数据表明,[3H]咪唑克生对小牛组织中的α2肾上腺素能受体具有最高亲和力,而[3H]育亨宾对人类额叶皮质中的α2肾上腺素能受体显示出最高亲和力。用肾上腺素能和血清素能药物进行的竞争结合实验进一步支持了以下观点:小牛额叶皮质和视网膜中的α2肾上腺素能受体相似,但与人类额叶皮质中的受体不同。在所研究的三种组织中,α2肾上腺素能受体对拮抗剂哌唑嗪的亲和力较低,这表明它们都属于α2A亚类。α2A肾上腺素能受体亚型选择性激动剂羟甲唑啉的竞争结合曲线较浅,但在存在GTP的情况下会发生右移和变陡。因此,浅曲线可归因于α2肾上腺素能受体与G蛋白的偶联。所研究的人类和牛组织中α2A肾上腺素能受体的不同结合特性可能反映了蛋白质结构中与物种相关的差异。[3H]咪唑克生还与这三种组织膜制剂中的非肾上腺素能位点结合。然而,[3H]咪唑克生对小牛皮质和视网膜中这些位点的亲和力明显低于对人类皮质中这些位点的亲和力。非肾上腺素能咪唑克生结合位点的物种相关差异可能是由于蛋白质结构的差异,甚至是基因产物的差异。

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