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胸腺中多巴胺 D1 样受体的药理学特性及放射自显影定位

Pharmacological characterization and autoradiographic localization of dopamine D1-like receptors in the thymus.

作者信息

Ricci A, Vega J A, Amenta F

机构信息

Sezione di Anatomia Umana, Università di Camerino, Italy.

出版信息

J Neuroimmunol. 1994 Mar;50(2):133-8. doi: 10.1016/0165-5728(94)90039-6.

Abstract

The present study was designed to identify the pharmacological profile and the anatomical localisation of dopamine D1-like receptor sites in the rat thymus using [3H]SCH 23390 as a ligand. [3H]SCH 23390 was specifically bound to sections of the thymus. Binding was time, temperature and concentration-dependent belonging in the range of concentrations of radioligand used to a single class of high affinity sites. The dissociation constant was 1.6 nM and the maximal density of binding sites averaged to 170 fmol/mg tissue. The pharmacological profile of [3H]SCH 23390 binding to sections of the rat thymus is consistent with the labelling of dopamine D1-like sites. Dopamine was able to compete with [3H]SCH 23390 binding to sections of rat thymus in the range of nanomolar concentrations. This suggests the labelling of dopamine D5 receptor sites. Light microscope autoradiography revealed the localisation of [3H]SCH 23390 binding sites primarily in the cortex of the thymus and in lesser amounts at the level of thymic corpuscles. The possible functional significance of dopamine D1-like receptors in the rat thymus is discussed.

摘要

本研究旨在使用[3H]SCH 23390作为配体,鉴定大鼠胸腺中多巴胺D1样受体位点的药理学特征和解剖定位。[3H]SCH 23390特异性结合于胸腺切片。结合具有时间、温度和浓度依赖性,在所使用的放射性配体浓度范围内属于单一类高亲和力位点。解离常数为1.6 nM,结合位点的最大密度平均为170 fmol/mg组织。[3H]SCH 23390与大鼠胸腺切片结合的药理学特征与多巴胺D1样位点的标记一致。多巴胺能够在纳摩尔浓度范围内与[3H]SCH 23390竞争结合大鼠胸腺切片。这表明标记的是多巴胺D5受体位点。光学显微镜放射自显影显示,[3H]SCH 23390结合位点主要位于胸腺皮质,在胸腺小体水平的含量较少。讨论了大鼠胸腺中多巴胺D1样受体可能的功能意义。

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