Svenningsson P, Hall H, Sedvall G, Fredholm B B
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Synapse. 1997 Dec;27(4):322-35. doi: 10.1002/(SICI)1098-2396(199712)27:4<322::AID-SYN6>3.0.CO;2-E.
Whole-hemisphere sections from six subjects were used in a quantitative autoradiographic study to characterize and to investigate the distribution of adenosine receptors, using [3H]DPCPX, [3H]CGS 21680, and [3H]SCH 58261 as radioligands. [3H]DPCPX-binding showed the pharmacology expected for adenosine A1 receptors and is therefore taken to mirror adenosine A1 receptors. Adenosine A1 receptors were widely distributed, with the highest densities in the stratum radiatum/pyramidale of the hippocampal region CA1. Adenosine A1 receptors were nonhomogeneously distributed in nucleus caudatus, globus pallidus, and cortical areas: In the cingulate and frontal cortex the deep layers showed the highest labeling, while in the occipital, parietal, temporal, and insular cortex it was highest in the superficial layers. In addition, we found very high levels of adenosine A1 receptors in structures known to be important for cholinergic transmission, especially the septal nuclei. The Bmax values and KD values for [3H]DPCPX-binding in stratum radiatum/pyramidale of CA1 and the superficial layer of insular cortex were 598 and 430 fmol/mg gray matter and 9.9 and 14.2 nM, respectively. [3H]CGS 21680-binding was multiphasic, but showed the pharmacology expected for adenosine A2A receptors and was taken to represent them. Adenosine A2A receptors were abundant in putamen, nucleus caudatus, nucleus accumbens, and globus pallidus pars lateralis. Specific [3H]CGS 21680-binding was also found in certain thalamic nuclei and throughout the cerebral cortex. The adenosine A2A receptor antagonist radioligand [3H]SCH 58261 was also found to label these extrastriatal structures. Thus, adenosine A2A receptors seem to be more widely distributed in the human brain than previously recognized.
在一项定量放射自显影研究中,使用[3H]DPCPX、[3H]CGS 21680和[3H]SCH 58261作为放射性配体,对6名受试者的全脑半球切片进行分析,以表征和研究腺苷受体的分布。[3H]DPCPX结合显示出腺苷A1受体预期的药理学特性,因此被认为反映了腺苷A1受体的情况。腺苷A1受体分布广泛,在海马区域CA1的辐射层/锥体层密度最高。腺苷A1受体在尾状核、苍白球和皮质区域分布不均:在扣带回和额叶皮质,深层标记最高,而在枕叶、顶叶、颞叶和岛叶皮质,表层标记最高。此外,我们发现在已知对胆碱能传递很重要的结构中,尤其是隔核,腺苷A1受体水平非常高。CA1辐射层/锥体层和岛叶皮质表层中[3H]DPCPX结合的Bmax值和KD值分别为598和430 fmol/mg灰质以及9.9和14.2 nM。[3H]CGS 21680结合是多相的,但显示出腺苷A2A受体预期的药理学特性,并被认为代表了这些受体。腺苷A2A受体在壳核、尾状核、伏隔核和苍白球外侧部丰富。在某些丘脑核和整个大脑皮质中也发现了特异性的[3H]CGS 21680结合。此外,腺苷A2A受体拮抗剂放射性配体[3H]SCH 58261也被发现标记这些纹状体以外的结构。因此,腺苷A2A受体在人类大脑中的分布似乎比以前认为的更广泛。