Ricci A, Zaccheo D, Amenta F
Dipartimento Scienze Cardiovascolari e Respiratorie, Università La Sapienza, Rome, Italy.
Synapse. 1995 Sep;21(1):37-44. doi: 10.1002/syn.890210106.
The present study was designed to characterize the pharmacological profile of dopamine D1-like receptors in the rat cerebellar cortex and to assess if these receptor sites undergo age-related changes. Cerebella of young (3 months), adult (12 months), and old (27 months) male Wistar rats were examined by using radioligand binding techniques and light microscope autoradiography. The non-selective dopamine D1-like radioligand [3H]SCH 23390 was specifically bound to sections of rat cerebellum. The findings that dopamine displaced [3H]SCH 23390 binding in the submicromolar range suggest that labelling of a dopamine D5 (or D1B) receptor subtype. The affinity of [3H]SCH 23390 for dopamine D1-like receptors was similar in the cerebellar cortex of the three animal groups investigated, whereas radioligand binding techniques revealed a gradual age-related reduction of the density of binding sites. Light microscope autoradiography showed the localization of [3H]SCH 23390 binding sites primarily in the molecular layer and to a lesser extent in the Purkinje neuron layer of the cerebellar cortex. Aging was accompanied by a loss of [3H]SCH 23390 binding sites affecting mainly the molecular layer. The age-dependent loss of dopamine D1-like receptors is more pronounced if detected with radioligand binding techniques than with light microscope autoradiography. This suggests that the decrease of dopamine D1-like receptors observed in aging rat cerebellar cortex may depend in part on changes in the receptor expression and in part on cortico-cerebellar structural changes.
本研究旨在表征大鼠小脑皮质中多巴胺D1样受体的药理学特征,并评估这些受体位点是否会发生与年龄相关的变化。通过放射性配体结合技术和光学显微镜放射自显影术,对年轻(3个月)、成年(12个月)和老年(27个月)雄性Wistar大鼠的小脑进行了检查。非选择性多巴胺D1样放射性配体[3H]SCH 23390特异性结合于大鼠小脑切片。多巴胺在亚微摩尔范围内取代[3H]SCH 23390结合的结果表明标记的是多巴胺D5(或D1B)受体亚型。在所研究的三个动物组的小脑皮质中,[3H]SCH 23390对多巴胺D1样受体的亲和力相似,而放射性配体结合技术显示结合位点密度随年龄逐渐降低。光学显微镜放射自显影显示[3H]SCH 23390结合位点主要定位于小脑皮质的分子层,在浦肯野神经元层中的定位较少。衰老伴随着[3H]SCH 23390结合位点的丧失,主要影响分子层。与光学显微镜放射自显影相比,用放射性配体结合技术检测到的多巴胺D1样受体随年龄的丧失更为明显。这表明在衰老大鼠小脑皮质中观察到的多巴胺D1样受体减少可能部分取决于受体表达的变化,部分取决于皮质 - 小脑结构的变化。