Gelbmann C M, Müller W E
Department of Psychopharmacology, Central Institute of Mental Health, Mannheim, Federal Republic of Germany.
J Neural Transm Gen Sect. 1990;79(1-2):131-6. doi: 10.1007/BF01251008.
Using the specific binding of the full alpha 2-adrenergic agonist 3H-UK-14,304 the contribution of high-affinity agonist states to the total number of alpha 2-adrenoceptors as labeled by the specific binding of the antagonist 3H-yohimbine has been investigated in the brain of young and aged mice. In contrast to findings with human platelet membranes, in young mice all central alpha 2-adrenoceptors are present in a high-affinity agonist conformation. While the total number of alpha 2-adrenoceptors was not changed in the brain of aged animals, a specific decline of the high-affinity agonist sites by about 30% was observed. It is suggested that the specific decrease of high-affinity agonist sites of central alpha 2-adrenoceptors might represent one of the mechanisms leading to a general impairment of central noradrenergic neurotransmission with aging.
利用全α2 - 肾上腺素能激动剂3H-UK-14,304的特异性结合,研究了高亲和力激动剂状态对以拮抗剂3H-育亨宾特异性结合标记的α2 - 肾上腺素能受体总数的贡献,实验对象为年轻和老年小鼠的大脑。与人类血小板膜的研究结果相反,在年轻小鼠中,所有中枢α2 - 肾上腺素能受体均以高亲和力激动剂构象存在。虽然老年动物大脑中α2 - 肾上腺素能受体的总数没有变化,但观察到高亲和力激动剂位点特异性下降了约30%。提示中枢α2 - 肾上腺素能受体高亲和力激动剂位点的特异性减少可能是导致衰老过程中中枢去甲肾上腺素能神经传递普遍受损的机制之一。