Parfitt K D, Bickford-Wimer P
Department of Pharmacology, University of Colorado Health Sciences Center, Denver 80262.
Neurobiol Aging. 1990 Nov-Dec;11(6):591-6. doi: 10.1016/0197-4580(90)90022-r.
Previous electrophysiological studies in aged rats have revealed a number of deficits in noradrenergic neurotransmission in the central nervous system. Such deficits include subsensitivity to the depressant effects of norepinephrine on cerebellar Purkinje neurons, which has been attributed specifically to altered beta adrenergic receptor-mediated processes. The objective of this study was to determine which beta adrenergic receptor subtype, beta 1 or beta 2, is responsible for this age-related subsensitivity. The effects of beta 1 and beta 2 agonists on spontaneous activity of Purkinje neurons was first examined in young rats and the selectivity of these agents was validated using selective beta 1 and beta 2 antagonists. The effects of the selective beta 1 and beta 2 agonists were then compared in young (3-month-old) and aged (18- and 26-month-old) Fischer 344 rats. These agents were applied to Purkinje neurons by pressure microejection from multibarreled micropipettes and the change in neuronal action potential discharge rate was recorded. Both dobutamine, a beta 1-selective agonist, and zinterol, a beta 2-selective agonist, induced dose-dependent inhibitions of Purkinje cell firing rate. Dobutamine-induced inhibitions were blocked by the selective beta 1 antagonist, ICI 89406 and not by the beta 2-selective antagonist, ICI 118551; conversely, zinterol-induced inhibitions were not blocked by ICI 89406 but were blocked by the presence of ICI 118551. Purkinje neurons of both groups of aged rats were significantly less sensitive to locally applied dobutamine than Purkinje cells of young rats.(ABSTRACT TRUNCATED AT 250 WORDS)
以往对老年大鼠的电生理研究表明,中枢神经系统中去甲肾上腺素能神经传递存在一些缺陷。这些缺陷包括对去甲肾上腺素对小脑浦肯野神经元抑制作用的敏感性降低,这一现象具体归因于β肾上腺素能受体介导的过程发生改变。本研究的目的是确定哪种β肾上腺素能受体亚型,β1还是β2,是导致这种与年龄相关的敏感性降低的原因。首先在年轻大鼠中研究了β1和β2激动剂对浦肯野神经元自发活动的影响,并使用选择性β1和β2拮抗剂验证了这些药物的选择性。然后比较了选择性β1和β2激动剂对年轻(3个月大)和老年(18个月和26个月大)Fischer 344大鼠的影响。通过多管微量移液器压力微注射将这些药物应用于浦肯野神经元,并记录神经元动作电位发放率的变化。β1选择性激动剂多巴酚丁胺和β2选择性激动剂齐特罗尔均诱导了浦肯野细胞发放率的剂量依赖性抑制。多巴酚丁胺诱导的抑制作用被选择性β1拮抗剂ICI 89406阻断,而未被β2选择性拮抗剂ICI 118551阻断;相反,齐特罗尔诱导的抑制作用未被ICI 89406阻断,但被ICI 118551阻断。两组老年大鼠的浦肯野神经元对局部应用的多巴酚丁胺的敏感性均显著低于年轻大鼠的浦肯野细胞。(摘要截短于250字)