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大鼠背侧海马中肾上腺素能受体的电生理学特征。III. 终末α2-肾上腺素能自身受体生理作用的证据。

Electrophysiological characterization of adrenoceptors in the rat dorsal hippocampus. III. Evidence for the physiological role of terminal alpha 2-adrenergic autoreceptors.

作者信息

Curet O, de Montigny C

机构信息

Department of Psychiatry, McGill University, Montreal, Que., Canada.

出版信息

Brain Res. 1989 Oct 9;499(1):18-26. doi: 10.1016/0006-8993(89)91131-1.

Abstract

The present electrophysiological studies were undertaken to assess the role of terminal alpha 2-adrenergic autoreceptors in regulating noradrenergic synaptic transmission in the rat CNS. The effectiveness of the electrical stimulation of the locus coeruleus (LC) in suppressing the firing activity of pyramidal neurons was determined in the dorsal hippocampus. Intravenous clonidine, an alpha 2-adrenergic agonist, decreased the effectiveness of the LC stimulation, without altering the effect of microiontophoretically applied norepinephrine. The subsequent i.v. administration of low doses of idazoxan, an alpha 2-adrenergic antagonist, reversed this effect of clonidine on the LC stimulation. To ascertain that the effect of clonidine administered i.v. was indeed attributable to its action on noradrenergic terminals, it was applied locally by microiontophoresis; it decreased the effectiveness of the LC stimulation. Another paradigm used to assess the function of terminal alpha 2-adrenoceptors was to increase the frequency of the LC stimulation from 1 to 5 Hz. This resulted in a 5-fold decrease of the effectiveness of the stimulation. That this was attributable to an enhanced activation of terminal alpha 2-adrenoceptors was suggested by the reversal of this effect of increasing the frequency of the LC stimulation by intravenous idazoxan. Furthermore, the degree of enhancement of the effectiveness of the LC stimulation by idazoxan was much greater at 5 than at 1 Hz. These results provide novel electrophysiological evidence for the potent regulatory role of terminal alpha 2-adrenoceptors on noradrenergic neurotransmission.

摘要

进行了目前的电生理研究,以评估终末α2-肾上腺素能自身受体在调节大鼠中枢神经系统去甲肾上腺素能突触传递中的作用。在背侧海马中确定了蓝斑(LC)电刺激抑制锥体神经元放电活动的有效性。静脉注射可乐定(一种α2-肾上腺素能激动剂)降低了LC刺激的有效性,而不改变微量离子电泳施加去甲肾上腺素的效果。随后静脉注射低剂量的咪唑克生(一种α2-肾上腺素能拮抗剂)可逆转可乐定对LC刺激的这种作用。为了确定静脉注射可乐定的作用确实归因于其对去甲肾上腺素能终末的作用,通过微量离子电泳将其局部应用;它降低了LC刺激的有效性。另一种用于评估终末α2-肾上腺素能受体功能的范式是将LC刺激的频率从1Hz增加到5Hz。这导致刺激有效性降低了5倍。静脉注射咪唑克生逆转增加LC刺激频率的这种作用,提示这归因于终末α2-肾上腺素能受体的激活增强。此外,咪唑克生对LC刺激有效性的增强程度在5Hz时比在1Hz时大得多。这些结果为终末α2-肾上腺素能受体对去甲肾上腺素能神经传递的有效调节作用提供了新的电生理证据。

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