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去甲肾上腺素摄取的识别位点:神经递质的调节作用

Recognition sites for norepinephrine uptake: regulation by neurotransmitter.

作者信息

Lee C M, Javitch J A, Snyder S H

出版信息

Science. 1983 May 6;220(4597):626-9. doi: 10.1126/science.6301013.

Abstract

Recognition sites for the uptake of norepinephrine on adrenergic neurons in the brain and periphery were labeled with [3H]desipramine. The number of these uptake sites varied with the concentration of transmitter; depletion of norepinephrine with reserpine reduced the number of uptake sites, whereas increasing the concentration of norepinephrine induced by treatment with monoamine oxidase inhibitors raised the number of binding sites. These dynamic alterations in norepinephrine uptake recognition sites may regulate synaptic function homeostatically, providing less inactivation of reuptake when the synaptic concentration of the transmitter is low and increased inactivation when it is high.

摘要

大脑和外周肾上腺素能神经元上去甲肾上腺素摄取的识别位点用[3H]地昔帕明进行标记。这些摄取位点的数量随递质浓度而变化;利血平使去甲肾上腺素耗竭会减少摄取位点的数量,而单胺氧化酶抑制剂治疗诱导去甲肾上腺素浓度增加则会提高结合位点的数量。去甲肾上腺素摄取识别位点的这些动态变化可能通过稳态调节突触功能,当递质的突触浓度较低时减少再摄取的失活,而当浓度较高时增加失活。

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