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去甲肾上腺素能终末兴奋性:阿片类药物的作用

Noradrenergic terminal excitability: effects of opioids.

作者信息

Nakamura S, Tepper J M, Young S J, Ling N, Groves P M

出版信息

Neurosci Lett. 1982 May 17;30(1):57-62. doi: 10.1016/0304-3940(82)90012-x.

Abstract

The local infusion of morphine or D-Ala2, Met5-enkephalinamide into the frontal cortical terminal fields of noradrenergic neurons of the nucleus locus coeruleus resulted in a decrease in the excitability of the axon terminal regions to direct electrical stimulation. These effects were concentration dependent and could be blocked or partially reversed by the local infusion of naloxone. Some evidence was obtained for a differential antagonizing effect of naloxone upon the effects of morphine and D-Ala2, Met5-enkephalinamide. These results are discussed with respect to an effect of opioids on the polarization and/or ionic conductance of the terminal fields of locus coeruleus neurons, and to the possible regulation of neurotransmitter release by presynaptic opiate receptors.

摘要

将吗啡或D-丙氨酸2、甲硫氨酸5-脑啡肽酰胺局部注入蓝斑核去甲肾上腺素能神经元的额叶皮质终末区,可导致轴突终末区域对直接电刺激的兴奋性降低。这些效应呈浓度依赖性,且可通过局部注入纳洛酮来阻断或部分逆转。有证据表明纳洛酮对吗啡和D-丙氨酸2、甲硫氨酸5-脑啡肽酰胺的作用具有差异性拮抗作用。本文就阿片类药物对蓝斑核神经元终末区极化和/或离子电导的影响,以及突触前阿片受体对神经递质释放的可能调节作用进行了讨论。

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