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来自巨细胞旁核的蓝斑激活:大脑中一条新的兴奋性氨基酸通路。

Activation of locus coeruleus from nucleus paragigantocellularis: a new excitatory amino acid pathway in brain.

作者信息

Ennis M, Aston-Jones G

机构信息

Department of Biology, New York University, New York 10003.

出版信息

J Neurosci. 1988 Oct;8(10):3644-57. doi: 10.1523/JNEUROSCI.08-10-03644.1988.

DOI:10.1523/JNEUROSCI.08-10-03644.1988
PMID:3193175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6569606/
Abstract

Recent anatomic and physiologic experiments revealed that a major afferent to the nucleus locus coeruleus (LC) is the nucleus paragigantocellularis (PGi) in the rostral ventrolateral medulla (Aston-Jones et al., 1986). In the present studies, responses of LC neurons to electrical activation of PGi were characterized in anesthetized rats. Low-intensity stimulation of PGi synaptically activated 73% of LC neurons at short latencies (mean onset, 11.3 msec), while a smaller population (16%) of LC neurons exhibited purely inhibitory responses. The excitatory transmission from PGi to LC was pharmacologically analyzed, revealing it to be resistant to cholinergic receptor antagonism, but completely abolished by the excitatory amino acid (EAA) antagonists kynurenic acid and gamma-D-glutamylglycine. The specific N-methyl-D-aspartate antagonist 2--amino-7-phosphonoheptanoic acid (AP7) and the preferential quisqualate receptor antagonist glutamate diethyl ester (GDEE) did not block LC responses to PGi stimulation, leading us to the tentative conclusion that EAAs may operate primarily at a kainate-type receptor on LC neurons to effect excitation from PGi. In addition to their blockade of PGi-evoked activity, kynurenic acid and DGG exerted a similar, simultaneous blockade of the characteristic excitation of LC neurons evoked by electrical stimulation of the hindpaw. These and other results indicate that the proposed EAA pathway from PGi may serve as a final link in a variety of sensory inputs to LC.

摘要

最近的解剖学和生理学实验表明,蓝斑核(LC)的主要传入神经是延髓头端腹外侧的巨细胞旁核(PGi)(阿斯顿 - 琼斯等人,1986年)。在本研究中,我们对麻醉大鼠中LC神经元对PGi电激活的反应进行了特征描述。低强度刺激PGi可在短潜伏期(平均起始时间为11.3毫秒)突触激活73%的LC神经元,而较小比例(16%)的LC神经元表现出纯抑制反应。对从PGi到LC的兴奋性传递进行了药理学分析,结果显示它对胆碱能受体拮抗剂有抗性,但被兴奋性氨基酸(EAA)拮抗剂犬尿氨酸和γ - D - 谷氨酰甘氨酸完全消除。特异性N - 甲基 - D - 天冬氨酸拮抗剂2 - 氨基 - 7 - 膦酰庚酸(AP7)和优先的quisqualate受体拮抗剂谷氨酸二乙酯(GDEE)并未阻断LC对PGi刺激的反应,这使我们初步得出结论,EAA可能主要作用于LC神经元上的海人藻酸型受体,以实现来自PGi的兴奋。除了阻断PGi诱发的活动外,犬尿氨酸和DGG还对后爪电刺激诱发的LC神经元特征性兴奋产生了类似的、同时的阻断作用。这些以及其他结果表明,所提出的从PGi发出的EAA通路可能是多种传入LC的感觉输入的最终环节。