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内源性谷氨酸在去甲肾上腺素和5-羟色胺对下丘脑-垂体-肾上腺皮质轴的刺激作用中的参与。

Involvement of endogeneous glutamate in the stimulatory effect of norepinephrine and serotonin on the hypothalamo-pituitary-adrenocortical axis.

作者信息

Feldman Shaul, Weidenfeld Joseph

机构信息

Department of Neurology, The Agnes Ginges Center for Human Neurogenetics, Hadassah University Hospital and Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Neuroendocrinology. 2004 Jan;79(1):43-53. doi: 10.1159/000076044.

Abstract

The effects of ionotropic glutamate receptor antagonists on the pituitary adrenal responses following injections of norepinephrine (NE) and serotonin (5-HT) receptor agonists into the hypothalamic paraventricular nucleus (PVN) or electrical stimulation of central NE and 5-HT pathways were studied in anesthetized male rats. PVN injections of an alpha(1)-adrenergic receptor agonist or a serotonergic 5-HT(1A) receptor agonist markedly increased both adrenocorticotropin (ACTH) and corticosterone (CS) serum levels. These responses were significantly inhibited by separate pre-injection of the selective non-NMDA and NMDA glutamate receptor subtype antagonists into the PVN in a dose-dependent manner. Electrical stimulation of either the ventral noradrenergic bundle or the dorsal raphe nucleus markedly increased serum ACTH and CS. These responses were also significantly attenuated by pre-injection of the above glutamate ionotropic receptor antagonists in a dose-dependent manner. These results suggest that glutamatergic interneurons in the PVN, acting via non-NMDA and NMDA receptors, may act as an excitatory mechanism in the NE and 5-HT control of hypothalamic ACTH secretagogues.

摘要

在麻醉的雄性大鼠中,研究了离子型谷氨酸受体拮抗剂对向下丘脑室旁核(PVN)注射去甲肾上腺素(NE)和5-羟色胺(5-HT)受体激动剂或电刺激中枢NE和5-HT通路后垂体-肾上腺反应的影响。向PVN注射α(1)-肾上腺素能受体激动剂或5-羟色胺能5-HT(1A)受体激动剂可显著提高促肾上腺皮质激素(ACTH)和皮质酮(CS)的血清水平。在PVN中预先分别注射选择性非NMDA和NMDA谷氨酸受体亚型拮抗剂,这些反应会以剂量依赖的方式受到显著抑制。电刺激腹侧去甲肾上腺素能束或背缝核可显著提高血清ACTH和CS水平。预先注射上述离子型谷氨酸受体拮抗剂也会以剂量依赖的方式使这些反应显著减弱。这些结果表明,PVN中的谷氨酸能中间神经元通过非NMDA和NMDA受体发挥作用,可能在下丘脑ACTH促分泌素的NE和5-HT调控中作为一种兴奋性机制。

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