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下丘脑去甲肾上腺素和5-羟色胺的耗竭增强了地塞米松对肾上腺皮质分泌的负反馈作用。

Depletion of hypothalamic norepinephrine and serotonin enhances the dexamethasone negative feedback effect on adrenocortical secretion.

作者信息

Feldman S, Weidenfeld J

机构信息

Department of Neurology, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Psychoneuroendocrinology. 1991;16(5):397-405. doi: 10.1016/0306-4530(91)90004-d.

Abstract

The role of norepinephrine (NE) and serotonin (5-HT) in the negative feedback effect of dexamethasone (DEX) on the adrenocortical response to ether stress was investigated. Injection of the catecholamine neurotoxin, 6-hydroxydopamine, into the ventral noradrenergic bundle or the paraventricular nucleus of the hypothalamus (PVN) which produced a very significant depletion in hypothalamic NE content enhanced the negative feedback effect of DEX. Injection of the 5-HT neurotoxin, 5,7-dihydroxytryptamine, into the raphé nuclei or PVN, which caused a depletion of hypothalamic 5-HT, produced a similar effect on the adrenocortical response to DEX. The degree of negative feedback may be viewed as a balance of neural stimulatory and glucocorticoid influences of the hypothalamus. Thus the removal of the stimulatory effects of NE and 5-HT on adrenocortical secretion, by the neurotoxic lesions, enhanced the inhibitory influence of DEX.

摘要

研究了去甲肾上腺素(NE)和5-羟色胺(5-HT)在地塞米松(DEX)对肾上腺皮质对应激反应的负反馈作用中的角色。向腹侧去甲肾上腺素能束或下丘脑室旁核(PVN)注射儿茶酚胺神经毒素6-羟基多巴胺,可导致下丘脑NE含量显著减少,而这增强了DEX的负反馈作用。向中缝核或PVN注射5-HT神经毒素5,7-二羟基色胺,导致下丘脑5-HT减少,对肾上腺皮质对DEX的反应产生了类似的影响。负反馈程度可被视为下丘脑神经刺激和糖皮质激素影响之间的平衡。因此,神经毒性损伤消除了NE和5-HT对肾上腺皮质分泌的刺激作用,增强了DEX的抑制作用。

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