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糖皮质激素反馈抵抗。

Glucocorticoid feedback resistance.

机构信息

Division of Medical Pharmacology, Leiden/Amsterdam Center for Drug Research, Leiden University, , 2300 RA Leiden, Netherlands.

出版信息

Trends Endocrinol Metab. 1997 Jan-Feb;8(1):26-33. doi: 10.1016/s1043-2760(96)00205-6.

Abstract

Glucocorticoid feedback resistance can be inherited or locally acquired. The implications of these two forms of resistance for disease are strikingly different. The inherited form is characterized by enhanced adrenocortical function and hypercorticism to compensate for a generalized deficit in the glucocorticoid receptor gene, but these individuals lack symptoms of Cushing's syndrome. By contrast, resistance acquired at the level of the hypothalamic corticotropin-releasing hormone (CRH) neurons is linked to hypercorticism, which is not compensatory but overexposes the rest of the body and the brain to glucocorticoids. This cell-specific glucocorticoid resistance can be acquired by genetically predisposed individuals failing to cope with (early) life events and causes enhanced vulnerability to disease-specific actions of glucocorticoids. (c) 1997, Elsevier Science Inc. (Trends Endocrinol Metab 1997; 8:26-33).

摘要

糖皮质激素反馈抵抗可以是遗传性的,也可以是局部获得性的。这两种形式的抵抗对疾病的影响有显著的不同。遗传性抵抗的特征是肾上腺皮质功能增强和皮质醇过多,以代偿糖皮质激素受体基因的普遍缺陷,但这些个体没有库欣综合征的症状。相比之下,在下丘脑促肾上腺皮质激素释放激素 (CRH) 神经元水平获得的抵抗与皮质醇过多有关,这种皮质醇过多不是代偿性的,而是使身体和大脑的其他部位过度暴露于糖皮质激素下。这种细胞特异性糖皮质激素抵抗可以被遗传易感性个体在无法应对(早期)生活事件时获得,并导致对糖皮质激素的特定疾病作用的易感性增强。(c)1997,Elsevier Science Inc.(Trends Endocrinol Metab 1997;8:26-33)。

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