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人类β-促黑素的正常与异常调节

Normal and abnormal regulation of beta-msh in man.

作者信息

Abe K, Nicholson W E, Liddle G W, Orth D N, Island D P

出版信息

J Clin Invest. 1969 Aug;48(8):1580-5. doi: 10.1172/JCI106123.

Abstract

The regulation of plasma beta-melanocyte-stimulating hormone (beta-MSH) in man has been studied utilizing a radioimmunoassay previously described (1). In normal subjects plasma beta-MSH values ranged from 20 to 110 pg/ml. Metyrapone increased and dexamethasone decreased plasma beta-MSH levels. Surgical stress stimulated beta-MSH secretion. Plasma beta-MSH levels were elevated in patients with untreated Addison's disease and untreated congenital adrenal hyperplasia, and these levels fell to normal during glucocorticoid therapy. In patients with Cushing's syndrome due to pituitary adrenocorticotropic hormone (ACTH) excess, plasma beta-MSH was slightly elevated before treatment. In those patients who developed pituitary tumors and hyperpigmentation after bilateral adrenalectomy, plasma beta-MSH was greatly elevated. In patients with Cushing's syndrome due to adrenal tumor, plasma beta-MSH was subnormal. In patients with the ectopic ACTH syndrome, the levels of plasma beta-MSH were high. Plasma beta-MSH had a diurnal variation in normal subjects, patients with Addison's disease, and patients with congenital adrenal hyperplasia; but the normal diurnal variation was lost in patients with Cushing's disease. In patients with high plasma beta-MSH, simultaneous determinations of plasma ACTH showed close correlation between the degree of elevation of ACTH and that of beta-MSH. In extracts of tumors from patients with the ectopic ACTH-MSH syndrome the quantities of the two hormones were roughly equivalent. In patients with hyperpigmentation due to a variety of disorders other than pituitary-adrenal abnormalities, plasma beta-MSH was normal. It is concluded that the secretion of beta-MSH is regulated by the same factors that regulate ACTH.

摘要

利用先前描述的放射免疫分析法(1)对人体血浆β-促黑素细胞激素(β-MSH)的调节进行了研究。正常受试者血浆β-MSH值范围为20至110 pg/ml。甲吡酮使血浆β-MSH水平升高,地塞米松则使其降低。手术应激刺激β-MSH分泌。未经治疗的艾迪生病和未经治疗的先天性肾上腺皮质增生患者血浆β-MSH水平升高,而在糖皮质激素治疗期间这些水平降至正常。在因垂体促肾上腺皮质激素(ACTH)过多导致的库欣综合征患者中,治疗前血浆β-MSH略有升高。在双侧肾上腺切除术后出现垂体肿瘤和色素沉着的患者中,血浆β-MSH大幅升高。在因肾上腺肿瘤导致的库欣综合征患者中,血浆β-MSH低于正常水平。在异位ACTH综合征患者中,血浆β-MSH水平较高。正常受试者、艾迪生病患者和先天性肾上腺皮质增生患者的血浆β-MSH有昼夜变化;但库欣病患者失去了正常的昼夜变化。在血浆β-MSH水平高的患者中,同时测定血浆ACTH显示ACTH升高程度与β-MSH升高程度密切相关。在异位ACTH-MSH综合征患者的肿瘤提取物中,这两种激素的量大致相当。在因垂体-肾上腺异常以外的各种疾病导致色素沉着的患者中,血浆β-MSH正常。结论是,β-MSH的分泌受调节ACTH的相同因素调控。

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Radioimmunoassay of ACTH in plasma.血浆促肾上腺皮质激素的放射免疫测定
J Clin Invest. 1968 Dec;47(12):2725-51. doi: 10.1172/JCI105955.

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