The CRFs and their control: Chemistry, physiology and clinical implications

Glenda Gillies, Ashley Grossman
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引用次数: 42

Abstract

The 41-amino acid CRF fulfils all the criteria for a corticotrophin releasing factor, although considerable evidence suggests that other factors, particularly VP, also play a physiologically significant role in controlling ACTH release. Although human CRF has now been identified as a 41-residue peptide, most studies to date have used oCRF-41 in their exploration of the physiology and pathology of the hypothalamic-pituitary-adrenal axis. Low doses of oCRF-41 appear to be safe, and for specific tests of the readily-releasable pool of ACTH and related peptides 100 μg is a practical dose for most purposes. Although serious side-effects have only been noted at doses above 100 μg, it is reasonable to monitor all patients administered CRF-41 with great care, and in particular to be alert to hypotension, especially in patients with corticosteroid deficiency. There is little doubt that, in combination with the standard insulin-tolerance test, the CRF test is a useful means of diagnosing hypothalamic or portal dysfunction in patients with secondary adrenal failure. However, in the diagnosis and differential diagnosis of Cushing's syndrome, the role of the CRF test remains unclear. In normal subjects, a high basal cortisol level usually inhibits the response to CRF, such that a greatly enhanced response is suggestive of pituitary-dependent Cushing's syndrome. In patients with diagnosed ACTH-dependent Cushing's syndrome, an absent response to CRF predisposes towards an ectopic source of ACTH. However, there are exceptions in all directions, and it is uncertain whether the CRF test will prove of greater value than the traditional procedures, such as the dexamethasone suppression test. The differential diagnosis of depression and Cushing's disease may be its greatest value.

In terms of treatment, there are as yet few data on the usefulness of CRF in expediting recovery of the pituitary-adrenal axis following long-term suppression, such as in patients with Cushing's syndrome treated by removal of a unilateral adenoma or trans-sphenoidal microadenomectomy. It is possible that such treatment may eventually be a useful application of CRF, although data are not yet available.

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CRFs及其对照:化学、生理和临床意义
41个氨基酸的CRF满足促肾上腺皮质激素释放因子的所有标准,尽管大量证据表明其他因素,特别是VP,在控制ACTH释放方面也起着重要的生理作用。虽然人类CRF现在已被确定为41-残基肽,但迄今为止大多数研究都使用CRF-41来探索下丘脑-垂体-肾上腺轴的生理和病理。低剂量的oCRF-41似乎是安全的,对于易释放的ACTH和相关肽库的特定测试,100 μg是大多数目的的实用剂量。虽然严重的副作用仅在剂量超过100 μg时才被发现,但非常谨慎地监测所有给予CRF-41的患者是合理的,尤其要警惕低血压,特别是皮质类固醇缺乏症患者。毫无疑问,结合标准胰岛素耐量试验,CRF试验是诊断继发性肾上腺衰竭患者下丘脑或门脉功能障碍的有效手段。然而,在库欣综合征的诊断和鉴别诊断中,CRF检测的作用尚不清楚。在正常受试者中,较高的基础皮质醇水平通常会抑制对CRF的反应,因此反应的显著增强提示垂体依赖性库欣综合征。在诊断为ACTH依赖性库欣综合征的患者中,对CRF的无反应易导致ACTH异位来源。然而,在所有方向上都有例外,目前尚不确定CRF试验是否会证明比传统方法(如地塞米松抑制试验)更有价值。对抑郁症和库欣病的鉴别诊断可能是其最大的价值。在治疗方面,关于CRF在长期抑制后加速垂体-肾上腺轴恢复方面的有用性的数据还很少,例如在库欣综合征患者中通过切除单侧腺瘤或经蝶窦微腺瘤切除术。这种治疗可能最终成为CRF的有用应用,尽管目前还没有数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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