肾上腺皮质类固醇:化学、合成和疾病中的干扰

V.H.T. James, J.D. Few
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引用次数: 24

摘要

肾上腺皮质类固醇的生物合成现在是一个相当好理解的过程,它是通过离散的、酶指导的步骤从胆固醇到各种激素类固醇进行的。然而,我们的大部分知识来自于对动物组织的研究,需要对人类腺体进行进一步的研究。特别是,单个酶系统的细节,以及类固醇中间体区隔化的程度和意义需要进一步探索。肾上腺代谢错误也值得进一步研究,以阐明先天性肾上腺增生的某些方面,并解释生化和临床观察之间的关系。用于测量血浆中类固醇激素水平的免疫测定方法的出现改变了诊断类固醇内分泌学的方法,现在较少强调尿液类固醇代谢物的测量,特别是关于雄激素。新的和灵敏的方法也允许测定唾液中的类固醇激素,这种液体的现成可用性,而且采样是一种非侵入性技术,这一事实使唾液类固醇测定成为其他有吸引力的替代方法,需要收集血液或尿液的传统调查方法。类固醇生物合成抑制剂和类固醇作用抑制剂已在诊断技术中取得了相当大的成功,并在有限程度上用于类固醇疾病的治疗。随着我们对类固醇生物合成细节、类固醇作用机制和类固醇分泌控制的了解的提高,在设计临床上有用的抑制剂方面应该有进一步的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adrenocorticosteroids: Chemistry, synthesis and disturbances in disease

The biosynthesis of adrenocortical steroids is now a reasonably well understood process, which proceeds by discrete, enzyme directed steps from cholesterol to the various hormonal steroids. However, much of our knowledge derives from studies of animal tissues and there is a need for further studies of human glands. In particular, the details of individual enzyme systems, and the extent and significance of compartmentalization of steroid intermediates requires further exploration. The adrenal metabolic errors also merit further study, to clarify some aspects of congenital adrenal hyperplasia and to explain the relationship between biochemical and clinical observations.

The advent of immunoassay methods for the measurement of steroid hormone levels in plasma has changed the approach to diagnostic steroid endocrinology, with less emphasis now on the measurement of urinary steroid metabolites, particularly in regard to androgens. The newer and sensitive methods available also allow the assay of steroid hormones in saliva, and the ready availability of this fluid, and the fact that sampling is a non-invasive technique makes salivary steroid assay an attractive alternative to other, traditional methods of investigation requiring blood or urine collection.

Inhibitors of steroid biosynthesis and of steroid action have been used with considerable success in diagnostic techniques and to a limited extent in the treatment of steroid disorders. As our understanding of the details of steroid biosynthesis, mechanism of steroid action, and control of steroid secretion improve, further progress in designing clinically useful inhibitors should be possible.

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