去氨加压素的临床应用历史

Lennox R. Ksido , Cassandra V. Heaney , Thomas F. Monaghan , Jeffrey P. Weiss
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引用次数: 0

摘要

去氨加压素是内源性肽类激素精氨酸血管加压素或抗利尿激素的合成类似物。这种药物最初开发于 1967 年,目的是创造一种可以治疗中枢性糖尿病的分子,中枢性糖尿病的特点是缺乏 ADH,会产生大量稀释尿液(Zaoral 等人,1967 年)。此后数年,去氨加压素的治疗用途已从中枢性糖尿病扩展到治疗许多其他疾病,特别是儿童夜尿症(尿床)、成人夜尿症、先天性出血性疾病等。本综述旨在回顾去氨加压素的历史,回顾其主要治疗适应症,并讨论该药物在药理学和药代动力学方面的重要注意事项。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
History of clinical applications of desmopressin
Desmopressin is a synthetic analog of the endogenous peptide hormone arginine vasopressin, or antidiuretic hormone. The drug was initially developed in 1967 with the intention of creating a molecule that could treat central diabetes insipidus, a condition characterized by a deficiency of ADH and results in the production of large volumes of dilute urine (Zaoral et al., 1967). In the years since, therapeutic use of desmopressin has expanded beyond central diabetes insipidus to include the treatment of many other conditions, notably nocturnal polyuria in children with enuresis (bed wetting), adult nocturia, congenital bleeding disorders, and more. The purpose of the present narrative review is to recount the history of desmopressin, review its key therapeutic indications, and discuss important pharmacologic and pharmacokinetic considerations of this medication.
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