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[儿科中的糖皮质激素]

[Glucocorticoids in pediatrics].

作者信息

Radmanović S Z

出版信息

Srp Arh Celok Lek. 1995 Jun;123 Suppl 1:58-62.

Abstract

Glucocorticoids (GCs) are among the most commonly used drugs. They have been employed to treat almost every known disease, from urticaria to leukemia. GCs are so termed because of their action to increase plasma glucose as a result of enhanced hepatic gluconeogenesis, but they play, also, key regulatory roles in a wide variety of physiologic processes. They are essential for survival under stress. GC effect is mediated through receptors localised in cytosol. Receptor-GC complexes bind to hormone response elements in nuclear DNA, affect transcription of genes, either stimulating or inhibiting mRNAs. Proteins so produced (enzymes, hormones) are responsible for the steroid response. There is one type of GC receptor and all GCs will affect all tissues in the same way. At present rational use of GCs falls into two categories: replacement therapy (in Addison's diseasse and in congenital adrenal hyperplasia) and pharmacotherapy, mostly for their anti-inflammatory and immunosuppressive properties, but also to lyse leukemic lymphocytes or to reduce brain edema. GC therapy does not cure the primary disease--it only ameliorates its manifestations and provides time for the body natural defenses to work. After the withdrawal of steroid therapy manifestations of primary process usually return. So, as a result, there is no positive effect on long-term prognosis. Most common indications for prologned high-dose GC therapy are in organ transplantation, tumour chemotherapy, collagen vascular syndromes, ulcerative colitis, nephrotic syndrome and regional enteritis. Asthma, allergic diseases, inflammatory eye diseases and blood dyscrasias are also often treated with GCs. Used in pharmacological doses GCs have a number of adverse side effects. The use of alternate 0 day therapy can decrease most GC side effects (less suppression of hypothalamic-pituitary-adrenal axis, growth inhibition, cushingoid features, infections and myopathy). Discontinuation of long-term therapy is potentially difficult ("steroid withdrawal syndrome"). It is necessary to reduce the total dose gradually, in small weekly decrements. Recent use of GCs in prenatal treatment of congenital adrenal hyperplasia is described.

摘要

糖皮质激素(GCs)是最常用的药物之一。它们已被用于治疗几乎所有已知疾病,从荨麻疹到白血病。之所以称其为糖皮质激素,是因为它们可通过增强肝脏糖异生作用来升高血糖,但它们在多种生理过程中也发挥着关键的调节作用。它们对于应激状态下的生存至关重要。GC的作用是通过位于细胞质中的受体介导的。受体 - GC复合物与核DNA中的激素反应元件结合,影响基因转录,刺激或抑制mRNA。如此产生的蛋白质(酶、激素)负责类固醇反应。只有一种类型的GC受体,所有GC都会以相同方式影响所有组织。目前,GC的合理使用分为两类:替代疗法(用于艾迪生病和先天性肾上腺增生)和药物治疗,主要利用其抗炎和免疫抑制特性,也用于溶解白血病淋巴细胞或减轻脑水肿。GC治疗并不能治愈原发性疾病——它只是改善其症状,并为机体的自然防御发挥作用争取时间。停用类固醇治疗后,原发性疾病的症状通常会复发。因此,对长期预后没有积极影响。长期大剂量GC治疗最常见的适应证是器官移植、肿瘤化疗、胶原血管综合征、溃疡性结肠炎、肾病综合征和局限性肠炎。哮喘、过敏性疾病、炎症性眼病和血液系统疾病也常使用GC治疗。以药理剂量使用GC会产生许多不良副作用。采用隔日疗法可减少大多数GC副作用(对下丘脑 - 垂体 - 肾上腺轴的抑制作用减轻、生长抑制、库欣样特征、感染和肌病)。长期治疗的停药可能很困难(“类固醇戒断综合征”)。有必要逐渐减少总剂量,每周少量递减。本文描述了GC在先天性肾上腺增生产前治疗中的最新应用。

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