Sönksen P H, Russell-Jones D, Jones R H
Department of Endocrinology and Chemical Pathology, United Medical School, Guy's Hospital, London, UK.
Horm Res. 1993;40(1-3):68-79. doi: 10.1159/000183770.
The diabetogenic action of pituitary extracts containing growth hormone has been recognised for more than 60 years and the importance of growth hormone in the development and progression of diabetic retinopathy for more than 30 years. Hypophysectomy was the first effective treatment for retinopathy but was discontinued because of the risk of severe hypoglycaemia that it produced and the development of an alternative, less dangerous therapy--photocoagulation. The precise role and significance of growth hormone in diabetes care, however, remains to this day a mystery. The fact that modern, highly purified biosynthetic preparations of growth hormone still retain full diabetogenic potency and the fact that diabetes develops in up to 25% of patients with acromegaly indicate growth hormone's potential for involvement in the aetiology of diabetes mellitus, although most will agree that this is not likely to be an important factor in the large majority of 'idiopathic' cases. There is strong evidence to indicate a substantial hypersecretion of growth hormone in 'idiopathic' diabetes mellitus (particularly insulin-dependent cases and those with retinopathy), which appears to be more related to residual pancreatic insulin secretion than to metabolic control. Since the advent of biosynthetic growth hormone in sufficient quantity to perform trials in adults, we are more aware of growth hormone's considerable potency in the regulation of body composition, growth factor production and intermediary metabolism. In this article, we review the literature and, from this and our own work, propose a new hypothesis which links the hypersecretion of growth hormone to reduced hepatic secretion of insulin-like growth-factor I (IGF-I) as a direct result of reduced portal insulin levels in diabetes mellitus. The hypersecretion of growth hormone exposes peripheral organs such as the retina and kidney to conditions favouring the expression of growth-hormone-dependent growth factors such as IGF-I which may contribute to the development of diabetic microvascular disease by autocrine and/or paracrine effects. If this hypothesis proves to be true, it offers new opportunities for the prevention of diabetic microvascular complications through suppression of growth hormone secretion which in turn will increase insulin sensitivity and facilitate good glycaemic control.
含有生长激素的垂体提取物的致糖尿病作用已被认识超过60年,而生长激素在糖尿病性视网膜病变发生和发展中的重要性也已被认识超过30年。垂体切除术是治疗视网膜病变的首个有效方法,但由于其会引发严重低血糖风险以及出现了替代的、危险性较小的疗法——光凝术,该方法已停止使用。然而,生长激素在糖尿病治疗中的精确作用和意义至今仍是个谜。现代高度纯化的生物合成生长激素制剂仍保留完全的致糖尿病效力,以及高达25%的肢端肥大症患者会患糖尿病这一事实,表明生长激素可能参与了糖尿病的病因学,尽管大多数人会认为在绝大多数“特发性”病例中这不太可能是一个重要因素。有强有力的证据表明,“特发性”糖尿病(尤其是胰岛素依赖型病例和伴有视网膜病变的病例)中生长激素大量分泌,这似乎与胰腺残余胰岛素分泌的关系比与代谢控制的关系更大。自从有足够数量的生物合成生长激素可用于成人试验以来,我们更加清楚生长激素在调节身体组成、生长因子产生和中间代谢方面具有相当大的效力。在本文中,我们回顾了文献,并基于此及我们自己的研究工作,提出了一个新的假说,该假说将生长激素的分泌过多与糖尿病时门静脉胰岛素水平降低导致的肝脏胰岛素样生长因子-I(IGF-I)分泌减少联系起来。生长激素分泌过多使视网膜和肾脏等外周器官处于有利于诸如IGF-I等生长激素依赖性生长因子表达的条件下,这些生长因子可能通过自分泌和/或旁分泌作用促成糖尿病微血管疾病的发展。如果这个假说被证明是正确的,那么通过抑制生长激素分泌为预防糖尿病微血管并发症提供了新的机会,这反过来又会提高胰岛素敏感性并促进良好的血糖控制。