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1型糖尿病微血管并发症中的血流动力学

Haemodynamics in microvascular complications in type 1 diabetes.

作者信息

Candido Riccardo, Allen Terri J

机构信息

Division of Diabetes, Lipoproteins and Metabolism, Baker Heart Research Institute, Melbourne, Victoria, Australia.

出版信息

Diabetes Metab Res Rev. 2002 Jul-Aug;18(4):286-304. doi: 10.1002/dmrr.313.

Abstract

Type 1 diabetes is commonly associated with microvascular complications. Most of the microvascular blood vessels are involved but those in the kidney, retina and large nerves exhibit the more significant pathology. Haemodynamic and metabolic factors both alone and through the activation of a common pathway contribute to the characteristic dysfunction observed in diabetic vasculopathy. The haemodynamic abnormalities in type 1 diabetes are characterized by increased systemic blood pressure and altered blood flow with subsequent activation of various vasoactive factors, which can contribute to the maintenance of the haemodynamic alterations and to the development and progression of the microvascular complications. These vasoactive factors include vasoconstrictors such as angiotensin II, and endothelin, as well as vasodilators such as nitric oxide (NO). Systemic hypertension and vasoactive factors independently and in interaction with the metabolic pathway activate intracellular second messengers, nuclear transcription factors and various growth factors which lead to the typical functional and structural alterations of diabetic microvascular complications. Therapeutic strategies involved in the management and prevention of diabetic complications currently include antihypertensive agents, particularly those that interrupt the renin-angiotensin system. Further understanding of the interactions among the vasoactive factors, the intracellular second messengers and the growth factors may help to identify novel strategies to influence the action of the vasoactive factors. These novel therapies, together with specific inhibitors of the metabolic pathway or the common pathway, may provide the possibility of preventing or even reversing the progression of diabetic microvascular complications.

摘要

1型糖尿病通常与微血管并发症相关。大多数微血管都会受累,但肾脏、视网膜和大神经中的血管病变更为显著。血流动力学和代谢因素单独作用以及通过共同途径的激活,都导致了糖尿病血管病变中观察到的特征性功能障碍。1型糖尿病中的血流动力学异常表现为全身血压升高和血流改变,随后激活各种血管活性因子,这可能有助于维持血流动力学改变以及微血管并发症的发生和发展。这些血管活性因子包括血管收缩剂,如血管紧张素II和内皮素,以及血管舒张剂,如一氧化氮(NO)。全身高血压和血管活性因子独立作用并与代谢途径相互作用,激活细胞内第二信使、核转录因子和各种生长因子,导致糖尿病微血管并发症典型的功能和结构改变。目前用于管理和预防糖尿病并发症的治疗策略包括抗高血压药物,尤其是那些阻断肾素-血管紧张素系统的药物。进一步了解血管活性因子、细胞内第二信使和生长因子之间的相互作用,可能有助于确定影响血管活性因子作用的新策略。这些新疗法,连同代谢途径或共同途径的特异性抑制剂,可能提供预防甚至逆转糖尿病微血管并发症进展的可能性。

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