Motoshima Hiroyuki, Araki Eiichi
Department of Metabolic Medicine, Faculty of Life Sciences, Kumamoto University.
Nihon Rinsho. 2012 Sep;70(9):1542-9.
The role of the renin-angiotensin-aldosterone system (RAAS) on the development of insulin resistance and type 2 diabetes (T2DM) is an area of growing interest. Most of the deleterious actions of the RAAS on insulin signals appear to be mediated through activation of the serine/threonine kinase, oxidative stress and tissue-inflammation in insulin-sensitive organs. Both experimental and clinical studies demonstrated that angiotensin II (Ang II) and aldosterone could play a role in the development of insulin resistance, diabetes and cardiovascular diseases. Large randomized clinical trials revealed that blockade of the RAAS with either angiotensin I converting enzyme inhibitors or AT1 receptor blockers results in decreased T2DM incidence, with a minor attenuation of markers for insulin resistance. This review focuses on the role of RAAS in the pathogenesis of insulin resistance, as well as on clinical relevance of RAAS blockade in the prevention and treatment of the metabolic syndrome and pre-diabetes.
肾素-血管紧张素-醛固酮系统(RAAS)在胰岛素抵抗和2型糖尿病(T2DM)发生发展中的作用是一个日益受到关注的领域。RAAS对胰岛素信号的大多数有害作用似乎是通过激活丝氨酸/苏氨酸激酶、氧化应激和胰岛素敏感器官中的组织炎症来介导的。实验研究和临床研究均表明,血管紧张素II(Ang II)和醛固酮可能在胰岛素抵抗、糖尿病和心血管疾病的发生发展中起作用。大型随机临床试验表明,使用血管紧张素I转换酶抑制剂或AT1受体阻滞剂阻断RAAS可降低T2DM发病率,同时胰岛素抵抗标志物略有减轻。本综述重点关注RAAS在胰岛素抵抗发病机制中的作用,以及RAAS阻断在预防和治疗代谢综合征及糖尿病前期中的临床意义。