Du Mei-Rong, Ju Gui-Xia, Li Nian-Sheng, Jiang Jun-Lin
*Department of Pharmacology, School of Pharmaceutical Sciences, Central South University, Changsha, China;†Department of Pharmacy, The Affiliated Hospital of Luzhou Medical College, Sichuan, China; and‡Provincial Key Laboratory of Cardiovascular Research, Central South University, Changsha, China.
J Cardiovasc Pharmacol. 2016 Oct;68(4):322-326. doi: 10.1097/FJC.0000000000000414.
Microvascular complications are the leading causes of acquired blindness, end-stage renal failure, and varieties of neuropathy associated with diabetes. Asymmetric dimethylarginine (ADMA), an endogenous nitric oxide synthase inhibitor, is involved in endothelial dysfunction, oxidative stress, and inflammation associated with the progression of diabetic microvascular complications. Elevated ADMA has been detected in experimental animals and patients with diabetic microangiopathy like retinopathy, nephropathy, and neuropathy. In the review, we focus on the role of ADMA in the pathobiology of major microvascular complications of diabetes.
微血管并发症是导致后天性失明、终末期肾衰竭以及各类糖尿病相关神经病变的主要原因。非对称二甲基精氨酸(ADMA)是一种内源性一氧化氮合酶抑制剂,参与了与糖尿病微血管并发症进展相关的内皮功能障碍、氧化应激和炎症反应。在实验动物以及患有糖尿病微血管病变(如视网膜病变、肾病和神经病变)的患者中均检测到ADMA水平升高。在本综述中,我们重点关注ADMA在糖尿病主要微血管并发症病理生物学中的作用。