Role of advanced glycation end products (AGEs) and its receptor (RAGE)-mediated diabetic vascular complications

Diwesh Chawla, A. Tripathi
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引用次数: 8

Abstract

Diabetes mellitus (DM) is one of the major epidemic disorders of the current century [1,2]. It is a group of metabolic disorders leading to defects in insulin secretion and action of insulin or both. Diabetes is influenced by a combination of both hereditary and environmental factors [3]. In the human body, blood glucose levels are controlled by a complex interaction of multiple chemicals and hormones, including insulin and glucagon. Insulin is one of the important peptide hormones produced from the beta cells of the pancreas that allows blood glucose to enter various cells of the body where it is oxidized to yield energy needed by the muscles and tissues to function [4]. Glucagon is also a peptide hormone, secreted from the alpha cells of the pancreas, which causes a rise in the blood glucose concentration. The effect of glucagon is opposite to that of insulin, which lowers the blood glucose concentration.
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晚期糖基化终产物(AGEs)及其受体(RAGE)介导的糖尿病血管并发症的作用
糖尿病(DM)是本世纪主要的流行疾病之一[1,2]。它是一组导致胰岛素分泌和胰岛素作用缺陷或两者兼而有之的代谢紊乱。糖尿病受遗传和环境因素共同影响[3]。在人体内,血糖水平是由多种化学物质和激素(包括胰岛素和胰高血糖素)的复杂相互作用控制的。胰岛素是胰腺β细胞产生的重要肽激素之一,它允许血糖进入身体的各种细胞,在那里它被氧化以产生肌肉和组织功能所需的能量[4]。胰高血糖素也是一种肽激素,由胰腺的α细胞分泌,它会导致血糖浓度升高。胰高血糖素的作用与胰岛素相反,后者能降低血糖浓度。
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