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2型糖尿病中的红细胞膜

Erythrocyte membrane in type 2 diabetes mellitus.

作者信息

Gabreanu Georgiana Roxana, Angelescu Silvana

机构信息

Hematology Department, Coltea Clinical Hospital, Bucharest, Romania.

出版信息

Discoveries (Craiova). 2016 Jun 30;4(2):e60. doi: 10.15190/d.2016.7.

Abstract

Type 2 diabetes mellitus represents a major public health challenge, due to the continuously growing prevalence and the complexity of the diabetic complications. Hyperglycemia seems to be the main mechanism for the disease progression. During erythrocyte's long life span, erythrocyte membranes are affected by the chronic exposure to glucose, which triggers several biochemical modifications that lead to both structural and functional disruption, which are further involved in the physiopathology of diabetes and its complications. Non-enzymatic protein glycation of red blood cell membrane proteins occur in two phases: early glycation, characterized by Schiff bases and Amadouri compounds formation, and advanced glycation, characterized by advanced glycation end products (AGEs). These products could be valuable tools for early diagnosis or biomarkers for disease progression, depending on how advanced they are in the glycation process. Advanced glycated end products were linked with diabetic complications. Also, lipid peroxidation and decreased activity of the enzyme pumps occur in the erythrocyte membrane of the diabetic patients. The investigation of lipid rafts and erythrocyte membrane fatty acids are a valuable tool for long-term monitoring of metabolic status. Further investigation of the erythrocyte membrane could provide novel biomarkers for monitoring of diabetes and its complications.

摘要

2型糖尿病是一项重大的公共卫生挑战,这是由于其患病率持续上升以及糖尿病并发症的复杂性。高血糖似乎是疾病进展的主要机制。在红细胞的漫长生命周期中,红细胞膜会受到长期暴露于葡萄糖的影响,这会引发多种生化修饰,导致结构和功能破坏,进而参与糖尿病及其并发症的病理生理过程。红细胞膜蛋白的非酶促蛋白糖基化分两个阶段发生:早期糖基化,其特征是席夫碱和阿马多里化合物的形成;晚期糖基化,其特征是晚期糖基化终产物(AGEs)。这些产物可能是早期诊断的有价值工具或疾病进展的生物标志物,这取决于它们在糖基化过程中的进展程度。晚期糖基化终产物与糖尿病并发症有关。此外,糖尿病患者的红细胞膜中还会发生脂质过氧化和酶泵活性降低。对脂筏和红细胞膜脂肪酸的研究是长期监测代谢状态的有价值工具。对红细胞膜的进一步研究可为监测糖尿病及其并发症提供新的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ef8/7159822/60015a1dca02/discoveries-04-060-g001.jpg

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