2型糖尿病的进展:部分原因是ASP-C5L2通路缺乏?

Wenlong Li, Rutai Hui
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引用次数: 0

摘要

2型糖尿病以胰岛素抵抗和β细胞功能障碍为特征。酰化刺激蛋白(ASP)及其特异性受体c5a样受体2 (C5L2)的途径参与了血浆葡萄糖和游离脂肪酸的有效清除。异常的ASP-C5L2通路可诱发胰岛素抵抗,引起高血糖和血浆游离脂肪酸升高。高水平的血浆葡萄糖和游离脂肪酸诱导β-细胞凋亡和功能障碍。我们提出ASP-C5L2通路异常参与了2型糖尿病的进展。
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The progression of type 2 diabetes: Partly caused by deficiency of ASP-C5L2 pathway?

Type 2 diabetes is characterized by insulin resistance and β-cell dysfunction. The pathway of acylation-stimulating protein (ASP) and its specific receptor, C5a-like receptor 2 (C5L2), involves in the effective clearance of plasma glucose and free fat acid. Abnormal ASP-C5L2 pathway may induce insulin resistance, as well as cause hyperglycemia and elevated plasma free fat acid. High levels of plasma glucose and free fat acid induce β-cell apoptosis and dysfunction. We proposed that the abnormality of ASP-C5L2 pathway contributes to progression of type 2 diabetes.

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