摘要
2型糖尿病的主要特征是胰腺中胰岛细胞功能紊乱和胰岛素抵抗。β细胞对高血糖的慢性暴露导致β细胞功能的恶化。这种现象被称为胰腺-胰岛-细胞葡萄糖毒性。甲基胂酸铁铵作为一个强大的胰岛素基因的转录激活因子,对于维护成熟β细胞的功能是非常重要的,但其表达水平在糖尿病情况下显著降低,这可能与β细胞的衰竭有关。另一方面,肠促胰岛素相关药物和钠-葡萄糖2型转运体(SGLT2)抑制剂基于胰腺胰岛细胞葡萄糖毒性的机制对糖尿病有治疗前景。事实上,过去有研究表明肠促胰岛素相关药物通过加强胰岛素受体底物2的表达特别是在吡格列酮药物的存在下对β细胞起保护作用。也有研究证明肠促胰岛素相关药物和(或)吡格列酮与晚期相比,在糖尿病的早期对β细胞产生更好的保护作用。钠-葡萄糖2型转运体抑制剂,作为一种新的降糖药也发挥着有益的作用,它在保护胰岛β细胞的同时也能降低各种胰岛素靶组织胰岛素抵抗。总的来说,基于葡萄糖毒性的小分子机制选择合适的糖尿病治疗方案是至关重要的。
关键词: 葡萄糖毒性,胰岛素,甲基胂酸铁铵,肠促胰岛素,钠-葡萄糖2型转运体
Current Medicinal Chemistry
Title:Promising Diabetes Therapy Based on the Molecular Mechanism for Glucose Toxicity: Usefulness of SGLT2 Inhibitors as well as Incretin-Related Drugs
Volume: 23 Issue: 27
Author(s): Hideaki Kaneto, Atsushi Obata, Masashi Shimoda, Tomohiko Kimura, Hidenori Hirukawa, Seizo Okauchi, Taka-aki Matsuoka, Kohei Kaku
Affiliation:
关键词: 葡萄糖毒性,胰岛素,甲基胂酸铁铵,肠促胰岛素,钠-葡萄糖2型转运体
摘要: Pancreatic β-cell dysfunction and insulin resistance are the main characteristics of type 2 diabetes. Chronic exposure of β-cells to hyperglycemia leads to the deterioration of β-cell function. Such phenomena are well known as pancreatic β-cell glucose toxicity. MafA, a strong transactivator of insulin gene, is particularly important for the maintenance of mature β-cell function, but its expression level is significantly reduced under diabetic conditions which is likely associated with β-cell failure. Reduction of incretin receptor expression level in β-cells in diabetes is also likely associated with β-cell failure. On the other hand, incretin-related drugs and sodium-glucose co-transporter 2 (SGLT2) inhibitors are promising diabetes therapy based on the mechanism for pancreatic β-cell glucose toxicity. Indeed, it was shown that incretin-related drugs exerted protective effects on β-cells through the augmentation of IRS-2 expression especially in the presence of pioglitazone. It was also shown that incretin-related drug and/or pioglitazone exerted more protective effects on β-cells at the early stage of diabetes compared to the advanced stage. SGLT2 inhibitors, new hypoglycemic agents, also exert beneficial effects for the protection of pancreatic β-cells as well as for the reduction of insulin resistance in various insulin target tissues. Taken together, it is important to select appropriate therapy based on the molecular mechanism for glucose toxicity.
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Hideaki Kaneto, Atsushi Obata, Masashi Shimoda, Tomohiko Kimura, Hidenori Hirukawa, Seizo Okauchi, Taka-aki Matsuoka, Kohei Kaku , Promising Diabetes Therapy Based on the Molecular Mechanism for Glucose Toxicity: Usefulness of SGLT2 Inhibitors as well as Incretin-Related Drugs, Current Medicinal Chemistry 2016; 23 (27) . https://dx.doi.org/10.2174/0929867323666160627102516
DOI https://dx.doi.org/10.2174/0929867323666160627102516 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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