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New oral antidiabetic agents

机译:新型口服降糖药

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摘要

The pathophysiology of hyperglycemia in type 2 diabetes (T2DM) involves 3 main defects: insulin deficiency, excess hepatic glucose output, and insulin resistance. Oral anti-diabetic agents act in a variety of ways. These include agents that stimulate insulin secretion, reduce hepatic glucose production, delay digestion and absorption of intestinal carbohydrate or improve insulin action. Because of improved knowledge of pathophysiology, new drugs with mechanisms of action focussed on specific pathophysiological alterations have appeared, in order to utilize all the possibilities of treating this condition. Here, we focus on the new agents used in the latest years and the overcoming ones in future, in particular incretin-based therapies, drugs inhibiting kidney glucose reabsorption (SGLT2 inhibitors), and glucokinase activators. The strategy for new drug development advocated here is to establish a broad range of anti-diabetic medicines with different mechanisms of action and potential opportunities for effective combination therapies.
机译:2型糖尿病(T2DM)中高血糖的病理生理学涉及3个主要缺陷:胰岛素缺乏,肝葡萄糖输出过多和胰岛素抵抗。口服抗糖尿病药以多种方式起作用。这些药物包括刺激胰岛素分泌,减少肝葡萄糖生成,延迟肠道碳水化合物的消化和吸收或改善胰岛素作用的药物。由于对病理生理学的了解不断增强,因此出现了针对特定病理生理学变化的作用机理的新药,以利用治疗这种疾病的所有可能性。在这里,我们重点关注最近几年使用的新药物以及将来要克服的药物,特别是基于肠降血糖素的疗法,抑制肾脏葡萄糖重吸收的药物(SGLT2抑制剂)和葡萄糖激酶激活剂。这里提倡的新药开发策略是建立具有不同作用机制和有效联合疗法潜在机会的广泛的抗糖尿病药。

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