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磺脲类药物在2型糖尿病管理中的作用。

The role of sulphonylureas in the management of type 2 diabetes mellitus.

作者信息

Rendell Marc

机构信息

Creighton Diabetes Center, 601 North 30th Street, Omaha, NE 68131, USA.

出版信息

Drugs. 2004;64(12):1339-58. doi: 10.2165/00003495-200464120-00006.

Abstract

The sulphonylureas act by triggering insulin release from the pancreatic beta cell. A specific site on the adenosine triphosphate (ATP)-sensitive potassium channels is occupied by sulphonylureas leading to closure of the potassium channels and subsequent opening of calcium channels. This results in exocytosis of insulin. The meglitinides are not sulphonylureas but also occupy the sulphonylurea receptor unit coupled to the ATP-sensitive potassium channel. Glibenclamide (glyburide), gliclazide, glipizide and glimepiride are the primary sulphonylureas in current clinical use for type 2 diabetes mellitus. Glibenclamide has a higher frequency of hypoglycaemia than the other agents. With long-term use, there is a progressive decrease in the effectiveness of sulphonylureas. This loss of effect is the result of a reduction in insulin-producing capacity by the pancreatic beta cell and is also seen with other antihyperglycaemic agents. The major adverse effect of sulphonylureas is hypoglycaemia. There is a theoretical concern that sulphonylureas may affect cardiac potassium channels resulting in a diminished response to ischaemia. There are now many choices for initial therapy of type 2 diabetes in addition to sulphonylureas. Metformin and thiazolidinediones affect insulin sensitivity by independent mechanisms. Disaccharidase inhibitors reduce rapid carbohydrate absorption. No single agent appears capable of achieving target glucose levels in the majority of patients with type 2 diabetes. Combinations of agents are successful in lowering glycosylated haemoglobin levels more than with a single agent. Sulphonylureas are particularly beneficial when combined with agents such as metformin that decrease insulin resistance. Sulphonylureas can also be given with a basal insulin injection to provide enhanced endogenous insulin secretion after meals. Sulphonylureas will continue to be used both primarily and as part of combined therapy for most patients with type 2 diabetes.

摘要

磺脲类药物通过触发胰腺β细胞释放胰岛素发挥作用。磺脲类药物占据三磷酸腺苷(ATP)敏感性钾通道上的一个特定位点,导致钾通道关闭,随后钙通道开放。这会导致胰岛素的胞吐作用。格列奈类药物虽不是磺脲类药物,但也占据与ATP敏感性钾通道偶联的磺脲类受体单元。格列本脲(优降糖)、格列齐特、格列吡嗪和格列美脲是目前临床上用于治疗2型糖尿病的主要磺脲类药物。格列本脲导致低血糖的发生率高于其他药物。长期使用后,磺脲类药物的疗效会逐渐降低。这种疗效丧失是胰腺β细胞胰岛素分泌能力下降的结果,其他降糖药物也会出现这种情况。磺脲类药物的主要不良反应是低血糖。理论上担心磺脲类药物可能影响心脏钾通道,导致对缺血的反应减弱。除了磺脲类药物外,目前2型糖尿病初始治疗还有很多选择。二甲双胍和噻唑烷二酮类药物通过独立机制影响胰岛素敏感性。双糖酶抑制剂可减少碳水化合物的快速吸收。没有一种单一药物似乎能够使大多数2型糖尿病患者达到目标血糖水平。联合用药比单一用药更能成功降低糖化血红蛋白水平。当磺脲类药物与二甲双胍等降低胰岛素抵抗的药物联合使用时,尤其有益。磺脲类药物也可与基础胰岛素注射联合使用,以增强餐后内源性胰岛素分泌。对于大多数2型糖尿病患者,磺脲类药物将继续作为主要治疗药物以及联合治疗的一部分使用。

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