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利拉利汀,一种基于黄嘌呤的二肽基肽酶-4 抑制剂,具有治疗 2 型糖尿病的独特特征。

Linagliptin, a xanthine-based dipeptidyl peptidase-4 inhibitor with an unusual profile for the treatment of type 2 diabetes.

机构信息

University of Copenhagen, Panum Institute, Department of Biomedical Sciences, DK-2200 Copenhagen N, Denmark.

出版信息

Expert Opin Investig Drugs. 2010 Jan;19(1):133-40. doi: 10.1517/13543780903463862.

Abstract

IMPORTANCE OF THE FIELD

Type 2 diabetes is a progressive disease for which current treatments are often unsatisfactory with respect to achieving therapeutic goals and unwanted side effects.

AREAS COVERED

Preclinical and clinical studies of linagliptin, a new oral antidiabetic agent, including data presented at Scientific Meetings and peer-reviewed studies published since 2007.

WHAT THE READER WILL GAIN

This article reviews pharmacokinetic and pharmacodynamic characteristics of linagliptin. Linagliptin belongs to a new chemical class of dipeptidyl pepidase-4 (DPP-4) inhibitors, which comprise xanthine-based compounds. It is a potent, long-acting inhibitor with high selectivity for DPP-4 versus the related enzymes DPP-8 and DPP-9. The drug has modest oral availability in humans, but is absorbed rapidly to inhibit plasma DPP-4 activity by > 80% over 24 h. It is not metabolized appreciably in vivo, but binds extensively to plasma proteins, with elimination occurring primarily in the liver. Linagliptin reduces degradation of the incretin hormone glucagon-like peptide-1 and is associated with reduced fasting and postprandial glucose in preclinical and clinical studies. Limited data from longer duration clinical trials show it improves glycemic control in patients with type 2 diabetes.

TAKE HOME MESSAGE

Linagliptin is a new oral antidiabetic agent associated with minimal risk of hypoglycemia, which holds promise for treatment of type 2 diabetes.

摘要

重要性领域

2 型糖尿病是一种进行性疾病,目前的治疗方法在实现治疗目标和避免不良副作用方面往往不尽如人意。

涵盖范围

新型口服抗糖尿病药物利格列汀的临床前和临床研究,包括科学会议上提交的数据和 2007 年以来发表的同行评议研究。

读者将获得的收益

本文综述了利格列汀的药代动力学和药效学特征。利格列汀属于二肽基肽酶-4(DPP-4)抑制剂的新化学类别,包括黄嘌呤类化合物。它是一种强效、长效抑制剂,对 DPP-4 具有高度选择性,而对相关酶 DPP-8 和 DPP-9 的选择性较低。该药物在人体中的口服生物利用度适中,但在 24 小时内可迅速吸收,使血浆 DPP-4 活性抑制超过 80%。它在体内不易代谢,但与血浆蛋白广泛结合,主要通过肝脏消除。利格列汀可减少肠促胰岛素激素胰高血糖素样肽-1 的降解,与降低空腹和餐后血糖有关,在临床前和临床研究中得到证实。来自更长时间临床试验的有限数据表明,它可改善 2 型糖尿病患者的血糖控制。

结论

利格列汀是一种新型口服抗糖尿病药物,低血糖风险低,有望用于治疗 2 型糖尿病。

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