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替尔泊肽:一种新型的每周一次的双重GIP和GLP-1受体激动剂,用于治疗2型糖尿病。

Tirzepatide: A Novel, Once-weekly Dual GIP and GLP-1 Receptor Agonist for the Treatment of Type 2 Diabetes.

作者信息

Kaneko Shizuka

机构信息

Division of Diabetes/Endocrinology/Lifestyle-Related Disease, Takatsuki Red Cross Hospital, Takatsuki, Japan.

出版信息

touchREV Endocrinol. 2022 Jun;18(1):10-19. doi: 10.17925/EE.2022.18.1.10. Epub 2022 Jun 16.

Abstract

Gastrointestinal hormones are currently used to treat type 2 diabetes mellitus (T2D). Incretin preparations with gastric inhibitory polypeptide (GIP) activity or glucagon-like peptide-1 (GLP-1) provide new means for controlling blood glucose levels, body weight, and lipid metabolism. GIP, an incretin, has not been used due to lack of promising action against diabetes. However, recent studies have shown that GIP has an important effect on glucagon and insulin secretion under normoglycaemic conditions. Co-existence of GIP with GLP-1 and glucagon signalling leads to a stronger effect than that of GLP-1 stimulation alone. The development of a GIP/GLP-1R unimolecular dual agonist with affinity for both GIP and GLP-1 receptors is under investigation, and the drug is expected to be clinically available in the near future. Tirzepatide, a GIP/GLP-1R unimolecular dual agonist, regulates metabolism via both peripheral organs and the central nervous system. The SURPASS phase III clinical trials conducted for tirzepatide comprise 10 clinical trials, including five global trials and the global SURPASS-CVOT trial, with >13,000 patients with T2D (ClinicalTrials.gov Identifier: NCT04255433). The clinical application of tirzepatide as a therapy for T2D may provide new insights into diabetic conditions and help clarify the role of GIP in its pathogenesis.

摘要

胃肠道激素目前被用于治疗2型糖尿病(T2D)。具有胃抑制多肽(GIP)活性或胰高血糖素样肽-1(GLP-1)的肠促胰岛素制剂为控制血糖水平、体重和脂质代谢提供了新方法。GIP作为一种肠促胰岛素,由于对糖尿病缺乏有效的治疗作用,尚未被应用。然而,最近的研究表明,在正常血糖条件下,GIP对胰高血糖素和胰岛素分泌具有重要作用。GIP与GLP-1及胰高血糖素信号共同存在时,其作用比单独刺激GLP-1更强。一种对GIP和GLP-1受体均具有亲和力的GIP/GLP-1R单分子双激动剂正在研发中,预计该药物在不久的将来可应用于临床。替尔泊肽是一种GIP/GLP-1R单分子双激动剂,可通过外周器官和中枢神经系统调节代谢。针对替尔泊肽开展的SURPASS III期临床试验包括10项临床试验,其中有5项全球试验和全球SURPASS-CVOT试验,纳入了超过13000例T2D患者(ClinicalTrials.gov标识符:NCT04255433)。替尔泊肽作为T2D治疗药物的临床应用可能为糖尿病病情提供新的见解,并有助于阐明GIP在其发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ca/9354517/3e4c668781fb/touchendo-18-10-g001.jpg

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