基于内泌素的双重和三重协同拮抗剂:肥胖症和糖尿病的新疗法

IF 3.8 3区 医学 Q2 Medicine Diabetes Therapy Pub Date : 2024-04-04 DOI:10.1007/s13300-024-01566-x
Robert M. Gutgesell, Rubén Nogueiras, Matthias H. Tschöp, Timo D. Müller
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摘要

长效胰高血糖素受体激动剂的发现标志着我们在应对肥胖和糖尿病双重流行病方面取得了重大进展。在这里,我们概述了基于增量素的药物疗法的发展历程,从外显素-4 到多重增量素激素受体激动剂的发现,这些激动剂有望成为我们治疗糖尿病和肥胖症的下一步。我们将讨论目前正在进行临床试验的多胰岛素受体激动剂,以及每一代新药带来的疗效改善。这些药物在临床前模型和临床试验中取得的成功表明,多拮抗剂在治疗代谢性疾病方面前景广阔,最新的葡萄糖依赖性胰岛素促肽受体:胰高血糖素样肽 1 受体:胰高血糖素受体(GIPR:GLP-1R:GCGR)三拮抗剂的疗效可与减肥手术相媲美。然而,要充分了解这些疗法是如何对体重产生影响的,还需要进一步的研究。在最后一节中,我们将讨论有关多拮抗剂药物潜在机制的未决问题,并了解如何利用肠脑沟通来实现无不良反应的持续体重减轻。
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Dual and Triple Incretin-Based Co-agonists: Novel Therapeutics for Obesity and Diabetes

The discovery of long-acting incretin receptor agonists represents a major stride forward in tackling the dual epidemic of obesity and diabetes. Here we outline the evolution of incretin-based pharmacotherapy, from exendin-4 to the discovery of the multi-incretin hormone receptor agonists that look set to be our next step toward curing diabetes and obesity. We discuss the multiagonists currently in clinical trials and the improvement in efficacy each new generation of these drugs bring. The success of these agents in preclinical models and clinical trials suggests a promising future for multiagonists in the treatment of metabolic diseases, with the most recent glucose-dependent insulinotropic peptide receptor:glucagon-like peptide 1 receptor:glucagon receptor (GIPR:GLP-1R:GCGR) triagonists rivaling the efficacy of bariatric surgery. However, further research is needed to fully understand how these therapies exert their effect on body weight and in the last section we cover open questions about the potential mechanisms of multiagonist drugs, and the understanding of how gut–brain communication can be leveraged to achieve sustained body weight loss without adverse effects.

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来源期刊
Diabetes Therapy
Diabetes Therapy Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
6.90
自引率
7.90%
发文量
130
审稿时长
6 weeks
期刊介绍: Diabetes Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all areas of diabetes. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Diabetes Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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