改变肥胖症:多受体药物的发展

IF 45.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Pub Date : 2024-07-25 DOI:10.1016/j.cell.2024.06.003
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引用次数: 0

摘要

一个多世纪以来,医生们一直在寻找通过药物减少体内多余脂肪的方法。最近,胰高血糖素样肽-1(GLP-1)受体的生化工程激动剂及其在基于 GLP-1 的多拮抗剂中的应用取得了进展,终于扭转了这一趋势。这些多拮抗剂通过结合胰高血糖素和/或葡萄糖依赖性促胰岛素多肽(GIP)受体的互补药理学来减轻体重。在最先进的形式中,肠道激素多拮抗剂可达到前所未有的减重效果,减重幅度可达 20%-30%,为减肥手术提供了一种药物替代方案。除了对血糖、脂肪肝和肾脏疾病产生有利影响外,它们还对心血管系统和脂肪组织产生有益影响。因此,这些新的干预措施为未来的抗肥胖药物带来了巨大的希望。
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Transforming obesity: The advancement of multi-receptor drugs

For more than a century, physicians have searched for ways to pharmacologically reduce excess body fat. The tide has finally turned with recent advances in biochemically engineered agonists for the receptor of glucagon-like peptide-1 (GLP-1) and their use in GLP-1-based polyagonists. These polyagonists reduce body weight through complementary pharmacology by incorporating the receptors for glucagon and/or the glucose-dependent insulinotropic polypeptide (GIP). In their most advanced forms, gut-hormone polyagonists achieve an unprecedented weight reduction of up to ∼20%–30%, offering a pharmacological alternative to bariatric surgery. Along with favorable effects on glycemia, fatty liver, and kidney disease, they also offer beneficial effects on the cardiovascular system and adipose tissue. These new interventions, therefore, hold great promise for the future of anti-obesity medications.

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来源期刊
Cell
Cell 生物-生化与分子生物学
CiteScore
110.00
自引率
0.80%
发文量
396
审稿时长
2 months
期刊介绍: Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO). The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries. In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.
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