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用于肥胖症和2型糖尿病的多靶点单分子肽:当前进展与未来方向

Multiagonist Unimolecular Peptides for Obesity and Type 2 Diabetes: Current Advances and Future Directions.

作者信息

Hasib Annie

机构信息

Division of Systems Medicine, School of Medicine, University of Dundee, Dundee, UK.

出版信息

Clin Med Insights Endocrinol Diabetes. 2020 Feb 14;13:1179551420905844. doi: 10.1177/1179551420905844. eCollection 2020.

DOI:10.1177/1179551420905844
PMID:32110131
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7025423/
Abstract

The ever-increasing prevalence of obesity and Type 2 diabetes has necessitated the development of newer and more effective approaches for achieving efficient glycemic control and weight loss. Conventional treatment methods often result in weight gain, further deteriorating the already impaired metabolic control in people with obesity/Type 2 diabetes. Alleviation of obesity and diabetes achieved after bariatric surgeries highlight the therapeutic importance of gut-brain axis and entails development of more patient-friendly approaches replicating the positive metabolic effects of bariatric surgery. Given the potential involvement of several gut hormones in the success of bariatric surgery, the therapeutic importance of synergistic interaction between these hormones for improved metabolism cannot be ignored. Many unimolecular multiagonist peptides are in preclinical and clinical trials as they maximize the combinatorial metabolic efficacy by concurrent activation of multiple gut hormone receptors. This review summarizes the ongoing developments of multiagonist peptides as novel therapeutic approaches against obesity-diabetes.

摘要

肥胖症和2型糖尿病的患病率不断上升,因此需要开发更新、更有效的方法来实现有效的血糖控制和体重减轻。传统治疗方法往往导致体重增加,进一步恶化肥胖症/2型糖尿病患者本已受损的代谢控制。减肥手术后肥胖症和糖尿病的缓解突出了肠-脑轴的治疗重要性,并需要开发更有利于患者的方法,以复制减肥手术的积极代谢作用。鉴于几种肠道激素可能参与减肥手术的成功,这些激素之间协同相互作用对改善新陈代谢的治疗重要性不容忽视。许多单分子多激动剂肽正处于临床前和临床试验阶段,因为它们通过同时激活多个肠道激素受体来最大化组合代谢功效。本综述总结了多激动剂肽作为治疗肥胖-糖尿病新方法的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/7025423/681917451c35/10.1177_1179551420905844-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/7025423/681917451c35/10.1177_1179551420905844-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607c/7025423/681917451c35/10.1177_1179551420905844-fig1.jpg

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本文引用的文献

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Ann Surg Treat Res. 2019 Jun;96(6):283-289. doi: 10.4174/astr.2019.96.6.283. Epub 2019 May 29.
2
Glucagon Receptor Signaling and Lipid Metabolism.胰高血糖素受体信号传导与脂质代谢
Front Physiol. 2019 Apr 24;10:413. doi: 10.3389/fphys.2019.00413. eCollection 2019.
3
PYY plays a key role in the resolution of diabetes following bariatric surgery in humans.
Cell. 2024 Jul 25;187(15):3829-3853. doi: 10.1016/j.cell.2024.06.003.
4
Structural analysis of the dual agonism at GLP-1R and GCGR.GLP-1R 和 GCGR 的双重激动剂的结构分析。
Proc Natl Acad Sci U S A. 2023 Aug 15;120(33):e2303696120. doi: 10.1073/pnas.2303696120. Epub 2023 Aug 7.
5
Novel Therapies for Cardiometabolic Disease: Recent Findings in Studies with Hormone Peptide-Derived G Protein Coupled Receptor Agonists.心脏代谢疾病的新型治疗方法:激素肽衍生的 G 蛋白偶联受体激动剂研究中的最新发现。
Nutrients. 2022 Sep 13;14(18):3775. doi: 10.3390/nu14183775.
6
How glucagon-like peptide 1 receptor agonists work.胰高血糖素样肽-1受体激动剂的作用机制。
Endocr Connect. 2021 Jul 17;10(7):R200-R212. doi: 10.1530/EC-21-0130.
7
Novel Approaches to Restore Pancreatic Beta-Cell Mass and Function.新型方法恢复胰腺β细胞的质量和功能。
Handb Exp Pharmacol. 2022;274:439-465. doi: 10.1007/164_2021_474.
8
Proglucagon-Derived Peptides as Therapeutics.胰高血糖素原衍生肽类作为治疗药物。
Front Endocrinol (Lausanne). 2021 May 18;12:689678. doi: 10.3389/fendo.2021.689678. eCollection 2021.
9
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5
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6
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Mol Metab. 2018 Dec;18:3-14. doi: 10.1016/j.molmet.2018.09.009. Epub 2018 Oct 3.
9
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10
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