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Sayaka Akieda-Asai Frontier Science Research Center, University of Miyazaki, Miyazaki 889-1692, Japan

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Paul-Emile Poleni Frontier Science Research Center, University of Miyazaki, Miyazaki 889-1692, Japan

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Kazuya Hasegawa Frontier Science Research Center, University of Miyazaki, Miyazaki 889-1692, Japan

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Yukari Date Frontier Science Research Center, University of Miyazaki, Miyazaki 889-1692, Japan

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( Bjorbaek & Kahn 2004 ). Leptin also inhibits AMP-activated protein kinase (AMPK) activity in the arcuate nucleus and in the paraventricular nucleus of the hypothalamus ( Minokoshi et al . 2004 ). Glucagon-like peptide-1 (GLP1), a gastrointestinal hormone

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Paige V Bauer Toronto General Hospital Research Institute and Department of Medicine, UHN, Toronto, ON, Canada
Department of Physiology, University of Toronto, Toronto, ON, Canada

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Frank A Duca Toronto General Hospital Research Institute and Department of Medicine, UHN, Toronto, ON, Canada

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. 2015 , Buse et al . 2016 ). Interestingly, this is not the only evidence for a therapeutic role of the gut in diabetes treatment. Over the past decade, incretin-based therapies including glucagon-like peptide-1 (GLP-1) receptor agonists and dipeptidyl

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Weiwei Xu Section of Endocrinology and Metabolism, Department of Medicine, Diabetes Discovery Research and Gender Medicine Laboratory, Tulane University Health Sciences Center, School of Medicine, and Southeast Louisiana Veterans Healthcare System Medical Center, New Orleans, Louisiana, USA

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Jamie Morford Section of Endocrinology and Metabolism, Department of Medicine, Diabetes Discovery Research and Gender Medicine Laboratory, Tulane University Health Sciences Center, School of Medicine, and Southeast Louisiana Veterans Healthcare System Medical Center, New Orleans, Louisiana, USA

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Franck Mauvais-Jarvis Section of Endocrinology and Metabolism, Department of Medicine, Diabetes Discovery Research and Gender Medicine Laboratory, Tulane University Health Sciences Center, School of Medicine, and Southeast Louisiana Veterans Healthcare System Medical Center, New Orleans, Louisiana, USA

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induces intra-islet glucagon-like peptide-1 (GLP-1) production and enhances beta cell survival . Diabetologia 54 2067 – 2076 . ( https://doi.org/10.1007/s00125-011-2181-x ) 10.1007/s00125-011-2181-x 21567300 Lubahn DB Joseph DR Sullivan PM Willard

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Alessandro Pocai Diabetes and Endocrinology, Merck Research Laboratories, Merck Sharp and Dohme Corp., 126 East Lincoln Avenue, Rahway, New Jersey 07065, USA

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insulin. Recent work on understanding the physiological function of proglucagon-derived peptides has renewed interest in glucagon-based therapeutics. One of these peptides is glucagon-like peptide-1 (GLP1), which is secreted from the L cells of the

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Neerav Mullur The University of Ottawa, Faculty of Medicine, Ottawa, Ontario, Canada

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Arianne Morissette The University of Ottawa Heart Institute, Ottawa, Ontario, Canada

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Nadya M Morrow The University of Ottawa Heart Institute, Ottawa, Ontario, Canada
Department of Biochemistry, Microbiology and Immunology, The University of Ottawa, Faculty of Medicine, Ottawa, Ontario, Canada

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Erin E Mulvihill The University of Ottawa Heart Institute, Ottawa, Ontario, Canada
Department of Biochemistry, Microbiology and Immunology, The University of Ottawa, Faculty of Medicine, Ottawa, Ontario, Canada

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administration ( McIntyre et al. 1965 ). The incretin hormones, glucose-dependent insulinotropic polypeptide (GIP), and glucagon-like peptide-1 (GLP-1) potentiate meal-stimulated insulin secretion through direct and indirect actions on islet β-cells. The first

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Tetsuhiro Kakimoto Safety Research Laboratory, Department I, Pharmacology Research Laboratories II, Research Division, Mitsubishi Tanabe Pharma Corporation, 2-2-50, Kawagishi, Toda-shi, Saitama 335-8505, Japan

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Hirotaka Kimata Safety Research Laboratory, Department I, Pharmacology Research Laboratories II, Research Division, Mitsubishi Tanabe Pharma Corporation, 2-2-50, Kawagishi, Toda-shi, Saitama 335-8505, Japan

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Satoshi Iwasaki Safety Research Laboratory, Department I, Pharmacology Research Laboratories II, Research Division, Mitsubishi Tanabe Pharma Corporation, 2-2-50, Kawagishi, Toda-shi, Saitama 335-8505, Japan

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Atsushi Fukunari Safety Research Laboratory, Department I, Pharmacology Research Laboratories II, Research Division, Mitsubishi Tanabe Pharma Corporation, 2-2-50, Kawagishi, Toda-shi, Saitama 335-8505, Japan

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Hiroyuki Utsumi Safety Research Laboratory, Department I, Pharmacology Research Laboratories II, Research Division, Mitsubishi Tanabe Pharma Corporation, 2-2-50, Kawagishi, Toda-shi, Saitama 335-8505, Japan

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, Yoon et al . 2003 ), suggesting that subjects with insulin resistance develop diabetes with the onset of β-cell dysfunction. Drugs to effectively increase insulin-secreting β-cells have been long-awaited. Glucagon-like peptide-1 (GLP-1), a member of

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Sehee Kim Department of Pharmacology, Biomedical Science Institute and Medical Research Center for Reactive Oxygen Species, Kyunghee University School of Medicine, Seoul 130-071, Republic of Korea

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Minho Moon Department of Pharmacology, Biomedical Science Institute and Medical Research Center for Reactive Oxygen Species, Kyunghee University School of Medicine, Seoul 130-071, Republic of Korea

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Seungjoon Park Department of Pharmacology, Biomedical Science Institute and Medical Research Center for Reactive Oxygen Species, Kyunghee University School of Medicine, Seoul 130-071, Republic of Korea

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pharmacological intervention of MMP-3 and microglial activation could be considered as plausible candidates for neuroprotective agents in PD. Glucagon-like peptide-1 (GLP-1), an endogenous 30-amino acid gut–brain peptide hormone, is synthesized from proglucagon

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Qiaoli Cui Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Yijing Liao Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Yaojing Jiang Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Xiaohang Huang Shanghai Yinuo Pharmaceutical Co., Ltd., Shanghai, China

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Weihong Tao Shanghai Yinuo Pharmaceutical Co., Ltd., Shanghai, China

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Quanquan Zhou Shanghai Yinuo Pharmaceutical Co., Ltd., Shanghai, China

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Anna Shao Shanghai Yinuo Pharmaceutical Co., Ltd., Shanghai, China

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Ying Zhao Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Jia Li Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Anran Ma Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Zhihong Wang Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Li Zhang Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China

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Zunyuan Yang Primed Non-Human Primate Research Centre (Sichuan Primed Shines Bio-tech Co., Ltd.), Chengdu, Sichuan, China

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Yinan Liang Primed Non-Human Primate Research Centre (Sichuan Primed Shines Bio-tech Co., Ltd.), Chengdu, Sichuan, China

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Minglin Wu Primed Non-Human Primate Research Centre (Sichuan Primed Shines Bio-tech Co., Ltd.), Chengdu, Sichuan, China

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Zhenyan Yang Primed Non-Human Primate Research Centre (Sichuan Primed Shines Bio-tech Co., Ltd.), Chengdu, Sichuan, China

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Wen Zeng Primed Non-Human Primate Research Centre (Sichuan Primed Shines Bio-tech Co., Ltd.), Chengdu, Sichuan, China

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Qinghua Wang Department of Endocrinology and Metabolism, Huashan Hospital, Fudan University, Shanghai, China
Shanghai Yinuo Pharmaceutical Co., Ltd., Shanghai, China
Keenan Research Centre for Biomedical Science, Division of Endocrinology and Metabolism, St. Michael’s Hospital, Toronto, Ontario, Canada

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Introduction Glucagon-like peptide 1 (GLP-1) is an incretin hormone produced and secreted by intestinal L cells in response to nutrients ingestion. GLP-1 regulates glucose metabolism mainly by stimulating postprandial insulin secretion and

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Benjamin J Lamont Department of Medicine (Austin Health), The University of Melbourne, Melbourne, Victoria, Australia

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Sofianos Andrikopoulos Department of Medicine (Austin Health), The University of Melbourne, Melbourne, Victoria, Australia

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Introduction The incretins glucagon-like peptide 1 (GLP1) and glucose-dependent insulinotropic polypeptide (GIP) act via specific G-protein-coupled receptors to potentiate insulin secretion from pancreatic β-cells in a glucose-dependent manner

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Bernard Khoo Endocrinology, Division of Medicine, University College London, Royal Free Campus, London, UK

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Tricia Mei-Mei Tan Department of Digestion, Metabolism and Reproduction, Imperial College London, Hammersmith Campus, London, UK

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gut hormone path-finder Glucagon-like peptide 1 (GLP-1) is the most extensively studied gut hormone with translational and clinical evidence for its efficacy ( Holst 2007 ). It is an alternatively processed product of the proglucagon peptide

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