Literature DB >> 26071095

Amylin: Pharmacology, Physiology, and Clinical Potential.

Debbie L Hay1, Steve Chen2, Thomas A Lutz2, David G Parkes2, Jonathan D Roth2.   

Abstract

Amylin is a pancreatic β-cell hormone that produces effects in several different organ systems. Here, we review the literature in rodents and in humans on amylin research since its discovery as a hormone about 25 years ago. Amylin is a 37-amino-acid peptide that activates its specific receptors, which are multisubunit G protein-coupled receptors resulting from the coexpression of a core receptor protein with receptor activity-modifying proteins, resulting in multiple receptor subtypes. Amylin's major role is as a glucoregulatory hormone, and it is an important regulator of energy metabolism in health and disease. Other amylin actions have also been reported, such as on the cardiovascular system or on bone. Amylin acts principally in the circumventricular organs of the central nervous system and functionally interacts with other metabolically active hormones such as cholecystokinin, leptin, and estradiol. The amylin-based peptide, pramlintide, is used clinically to treat type 1 and type 2 diabetes. Clinical studies in obesity have shown that amylin agonists could also be useful for weight loss, especially in combination with other agents.
Copyright © 2015 by The American Society for Pharmacology and Experimental Therapeutics.

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Year:  2015        PMID: 26071095     DOI: 10.1124/pr.115.010629

Source DB:  PubMed          Journal:  Pharmacol Rev        ISSN: 0031-6997            Impact factor:   25.468


  92 in total

1.  Amyloidogenicity and cytotoxicity of des-Lys-1 human amylin provides insight into amylin self-assembly and highlights the difficulties of defining amyloidogenicity.

Authors:  Kyung-Hoon Lee; Alexander Zhyvoloup; Daniel Raleigh
Journal:  Protein Eng Des Sel       Date:  2019-12-13       Impact factor: 1.650

2.  N-Glycosylation of Asparagine 130 in the Extracellular Domain of the Human Calcitonin Receptor Significantly Increases Peptide Hormone Affinity.

Authors:  Sang-Min Lee; Jason M Booe; Joseph J Gingell; Virginie Sjoelund; Debbie L Hay; Augen A Pioszak
Journal:  Biochemistry       Date:  2017-06-26       Impact factor: 3.162

3.  Evolutionary Adaptation and Amyloid Formation: Does the Reduced Amyloidogenicity and Cytotoxicity of Ursine Amylin Contribute to the Metabolic Adaption of Bears and Polar Bears?

Authors:  Rehana Akter; Andisheh Abedini; Zachary Ridgway; Xiaoxue Zhang; Joel Kleinberg; Ann Marie Schmidt; Daniel P Raleigh
Journal:  Isr J Chem       Date:  2016-12-19       Impact factor: 3.333

Review 4.  Bone Health following Bariatric Surgery: Implications for Management Strategies to Attenuate Bone Loss.

Authors:  Tair Ben-Porat; Ram Elazary; Shiri Sherf-Dagan; Ariela Goldenshluger; Ronit Brodie; Yoav Mintz; Ram Weiss
Journal:  Adv Nutr       Date:  2018-03-01       Impact factor: 8.701

5.  Human amylin proteotoxicity impairs protein biosynthesis, and alters major cellular signaling pathways in the heart, brain and liver of humanized diabetic rat model in vivo.

Authors:  Amro Ilaiwy; Miao Liu; Traci L Parry; James R Bain; Christopher B Newgard; Jonathan C Schisler; Michael J Muehlbauer; Florin Despa; Monte S Willis
Journal:  Metabolomics       Date:  2016-04-23       Impact factor: 4.290

Review 6.  Amylin and its G-protein-coupled receptor: A probable pathological process and drug target for Alzheimer's disease.

Authors:  Wei Qiao Qiu
Journal:  Neuroscience       Date:  2017-05-19       Impact factor: 3.590

Review 7.  Diabetes pharmacotherapy and effects on the musculoskeletal system.

Authors:  Evangelia Kalaitzoglou; John L Fowlkes; Iuliana Popescu; Kathryn M Thrailkill
Journal:  Diabetes Metab Res Rev       Date:  2018-12-20       Impact factor: 4.876

8.  Analysis of Amylin Consensus Sequences Suggests That Human Amylin Is Not Optimized to Minimize Amyloid Formation and Provides Clues to Factors That Modulate Amyloidogenicity.

Authors:  Daeun Noh; Rebekah L Bower; Debbie L Hay; Alexander Zhyvoloup; Daniel P Raleigh
Journal:  ACS Chem Biol       Date:  2020-06-03       Impact factor: 5.100

9.  Differential effects of serine side chain interactions in amyloid formation by islet amyloid polypeptide.

Authors:  Rehana Akter; Junjie Zou; Daniel P Raleigh
Journal:  Protein Sci       Date:  2020-02       Impact factor: 6.725

10.  Distinct Patterns of Internalization of Different Calcitonin Gene-Related Peptide Receptors.

Authors:  Joseph J Gingell; Tayla A Rees; Erica R Hendrikse; Andrew Siow; David Rennison; John Scotter; Paul W R Harris; Margaret A Brimble; Christopher S Walker; Debbie L Hay
Journal:  ACS Pharmacol Transl Sci       Date:  2020-02-26
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