GLP-1/glucagon receptor co-agonism for treatment of obesity

Research output: Contribution to journalReviewResearchpeer-review

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GLP-1/glucagon receptor co-agonism for treatment of obesity. / Sánchez-Garrido, Miguel A.; Brandt, Sara J; Clemmensen, Christoffer; Müller, Timo D; DiMarchi, Richard D; Tschöp, Matthias H.

In: Diabetologia, Vol. 60, No. 10, 10.2017, p. 1851-1861.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Sánchez-Garrido, MA, Brandt, SJ, Clemmensen, C, Müller, TD, DiMarchi, RD & Tschöp, MH 2017, 'GLP-1/glucagon receptor co-agonism for treatment of obesity', Diabetologia, vol. 60, no. 10, pp. 1851-1861. https://doi.org/10.1007/s00125-017-4354-8

APA

Sánchez-Garrido, M. A., Brandt, S. J., Clemmensen, C., Müller, T. D., DiMarchi, R. D., & Tschöp, M. H. (2017). GLP-1/glucagon receptor co-agonism for treatment of obesity. Diabetologia, 60(10), 1851-1861. https://doi.org/10.1007/s00125-017-4354-8

Vancouver

Sánchez-Garrido MA, Brandt SJ, Clemmensen C, Müller TD, DiMarchi RD, Tschöp MH. GLP-1/glucagon receptor co-agonism for treatment of obesity. Diabetologia. 2017 Oct;60(10):1851-1861. https://doi.org/10.1007/s00125-017-4354-8

Author

Sánchez-Garrido, Miguel A. ; Brandt, Sara J ; Clemmensen, Christoffer ; Müller, Timo D ; DiMarchi, Richard D ; Tschöp, Matthias H. / GLP-1/glucagon receptor co-agonism for treatment of obesity. In: Diabetologia. 2017 ; Vol. 60, No. 10. pp. 1851-1861.

Bibtex

@article{24cda13851844706ae54b796d17ea305,
title = "GLP-1/glucagon receptor co-agonism for treatment of obesity",
abstract = "Over a relatively short period, obesity and type 2 diabetes have come to represent a large medical and economic burden to global societies. The epidemic rise in the prevalence of obesity has metabolic consequences and is paralleled by an increased occurrence of other diseases, such as diabetes, cancer and cardiovascular complications. Together, obesity and type 2 diabetes constitute one of the more preventable causes of premature death and the identification of novel, safe and effective anti-obesity drugs is of utmost importance. Pharmacological attempts to treat obesity have had limited success, with notable adverse effects, rendering bariatric surgery as the only current therapy for substantially improving body weight. Novel unimolecular, multifunctional peptides have emerged as one of the most promising medicinal approaches to enhance metabolic efficacy and restore normal body weight. In this review, we will mainly focus on the discovery and translational relevance of dual agonists that pharmacologically function at the receptors for glucagon and glucagon-like peptide-1. Such peptides have advanced to clinical evaluation and inspired the pursuit of multiple related approaches to achieving polypharmacy within single molecules.",
keywords = "Journal Article, Review",
author = "S{\'a}nchez-Garrido, {Miguel A.} and Brandt, {Sara J} and Christoffer Clemmensen and M{\"u}ller, {Timo D} and DiMarchi, {Richard D} and Tsch{\"o}p, {Matthias H}",
year = "2017",
month = oct,
doi = "10.1007/s00125-017-4354-8",
language = "English",
volume = "60",
pages = "1851--1861",
journal = "Diabetologia",
issn = "0012-186X",
publisher = "Springer",
number = "10",

}

RIS

TY - JOUR

T1 - GLP-1/glucagon receptor co-agonism for treatment of obesity

AU - Sánchez-Garrido, Miguel A.

AU - Brandt, Sara J

AU - Clemmensen, Christoffer

AU - Müller, Timo D

AU - DiMarchi, Richard D

AU - Tschöp, Matthias H

PY - 2017/10

Y1 - 2017/10

N2 - Over a relatively short period, obesity and type 2 diabetes have come to represent a large medical and economic burden to global societies. The epidemic rise in the prevalence of obesity has metabolic consequences and is paralleled by an increased occurrence of other diseases, such as diabetes, cancer and cardiovascular complications. Together, obesity and type 2 diabetes constitute one of the more preventable causes of premature death and the identification of novel, safe and effective anti-obesity drugs is of utmost importance. Pharmacological attempts to treat obesity have had limited success, with notable adverse effects, rendering bariatric surgery as the only current therapy for substantially improving body weight. Novel unimolecular, multifunctional peptides have emerged as one of the most promising medicinal approaches to enhance metabolic efficacy and restore normal body weight. In this review, we will mainly focus on the discovery and translational relevance of dual agonists that pharmacologically function at the receptors for glucagon and glucagon-like peptide-1. Such peptides have advanced to clinical evaluation and inspired the pursuit of multiple related approaches to achieving polypharmacy within single molecules.

AB - Over a relatively short period, obesity and type 2 diabetes have come to represent a large medical and economic burden to global societies. The epidemic rise in the prevalence of obesity has metabolic consequences and is paralleled by an increased occurrence of other diseases, such as diabetes, cancer and cardiovascular complications. Together, obesity and type 2 diabetes constitute one of the more preventable causes of premature death and the identification of novel, safe and effective anti-obesity drugs is of utmost importance. Pharmacological attempts to treat obesity have had limited success, with notable adverse effects, rendering bariatric surgery as the only current therapy for substantially improving body weight. Novel unimolecular, multifunctional peptides have emerged as one of the most promising medicinal approaches to enhance metabolic efficacy and restore normal body weight. In this review, we will mainly focus on the discovery and translational relevance of dual agonists that pharmacologically function at the receptors for glucagon and glucagon-like peptide-1. Such peptides have advanced to clinical evaluation and inspired the pursuit of multiple related approaches to achieving polypharmacy within single molecules.

KW - Journal Article

KW - Review

U2 - 10.1007/s00125-017-4354-8

DO - 10.1007/s00125-017-4354-8

M3 - Review

C2 - 28733905

VL - 60

SP - 1851

EP - 1861

JO - Diabetologia

JF - Diabetologia

SN - 0012-186X

IS - 10

ER -

ID: 182328162