4.4 Article

Problem or solution: The strange story of glucagon

Journal

PEPTIDES
Volume 100, Issue -, Pages 36-41

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.peptides.2017.11.013

Keywords

Glucagon; Diabetes; Obesity; Energy expenditure; Incretin; Oxyntomodulin

Funding

  1. MRC
  2. BBSRC
  3. NIHR
  4. Integrative Mammalian Biology (IMB) Capacity Building Award
  5. EuroCHIP grant [FP7- HEALTH- 2009-241592]
  6. NIHR Biomedical Research Centre Funding Scheme
  7. Wellcome Trust
  8. National Institute for Health Research [NF-SI-0507-10337, NF-SI-0513-10080, ACF-2011-21-005] Funding Source: researchfish

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Globally, 13% of the world's adult population is obese, and more than 400 million people suffer from diabetes. These conditions are both associated with significant morbidity, mortality and financial cost. Therefore, finding new pharmacological treatments is an imperative. Relative hyperglucagonaemia is seen in all types of diabetes, and has been implicated in its pathogenesis. Consequently, clinical trials are underway using drugs which block glucagon activity to treat type 2 diabetes. Conversely, exogenous glucagon can increase energy expenditure. Therefore, researchers are designing peptides that combine activation of the glucagon receptor with further incretin properties, which will treat obesity while mitigating the hyperglycaemic effects of glucagon. This review will discuss these conflicting physiological properties of glucagon, and the attempts to harness these effects pharmacologically.

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