2015
DOI: 10.1038/nrendo.2015.3
|View full text |Cite
|
Sign up to set email alerts
|

A new paradigm for treating obesity and diabetes mellitus

Abstract: Standfirst :An innovative unimolecular, polypharmaceutical strategy using a well-balanced monomeric peptide triagonist targeting three metabolically-related hormone receptors (glucagon-like peptide-1, glucose-dependent insulinotropic poplypeptide and glucagon) appears the most effective pharmacological approach to reversing obesity and metabolic comorbidities in rodents and could open new perspective to tackle the dual obesity-diabetes burden in humans.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
5
0
1

Year Published

2015
2015
2023
2023

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 19 publications
(9 citation statements)
references
References 14 publications
(18 reference statements)
1
5
0
1
Order By: Relevance
“…Of particular significance, unlike the GIPR/GLP-1R dual agonist, the triagonist increased energy expenditure and endogenous circulating FGF21, which are contributed by the GcgR agonism component within the triagonist. The successful in vivo validation of the GcgR/GLP-1R/GIPR triagonist confirms the previously unappreciated yet unique virtues of GcgR and GIPR agonism for the treatment and prevention of obesity and T2D (Scheen and Paquot, 2015). Triagonism offers a number of potential advantages that distinguishes it from either of the respective co-agonists.…”
Section: Get a Gip: ''Twincretins''supporting
confidence: 53%
“…Of particular significance, unlike the GIPR/GLP-1R dual agonist, the triagonist increased energy expenditure and endogenous circulating FGF21, which are contributed by the GcgR agonism component within the triagonist. The successful in vivo validation of the GcgR/GLP-1R/GIPR triagonist confirms the previously unappreciated yet unique virtues of GcgR and GIPR agonism for the treatment and prevention of obesity and T2D (Scheen and Paquot, 2015). Triagonism offers a number of potential advantages that distinguishes it from either of the respective co-agonists.…”
Section: Get a Gip: ''Twincretins''supporting
confidence: 53%
“…Furthermore, sulfonylureas and other long established therapeutics, including the insulin-sensitizer metformin, do not prevent the continuing loss of beta cell function observed in T2DM [91]. Incretin-based therapies are increasingly being used in clinical practice for the management of T2DM [92,93] that address a different aspect of beta cell dysfunction: the lack of potentiation of insulin secretion in response to an oral glucose/nutrient challenge [94]. This potentiation occurs because of incretins that act on the pancreas and other peripheral tissues to elicit biological effects, including augmenting nutrient-stimulated insulin secretion.…”
Section: Prevention and Therapymentioning
confidence: 99%
“…For example, the influence of abdominal obesity on the risk of diabetes was found to be more important than that of general obesity [ 10 ]. Given the striking parallel increases in the incidences of these two conditions, obesity is likely an important contributing factor to the manifestation of diabetes and the complications, mortality, and morbidity related to this disease [ 11 ].…”
Section: Prevalence Of Diabetes and Obesitymentioning
confidence: 99%