How May GIP Enhance the Therapeutic Efficacy of GLP-1?
LY3298176
NNC00902746
glucagon-like peptide-1
glucose-dependent insulinotropic polypeptide
tirzepatide
type 2 diabetes mellitus
Journal
Trends in endocrinology and metabolism: TEM
ISSN: 1879-3061
Titre abrégé: Trends Endocrinol Metab
Pays: United States
ID NLM: 9001516
Informations de publication
Date de publication:
06 2020
06 2020
Historique:
received:
08
11
2019
revised:
30
01
2020
accepted:
06
02
2020
entrez:
13
5
2020
pubmed:
13
5
2020
medline:
4
8
2021
Statut:
ppublish
Résumé
Glucagon-like peptide-1 (GLP-1) receptor agonists improve glucose homeostasis, reduce bodyweight, and over time benefit cardiovascular health in type 2 diabetes mellitus (T2DM). However, dose-related gastrointestinal effects limit efficacy, and therefore agents possessing GLP-1 pharmacology that can also target alternative pathways may expand the therapeutic index. One approach is to engineer GLP-1 activity into the sequence of glucose-dependent insulinotropic polypeptide (GIP). Although the therapeutic implications of the lipogenic actions of GIP are debated, its ability to improve lipid and glucose metabolism is especially evident when paired with the anorexigenic mechanism of GLP-1. We review the complexity of GIP in regulating adipose tissue function and energy balance in the context of recent findings in T2DM showing that dual GIP/GLP-1 receptor agonist therapy produces profound weight loss, glycemic control, and lipid lowering.
Identifiants
pubmed: 32396843
pii: S1043-2760(20)30048-5
doi: 10.1016/j.tem.2020.02.006
pii:
doi:
Substances chimiques
Glucagon-Like Peptide-1 Receptor
0
Hypoglycemic Agents
0
Receptors, Gastrointestinal Hormone
0
Gastric Inhibitory Polypeptide
59392-49-3
Glucagon-Like Peptide 1
89750-14-1
gastric inhibitory polypeptide receptor
D6H00MV7K8
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
410-421Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.