Kidney effects of Glucagon-Like Peptide 1 (GLP1): from molecular foundations to a pharmacophysiological perspective

GLP1 receptor agonists (GLP1-RAs) are drugs that mimic the effects of the incretin hormone GLP1 and were initially introduced in medicine for the treatment of diabetes in 2005 and for obesity in 2014. Over time, data from secondary and exploratory objectives of large randomized controlled-trials sug...

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Autores:
Rico-Fontalvo, Jorge
Reina, Maricely
Soler, María José
Unigarro-Palacios, Mario
Castañeda González, Juan Pablo
Jiménez Quintero, Javier
Raad Sarabia, Maria Isabel
Proenca de Moraes, Thyago
Daza-Arnedo, Rodrigo
Tipo de recurso:
Fecha de publicación:
2024
Institución:
Universidad Simón Bolívar
Repositorio:
Repositorio Digital USB
Idioma:
spa
OAI Identifier:
oai:bonga.unisimon.edu.co:20.500.12442/15936
Acceso en línea:
https://hdl.handle.net/20.500.12442/15936
https://doi.org/10.1590/2175-8239-JBN-2024-0101en
https://www.bjnephrology.org/en/article/kidney-effects-of-glucagon-like-peptide-1-glp1-from-molecular-foundations-to-a-pharmacophysiological-perspective/
Palabra clave:
Albuminuria
Diabetes
Incretins
Obesity
Kidney disease
Albuminúria
Diabetes
Incretinas
Obesidade
Doença Renal
Rights
openAccess
License
Attribution-NonCommercial-NoDerivs 3.0 United States
Description
Summary:GLP1 receptor agonists (GLP1-RAs) are drugs that mimic the effects of the incretin hormone GLP1 and were initially introduced in medicine for the treatment of diabetes in 2005 and for obesity in 2014. Over time, data from secondary and exploratory objectives of large randomized controlled-trials suggested that GLP1-RAs could also exert renal action by slowing the progression of kidney disease in patients with and without diabetes. Based on this rationale, the Flow study (1 mg semaglutide vs placebo) was designed and recruitment began in 2019 until May 2021. The recently published results confirmed the effect of semaglutide in reducing the composite renal outcome. However, similar to SGLT2 inhibitors, the potential mechanisms behind the renal effects of GLP1-RAs still need to be elucidated. The aim of this review is to address the different physiological mechanisms of GLP1-RAs at the renal level, using evidence from experimental studies and current scientific literature.