Beneficial effects of murtilla extract and madecassic acid on insulin sensitivity and endothelial function in a model of diet-induced obesity

Autor: Marta Gil-Ortega, María S. Fernández-Alfonso, Miriam Martín-Ramos, Marta Viana, Silvia M. Arribas, Carla Delporte, Jorge Arancibia-Radich, Martín Alcalá, Raquel González-Blázquez, Beatriz Somoza
Přispěvatelé: USPCEU. Departamento de Química y Bioquímica, USPCEU. Grupo de Metabolismo y Función Vascular (MET-VASC)
Rok vydání: 2019
Předmět:
Male
0301 basic medicine
Antioxidant
Myrtaceae
medicine.medical_treatment
lcsh:Medicine
Pharmacology
Mice
chemistry.chemical_compound
0302 clinical medicine
Insulin
Extrac
Phosphorylation
Endothelial dysfunction
lcsh:Science
Aorta
Protein Tyrosine Phosphatase
Non-Receptor Type 1

Multidisciplinary
myr
Murtilla
Insulin sensitivity
Endothelial function
Myricetin
Nitric Oxide Synthase Type III
Medicina
Diet
High-Fat

Nitric Oxide
Article
Nitric oxide
03 medical and health sciences
Insulin resistance
medicine.artery
Beneficial effect
Ethyl acetate extract
medicine
Animals
Obesity
Plant Extracts
lcsh:R
medicine.disease
Triterpenes
Mice
Inbred C57BL

Plant Leaves
Disease Models
Animal

030104 developmental biology
chemistry
lcsh:Q
Endothelium
Vascular

Insulin Resistance
Proto-Oncogene Proteins c-akt
030217 neurology & neurosurgery
Zdroj: Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
ISSN: 2045-2322
DOI: 10.1038/s41598-018-36555-1
Popis: Infusions of murtilla leaves exhibit antioxidant, analgesic, and anti-inflammatory properties. Several compounds that are structurally similar to madecassic acid (MA), a component of murtilla leaf extract (ethyl acetate extract, EAE), have been shown to inhibit protein tyrosine phosphatase 1B (PTP1P). The aim of this study was to evaluate if EAE and two compounds identified in EAE (MA and myricetin [MYR]) could have a beneficial effect on systemic and vascular insulin sensitivity and endothelial function in a model of diet-induced obesity. Experiments were performed in 5-week-old male C57BL6J mice fed with a standard (LF) or a very high-fat diet (HF) for 4 weeks and treated with EAE, MA, MYR, or the vehicle as control (C). EAE significantly inhibited PTP1B. EAE and MA, but not MYR, significantly improved systemic insulin sensitivity in HF mice and vascular relaxation to Ach in aorta segments, due to a significant increase of eNOS phosphorylation and enhanced nitric oxide availability. EAE, MA, and MYR also accounted for increased relaxant responses to insulin in HF mice, thus evidencing that the treatments significantly improved aortic insulin sensitivity. This study shows for the first time that EAE and MA could constitute interesting candidates for treating insulin resistance and endothelial dysfunction associated with obesity.
This study was supported by BFU2011-25303, GR921645-Santander, Fundación Mutua Madrileña, Fundación Eugenio Rodríguez Pascual, SESCAMET, project FONDECYT1130155, grant CONICYT de Doctorado Nacional, grant CONICYT de Apoyo de Tesis 21130672, and grant CONICYT de Pasantía Doctoral
Databáze: OpenAIRE