Activation of AT


Journal

British journal of pharmacology
ISSN: 1476-5381
Titre abrégé: Br J Pharmacol
Pays: England
ID NLM: 7502536

Informations de publication

Date de publication:
10 2020
Historique:
received: 05 04 2020
revised: 08 08 2020
accepted: 16 08 2020
pubmed: 28 8 2020
medline: 22 6 2021
entrez: 28 8 2020
Statut: ppublish

Résumé

The AT Female diabetic (db/db) and non-diabetic (db/+) mice were treated for 1 month with the selective AT C21-treated db/db mice displayed improved glucose and pyruvate tolerance compared with saline-treated db/db mice. Also, C21-treated db/db mice showed reduced liver weight and decreased hepatic lipid accumulation compared with saline-treated db/db mice. Insulin signalling analysis showed increased phosphorylation of the insulin receptor, Akt and FOXO1 in the livers of C21-treated db/db mice compared with saline-treated counterparts. These findings were associated with increased adiponectin levels in plasma and adipose tissue and reduced adipocyte size in inguinal fat. The beneficial effects of AT Chronic C21 infusion exerts beneficial metabolic effects in female diabetic db/db mice, alleviating type 2 diabetes complications, through a mechanism that involves NO production.

Sections du résumé

BACKGROUND AND PURPOSE
The AT
EXPERIMENTAL APPROACH
Female diabetic (db/db) and non-diabetic (db/+) mice were treated for 1 month with the selective AT
KEY RESULTS
C21-treated db/db mice displayed improved glucose and pyruvate tolerance compared with saline-treated db/db mice. Also, C21-treated db/db mice showed reduced liver weight and decreased hepatic lipid accumulation compared with saline-treated db/db mice. Insulin signalling analysis showed increased phosphorylation of the insulin receptor, Akt and FOXO1 in the livers of C21-treated db/db mice compared with saline-treated counterparts. These findings were associated with increased adiponectin levels in plasma and adipose tissue and reduced adipocyte size in inguinal fat. The beneficial effects of AT
CONCLUSION AND IMPLICATIONS
Chronic C21 infusion exerts beneficial metabolic effects in female diabetic db/db mice, alleviating type 2 diabetes complications, through a mechanism that involves NO production.

Identifiants

pubmed: 32851652
doi: 10.1111/bph.15241
pmc: PMC7520448
doi:

Substances chimiques

Receptor, Angiotensin, Type 2 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4766-4781

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI134714
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI132599
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30DK063491
Pays : United States
Organisme : American Heart Association
ID : 17GRNT33661206
Organisme : NHLBI NIH HHS
ID : P01 HL129941
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007770
Pays : United States
Organisme : American Heart Association
ID : 16SDG30130015
Organisme : NIDDK NIH HHS
ID : P30 DK063491
Pays : United States
Organisme : Universidad de Buenos Aires
ID : UBACYT 20020130100218BA
Organisme : NHLBI NIH HHS
ID : R01 HL142672
Pays : United States
Organisme : Fondo para la Investigación Científica y Tecnológica
ID : PICT-2014-0362

Informations de copyright

© 2020 The British Pharmacological Society.

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Auteurs

Fernando P Dominici (FP)

Facultad de Farmacia y Bioquímica, Departamento de Química Biológica, IQUIFIB (UBA-CONICET), Universidad de Buenos Aires, Buenos Aires, Argentina.

Luciana C Veiras (LC)

Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Justin Z Y Shen (JZY)

Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Ellen A Bernstein (EA)

Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Diego T Quiroga (DT)

Facultad de Farmacia y Bioquímica, Departamento de Química Biológica, IQUIFIB (UBA-CONICET), Universidad de Buenos Aires, Buenos Aires, Argentina.

Ulrike M Steckelings (UM)

IMM-Department of Cardiovascular & Renal Research, University of Southern Denmark, Odense, Denmark.

Kenneth E Bernstein (KE)

Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Jorge F Giani (JF)

Department of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

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Classifications MeSH