A readout of metabolic efficiency in arylamine N-acetyltransferase-deficient mice reveals minor energy metabolism changes.


Journal

FEBS letters
ISSN: 1873-3468
Titre abrégé: FEBS Lett
Pays: England
ID NLM: 0155157

Informations de publication

Date de publication:
04 2019
Historique:
received: 12 02 2019
revised: 26 02 2019
accepted: 07 03 2019
pubmed: 19 3 2019
medline: 16 5 2020
entrez: 19 3 2019
Statut: ppublish

Résumé

Recent studies have revealed a possible link between the activities of polymorphic arylamine N-acetyltransferases (NATs) and energy metabolism. We used a Nat1/Nat2 double knockout (KO) mouse model to demonstrate that ablation of the two Nat genes is associated with modest, intermittent alterations in respiratory exchange rate. Pyruvate tolerance tests show that double KO mice have attenuated hepatic gluconeogenesis when maintained on a high-fat/high-sucrose diet. Absence of the two Nat genes also leads to an increase in the hepatic concentration of coenzyme A in mice fed a high-fat/high-sucrose diet. Our results suggest a modest involvement of NAT in energy metabolism in mice, which is consistent with the absence of major phenotypic deregulation of energy metabolism in slow human acetylators.

Identifiants

pubmed: 30883722
doi: 10.1002/1873-3468.13357
doi:

Substances chimiques

Arylamine N-Acetyltransferase EC 2.3.1.5
Coenzyme A SAA04E81UX

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

831-841

Subventions

Organisme : Longstaffe Trust
Pays : International
Organisme : Centre for Collaborative Drug Research of the University of Toronto
Pays : International
Organisme : Université Paris Diderot
Pays : International
Organisme : Centre National de la Recherche Scientifique
Pays : International
Organisme : China Scholarship Council
ID : 201606180082
Pays : International

Informations de copyright

© 2019 Federation of European Biochemical Societies.

Auteurs

Raphaël G P Denis (RGP)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Florent Busi (F)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Julien Castel (J)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Chloé Morel (C)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Wenchao Zhang (W)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.
School of Life Sciences, Lanzhou University, China.

Linh-Chi Bui (LC)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Kim S Sugamori (KS)

Department of Pharmacology & Toxicology, University of Toronto, Canada.

Stephenie D Prokopec (SD)

Ontario Institute for Cancer Research, Toronto, Canada.

Paul C Boutros (PC)

Department of Pharmacology & Toxicology, University of Toronto, Canada.
Ontario Institute for Cancer Research, Toronto, Canada.
Department of Medical Biophysics, University of Toronto, Canada.

Denis M Grant (DM)

Department of Pharmacology & Toxicology, University of Toronto, Canada.

Fernando Rodrigues-Lima (F)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Serge Luquet (S)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

Jean-Marie Dupret (JM)

Université Paris Diderot, Sorbonne Paris Cité, Unité BFA, CNRS, UMR 8251, Paris, France.

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Classifications MeSH