Upregulation of hepatic autophagy under nutritional ketosis.


Journal

The Journal of nutritional biochemistry
ISSN: 1873-4847
Titre abrégé: J Nutr Biochem
Pays: United States
ID NLM: 9010081

Informations de publication

Date de publication:
07 2021
Historique:
received: 07 05 2020
revised: 15 12 2020
accepted: 20 01 2021
pubmed: 12 3 2021
medline: 15 9 2021
entrez: 11 3 2021
Statut: ppublish

Résumé

Many of the metabolic effects evoked by the ketogenic diet mimic the actions of fasting and the benefits of the ketogenic diet are often attributed to these similarities. Since fasting is a potent autophagy inductor in vivo and in vitro it has been hypothesized that the ketogenic diet may upregulate autophagy. The aim of the present study was to provide a comprehensive evaluation of the influence of the ketogenic diet on the hepatic autophagy. C57BL/6N male mice were fed with two different ketogenic chows composed of fat of either animal or plant origin for 4 weeks. To gain some insight into the time frame for the induction of autophagy on the ketogenic diet, we performed a short-term experiment in which animals were fed with ketogenic diets for only 24 or 48 h. The results showed that autophagy is upregulated in the livers of animals fed with the ketogenic diet. Moreover, the size of the observed effect was likely dependent on the diet composition. Subsequently, the markers of regulatory pathways that may link ketogenic diet action to autophagy were measured, i.e., the activity of mTORC1, activation of AMPK, and the levels of SIRT1, p53, and FOXO3. Overall, observed treatment-specific effects including the upregulation of SIRT1 and downregulation of FOXO3 and p53. Finally, a GC/MS analysis of the fatty acid composition of animals' livers and the chows was performed in order to obtain an idea about the presence of specific compounds that may shape the effects of ketogenic diets on autophagy.

Identifiants

pubmed: 33705944
pii: S0955-2863(21)00040-1
doi: 10.1016/j.jnutbio.2021.108620
pii:
doi:

Substances chimiques

Dietary Fats 0
Forkhead Box Protein O3 0
FoxO3 protein, mouse 0
Tumor Suppressor Protein p53 0
AMP-Activated Protein Kinases EC 2.7.11.31
Sirt1 protein, mouse EC 3.5.1.-
Sirtuin 1 EC 3.5.1.-

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

108620

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Daniela Liśkiewicz (D)

Laboratory of Molecular Biology, Institute of Physiotherapy and Health Sciences, The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland. Electronic address: d.liskiewicz@awf.katowice.pl.

Arkadiusz Liśkiewicz (A)

Department of Physiology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.

Mateusz Grabowski (M)

Department for Experimental Medicine, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.

Marta Maria Nowacka-Chmielewska (MM)

Laboratory of Molecular Biology, Institute of Physiotherapy and Health Sciences, The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland.

Konstancja Jabłońska (K)

Department for Experimental Medicine, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.

Anna Wojakowska (A)

Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.

Łukasz Marczak (Ł)

Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland.

Jarosław J Barski (JJ)

Department of Physiology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland; Department for Experimental Medicine, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.

Andrzej Małecki (A)

Laboratory of Molecular Biology, Institute of Physiotherapy and Health Sciences, The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland.

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Classifications MeSH