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Original research
Intestinal gluconeogenesis prevents obesity-linked liver steatosis and non-alcoholic fatty liver disease
  1. Justine Vily-Petit1,2,
  2. Maud Soty-Roca1,2,
  3. Marine Silva1,2,
  4. Margaux Raffin1,2,
  5. Amandine Gautier-Stein1,2,
  6. Fabienne Rajas1,2,
  7. Gilles Mithieux1,2
  1. 1U1213 Nutrition, Diabetes and the Brain, Institut national de la santé et de la recherche médicale, Lyon, France
  2. 2U1213 Nutrition, Diabetes and the Brain, Université Lyon 1 Faculté de Médecine Lyon-Est, Lyon, France
  1. Correspondence to Dr Gilles Mithieux, U1213, Institut national de la santé et de la recherche médicale, Lyon 69372, France; gilles.mithieux{at}inserm.fr

Abstract

Objective Hepatic steatosis accompanying obesity is a major health concern, since it may initiate non-alcoholic fatty liver disease (NAFLD) and associated complications like cirrhosis or cancer. Intestinal gluconeogenesis (IGN) is a recently described function that contributes to the metabolic benefits of specific macronutrients as protein or soluble fibre, via the initiation of a gut-brain nervous signal triggering brain-dependent regulations of peripheral metabolism. Here, we investigate the effects of IGN on liver metabolism, independently of its induction by the aforementioned macronutrients.

Design To study the specific effects of IGN on hepatic metabolism, we used two transgenic mouse lines: one is knocked down for and the other overexpresses glucose-6-phosphatase, the key enzyme of endogenous glucose production, specifically in the intestine.

Results We report that mice with a genetic overexpression of IGN are notably protected from the development of hepatic steatosis and the initiation of NAFLD on a hypercaloric diet. The protection relates to a diminution of de novo lipogenesis and lipid import, associated with benefits at the level of inflammation and fibrosis and linked to autonomous nervous system. Conversely, mice with genetic suppression of IGN spontaneously exhibit increased hepatic triglyceride storage associated with activated lipogenesis pathway, in the context of standard starch-enriched diet. The latter is corrected by portal glucose infusion mimicking IGN.

Conclusion We conclude that IGN per se has the capacity of preventing hepatic steatosis and its eventual evolution toward NAFLD.

  • intestinal gluconeogenesis
  • gut-brain neural communication
  • hepatic steatosis
  • obesity
  • diabetes
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Footnotes

  • Contributors JV-P and MS-R conceived and carried out the experiments, and wrote the paper. MS and MR contributed to the experimental studies. AG-S and FR interpreted the data and edited the manuscript. GM supervised the study and wrote the manuscript.

  • Funding This work was supported by research grants from the Agence Nationale de la Recherche (ANR-17-CE14-0020-01), the Fondation pour la Recherche Médicale (Equipe FRM DEB20160334898) and the company Servier.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting or dissemination plans of this research.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available upon reasonable request. Unpublished results mentioned in the text may be communicated on request.

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