Brown adipose tissue activity impacts systemic lactate clearance in male mice

Non-shivering thermogenesis in brown adipose tissue (BAT) is linked to metabolic health. Yet, how its activity states impact on systemic metabolism and in particular on lactate, a highly abundant metabolite increasingly recognized as a critical player in energy metabolism, remains unresolved. The goal of this study was to investigate the impact of BAT activity on lactate metabolism at the whole organism level. To activate or inactivate non-shivering thermogenesis in BAT, we housed C57Bl6/J male mice at 4, 21 and 30°C and then conducted lactate tolerance tests. In mice exposed to cold exposure (4°C), systemic lactate clearance was elevated. In contrast, clearance of systemic lactate was poor in mice housed under thermoneutral conditions (30°C) that inactivate BAT thermogenesis, as well as in mice deficient for the mitochondrial uncoupling protein-1. To better understand lactate metabolic fate during the clearance phase, in vivo stable isotope tracing experiments with labelled <sup>13</sup>C-lactate and analyses by mass spectrometry were performed. These experiments revealed that lactate contribution to gluconeogenesis was increased under cold exposure while its contribution to the tricarboxylic acid cycle was reduced in BAT under thermoneutrality. Remarkably, we also identified that lactate entered a pyruvate cycling process that was highly active in BAT, and repressed at thermoneutrality. Our study shows that inactivation of non-shivering thermogenesis decreased systemic lactate clearance, concomitantly with changes in metabolic fate of lactate in BAT and in gluconeogenic organs, in male mice. KEY POINTS: Lactate clearance is enhanced upon cold exposure and reduced at thermoneutrality. UCP1-deficient mice exhibit impaired lactate clearance. Oxidative utilization of lactate in brown fat is decreased at thermoneutrality. Prolonged cold exposure increases lactate contribution to gluconeogenesis. Lactate enters a highly active pyruvate cycling process in brown adipose tissue.

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Publication Details

Journal
The Journal of Physiology
Published
2025-09-22
DOI
https://doi.org/10.1113/jp288871
Citations
2
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
2.33

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article

Brown adipose tissue activity impacts systemic lactate clearance in male mice

Mélissa Parny, Isabelle Raymond‐Letron, Jean Nakhle, Jean‐Philippe Pradère et al.
2 citations
The Journal of Physiology
Adipose Tissue and Metabolism
2.33
article

Brown adipose tissue activity impacts systemic lactate clearance in male mice

Mélissa Parny, Isabelle Raymond‐Letron, Jean Nakhle, Jean‐Philippe Pradère, Isabelle Ader, Cédric Moro, Audrey Carrière, Cédric Dray, Luc Pellerin, Yannick Jeanson, Rémi Montané, Armelle Yart, Spiro Khoury, Damien Lagarde, Jean‐Charles Portais, Rogério Souza, Louis Casteilla, Anne Galinier, Marie Sallese, Léana Porcher‐Bibes, Anne‐Karine Bouzier Sore, Emma Huard
article en
2 citations

Abstract

Non-shivering thermogenesis in brown adipose tissue (BAT) is linked to metabolic health. Yet, how its activity states impact on systemic metabolism and in particular on lactate, a highly abundant metabolite increasingly recognized as a critical player in energy metabolism, remains unresolved. The goal of this study was to investigate the impact of BAT activity on lactate metabolism at the whole organism level. To activate or inactivate non-shivering thermogenesis in BAT, we housed C57Bl6/J male mice at 4, 21 and 30°C and then conducted lactate tolerance tests. In mice exposed to cold exposure (4°C), systemic lactate clearance was elevated. In contrast, clearance of systemic lactate was poor in mice housed under thermoneutral conditions (30°C) that inactivate BAT thermogenesis, as well as in mice deficient for the mitochondrial uncoupling protein-1. To better understand lactate metabolic fate during the clearance phase, in vivo stable isotope tracing experiments with labelled <sup>13</sup>C-lactate and analyses by mass spectrometry were performed. These experiments revealed that lactate contribution to gluconeogenesis was increased under cold exposure while its contribution to the tricarboxylic acid cycle was reduced in BAT under thermoneutrality. Remarkably, we also identified that lactate entered a pyruvate cycling process that was highly active in BAT, and repressed at thermoneutrality. Our study shows that inactivation of non-shivering thermogenesis decreased systemic lactate clearance, concomitantly with changes in metabolic fate of lactate in BAT and in gluconeogenic organs, in male mice. KEY POINTS: Lactate clearance is enhanced upon cold exposure and reduced at thermoneutrality. UCP1-deficient mice exhibit impaired lactate clearance. Oxidative utilization of lactate in brown fat is decreased at thermoneutrality. Prolonged cold exposure increases lactate contribution to gluconeogenesis. Lactate enters a highly active pyruvate cycling process in brown adipose tissue.

The Journal of PhysiologyVol. 603(22)
Centre National de la Recherche Scientifique (FR), Université de Bordeaux (FR), Inserm (FR), École Nationale Vétérinaire de Toulouse (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Institut Universitaire de France (FR), Institut National des Sciences Appliquées de Toulouse (FR), Université de Poitiers (FR), Centre de Résonance Magnétique des Systèmes Biologiques (FR), Laboratoire Hétérochimie Fondamentale et Appliquée (FR), Institut des Maladies Métaboliques et Cardiovasculaires (FR)
Biogen, Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Lausanne, Région Occitanie Pyrénées-Méditerranée
Openalex Percentile: Top 10%
Adipose Tissue and Metabolism
2.33
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