Exercise-induced BDNF promotes PPARδ-dependent reprogramming of lipid metabolism in skeletal muscle during exercise recovery

Author:

Chan Wing Suen1ORCID,Ng Chun Fai1ORCID,Pang Brian Pak Shing1,Hang Miaojia1,Tse Margaret Chui Ling1ORCID,Iu Elsie Chit Yu1,Ooi Xin Ci1,Yang Xiuying2ORCID,Kim Jason K.34ORCID,Lee Chi Wai5ORCID,Chan Chi Bun16ORCID

Affiliation:

1. School of Biological Sciences, University of Hong Kong, 5N10 Kadoorie Biological Sciences Building, Pokfulam Road, Hong Kong, China.

2. Beijing Key Laboratory of Drug Target and Screening Research, Institute of Materia Medica of Peking Union Medical College, Beijing 101399, China.

3. Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.

4. Division of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.

5. Department of Biology, Hong Kong Baptist University, Hong Kong, China.

6. State Key Laboratory of Pharmaceutical Biotechnology, University of Hong Kong, Hong Kong, China.

Abstract

Post-exercise recovery is essential to resolve metabolic perturbations and promote long-term cellular remodeling in response to exercise. Here, we report that muscle-generated brain-derived neurotrophic factor (BDNF) elicits post-exercise recovery and metabolic reprogramming in skeletal muscle. BDNF increased the post-exercise expression of the gene encoding PPARδ (peroxisome proliferator–activated receptor δ), a transcription factor that is a master regulator of lipid metabolism. After exercise, mice with muscle-specific Bdnf knockout ( MBKO ) exhibited impairments in PPARδ-regulated metabolic gene expression, decreased intramuscular lipid content, reduced β-oxidation, and dysregulated mitochondrial dynamics. Moreover, MBKO mice required a longer period to recover from a bout of exercise and did not show increases in exercise-induced endurance capacity. Feeding naïve mice with the bioavailable BDNF mimetic 7,8-dihydroxyflavone resulted in effects that mimicked exercise-induced adaptations, including improved exercise capacity. Together, our findings reveal that BDNF is an essential myokine for exercise-induced metabolic recovery and remodeling in skeletal muscle.

Publisher

American Association for the Advancement of Science (AAAS)

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