Abstract

Peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) is expressed in skeletal muscles and regulates systemic metabolism. Thus, nutraceuticals targeting skeletal muscle PGC-1α have attracted attention to modulate systemic metabolism. As auraptene contained in citrus fruits promotes lipid metabolism and improves mitochondrial respiration, it could increase mitochondrial function through PGC-1α. Therefore, we hypothesized that PGC-1α is activated by auraptene and investigated its effect using Citrus hassaku extract powder (CHEP) containing >80% of auraptene. C2C12 myotubes were incubated with vehicle or CHEP for 24 h; C57BL/6J mice were fed a control diet or a 0.25% (w/w) CHEP-containing diet for 5 weeks. PGC-1α protein level and mitochondrial content increased following CHEP treatment in cultured myotubes and skeletal muscles. In addition, the number of oxidative fibers increased in CHEP-fed mice. These findings suggest that CHEP-mediated PGC-1α upregulation induced mitochondrial biogenesis and fiber transformation to oxidative fibers. Furthermore, as CHEP increased the expression of the protein sirtuin 3 and of phosphorylated AMP-activated protein kinase (AMPK) and the transcriptional activity of PGC-1α, these molecules might be involved in CHEP-induced effects in skeletal muscles. Collectively, our findings indicate that CHEP mediates PGC-1α expression in skeletal muscles and may serve as a dietary supplement to prevent metabolic disorders.

Highlights

  • Peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) functions as an inducible co-regulator of energy homeostasis [1,2,3,4]

  • We demonstrated that Citrus hassaku extract powder (CHEP) increased mitochondrial content and the number of oxidative fibers in murine skeletal muscle

  • As overexpression of PGC-1α in skeletal muscle stimulates the switch of muscle fiber type from glycolytic fibers to oxidative fibers [7], we investigated whether CHEP alters the muscle fiber type in murine skeletal muscle

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Summary

Introduction

Peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) functions as an inducible co-regulator of energy homeostasis [1,2,3,4]. It is abundantly expressed in tissues with high energy demand, including skeletal muscle, brown adipose tissue, heart, kidney, and brain [5]. PGC-1α affects energy metabolism by interacting with transcription factors such as peroxisome proliferator-activated receptors (PPARs) [6]. We revealed that overexpression of skeletal muscle-specific PGC-1α increases mitochondrial content, the transformation of glycolytic fibers to oxidative fibers, fatty acid oxidation, and exercise capacity [7] and inhibits the progression of atherosclerosis [8]. Upregulation of PGC-1α to modulate metabolic pathways is an interesting strategy for preventing metabolic disorders

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