4.6 Article

Paeoniflorin Alleviates Skeletal Muscle Atrophy in Ovariectomized Mice through the ERα/NRF1 Mitochondrial Biogenesis Pathway

Journal

PHARMACEUTICALS
Volume 15, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/ph15040390

Keywords

muscle atrophy; post-menopausal women; estrogen insufficiency; paeoniflorin; mitochondrial biogenesis; anti-inflammation; muscle differentiation

Funding

  1. National Research Foundation of Korea (NRF) - Korea government (MIST) [2020R1A2C1102078]
  2. National Research Foundation of Korea [2020R1A2C1102078] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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In this study, it was demonstrated that Paeoniflorin (PNF) can inhibit TNF-α-induced skeletal muscle atrophy in postmenopausal women by restoring mitochondrial biosynthesis. PNF treatment restored differentiated myoblasts damaged by TNF-α and the diameter of atrophied myotubes. This mechanism was mediated through the regulation of estrogen receptor alpha (ERα) and the restoration of nuclear respiratory factor 1 (NRF1) and mitochondrial transcription factor A (TFAM).
Muscle atrophy in postmenopausal women is caused by estrogen deficiency and a variety of inflammatory factors, including tumor necrosis factor alpha (TNF alpha). Paeoniflorin (PNF), a natural compound with anti-inflammatory properties, improves estradiol synthesis. Here, we demonstrate that PNF inhibits the progression of TNF alpha-induced skeletal muscle atrophy after menopause by restoring mitochondrial biosynthesis. Differentiated myoblasts damaged by TNF alpha were restored by PNF, as evident by the increase in the expression of myogenin (MyoG) and myosin heavy chain 3 (Myh3)-the markers of muscle differentiation. Moreover, diameter of atrophied myotubes was restored by PNF treatment. TNF alpha-repressed nuclear respiratory factor 1 (NRF1) and mitochondrial transcription factor A (TFAM) (a major regulator of mitochondrial biosynthesis) were restored by PNF, via regulation by estrogen receptor alpha (ER alpha), an upregulator of NRF1. This mechanism was confirmed in ovariectomized (OVX) mice with a similar to 40% reduction in the cross-sectional area of the anterior tibialis muscle. OVX mice administered PNF (100, 300 mg/kg/day) for 12 weeks recovered more than similar to 20%. Behavioral, rotarod, and inverted screen tests showed that PNF enhances reduced muscle function in OVX mice. ER alpha restored expression of mitofusin 1 (MFN1) and mitofusin 2 (MFN2) (mitochondrial fusion markers) and dynamin-related protein (DRP1) and fission 1 (FIS1) (mitochondrial fission markers). Therefore, PNF can prevent muscle atrophy in postmenopausal women by inhibiting dysfunctional mitochondrial biogenesis.

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