| First Author | Yoh K | Year | 2022 |
| Journal | Biochem Biophys Res Commun | Volume | 628 |
| Pages | 11-17 | PubMed ID | 36063597 |
| Mgi Jnum | J:328541 | Mgi Id | MGI:7336421 |
| Doi | 10.1016/j.bbrc.2022.08.064 | Citation | Yoh K, et al. (2022) Constitutive activation of estrogen receptor alpha signaling in muscle prolongs exercise endurance in mice. Biochem Biophys Res Commun 628:11-17 |
| abstractText | Estrogen is a female hormone that plays a role in various tissues, although the mechanism in skeletal muscle has not been fully clarified. We previously showed that systemic administration of estrogen for 10 weeks ameliorated decreased exercise endurance in ovariectomized mice. To assess whether a long-term and muscle-specific activation of estrogen signaling modulates muscle function, we constructed an expression plasmid for a constitutively active estrogen receptor alpha (caERalpha) under the control of muscle creatine kinase (Mck) gene promoter/enhancer. In C2C12 mouse myoblastic cells, transfection of the Mck-caERalpha plasmid elevated the estrogen response element-driven transcription in a ligand-independent manner. Using this construct, we generated Mck-caERalpha transgenic mice, in which caERalpha is predominantly expressed in muscle. Treadmill running test revealed that female Mck-caERalpha mice exhibit a prolonged running time and distance compared with the wild-type mice. Moreover, microarray expression analysis revealed that the genes related to lipid metabolism, insulin signaling, and growth factor signaling were particularly upregulated in the quadriceps femoris muscle of Mck-caERalpha mice. These results suggest that estrogen signaling potentiates exercise endurance in skeletal muscle through modulating the expression of metabolism-associated genes. |
