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자료유형
학술저널
저자정보
저널정보
한국운동생리학회 운동과학 운동과학 제24권 제2호
발행연도
2015.1
수록면
153 - 160 (8page)

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PURPOSE: The propose of this study was to evaluate whether PPARβ/δ can increase mitochondrial enzymes and GLUT4 through NRF-1 promoter activity. METHODS: To evaluate, PPARβ/δ and NRF-1 protein expression in mouse skeletal muscle, TA muscle were dissect at 24h after 10 day swimming exercise(Ex). To evaluate PPARβ/δ effects on gene regulation, PPARβ/δ was overexpressed in mouse TA muscle using electrical pulse-mediated gen transfer(electroporation; EPO) method. We conducted chip and promoter reporter assay to confirm of PPARβ/δ can bind NRF-1 promoter and activates NRF-1 promoter in mouse muscle cell. RESULTS: PPARβ/δ and NRF-1 protein expression in skeletal muscle of 10 day Ex group were increased 2.2 and 2.7 fold respectively when compare to non-exercise muscle. PGC-1α protein expression in PPARβ/δ overexpression skeletal muscle were not different, but NRF-1, MEF2A, GLUT4, ATP syn and Cyt C expression were increased 2.2, 2.3, 2.1, 2 and 1.7 fold respectively when compare to empty vector(EV) treated muscle. Our ChiP and promoter activity assay result show that NRF-1 promoter has a PPARβ/δ binding site(PPRE) and PPARβ/δ can activates NRF-1 promoter through the PPRE. CONCLUSIONS: The increased PPARβ/δ by endurance exercise can control MEF2A-GLUT4 and mitochodrial enzymes such as ATP syn and Cyt C through NRF-1 promoter activity.

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