有氧训练强度对肥胖雄性Wistar大鼠骨骼肌PGC-1α、干扰素调节因子4和动脉粥样硬化指数的影响

Q4 Veterinary
K. Hejazi, M. Ziaaldini, S. A. Hosseini, M. Fathei
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引用次数: 1

摘要

过氧化物酶体增殖物激活受体γ共激活因子1-α(PGC-1α)是能量代谢的主要调节因子。训练刺激许多过程,如线粒体生物发生、葡萄糖代谢和脂肪酸代谢。它还增加了脂肪氧化的能力。本研究旨在研究8周不同强度有氧训练对肥胖雄性Wistar大鼠PGC-1α、干扰素调节因子4(IRF4)和动脉粥样硬化指数的影响。将24只高脂饮食诱导的肥胖雄性大鼠(体重:250至300gr,BMI>30g/cm2)分为三组:中等强度有氧训练(MI)、高强度有氧运动(HI)和对照组(C)。MI和HI训练组分别以28米/分钟和34米/分钟的速度在跑步机上行走8周,每周5次,每次60分钟。MI和HI组的PGC-1a水平与C组相比显著升高(p 0.05)。血清HDL-C水平仅在MI组与C组比较升高(p<0.05),MI组和HI组的动脉粥样硬化指数水平比C组降低得更显著(p<0.05)。结果表明,8周的中高强度有氧训练可能是激活骨骼肌PGC-1a蛋白(即能量代谢和线粒体生物发生的关键调节因子)的信号通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The impact of aerobic training intensity on skeletal muscle PGC-1α, interferon regulatory factor 4, and atherogenic index in obese male Wistar rats
Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) is the main regulator in energy metabolism. Training stimulates many processes like mitochondrial biogenesis, glucose metabolism, and fatty acids metabolism. It also increases the capacity of fat oxidation. The purpose of this study was to investigate the effects of eight-week aerobic training of different intensities on PGC-1α, interferon regulatory factor 4 (IRF4), and atherogenic index in obese male Wistar rats. Twenty-four obese male rats induced by a high-fat diet (weight: 250 to 300 gr, BMI >30g/cm2) were divided into three groups: aerobic training of moderate intensity (MI), aerobic training of high intensity (HI), and the control group (C). The MI and HI training groups carried out exercise training by eight weeks of walking on a treadmill for five sessions/week, 60 min per session, and at a speed of 28 m/min and 34 m/min, respectively. The levels of PGC-1a in the MI and HI groups significantly increased compared to the C group (p 0.05). The serum HDL-C levels increased only in the MI group compared to the C group (p  < 0.05). The LDL-C, TG, TC, and atherogenic index levels reduced more significantly in MI and HI groups than in the C group (p  < 0.05). The results show that eight-week aerobic training of two moderate and high intensities may be the signaling pathways to the activation of the PGC-1a protein (i.e., a key regulator of energy metabolism and mitochondrial biogenesis) in skeletal muscle.
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