Evangelista Fabiana S, Muller Cynthia R, Stefano Jose T, Torres Mariana M, Muntanelli Bruna R, Simon Daniel, Alvares-da-Silva Mario R, Pereira Isabel V, Cogliati Bruno, Carrilho Flair J, Oliveira Claudia P
School of Arts, Science and Humanities, University of Sao Paulo Brazil.
Experimental Pathophysiology Dept, Faculty of Medicine, University of Sao Paulo Brazil.
Int J Clin Exp Med. 2015 Jul 15;8(7):10911-9. eCollection 2015.
This study sought to determine the role of physical training (PT) on body weight (BW), energy balance, histological markers of nonalcoholic fatty liver disease (NAFLD) and metabolic gene expression in the liver of ob/ob mice. Adult male ob/ob mice were assigned into groups sedentary (S; n = 8) and trained (T; n = 9). PT consisted in running sessions of 60 min at 60% of maximal speed conducted five days per week for eight weeks. BW of S group was higher from the 4(th) to 8(th) week of PT compared to their own BW at the beginning of the experiment. PT decreased daily food intake and increased resting oxygen consumption and energy expenditure in T group. No difference was observed in respiratory exchange ratio, but the rates of carbohydrate and lipids oxidation, and maximal running capacity were greater in T than S group. Both groups showed liver steatosis but not inflammation. PT increased CPT1a and SREBP1c mRNA expression in T group, but did not change MTP, PPAR-α, PPAR-γ, and NFKB mRNA expression. In conclusion, PT prevented body weight gain in ob/ob mice by inducing negative energy balance and increased physical exercise tolerance. However, PT did not change inflammatory gene expression and failed to prevent liver steatosis possible due to an upregulation in the expression of SREBP1c transcription factor. These findings reveal that PT has positive effect on body weight control but not in the liver steatosis in a leptin deficiency condition.
本研究旨在确定体育锻炼(PT)对ob/ob小鼠体重(BW)、能量平衡、非酒精性脂肪性肝病(NAFLD)组织学标志物以及肝脏代谢基因表达的作用。成年雄性ob/ob小鼠被分为久坐组(S;n = 8)和训练组(T;n = 9)。PT包括以最大速度的60%进行60分钟的跑步训练,每周进行五天,持续八周。与实验开始时自身的体重相比,PT第4至8周时S组的体重更高。PT使T组的每日食物摄入量减少,静息耗氧量和能量消耗增加。两组的呼吸交换率无差异,但T组的碳水化合物和脂质氧化率以及最大跑步能力均高于S组。两组均出现肝脏脂肪变性但无炎症。PT使T组的CPT1a和SREBP1c mRNA表达增加,但未改变MTP、PPAR-α、PPAR-γ和NFKB mRNA表达。总之,PT通过诱导负能量平衡防止ob/ob小鼠体重增加,并提高了身体运动耐力。然而,PT未改变炎症基因表达,且由于SREBP1c转录因子表达上调可能未能预防肝脏脂肪变性。这些发现表明,在瘦素缺乏的情况下,PT对体重控制有积极作用,但对肝脏脂肪变性无效。