Arazi Hamid, Asadi Abbas, Suzuki Katsuhiko
Department of Exercise Physiology, Faculty of Sports Sciences, University of Guilan, Rasht 1438, Iran.
Faculty of Sport Sciences, Waseda University, Tokorozawa 359-1192, Japan.
Antioxidants (Basel). 2018 Jun 11;7(6):76. doi: 10.3390/antiox7060076.
The aim of this study was to investigate the effects of 6-week beta-hydroxy-beta methylbutyrate-free acid (HMB-FA) supplementation on oxidative stress and biochemical variables in responses to resistance training. Sixteen healthy young males participated in this study and were randomly assigned to a HMB-FA supplementation group ( = 8) or a placebo supplementation group ( = 8). The resistance training program was applied for 6 weeks with two sessions per week. Blood samples were collected before and after training, and 8-hydroxy-2-deoxyguanosine (8-OHdG), malondialdehyde (MDA), protein carbonyl (PC), and biochemical variables, such as alanine transaminase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and the numbers of total white blood cells (WBC), neutrophils, lymphocytes, and monocytes were analyzed. Following intervention, both the HMB-FA and placebo supplementation groups showed significant decreases in MDA (effect size [ES]; −0.39, −0.33) and PC (ES; −1.37, −1.41), respectively. However, 8-OHdG did not change after 6 weeks of training in any of the groups. In addition, both groups showed similar training effects on biochemical variables after 6 weeks of intervention. It was concluded that HMB-FA supplementation during resistance training did not add further adaptive changes related to oxidative stress markers.
本研究的目的是调查补充6周β-羟基-β-甲基丁酸游离酸(HMB-FA)对抵抗训练反应中氧化应激和生化指标的影响。16名健康年轻男性参与了本研究,并被随机分为HMB-FA补充组(n = 8)或安慰剂补充组(n = 8)。抵抗训练计划为期6周,每周进行两次训练。在训练前后采集血样,分析8-羟基-2'-脱氧鸟苷(8-OHdG)、丙二醛(MDA)、蛋白质羰基(PC)以及生化指标,如丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、碱性磷酸酶(ALP)和白细胞总数(WBC)、中性粒细胞、淋巴细胞及单核细胞数量。干预后,HMB-FA补充组和安慰剂补充组的MDA(效应量[ES];-0.39,-0.33)和PC(ES;-1.37,-1.41)均显著降低。然而,6周训练后,任何一组的8-OHdG均未发生变化。此外,干预6周后,两组在生化指标上显示出相似的训练效果。得出的结论是,在抵抗训练期间补充HMB-FA并未带来与氧化应激标志物相关的进一步适应性变化。