Department of Sport and Exercise Science, Aberystwyth University, Aberystwyth, UK; Clinical Research Centre, Prince Phillip Hospital, Llanelli, UK.
Institute of Biological, Environmental and Rural Sciences, Aberystwyth University, Aberystwyth, UK.
Brain Behav Immun. 2014 Jul;39:194-203. doi: 10.1016/j.bbi.2013.10.032. Epub 2013 Nov 4.
Bovine colostrum (COL) has been advocated as a nutritional countermeasure to exercise-induced immune dysfunction and increased risk of upper respiratory illness (URI) in athletic populations, however, the mechanisms remain unclear. During winter months, under double-blind procedures, 53 males (mean training load±SD, 50.5±28.9 MET-hweek(-1)) were randomized to daily supplementation of 20g of COL (N=25) or an isoenergetic/isomacronutrient placebo (PLA) (N=28) for 12weeks. Venous blood was collected at baseline and at 12weeks and unstimulated saliva samples at 4 weeks intervals. There was a significantly lower proportion of URI days and number of URI episodes with COL compared to PLA over the 12weeks (p<0.05). There was no effect of COL on in vitro neutrophil oxidative burst, salivary secretory IgA or salivary antimicrobial peptides (p>0.05), which does not support previously suggested mechanisms. In a subset of participants (COL=14, PLA=17), real-time quantitative PCR, targeting the 16S rRNA gene showed there was an increase in salivary bacterial load over the 12 weeks period with PLA (p<0.05) which was not as evident with COL. Discriminant function analysis of outputs received from serum metabolomics showed changes across time but not between groups. This is the first study to demonstrate that COL limits the increased salivary bacterial load in physically active males during the winter months which may provide a novel mechanism of immune-modulation with COL and a relevant marker of in vivo (innate) immunity and risk of URI.
牛初乳(COL)一直被认为是一种营养对策,可以对抗运动引起的免疫功能障碍和增加运动员上呼吸道疾病(URI)的风险,然而,其机制尚不清楚。在冬季,53 名男性(平均训练负荷±标准差,50.5±28.9 MET-hweek(-1))以双盲程序随机分为每天补充 20g COL(N=25)或等能量/等宏量营养素安慰剂(PLA)(N=28),持续 12 周。在基线和 12 周时采集静脉血,在 4 周间隔时采集非刺激唾液样本。与 PLA 相比,COL 在 12 周内 URI 天数和 URI 发作次数明显减少(p<0.05)。COL 对体外中性粒细胞氧化爆发、唾液分泌型 IgA 或唾液抗菌肽没有影响(p>0.05),这与之前提出的机制不一致。在部分参与者(COL=14,PLA=17)中,针对 16S rRNA 基因的实时定量 PCR 显示,PLA 组在 12 周内唾液细菌负荷增加(p<0.05),而 COL 组则不明显。来自血清代谢组学的输出的判别函数分析显示,随着时间的推移发生了变化,但组间没有变化。这是第一项研究表明,COL 可限制冬季活跃男性唾液中细菌负荷的增加,这可能为 COL 提供了一种新的免疫调节机制,以及一种与体内(先天)免疫和 URI 风险相关的新型标志物。