Beverage Content Influences Voluntary Fluid Intake During Exercise: A Systematic Review: 2034 Board #186 June 2, 2: 00 PM - 3: 30 PM.

Lesley W. Vandermark, Pryor Jl, Riana R. Pryor, Lindsay J. DiStefano, D. Casa
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Abstract

Oxidative stress is known to be involved in many adverse mechanisms. Few studies have examined the effects of dehydration on oxidative stress. PURPOSE: Examine the effect of dehydration on plasma oxidative stress and antioxidant capacity in collegiate athletes. METHODS: Eighty-two athletes (56 male, 26 female) were recruited to undergo an acute dehydration (3% body weight), rehydration protocol. Subjects reported to the lab for baseline anthropometrics and blood sampling. The dehydration protocol required subjects to participate in their respective training until 3% of pre-weight body mass was lost. They reported back to the lab where a blood sample was immediately collected. Subjects then drank Gatorade until body weight was reestablished to baseline values. Plasma was collected at 80 min post full re-hydration (PFR) and snap frozen in liquid nitrogen and stored at -80 degrees Celsius until analysis. Oxidative stress was determined by measuring F2-isoprostane lipid oxidation via EIA kit. Ferric reducing ability of plasma (FRAP) was used to measure plasma antioxidant potential. Plasma osmolality was determined by freezing point depression by an osmometer. Statistical analysis consisted of 1-way ANOVA. All values are reported as mean ± SD. RESULTS: Plasma osmolality (280.9 mOsm ± 14.2) significantly elevated (286.2 mOsm ± 15.8) post exercise (p= 0.031), but returned to below normal values (282.1 mOsm ± 15.3) PFR. Plasma FRAP (uM/L ascorbate equivalents) values also increased post dehydration (pre: 0.237 ± 0.068, post: 0.286 ± 0.279), and decreased to near baseline levels PFR (0.247 ± 0.150) but only exhibited a statistical trend (P=0.08). Mean concentrations of F2-isoprostanes (pg/mL) declined from (437.6 ± 125.5) at baseline to (77.5 ± 496) post dehydration, and then rose to (699.73 ± 154.2) PFR (p<0.001). CONCLUSIONS: This study indicates that dehydration causes dramatic increases in plasma osmolality and antioxidant potential. Increased concentrations of antioxidants might be responsible for the reduction in F2-isoprostanes immediately post exercise. This decrease is followed by a large increase at 80 min post full rehydration despite normalization of plasma osmolality. The reasons for the decrease post dehydration and increase after rehydration in F2-isoprostanes warrants further examination.
饮料含量影响运动期间的自愿液体摄入量:系统评价:2034 Board #186 6月2日,下午2:00 -下午3:30。
众所周知,氧化应激参与了许多不良机制。很少有研究检查脱水对氧化应激的影响。目的:探讨脱水对大学生运动员血浆氧化应激和抗氧化能力的影响。方法:招募82名运动员(男56名,女26名)进行急性脱水(体重3%),补液方案。受试者到实验室进行基线人体测量和血液采样。脱水方案要求受试者参加各自的训练,直到体重减少3%。他们向实验室报告,实验室立即采集了血液样本。然后受试者喝佳得乐,直到体重恢复到基线值。血浆在完全再水化(PFR)后80分钟收集,并在液氮中快速冷冻,并在-80摄氏度保存直至分析。采用EIA试剂盒测定f2 -异前列腺烷脂质氧化水平,测定氧化应激水平。采用血浆铁还原能力(FRAP)测定血浆抗氧化电位。血浆渗透压是用渗透计降低冰点来测定的。统计分析采用单因素方差分析。所有数值均以均数±标准差报告。结果:运动后血浆渗透压(280.9 mOsm±14.2)明显升高(286.2 mOsm±15.8)(p= 0.031),但PFR恢复到正常值(282.1 mOsm±15.3)以下。血浆FRAP (uM/L抗坏血酸当量)值在脱水后也增加(脱水前为0.237±0.068,脱水后为0.286±0.279),PFR降至接近基线水平(0.247±0.150),但仅呈现统计学趋势(P=0.08)。f2 -异前列腺素平均浓度(pg/mL)从基线时的(437.6±125.5)下降到脱水后的(77.5±496),再上升到(699.73±154.2)PFR (p<0.001)。结论:该研究表明,脱水可导致血浆渗透压和抗氧化潜能急剧增加。抗氧化剂浓度的增加可能是运动后f2 -异前列腺素立即减少的原因。尽管血浆渗透压恢复正常,但在完全补液后80分钟,血浆渗透压会大幅升高。f2 -异前列腺素在脱水后减少而在复水后增加的原因值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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