Effect of Ibuprofen on Markers of Acute Kidney Injury, Intestinal Injury, and Endotoxemia after Running in the Heat.

Jonathan W Specht,Alyssa R Bailly,Serena Garcia,Steven Klepacz,Suzana Andrade De Oliveira,David Lucero,Zachary J McKenna,Zachary J Schlader,Fabiano T Amorim
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Abstract

PURPOSE To test the hypothesis that ibuprofen ingestion exacerbates markers of acute kidney injury (AKI), gastrointestinal (GI) injury, and endotoxemia after running in the heat. METHODS Using a randomized double-blind crossover design, eleven physically active individuals (six women) ingested 600 mg of ibuprofen or placebo 12- and one-hour prior to running one-hour in a heated chamber (35 °C, 20%-60% R.H.) at an intensity of 60% V̇O2peak. Blood and urine samples were collected pre-, post-, and one-hour post-exercise to assess cytokines and markers of AKI, GI injury, and endotoxemia. RESULTS One hour of running in the heat increased markers of AKI (urinary product of IGFBP7•TIMP2 [Placebo: ∆ 1.8 ± 0.8 log10(ng/ml)2/1000, Ibuprofen: ∆ 1.8 ± 0.9 log10(ng/ml)2/1000], urinary NGAL, and serum cystatin C), GI damage (I-FABP [Placebo: ∆ 631 ± 446 pg/ml, Ibuprofen: ∆ 576 ± 455 pg/ml]), and inflammatory cytokines (TNFα [Placebo: ∆ 5.2 ± 3.5 pg/ml, Ibuprofen: ∆ 6.2 ± 4.9 pg/ml], IL-6, IL-10, and MCP-1), but these changes were not exacerbated by ibuprofen ingestion. There were effects of time (p < 0.001) and condition (p = 0.03) for serum IL-8, with greater concentrations in the ibuprofen (pre: 11.4 ± 5.1 pg/mL, post: 15.5 ± 7.3 pg/ml) trials than placebo (pre: 9.7 ± 4.2 pg/mL, post: 11.7 ± 5.4 pg/mL). There were no effects of time or condition on markers of endotoxemia (LBP [Placebo: ∆ -1.2 ± 3.2 μg/ml, Ibuprofen: ∆ 1.0 ± 1.6 μg/ml], sCD14). CONCLUSIONS These findings indicate that ibuprofen ingestion does not worsen intestinal or renal injury experienced during one hour of exercise in the heat, but increases pro-inflammatory IL-8.
布洛芬对高温跑步后急性肾损伤、肠损伤和内毒素血症指标的影响。
目的验证摄入布洛芬可加重高温跑步后急性肾损伤(AKI)、胃肠道损伤(GI)和内毒素血症指标的假说。方法采用随机双盲交叉设计,11名体力活动者(6名女性)在35°C, 20%-60% R.H.的加热室中以60%的峰值强度跑步1小时前12和1小时服用600mg布洛芬或安慰剂。在运动前、运动后和运动后1小时采集血液和尿液样本,以评估AKI、GI损伤和内毒素血症的细胞因子和标志物。RESULTSOne小时的运行热增加标记的阿基(尿IGFBP7•TIMP2产品(安慰剂:∆1.8±0.8 log10 (ng / ml) 2/1000,布洛芬:∆1.8±0.9 log10 (ng / ml) 2/1000),尿NGAL,和血清半胱氨酸蛋白酶抑制物C),胃肠道损伤(I-FABP(安慰剂:∆631±446 pg / ml,布洛芬:∆576±455 pg / ml)),和炎性细胞因子(肿瘤坏死因子α(安慰剂:∆5.2±3.5 pg / ml,布洛芬:∆6.2±4.9 pg / ml), il - 6、il - 10,和MCP-1),但是这些改变并非加剧了布洛芬摄入。对血清IL-8有时间(p < 0.001)和条件(p = 0.03)的影响,布洛芬组(治疗前:11.4±5.1 pg/mL,治疗后:15.5±7.3 pg/mL)高于安慰剂组(治疗前:9.7±4.2 pg/mL,治疗后:11.7±5.4 pg/mL)。时间和条件对内毒素血症标志物(LBP[安慰剂:∆-1.2±3.2 μg/ml,布洛芬:∆1.0±1.6 μg/ml], sCD14)无影响。结论:摄入布洛芬不会加重高温运动1小时后的肠道或肾脏损伤,但会增加促炎IL-8。
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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