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布洛芬增加肠道屏障损伤标志物,但在缺氧休息和运动后抑制炎症。

Ibuprofen Increases Markers of Intestinal Barrier Injury But Suppresses Inflammation at Rest and After Exercise in Hypoxia.

机构信息

Department of Health, Exercise and Sports Sciences, University of New Mexico, Albuquerque, NM.

Department of Kinesiology, California Baptist University, Riverside, CA.

出版信息

Med Sci Sports Exerc. 2023 Jan 1;55(1):141-150. doi: 10.1249/MSS.0000000000003032. Epub 2022 Sep 5.

Abstract

PURPOSE

The purpose of this study was to evaluate the effects of acute ibuprofen consumption (2 × 600-mg doses) on markers of enterocyte injury, intestinal barrier dysfunction, inflammation, and symptoms of gastrointestinal (GI) distress at rest and after exercise in hypobaric hypoxia.

METHODS

Using a randomized double-blind placebo-controlled crossover design, nine men (age, 28 ± 3 yr; weight, 75.4 ± 10.5 kg; height, 175 ± 7 cm; body fat, 12.9% ± 5%; V̇O 2 peak at 440 torr, 3.11 ± 0.65 L·min -1 ) completed a total of three visits including baseline testing and two experimental trials (placebo and ibuprofen) in a hypobaric chamber simulating an altitude of 4300 m. Preexercise and postexercise blood samples were assayed for intestinal fatty acid binding protein (I-FABP), ileal bile acid binding protein, soluble cluster of differentiation 14, lipopolysaccharide binding protein, monocyte chemoattractant protein-1, tumor necrosis factor α (TNF-α), interleukin-1β, and interleukin-10. Intestinal permeability was assessed using a dual sugar absorption test (urine lactulose-to-rhamnose ratio).

RESULTS

Resting I-FABP (906 ± 395 vs 1168 ± 581 pg·mL -1 ; P = 0.008) and soluble cluster of differentiation 14 (1512 ± 297 vs 1642 ± 313 ng·mL -1 ; P = 0.014) were elevated in the ibuprofen trial. Likewise, the urine lactulose-to-rhamnose ratio (0.217 vs 0.295; P = 0.047) and the preexercise to postexercise change in I-FABP (277 ± 308 vs 498 ± 479 pg·mL -1 ; P = 0.021) were greater in the ibuprofen trial. Participants also reported greater upper GI symptoms in the ibuprofen trial ( P = 0.031). However, monocyte chemoattractant protein-1 ( P = 0.007) and TNF-α ( P = 0.047) were lower throughout the ibuprofen trial compared with placebo (main effect of condition).

CONCLUSIONS

These data demonstrate that acute ibuprofen ingestion aggravates markers of enterocyte injury and intestinal barrier dysfunction at rest and after exercise in hypoxia. However, ibuprofen seems to suppress circulating markers of inflammation.

摘要

目的

本研究旨在评估急性布洛芬摄入(2×600mg 剂量)对低压缺氧下静息和运动后肠上皮细胞损伤、肠道屏障功能障碍、炎症和胃肠道(GI)不适症状标志物的影响。

方法

采用随机双盲安慰剂对照交叉设计,9 名男性(年龄 28±3 岁;体重 75.4±10.5kg;身高 175±7cm;体脂 12.9%±5%;4300m 模拟高原条件下的峰值摄氧量 440 托,3.11±0.65L·min-1)在低压舱中完成了总共 3 次访问,包括基线测试和 2 次实验(安慰剂和布洛芬)。在运动前和运动后采集血样,测定肠脂肪酸结合蛋白(I-FABP)、回肠胆酸结合蛋白、可溶性 CD14、脂多糖结合蛋白、单核细胞趋化蛋白-1、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β和白细胞介素-10。通过双糖吸收试验(尿乳果糖/鼠李糖比值)评估肠道通透性。

结果

在布洛芬试验中,静息时的 I-FABP(906±395 与 1168±581pg·mL-1;P=0.008)和可溶性 CD14(1512±297 与 1642±313ng·mL-1;P=0.014)升高。同样,尿乳果糖/鼠李糖比值(0.217 与 0.295;P=0.047)和运动前到运动后的 I-FABP 变化(277±308 与 498±479pg·mL-1;P=0.021)在布洛芬试验中更大。参与者在布洛芬试验中也报告了更多的上胃肠道症状(P=0.031)。然而,与安慰剂相比,整个布洛芬试验中单核细胞趋化蛋白-1(P=0.007)和 TNF-α(P=0.047)水平较低(条件的主要作用)。

结论

这些数据表明,急性布洛芬摄入会加重低压缺氧下静息和运动后肠上皮细胞损伤和肠道屏障功能障碍的标志物。然而,布洛芬似乎抑制了循环炎症标志物。

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