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急性摄入布洛芬并不会影响白细胞介素-6 的释放,也不能改善热环境下的自主运动能力,尽管它改变了皮质活动。

Acute ingestion of Ibuprofen does not influence the release of IL-6 or improve self-paced exercise in the heat despite altering cortical activity.

机构信息

School of Medicine and Psychology, College of Health and Medicine, Australian National University, 54 Mills Rd, Florey Building, Canberra, ACT, 2601, Australia.

Griffith Centre For Mental Health and ALIVE National Centre for Mental Health Research Translation, Griffith University, Nathan, QLD, Australia.

出版信息

Eur J Appl Physiol. 2024 Aug;124(8):2303-2313. doi: 10.1007/s00421-024-05452-z. Epub 2024 Mar 6.

Abstract

The present study tested the hypothesis that ingesting 800 mg Ibuprofen prior to self-paced cycling at a fixed rating of perceived exertion (RPE) improves performance by attenuating the release of Interleukin (IL)-6 and its signalling molecules, whilst simultaneously modulating cortical activity and cerebral oxygenation to the brain. Eight healthy, recreationally active males ingested 800 mg Ibuprofen or a placebo ~ 1 h prior to performing fixed RPE cycling for 60 min in 35 °C and 60% relative humidity at an intensity of hard to very hard (RPE = 16) with intermittent maximal (RPE = 20) sprints every 10 min. Power output (PO), core and mean skin temperatures (T, T), respectively, and heart rate (HR) were measured continuously. Electroencephalography (EEG) recordings at the frontal (Fz), motor (Cz) and Parietal (Pz) areas (90 s) were collected every 5 min. IL-6, soluble glycoprotein receptor (sgp130) and IL-6 receptor (R) were collected at pre-, 30 min and immediately post-exercise. Mean PO, HR, T and T, and RPE were not different between trials (P ≥ 0.33). At end-exercise, the change in IL-6, sgp130 and sIL-6R was not different between trials (P ≥ 0.12). The increase in α and β activity did not differ in any cortices between trials (P ≥ 0.07); however, there was a significant reduction in α/β activity in the Ibuprofen compared to placebo trials at all sites (P ≤ 0.05). Ingesting a maximal, over-the-counter dose of Ibuprofen prior to exercise in the heat does not attenuate the release of IL-6, nor improve performance, but may influence cortical activity evidenced by a greater reduction in α/β activity.

摘要

本研究旨在验证以下假设

在固定自我感知用力程度(RPE)下进行自行调节的自行车运动前摄入 800 毫克布洛芬,通过减轻白细胞介素(IL)-6 的释放及其信号分子,同时调节大脑的皮质活动和脑氧合,从而改善运动表现。8 名健康、有规律运动的男性在 35°C 和 60%相对湿度的环境下,以努力到非常努力的强度(RPE=16)进行固定 RPE 自行车运动 60 分钟,每隔 10 分钟进行一次间歇性最大强度(RPE=20)冲刺,分别在运动前 1 小时和运动前 30 分钟和运动后即刻,服用 800 毫克布洛芬或安慰剂。持续测量功率输出(PO)、核心温度(T)和平均皮肤温度(T)以及心率(HR)。每 5 分钟收集一次额区(Fz)、运动区(Cz)和顶区(Pz)的脑电图(EEG)记录(90s)。在运动前、30 分钟和运动后即刻收集白细胞介素(IL)-6、可溶性糖蛋白受体(sgp130)和白细胞介素(IL)-6 受体(R)。运动结束时,试验间 IL-6、sgp130 和 sIL-6R 的变化无差异(P≥0.33)。运动结束时,试验间 IL-6、sgp130 和 sIL-6R 的变化无差异(P≥0.12)。在任何皮质区,试验间的α和β活动增加均无差异(P≥0.07);然而,与安慰剂组相比,布洛芬组在所有部位的α/β 活性均显著降低(P≤0.05)。在热环境中进行运动前摄入最大剂量的非处方布洛芬不会减轻 IL-6 的释放,也不会提高运动表现,但可能会影响皮质活动,表现为α/β 活性的降低更为明显。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0689/11322222/b0ee6b23c4b8/421_2024_5452_Fig1_HTML.jpg

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