Effects of Cannabidiol Ingestion on Thermoregulatory and Inflammatory Responses to Treadmill Exercise in the Heat in Recreationally Active Males.

Drusus A Johnson,Thomas G Cable,Mark P Funnell,Donald L Peden,Josh Thorley,Mafalda Ferreira de Cunha,Kirsty M Reynolds,Luke Harris,Matt Wood,Tom Chavez-O'Reilly,Joe Carrington,Stephen J Bailey,Tom Clifford,Liam M Heaney,Lewis J James
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Abstract

PURPOSE Exertional heat stress can induce systemic endotoxin exposure and a pro-inflammatory cascade, likely impairing thermoregulation. Cannabidiol (CBD) is protective in pre-clinical models of tissue ischaemia and inflammation. Therefore, this study examined the effects of CBD ingestion on exercise-induced thermoregulatory and inflammatory responses. METHODS In a randomised, double-blinded study, thirteen active males (age 25 ± 5 y; peak oxygen uptake [V̇O2peak] 50.4 ± 3.2 mL/kg/min) ingested 298 mg CBD or placebo 105 minutes before 1 h treadmill exercise (60-65% V̇O2peak) in 32 °C and 50% relative humidity. Core temperature, skin temperature, heart rate, subjective outcomes and sweat loss were assessed during/after exercise. Plasma osmolality, plasma volume changes and plasma markers of intestinal damage (I-FABP), monocyte activation (CD14) and inflammatory cytokine responses (IL-6, IL-8 and TNF-α) were assessed at baseline, pre-exercise, 20- and 90-min post-exercise. RESULTS Core temperature (∆ 1.69 ± 0.48 °C [CBD] and 1.79 ± 0.53 °C [Placebo]) and I-FABP increased during exercise, with no differences between conditions (p > 0.050). Mean (95% CI) CD14 was 1776 (463 to 3090) pg/mL greater 90 min post-exercise in placebo (p = 0.049). Median (interquartile range) peak IL-6 concentration was -0.8 (-1.1, -0.3) pg/mL less in CBD (p = 0.050), whilst the between-conditions difference in IL-6 area under curve was -113 (-172, 27) pg/mL·270 min (p = 0.054). CONCLUSIONS CBD did not affect thermoregulation during exertional heat stress but appeared to elicit minor immunosuppressive effects, reducing CD14 and IL-6 responses, warranting investigation in humans under more severe heat strain and other pro-inflammatory scenarios.
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摄入大麻二酚对热量调节和炎症反应的影响--运动量大的男性在高温下进行跑步机运动时的热量调节和炎症反应
目的劳累性热应激可诱发全身性内毒素暴露和促炎症级联反应,并可能损害体温调节功能。大麻二酚(CBD)在组织缺血和炎症的临床前模型中具有保护作用。方法在一项随机、双盲研究中,13 名活跃的男性(年龄 25 ± 5 岁;峰值摄氧量[V.M.O.peak] 50.4 ± 3.2 mL/kg/min)在 32 °C、50% 相对湿度条件下进行 1 小时跑步机运动(V.M.O.peak 为 60-65% )前 105 分钟摄入 298 毫克大麻二酚或安慰剂。在运动过程中/后对核心温度、皮肤温度、心率、主观结果和出汗量进行了评估。在基线、运动前、运动后 20 分钟和 90 分钟评估血浆渗透压、血浆容量变化以及肠道损伤(I-FABP)、单核细胞活化(CD14)和炎症细胞因子反应(IL-6、IL-8 和 TNF-α)的血浆标志物。结果运动时核心温度(∆ 1.69 ± 0.48 °C[CBD]和 1.79 ± 0.53 °C[安慰剂])和 I-FABP 升高,不同条件下无差异(p > 0.050)。安慰剂组运动后 90 分钟 CD14 的平均值(95% CI)比安慰剂组高 1776(463 至 3090) pg/mL(p = 0.049)。CBD的IL-6峰值浓度中位数(四分位数间距)为-0.8(-1.1,-0.3)皮克/毫升(p = 0.050),而IL-6曲线下面积的条件间差异为-113(-172,27)皮克/毫升-270分钟(p = 0.054)。结论SCBD 不会影响劳累性热应激期间的体温调节,但似乎会引起轻微的免疫抑制作用,降低 CD14 和 IL-6 反应,值得在更严重的热应激和其他促炎情况下对人体进行研究。
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