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吸入用福莫特罗会损害耐力训练者的有氧运动能力:一项随机对照试验。

Inhaled formoterol impairs aerobic exercise capacity in endurance-trained individuals: a randomised controlled trial.

作者信息

Jessen Søren, Lemminger Anders, Backer Vibeke, Fischer Mads, Di Credico Andrea, Breenfeldt Andersen Andreas, Bangsbo Jens, Hostrup Morten

机构信息

August Krogh Section for Human Physiology, Department of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, Denmark.

Department of Otorhinolaryngology, Head and Neck Surgery, and Audiology, Rigshospitalet, Copenhagen, Denmark.

出版信息

ERJ Open Res. 2023 Apr 24;9(2). doi: 10.1183/23120541.00643-2022. eCollection 2023 Mar.

Abstract

BACKGROUND

The 2022 Global Initiative for Asthma guidelines emphasise the inhaled long-acting β-agonist formoterol as part of the first treatment step, and therefore formoterol use among athletes will probably increase. However, prolonged supratherapeutic use of inhaled β-agonists impairs training outcomes in moderately trained men. We investigated whether inhaled formoterol, at therapeutic doses, imposes detrimental effects in endurance-trained individuals of both sexes.

METHODS

51 endurance-trained participants (31 male, 20 female; mean±sd maximal oxygen consumption ( ) 62±6 mL·min·kg bw and 52±5 mL·min·kg bw, respectively) inhaled formoterol (24 µg; n=26) or placebo (n=25) twice daily for 6 weeks. At baseline and follow-up, we assessed and incremental exercise performance during a bike-ergometer ramp-test; body composition by dual-energy X-ray absorptiometry; muscle oxidative capacity by high-resolution mitochondrial respirometry, enzymatic activity assays and immunoblotting; intravascular volumes by carbon monoxide rebreathing; and cardiac left ventricle mass and function by echocardiography.

RESULTS

Compared to placebo, formoterol increased lean body mass by 0.7 kg (95% CI 0.2-1.2 kg; treatment×trial p=0.022), but decreased by 5% (treatment×trial p=0.013) and incremental exercise performance by 3% (treatment×trial p<0.001). In addition, formoterol lowered muscle citrate synthase activity by 15% (treatment×trial p=0.063), mitochondrial complex II and III content (treatment×trial p=0.028 and p=0.007, respectively), and maximal mitochondrial respiration through complexes I and I+II by 14% and 16% (treatment×trial p=0.044 and p=0.017, respectively). No apparent changes were observed in cardiac parameters and intravascular blood volumes. All effects were sex-independent.

CONCLUSION

Our findings demonstrate that inhaled therapeutic doses of formoterol impair aerobic exercise capacity in endurance-trained individuals, which is in part related to impaired muscle mitochondrial oxidative capacity. Thus, if low-dose formoterol fails to control respiratory symptoms in asthmatic athletes, physicians may consider alternative treatment options.

摘要

背景

2022年全球哮喘防治创议指南强调,吸入长效β受体激动剂福莫特罗是初始治疗步骤的一部分,因此运动员使用福莫特罗的情况可能会增加。然而,长期超治疗剂量使用吸入性β受体激动剂会损害中度训练男性的训练效果。我们调查了治疗剂量的吸入性福莫特罗是否会对男女耐力训练个体产生有害影响。

方法

51名耐力训练参与者(31名男性,20名女性;平均±标准差最大耗氧量分别为62±6 mL·min·kg体重和52±5 mL·min·kg体重)每天两次吸入福莫特罗(24μg;n = 26)或安慰剂(n = 25),持续6周。在基线和随访时,我们评估了自行车测力计递增负荷试验期间的最大耗氧量和递增运动表现;通过双能X线吸收法评估身体成分;通过高分辨率线粒体呼吸测定法、酶活性测定和免疫印迹法评估肌肉氧化能力;通过一氧化碳重复呼吸法评估血管内容量;通过超声心动图评估心脏左心室质量和功能。

结果

与安慰剂相比,福莫特罗使去脂体重增加了0.7 kg(95%可信区间0.2 - 1.2 kg;治疗×试验p = 0.022),但最大耗氧量降低了约5%(治疗×试验p = 0.013),递增运动表现降低了3%(治疗×试验p < 0.001)。此外,福莫特罗使肌肉柠檬酸合酶活性降低了15%(治疗×试验p = 0.063),线粒体复合物II和III含量分别降低(治疗×试验p = 0.028和p = 0.007),通过复合物I和I + II的最大线粒体呼吸分别降低了14%和16%(治疗×试验p = 0.044和p = 0.017)。心脏参数和血管内容量未观察到明显变化。所有影响均与性别无关。

结论

我们的研究结果表明,吸入治疗剂量的福莫特罗会损害耐力训练个体有氧运动能力,这部分与肌肉线粒体氧化能力受损有关。因此,如果低剂量福莫特罗未能控制哮喘运动员的呼吸道症状,医生可考虑其他治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10123513/676d4525f73d/00643-2022.01.jpg

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