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有氧训练与二氯乙酸联合应用可改善肌肉细胞色素氧化酶缺乏症患者的运动能力和有氧代谢指标。

Combined aerobic training and dichloroacetate improve exercise capacity and indices of aerobic metabolism in muscle cytochrome oxidase deficiency.

作者信息

Taivassalo T, Matthews P M, De Stefano N, Sripathi N, Genge A, Karpati G, Arnold D L

机构信息

Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, Quebec, Canada.

出版信息

Neurology. 1996 Aug;47(2):529-34. doi: 10.1212/wnl.47.2.529.

Abstract

There is no generally effective therapy for mitochondrial myopathies. In this study, we measured responses to combined aerobic training and oral dichloroacetate (DCA) therapy in a 25-year-old woman with a mitochondrial myopathy caused by cytochrome oxidase deficiency. The patient trained for 14 weeks, and DCA therapy was begun after 8 weeks. Independent indices of aerobic capacity and oxidative metabolism showed substantial improvement. Venous lactate concentrations at rest, and after a constant amount of work, decreased by approximately 50% after 8 weeks of aerobic training, and by more than 70% with the combination of training and DCA treatment. Heart rate at rest and after a constant amount of submaximal work decreased progressively. Aerobic capacity on a graded submaximal exercise test improved by 71% from baseline by the end of the treatment period. 31P magnetic resonance spectroscopy measurements of rate constants for recovery of muscle phosphocreatine increased 1.7-fold and metabolically active adenine diphosphate increased 2.8-fold after 8 weeks of training alone, and 4.5-fold and 23.0-fold after 14 weeks of training plus DCA treatment. Responses to the SF-36 Health Survey suggested a marked reduction in handicap. Thus, in this open study of a patient with cytochrome oxidase deficiency, a combination of aerobic training and DCA treatment resulted in substantial improvements in biochemical indices, exercise performance, and handicap. We conclude that exercise limitation in patients with mitochondrial myopathy may arise from effects of chronic deconditioning in addition to the effects of primary mitochondrial dysfunction and may be partially reversed by training and administration of DCA.

摘要

线粒体肌病目前尚无普遍有效的治疗方法。在本研究中,我们对一名因细胞色素氧化酶缺乏导致线粒体肌病的25岁女性,测量了其联合有氧运动训练和口服二氯乙酸(DCA)治疗的反应。患者进行了14周的训练,DCA治疗在8周后开始。有氧运动能力和氧化代谢的独立指标显示有显著改善。静息时以及完成一定量工作后的静脉血乳酸浓度,在有氧运动训练8周后下降了约50%,在训练与DCA治疗联合应用后下降超过70%。静息时以及完成一定量次最大运动后的心率逐渐降低。在分级次最大运动试验中,到治疗期结束时,有氧运动能力较基线提高了71%。仅训练8周后,通过31P磁共振波谱测量的肌肉磷酸肌酸恢复速率常数增加了1.7倍,代谢活跃的二磷酸腺苷增加了2.8倍;在训练加DCA治疗14周后,分别增加了4.5倍和23.0倍。SF-36健康调查的反应表明残疾程度显著降低。因此,在这项针对细胞色素氧化酶缺乏患者的开放性研究中,有氧运动训练和DCA治疗相结合使生化指标、运动表现和残疾程度有了显著改善。我们得出结论,线粒体肌病患者的运动受限可能除了原发性线粒体功能障碍的影响外,还源于慢性失健的影响,并且可能通过训练和给予DCA得到部分逆转。

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