Murakami H, Soma R, Hayashi J, Katsuta S, Matsuda M, Ajisaka R, Okada M, Kuno S
Center for Tsukuba Advanced Research Alliance, University of Tsukuba, Tsukuba, 305-8574 Japan.
Jpn J Physiol. 2001 Oct;51(5):563-8. doi: 10.2170/jjphysiol.51.563.
This study focused on the mitochondrial DNA (mtDNA) as the genetic factor most likely to bring about the individual difference in endurance capacity or its trainability. Platelets contain mtDNA but no nuclear DNA, whereas rho(0)-HeLa cells have nuclear DNA but no mtDNA. The oxidative capacity of mitochondria in the cultured cells, which were fused rho(0)-HeLa cell with platelets obtained from individual subjects (the so-called "cybrids"), reflects the individual mtDNA polymorphism in the gene-coding region. The purpose of this study was to investigate the relationship between the oxidative capacity of cybrids and the individual difference in endurance capacity, or its trainability. Forty-one sedentary young males took part in an 8-week endurance training program. They were determined by using their VO(2 max) as an index of endurance capacity on an ergocycle before and after the endurance training program. The relations between VO(2 max) before endurance training or the change of it by endurance training and the oxidative capacity of cybrids were investigated. There was no relation between them, and two groups were drawn from all subjects, based on one standard division of their initial VO(2 max): the higher pre-VO(2 max) group (n = 6) and the lower pre-VO(2 max) group (n = 5) (51.8 +/- 3.5 ml/min/kg vs. 33.3 +/- 3.8 ml/min/kg, p < 0.01). No significant difference was found between the O(2) consumption of the cybrids in the higher initial VO(2 max) group and that in the lower initial VO(2 max) group (16.3 +/- 4.9 vs. 15.9 +/- 2.0 nmol O(2)/min/10(7) cells, NS). Furthermore, neither the cytochrome c oxidase (COX) activity nor the complex I + III activity of cybrids showed a significant difference between the two groups. The oxidative capacity of cybrids between the high trainability group (n = 6) (Delta VO(2 max) 12.1 +/- 1.6 ml/min/kg) and the low trainability group (n = 9) (Delta VO(2 max) 2.3 +/- 0.5 ml/min/kg) was also similar. Thus the mtDNA polymorphism is very unlikely to relate to the individual difference in endurance capacity or its trainability in young sedentary healthy subjects.
本研究聚焦于线粒体DNA(mtDNA),其作为最有可能导致耐力能力个体差异或其可训练性个体差异的遗传因素。血小板含有mtDNA但不含核DNA,而ρ⁰-HeLa细胞含有核DNA但不含mtDNA。将来自个体受试者的血小板与ρ⁰-HeLa细胞融合(即所谓的“胞质杂种”)后,培养细胞中线粒体的氧化能力反映了基因编码区域的个体mtDNA多态性。本研究的目的是调查胞质杂种的氧化能力与耐力能力个体差异或其可训练性之间的关系。41名久坐不动的年轻男性参加了为期8周的耐力训练计划。在耐力训练计划前后,以他们的最大摄氧量(VO₂max)作为耐力能力指标,通过测力计来测定。研究了耐力训练前的VO₂max或耐力训练导致的VO₂max变化与胞质杂种氧化能力之间的关系。它们之间没有关系,根据初始VO₂max的一个标准划分,从所有受试者中分为两组:初始VO₂max较高组(n = 6)和初始VO₂max较低组(n = 5)(51.8±3.5毫升/分钟/千克对33.3±3.8毫升/分钟/千克,p < 0.01)。初始VO₂max较高组的胞质杂种的氧气消耗量与初始VO₂max较低组的相比未发现显著差异(16.3±4.9对15.9±2.0纳摩尔氧气/分钟/10⁷个细胞,无显著性差异)。此外,两组之间胞质杂种的细胞色素c氧化酶(COX)活性和复合物I + III活性均未显示出显著差异。高可训练性组(n = 6)(VO₂max变化12.1±1.6毫升/分钟/千克)和低可训练性组(n = 9)(VO₂max变化2.3±0.5毫升/分钟/千克)之间的胞质杂种氧化能力也相似。因此,在久坐不动的年轻健康受试者中,mtDNA多态性极不可能与耐力能力个体差异或其可训练性相关。