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低运动能力和高运动能力近交系大鼠遗传模型中的心脏功能

Cardiac performance in inbred rat genetic models of low and high running capacity.

作者信息

Chen J, Feller G M, Barbato J C, Periyasamy S, Xie Z J, Koch L G, Shapiro J I, Britton S L

机构信息

Functional Genomics Laboratory, Medical College of Ohio, Toledo, OH 43614-5804, USA.

出版信息

J Physiol. 2001 Sep 1;535(Pt 2):611-7. doi: 10.1111/j.1469-7793.2001.00611.x.

Abstract
  1. Previous work demonstrating that DA inbred rats are superior to COP inbred rats in aerobic treadmill running capacity has indicated their utility as genetic models to explore this trait. We tested the general hypothesis that intermediate phenotypes of cardiac function and calcium metabolism are responsible for the difference in capacity between these strains. 2. Logical cardiac trait differences were estimated at a tissue (isolated papillary muscle), cellular (isolated left ventricular cells), and biochemical level of organization. 3. DA hearts were found to give significantly higher values than COP hearts for: (1) maximal developed tension (38.3 % greater), and rates of tension change in contraction (61 %) or relaxation (59 %) of isolated papillary muscle, (2) fractional shortening (50 %), amplitude of the Ca(2+) transient (78.6 %), and caffeine-induced release of Ca(2+) from the sarcoplasmic reticulum (SR; 260 %) in isolated ventricular myocytes, and (3) Na(+),K(+)-ATPase activity of isolated myocytes (17.3 %). 4. Our results suggest that these trait differences may prove useful for further studies into the genes responsible for natural variations in both ventricular function and aerobic endurance capacity. Understanding the genetic basis of aerobic capacity will help define the continuum between health and disease.
摘要
  1. 先前的研究表明,在有氧跑步机跑步能力方面,DA近交系大鼠优于COP近交系大鼠,这表明它们可作为探索该性状的遗传模型。我们检验了一个总体假设,即心脏功能和钙代谢的中间表型是造成这些品系之间能力差异的原因。2. 在组织(离体乳头肌)、细胞(离体左心室细胞)和生化组织水平上估计了合理的心脏性状差异。3. 发现DA心脏在以下方面的值显著高于COP心脏:(1)离体乳头肌的最大舒张张力(高38.3%)、收缩期(61%)或舒张期(59%)的张力变化率;(2)离体心室肌细胞的缩短分数(50%)、Ca(2+)瞬变幅度(78.6%)以及咖啡因诱导的肌浆网(SR)Ca(2+)释放(260%);(3)离体心肌细胞的Na(+)、K(+)-ATP酶活性(17.3%)。4. 我们的结果表明,这些性状差异可能有助于进一步研究负责心室功能和有氧耐力能力自然变异的基因。了解有氧能力的遗传基础将有助于界定健康与疾病之间的连续统一体。

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