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卡维地洛与有氧运动训练疗法联合改善心力衰竭小鼠心脏收缩力和重塑的综合作用。

Integrative effect of carvedilol and aerobic exercise training therapies on improving cardiac contractility and remodeling in heart failure mice.

机构信息

School of Physical Education and Sport, University of São Paulo, São Paulo, Brazil.

出版信息

PLoS One. 2013 May 1;8(5):e62452. doi: 10.1371/journal.pone.0062452. Print 2013.

Abstract

The use of β-blockers is mandatory for counteracting heart failure (HF)-induced chronic sympathetic hyperactivity, cardiac dysfunction and remodeling. Importantly, aerobic exercise training, an efficient nonpharmacological therapy to HF, also counteracts sympathetic hyperactivity in HF and improves exercise tolerance and cardiac contractility; the latter associated with changes in cardiac Ca(2+) handling. This study was undertaken to test whether combined β-blocker and aerobic exercise training would integrate the beneficial effects of isolated therapies on cardiac structure, contractility and cardiomyocyte Ca(2+) handling in a genetic model of sympathetic hyperactivity-induced HF (α2A/α2C- adrenergic receptor knockout mice, KO). We used a cohort of 5-7 mo male wild-type (WT) and congenic mice (KO) with C57Bl6/J genetic background randomly assigned into 5 groups: control (WT), saline-treated KO (KOS), exercise trained KO (KOT), carvedilol-treated KO (KOC) and, combined carvedilol-treated and exercise-trained KO (KOCT). Isolated and combined therapies reduced mortality compared with KOS mice. Both KOT and KOCT groups had increased exercise tolerance, while groups receiving carvedilol had increased left ventricular fractional shortening and reduced cardiac collagen volume fraction compared with KOS group. Cellular data confirmed that cardiomyocytes from KOS mice displayed abnormal Ca(2+) handling. KOT group had increased intracellular peak of Ca(2+) transient and reduced diastolic Ca(2+) decay compared with KOS group, while KOC had increased Ca(2+) decay compared with KOS group. Notably, combined therapies re-established cardiomyocyte Ca(2+) transient paralleled by increased SERCA2 expression and SERCA2:PLN ratio toward WT levels. Aerobic exercise trained increased the phosphorylation of PLN at Ser(16) and Thr(17) residues in both KOT and KOCT groups, but carvedilol treatment reduced lipid peroxidation in KOC and KOCT groups compared with KOS group. The present findings provide evidence that the combination of carvedilol and aerobic exercise training therapies lead to a better integrative outcome than carvedilol or exercise training used in isolation.

摘要

β受体阻滞剂的应用对于拮抗心力衰竭(HF)引起的慢性交感神经活性亢进、心功能障碍和重构是强制性的。重要的是,有氧运动训练是一种有效的非药物治疗HF 的方法,也能拮抗 HF 中的交感神经活性亢进,并提高运动耐量和心肌收缩力;后者与心脏 Ca(2+)处理的变化有关。本研究旨在测试β受体阻滞剂和有氧运动训练的联合治疗是否会整合单独治疗对交感神经活性亢进诱导的 HF (α2A/α2C-肾上腺素能受体敲除小鼠,KO)遗传模型中心脏结构、收缩性和心肌细胞 Ca(2+)处理的有益影响。我们使用了一组 5-7 月龄的雄性野生型(WT)和同基因小鼠(KO),它们具有 C57Bl6/J 遗传背景,随机分为 5 组:对照组(WT)、盐水处理的 KO 组(KOS)、运动训练的 KO 组(KOT)、卡维地洛处理的 KO 组(KOC)和卡维地洛联合运动训练的 KO 组(KOCT)。与 KOS 小鼠相比,单独和联合治疗降低了死亡率。KOT 和 KOCT 组的运动耐量均增加,而接受卡维地洛治疗的组的左心室短轴缩短分数增加,心脏胶原容积分数降低。细胞数据证实,KOS 小鼠的心肌细胞显示出异常的 Ca(2+)处理。与 KOS 组相比,KOT 组的细胞内 Ca(2+)瞬变峰值增加,舒张期 Ca(2+)衰减减少,而 KOC 组的 Ca(2+)衰减增加。值得注意的是,联合治疗使心肌细胞 Ca(2+)瞬变恢复正常,同时 SERCA2 表达和 SERCA2:PLN 比值增加至 WT 水平。有氧运动训练增加了 KOT 和 KOCT 两组中 PLN 在 Ser(16)和 Thr(17)残基的磷酸化,但与 KOS 组相比,卡维地洛治疗降低了 KOC 和 KOCT 组的脂质过氧化。本研究结果提供了证据,表明卡维地洛和有氧运动训练联合治疗比单独使用卡维地洛或运动训练的整合效果更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea7/3641040/dcad027abb08/pone.0062452.g001.jpg

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