首页> 外文期刊>The Journal of Experimental Biology >Increase in cardiac myosin heavy-chain (MyHC) alpha protein isoform in hibernating ground squirrels, with echocardiographic visualization of ventricular wall hypertrophy and prolonged contraction
【24h】

Increase in cardiac myosin heavy-chain (MyHC) alpha protein isoform in hibernating ground squirrels, with echocardiographic visualization of ventricular wall hypertrophy and prolonged contraction

机译:超声心动图显示室壁肥厚和延长收缩时,冬眠松鼠中心肌肌球蛋白重链(MyHC)α蛋白同工型增加

获取原文
获取原文并翻译 | 示例
           

摘要

Deep hibernators such as golden-mantled ground squirrels (Callospermophilus lateralis) have multiple challenges to cardiac function during low temperature torpor and subsequent arousals. As heart rates fall from over 300 beats min(-1) to less than 10, chamber dilation and reduced cardiac output could lead to congestive myopathy. We performed echocardiography on a cohort of individuals prior to and after several months of hibernation. The left ventricular chamber exhibited eccentric and concentric hypertrophy during hibernation and thus calculated ventricular mass was similar to 30% greater. Ventricular ejection fraction was mildly reduced during hibernation but stroke volumes were greater due to the eccentric hypertrophy and dramatically increased diastolic filling volumes. Globally, the systolic phase in hibernation was similar to 9.5 times longer, and the diastolic phase was 28x longer. Left atrial ejection generally was not observed during hibernation. Atrial ejection returned weakly during early arousal. Strain echocardiography assessed the velocity and total movement distance of contraction and relaxation for regional ventricular segments in active and early arousal states. Myocardial systolic strain during early arousal was significantly greater than the active state, indicating greater total contractile movement. This mirrored the increased ventricular ejection fraction noted with early arousal. However, strain rates were slower during early arousal than during the active period, particularly systolic strain, which was 33% of active, compared with the rate of diastolic strain, which was 67% of active. As heart rate rose during the arousal period, myocardial velocities and strain rates also increased; this was matched closely by cardiac output. Curiously, though heart rates were only 26% of active heart rates during early arousal, the cardiac output was nearly 40% of the active state, suggesting an efficient pumping system. We further analyzed proportions of cardiac myosin heavy-chain (MyHC) isoforms in a separate cohort of squirrels over 5 months, including time points before hibernation, during hibernation and just prior to emergence. Hibernating individuals were maintained in both a 4 degrees C cold room and a 20 degrees C warm room. Measured by SDS-PAGE, relative percentages of cardiac MyHC alpha were increased during hibernation, at both hibernacula temperatures. A potential increase in contractile speed, and power, from more abundant MyHC alpha may aid force generation at low temperature and at low heart rates. Unlike many models of cardiomyopathies where the alpha isoform is replaced by the beta isoform in order to reduce oxygen consumption, ground squirrels demonstrate a potential cardioprotective mechanism to maintain cardiac output during torpor.
机译:深层冬眠动物,如金黄色的地面松鼠(Callospermophiluslateralis),在低温煎熬和随后的唤醒过程中对心脏功能有多重挑战。当心率从300次以上min-1降至10次以下时,心室扩张和心输出量减少可能导致充血性肌病。我们对数月的冬眠前后的人群进行了超声心动图检查。冬眠期间,左心室表现出偏心和同心肥大,因此计算出的心室质量增加了30%。冬眠期间心室射血分数轻度降低,但由于偏心肥大和舒张期充盈量显着增加,使卒中量更大。在全球范围内,冬眠的收缩期延长了9.5倍,舒张期延长了28倍。冬眠期间通常未观察到左心房射血。在早期唤醒中,心房排出微弱地返回。应变超声心动图评估活跃和早期唤醒状态下局部心室节段收缩和放松的速度和总运动距离。早期唤醒时的心肌收缩力明显大于活动状态,表明总收缩运动更大。这反映了早期唤醒引起的心室射血分数增加。但是,早期唤醒时的应变率比活跃期要慢,尤其是收缩期应变,活跃期为33%,而舒张期应变为活跃期67%。随着唤醒期间心率的上升,心肌速度和应变率也增加;这与心输出量紧密匹配。奇怪的是,尽管在早期唤醒时心率仅是活跃心率的26%,但心输出量却接近活跃状态的40%,这表明有一个有效的泵系统。我们进一步分析了一个独立的松鼠群在5个月内(包括冬眠之前,冬眠期间和刚出现之前的时间点)在一个单独的松鼠群中心肌肌球蛋白重链(MyHC)同工型的比例。处于冬眠状态的人被关在4摄氏度的冷室和20摄氏度的暖室中。通过SDS-PAGE测量,在两个冬眠温度下,冬眠期间心脏MyHCα的相对百分比都增加了。来自更丰富的MyHCα的收缩速度和力量的潜在增加可能有助于在低温和低心率时产生力量。与许多心肌病模型不同,在这些模型中,α亚型被β亚型取代以减少氧气消耗,地松鼠表现出了潜在的心脏保护机制,可以在躯干过程中维持心输出量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号