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模拟微重力与左右心室恢复诱导重塑

Simulated Microgravity and Recovery-Induced Remodeling of the Left and Right Ventricle.

作者信息

Zhong Guohui, Li Yuheng, Li Hongxing, Sun Weijia, Cao Dengchao, Li Jianwei, Zhao Dingsheng, Song Jinping, Jin Xiaoyan, Song Hailin, Yuan Xinxin, Wu Xiaorui, Li Qi, Xu Qing, Kan Guanghan, Cao Hongqing, Ling Shukuan, Li Yingxian

机构信息

State Key Laboratory of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center Beijing, China.

Key Laboratory of Molecular and Cellular Biology of Ministry of Education, College of Life Science, Hebei Normal University Shijiazhuang, China.

出版信息

Front Physiol. 2016 Jun 29;7:274. doi: 10.3389/fphys.2016.00274. eCollection 2016.

Abstract

Physiological adaptations to microgravity involve alterations in cardiovascular systems. These adaptations result in cardiac remodeling and orthostatic hypotension. However, the response of the left ventricle (LV) and right ventricle (RV) following hindlimb unloading (HU) and hindlimb reloading (HR) is not clear and the underlying mechanism remains to be understood. In this study, three groups of mice were subjected to HU by tail suspension for 28 days. Following this, two groups were allowed to recover for 7 or 14 days. The control group was treated equally, with the exception of tail suspension. Echocardiography was performed to detect the structure and function changes of heart. Compared with the control, the HU group of mice showed reduced LV-EF (ejection fraction), and LV-FS (fractional shortening). However, mice that were allowed to recover for 7 days after HU (HR-7d) showed increased LVIDs (systolic LV internal diameter) and LV Vols (systolic LV volume). Mice that recovered for 14 days (HR-14d) returned to the normal state. In comparison, RV-EF and RV-FS didn't recover to the normal conditions till being reloaded for 14 days. Compared with the control, RVIDd (diastolic RV internal diameter), and RV Vold (diastolic RV volume) were reduced in HU group and recovered to the normal conditions in HR-7d and HR-14d groups, in which groups RVIDs (systolic RV internal diameter) and RV Vols (systolic RV volume) were increased. Histological analysis and cardiac remodeling gene expression results indicated that HU induces left and right ventricular remodeling. Western blot demonstrated that the phosphorylation of HDAC4 and ERK1/2 and the ratio of LC3-II / LC3-I, were increased following HU and recovered following HR in both LV and RV, and the phosphorylation of AMPK was inhibited in both LV and RV following HU, but only restored in LV following HR for 14 days. These results indicate that simulated microgravity leads to cardiac remodeling, and the remodeling changes can be reversed. Furthermore, in the early stages of recovery, cardiac remodeling may be intensified. Finally, compared with the LV, the RV is not as easily reversed. Cardiac remodeling pathways, such as, HDAC4, ERK1/2, LC3-II, and AMPK were involved in the process.

摘要

对微重力的生理适应涉及心血管系统的改变。这些适应导致心脏重塑和体位性低血压。然而,后肢卸载(HU)和后肢重新加载(HR)后左心室(LV)和右心室(RV)的反应尚不清楚,其潜在机制仍有待了解。在本研究中,三组小鼠通过尾部悬吊进行28天的HU。在此之后,两组小鼠被允许恢复7天或14天。对照组除尾部悬吊外接受相同处理。进行超声心动图检查以检测心脏的结构和功能变化。与对照组相比,HU组小鼠的左室射血分数(LV-EF)和左室短轴缩短率(LV-FS)降低。然而,HU后恢复7天的小鼠(HR-7d)左室收缩末期内径(LVIDs)和左室收缩末期容积(LV Vols)增加。恢复14天的小鼠(HR-14d)恢复到正常状态。相比之下,右室射血分数(RV-EF)和右室短轴缩短率(RV-FS)直到重新加载14天才恢复到正常状态。与对照组相比,HU组右室舒张末期内径(RVIDd)和右室舒张末期容积(RV Vold)减小,在HR-7d和HR-14d组恢复到正常状态,这两组右室收缩末期内径(RVIDs)和右室收缩末期容积(RV Vols)增加。组织学分析和心脏重塑基因表达结果表明,HU诱导左、右心室重塑。蛋白质印迹法显示,HU后左、右心室中组蛋白去乙酰化酶4(HDAC4)和细胞外信号调节激酶1/2(ERK1/2)的磷酸化以及微管相关蛋白1轻链3-II(LC3-II)/微管相关蛋白1轻链3-I(LC3-I)的比值增加,HR后恢复,HU后左、右心室中腺苷酸活化蛋白激酶(AMPK)的磷酸化受到抑制,但仅在HR 14天后左心室中恢复。这些结果表明,模拟微重力导致心脏重塑,且重塑变化可以逆转。此外,在恢复的早期阶段,心脏重塑可能会加剧。最后,与左心室相比,右心室不太容易逆转。心脏重塑途径,如HDAC4、ERK1/2、LC3-II和AMPK参与了这一过程。

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