Chronic intermittent hypobaric hypoxia attenuates radiation induced heart damage in rats

被引:11
作者
Wang, Jun [1 ]
Wu, Yajing [1 ]
Yuan, Fang [2 ]
Liu, Yixian [2 ]
Wang, Xuefeng [1 ]
Cao, Feng [1 ]
Zhang, Yi [2 ,3 ]
Wang, Sheng [2 ,3 ]
机构
[1] Hebei Med Univ, Hosp 4, Dept Radiat Oncol, Shijiazhuang 050011, Peoples R China
[2] Hebei Med Univ, Dept Physiol, 361 East Zhongshan Rd, Shijiazhuang 050017, Hebei, Peoples R China
[3] Hebei Collaborat Innovat Ctr Cardiocerebrovasc Di, Shijiazhuang 050000, Peoples R China
关键词
Radiation induced heart damage; Chronic intermittent hypobaric hypoxia; Oxidative stress; Endoplasmic reticulum stress; ENDOPLASMIC-RETICULUM STRESS; INFLAMMATION; DYSFUNCTION; PREVENTION; FRUCTOSE; INJURY;
D O I
10.1016/j.lfs.2016.07.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aims: Radiation-induced heart damage (RIHD) is becoming an increasing concern for patients and clinicians due to the use of radiotherapy for thoracic tumor. Chronic intermittent hypobaric hypoxia (CIHH) preconditioning has been documented to exert a cardioprotective effect. Here we hypothesized that CIHH was capable of attenuating functional and structural damage in a rat model of RIHD. Main methods: Male adult Sprague-Dawley rats were randomly divided into 4 groups: control, radiation, CIHH and CIHH plus radiation. Cardiac function was measured using Langendorff perfusion in in vitro rat hearts. Cardiac fibrosis, oxidative stress and endoplasmic reticulum stress (ERS) was assessed by quantitative analysis of protein expression. Key findings: No significant difference between any two groups was observed in baseline cardiac function as assessed by left ventricular end diastolic pressure (LVEDP), left ventricular developing pressure (LVDP) and the derivative of left ventricular pressure (+/- LVdp/dt). When challenged by ischemia/reperfusion, LVEDP was increased but LVDP and +/- LVdp/dt was decreased significantly in radiation group compared with controls, accompanied by an enlarged infarct size and decreased coronary flow. Importantly, CIHH dramatically improved radiation-induced damage of cardiac function and blunted radiation-induced cardiac fibrosis in the perivascular and interstitial area. Furthermore, CIHH abrogated radiation-induced increase in malondialdehyde and enhanced total superoxide dismutase activity, as well as downregulated expression levels of ERS markers like GRP78 and CHOP. Significance: CIHH pretreatment alleviated radiation-induced damage of cardiac function and fibrosis. Such a protective effect was closely associated with suppression of oxidative stress and ERS responses. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:57 / 63
页数:7
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