JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES) ›› 2013, Vol. 51 ›› Issue (12): 11-14.

• Articles • Previous Articles     Next Articles

Research on cardiac dysfunction induced by trastuzumab and the possible mechanisms

SHEN Xiao-qian1, ZHANG Wen-dong2, HE Yuan-liu3, CONG Xiao4, SU Guo-hai4, HAO En-kui1   

  1. 1. Department of Cardiology, Qianfoshan Hospital Affiliated to Shandong University, Jinan 250014, China;  
    2. Department of Chemotherapy, Center for Cancer, Qilu Hospital of Shandong University, Jinan 250012, China;
    3. Department of Ultrasound, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, China;
    4. Department of Cardiology, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, China
  • Received:2013-09-22 Online:2013-12-10 Published:2013-12-10

Abstract:

Objective   To observe the effect of trastuzumab on cardiac function of rats and to investigate the possible mechanisms. Methods   A total of 20 Wistar rats were randomly divided into the experimental and control group, with 10 in each. Rats in the experimental group received daily intraperitoneal injection of trastuzumab (12mg/kg in the first day and then 6 mg/kg in the following 6 days). The cumulative dose of trastuzumab was 48mg/kg. Rats in the control group were given the same volume of saline. The cardiac function was evaluated with echocardiogram before and after trastuzumab administration. Myocardial cell apoptosis was determined with terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining. Apoptotic index was calculated with reference to the results of TUNEL staining. The activity of Caspsase-3 was measured with colorimetic assay. Results   Compared with the control group, in the experimental group, the left ventricular end systolic diameter (LVED) significantly increased; the left ventricle posterior wall (LVPW) became thinner; the left ventricular ejection fraction (LVEF) reduced; the left ventricular fractional shortening (LVFS) declined(P<0.01); the number of apoptotic myocardial cells and activity of Caspase-3 were both significantly higher (P<0.001). The degree of myocardial cell apoptosis was positively associated with left ventricular diameter and negatively correlated with left ventricular wall thickness. Conclusion    Consecutive multiple intraperitoneal injections of trastuzumab could impair cardiac function in rats, which may be associated with the apoptosis of myocardial cells.

Key words: Wistar rats; Trastuzumab; Cardiotoxicity; Echocardiogram; Apoptosis

CLC Number: 

  • R542.2
[1] KAN Li-li1, JIANG Fang-guo1, AN Feng-shuang2. Effect and expression of GRK2 on collagen synthesis in myocardial fibrosis rat model [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2013, 51(9): 22-25.
[2] WANG Fu1, LIU Shan-wen1, LI Bin2, GENG Hai-hua3, SUN Shuai1, LI Rui1, XIAO Jie1, JI Xiao-ping1. Protective effects of rhEPO on oxidative stress damage in cardiomyocytes and on heart after myocardial infarction [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2013, 51(7): 1-5.
[3] SUO Fei1, HU He-sheng2, XUE Mei2, WANG Ye1, XUAN Yong-li1, YAN Su-hua2 . Relationship between neurturin dynamic expression after myocardial infarction and cardiac vagal neural remodeling [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2013, 51(5): 1-5.
[4] ZHAO Li-xiang, WU Xin-ning, WANG Xi, LI Na, CHEN Tong-shuai, LIU Jun-ni, BU Pei-li. Effects of NAD on the mRNA expression of collagen  type I induced by Angiotensin II in cardiac fibroblasts [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2013, 51(3): 1-5.
[5] LU Guan-yan1, CUI Bin2, LIU Zhong-liang3, LI Yu-tang4, LIU Xue-fei3, MA Xiao-jing1, ZHU Gui-yue1, YUAN Hai-tao1. Valsartan alters the balance of Th17 cells to regulatory T cells in chronic viral  myocarditis [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2013, 51(2): 1-.
[6] WANG Qi-lei1, REN Man-yi2, WANG De-jin1, XU Dong-ling1, DU Yi-meng1, WANG Xu-ping3, SUI Shu-jian1. TWEAK promotes expressions of collagen I and matrix metalloproteinase1
in rat cardiac fibroblasts via P38MAPK pathway
[J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2012, 50(11): 43-47.
[7] WANG De-jin1, REN Man-yi2, CHEN Hui-na1, WANG Xu-ping3, SUI Shu-jian1. Tumor necrosis factor-like weak inducer of apoptosis promotes expression of matrix metalloproteinase 9 in rat cardiac fibroblasts via the nuclear factor-κB pathway [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(11): 13-17.
[8] KAN Li-li1,2, AN Feng-shuang2. Evaluation of E/E′ on left ventricular diastolic function affected by  drug-treatment in the patients with hypertrophic cardiomyopathy [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(7): 105-108.
[9] MA Li-na1, YAO Min-qiang2, WANG Pei-xian1. Echocardiographic evaluation on cardiac structure and function in patients with symptomatic alcoholic cardiomyopathy [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2011, 49(1): 82-85.
[10] . Prevalence of Fabry disease in patients with  hypertrophic cardiomyopathy [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2010, 48(3): 116-119.
[11] . Quantitative analysis of cardiac troponin T and the risk factors of myocardial infarction [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2009, 47(11): 114-117.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!