Insight into the role of DL-α-lipoic acid against cyclophosphamide induced alterations in calcium sensitivity of cardiac myofilaments

被引:2
作者
Mythili, Y. [1 ]
Sudharsan, P. T. [1 ]
Varalakshmi, P. [1 ]
机构
[1] Univ Madras, Dept Med Biochem, Dr ALM Post Grad Inst Basic Med Sci, Madras 600113, Tamil Nadu, India
关键词
cyclophosphamide; myofibrillar calcium sensitivity; heart; lipoic acid; ultrastructure;
D O I
10.1007/s11010-006-9144-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cyclophosphamide (CP), a potent antitumor drug, is known to cause severe cardiotoxicity. The present study is aimed at evaluating the role of DL-alpha-Lipoic acid (LA) on the calcium responsiveness of cardiac myofilaments isolated from CP treated rats. Adult male Wistar rats were divided into four treatment groups. Two groups received single intraperitoneal injection of CP (200 mg/kg b.wt.) to induce cardiotoxicity, one of these groups received LA treatment (25 mg/kg b.wt. for 10 days). A vehicle treated control group and a LA drug control were also included. Cardiotoxicity was evident from increased levels of cardiac Troponin I in serum of CP treated rats. The pCa-actomyosin ATPase relationship of myofilaments demonstrated a rightward shift indicating diminished responsiveness in CP treated rats. The hill coefficient was reduced and the myofibrillar myosin Ca2+-ATPase and K+-(EDTA) activities were also significantly (P < 0.05) reduced. Ultrastuctural observations were also in agreement with the above abnormal changes, wherein loss of myofilaments occurred. LA effectively normalized these abnormalities and restored the cardiac function in CP administered rats.
引用
收藏
页码:31 / 37
页数:7
相关论文
共 31 条
  • [1] APPELBAUM FR, 1976, LANCET, V1, P58
  • [2] BODOR GS, 1992, CLIN CHEM, V38, P2203
  • [3] Functional consequences of caspase activation in cardiac myocytes
    Communal, C
    Sumandea, M
    de Tombe, P
    Narula, J
    Solaro, RJ
    Hajjar, RJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) : 6252 - 6256
  • [4] Altered contractile function in heart failure
    de Tombe, PP
    [J]. CARDIOVASCULAR RESEARCH, 1998, 37 (02) : 367 - 380
  • [5] Dollery C., 1999, THERAPEUTIC DRUGS, P349
  • [6] Fiske CH, 1925, J BIOL CHEM, V66, P375
  • [7] Lipoic acid reduces ischemia-reperfusion injury in animal models
    Freisleben, HJ
    [J]. TOXICOLOGY, 2000, 148 (2-3) : 159 - 171
  • [8] Role of troponin I proteolysis in the pathogenesis of stunned myocardium
    Gao, WD
    Atar, D
    Liu, YG
    Perez, NG
    Murphy, AM
    Marban, E
    [J]. CIRCULATION RESEARCH, 1997, 80 (03) : 393 - 399
  • [9] Chemo therapy-induced cardiotoxicity: current practice and prospects of prophylaxis
    Gharib, MI
    Burnett, AK
    [J]. EUROPEAN JOURNAL OF HEART FAILURE, 2002, 4 (03) : 235 - 242
  • [10] Oxygen, oxidative stress, hypoxia, and heart failure
    Giordano, FJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (03) : 500 - 508