The protective effect of thiamine pyrophosphate, but not thiamine, against cardiotoxicity induced with cisplatin in rats

被引:31
作者
Coskun, Resit [2 ]
Turan, Mehmet Ibrahim [1 ,3 ]
Turan, Isil Siltelioglu [4 ]
Gulaboglu, Mine [5 ]
机构
[1] Ataturk Univ, Fac Med, Dept Pediat, TR-25240 Erzurum, Turkey
[2] Numune State Hosp, Dept Cardiol, Ankara, Turkey
[3] Ataturk Univ, Dept Pediat, TR-25240 Erzurum, Turkey
[4] Pasinler State Hosp, Dept Internal Med, Erzurum, Turkey
[5] Ataturk Univ, Dept Pharmacol, TR-25240 Erzurum, Turkey
关键词
Cisplatin; rat; heart; toxicity; thiamine; OXIDATIVE DNA-DAMAGE; ALPHA-LIPOIC ACID; INDUCED NEPHROTOXICITY; STRESS; CHROMATOGRAPHY; LEUKOCYTES; ENZYMES; KIDNEY; INJURY; ASSAYS;
D O I
10.3109/01480545.2013.851688
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study investigated the effect of thiamine pyrophosphate on oxidative damage associated with cardiotoxicity caused by cisplatin (CIS), an antineoplastic agent, in rats, and compared this with thiamine. Animals used in the study were divided into four groups of 6 rats each. These represented a control group receiving 5 mg/kg of CIS, study groups receiving 20 mg/kg of thiamine pyrophosphate plus 5 mg/kg of cisplatin (CTPG) or 20 mg/kg of thiamine plus 5 mg/kg of cisplatin and a healthy (H) group. All doses were administered intraperitoneally once a day for 14 days. Malondialdehyde, total glutathione and products of DNA injury results were similar in the CTPG and H groups (p > 0.05). Creatinine kinase, creatine kinase MB and troponin 1 levels were similar in the CTPG and H groups (p > 0.05). Thiamine pyrophosphate prevented CIS-associated oxidative stress and heart injury, whereas thiamine did not prevent these.
引用
收藏
页码:290 / 294
页数:5
相关论文
共 38 条
[21]   CISPLATIN NEUROTOXICITY [J].
MOLLMAN, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (02) :126-127
[22]   Assay of coenzyme Q10 in plasma by a single dilution step [J].
Mosca, F ;
Fattorini, D ;
Bompadre, S ;
Littarru, GP .
ANALYTICAL BIOCHEMISTRY, 2002, 305 (01) :49-54
[23]   ASSAY FOR LIPID PEROXIDES IN ANIMAL-TISSUES BY THIOBARBITURIC ACID REACTION [J].
OHKAWA, H ;
OHISHI, N ;
YAGI, K .
ANALYTICAL BIOCHEMISTRY, 1979, 95 (02) :351-358
[24]   Cisplatin nephrotoxicity: Mechanisms and renoprotective strategies [J].
Pabla, N. ;
Dong, Z. .
KIDNEY INTERNATIONAL, 2008, 73 (09) :994-1007
[25]  
Pavia D.L., 2006, INTRO ORGANIC LAB TE, V4th
[26]   Hepatotoxicity due to mitochondrial dysfunction [J].
Pessayre, D ;
Mansouri, A ;
Haouzi, D ;
Fromenty, B .
CELL BIOLOGY AND TOXICOLOGY, 1999, 15 (06) :367-373
[27]   Mitochondrial density determines the cellular sensitivity to cisplatin-induced cell death [J].
Qian, W ;
Nishikawa, M ;
Haque, AM ;
Hirose, M ;
Mashimo, M ;
Sato, E ;
Inoue, M .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2005, 289 (06) :C1466-C1475
[28]  
Rybak LP, 2000, AM J OTOL, V21, P513
[29]  
Salman S, 2011, INT J FERTIL STERIL, V5, P96
[30]   ESTIMATION OF TOTAL PROTEIN-BOUND AND NONPROTEIN SULFHYDRYL GROUPS IN TISSUE WITH ELLMANS REAGENT [J].
SEDLAK, J ;
LINDSAY, RH .
ANALYTICAL BIOCHEMISTRY, 1968, 25 (1-3) :192-&