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
[1]  
Antunes LMG, 2000, PHARMACOL RES, V41, P405, DOI 10.1006/phrs.1999.0600
[2]  
Asami S, 1996, CANCER RES, V56, P2546
[3]   Oxidative stress in allergic respiratory diseases [J].
Bowler, RP ;
Crapo, JD .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (03) :349-356
[4]  
Butterworth RF., 2005, MODERN NUTR HLTH DIS
[5]   Ultrastructural changes in the albino guinea pig cochlea at different survival times following cessation of 8-day cisplatin administration [J].
Cardinaal, RM ;
de Groot, JCMJ ;
Huizing, EH ;
Smoorenburg, GF ;
Veldman, JE .
ACTA OTO-LARYNGOLOGICA, 2004, 124 (02) :144-154
[6]   L-Carnitine inhibits cisplatin-induced injury of the kidney and small intestine [J].
Chang, BJ ;
Nishikawa, M ;
Sato, E ;
Utsumi, K ;
Inoue, M .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2002, 405 (01) :55-64
[7]   Role of oxidative and nitrosative stress in cisplatin-induced nephrotoxicity [J].
Chirino, Yolanda I. ;
Pedraza-Chaverri, Jose .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 2009, 61 (03) :223-242
[8]   The effect of thiamine supplementation on tumour proliferation - A metabolic control analysis study [J].
Comin-Anduix, B ;
Boren, J ;
Martinez, S ;
Moro, C ;
Centelles, JJ ;
Trebukhina, R ;
Petushok, N ;
Lee, WNP ;
Boros, LG ;
Cascante, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (15) :4177-4182
[9]   Biochemically and histopathologically comparative review of thiamine's and thiamine pyrophosphate's oxidative stress effects generated with methotrexate in rat liver [J].
Demiryilmaz, Ismail ;
Sener, Ebru ;
Cetin, Nihal ;
Altuner, Durdu ;
Suleyman, Bahadir ;
Albayrak, Fatih ;
Akcay, Fatih ;
Suleyman, Halis .
MEDICAL SCIENCE MONITOR, 2012, 18 (12) :BR475-BR481
[10]   Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95