Serum paraoxonase 1 status and its association with atherogenic indexes in gentamicin-induced nephrotoxicity in rats treated with coenzyme Q10

被引:17
作者
Ahmadvand, Hassan [1 ,2 ]
Dehnoo, Maryam Ghasemi [3 ]
Dehghani, Akram [2 ]
Bagheri, Shahrokh [2 ]
Cheraghi, Rooh Angiz [2 ]
机构
[1] Lorestan Univ Med Sci, Razi Herbal Res Ctr, Khorramabad, Iran
[2] Lorestan Univ Med Sci, Dept Biochem, Fac Med, Khorramabad, Iran
[3] Islamic Azad Univ, Sci & Res Branch, Dept Biol, Tehran, Iran
基金
英国医学研究理事会;
关键词
Atherogenic index; coenzyme Q10; gentamicin; lipid profile; nephrotoxicity; paraoxonase; 1; activity; rat; DENSITY-LIPOPROTEIN CHOLESTEROL; INDUCED OXIDATIVE STRESS; CORONARY-ARTERY-DISEASE; ENZYME-ACTIVITY; NITRIC-OXIDE; ARYLESTERASE; Q(10); ATHEROSCLEROSIS; BALANCE; HUMANS;
D O I
10.3109/0886022X.2013.865154
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Coenzyme Q10 is a natural antioxidant and scavenger of free radicals. In the present study, we examined the effect of coenzyme Q10 on paraoxonase 1 (PON1) activity, lipid profile, atherogenic indexes and relationship of PON 1 activity by high-density lipoprotein (HDL) and atherogenic indexes in gentamicin (GM)-induced nephrotoxicity rats. Thirty Sprague-Dawley rats were divided into three groups to receive saline; GM, 100 mg/kg/d; and GM plus coenzyme Q10 by 15 mg/kg i.p daily, respectively. After 12 days, animals were anaesthetized, blood samples were also collected before killing to measure the levels of triglyceride (TG), cholesterol (C), low-density lipoprotein (LDL), very low density lipoprotein (VLDL), HDL, atherogenic indexes and the activities of PON1 of all groups were analyzed. Data were analyzed by non-parametric Mann-Whitney test (using SPSS 13 software). Coenzyme Q10 significantly decreased TG, C, LDL, VLDL, atherogenic index, atherogenic coefficient and cardiac risk ratio. HDL level and PON1 activity were significantly increased when treated with coenzyme Q10. Also, the activity of PON 1 correlated positively with HDL and negatively with atherogenic coefficient, cardiac risk ratio 1 and cardiac risk ratio 2. This study showed that coenzyme Q10 exerts beneficial effects on PON1 activity, lipid profile, atherogenic index and correlation of PON 1 activity with HDL and atherogenic index in GM -induced nephrotoxicity rats.
引用
收藏
页码:413 / 418
页数:6
相关论文
共 44 条
[1]  
Ahmadvand H, 2012, IRAN J PHARM THER, V11, P64
[2]   Amelioration of altered antioxidant enzymes activity and glomerulosclerosis by coenzyme Q10 in alloxan-induced diabetic rats [J].
Ahmadvand, Hassan ;
Tavafi, Majid ;
Khosrowbeygi, Ali .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2012, 26 (06) :476-482
[3]  
[Anonymous], 2012, SULTAN QABOOS U MED, DOI [DOI 10.12816/0003082, 10.12816/0003082]
[4]  
Askari G, 2013, INT J PREVENTIVE MED, V4, pS58
[5]  
Aviram M, 2005, HANDB EXP PHARM, V170, P263
[6]   Association of lipids, lipoproteins, apolipoproteins and paraoxonase enzyme activity with premature coronary artery disease [J].
Azizi, F ;
Rahmani, M ;
Raiszadeh, F ;
Solati, M ;
Navab, M .
CORONARY ARTERY DISEASE, 2002, 13 (01) :9-16
[7]   Time dependent effects of gentamicin on the enzymes of carbohydrate metabolism, brush border membrane and oxidative stress in rat kidney tissues [J].
Banday, Anees A. ;
Farooq, Neelam ;
Priyarnvada, Shublia ;
Yusufi, Ahad N. K. ;
Khan, Farah .
LIFE SCIENCES, 2008, 82 (9-10) :450-459
[8]   Environmental contaminants and redox status of coenzyme Q10 and vitamin E in Inuit from Nunavik [J].
Belanger, Marie-Claire ;
Mirault, Marc-Edouard ;
Dewailly, Eric ;
Berthiaume, Line ;
Julien, Pierre .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2008, 57 (07) :927-933
[9]   Diagnostic value of thiols, paraoxonase 1, arylesterase and oxidative balance in colorectal cancer in human [J].
Bulbuller, N. ;
Eren, E. ;
Ellidag, H. Y. ;
Oner, O. Z. ;
Sezer, C. ;
Aydin, O. ;
Yilmaz, N. .
NEOPLASMA, 2013, 60 (04) :419-424
[10]   Treatment of massive hypertriglyceridemia resistant to PUFA and fibrates: A possible role for the coenzyme Q10? [J].
Cicero, AFG ;
Derosa, G ;
Miconi, A ;
Laghi, L ;
Nascetti, S ;
Gaddi, A .
BIOFACTORS, 2005, 23 (01) :7-14