The therapeutic applications of celery oil seed extract on the plasticizer di(2-ethylhexyl) phthalate toxicity

被引:16
作者
El-Shinnawy, Nashwa A. [1 ]
机构
[1] Ain Shams Univ, Women Coll Arts Sci & Educ, Dept Zool, Cairo 11757, Egypt
关键词
Apium graveolens (celery oil); di(2-ethylhexyl) phthalate; endothelin; 1; obesity; PPAR; JUNCTIONAL INTERCELLULAR COMMUNICATION; ACTIVATED-RECEPTOR-ALPHA; OXIDATIVE STRESS; CIRCULATING LEVELS; APIUM-GRAVEOLENS; BISPHENOL-A; PPAR-ALPHA; RATS; LIVER; DEHP;
D O I
10.1177/0748233713475515
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The present study investigated the impact of two doses, 500mg/kg and 1000mg/kg, of di(2-ethylhexyl) phthalate (DEHP) and studied the possible therapeutic dose of celery oil seed extract for 6weeks on some atheroscelerogenic, obesogenic, antioxidant and liver functions in rats. Both doses of DEHP caused over-expression of peroxisome proliferator-activated receptor alpha (PPAR) messenger RNA with significant increase in liver weights, relative liver weights, serum cholesterol (Chol), triglycerides, low-density lipoprotein Chol, liver total lipids, along with an increase in the activities of serum aspartate aminotransferase, alanine aminotransferase, serum endothelin 1 and liver tissue thiobarbituric acid reactive substances (TBARS). Additionally, DEHP administration to rats resulted in significant decrease in final body weights, serum total protein, albumin, liver total protein and serum total nitric oxide. Our study confirmed the role of oral combination of Apium graveolens (celery) oil seed extract at small cumulative doses (50 mu l/kg for 6weeks) with DEHP in ameliorating the toxicological effects of DEHP, which was revealed in reducing the expression of PPAR, lipid profile, with restoring liver functions, vascular oxidative stress and inhibition of TBARS activity.
引用
收藏
页码:355 / 366
页数:12
相关论文
共 57 条
[1]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[2]   Metabolic syndrome in men with prostate cancer undergoing long-term androgen-deprivation therapy [J].
Braga-Basaria, Milena ;
Dobs, Adrian S. ;
Muller, Denis C. ;
Carducci, Michael A. ;
John, Majnu ;
Egan, Josephine ;
Basaria, Shehzad .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (24) :3979-3983
[3]  
Chevalier A., 1998, ENCY MED PLANTS, P61
[4]   Gene ontology mapping as an unbiased method for identifying molecular pathways and processes affected by toxicant exposure: Application to acute effects caused by the rodent non-genotoxic carcinogen diethylhexylphthalate [J].
Currie, RA ;
Bombail, V ;
Oliver, JD ;
Moore, DJ ;
Lim, FL ;
Gwilliam, V ;
Kimber, I ;
Chipman, K ;
Moggs, JG ;
Orphanides, G .
TOXICOLOGICAL SCIENCES, 2005, 86 (02) :453-469
[5]   Chronic toxicity of di(2-ethylhexyl)phthalate in rats [J].
David, RM ;
Moore, MR ;
Finney, DC ;
Guest, D .
TOXICOLOGICAL SCIENCES, 2000, 55 (02) :433-443
[6]   Reversibility of the chronic effects of di(2-ethylhexyl) phthalate [J].
David, RM ;
Moore, MR ;
Finney, DC ;
Guest, D .
TOXICOLOGIC PATHOLOGY, 2001, 29 (04) :430-439
[7]   PPAR-mediated activity of phthalates: A link to the obesity epidemic? [J].
Desvergne, Beatrice ;
Feige, Jerome N. ;
Casals-Casas, Cristina .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2009, 304 (1-2) :43-48
[8]  
DOUMAS BT, 1975, CLIN CHEM, V21, P1159
[9]   ALBUMIN STANDARDS AND MEASUREMENT OF SERUM ALBUMIN WITH BROMCRESOL GREEN [J].
DOUMAS, BT ;
WATSON, WA ;
BIGGS, HG .
CLINICA CHIMICA ACTA, 1971, 31 (01) :87-&
[10]  
Dryer R.L., 1970, FUNDAMENTAL CLIN CHE, P329