Cinnamic Acid and Cinnamaldehyde Ameliorate Cisplatin-Induced Splenotoxicity in Rats

被引:33
作者
Abd El-Raouf, Ola M. [1 ]
El-Sayed, El-Sayed M. [2 ]
Manie, Mohamed F. [1 ]
机构
[1] NODCAR, Pharmacolgy Dept, Cairo, Egypt
[2] Al Azhar Univ, Fac Pharm, Pharmacolgy & Toxicol Dept, Cairo, Egypt
关键词
Cinnamic acid; Cinnamaldehyde; Cisplatin; Splenotoxicity; Antioxidant; INDUCED NEPHROTOXICITY; BLOOD SMEARS; LIPOIC ACID; ACCUMULATION; RESISTANCE; STRESS; ALPHA; LIVER; MICE;
D O I
10.1002/jbt.21715
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cinnamic acid (CA) and cinnamaldehyde (CD) are major constituents of cinnamon species. They possess various pharmacological properties of which their antioxidant activity is a prime one. This study aims to investigate potential protective effects against cisplatin (CP)-induced splenotoxicity in rats. A single dose of CP (5 mg/kg) injected i.p. caused a significant decrease in hemoglobin content (18%), total leucocytic count (46%), neutrophils (78%), and catalase (CAT) splenic activity (64%) with a marked increase in lymphocytes (26%) and splenic content of malondialdehyde (68%) and TNF- (69%) as compared with the control group. Contrarily, CA (50 mg/kg, p.o.) or CD (40 mg/kg, p.o.) administration for 7 days before CP ameliorated CP-induced splenotoxicity as indicated by mitigation of the biochemical parameters and histopathological changes. These results revealed the promising protective effects of CA and CD on CP-induced splenotoxicity in rats; an effect that might be attributed to antioxidant and anti-inflammatory activities.
引用
收藏
页码:426 / 431
页数:6
相关论文
共 37 条
[1]  
Akao Y, 2003, BIOL PHARM BULL, V26, P1057, DOI 10.1248/bpb.26.1057
[2]  
[Anonymous], 1996, GUIDE CARE USE LAB A
[3]  
[Anonymous], Int. J. Pharm. Sci. Rev. Res.
[4]   Protective effects of vitamin E and vitamin C on cisplatin nephrotoxicity in developing rats [J].
Appenroth, D ;
Frob, S ;
Kersten, L ;
Splinter, K ;
Winnefeld, K .
ARCHIVES OF TOXICOLOGY, 1997, 71 (11) :677-683
[5]  
Banchroft JD, 1996, THEORY PRACTICE HIST
[6]  
Barceloux DG, 2009, DM-DIS MON, V55, P318, DOI [10.1016/j.disamonth.2009.03.006, 10.1016/j.disamonth.2009.03.005, 10.1016/j.disamonth.2009.03.003, 10.1016/j.disamonth.2009.03.004, 10.1016/j.disamonth.2009.03.008, 10.1016/j.disamonth.2009.03.002, 10.1016/j.disamonth.2009.03.007, 10.1016/j.disamonth.2009.03.010, 10.1016/j.disamonth.2009.03.011]
[7]   L-METHIONINE ANTAGONISM OF CIS-PLATINUM NEPHROTOXICITY [J].
BASINGER, MA ;
JONES, MM ;
HOLSCHER, MA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (01) :1-15
[8]   PROLONGED ACTIVATION OF JUN AND COLLAGENASE GENES BY TUMOR NECROSIS FACTOR-ALPHA [J].
BRENNER, DA ;
OHARA, M ;
ANGEL, P ;
CHOJKIER, M ;
KARIN, M .
NATURE, 1989, 337 (6208) :661-663
[9]   Transformation of cinnamic acid from trans- to cis-form raises a notable bactericidal and synergistic activity against multiple-drug resistant Mycobacterium tuberculosis [J].
Chen, Yen-Ling ;
Huang, Shao-Tsung ;
Sun, Fang-Ming ;
Chiang, Yu-Ling ;
Chiang, Chia-Jung ;
Tsai, Chiung-Man ;
Weng, Chia-Jui .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 43 (03) :188-194
[10]   Protective effects of apocynin against cisplatin-induced oxidative stress and nephrotoxicity [J].
Chirino, Yolanda I. ;
Sanchez-Gonzalez, Dolores Javier ;
Martinez-Martinez, Claudia Maria ;
Cruz, Cristino ;
Pedraza-Chaverri, Jose .
TOXICOLOGY, 2008, 245 (1-2) :18-23