The protective action of thymol against carbon tetrachloride hepatotoxicity in mice

被引:49
作者
Alam, K
Nagi, MN
Badary, OA
Al-Shabanah, OA
Al-Rikabi, AC
Al-Bekairi, AM
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacol, Riyadh 11451, Saudi Arabia
[2] King Saud Univ, Coll Med, Dept Pathol, Riyadh 11461, Saudi Arabia
关键词
thymol; carbon tetrachloride; hepatotoxicity; lipid peroxides;
D O I
10.1006/phrs.1999.0472
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The protective action of thymol (paramethyl-isopropyl-phenol) was investigated against carbon tetrachloride (CCl4)-induced hepatotoxicity in male Swiss albino mice. The CCl4 at a dose of 20 mu l kg(-1) produced damage to liver cells and was followed by the significant increase (P < 0.001) in serum alanine aminotransferase (ALT) activity and hepatic lipid peroxidation after 24 h. The hepatocellular necrosis was further confirmed by histopathological examination of liver section. Oral administration of thymol in a single dose (300 mg kg(-1)) resulted in significant (P < 0.05) amelioration of CCl4-induced hepatotoxicity. Thymol also inhibited lipid peroxidation induced by CCl4 in vivo. The protection offered by thymol was also evident from histopathology photomicrograph. In a separate in vitro assay, thymol inhibited the non-enzymatic lipid peroxidation of normal mice liver homogenate induced by Fe3+-ascorbate. The present study suggests that thymol protects the liver against CCl4-induced toxicity and the protection may be mediated through its ability to inhibit lipid peroxidation. However, other interactions between thymol and CCl4 remains to be elucidated. (C) 1999 Academic Press.
引用
收藏
页码:159 / 163
页数:5
相关论文
共 17 条
[1]   ANTIOXIDANT ACTIONS OF THYMOL, CARVACROL, 6-GINGEROL, ZINGERONE AND HYDROXYTYROSOL [J].
AESCHBACH, R ;
LOLIGER, J ;
SCOTT, BC ;
MURCIA, A ;
BUTLER, J ;
HALLIWELL, B ;
ARUOMA, OI .
FOOD AND CHEMICAL TOXICOLOGY, 1994, 32 (01) :31-36
[2]   EFFECTS OF DISULFIRAM ON HEPATIC P450IIE1, OTHER MICROSOMAL-ENZYMES, AND HEPATOTOXICITY IN RATS [J].
BRADY, JF ;
XIAO, F ;
WANG, MH ;
LI, Y ;
NING, SM ;
GAPAC, JM ;
YANG, CS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1991, 108 (02) :366-373
[3]   MECHANISMS OF CARBON-TETRACHLORIDE HEPATOTOXICITY [J].
CLAWSON, GA .
PATHOLOGY AND IMMUNOPATHOLOGY RESEARCH, 1989, 8 (02) :104-112
[4]  
HANDA SS, 1990, INDIAN J MED RES-B, V92, P276
[5]   FIXED OIL OF NIGELLA-SATIVA AND DERIVED THYMOQUINONE INHIBIT EICOSANOID GENERATION IN LEUKOCYTES AND MEMBRANE LIPID-PEROXIDATION [J].
HOUGHTON, PJ ;
ZARKA, R ;
DELASHERAS, B ;
HOULT, JRS .
PLANTA MEDICA, 1995, 61 (01) :33-36
[6]   The crucial antioxidant action of schisandrin B in protecting against carbon tetrachloride hepatotoxicity in mice: A comparative study with butylated hydroxytoluene [J].
Ip, SP ;
Ko, KM .
BIOCHEMICAL PHARMACOLOGY, 1996, 52 (11) :1687-1693
[7]  
KALF GF, 1987, ANNU REV PHARMACOL, V27, P399
[8]  
Kim SG, 1996, J PHARMACOL EXP THER, V277, P1058
[9]  
KORNBRUST DJ, 1980, MOL PHARMACOL, V17, P408
[10]   MECHANISM FOR THE PROTECTIVE EFFECTS OF SILYMARIN AGAINST CARBON TETRACHLORIDE-INDUCED LIPID-PEROXIDATION AND HEPATOTOXICITY IN MICE - EVIDENCE THAT SILYMARIN ACTS BOTH AS AN INHIBITOR OF METABOLIC-ACTIVATION AND AS A CHAIN-BREAKING ANTIOXIDANT [J].
LETTERON, P ;
LABBE, G ;
DEGOTT, C ;
BERSON, A ;
FROMENTY, B ;
DELAFORGE, M ;
LARREY, D ;
PESSAYRE, D .
BIOCHEMICAL PHARMACOLOGY, 1990, 39 (12) :2027-2034