Hepatoprotective effects of rubiadin, a major constituent of Rubia cordifolia Linn.

被引:136
作者
Rao, GMM [1 ]
Rao, CV
Pushpangadan, P
Shirwaikar, A
机构
[1] Natl Bot Res Inst, Pharmacognosy & Ethnopharmacol Div, Lucknow 226001, Uttar Pradesh, India
[2] Coll Pharmaceut Sci, Dept Pharmacognosy, Manipal 576119, India
关键词
Rubia cordifolia; rubiadin; carbon tetrachloride; hepatoprotective effect; silymarin; histopathology;
D O I
10.1016/j.jep.2005.08.073
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The hepatoprotective effects of rubiadin, a major constituent isolated from Rubia cordifolia Linn., were evaluated against carbon tetrachloride (CCI4)-induced hepatic damage in rats. Rubiadin at a dose of 50, 100 and 200 mg/kg was administered orally once daily for 14 days. The substantially elevated serum enzymatic activities of serum glutamic oxaloacetic transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), serum alkaline phosphatase (SALP) and gamma-glutmyltransferase (gamma-GT) due to carbontetrachloride treatment were dose dependently restored towards normalization. Meanwhile, the decreased activities of glutathione S-transferase and glutathione ruductase were also restored towards normalization. In addition, rubiadin also significantly prevented the elevation of hepatic melondialdehyde formation and depletion of reduced glutathione content in the liver Of CCl4 intoxicated rats in a dose dependent manner. Silymarin used as standard reference also exhibited significant hepatopretective activity on post treatment against carbon tetrachloride induced hepatotoxicity in rats. The biochemical observations were supplemented with histopathological examination of rat liver sections. The results of this study strongly indicate that rubiadin has a potent hepatoprotective action against carbon tetrachloride induced hepatic damage in rats. (c) 2005 Published by Elsevier Ireland Ltd.
引用
收藏
页码:484 / 490
页数:7
相关论文
共 40 条
[21]  
Mitra S. K., 2000, Indian Journal of Physiology and Pharmacology, V44, P82
[22]  
MIZE CE, 1962, J BIOL CHEM, V237, P1589
[23]  
Okhawa H, 1979, ANAL BIOCHEM, V95, P351
[24]  
PANDEY GS, 1967, BHAV PRAKASH NIGHANI, P570
[25]  
Pandey Savita, 1994, Indian Journal of Experimental Biology, V32, P180
[26]   MECHANISMS OF CARBON-TETRACHLORIDE TOXICITY [J].
RECKNAGEL, RO ;
GLENDE, EA ;
DOLAK, JA ;
WALLER, RL .
PHARMACOLOGY & THERAPEUTICS, 1989, 43 (01) :139-154
[27]  
RECKNAGEL RO, 1973, CRITICAL REV TOXICOL, V2, P263
[28]  
Recknagel RO., 1991, Hepatotoxicology, P401
[29]   PREVENTION OF ALLERGIC CONTACT-DERMATITIS WITH ALTERNATIVE PRODUCTS [J].
SERTOLI, A ;
FRANCALANCI, S ;
GIORGINI, S ;
BRUSI, C ;
ACCIAI, MC .
CONTACT DERMATITIS, 1994, 31 (05) :322-323
[30]  
SHIANG SH, 1995, J NAT PRODUCTS, V58, P1365