Evaluation of the hepatoprotective activity of standardized ethanolic extract of Curcuma xanthorrhiza Roxb.

被引:12
作者
Devaraj, Sutha [1 ]
Ismail, Sabariah [1 ]
Ramanathan, Surash [1 ]
Marimuthu, Santhini [2 ]
Fei, Yam Mun [3 ]
机构
[1] Univ Sains Malaysia, Ctr Drug Res, George Town 11800, Malaysia
[2] Univ Sains Malaysia, Sch Biol Sci, George Town 11800, Malaysia
[3] Univ Sains Malaysia, Sch Pharmaceut Sci, George Town 11800, Malaysia
来源
JOURNAL OF MEDICINAL PLANTS RESEARCH | 2010年 / 4卷 / 23期
关键词
Curcuma xanthorrhiza; hepatoprotective activity; ethanol; serum enzyme; LIVER-INJURY; CONSUMPTION;
D O I
10.5897/JMPR10.453
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Curcuma xanthorrhiza is widely used in Indonesia folk medicine to treat liver disorders. This study has evaluated the hepatoprotective activity of standardized ethanolic extract of C. xanthorrhiza. The extract was standardized using GC-MS. The hepatoprotective activity of this extract was studied using ethanol-induced liver toxicity in rats. This respective activity was assessed through monitoring liver function tests through the measurement of alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP) and protein content. Further, hepatic tissues were also subjected to histopathological studies. Pretreatment of the standardized C. xanthorrhiza ethanolic extract (500 mg/kg) reduced the fatty liver symptoms and significantly (p < 0.05) inhibit the increase of respective serum enzyme levels. The results of the present study indicated that C. xanthorrhiza possess hepatoprotective effects which could act as an effective treatment for acute hepatic diseases.
引用
收藏
页码:2512 / 2517
页数:6
相关论文
共 26 条
[11]   Saponins isolated from the root of Platycodon grandiflorum protect against acute ethanol-induced hepatotoxicity in mice [J].
Khanal, Tilak ;
Choi, Jae Ho ;
Hwang, Yong Pil ;
Chung, Young Chul ;
Jeong, Hye Gwang .
FOOD AND CHEMICAL TOXICOLOGY, 2009, 47 (03) :530-535
[12]   Abrogation of cisplatin-induced hepatotoxicity in mice by xanthorrhizol is related to its effect on the regulation of gene transcription [J].
Kim, SH ;
Hong, KO ;
Chung, WY ;
Hwang, JK ;
Park, KK .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2004, 196 (03) :346-355
[13]   CIRRHOSIS IN ALCOHOLIC AND ITS RELATION TO VOLUME OF ALCOHOL-ABUSE [J].
LELBACH, WK .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1975, 252 (APR25) :85-105
[14]   ACUTE CHOLESTASIS, HEPATIC-FAILURE, AND FATTY LIVER IN ALCOHOLIC [J].
MORGAN, MY ;
SHERLOCK, S ;
SCHEUER, PJ .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1978, 13 (03) :299-303
[15]   High AST/ALT ratio may indicate advanced alcoholic liver disease rather than heavy drinking [J].
Nyblom, H ;
Berggren, U ;
Balldin, J ;
Olsson, R .
ALCOHOL AND ALCOHOLISM, 2004, 39 (04) :336-339
[16]   Hepatocellular carcinoma: Clinicopathological aspects [J].
Okuda, K .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1997, 12 (9-10) :S314-S318
[17]   Evaluation of hepatoprotective effect of Gentiana olivieri herbs on subacute administration and isolation of active principle [J].
Orhan, DD ;
Aslan, M ;
Aktay, G ;
Ergun, E ;
Yesilada, E ;
Ergun, F .
LIFE SCIENCES, 2003, 72 (20) :2273-2283
[18]   ASPARTATE-AMINOTRANSFERASE ISOENZYMES [J].
PANTEGHINI, M .
CLINICAL BIOCHEMISTRY, 1990, 23 (04) :311-319
[19]   TRANSFERENCE OF HEPATIC-COMA TO NORMAL RATS FROM GALACTOSAMINE TREATED DONORS BY REVERSE PLASMA-EXCHANGE [J].
RYAN, CJ ;
ASLAM, M ;
COURTNEY, JM .
BIOMATERIALS ARTIFICIAL CELLS AND ARTIFICIAL ORGANS, 1990, 18 (04) :477-482
[20]   ATTENUATION OF THE ETHANOL-INDUCED HEPATIC REDOX CHANGE AFTER CHRONIC ALCOHOL-CONSUMPTION IN BABOONS - METABOLIC CONSEQUENCES INVIVO AND INVITRO [J].
SALASPURO, MP ;
SHAW, S ;
JAYATILLEKE, E ;
ROSS, WA ;
LIEBER, CS .
HEPATOLOGY, 1981, 1 (01) :33-38