Author, Subjects, Keywords

Cited Author

 

 
   » By Author or Editor
 » Browse Author by Alphabet
 » By Journal
 » By Subjects
 » By Affiliations
 » By Type
 » By Year
 » By Latest Additions
 
 
   » By Author
 » Top 20 Authors
 » Top 20 Article
 » Top 20 Journal Cited
 » Top 20 Cited
 » Top 20 Author Cited
 » Usage Since Sept 2007


 
 
 

Login | Create Account

Effects of Ginger Extract (Zingiber officinale Roscoe) on Antioxidant Status of Hepatocarcinoma Indu

Norliza Ahmad, and Suhaniza Sulaiman, and Nor Ashikeen Mukti, and Nor Azian Murad, and Noor Aini Abd Hamid, and Yasmin Anum Mohd Yusof, (2006) Effects of Ginger Extract (Zingiber officinale Roscoe) on Antioxidant Status of Hepatocarcinoma Indu. Malaysian Journal of Biochemistry and Molecular Biology, 14 (1). pp. 7-12. ISSN ISSN 1511-2616

Full text not available from this repository.

Official URL: http://ejum.fsktm.um.edu.my/ArticleInformation.aspx?ArticleID=581

Affiliations

Universiti Kebangsaan Malaysia. Faculty of Medicine. Dept. of Biochemistry
Universiti Kebangsaan Malaysia. Faculty of Medicine. Dept. of Biochemistry
Universiti Kebangsaan Malaysia. Faculty of Medicine. Dept. of Biochemistry
Universiti Teknologi Malaysia. Centre of Lipids, Engineering and Applied Research
Universiti Kebangsaan Malaysia. Faculty of Medicine. Dept. of Biochemistry
Universiti Kebangsaan Malaysia. Faculty of Medicine. Dept. of Biochemistry

Abstract

Ginger or Zingiber officinale which is used in traditional medicine has been found to possess antioxidant effect that can control the generation of free radicals. Free radical level has been reported to be high in cancer cells. The aim of this study was to observe the effect of ginger extract on antioxidant status in rats induced with liver cancer. Twenty-six male Wistar rats were divided into 5 groups: 2 control groups were fed with normal rat chow and olive oil respectively. Treatment groups consisted of rats fed with ginger extract at 100 mg/kg body weight (ginger group), rats induced with liver cancer by choline deficient diet plus ethionine in drinking water (CDE group) and rats with CDE diet plus ginger extract (CDE + ginger group) . Blood samples were taken from the orbital sinus at 0 and 8 weeks of experiment for the determination of antioxidant enzyme activities and MDA level. Comparison between the control group and the CDE group showed significant increase (p<0.05) in SOD activity at 8 week of experiment, whereas no significant differences were observed in the activities of GPx, catalase and the MDA level. Antioxidant effect of ginger extract was observed by the significant decrease (p<0.05) in SOD activity and the level of MDA in CDE group after treatment with ginger when compared to CDE group alone and with the control group. Catalase activity increased significantly (p<0.05) in CDE group after supplementation with ginger at week 8 of experiment when compared to CDE group alone, while there were no significant changes observed for GPx. From this study, it can be concluded that free radicals are increased in liver carcinogenesis (as evidenced by an increase in SOD activity) and ginger extract exhibits anticancer effect by scavenging the free radicals (decrease in SOD activity).

Item Type:Journal
Keywords:Zingiber officinale, antioxidant, hepatocarcinoma induced rats
Subjects:Q Science, Computer Science
R Medicine, Dentistry, Pharmacy, Nursing
ID Code:2189

1. Haydon GH & Hayaes PC. Hepatocellular carcinoma. Br. J. Hosp. Med. 1995; 53(3): 74-81.

2. Kementerian Kesihatan Malaysia. 2003

3. Chen CJ, Yu MW & Liaw YF. Epidemiological characteristic and risk factors of hepatocellular carcinoma. J. Gastroenterol. Hepatol. 1997; 12: S294-S308.

4. Tee LBG, Kirilak Y, Huang W, Morgan RH & Yeoh GCT. Differentiation of Oval Cell Into Duct-like Cells in Preneoplastic Liver of Rats Placed on a Choline Deficient Diet Supplemented with Ethionine. University of Western Australia, Nedlands, Australia. 1992; pp. 1-35.

5. Chandrasoma P & Taylor CR. The Liver: II. Toxic & metabolic diseases; neoplasms, Concise Pathology, 3rd Ed Intern Ed Connecticut: Appleton & Lange. 2001; pp. 649-662.

6. Packer L & Colman, C.. The Antioxidant Miracle. Canada. John Wiley & Sons Inc. Pub. 1999.

7. Halliwell B. Free radical and metal ions in health and disease. Proc. Nutr. Soc. 1987; 46: 13-26.

8. Kemper KJ 1999. Ginger (Zingiber officinale). The Logwood Herbal Task Force. (online) http://www.mep.edu/herbal/ginger.pdf (16 September 2003).

9. Saidin I. Halia Sayuran tradisional, ulam dan penyedap rasa. Universiti Kebangsaan Malaysia, Bangi, Selangor. 2000.

10. Foster S. Ginger (Zingiber officinale): Your Food is your Medicine. (online) http://www.stevenfoster.com/education/monograph/ginger.htm (16 September 2003).

11. Aeschbach R, Loliger J, Scott BC, Murcia A, Butler B, Halliwell B & Aruoma OI.. Antioxidant actions of thymol, carbacrol, 6-gingerol, zingerone and hydroxytyrosol. Food Chem. Toxicol. 1994; 32: 31-36.

12. Chang W-S, Chang Y-H, Lu F-J & Chiang H-C. Inhibitory effects of phenolics on xanthine oxidase. Anticancer Res. 1994; 14: 501-506

13. Jeyakumar S, Nalini N & Venugopal M. Antioxidant activity of ginger in rats fed a high fat diet. Med. Sci. Res. 1999; 27: 341-344.

14. Manju V & Nalini N. Chemopreventive efficacy of ginger, a naturally occurring anticarcinogen during the initiation, post-initiation stages of 1,2 dimethylhydrazine-induced colon cancer. Clin, Chim. Acta 2005; 358: 60-67

15. Beyer WF & Fridovich I. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Analyt. Biochem. 1987; 161: 559-566.

16. Paglia DE & Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroksidase. J. Lab. Clin. Med. 1967 ; 70(1): 158-169

17. Aebi H. Catalase. In: Bergmayer HU eds. Methods of Enzymatic Analysis. London: Academic Press 1984 pp671-684.

18. Ledwozyw A, Michalak J, Stepian A & Kadziolka. The relationship between plasma TG, cholesterol, total lipid peroxidation product during human atherosclerosis. Clin. Chim. Acta 1986; 155:272-284.

19. Halliwell B & Gutteridge JMC eds.. Free Radicals in Biology and Medicine. Oxford: Oxford Univ. Press 1999

20. Hazelton GA & Lang CA. Glutathion peroxidase and reductase activities in the aging mouse. Mech. Ageing and Dev. 1985; 29: 71-81.

21. Cerutti PA. Oxyradicals and cancer. Lancet. 1994; 344: 862-868.

22. Capel I, Pinnock M, Willimas D & Hanham IW. The serum levels of some trace and bulk element in cancer patients. Oncology. 1982; 39:38-41.

23. Park KK, Chun KS, Lee JM, Lee SS & Surh YJ. Inhibitory effects of [6]-gingerol, a major pungent principle of ginger, on phorbol ester-induced inflammation, epidermal ornithine decarboxylase activity and skin tumor promotion in ICR mice. Cancer Lett. 1998; 129(2): 139-144.

24. Zhan H, Sun CP, Liu CG & Zhou JH. Age-related change of free radical generation in liver and sex glands of rats. Mech. Ageing Dev. 1992; 62: 111-116

25. Chandra Mohan KVP & Nagini S. Dose-response effect of tomato lycopene on lipid peroxidation and enzymic antioxidant in the hamster buccal pouch carcinogenesis model. Nutr. Res. 2003; 23:1403-1416

26. Sohal RS, Svensson I & Brunk UT. Hydrogen peroxide production by liver mitochondria in different species. Mech. Ageing Dev. 1990; 53: 209-215.

27. Matés JM, Perez-Gomez C & Nunez de Castro I. Antioxidant enzymes and human diseases. Clin. Biochem. 1999; 32(8): 595- 603.

28. Pigeolet E, Corbisier P, Houbion A, Lambert D, Michiels C, Raes M, Zachary MD & Remacle J. Glutathion peroxidase, superoxide dismutase, and catalase inactivation by peroxidase and oxygen derived free radicals. Mech. Ageing Dev. 1990; 51: 283-297.

29. Faber E. Ethionine Carcinogenesis. Adv. Cancer Res. 963; 7: 383-474.

30. Huang YL, Sheu JY & Lin TH. Association between oxidative stress and changes of trace elements in patient with breast cancer. Clin. Biochem. 1999; 32: 131-136.

31. Sabitha KE & Shyamaladevi CS. Oxidant and antioxidant activity changes in patients with oral cancer and treated with radiotherapy. Oral Oncol. 1998; 35: 273-277.

32. Szatrowski TP & Nathan CF. Production of large amount of H2O2 by human tumor cells. Cancer Res. 1991; 51:794-798.

Repository Staff Only: item control page