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Protective Effect of Zingiber officinale Against Dalton’s Lymphoma Ascites Tumour by Regulating Inflammatory Mediator and Cytokines

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Abstract

The aim of the present investigation was to evaluate Zingiber officinale paste against Dalton’s lymphoma ascites (DLA)-induced tumours in Swiss albino mice. Experimental animals received Z. officinale paste (low dose 100 mg/kg bw and high dose 500 mg/kg bw) orally for eight alternative days. Treatment with Z. officinale paste showed significant increase in haemoglobin level and decrease in aspartate amino transferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP) and gamma glutamyl transferase (γ-GT) level. Z. officinale paste reduced the inflammatory mediators and cytokine levels, such as inducible nitric oxide (iNOS), tumour necrosis factor level (TNF-α) and interleukin-1β (IL-1β). Treatment with Z. officinale paste also significantly increased the antioxidant enzyme level, such as superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH) and glutathione transferase (GST), and decreased the lipid peroxidation. Treatment also increased the vitamin C and E levels in treated animals compared with the DLA-bearing host. Histopathological studies also confirmed the protective influence of Z. officinale paste against DLA. The present study suggested that Z. officinale paste could be used as natural spice and a potent antitumour agent.

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References

  1. Sreenivas, S. A., Venu Gopal, Y., Ravidranath, A., Kalpana, G. & Kapoor, R. (2012). Anti-tumour and antioxidant activity of Capparis Sepiaria against Dalton’s ascites lymphoma in rodents. Academic Journal of Cancer Research, 5, 46–52.

    Google Scholar 

  2. Muthumani, P., Venkatraman, S., Ramseshu, K. V., Meera, R., Devi, P., Kameswari, B. & Eswarapriya, B. (2009). Pharmacological studies of anticancer, anti-inflammatory activities of Murraya koenigii (Linn) Spreng in experimental animals C/I. Journal of Pharmaceutical Sciences and Research, 3137–3141.

  3. Gennari, C. D., Castoldi, D., & Sharon, O. (2007). Natural products with taxol-like anti-tumour activity: synthetic approaches to elutherobin and dictyostatin. Pure and Applied Chemistry, 79(2), 173–180.

    Article  CAS  Google Scholar 

  4. Prasad, S. B., Rosangkima, G., & Kharbangar, A. (2010). Structural and biochemical changes in mitochondria after cisplantin treatment of Dalton’s lymphoma-bearing mice. Mitochondrion, 10, 38–45.

    Article  CAS  Google Scholar 

  5. Lan-Sook Lee, L., Cho, C., Hong, H., Lee, Y. C., Choi, U. K. & Kim, Y. C. (2013). Hypolipidemic and antioxidant properties of phenolic compound rich extracts from white gingseng in cholesterol red rabbit. Molecules, 18, 12548–12560.

    Article  Google Scholar 

  6. Ho, Y., Huang, S., Deng, J., Lin, Y. H., Chang, Y. S. & Huang, G. J. (2012). In vitro antioxidant properties and total phenolic contents of wetland medicinal plants in Taiwan. Botanical Studies, 53, 55–66.

    CAS  Google Scholar 

  7. Sakthivel, K. M., Kannan, N., Angeline, A., & Guruvayoorappan, C. (2012). Anticancer activity of Acacia nilotica (L.) wild. Ex. Delile Subsp. indica against Dalton’s ascitic lymphoma induced solid and ascitic tumor model. Asian Pacific Journal of Cancer Prevention, 113, 3989–3995.

    Article  Google Scholar 

  8. Surh, Y. J. (2003). Cancer chemoprevention with dietary phytochemicals. Nature Reviews Cancer, 3, 68–780.

    Article  Google Scholar 

  9. Lai, P. K., & Roy, J. (2004). Antimicrobial and chemopreventive properties of herbs and spices. Current Medicinal Chemistry, 11, 1451–1460.

    Article  CAS  Google Scholar 

  10. Agarwal, N., Majee, C., & Chakraborthy, G. S. (2012). Natural herbs as anticancer drugs. International Journal of PharmTech Research, 4(3), 1142–1153.

    Google Scholar 

  11. Shukla, Y., & Singh, M. (2007). Cancer preventive properties of ginger a brief review. Food and Chemical Toxicology, 45, 683–690.

    Article  CAS  Google Scholar 

  12. Shakya, S. R. (2015). Medicinal uses of ginger (Zingiber officinale Roscoe) improves growth and enhances immunity in aquaculture. International Journal of Chemical Studies, 3(2), 83–87.

    Google Scholar 

  13. Anisha, C., & Radhakrishnan, E. K. (2015). Gliotoxin-producing endophytic Acremonium sp. from Zingiber officinale found antagonistic to soft rot pathogen Pythium myriotylum. Applied Biochemistry and Biotechnology, 175(7), 3458–3467.

    Article  CAS  Google Scholar 

  14. Keerthi, D., Geethu, C., Nair, R. A., & Pillai, P. (2014). Metabolic profiling of Zingiber zerumbet following Pythium myriotylum infection: investigations on the defensive role of the principal secondary metabolite, zerumbone. Applied Biochemistry and Biotechnology, 172(5), 2593–2603.

    Article  CAS  Google Scholar 

  15. Ahmed, J. (2004). Rheological behaviour and colour changes of ginger paste during storage. International Journal of Food Science and Technology, 39, 325–330.

    Article  CAS  Google Scholar 

  16. Gothoskar, S. V., & Ranadive, K. J. (1971). Anticancer screening of SAN-AB; an extract of marking nut, Semicarpus anacarium. Indian Journal of Experimental Biology, 9, 372–375.

    CAS  Google Scholar 

  17. Iman Elkhishin, A., & Ibrahim Awwad, A. (2009). A study of the cardiovascular toxic effects of Zingiber officinale (ginger) in adult male albino rats and its possible mechanisms of action. Mansourora Journal Forensic Medicine Clinical Toxicology, 17, 109–127.

    Google Scholar 

  18. Ellman, G. L. (1959). Tissue sulfhydryl groups. Archives of Biochemistry and Biophysics, 82, 70–77.

    Article  CAS  Google Scholar 

  19. Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1974). Glutathione-S-transferase: the first step in mercapturic acid formation. Journal of Biological Chemistry, 249, 7130–7139.

    CAS  Google Scholar 

  20. Omaye, S. T., Turbull, T. D., & Sauberlich, H. C. (1979). Selected method for the determination of ascorbic acid in animal cells, tissues and fluids. In D. B. McCormic & D. L. Wright (Eds.), Methods Enzymol, 62 (pp. 3–11). New York: Academic Press.

    Google Scholar 

  21. Baker, H., Frank, O., Angelis, B., & Feingold, S. (1951). Plasma tocopherol in man at various times after ingesting free or acetylated tocopherol. Nutrition Reports International, 21, 531–536.

    Google Scholar 

  22. Lowry, O. H., Roesborough, M. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with Folin-phenol reagent. Journal of Biological Chemistry, 193, 265–275.

    CAS  Google Scholar 

  23. Kakkar, P., Das, B., & Viswanathan, P. N. (1984). A modified spectrophotometric assay of superoxide dismutase. Indian Journal of Biochemistry & Biophysics, 21, 130–132.

    CAS  Google Scholar 

  24. Sinha, K. A. (1972). Colorimetric assay of catalase. Analytical Biochemistry, 47, 389–394.

    Article  CAS  Google Scholar 

  25. Niehius, W. G., & Samuelsson, D. (1968). Formation of malondialdehyde from phospholipid arachidonate during microsomal lipid peroxidation. European Journal of Biochemistry, 6, 126–130.

    Article  Google Scholar 

  26. Guruvayoorappan, C., & Girija, K. (2007). β-carotene down regulates inducible nitric oxide synthase gene expression and induce apoptosis by suppressing bcl-2 expression and activating caspase-3 and p53 in B16F- 10 melanoma cells. Nutrition Research, 27, 336–342.

    Article  CAS  Google Scholar 

  27. Rahman, K. (2003). Garlic and aging: new insights into an old remedy. Aging Research Reviews, 2, 39–56.

    Article  Google Scholar 

  28. Lai, F. Y. C., Chyau, C. C., Mau, J. L., Chen, C. C., Lai, Y. J., Shih, C. F. & Lin, L. L. (2004). Antimicrobial activity and cytotoxicity of the essential oil of Curcuma zedoaria. The American Journal of Chinese Medicine, 32(2), 281–290.

    Article  CAS  Google Scholar 

  29. Radha, R., Kavimani, S., & Ravichandran, V. (2008). Anti-tumour activity of methanolic extract of Plumeria alba L. Leaves against Dalton lymphoma ascites in mice. International Journal of Health Research, 1, 79–85.

    Google Scholar 

  30. Kumar, G., Karthik, L., & Bhaskar Rao K. V. (2011). Review on pharmacological and phytochemical properties of Zingiber officinale Roscoe. Journal of Pharmacy Research, 4(9), 2963–2966.

    CAS  Google Scholar 

  31. Surh, Y. J. (2002). Anti-tumor promoting potential of selected spice ingredients with anti-oxidative and anti-inflammatory activities: a short review. Food and Chemical Toxicology, 40, 1091–1097.

    Article  CAS  Google Scholar 

  32. Lakshmi, S., Padmaja, G., & Remani, P. (2011). Antitumor effects of iso-curcumenol isolated from Curcuma zedoaria rhizomes on human and murine cancer cells. International Journal of Medicinal Chemistry, 1–13.

  33. Bhandari, U., Shamsher, A. A., Pillai, K. K., & Khan, M. S. Y. (2008). Anti-hepatotoxic activity of ginger ethanol extracts in rats. Pharmaceutical Biology, 41, 68–71.

    Article  Google Scholar 

  34. Erat, M., Ciftci, M., Gumustekin, K., & Gul, M. (2007). Effects of nicotine and vitamin E on glutathione reductase activity in some rat tissue in vivo and in vitro. European Journal of Pharmacology, 554, 92–97.

  35. Prasad, S. B., Rosangkima, G., & Nicol, B. M. (2010). Cyclophosphamide and ascorbic acid mediated ultrastructural and biochemical changes in Dalton’s lymphoma cells in vivo. European Journal of Pharmacology, 645, 47–54.

    Article  CAS  Google Scholar 

  36. Nagendra Chari, K. L., Manasa, D., Srinivas, P., & Sowbhagya, H. B. (2013). Enzyme assisted extraction of bioactive compounds from ginger. Food Chemistry, 139, 509–514.

  37. Dorai, T., & Aggarwal, B. B. (2004). Role of chemopreventive agents in cancer therapy. Cancer Letters, 215, 129–140.

    Article  CAS  Google Scholar 

  38. Jeong, C. H., Bode, A. M., Pugliese, A., Cho, Y. Y., Kim, H. G., Shim, J. H., et al. (2009). [6]-gingerol suppresses colon cancer growth by targeting leukotriene a4 hydrolase. Cancer Research, 69(13), 5584–5591.

    Article  CAS  Google Scholar 

  39. Singh, R. P., Banerjee, S., Kumar, P. V., Raveesha, K. A., & Rao, A. R. (2006). Tinosporacordifolia induces enzymes of carcinogen/drug metabolism and antioxidant system, and inhibits lipid peroxidation in mice. Phytomedicine, 13, 74–84.

    Article  CAS  Google Scholar 

  40. Verma, N., & Vinayak, M. (2009). Semecarpus anacardium nut extract promotes the antioxidant defence system and inhibits anaerobic metabolism during development of lymphoma. Bioscience Reports, 29, 151–164.

    Article  CAS  Google Scholar 

  41. Bak, M. J., Ok, S., Jun, M., & Jeong, W. S. (2012). 6-shogaol rich extract from ginger up-regulates the antioxidant defense systems in cell and mice. Molecules, 171, 8037–8055.

    Article  Google Scholar 

  42. Hung, J. Y., Hsu, Y. L., Li, C. T., Ko, Y. C., Ni, W. C., Huang, M. S., & Kuo, P. L. (2009). [6]-shogaol, an active constituent of dietary ginger, induces autophagy by inhibiting the AKT/mTOR pathway in human non-small cell lung cancer A549 cells. Journal of Agricultural and Food Chemistry, 57(20), 9809–9816.

    Article  CAS  Google Scholar 

  43. Selvendiran, K., Singh, J. P. V., Krishnan, K. B., & Sakthisekaran, D. (2003). Cytoprotective effect of piperine against benzo(a)pyrene induced lung cancer with reference to lipid peroxidation and antioxidant system in Swiss albino mice. Fitoterapia, 74, 109–115.

    Article  CAS  Google Scholar 

  44. Khanom, F., Kayahara, H., Hirota, M., & Tadasa K. (2003). Superoxide scavenging and Tyrosinase inhibitory active compound in ginger. Pakistan Journal of Biological Sciences, 6(24), 1996–2000.

    Article  Google Scholar 

  45. Haniadka, R., Saxena, A., Shivashankara, A. R., Fayad, R., Princy, P. L., Nazreth, N., et al. (2013). Ginger protects the liver against the toxic effects of xenobiotic compounds preclinical observations. Journal of Nutrition & Food Sciences, 1–6.

  46. Habib, S. H., Makpol, S., Abdul Hamid, N. A., Das S., Ngah W. Z. W., & Yusof Y. A. M. (2008). Ginger extract (Zingiber officinale) has anti-cancer and anti-inflammatory effects on ethionine-induced hepatoma rats. Clinics, 63(6), 807–813.

    Article  Google Scholar 

  47. Ippoushi, K., Azuma, K., Ito, H., Horie, H. & Higashio, H. (2003). 6-gingerol inhibits the nitric oxide synthesis in activated J774. 1 mouse macrophages and prevents peroxynitrite induced oxidation and nitration reactions. Life Sciences, 73, 3427–3437.

    Article  CAS  Google Scholar 

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Acknowledgments

The authors are grateful to Dr. C. Guruvayoorappan, Assistant Professor, Division of Cancer Research, Regional Cancer Center, Thiruvananthapuram, for his help and guidance during the course of this study.

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Correspondence to Thottiam Vasudevan Ranganathan.

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Rubila, S., Ranganathan, T.V. & Sakthivel, K.M. Protective Effect of Zingiber officinale Against Dalton’s Lymphoma Ascites Tumour by Regulating Inflammatory Mediator and Cytokines. Appl Biochem Biotechnol 180, 1482–1496 (2016). https://doi.org/10.1007/s12010-016-2181-x

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  • DOI: https://doi.org/10.1007/s12010-016-2181-x

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