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Antilipoxygenase and Antihelmintic Activity of Ginger (Zingiber Officinale) Enriched Cane Jaggery

Author Affiliations

  • 1Department of Sugar Technology, Sir. M. Visvesvaraya Post Graduate Centre, University of Mysore, Mandya, 571 402, Karnataka, INDIA
  • 2Department of Biochemistry, Adichunchanagiri Biotechnology and Cancer Research Institute, Balagangadharanatha Nagara, 571 448, Nagamangala Taluk, Mandya, Karnataka, INDIA

Res. J. Recent Sci., Volume 4, Issue (8), Pages 62-66, August,2 (2015)

Abstract

Zingiber Officinale enriched jaggery (ZOEJ) at 0.05 %, 0.1 % and 0.2 % concentrations from Co 86032, Co419 and Co 62175 sugarcane varieties were evaluated for lipoxygenase inhibitory and antihelmintic activity. In addition total phenol content of the ZOEJ samples were quantified. Total phenol content of ZOEJ indicated significant difference between enriched and control jaggery and showed a dose dependent increase for all the varieties. ZOEJ showed inhibition of lipoxygenase activity with an EC50 of 0.34, 0.33 and 0.31 mg/mL at 0.05 % Z. officinale enrichment for Co 86032, Co419 and Co 62175 sugarcane varieties, respectively. A positive correlation (r = 0.961, 0.900 and 0.970) was observed between total phenolics and antilipoxygenase activity of ZOEJ for Co 86032, Co419 and Co 62175 varieties. However, ZOEJexhibited antihelmintic activity at 0.5g/mL concentration in all sugarcane varieties but indicated no significant difference in both paralysis and death time of helmintis upon spice enrichment. Hence, dietary supplementation of Z. officinale enriched jaggery may contribute better health benefits.

References

  1. Saarela M., Functional foods: Concept to product, Woodhead Publishing Series in Food Science, Technology and Nutrition No. 205. Oxford Woodhead Publishing Limited, (2011)
  2. Hasler C.M., Functional foods: benefits, concerns and challenges: A position paper from the American council on science and health, J.Nutr., 132, 3772–3781 (2002)
  3. Walter Jaffe R., Health effects of non-centrifugal sugar (NCS): A review, Sugar Tech., 14, 87-94 (2012)
  4. Sahu A.P. and Saxena A.K., Enhanced translocation of particles from lungs by jaggery, Environ. Health Perspect., 102, 211–214 (1994)
  5. Nrashant S., Kumar D., Raisuddin S. and Anand P Sahu., Genotoxic effects of arsenic: Prevention by functional food-Jaggery, Cancer Lett., 268, 325-330 (2008)
  6. Okabe., Toda T.T., Inafuku M., Wada K., Iwasaki H. and Oku H., Antiatherosclerotic functions of kokuto, Okinawan non-centrifuged cane sugar, J. Agric. Food Chem., 57, 69–75 (2009)
  7. Harish Nayaka M.A., Sathisha U.V., Manohar M.P., Chandrashekar K.B. and Shylaja M.D., Cytoprotective and antioxidant activity studies of jaggery sugar, Food Chem., 115, 113-118 (2009)
  8. Dugasani S., Pichika M.R., Nadarajah V.D., Balijepalli M.K., Tandra S. and Korlakunta J.N., Comparative antioxidant and anti-inflammatory effects of [6]-gingerol, [8]-gingerol, [10]-gingerol and [6]-shogaol, J. Ethnopharmacol., 127, 515–520 (2010)
  9. Jung H.W., Yoon C.H., Park K.M., Han H.S. and Park Y.K., Hexane fraction of Zingiberis Rhizoma Crudus extract inhibits the production of nitric oxide and proinflammatory cytokines in LPS-stimulated BV2 microglial cells via the NF-kappaB pathway, Food Chem.Toxicol., 47, 1190–1197 (2009)
  10. Park M., Bae J. and Lee D.S., Antibacterial activity of [10]-gingerol and [12]-gingerol isolated from ginger rhizome against periodontal bacteria, Phytother Res., 22, 1446–1449 (2008)
  11. Matsuda A., Wang Z., Takahashi S., Tokuda T., Miura N. and Hasegawa J., Upregulation of mRNA of retinoid binding protein and fatty acid binding protein by cholesterol enriched-diet and effect of ginger on lipid metabolism, Life Sci., 84, 903–907 (2009)
  12. Sreejayan N. and Rao M.N.A., Free radical scavenging activity of curcuminoids, Arzneimittel-Forschung., 46, 169–171 (1996)
  13. Jagannadha Rao P.V.K., Madhusweta Das and Das S.K., Jaggery: A Traditional Indian Sweetener, Indian J.Tradit. Know., , 95-102 (2007)
  14. Singleton V.L., Orthofer R. and Lamuela-Raventos R.M., Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Ciocalteu reagent, Methods Enzymol., 299, 152-178 (1999)
  15. Vineet Kumar, Anita Rani, Vimal Pandey G.S. and Chauhan, Changes in lipoxygenaseisozymes and trypsin inhibitor activity in soybean during germination at different temperatures, Food Chem., 99, 563–568 (2006)
  16. NAIDU K.A., Eugenol: An inhibitor of lipoxygenase dependent lipid peroxidation, Prostaglandins Leukot. Essen. Fatty Acids., 53, 381–383 (1995)
  17. Ajaiyeoba E.O., Onocha P.A. and Olarenwaju O.T., In vitro Anthelmintic Properties of Buchholziacoriaceae and Gynandropsisgynandra Extracts, Pharm. Biol., 39, 217-220 (2001)
  18. Ammon H.P.T., Annazodo M.I., Safayhi H., Dhawan B.N. and Scrimal R., Curcumin : a potent inhibitor of leukotriene B4 formation in rat peritoneal polymorphonuclear neutrophils (PMNL), Planta Medica., 58, 226 (1992)
  19. Kuhn H., Romisch I. and Belkner J., The role of lipoxygenase-isoforms in atherogenesis, Mol.Nutr. Food Res., 49, 1014–1029 (2005)
  20. Flynn D.L., Rafferty M.F. and Boctor A.M., Inhibition of human neutrophil 5-lipoxygenase activity by gingerdione, shogaol, capsaicin and related pungent compounds, Prostaglandins Leukot. Med., 24, 195 (1986)
  21. Kiuchi F., Iwakami S., Shibuya M., Hanaoka F. and Sankawa, Inhibition of prostaglandin and leukotriene biosynthesis by gingerols and diarylheptanoids, Chem. Pharm. Bull. (Tokyo)., 40, 387–391 (1992)
  22. Ammon H.P.T., Safayhi H., Mack T. and Sabieraj J., Mechanism of anti inflammatory actions of curcumine and boswellic acids, J. Ethnopharmacol., 38, 113–119 (1993)
  23. GIBBS H.C., Epidemiology, Diagnosis and Control of Gastrointestinal parasitism, Kenya, ILARD. pp 121, (1986)
  24. Prasad P., Praveen Kumar P., Satyavathi K. and Prabhakar M.C., Comparatives studies on anthelmintic activity of natural sweeteners, Res. J. Pharm. Biol. Chem. Sci., , 510-514 (2010)
  25. Bate-Smith E.C., The phenolic constituent of plants and their taxonomic significance, dicotyledons, J. Linn. Soc. Bot., 58, 95-103 (1962)
  26. Martin R.J., Mode of action of anthelmintic drugs, Vet. J., 154,11-34 (1997)