Antiviral activity of sulfated polysaccharide of Adenanthera pavonina against Poliovirus in HEp-2 Cells

Evidence-based Complementary and Alternative Medicine

Volumn 2014, Issue , 2014, Pages

  Godoi, Ananda Marques De ^a   Faccin Galhardi, Lígia Carla ^a   Lopes, Nayara ^a   Rechenchoski, Daniele Zendrini ^a   De Almeida, Raimundo Rafael ^b   Ricardo, Nágila Maria Pontes Silva ^b   Nozawa, Carlos ^a   Linhares, Rosa Elisa Carvalho ^a  

^a STATE UNIVERSITY OF LONDRINA   (Brazil)

^b FEDERAL UNIVERSITY OF CEARÁ   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVIRUS AGENT; POLYSACCHARIDE SULFATE;

ADENANTHERA PAVONINA; ANTIVIRAL ACTIVITY; ARTICLE; CYTOTOXICITY ASSAY; HEP 2 CELL LINE; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; IC50; IMMUNOFLUORESCENCE TEST; INFECTION CONTROL; PLANT; PLANT SEED; POLIOMYELITIS VIRUS 1; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; VIRUS INFECTION;

EID: 84907246615     PISSN: 1741427X     EISSN: 17414288     Source Type: Journal    
DOI: 10.1155/2014/712634     Document Type: Article

References (36)

1. Hupfeld J., Efferth T., Drug resistance of human immunodeficiency virus and overcoming it by natural products. In Vivo 2009 23 1 1 6 2-s2.0-63049094312
2. Ghosh T., Chattopadhyay K., Marschall M., Karmakar P., Mandal P., Ray B., Focus on antivirally active sulfated polysaccharides: from structure-activity analysis to clinical evaluation. Glycobiology 2009 19 1 2 15 10.1093/glycob/cwn092 2-s2.0-57649225479
3. Josephine A., Amudha G., Veena C. K., Preetha S. P., Rajeswari A., Varalakshmi P., Beneficial effects of sulfated polysaccharides from Sargassum wightii against mitochondrial alterations induced by Cyclosporine A in rat kidney. Molecular Nutrition & Food Research 2007 51 11 1413 1422 10.1002/mnfr.200700127 2-s2.0-36649007656
4. Cunha P. L. R., Paula R. C. M., Feitosa J. P. A., Polissacarídeos da biodiversidade brasileira: uma oportunidade de transformar conhecimento em valor econômico. Química Nova 2009 32 3 649 660 10.1590/S0100-40422009000300009
5. Sultana R., Gulzar T., Proximate analysis of Adenanthera pavonina L. seed oil, a source of lignoceric acid grown in Pakistan. Journal of the American Oil Chemists' Society 2012 89 9 1611 1618 10.1007/s11746-012-2073-3 2-s2.0-84865271438
6. Fonseca S., Perez S., Ação do polietilenoglicol na germinação de sementes de Adenanthera pavonina L. e o uso de poliaminas na atenuação do estresse hídrico sob diferentes temperaturas. Revista Brasileira de Sementes 2003 25 1 1 6
7. Soomro R. K., Sherazi S. T. H., Spectroscopic and chromatographic evaluation of the wax ester fraction of Adenanthera pavonina oil. Industrial Crops and Products 2012 36 1 294 298 10.1016/j.indcrop.2011.10.012 2-s2.0-82055202807
8. Krishnaveni A., Selvi S., Mohandass S., Antidiabetic, hypolipidemic activity of Adenanthera pavonina seeds in alloxan induced diabetic rats. Journal of Pharmacy Research 2011 4 5 1440 1442
9. Adedapo A. D. A., Osude Y. O., Adedapo A. A., Moody J. O., Adeagbo A. S., Olajide O. A., Makinde J. M., Blood pressure lowering effect of Adenanthera pavonina seed extract on normotensive rats. Records of Natural Products 2009 3 2 82 89
10. Ara A., Saleh-e-In M. M., Ahmed N. U., Ahmed M., Hashem M. A. H., Bachar S. C., Phytochemical screening, analgesic, antimicrobial and anti-oxidant activities of bark extracts of Adenanthera pavonina l. (Fabaceae). Advances in Natural and Applied Sciences 2010 4 3 352 360 2-s2.0-79960444570
11. Soares J. R., de Carvalho A. Q., Dos Santos I. S., MacHado O. L. T., Nascimento V. V., Vasconcelos I. M., da Ferreira A. T. S., de Perales J. E. A., Gomes V. M., Antimicrobial peptides from Adenanthera pavonina L. Seeds: characterization and antifungal activity. Protein and Peptide Letters 2012 19 5 520 529 10.2174/092986612800191062 2-s2.0-84860546822
12. Racaniello V. R., Knipe D. M., Howley P. M., Picornaviridae: the viruses and their replication. Fields Virology 2007 5th Philadelphia, Pa, USA Lippincott Williams & Wilkins 796 837
13. Global Polio Eradication Iniciative, Annual report 2014. WHO press, World Health Organization, Geneva, Switzerland, 2014
14. Vieira Í. G. P., Mendes F. N. P., Gallão M. I., de Brito E. S., NMR study of galactomannans from the seeds of mesquite tree (Prosopis juliflora (Sw) DC). Food Chemistry 2007 101 1 70 73 10.1016/j.foodchem.2005.11.052 2-s2.0-33746877110
15. O'Neill A. N., Sulphated derivatives of laminarin. Canadian Journal of Chemistry 1995 33 6 1097 1101
16. Ono L., Wollinger W., Rocco I. M., Coimbra T. L. M., Gorin P. A. J., Sierakowski M., In vitro and in vivo antiviral properties of sulfated galactomannans against yellow fever virus (BeH111 strain) and dengue 1 virus (Hawaii strain). Antiviral Research 2003 60 3 201 208 10.1016/S0166-3542(03)00175-X 2-s2.0-0344153732
17. Wang L., Li X., Chen Z., Sulfated modification of the polysaccharides obtained from defatted rice bran and their antitumor activities. International Journal of Biological Macromolecules 2009 44 2 211 214 10.1016/j.ijbiomac.2008.12.006 2-s2.0-58849088039
18. Yamamoto K. A., Galhardi L. C. F., Rincão V. P., Soares S. D. A., Vieira Í. G. P., Ricardo N. M. P. S., Nozawa C., Linhares R. E. C., Antiherpetic activity of an Agaricus brasiliensis polysaccharide, its sulfated derivative and fractions. International Journal of Biological Macromolecules 2013 52 1 9 13 10.1016/j.ijbiomac.2012.09.029 2-s2.0-84868571785
19. Lopes N., Faccin-Galhardi L. C., Espada S. F., Pacheco A. C., Ricardo N. M. P. S., Linhares R. E. C., Nozawa C., Sulfated polysaccharide of Caesalpinia ferrea inhibits herpes simplex virus and poliovirus. International Journal of Biological Macromolecules 2013 60 93 99 10.1016/j.ijbiomac.2013.05.015 2-s2.0-84879171230
20. Nishimura T., Toku H., Fukuyasu H., Antiviral compounds. XII. Antiviral activity of amidinohydrazones of alkoxyphenyl-substituted carbonyl compounds against influenza virus in eggs and in mice. Kitazato Archives of Experimental Medicine 1977 50 1-2 39 46 2-s2.0-0017569703
21. Minari M. C., Rincão V. P., Soares S. A., Ricardo N. M. P. S., Nozawa C., Linhares R. E. C., Antiviral properties of polysaccharides from Agaricus brasiliensis in the replication of bovine herpesvirus 1. Acta Virologica 2011 55 3 255 259 10.4149/av-2011-03-255 2-s2.0-84855931929
22. Faccin L. C., Benati F., Rincão V. P., Mantovani M. S., Soares S. A., Gonzaga M. L., Nozawa C., Carvalho Linhares R. E., Antiviral activity of aqueous and ethanol extracts and of an isolated polysaccharide from Agaricus brasiliensis against poliovirus type 1. Letters in Applied Microbiology 2007 45 1 24 28 10.1111/j.1472-765X.2007.02153.x 2-s2.0-34347339602
23. Faccin-Galhardi L. C., Aimi Yamamoto K., Ray S., Ray B., Carvalho Linhares R. E., Nozawa C., The in vitro antiviral property of Azadirachta indica polysaccharides for poliovirus. Journal of Ethnopharmacology 2012 142 1 86 90 10.1016/j.jep.2012.04.018 2-s2.0-84861964245
24. Mähner C., Lechner M. D., Nordmeier E., Synthesis and characterisation of dextran and pullulan sulphate. Carbohydrate Research 2001 331 2 203 208 10.1016/S0008-6215(00)00315-3 2-s2.0-0035932542
25. Yang J., Du Y., Wen Y., Li T., Hu L., Sulfation of Chinese lacquer polysaccharides in different solvents. Carbohydrate Polymers 2003 52 4 397 403 10.1016/S0144-8617(02)00330-2 2-s2.0-0037410658
26. Cerqueira M. A., Souza B. W. S., Simões J., Teixeira J. A., Domingues M. R. M., Coimbra M. A., Vicente A. A., Structural and thermal characterization of galactomannans from non-conventional sources. Carbohydrate Polymers 2011 83 1 179 185 10.1016/j.carbpol.2010.07.036 2-s2.0-77957309542
27. Hu C., Kong Q., Yang D., Pan Y., Isolation and structural characterization of a novel galactomannan from Eremurus anisopterus (Ker. et Kir) Regel roots. Carbohydrate Polymers 2011 84 1 402 406 10.1016/j.carbpol.2010.11.054 2-s2.0-78951482364
28. Shobha M. S., Vishu Kumar A. B., Tharanathan R. N., Koka R., Gaonkar A. K., Modification of guar galactomannan with the aid of Aspergillus niger pectinase. Carbohydrate Polymers 2005 62 3 267 273 10.1016/j.carbpol.2005.07.031 2-s2.0-28444475255
29. Mudgil D., Barak S., Khatkar B. S., X-ray diffraction, IR spectroscopy and thermal characterization of partially hydrolyzed guar gum. International Journal of Biological Macromolecules 2012 50 4 1035 1039 10.1016/j.ijbiomac.2012.02.031 2-s2.0-84860238193
30. Figueiró S. D., Góes J. C., Moreira R. A., Sombra A. S. B., On the physico-chemical and dielectric properties of glutaraldehyde crosslinked galactomannan-collagen films. Carbohydrate Polymers 2004 56 3 313 320 10.1016/j.carbpol.2004.01.011 2-s2.0-2942675033
31. Chrestani F., Sierakowski M. R., de Andrade Uchoa D. E., Nozawa C., Sassaki G. L., Gorin P. A. J., Ono L., In vitro antiherpetic and antirotaviral activities of a sulfate prepared from Mimosa scabrella galactomannan. International Journal of Biological Macromolecules 2009 45 5 453 457 10.1016/j.ijbiomac.2009.09.003 2-s2.0-70350342869
32. Soltan M. M., Zaki A. K., Antiviral screening of forty-two Egyptian medicinal plants. Journal of Ethnopharmacology 2009 126 1 102 107 10.1016/j.jep.2009.08.001 2-s2.0-70349959903
33. Zandi K., Taherzadeh M., Tajbakhsh S., Yaghoubi R., Rastian Z., Sartavi K., Antiviral activity of Avicennia marina leaf extract on HSV-1 and vaccine strain of polio virus in vero cells. International Journal of Infectious Diseases 2008 12 supplement 1 e298 10.1016/j.ijid.2008.05.800
34. Song X., Yin Z., Li L., Cheng A., Jia R., Xu J., Wang Y., Yao X., Lv C., Zhao X., Antiviral activity of sulfated Chuanminshen violaceum polysaccharide against duck enteritis virus in vitro. Antiviral Research 2013 98 2 344 351 10.1016/j.antiviral.2013.03.012 2-s2.0-84880437114
35. Saha S., Galhardi L. C. F., Yamamoto K. A., Linhares R. E. C., Bandyopadhyay S. S., Sinha S., Nozawa C., Ray B., Water-extracted polysaccharides from Azadirachta indica leaves: structural features, chemical modification and anti-bovine herpesvirus type 1 (BoHV-1) activity. International Journal of Biological Macromolecules 2010 47 5 640 645 10.1016/j.ijbiomac.2010.08.011 2-s2.0-77958167443
36. Biesert L., Adamski M., Zimmer G., Suhartono H., Fuchs J., Unkelbach U., Melhorn R. J., Hideg K., Milbradt R., Rubsamen-Waigmann H., Anti-human immunodeficiency virus (HIV) drug HOE/BAY 946 increases membrane hydrophobicity of human lymphocytes and specifically suppresses HIV-protein synthesis. Medical Microbiology and Immunology 1990 179 6 307 321 2-s2.0-0025668207