Physico-chemical characterization and pharmacological activities of sulfated polysaccharide from sea urchin, Paracentrotus lividus

International Journal of Biological Macromolecules

Volumn 97, Issue , 2017, Pages 8-15

  Salem, Yosra Ben ^a   Amri, Safa ^b   Hammi, Khaoula Mkadmini ^c   Abdelhamid, Amal ^b   Cerf, Didier Le ^d   Bouraoui, Abderrahman ^b   Majdoub, Hatem ^a  

^a FACULTÉ DES SCIENCES DE MONASTIR   (Tunisia)

^b UNIVERSITY OF MONASTIR   (Tunisia)

^c CENTRE DE BIOTECHNOLOGIE DE BORJ CÉDRIA   (Tunisia)

^d UNIVERSITÉ ET INSA DE ROUEN   (France)

Author keywords

Paracentrotus lividus; Pharmacological activities; Physico chemical characterization; Sulfated polysaccharide

Indexed keywords

ARABINOSE; CARBOHYDRATE; FUCOSE; GALACTOSE; GLUCOSE; LYSINE ACETYLSALICYLATE; OMEPRAZOLE; POLYSACCHARIDE SULFATE; PROTEIN; RANITIDINE; SULFATE; TRAMADOL; URONIC ACID; ANALGESIC AGENT; MONOSACCHARIDE; NONSTEROID ANTIINFLAMMATORY AGENT; POLYSACCHARIDE;

ANALGESIC ACTIVITY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIINFLAMMATORY ACTIVITY; ANTIULCER ACTIVITY; ARTICLE; CARRAGEENAN-INDUCED PAW EDEMA; CONTROLLED STUDY; DRUG MECHANISM; EXPERIMENTAL GASTRIC ULCER; FEMALE; HOT PLATE TEST; IN VIVO STUDY; INFRARED SPECTROSCOPY; LATENT PERIOD; LIGHT SCATTERING; MALE; MASS FRAGMENTOGRAPHY; MOLECULAR WEIGHT; MOUSE; NOCICEPTION; NONHUMAN; PARACENTROTUS LIVIDUS; PHYSICAL CHEMISTRY; RAT; REACTION TIME; SALINITY; SIZE EXCLUSION CHROMATOGRAPHY; STOMACH PROTECTION; SWISS WEBSTER MOUSE; TEMPERATURE; VISCERAL PAIN; WRITHING TEST; ANIMAL; CHEMICAL PHENOMENA; CHEMISTRY; EDEMA; PARACENTROTUS;

ANALGESICS; ANIMALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; CHEMICAL PHENOMENA; EDEMA; MICE; MOLECULAR WEIGHT; MONOSACCHARIDES; PARACENTROTUS; POLYSACCHARIDES; RATS; SULFATES;

EID: 85008693003     PISSN: 01418130     EISSN: 18790003     Source Type: Journal    
DOI: 10.1016/j.ijbiomac.2017.01.007     Document Type: Article

References (56)

1. [1] Tian, H., Yin, X., Zeng, Q., Zhu, L., Chen, J., Isolation, structure, and surfactant properties of polysaccharides from Ulva lactuca L. from South China Sea. Int. J. Biol. Macromol. 79 (2015), 577–582.
2. [2] Shao, P., Chen, X., Sun, P., Chemical characterization, antioxidant and antitumor activity of sulfated polysaccharide from Sargassum horneri. Carbohydr. Polym. 105 (2014), 260–269.
3. [3] Souza, B.W., Cerqueira, M.A., Bourbon, A.I., Pinheiro, A.C., Martins, J.T., Teixeira, J.A., Coimbra, M.A., Vicente, A.A., Chemical characterization and antioxidant activity of sulfated polysaccharide from the red seaweed Gracilaria birdiae. Food Hydrocolloids 27:2 (2012), 287–292.
4. [4] de Jesus Raposo, M.F., de Morais, A.M.B., de Morais, R.M.S.C., Marine polysaccharides from algae with potential biomedical applications. Mar. Drugs 13:5 (2015), 2967–3028.
5. [5] Chi, A., Li, H., Kang, C., Guo, H., Wang, Y., Guo, F., Tang, L., Anti-fatigue activity of a novel polysaccharide conjugates from Ziyang green tea. Int. J. Biol. Macromol. 80 (2015), 566–572.
6. [6] Jiao, H., Shang, X., Dong, Q., Wang, S., Liu, X., Zheng, H., Lu, X., Polysaccharide constituents of three types of sea urchin shells and their anti-inflammatory activities. Mar. Drugs 13:9 (2015), 5882–5900.
7. [7] Zhu, B.-W., Qin, L., Zhou, D.-Y., Wu, H.-T., Wu, J., Yang, J.-F., Li, D.-M., Dong, X.-P., Murata, Y., Extraction of lipid from sea urchin (Strongylocentrotus nudus) gonad by enzyme-assisted aqueous and supercritical carbon dioxide methods. Eur. Food Res. Technol. 230:5 (2010), 737–743.
8. [8] de Quiros, A.R.-B., Lopez-Hernandez, J., Simal-Lozano, J., Separation of phospholipid classes in sea urchin, Paracentrotus lividus by high-performance liquid chromatography. J. Chromatogr. B 770:1 (2002), 71–75.
9. [9] Zar, J., Biostatistical Analysis. 2nd edition, 1984, Printice Hall, New York.
10. [10] Qin, L., Zhu, B.-W., Zhou, D.-Y., Wu, H.-T., Tan, H., Yang, J.-F., Li, D.-M., Dong, X.-P., Murata, Y., Preparation and antioxidant activity of enzymatic hydrolysates from purple sea urchin (Strongylocentrotus nudus) gonad. LWT-Food Sci. Technol. 44:4 (2011), 1113–1118.
11. [11] Cinelli, L.P., Andrade, L., Valente, A.P., Mourão, P.A., Sulfated α-L-galactans from the sea urchin ovary: selective 6-desulfation as eggs are spawned. Glycobiology 20:6 (2010), 702–709.
12. [12] Wrolstad, R.E., Acree, T.E., Decker, E.A., Penner, M.H., Reid, D.S., Schwartz, S.J., Shoemaker, C.F., Smith, D.M., Sporns, P., Handbook of food analytical chemistry. Water, Proteins, Enzymes, Lipids, and Carbohydrates, vol 1, 2005, John Wiley & Sons.
13. [13] la Cruz‐García, D., López‐Hernández, J., González‐Castro, M.J., Rodríguez‐BernaldoD De Quirós, A.I., Simal‐Lozano, J., Protein, amino acid and fatty acid contents in raw and canned sea urchin (Paracentrotus lividus) harvested in Galicia (NW Spain). J. Sci. Food Agric. 80:8 (2000), 1189–1192.
14. [14] Dincer, T., Cakli, S., Chemical composition and biometrical measurements of the Turkish sea urchin (Paracentrotus lividus, Lamarck, 1816). Crit. Rev. Food Sci. Nutr. 44:7 (2007), 21–26.
15. [15] Mansour, M.B., Majdoub, H., Bataille, I., Roudesli, M.S., Hassine, M., Ajzenberg, N., Chaubet, F., Maaroufi, R.M., Polysaccharides from the skin of the ray Raja radula. Partial characterization and anticoagulant activity. Thromb. Res. 123:4 (2009), 671–678.
16. [16] Dubois, M., Gilles, K.A., Hamilton, J.K., Rebers, P., Smith, F., Colorimetric method for determination of sugars and related substances. Anal. Chem. 28:3 (1956), 350–356.
17. [17] Lowry, O.H., Rosebrough, N.J., Farr, A.L., Randall, R.J., Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193:1 (1951), 265–275.
18. [18] Bitter, T., Muir, H.M., A modified uronic acid carbazole reaction. Anal. Biochem. 4:4 (1962), 330–334.
19. [19] Dodgson, K., Price, R., A note on the determination of the ester sulphate content of sulphated polysaccharides. Biochem. J., 84(1), 1962, 106.
20. [20] Chaouch, M.A., Hafsa, J., Rihouey, C., Le Cerf, D., Majdoub, H., Depolymerization of polysaccharides from Opuntia ficus indica: antioxidant and antiglycated activities. Int. J. Biol. Macromol. 79 (2015), 779–786.
21. [21] Zimm, B.H., The scattering of light and the radial distribution function of high polymer solutions. J. Chem. Phys. 16:12 (1948), 1093–1099.
22. [22] Majdoub, H., Roudesli, S., Deratani, A., Polysaccharides from prickly pear peel and nopals of Opuntia ficus‐indica: extraction, characterization and polyelectrolyte behaviour. Polym. Int. 50:5 (2001), 552–560.
23. [23] Ali, G., Rihouey, C., Larreta-Garde, V.r., Le Cerf, D., Picton, L., Molecular size characterization and kinetics studies on hydrolysis of pullulan by pullulanase in an entangled alginate medium. Biomacromolecules 14:7 (2013), 2234–2241.
24. [24] Mkadmini Hammi, K., Hammami, M., Rihouey, C., Le Cerf, D., Ksouri, R., Majdoub, H., Optimization extraction of polysaccharide from Tunisian Zizyphus lotus fruit by response surface methodology: composition and antioxidant activity. Food Chem. 212 (2016), 476–484.
25. [25] Guentas, L., Pheulpin, P., Michaud, P., Heyraud, A., Gey, C., Courtois, B., Courtois, J., Structure of a polysaccharide from a Rhizobium species containing 2-deoxy-β-d-arabino-hexuronic acid. Carbohydr. Res. 332:2 (2001), 167–173.
26. [26] Medeiros, P.M., Simoneit, B.R.T., Analysis of sugars in environmental samples by gas chromatography–mass spectrometry. J. Chromatogr. A 1141:2 (2007), 271–278.
27. [27] Winter, C.A., Risley, E.A., Nuss, G.W., Carrageenin-induced edema in hind paw of the rat as an assay for antiinflammatory drugs. Exp. Biol. Med. 111:3 (1962), 544–547.
28. [28] Lanhers, M.-C., Fleurentin, J., Dorfman, P., Mortier, F., Pelt, J.-m., Analgesic, antipyretic and anti-inflammatory properties of Euphorbia hirta. Planta Med. 57:3 (1991), 225–231.
29. [29] Amir, M., Shikha, K., Synthesis and analgesic anti-inflammatory ulcerogenic and lipid peroxidation activities of some new 2-[(2, 6-dichloroanilino) phenyl] acetic acid derivatives. Eur. J. Med. Chem. 39:6 (2004), 535–545.
30. [30] Eddy, N.B., Leimbach, D., Synthetic analgesics. II. dithienylbutenyl-and dithienylbutylamines. J. Pharmacol. Exp. Ther. 107:3 (1953), 385–393.
31. [31] Colucci, M., Maione, F., Bonito, M.C., Piscopo, A., Di Giannuario, A., Pieretti, S., New insights of dimethyl sulphoxide effects (DMSO) on experimental in vivo models of nociception and inflammation. Pharmacol. Res. 57:6 (2008), 419–425.
32. [32] Lajili, S., Deghrigue, M., Bel, H., Haj Amor, Muller, A., In vitro immunomodulatory activity and in vivo anti-inflammatory and analgesic potential with gastroprotective effect of the Mediterranean red alga Laurencia obtusa. Pharm. Biol., 2016, 1–10.
33. [33] Hara, N., Okabe, S., [Effects of gefarnate on acute gastric lesions in rats]: Nihon yakurigaku zasshi. Folia Pharmacologica Japonica 85:6 (1985), 443–446.
34. [34] Liu, X., Sun, Z., Zhang, M., Meng, X., Xia, X., Yuan, W., Xue, F., Liu, C., activities, Antioxidant and antihyperlipidemic activities of polysaccharides from sea cucumber Apostichopus japonicus. Carbohydr. Polym. 90:4 (2012), 1664–1670.
35. [35] Zhu, B.-W., Zhou, D.-y., Li, T., Yan, S., Yang, J.-f., Li, D.-m., Dong, X.-p., Murata, Y., Chemical composition and free radical scavenging activities of a sulphated polysaccharide extracted from abalone gonad (Haliotis Discus Hannai Ino). Food Chem. 121:3 (2010), 712–718.
36. [36] Liu, C., Lin, Q., Gao, Y., Ye, L., Xing, Y., Xi, T., Characterization and antitumor activity of a polysaccharide from Strongylocentrotus nudus eggs. Carbohydr. Polym. 67:3 (2007), 313–318.
37. [37] Vilela-Silva, A.-C.E., Hirohashi, N., Mourão, P.A., The structure of sulfated polysaccharides ensures a carbohydrate-based mechanism for species recognition during sea urchin fertilization. Int. J. Dev. Biol. 52:5-6 (2004), 551–559.
38. [38] Cinelli, L.P., Vilela-Silva, A.-C.E., Mourão, P.A., Seminal fluid from sea urchin (Lytechinus variegatus) contains complex sulfated polysaccharides linked to protein. Comp. Biochem. Physiol. B: Biochem. Mol. Biol. 154:1 (2009), 108–112.
39. [39] Alves, A.-P., Mulloy, B., Moy, G.W., Vacquier, V.D., Mourão, P.A., Females of the sea urchin Strongylocentrotus purpuratus differ in the structures of their egg jelly sulfated fucans. Glycobiology 8:9 (1998), 939–946.
40. [40] Yang, X., Wang, R., Zhang, S., Zhu, W., Tang, J., Liu, J., Chen, P., Zhang, D., Ye, W., Zheng, Y., Polysaccharides from Panax japonicus CA Meyer and their antioxidant activities. Carbohydr. Polym. 101 (2014), 386–391.
41. [41] Kacurakova, M., Capek, P., Sasinkova, V., Wellner, N., Ebringerova, A., FT-IR study of plant cell wall model compounds: pectic polysaccharides and hemicelluloses. Carbohydr. Polym. 43:2 (2000), 195–203.
42. [42] Pawlaczyk, I., Czerchawski, L., Kuliczkowski, W., Karolko, B., Pilecki, W., Witkiewicz, W., Gancarz, R., Anticoagulant and anti-platelet activity of polyphenolic-polysaccharide preparation isolated from the medicinal plant Erigeron canadensis L. Thromb. Res. 127:4 (2011), 328–340.
43. [43] Villay, A., de Filippis, F.L., Picton, L., Le Cerf, D., Vial, C., Michaud, P., Comparison of polysaccharide degradations by dynamic high-pressure homogenization. Food Hydrocolloids 27:2 (2012), 278–286.
44. [44] Ammar, H.H., Lajili, S., Said, R.B., Le Cerf, D., Bouraoui, A., Majdoub, H., Physico-chemical characterization and pharmacological evaluation of sulfated polysaccharides from three species of Mediterranean brown algae of the genus Cystoseira. DARU J. Pharm. Sci., 23(1), 2015, 1.
45. [45] Weiner, R., Thakur, M., Imaging infection/inflammations: pathophysiologic basis and radiopharmaceuticals. Q. J. Nucl. Med. Mol. Imaging, 43(1), 1999, 2.
46. [46] Kang, S.-M., Kim, K.-N., Lee, S.-H., Ahn, G., Cha, S.-H., Kim, A.-D., Yang, X.-D., Kang, M.-C., Jeon, Y.-J., Anti-inflammatory activity of polysaccharide purified from AMG-assistant extract of Ecklonia cava in LPS-stimulated RAW 264.7 macrophages. Carbohydr. Polym. 85:1 (2011), 80–85.
47. [47] Park, H.Y., Han, M.H., Park, C., Jin, C.-Y., Kim, G.-Y., Choi, I.-W., Kim, N.D., Nam, T.-J., Kwon, T.K., Choi, Y.H., Anti-inflammatory effects of fucoidan through inhibition of NF-κB, MAPK and Akt activation in lipopolysaccharide-induced BV2 microglia cells. Food Chem. Toxicol. 49:8 (2011), 1745–1752.
48. [48] Collier, H., Dinneen, L., JOHNSON, C.A., Schneider, C., The abdominal constriction response and its suppression by analgesic drugs in the mouse. Brit. J. Pharmacol. Chemother. 32:2 (1968), 295–310.
49. [49] Rodrigues, J.A., de SO, E., Vanderlei, L.M., Silva, I.W., de Araújo, I.N., de Queiroz, G.A., de Paula, T.M., Abreu, N.A., Ribeiro, M.M., Bezerra, H.V., Antinociceptive Chaves anti-inflammatory activities of a sulfated polysaccharide isolated from the green seaweed Caulerpa cupressoides. Pharmacol. Rep. 64:2 (2012), 282–292.
50. [50] Mellinger-Silva, C., Simas-Tosin, F.F., Schiavini, D.N., Werner, M.F., Baggio, C.H., Pereira, I.T., Da Silva, L.M., Gorin, P.A., Iacomini, M., Isolation of a gastroprotective arabinoxylan from sugarcane bagasse. Bioresour. Technol. 102:22 (2011), 10524–10528.
51. [51] Nergard, C.S., Diallo, D., Inngjerdingen, K., Michaelsen, T.E., Matsumoto, T., Kiyohara, H., Yamada, H., Paulsen, B.S., Medicinal use of Cochlospermum tinctorium in Mali: anti-ulcer-, radical scavenging-and immunomodulating activities of polymers in the aqueous extract of the roots. J. Ethnopharmacol. 96:1 (2005), 255–269.
52. [52] Cipriani, T.R., Mellinger, C.G., Bertolini, M.L., Baggio, C.H., Freitas, C.S., Marques, M.C.A., Gorin, P.A., Sassaki, G.L., Iacomini, M., Gastroprotective effect of a type I arabinogalactan from soybean meal. Food Chem. 115:2 (2009), 687–690.
53. [53] Shibata, H., Kimura-Takagi, I., Nagaoka, M., Hashimoto, S., Aiyama, R., Iha, M., Ueyama, S., Yokokura, T., Properties of fucoidan from Cladosiphon okamuranus tokida in gastric mucosal protection. Biofactors 11:4 (2000), 235–245.
54. [54] Itsuko, K., Masato, N., Shusuke, H., Haruji, S., Teruo, Y., Antiulcer Agent and Adhesion Inhibitor for. 1994, Helicobacter pylori.
55. [55] Choi, J.-i., Raghavendran, H.R.B., Sung, N.-Y., Kim, J.-H., Chun, B.S., Ahn, D.H., Choi, H.-S., Kang, K.-W., Lee, J.-W., Effect of fucoidan on aspirin-induced stomach ulceration in rats. Chem. Biol. Interact. 183:1 (2010), 249–254.
56. [56] Pomin, V.H., Fucanomics and galactanomics. Marine distribution, medicinal impact, conceptions, and challenges. Marine drugs 10:4 (2012), 793–811.