Protective effect of Anoectochilus roxburghii polysaccharide against CCl4-induced oxidative liver damage in mice

International Journal of Biological Macromolecules

Volumn 96, Issue , 2017, Pages 442-450

  Li, Juan ^d   Zhang, Xiaohui ^c   Yang, Lawei ^a,c   Pan, Qunwen ^a,c   Chen, Meizhen ^c   Cui, Shichao ^b,c   Yu, Jie ^c  

^a GUANGDONG MEDICAL UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

^c SHANTOU UNIVERSITY   (China)

^d Shantou Ecological Environment Technology Center   (China)

Author keywords

Anoectochilus roxburghii; Hepatoprotective effects; Polysaccharide

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; ALANINE AMINOTRANSFERASE; ANOECTOCHILUS ROXBURGHII EXTRACT; ASCORBIC ACID; ASPARTATE AMINOTRANSFERASE; CARBON TETRACHLORIDE; GALACTOSE; GLUCOSE; GLUTATHIONE; HYDROXYL RADICAL; MALONALDEHYDE; PLANT EXTRACT; POLYSACCHARIDE; SUPEROXIDE; SUPEROXIDE DISMUTASE; TRIACYLGLYCEROL; UNCLASSIFIED DRUG; ANTIOXIDANT; MONOSACCHARIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANOECTOCHILUS ROXBURGHII; ANTIOXIDANT ACTIVITY; ARTICLE; CARBOHYDRATE ANALYSIS; CONCENTRATION RESPONSE; CONTROLLED STUDY; DOWN REGULATION; DRUG DETERMINATION; DRUG EFFECT; DRUG IDENTIFICATION; DRUG ISOLATION; DRUG MECHANISM; DRUG PURIFICATION; DRUG SCREENING; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; FEMALE; HISTOPATHOLOGY; IN VITRO STUDY; IN VIVO STUDY; LIPID OXIDATION; LIVER INJURY; LIVER PROTECTION; MALE; MOLECULAR WEIGHT; MOUSE; NONHUMAN; ORCHIDACEAE; PROTEIN EXPRESSION; TRIACYLGLYCEROL BLOOD LEVEL; UPREGULATION; ANIMAL; BLOOD; CHEMICAL AND DRUG INDUCED LIVER INJURY; CHEMISTRY; DRUG EFFECTS; LIVER; METABOLISM; OXIDATIVE STRESS; PATHOLOGY;

ANIMALS; ANTIOXIDANTS; CARBON TETRACHLORIDE; CHEMICAL AND DRUG INDUCED LIVER INJURY; GLUTATHIONE; LIVER; MALONDIALDEHYDE; MICE; MONOSACCHARIDES; ORCHIDACEAE; OXIDATIVE STRESS; POLYSACCHARIDES; SUPEROXIDE DISMUTASE;

EID: 85007439875     PISSN: 01418130     EISSN: 18790003     Source Type: Journal    
DOI: 10.1016/j.ijbiomac.2016.12.039     Document Type: Article

References (44)

1. [1] Sun, B., Karin, M., Nf-Kappab signaling, liver disease and hepatoprotective agents. Oncogene 27 (2008), 6228–6244.
2. [2] Na, J.Y., Song, K., Kim, S., Kwon, J., Hepatoprotective effect of phosphatidylcholine against carbon tetrachloride liver damage in mice. Biochem. Biophys. Res. Commun. 460 (2015), 308–313.
3. [3] Haretskaya, M.V., Sheibak, V.M., Hepatoprotective properties of taurine during carbon tetrachloride intoxication. Biochem. (Moscow) Suppl. Ser. B: Biomed. Chem. 8 (2014), 286–292.
4. [4] Recknagel, R.O., Glende, E.A. Jr., Dolak, J.A., Waller, R.L., Mechanisms of carbon tetrachloride toxicity. Pharmacol. Ther. 43 (1989), 139–154.
5. 4 by cytochrome P450 enzymes and the ccl4-dependent suicidal inactivation of P450. Dalton Trans. (Cambridge, England: 2003) 43 (2014), 14833–14840.
6. [6] Sato, A., Nakashima, H., Nakashima, M., Ikarashi, M., Nishiyama, K., Kinoshita, M., Seki, S., Involvement of the tnf and fasl produced by cd11b kupffer cells/macrophages in ccl4-induced acute hepatic injury. PLoS One, 9, 2014, e92515.
7. [7] Kim, Y., You, Y., Yoon, H.G., Lee, Y.H., Kim, K., Lee, J., Kim, M.S., Kim, J.C., Jun, W., Hepatoprotective effects of fermented Curcuma longa L. on carbon tetrachloride-induced oxidative stress in rats. Food Chem. 151 (2014), 148–153.
8. [8] Liu, J., Lu, J.F., Wen, X.Y., Kan, J., Jin, C.H., Antioxidant and protective effect of inulin and catechin grafted inulin against ccl4-induced liver injury. Int. J. Biol. Macromol. 72 (2015), 1479–1484.
9. [9] Colak, E., Ustuner, M.C., Tekin, N., Colak, E., Burukoglu, D., Degirmenci, I., Gunes, H.V., The hepatocurative effects of Cynara scolymus L. leaf extract on carbon tetrachloride-induced oxidative stress and hepatic injury in rats. SpringerPlus, 5, 2016, 216.
10. [10] Yang, L.-C., Lu, T.-J., Lin, W.-C., The prebiotic arabinogalactan of anoectochilus formosanus prevents ovariectomy-induced osteoporosis in mice. J. Funct. Foods 5 (2013), 1642–1653.
11. [11] Cui, S.C., Yu, J., Zhang, X.H., Cheng, M.Z., Yang, L.W., Xu, J.Y., Antihyperglycemic and antioxidant activity of water extract from anoectochilus roxburghii in experimental diabetes. Exp. Toxicol. Pathol. 65 (2013), 485–488.
12. [12] Tseng, C.C., Shang, H.F., Wang, L.F., Su, B., Hsu, C.C., Kao, H.Y., Cheng, K.T., Antitumor and immunostimulating effects of anoectochilus formosanus hayata. Phytomedicine 13 (2006), 366–370.
13. [13] Li, L., Li, Y.M., Liu, Z.L., Zhang, J.G., Liu, Q., Yi, L.T., The renal protective effects of anoectochilus roxburghii polysaccharose on diabetic mice induced by high-fat diet and streptozotocin. J.Ethnopharmacol 178 (2016), 58–65.
14. [14] Du, X.M., Sun, N.Y., Hayashi, J., Chen, Y., Sugiura, M., Shoyama, Y., Hepatoprotective and antihyperliposis activities of in vitro cultured anoectochilus formosanus. Phytother. Res. 17 (2003), 30–33.
15. [15] Shih, C.C., Wu, Y.W., Lin, W.C., Aqueous extract of anoectochilus formosanus attenuate hepatic fibrosis induced by carbon tetrachloride in rats. Phytomedicine 12 (2005), 453–460.
16. [16] Wu, J.B., Lin, W.L., Hsieh, C.C., Ho, H.Y., Tsay, H.S., Lin, W.C., The hepatoprotective activity of kinsenoside from anoectochilus formosanus. Phytother. Res. 21 (2007), 58–61.
17. [17] Hsieh, W.T., Tsai, C.T., Wu, J.B., Hsiao, H.B., Yang, L.C., Lin, W.C., Kinsenoside, a high yielding constituent from anoectochilus formosanus inhibits carbon tetrachloride induced kupffer cells mediated liver damage. J. Ethnopharmacol. 135 (2011), 440–449.
18. [18] Shim, J.Y., Kim, M.H., Kim, H.D., Ahn, J.Y., Yun, Y.S., Song, J.Y., Protective action of the immunomodulator ginsan against carbon tetrachloride-Induced liver injury via control of oxidative stress and the inflammatory response. Toxicol. Appl. Pharmacol. 242 (2010), 318–325.
19. [19] Zhang, L., Zhang, W., Wang, Q., Wang, D., Dong, D., Mu, H., Ye, X.S., Duan, J., Purification, antioxidant and immunological activities of polysaccharides from actinidia chinensis roots. Int. J. Biol. Macromol. 72 (2015), 975–983.
20. [20] Zhang, Z., Lv, G., Pan, H., Pandey, A., He, W., Fan, L., Antioxidant and hepatoprotective potential of endo-polysaccharides from hericium erinaceus grown on tofu whey. Int. J. Biol. Macromol. 51 (2012), 1140–1146.
21. [21] Yang, L.C., Lin, W.C., Lu, T.J., Characterization and prebiotic activity of aqueous extract and indigestible polysaccharide from anoectochilus formosanus. J. Agric. Food Chem. 60 (2012), 8590–8599.
22. [22] Vilkas, E., Radjabi-Nassab, F., The glucomannan system from aloe vahombe (Liliaceae). iii. Comparative studies on the glucomannan components isolated from the leaves. Biochimie 68 (1986), 1123–1127.
23. [23] DuBois, M., Gilles, K.A., Hamilton, J.K., Rebers, P.A., Smith, F., Colorimetric method for determination of sugars and related substances. Anal. Chem. 28 (1956), 350–356.
24. [24] Compton, S.J., Jones, C.G., Mechanism of dye response and interference in the bradford protein assay. Anal. Biochem. 151 (1985), 369–374.
25. [25] Yuan, Q., Xie, Y., Wang, W., Yan, Y., Ye, H., Jabbar, S., Zeng, X., Extraction optimization, characterization and antioxidant activity in vitro of polysaccharides from mulberry (Morus alba L.) leaves. Carbohydr. Polym. 128 (2015), 52–62.
26. [26] Chen, G.T., Ma, X.M., Liu, S.T., Liao, Y.L., Zhao, G.Q., Isolation, purification and antioxidant activities of polysaccharides from grifola frondosa. Carbohydr. Polym. 89 (2012), 61–66.
27. [27] Tian, L., Zhao, Y., Guo, C., Yang, X., A comparative study on the antioxidant activities of an acidic polysaccharide and various solvent extracts derived from herbal houttuynia cordata. Carbohydr. Polym. 83 (2011), 537–544.
28. [28] Reitman, S., Frankel, S., A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am. J. Clin. Pathol. 28 (1957), 56–63.
29. [29] Wang, R., Chen, P., Jia, F., Tang, J., Ma, F., Optimization of polysaccharides from panax japonicus C.A. meyer by rsm and its anti-oxidant activity. Int. J. Biol. Macromol. 50 (2012), 331–336.
30. [30] Zhao, M., Yang, N., Yang, B., Jiang, Y., Zhang, G., Structural characterization of water-soluble polysaccharides from opuntia monacantha cladodes in relation to their anti-glycated activities. Food Chem. 105 (2007), 1480–1486.
31. [31] Černá, M., Barros, A.S., Nunes, A., Rocha, S.l.M., Delgadillo, I., Čopı́ková, J., Coimbra, M.A., Use of Ft-Ir spectroscopy as a tool for the analysis of polysaccharide food additives. Carbohydr. Polym. 51 (2003), 383–389.
32. [32] Luo, J., Liu, J., Sun, Y., Ye, H., Zhou, C., Zeng, X., Medium optimization, preliminary characterization and antioxidant activity in vivo of mycelial polysaccharide from phellinus baumii pilát. Carbohydr. Polym. 81 (2010), 533–540.
33. [33] Lai, F., Wen, Q., Li, L., Wu, H., Li, X., Antioxidant activities of water-soluble polysaccharide extracted from mung bean (Vigna radiata L.) hull with ultrasonic assisted treatment. Carbohydr. Polym. 81 (2010), 323–329.
34. [34] Han, X., Shen, S., Liu, T., Du, X., Cao, X., Feng, H., Zeng, X., Characterization and antioxidant activities of the polysaccharides from radix cyathulae officinalis kuan. Int. J. Biol. Macromol. 72 (2015), 544–552.
35. [35] Ma, L., Gan, D., Wang, M., Zhang, Z., Jiang, C., Zeng, X., Optimization of extraction, preliminary characterization and hepatoprotective effects of polysaccharides from stachys floridana schuttl. Ex Benth. Carbohydr. Polym. 87 (2012), 1390–1398.
36. [36] Campo, G.M., Avenoso, A., Campo, S., Nastasi, G., Traina, P., D'Ascola, A., Rugolo, C.A., Calatroni, A., The antioxidant activity of chondroitin-4-sulphate, in carbon tetrachloride-induced acute hepatitis in mice involves Nf-kappab and caspase activation. Br. J. Pharmacol. 155 (2008), 945–956.
37. [37] Yu, J., Cui, P.-J., Zeng, W.-L., Xie, X.-L., Liang, W.-J., Lin, G.-B., Zeng, L., Protective effect of selenium-polysaccharides from the mycelia of coprinus comatus on alloxan-induced oxidative stress in mice. Food Chem. 117 (2009), 42–47.
38. [38] Goldberg, D.M., Watts, C., Serum enzyme changes as evidence of liver reaction to oral alcohol. Gastroenterology 49 (1965), 256–261.
39. [39] Recknagel, R.O., Glende, E.A. Jr., Dolak, J.A., Waller, R.L., Mechanisms of carbon tetrachloride toxicity. Pharmacol. Ther. 43 (1989), 139–154.
40. [40] Abuja, P.M., Albertini, R., Methods for monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins. Clin. Chim. Acta 306 (2001), 1–17.
41. [41] Freeman, B.A., Crapo, J.D., Biology of disease: free radicals and tissue injury. Lab. Invest. 47 (1982), 412–426.
42. [42] Cemek, M., Aymelek, F., Buyukokuroglu, M.E., Karaca, T., Buyukben, A., Yilmaz, F., Protective potential of royal jelly against carbon tetrachloride induced-Toxicity and changes in the serum sialic acid levels. Food Chem. Toxicol. 48 (2010), 2827–2832.
43. [43] Shafi, A., Gill, T., Sreenivasulu, Y., Kumar, S., Ahuja, P.S., Singh, A.K., Improved callus induction, shoot regeneration, and salt stress tolerance in arabidopsis overexpressing superoxide dismutase from potentilla atrosanguinea. Protoplasma 252 (2015), 41–51.
44. [44] Salvi, M., Battaglia, V., Brunati, A.M., La Rocca, N., Tibaldi, E., Pietrangeli, P., Marcocci, L., Mondovi, B., Rossi, C.A., Toninello, A., Catalase takes part in rat liver mitochondria oxidative stress defense. J. Biol. Chem. 282 (2007), 24407–24415.