Pleurotus ostreatus, an edible mushroom, enhances glucose 6-phosphate dehydrogenase, ascorbate peroxidase and reduces xanthine dehydrogenase in major organs of aged rats

References

• Arivazhagan P, Shila S, Kumaran S, Panneerselvam C. (2002). Effect of dl-α-lipoic acid on the status of lipid peroxidation and antioxidant enzymes in various brain regions of aged rats. Exp Gerontol 37:803–11
   PubMed Web of Science ®Google Scholar
• Asada K. (1999). The water-water cycle in chloroplasts: Scavenging of active oxygen and dissipation of excess photons. Annu Rev Plant Mol Biol 50:601–39
   PubMed Web of Science ®Google Scholar
• Balu M, Sangeetha P, Murali G, Panneerselvam C. (2005). Age-related oxidative protein damages in central nervous system of rats: Modulatory role of grape seed extract. Int J Devl Neurosci 23:501–7
   PubMed Web of Science ®Google Scholar
• Cheng HY, Kim HJ, Kim KW, et al. (2002). Molecular inflammation hypothesis of aging based on the anti-aging mechanism of calorie restriction. Microsc Res Tech 59:264–72
   PubMedGoogle Scholar
• Cos P, Ying L, Calomme M, et al. (1998). Structure–activity relationship and classification of flavonoids as inhibitors of xanthine oxidase and superoxide scavengers. J Nat Prod 61:71–6
   PubMed Web of Science ®Google Scholar
• Dew TP, Day AJ, Morgan MR. (2005). Xanthine oxidase activity in vitro: Effects of food extracts and components. J Agric Food Chem 53:6510–15
   PubMed Web of Science ®Google Scholar
• Diaz-Vivancos P, Rubio M, Mesonero V, et al. (2006). The apoplastic antioxidant system in Prunus: Response to plum pox virus. J Exp Bot 57:3813–24
   PubMed Web of Science ®Google Scholar
• El-baky A, Hanaa H, Mohamed A, et al. (2003). Influence of salinity on lipid peroxidation, antioxidant enzyme and electrophoretic patterns of protein and isozymes in leaves of some onion cultivars. Asi J Plant Sci 2:1220–7
   Google Scholar
• Ellis HA, Kirkman HN. (1961). A colorimetric method for assay of erythrocyte glucose-6-phosphate dehydrogenase. Proc Soc Exp Biol Med 106:607–9
   PubMed Web of Science ®Google Scholar
• Enander K, Rydstrom J. (1982). Energy-linked nicotinamide nucleotide transhydrogenase. Kinetics and regulation of purified and reconstituted transhydrogenase from beef heart mitochondria. J Biol Chem 257:14760–6
   PubMedGoogle Scholar
• Goto S, Takahashi R, Kumiyama AA, et al. (2001). Implications of protein degradation in aging. Ann N Y Acad Sci 928:54–64
   PubMedGoogle Scholar
• Gulcin I, Oktay M, Kirecci E, Kurrevioglu OI. (2003). Screening of antioxidant and antimicrobial activities of anise (Pimpinella anisum L.) seed extracts. Food Chem 83:371–82
   Web of Science ®Google Scholar
• Irie S, Kato Y. (1984). Developmental changes in the activity of xanthine dehydrogenase and closely related enzyme in chick tissues. Develop Growth Differ 26:205–15
   Google Scholar
• Jayakumar T, Ramesh E, Geraldine P. (2006). Antioxidant activity of the oyster mushroom, Pleurotus ostreatus, on CCl4-induced liver injury in rats. Food Chem Toxicol 44:1989–96
   PubMed Web of Science ®Google Scholar
• Jayakumar T, Sakthivel M, Thomas PA, Geraldine P. (2008). Pleurotus ostreatus, an oyster mushroom, decreases the oxidative stress induced by carbon tetrachloride in rat kidneys, heart and brain. Chem Biol Interact 176:108–20
   PubMed Web of Science ®Google Scholar
• Jayakumar T, Thomas PA, Geraldine P. (2007). Protective effect of an extract of the oyster mushroom, Pleurotus ostreatus, on antioxidants of major organs of aged rats. Exp Gerontol 42:183–91
   PubMed Web of Science ®Google Scholar
• Jayakumar T, Thomas PA, Ramesh E, Geraldine P. (2010). An extract of the mushroom, Pleurotus ostreatus, bolsters the glutathione redox system in various organs of aged rats. J Med Food 13:1–8
   PubMedGoogle Scholar
• Jesenak M, Hrubisko M, Majtan J, et al. (2013). Anti-allergic effect of pleuran (β-glucan from Pleurotus ostreatus) in children with recurrent respiratory tract infections. Phytother Res. [Epub ahead of print]. doi: 10.1002/ptr.5020
   Google Scholar
• Kumaran S, Subathra M, Balu M, Panneerselvam C. (2004). Age-associated decreased activities of mitochondrial electron transport chain complexes in heart and skeletal muscle: Role of L-carnitine. Chem Biol Interact 30:11–18
   Google Scholar
• Laemmli UK. (1970). Cleavage of structural proteins during the assemblage of the head of bacteriophage T4. Nature 227:680–5
   PubMed Web of Science ®Google Scholar
• Lee GR, Bithell TC, Foerster J, et al. (1993). Glucose-6-phosphate dehydrogenase deficiency and related deficiencies involving the pentose phosphate pathway and glutathione metabolism. In: Lee GR, ed. Wintrobe’s Clinical Hematology. Philadelphia: Lea and Febiger, 1006–16
   Google Scholar
• Lowry OH, Rosebrough NJ, Farr AL, et al. (1951). Protein measurement with Folin phenol reagent. J Boil Chem 193:265–75
   PubMed Web of Science ®Google Scholar
• Mahesh R, Bhuvana S, Hazeena Begum VM. (2009). Effect of Terminalia chebula aqueous extract on oxidative stress and antioxidant status in the liver and kidney of young and aged rats. Cell Biochem Funct 27:358–63
   PubMed Web of Science ®Google Scholar
• Mattila P, Vaananen PS, Kongo K, et al. (2002). Basic composition and amino acid contents of mushrooms cultivated in Finland. J Agric Food Chem 50:6419–22
   PubMed Web of Science ®Google Scholar
• McCord JM. (1985). Oxygen-derived free radicals in postischemic tissue injury. New Engl J Med 313:159–63
   Google Scholar
• Mittler R, Zilinskas BA. (1993). Detection of ascorbate peroxidase activity in native gels by inhibition of the ascorbate-dependent reduction of nitroblue tetrazolium. Anal Biochem 212:540–6
   PubMed Web of Science ®Google Scholar
• Nagao A, Seki M, Kobayashi H. (1999). Inhibition of xanthine oxidase by flavonoids. Biosci Biotech Biochem 63:1787–90
   PubMed Web of Science ®Google Scholar
• Nakano Y, Asada K. (1987). Purification of ascorbate peroxidase in spinach chloroplast: Its inactivation in ascorbate-depleted medium and reactivation by monodehydroascorbate radical. Plant Cell Physiol 28:131–40
   Web of Science ®Google Scholar
• Ogawa N. (1994). Free radical and neural cell damage. Rinsho Shinkeigaku 34:1266–8
   PubMedGoogle Scholar
• Ramesh T, Kim SW, Sung JH, et al. (2012). Effect of fermented Panax ginseng extract (GINST) on oxidative stress and antioxidant activities in major organs of aged rats. Exp Gerontol 47:77–84
   PubMed Web of Science ®Google Scholar
• Ravi B, Renitta RE, Lakshmi Prabha M, et al. (2013). Evaluation of antidiabetic potential of oyster mushroom (Pleurotus ostreatus) in alloxan-induced diabetic mice. Immunopharmacol Immunotoxicol 35:101–9
   PubMed Web of Science ®Google Scholar
• Reiter RJ. (1995). Oxidative process and antioxidative defense mechanism in aging brain. FASEB J 9:526–33
   PubMed Web of Science ®Google Scholar
• Sang YK, Jung-Hyun L, Myoung RP, et al. (2005). Enhanced antioxidant enzymes are associated with reduced hydrogen peroxide in Barley roots under saline stress. J Biochem Mol Biol 38:218–24
   PubMedGoogle Scholar
• Satav JG, Dave KR, Katyare SS. (2000). Influence of insulin status on extra-mitochondrial oxygen metabolism in the rat. Horm Metab Res 32:57–61
   PubMed Web of Science ®Google Scholar
• Schrader T, Rienhofer A, Andreesen JR. (1999). Selenium-containing xanthine dehydrogenase from Eubacterium barkeri. Eur J Biochem 264:862–71
   PubMedGoogle Scholar
• Sies H, Ed. (1985). Oxidative Stress. London: Academic Press
   Google Scholar
• Singh RP, Khanna R, Kaw JL. (2003). Comparative effect of benzanthrone and 3-bromobenzanthrone on hepatic xenobiotic metabolism and antioxidative defense system in guinea pigs. Arch Toxicol 77:94–9
   PubMed Web of Science ®Google Scholar
• Srinivasan V. (1999). Melatonin, oxidative stress and ageing. Curr Sci 76:46–54
   Google Scholar
• Steinhiller D, Brunga M, Werz O, et al. (1995). The nuclear receptor for melatonin represses 5-lipoxygenase gene expression in human B lymphocytes. J Biol Chem 270:7037–40
   PubMedGoogle Scholar
• Subbarao KV, Richardson IS. (1990). Iron dependent peroxidation of rat brain: A regional study. J Neurosci Res 26:224–32
   PubMed Web of Science ®Google Scholar
• Unyayar A, Demirbilek M, Turkoglu M, et al. (2006). Evaluation of cytotoxic and mutagenic effects of Coriolus versicolor and Funalia trogii extracts on mammalian cells. Drug Chem Toxicol 29:69–83
   PubMed Web of Science ®Google Scholar
• Vamanu E. (2013). Antioxidant properties of polysaccharides obtained by batch cultivation of Pleurotus ostreatus mycelium. Nat Prod Res Formerly Nat Prod Lett 27:1115–18
   PubMed Web of Science ®Google Scholar
• Wendel JF, Weeden NF. (1989). Visualization and interpretation of plant isozymes. In: Solitis DF, Solitis PS, ed. Isozymes in Plant Biology. London: Chapman and Hall, 5–45
   Google Scholar
• Yan B, Dai Q, Liu X, et al. (1996). Flooding-induced membrane damage, lipid oxidation and activated oxygen generation in corn leaves. Plant Soil 179:261–8
   Web of Science ®Google Scholar
• Yang Q, Huang B, Li H, et al. (2012). Gastroprotective activities of a polysaccharide from the fruiting bodies of Pleurotus ostreatus in rats. Intl J Biol Macromol 50:1224–8
   PubMedGoogle Scholar