References
- Francis PT, Palmer AM, Snape M, Wilcock GK. The cholinergic hypothesis of alzheimer's disease: a review of progress. J Neurol Neurosurg Psychiatry. 1999;66:137-147. https://doi.org/10.1136/jnnp.66.2.137
- Beal F. Aging, energy and oxidative stress in neurodegenerative diseases. Ann Neurol. 1995;38:357-366. https://doi.org/10.1002/ana.410380304
- Coyle JT, Price DL, DeLong MR. Alzheimer's disease: a disorder of cholinergeric innervation. Science. 1983;219:1184-1190. https://doi.org/10.1126/science.6338589
- Talesa VN. Acetylcholinesterase in Alzheimer's disease. Mech Aging Dev. 2001;122:1961-1969. https://doi.org/10.1016/S0047-6374(01)00309-8
- Block F, Pergande G, Schwarz M. Flupirtine reduces functional deficits and neuronal damage after global ischemia in rats. Brain Res. 1997;754:279-284. https://doi.org/10.1016/S0006-8993(97)00096-6
- Colovic MB, Krstic DZ, Lazarevic-Pasti TD, Bondzic AM, Vasic VM. Acetylcholinesterase inhibitors: pharmacology and toxicology. Curr Neuropharmacol. 2013;11:315-335. https://doi.org/10.2174/1570159X11311030006
-
Xie QW, Whisnant R, Nathan C. Promoter of the mouse gene encoding calcium-independent nitric oxide synthase confers inducibility by interferon
$\gamma$ and bacterial lipopolysaccharide. J Exper Medi. 1993;177:1779-1784. https://doi.org/10.1084/jem.177.6.1779 - Medzhitov R. Origin and physiological roles of inflammation. Nature. 2008:454:428-435. https://doi.org/10.1038/nature07201
- MacMicking J, Xie QW, Nathan C. Nitric oxide and macrophage function. Annu Rev Immunol. 1997;15:323-350. https://doi.org/10.1146/annurev.immunol.15.1.323
- Hippeli S, Elstner EF. Inhibition of biochemical model reactions for inflammatory processes by plant extracts: a review on recent developments. Free Radi Res. 1999;31(Suppl):S81-S87. https://doi.org/10.1080/10715769900301361
- Boumpas DT, Chrousos GP, Wilder RL, Cupps TR, Balow JE. Glucocorticoid therapy of immune-mediated diseases:basic and clinical correlates. Ann Intern Med. 1993;119:1198-1208. https://doi.org/10.7326/0003-4819-119-12-199312150-00007
- Wasser SP, Weis AL. Therapeutic effects of substances occurring in higher Basidiomycetes mushrooms: a modern perspective. Crit Rev Immunol. 1999;19:65-96.
- Lindequist U, Niedermeyer THJ, Julich WD. The pharmacological potential of mushrooms. eCAM. 2005;2:285-299.
- Yoon KN, Jang HS, Jin GH. Antioxidant, anti-diabetic, anti-cholinesterase, and nitric oxide inhibitory activities of fruiting bodies of Agaricus brasiliensis. Korean J Clin Lab Sci. 2015; 47:194-202. https://doi.org/10.15324/kjcls.2015.47.4.194
- Park WH, Lee HD. Illustrated book of Korean medicinal mushrooms. 2nd ed. Seoul: Kyohak Publishing; 2003. p359-360.
- Bae JS, Jang KH, Yim H, Jin HK. Polysaccharide isolated from Phellinus gilvus inhibit melanoma growth in mouse. Caner Lett. 2005;218:43-52. https://doi.org/10.1016/j.canlet.2004.08.002
- Yoon KN, Jang HS. Antioxidant and antimicrobial activities of fruiting bodies of Phellinus gilvus collected in Korea. Korean J Clin Lab Sci. 2016;48:355-364. https://doi.org/10.15324/kjcls.2016.48.4.355
- Shim SM, Im KH, Kim JW, Shim MJ, Lee MW, Lee TS. Studies on immuno-modulatory and antitumor effects of crude polysaccharides extracted from Paecilomyces sinclairii. Korean J Mycol. 2003;31:155-160. https://doi.org/10.4489/KJM.2003.31.3.155
- Swain T, Hillis WE, Ortga M. Phenolic constituents of Prunus domestica. I. Quantitative analysis of phenolic constituents. J Sci Food Agric. 1959;10:83-88.
- Moreno MIN, Isla MI, Sampietro AR, Vattuone MA. Comparison of the free radical scavenging activity of propolis from several region of Argentina. J Enthnopharmcol. 2000;71:109-114. https://doi.org/10.1016/S0378-8741(99)00189-0
- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Immunol Meth. 1983;65:55-63. https://doi.org/10.1016/0022-1759(83)90303-4
- Stirpe F, Corte Della E. The regulation of rat liver xanthine oxidase. Conversion in vitro of the enzyme activity from dehydrogenase (type D) to oxidase (type O). J Biol Chem. 1969;244:3855-3863.
- Ellman GL, Courtney KD, Andres V Jr, Featherstone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. 1961;7:88-95. https://doi.org/10.1016/0006-2952(61)90145-9
- Greene LA, Tischler AS. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc Natl Acad Sci. 1976;73:2424-2428. https://doi.org/10.1073/pnas.73.7.2424
-
Ma S, Liu H, Jiao H, Wang L, Chen L, Liang J, et al. Neuroprotective effect of ginkgolide K on glutamate-induced cytotoxicity in PC 12 cells via inhibition of ROS generation and
$Ca^{2+}$ influx. Neurotoxicol. 2012;33:59-69. https://doi.org/10.1016/j.neuro.2011.11.003 - Ryu JH, Ahn H, Kim JY, Kim YK. Inhibitory activity of plant extracts on nitric oxide synthesis in LPS-activated macrophage. Phytother Res. 2003;17:485-489. https://doi.org/10.1002/ptr.1180
- Winter CA, Risley EA, Nuss GW. Carrageenan induced edema in the hind paw of rat as an assay for anti-inflammatory activity. Proc Soc Exp Biol Med. 1962;111:544-547. https://doi.org/10.3181/00379727-111-27849
- Rocha-Guzmn NE, Gonzlez-Laredo JA, Conzalez-Laredo RF, Reynoso-Camacho R, Ramos-Gmez M, Garcia-Gasca T, et al. Antioxidant activity and genotoxic effect on HeLa cells of phenolic compounds from infusions of Quercus resinosa leaves. Food Chem. 2009;115:1320-1325. https://doi.org/10.1016/j.foodchem.2009.01.050
- Yim HS, Chye FY, Ho SK, Ho WC. Phenolic profiles of selected edible wild mushrooms as affected by extraction solvent, time and temperature. Asian J Food Ag-Ind. 2009;2:392-401.
- Ling X, Bochu W. A review of phytotherapy of gout: perspective of new pharmacological treatments. Pharmazie. 2014;69:243-256.
- Storch I, Ferber E. Detergent-amplified chemiluminescence of lucigenin for determination of superoxide amino production by NADPH oxidase and xanthine oxidase. Anal Biochem. 1988; 169:262-267. https://doi.org/10.1016/0003-2697(88)90283-7
- Costantino L, Albasini A, Rastelli G, Benvenuti S. Activity of polyphenolic crude extracts as scavengers of superoxide radicals and inhibitors of xanthine oxidase. Planta Med. 1992;58: 342-344. https://doi.org/10.1055/s-2006-961481
- Alam N, Yoon KN, Lee JS, Cho HJ, Lee TS. Consequence of the antioxidant activities and tyrosinase inhibitory effects of various extracts from the fruiting bodies of Pleurotus ferulae. Saudi J Biol Sci. 2012;19:111-118. https://doi.org/10.1016/j.sjbs.2011.11.004
- Tayebati SK, Di Tullio MA, Amenta F. Effect of treatment with the cholinesterase inhibitor rivastigmine on vesicular acetylcholine transporter and choline acetyltransferase in rat brain. Clin Exp Hypertens. 2004;26:363-373. https://doi.org/10.1081/CEH-120034140
- Nguyen TK, Shin DB, Lee KR, Shin PG, Cheong JC, Yoo YB, et al. Antioxidant, anti-inflammatory and anti-acetylcholinesterase activities of fruiting bodies of Phellinus xeranticus. J Mushroom Sci Prod. 2013;11:278-286. https://doi.org/10.14480/JM.2013.11.4.278
- Yoon KN, Lee TS. In vitro antioxidant, anti-hyperglycemic, anti- cholinesterase, and inhibition of nitric oxide production activities of methanol and hot water extracts of Russula rosacea mushroom. J Mushrooms. 2015;13:1-10. https://doi.org/10.14480/JM.2015.13.1.1
- Choi DW. Excitotoxic cell death. J Neurologic. 1991;23: 1262-1276.
- Naito M, Umegaki H, Iguchi A. Protective effects of probucol against glutamate-induced cytotoxicity in neuronal cell line PC 12. Neurosci Lett. 1995;186:211-213. https://doi.org/10.1016/0304-3940(95)11321-M
- Beal MF. Mechanisms of excitotoxicity in neurologic diseases. PASEB J. 1992;6: 3338-3344.
- Choi WH, Oh YS, Ahn JY, Kim SR, Ha TY. Antioxidative and protective effects of Ulmus davidiana var. japonicus extracts on glutamate-induced cytotoxicity in PC 12 cells. Korean J Food Sci Technol. 2005;37:479-483.
- Abbas AK, Lichtman AH, et al. Celluar and molecular immunology. 6th ed. Philadelphia: Saunders Elsevier; 2006. p75-77.
- Nathan C. Nitric oxide as a secretory product of mammalian cell. The FASEB J. 1992;6:3051-3064. https://doi.org/10.1096/fasebj.6.12.1381691
- Willeaume V, Kruys V, Mijatovic T, Huez G. Tumor necrosis factor-alpha production induced by viruses and by lipopolysaccharides in macrophages: similarities and differences. J Inflamm. 1996;46:1-12.
- Jang HJ, Kim AK, Pyo MY. Yang KS. Inhibitors ofnnitric oxide syntheasis from Phellinus pini in murine macrophages. J Pharm Soc Korea. 2007;51:430-434.
- Fangkrathok N, Junlatat J, Sripanidkulchai B. In vivo and in vitro anti-inflammatory activity of Lentinus polychrous extract. J Ethnopharm. 2013;147:631-637. https://doi.org/10.1016/j.jep.2013.03.055
- Lee IG. Differential diagnosis and treatment of generalized edema. J Korean Acad Fam Med. 2003;24:6-10.
- Cho YS, Kim ND, Kim SA. Effects of concurrent administration of aspirin and prednisolone on the anti-inflammatory and antipyretic activities in rats. J Pharm Soc Korea. 1978;22:128-137.
- Seibert K, Zhang Y, Leahy K, Hauser S, Masferrer J, Perkins W, Lee L, Isakson P. Pharmacological and biochemical demonstration of the role of cyclooxygenase 2 in inflammation and pain. Proc Natl Acad Sci USA. 1994;91:12013-12017. https://doi.org/10.1073/pnas.91.25.12013
- Lim JH, Kim SH, Park NH, Moon CG, Kang, SS, Kim SH, Shin DH, Kim JC. Acute and chronic antiinflammatory effects of Phellinus linteus water extract in rats. J Biomed Res. 2010; 11:27-35.
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