Neuroprotective compounds from Salix pseudo-lasiogyne twigs and their anti-amnesic effects on scopolamine-induced memory deficit in mice

Planta Medica

Volumn 79, Issue 1, 2013, Pages 79-82

  Yang, Heejung ^a   Lee, Sang Hoon ^a   Sung, Sang Hyun ^a   Kim, Jinwoong ^a   Kim, Young Choong ^a  

^a Seoul National University   (South Korea)

Author keywords

1 hydroxy 6 oxo 2 cyclohexenecarboxylate; BV2 microglial cell; passive avoidance test; Salicaceae; salicortin; Salix pseudo lasiogyne

Indexed keywords

1 HYDROXY 6 OXO 2 CYCLOHEXENECARBOXYLATE; 2' O 4 COUMAROYLSALICORTIN; 2' O ACETYLSALICIN; 2' O ACETYLSALICORTIN; 2',6' O ACETYLSALICORTIN; 3' O ACETYLSALICIN; 3' O ACETYLSALICORTIN; 6' O ACETYLSALICORTIN; GLUTATHIONE; GLUTATHIONE REDUCTASE; GRANDIDENTATIN; HERBACEOUS AGENT; ISOGRANDIDENTATIN; LIPOPOLYSACCHARIDE; METHANOL; NITRIC OXIDE; PLANT EXTRACT; SALICIN; SALICORTIN; SALIGENIN; SALIX PSEUDO LASIOGYNE EXTRACT; SCOPOLAMINE; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG; ANTIOXIDANT; NEUROPROTECTIVE AGENT; NOOTROPIC AGENT; SCOPOLAMINE BROMIDE;

AMNESIA; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANTIINFLAMMATORY ACTIVITY; ARTICLE; BRAIN CORTEX; COGNITION; CONTROLLED STUDY; DRUG STRUCTURE; HIPPOCAMPUS; IC 50; MALE; MICROGLIA; MOUSE; NEUROPROTECTION; NONHUMAN; PASSIVE AVOIDANCE; SOLVENT EXTRACTION; SPECTROSCOPY; ANIMAL; AVOIDANCE BEHAVIOR; CELL CULTURE; CHEMICAL STRUCTURE; CHEMICALLY INDUCED DISORDER; CHEMISTRY; DRUG EFFECT; ENZYMOLOGY; IN VITRO STUDY; ISOLATION AND PURIFICATION; METABOLISM; PHYTOTHERAPY; PLANT STEM; SPRAGUE DAWLEY RAT; WILLOW;

MUS; SALICACEAE; SALIX;

AMNESIA; ANIMALS; ANTIOXIDANTS; AVOIDANCE LEARNING; CELLS, CULTURED; CEREBRAL CORTEX; GLUTATHIONE; HIPPOCAMPUS; INHIBITORY CONCENTRATION 50; MALE; MICE; MICROGLIA; MOLECULAR STRUCTURE; NEUROPROTECTIVE AGENTS; NOOTROPIC AGENTS; PHYTOTHERAPY; PLANT EXTRACTS; PLANT STEMS; RATS, SPRAGUE-DAWLEY; SALIX; SCOPOLAMINE HYDROBROMIDE; SUPEROXIDE DISMUTASE;

MLCS; MLOWN;

EID: 84872086428     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0032-1327949     Document Type: Article

References (27)

1. Mahdi J. G., Mahdi A. J., Mahdi A. J., Bowen I. D. The historical analysis of aspirin discovery, its relation to the willow tree and antiproliferative and anticancer potential. Cell Prolif: 2006; 39 147 155
2. Koh K. S., Jeon E. S. Ferns, fern-allies and seed-bearing plants of Korea. Seoul Iljin-sa: 2003
3. Jung W. K., Lee D. Y., Park C., Choi Y. H., Choi I., Park S. G., Seo S. K., Lee S. W., Yea S. S., Ahn S. C., Lee C. M., Park W. S., Ko J. H., Choi I. W. Cilostazol is anti-inflammatory in BV2 microglial cells by inactivating nuclear factor-kappaB and inhibiting mitogen-activated protein kinases. Br J Pharmacol: 2010; 159 1274 1285
4. Henn A., Lund S., Hedtjarn M., Schrattenholz A., Porzgen P., Leist M. The suitability of BV2 cells as alternative model system for primary microglia cultures or for animal experiments examining brain inflammation. ALTEX: 2009; 26 83 94
5. Aquilano K., Baldelli S., Rotilio G., Ciriolo M. R. Role of nitric oxide synthases in Parkinsons disease: a review on the antioxidant and anti-inflammatory activity of polyphenols. Neurochem Res: 2008; 33 2416 2426
6. Shimomura H., Sashida Y., Yoshinari K. Phenolic glucosides from the heartwood of Prunus grayana. Phytochemistry: 1989; 28 1499 1502
7. Zapesochnaya G. G., Kurkin V. A., Braslavskii V. B., Filatova N. V. Phenolic compounds of Salix acutifolia bark. Chem Nat Compd: 2002; 38 314 318
8. Reichardt P. B., Merken H. M., Clausen T. P., Wu J. Phenolic glycosides from Salix lasiandra. J Nat Prod: 1992; 55 970 973
9. Thieme H. The phenol glycosides in Salicaceae. 2. Isolation and demonstration. Pharmazie: 1964; 19 471 475
10. Ruuhola T., Julkunen-Tiitto R., Vainiotalo P. In vitro degradation of willow salicylates. J Chem Ecol: 2003; 29 1083 1097 (Pubitemid 36712747)
11. Dommisse R. A., Van Hoof L., Vlietinck A. J. Structural analysis of phenolic glucosides from Salicaceae by NMR spectroscopy. Phytochemistry: 1986; 25 1201 1204
12. Ikonen A., Tahvanainen J., Roininen H. Phenolic secondary compounds as determinants of the host plant preferences of the leaf beetle Agelastica alni. Chemoecology: 2002; 12 125 131
13. Dagvadorj E., Shaker K. H., Windsor D., Schneider B., Boland W. Phenolic glucosides from Hasseltia floribunda. Phytochemistry: 2010; 71 1900 1907
14. Shen C. C., Chang Y. S., Hott L. K. Nuclear magnetic resonance studies of 5,7-dihydroxyflavonoids. Phytochemistry: 1993; 34 843 845
15. Fisher T. H., Chao P., Upton C. G., Day A. J. One- and two-dimensional NMR study of resol phenol-formaldehyde prepolymer resins. Magn Reson Chem: 1995; 33 717 723
16. Andersen J. K. Oxidative stress in neurodegeneration: cause or consequence? Nat Med: 2004; 10 (Suppl.) S18 S25 (Pubitemid 38901863)
17. Ienco E. C., Logerfo A., Carlesi C., Orsucci D., Ricci G., Mancuso M., Siciliano G. Oxidative stress treatment for clinical trials in neurodegenerative diseases. J Alzheimers Dis: 2011; 24 02 111 126
18. Lu S. C. Regulation of hepatic glutathione synthesis: current concepts and controversies. Faseb J: 1999; 13 1169 1183 (Pubitemid 29300363)
19. Junio H. A., Sy-Cordero A. A., Ettefagh K. A., Burns J. T., Micko K. T., Graf T. N., Richter S. J., Cannon R. E., Oberlies N. H., Cech N. B. Synergy-directed fractionation of botanical medicines: a case study with goldenseal (Hydrastis canadensis). J Nat Prod: 2011; 74 1621 1629
20. Wagner H., Ulrich-Merzenich G. Synergy research: approaching a new generation of phytopharmaceuticals. Phytomedicine: 2009; 16 97 110
21. Spelman K., Duke J. A., Bogenschutz-Godwin M. J. Natural products from plants. 2nd edition. Boca Raton CRC Taylor and Francis: 2006
22. Dawson V. L., Brahmbhatt H. P., Mong J. A., Dawson T. M. Expression of inducible nitric oxide synthase causes delayed neurotoxicity in primary mixed neuronal-glial cortical cultures. Neuropharmacology: 1994; 33 1425 1430 (Pubitemid 24353737)
23. Jeong E. J., Ma C. J., Lee K. Y., Kim S. H., Sung S. H., Kim Y. C. KD-501, a standardized extract of Scrophularia buergeriana has both cognitive-enhancing and antioxidant activities in mice given scopolamine. J Ethnopharmacol: 2009; 121 98 105
24. McCord J. M., Fridovich I. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). J Biol Chem: 1969; 244 6049 6055
25. Carlberg I., Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J Biol Chem: 1975; 250 5475 5480
26. Flohe L., Gunzler W. A. Assays of glutathione peroxidase. Methods Enzymol: 1984; 105 114 121 (Pubitemid 14165378)
27. Tietze F. Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues. Anal Biochem: 1969; 27 502 522