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      KCI등재

      아밀로이드 베타 단백질에 의해 유도된 신경세포 독성에 대한 황정의 억제 효과 탐색 = Protective Effects of Polygonatum odoratum Extracts on Amyloid β-protein-induced Death in Neuronal Cells

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      https://www.riss.kr/link?id=A104744715

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      다국어 초록 (Multilingual Abstract)

      The amyloid β-protein (Aβ) is the principal component of the senile plaques characteristic of Alzheimer’s disease (AD) and elicits a toxic effect on neurons in vitro and in vivo. Many environmental factors including antioxidants and proteoglycans ...

      The amyloid β-protein (Aβ) is the principal component of the senile plaques characteristic of Alzheimer’s disease (AD) and elicits a toxic effect on neurons in vitro and in vivo. Many environmental factors including antioxidants and proteoglycans modify Aβ toxicity. In this study, we have investigated the protective effects of organic solvent-extracts of Polygonatum odoratum fractions pre-extracted with methanol on Aβ-induced oxidative cell death in cultured rat pheochromocytoma (PC12) cells. For this study, we used MTT reduction assay for detection of protective effects of organic solvent-extracts of Polygonatum odoratum fractions pre-extracted with methanol on Aβ25-35-induced cytotoxicity to PC12 cells. We also used cell-based β-secretase assay system to investigate the inhibitory effect of organic solvent-extracts of Polygonatum odoratum on β-secretase activity. We previously reported that methanol extracts of Polygonatum odoratum strongly attenuated cytotoxicity induced by the three A fragments (Aβ25-35, Aβ1-42 Aβ1-43) to both SK-N-MC and PC12 cells. In the present study, we found that the organic solvent extracts of Polygonatum odoratum fractions pre-extracted with methanol had the strong protective effects against Aβ25-35-induced cytotoxicity to PC12 cells and inhibitory potency to β-secretase activity. These results suggest that organic solvent extracts of Polygonatum odoratum fractions pre-extracted with methanol may contain the protective component(s) against Aβ-induced cell death in PC12 cells as well as inhibitory component(s) to β-secretase activity. (Cancer Prev Res 13, 197-204, 2008)

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      참고문헌 (Reference)

      1 문자영, "아밀로이드 베타 단백질에 의해 유도된 신경세포 독성에 대한 백합과 숙근류의 억제 효과 탐색" 대한암예방학회 10 (10): 242-250, 2005

      2 康秉秀, "本草學" 永林社 594-595, 1995

      3 陶弘景, "名醫別錄" 人民衛生出版社 23-, 1986

      4 Selkoe, D.J., "Translating cell biology into therapeutic advances in Alzheimer's disease" 399 (399): A23-A31, 1999

      5 Andrea Zangara, "The psychopharmacology of huperzine A: an alkaloid with cognitive enhancing and neuroprotective properties of interest in the treatment of Alzheimer’s disease" 75 : 675-686, 2003

      6 Bastinetto, S., "The ginkgo biloba extract (EGb 761) protects hippocampal neurons against cell death induced by β- amyloid" 12 : 1882-1890, 2000

      7 Henderson, V.W., "The epidemiology of estrogen replacement therapy and Alzheimer's disease" 48 (48): S27-S35, 1997

      8 Oken, B.S., "The efficacy of Ginkgo biloba on cognitive function in Alzheimer disease" 55 : 1409-1415, 1998

      9 Badia, A., "Synthesis and evaluation of tarcrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer’s disease" 6 : 427-440, 1998

      10 Kihara, T., "Stimulation of alpha4beta2 nicotinic acetylcholine receptors inhibits beta-amyloid toxicity" 792 : 331-334, 1998

      1 문자영, "아밀로이드 베타 단백질에 의해 유도된 신경세포 독성에 대한 백합과 숙근류의 억제 효과 탐색" 대한암예방학회 10 (10): 242-250, 2005

      2 康秉秀, "本草學" 永林社 594-595, 1995

      3 陶弘景, "名醫別錄" 人民衛生出版社 23-, 1986

      4 Selkoe, D.J., "Translating cell biology into therapeutic advances in Alzheimer's disease" 399 (399): A23-A31, 1999

      5 Andrea Zangara, "The psychopharmacology of huperzine A: an alkaloid with cognitive enhancing and neuroprotective properties of interest in the treatment of Alzheimer’s disease" 75 : 675-686, 2003

      6 Bastinetto, S., "The ginkgo biloba extract (EGb 761) protects hippocampal neurons against cell death induced by β- amyloid" 12 : 1882-1890, 2000

      7 Henderson, V.W., "The epidemiology of estrogen replacement therapy and Alzheimer's disease" 48 (48): S27-S35, 1997

      8 Oken, B.S., "The efficacy of Ginkgo biloba on cognitive function in Alzheimer disease" 55 : 1409-1415, 1998

      9 Badia, A., "Synthesis and evaluation of tarcrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer’s disease" 6 : 427-440, 1998

      10 Kihara, T., "Stimulation of alpha4beta2 nicotinic acetylcholine receptors inhibits beta-amyloid toxicity" 792 : 331-334, 1998

      11 Skolnick, A.A., "Old Chinese herbal medicine used for fever yields possible new Alzheimer disease therapy" 277 : 776-, 1997

      12 Hoshi, M., "Nontoxic amyloid beta peptide 1-42 suppresses acetylcholine synthesis. Possible role in cholinergic dysfunction in Alzheimer's disease" 272 : 2038-2041, 1997

      13 Mattson, M.P., "Neuroprotective signal transduction: relevance to stroke" 21 : 193-206, 1997

      14 Scott, S.A., "Nerve growth factor and Alzheimer's disease" 5 : 179-211, 1994

      15 Gooch, M.D., "Molecular basis of Alzheimer's disease" 53 : 1545-1557, 1996

      16 Seiger, A., "Intracranial infusion of purified nerve growth factor to an Alzheimer patient: the first attempt of a possible future treatment strategy" 57 : 255-261, 1993

      17 Park, S.Y., "Discovery of natural products from Curcuma longa that protect cells from beta-amyloid insult: A drug discovery effort against Alzheimer's disease" 65 : 1227-1231, 2002

      18 Pasinetti, G.M., "Cyclooxygenase-2 expression is increased in frontal cortex of Alzheimer's disease brain" 87 : 319-324, 1998

      19 Harkany, T., "Cholinotoxic effects of beta-amyloid (1-42) peptide on cortical projections of the rat nucleus basalis magnocellularis" 695 : 71-75, 1995

      20 Haass, C., "Cellular processing of beta-amyloid precursor protein and the genesis of amyloid beta-peptide" 75 : 1039-1042, 1993

      21 Oh, M., "Cell-based assay for β-secretase activity" 323 : 7-11, 2003

      22 Pike, C.J., "Beta-amyloid neurotoxicity in vitro: evidence of oxidative stress but not protection by antioxidants" 69 : 1601-1611, 1997

      23 Yan, S.D., "An intracellular protein that binds amyloid- peptide and mediates neurotoxicity in Alzheimer's disease" 389 : 689-695, 1997

      24 Lorenzo, A., "Amyloid fibril toxicity in Alzheimer's disease and diabetes" 777 : 89-95, 1996

      25 Le Bars, P.L., "A placebo-controlled, double-blind, randomized trial of an extract of Ginko biloba for dementia, North American Egb Study Group" 278 : 1327-1332, 1997

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 재인증평가 신청대상 (재인증)
      2019-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2018-12-01 평가 등재후보로 하락 (계속평가) KCI등재후보
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2013-10-14 학술지명변경 외국어명 : Cancer Prevention Research -> Journal of Cancer Prevention KCI등재
      2012-10-15 학회명변경 영문명 : Korean Association of Cancer Prevention -> Korean Society of Cancer Preveniton KCI등재
      2011-04-04 학술지명변경 외국어명 : Journal of Korean Association of Cancer Prevention -> Cancer Prevention Research KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.22 0.22 0.18
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.15 0.12 0.405 0.13
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