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      독활지황탕(獨活地黃湯)이 βA로 유도된 Alzheimer`s Disease 병태 모델에 미치는 영향 = The Effects of Dokhwaljihwang-tang(Duhuodihuangtang) on the Alzheimer`s Disease Model Induced by βA

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      https://www.riss.kr/link?id=A82704139

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      다국어 초록 (Multilingual Abstract)

      Objectives: This research investigates the effect of the DHJHT extract on Alzheimer`s disease. Specifically, the effects of the DHJHT extract on (1) the behavior (2) the infarction area of the hippocampus, and brain tissue injury in AD mice induced with βA were investigated. Methods: The effects of the DHJHT extract on the proinflammation cytokines mRNA expression and production of BACE, APP and βA in in BV2 microglial cell line treated by lipopolysacchaide(LPS) plus βA were investigated. The effects of the DHJHT extract on the behavior of the memory deficit mice induced by scopolamine were investigated. Results: 1. The DHJHT extract suppressed the expression of IL-1β, IL-6, TNF-α, COX-2, and NOS-II, BACE and APP mRNA in BV2 microglial cell line treated by LPS plus βA. 2. The DHJHT extract suppressed the expression of βA production in BV2 microglial cell line treated with LPS plus βA. 3. The DHJHT extract showed significantly inhibitory effect on the scopolamine-induced impairment of memory in the experiment of Morris water maze. 4. The DHJHT group suppressed the expression of IL-1β, TNF-α, MDA, and CD68+/CD11b+ in the brain tissue of the mice with AD induced by βA. 5. The DHJHT group reduced the infarction area of hippocampus, and controlled the injury of the brain tissue in the mice with AD induced by βA. 6. The DHJHT group reduced tau protein, and GFAP in the brain tissue of the mice with AD induced by βA. Conclusions: These results suggest that the DHJHT group may be effective for the treatment of AD. Thus, DHJHT could be considered among the future therapeutic drugs indicated for the treatment of AD.
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      Objectives: This research investigates the effect of the DHJHT extract on Alzheimer`s disease. Specifically, the effects of the DHJHT extract on (1) the behavior (2) the infarction area of the hippocampus, and brain tissue injury in AD mice induced wi...

      Objectives: This research investigates the effect of the DHJHT extract on Alzheimer`s disease. Specifically, the effects of the DHJHT extract on (1) the behavior (2) the infarction area of the hippocampus, and brain tissue injury in AD mice induced with βA were investigated. Methods: The effects of the DHJHT extract on the proinflammation cytokines mRNA expression and production of BACE, APP and βA in in BV2 microglial cell line treated by lipopolysacchaide(LPS) plus βA were investigated. The effects of the DHJHT extract on the behavior of the memory deficit mice induced by scopolamine were investigated. Results: 1. The DHJHT extract suppressed the expression of IL-1β, IL-6, TNF-α, COX-2, and NOS-II, BACE and APP mRNA in BV2 microglial cell line treated by LPS plus βA. 2. The DHJHT extract suppressed the expression of βA production in BV2 microglial cell line treated with LPS plus βA. 3. The DHJHT extract showed significantly inhibitory effect on the scopolamine-induced impairment of memory in the experiment of Morris water maze. 4. The DHJHT group suppressed the expression of IL-1β, TNF-α, MDA, and CD68+/CD11b+ in the brain tissue of the mice with AD induced by βA. 5. The DHJHT group reduced the infarction area of hippocampus, and controlled the injury of the brain tissue in the mice with AD induced by βA. 6. The DHJHT group reduced tau protein, and GFAP in the brain tissue of the mice with AD induced by βA. Conclusions: These results suggest that the DHJHT group may be effective for the treatment of AD. Thus, DHJHT could be considered among the future therapeutic drugs indicated for the treatment of AD.

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      참고문헌 (Reference)

      1 전국한의과대학 신경정신과 교과서편찬위원회, "한의신경정신과학" 집문당 236-333, 2007

      2 오영선, "치매의 병리, 연구동향과 향후 연구전략에 대한 고찰" 8 (8): 793-822, 1999

      3 이광우, "임상신경학" 고려의학 199-210, 1997

      4 이정찬, "신 사상의학론2" 목과토 178-249, 2003

      5 전국한의과대학 사상의학교실, "사상의학" 집문당 512-, 1997

      6 전국한의과대학본초학교실, "본초학" 성보사 131-627, 1994

      7 진현철, "독활지황탕의 위장관 및 중추신경에 미치는 효능에 관한 실험적 연구" 9 (9): 187-201, 1997

      8 錢鏡湖, "辨證奇問全書" 甘地出版社 222-225, 1990

      9 陳士鐸, "石室秘錄" 中國中醫藥出版社 125-, 1991

      10 Louise B, "β-AmyloidPeptideSecretionby a MicroglialCellLine Is Induced by β -Amyloid (25-35)and Lipopolysaccharide" 271 (271): 16084-16089, 1996

      1 전국한의과대학 신경정신과 교과서편찬위원회, "한의신경정신과학" 집문당 236-333, 2007

      2 오영선, "치매의 병리, 연구동향과 향후 연구전략에 대한 고찰" 8 (8): 793-822, 1999

      3 이광우, "임상신경학" 고려의학 199-210, 1997

      4 이정찬, "신 사상의학론2" 목과토 178-249, 2003

      5 전국한의과대학 사상의학교실, "사상의학" 집문당 512-, 1997

      6 전국한의과대학본초학교실, "본초학" 성보사 131-627, 1994

      7 진현철, "독활지황탕의 위장관 및 중추신경에 미치는 효능에 관한 실험적 연구" 9 (9): 187-201, 1997

      8 錢鏡湖, "辨證奇問全書" 甘地出版社 222-225, 1990

      9 陳士鐸, "石室秘錄" 中國中醫藥出版社 125-, 1991

      10 Louise B, "β-AmyloidPeptideSecretionby a MicroglialCellLine Is Induced by β -Amyloid (25-35)and Lipopolysaccharide" 271 (271): 16084-16089, 1996

      11 Brandeis R, "use of the Morris Water Maze in the study of memory and learning" 48 (48): 29-69, 1989

      12 Yankner B, "and neurotoxic effects of amyloid beta protein: reversal by tachykinin neuropeptides" 250 (250): 279-282, 1990

      13 이수영, "Wistarrat의 노화에 따른 체중, 혈액학적 및 혈청생화학적 변화에 미치는 독활지황탕에 대한 실험적 고찰" 13 (13): 332-334, 2004

      14 LemereCA, "The E280A presenilin 1Alzheimermutation produces increased Aβ 42 deposition and severe erebellarpathology" 2 (2): 1146-1150, 1996

      15 Tabaton M, "Senile plaques in cerebral amyloid angiopathy show accumulation of amyloid precursor protein without cytoskeletal abnormalities" 593 (593): 299-303, 1992

      16 Gertsch J, "Relative quantification of mRNA levels in Jurkat T cells with RT-real time-PCR (RT-rt-PCR): new possibilities for the screening of anti-inflammatory and cytotoxic compounds" 19 (19): 1236-1243, 2002

      17 Bouras C, "Regional distribution of neurofibrillary tangles and senile plaques in the cerebral cortex of elderly patients: a quantitative evaluation of a one-year autopsy population from a geriatric hospital" 4 (4): 138-150, 1994

      18 Araga S, "Reduced natural killer cell activity in patients with dementia of the Alzheimer type" 84 (84): 259-263, 1991

      19 Bradford MA, "Rapidand Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding" 72 : 248-254, 1976

      20 Perri BR, "Metabolic Quantification of Lesion Volume following Experimental Traumatic Brain Injuryin the Rat" 14 (14): 15-22, 1997

      21 Tariot PN, "Memantine Study Group. Memantine Treatment in Patients With Moderate to Severe Alzheimer Disease Already Receiving Donepezil: A Randomized Controlled Trial" 291 (291): 317-324, 2004

      22 Magnottl RA, "Measurement of Acetylcholinesterase in Erythrocytes in the Field" 33 (33): 1731-1735, 1987

      23 Suematsu T, "Lipid peroxidation in alcoholic liver disease in humans" 5 (5): 427-430, 1981

      24 Dickson DW, "Immunocytochemistry of neurofibrillary tangles with antibodies to subregions of tau protein ; identification of hidden and cleaved tau epitopes and a new phosphorylation site" 84 (84): 5596-605, 1992

      25 Blasi E, "Immortalization of murine microglial cells by a v-raf/v-myc carrying retrovirus" 27 (27): 229-237, 1990

      26 Vosselera MN, "Area at Risk and Viability after Myocardial Ischemia and Reperfusion Can Be Determined by Contrast-Enhanced Cardiac Magnetic Resonance Imaging" 43 (43): 13-23, 2009

      27 SuzukiN, "An increased percentageoflong amyloid β protein secreted by familialamyloid β protein precursor (βAPP717) mutants" 264 (264): 1336-1340, 1994

      28 Bocchini V, "An immortalized cell line expresses properties of activated microglial cells" 31 (31): 616-621, 1992

      29 Brockmann K, "A novel GFAP mutation and disseminated white matter lesions:adult Alexander disease?" 50 (50): 100-105, 2003

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      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
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      2007-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.77 0.77 0.77
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.73 0.7 0.915 0
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