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논문 기본 정보

자료유형
학술저널
저자정보
Lee, Hyung Eun (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Lee, So Young (Natural Products Research Institute and College of Pharmacy, Seoul National University) Kim, Ju Sun (Natural Products Research Institute and College of Pharmacy, Seoul National University) Park, Se Jin (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Kim, Jong Min (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Lee, Young Woo (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Jung, Jun Man (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Kim, Dong Hyun (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Shin, Bum Young (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Jang, Dae Sik (Department of Life and Nanopharmaceutical Science, College of Pharmacy, Kyung Hee University) Kang, Sam Sik (Natural Products Research Institute and College of Pharmacy, S) Ryu, Jong Hoon
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제21권 제4호
발행연도
2013.1
수록면
299 - 306 (8page)

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In the present study, we investigated the effect of ethanolic extract of the seed of Zizyphus jujuba var. spinosa (EEZS) on cholinergic blockade-induced memory impairment in mice. Male ICR mice were treated with EEZS. The behavioral tests were conducted using the passive avoidance, the Y-maze, and the Morris water maze tasks. EEZS (100 or 200 mg/kg, p.o.) significantly ameliorated the scopolamine-induced cognitive impairment in our present behavioral tasks without changes of locomotor activity. The ameliorating effect of EEZS on scopolamine-induced memory impairment was significantly reversed by a sub-effective dose of MK-801 (0.0125 mg/kg, s.c.). In addition, single administration of EEZS in normal naive mouse enhanced latency time in the passive avoidance task. Western blot analysis was employed to confirm the mechanism of memory-ameliorating effect of EEZS. Administration of EEZS (200 mg/kg) increased the level of memory-related signaling molecules, including phosphorylation of extracellular signal-regulated kinase or cAMP response element-binding protein in the hippocampal region. Also, the time-dependent expression level of brain-derived neurotrophic factor by the administration of EEZS was markedly increased from 3 to 9 h. These results suggest that EEZS has memory-ameliorating effect on scopolamine-induced cognitive impairment, which is mediated by the enhancement of the cholinergic neurotransmitter system, in part, via NMDA receptor signaling, and that EEZS would be useful agent against cognitive dysfunction such as Alzheimer's disease.

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