단삼이 활성산소에 의하여 손상된 배양 해마신경세포에 미치는 영향

In order to evaluate the cytotoxic effect of reactive oxygen species(AOS), the cell viability was measured by MTT assay after cultured mouse hippocampal neurons were treated with various concentrations of xanthine oxidase(XO) and hypoxanthine (HX) for 5 hours. And also, the protective effect of Salv...

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Published in동의생리병리학회지 Vol. 17; no. 4; pp. 1008 - 1012
Main Authors 이병찬(Byung Chan Lee), 한선희(Sun Hee Han), 송인영(In Young Song), 이강창(Kang Chang Lee)
Format Journal Article
LanguageKorean
Published 한의병리학회 2003
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ISSN1738-7698
2288-2529
2283-2529

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Abstract In order to evaluate the cytotoxic effect of reactive oxygen species(AOS), the cell viability was measured by MTT assay after cultured mouse hippocampal neurons were treated with various concentrations of xanthine oxidase(XO) and hypoxanthine (HX) for 5 hours. And also, the protective effect of Salviae Mutiorrhizae Radix(SMR) on XO/HX-induced neurotoxicity was examined in these cultures. XO/HX significantly decreased cell viability in dose-and time dependent manners when cultured mouse hippocampal neurons were treated with 5~40 mU/ml XO for 5 hours. In the protective effect of SMA, SMR increased cell viability dose-dependently after cultured mouse hippocampal neurons were preincubated with 30~120 ㎍/ml SMR for 2 hours. From these results, it is suggested that XO/HX is toxic on cultured mouse hippocampal neurons, and herbe medicine such as SMR is very effective in blocking the cytotoxicity induced by AOS.
AbstractList In order to evaluate the cytotoxic effect of reactive oxygen species(AOS), the cell viability was measured by MTT assay after cultured mouse hippocampal neurons were treated with various concentrations of xanthine oxidase(XO) and hypoxanthine (HX) for 5 hours. And also, the protective effect of Salviae Mutiorrhizae Radix(SMR) on XO/HX-induced neurotoxicity was examined in these cultures. XO/HX significantly decreased cell viability in dose-and time dependent manners when cultured mouse hippocampal neurons were treated with 5~40 mU/ml XO for 5 hours. In the protective effect of SMA, SMR increased cell viability dose-dependently after cultured mouse hippocampal neurons were preincubated with 30~120 ㎍/ml SMR for 2 hours. From these results, it is suggested that XO/HX is toxic on cultured mouse hippocampal neurons, and herbe medicine such as SMR is very effective in blocking the cytotoxicity induced by AOS.
KCI Citation Count: 1
Author 이병찬(Byung Chan Lee)
한선희(Sun Hee Han)
송인영(In Young Song)
이강창(Kang Chang Lee)
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DocumentTitleAlternate Effect of Salviae Multiorrhizae Radix on the Cultured Mouse Hippocampal Neurons Damaged by Reactive Oxygen Species
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Xanthine oxidase
Cultured hippocampal neuron
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Title 단삼이 활성산소에 의하여 손상된 배양 해마신경세포에 미치는 영향
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