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      KCI등재후보

      간질 발작시에 나타나는 조기유전자 발현의 변화 = Changes of Immediate Early Gene Induction in the Drug-Induced Seizure Models

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      https://www.riss.kr/link?id=A2026122

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      다국어 초록 (Multilingual Abstract)

      Cellular immediate early gene expressions have been demonstrated to be modulated in response to a variety of seizure-inducing stimuli. In this study, two immediate early genes, c-fos and c-myc were investigated in response to the convulsants such as kainic acid(KA, 10mg/kg, ip). pentylenetetrazole(PTZ, 40mg/kg, ip), and N-methy1-D-aspartate(NMEA, 60mg/kg, ip) in three regions of rat brain : cerebral cortex, striatum, and brain stem. The KA and PTZ treatment slightly increased the transcription of c-fos in cerebral cortex, striatum, and brain stem. The MK-801 or baclofen pretreatment did not block the elevated expression of c-fos by KA and PTZ treatment. The NMDA treatment showed a reversal response of KA and PTZ treatment. The c-myc expression did not show a significant change in each of convulsant treatment groups and MK-801 or baclofen pretreatment did not exhibit considerable differenes.
      Therefore, c-fos could be one of the first seizure-related genes expressed in a cascade of events underlying different post-translational products, which result in diverse functional consequences depending on the brain sites.
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      Cellular immediate early gene expressions have been demonstrated to be modulated in response to a variety of seizure-inducing stimuli. In this study, two immediate early genes, c-fos and c-myc were investigated in response to the convulsants such as k...

      Cellular immediate early gene expressions have been demonstrated to be modulated in response to a variety of seizure-inducing stimuli. In this study, two immediate early genes, c-fos and c-myc were investigated in response to the convulsants such as kainic acid(KA, 10mg/kg, ip). pentylenetetrazole(PTZ, 40mg/kg, ip), and N-methy1-D-aspartate(NMEA, 60mg/kg, ip) in three regions of rat brain : cerebral cortex, striatum, and brain stem. The KA and PTZ treatment slightly increased the transcription of c-fos in cerebral cortex, striatum, and brain stem. The MK-801 or baclofen pretreatment did not block the elevated expression of c-fos by KA and PTZ treatment. The NMDA treatment showed a reversal response of KA and PTZ treatment. The c-myc expression did not show a significant change in each of convulsant treatment groups and MK-801 or baclofen pretreatment did not exhibit considerable differenes.
      Therefore, c-fos could be one of the first seizure-related genes expressed in a cascade of events underlying different post-translational products, which result in diverse functional consequences depending on the brain sites.

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