The Mechanism of Anti-Epileptogenesis by Levetiracetam Treatment is Similar to the Spontaneous Recovery of Idiopathic Generalized Epilepsy during Adolescence
The anti-epileptogenic drug levetiracetam has anticonvulsant and anti-epileptogenesis effects. Synergy between cell death and inflammation can lead to increased levels of apoptosis inhibitory factors and brain-derived neurotrophic factor, aberrant neurogenesis and extended axon sprouting. Once hyper...
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Published in | Psychiatry investigation Vol. 14; no. 6; pp. 844 - 850 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Korea (South)
Korean Neuropsychiatric Association
01.11.2017
대한신경정신의학회 |
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Abstract | The anti-epileptogenic drug levetiracetam has anticonvulsant and anti-epileptogenesis effects. Synergy between cell death and inflammation can lead to increased levels of apoptosis inhibitory factors and brain-derived neurotrophic factor, aberrant neurogenesis and extended axon sprouting. Once hyperexcitation of the neural network occurs, spontaneous seizures or epileptogenesis develops. This study investigated whether the anti-epileptogenic effect of levetiracetam is due to its alternate apoptotic activity.
Adult male Noda epileptic rats were treated with levetiracetam or vehicle control for two weeks. mRNA quantification of Bax, Bcl-2 and GAPDH expression were performed from prefrontal cortex and hippocampus tissue samples.
The levetiracetam-treated group showed a significant increase of Bax/Bcl-2 mRNA expression ratio in the prefrontal cortex than the control group, but no change in the Bax/Bcl-2 mRNA expression ratio in hippocampus.
Idiopathic generalized epilepsy including childhood absence epilepsy develop at childhood and recover spontaneously during adolescence. The aberrant neural excitable network is pruned by a neural-maturing action. This study suggests the mechanism of acquired anti-epileptogenesis by levetiracetam treatment may be similar to spontaneous recovery of idiopathic generalized epilepsy during adolescence. |
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AbstractList | The anti-epileptogenic drug levetiracetam has anticonvulsant and anti-epileptogenesis effects. Synergy between cell death and inflammation can lead to increased levels of apoptosis inhibitory factors and brain-derived neurotrophic factor, aberrant neurogenesis and extended axon sprouting. Once hyperexcitation of the neural network occurs, spontaneous seizures or epileptogenesis develops. This study investigated whether the anti-epileptogenic effect of levetiracetam is due to its alternate apoptotic activity.
Adult male Noda epileptic rats were treated with levetiracetam or vehicle control for two weeks. mRNA quantification of Bax, Bcl-2 and GAPDH expression were performed from prefrontal cortex and hippocampus tissue samples.
The levetiracetam-treated group showed a significant increase of Bax/Bcl-2 mRNA expression ratio in the prefrontal cortex than the control group, but no change in the Bax/Bcl-2 mRNA expression ratio in hippocampus.
Idiopathic generalized epilepsy including childhood absence epilepsy develop at childhood and recover spontaneously during adolescence. The aberrant neural excitable network is pruned by a neural-maturing action. This study suggests the mechanism of acquired anti-epileptogenesis by levetiracetam treatment may be similar to spontaneous recovery of idiopathic generalized epilepsy during adolescence. Objective: The anti-epileptogenic drug levetiracetam has anticonvulsant and anti-epileptogenesis effects. Synergy between cell death and inflammation can lead to increased levels of apoptosis inhibitory factors and brain-derived neurotrophic factor, aberrant neurogenesis and extended axon sprouting. Once hyperexcitation of the neural network occurs, spontaneous seizures or epileptogenesis develops. This study investigated whether the anti-epileptogenic effect of levetiracetam is due to its alternate apoptotic activity. Methods: Adult male Noda epileptic rats were treated with levetiracetam or vehicle control for two weeks. mRNA quantification of Bax, Bcl-2 and GAPDH expression were performed from prefrontal cortex and hippocampus tissue samples. Results: The levetiracetam-treated group showed a significant increase of Bax/Bcl-2 mRNA expression ratio in the prefrontal cortex than the control group, but no change in the Bax/Bcl-2 mRNA expression ratio in hippocampus. Conclusion: Idiopathic generalized epilepsy including childhood absence epilepsy develop at childhood and recover spontaneously during adolescence. The aberrant neural excitable network is pruned by a neural-maturing action. This study suggests the mechanism of acquired anti-epileptogenesis by levetiracetam treatment may be similar to spontaneous recovery of idiopathic generalized epilepsy during adolescence. KCI Citation Count: 0 OBJECTIVEThe anti-epileptogenic drug levetiracetam has anticonvulsant and anti-epileptogenesis effects. Synergy between cell death and inflammation can lead to increased levels of apoptosis inhibitory factors and brain-derived neurotrophic factor, aberrant neurogenesis and extended axon sprouting. Once hyperexcitation of the neural network occurs, spontaneous seizures or epileptogenesis develops. This study investigated whether the anti-epileptogenic effect of levetiracetam is due to its alternate apoptotic activity. METHODSAdult male Noda epileptic rats were treated with levetiracetam or vehicle control for two weeks. mRNA quantification of Bax, Bcl-2 and GAPDH expression were performed from prefrontal cortex and hippocampus tissue samples. RESULTSThe levetiracetam-treated group showed a significant increase of Bax/Bcl-2 mRNA expression ratio in the prefrontal cortex than the control group, but no change in the Bax/Bcl-2 mRNA expression ratio in hippocampus. CONCLUSIONIdiopathic generalized epilepsy including childhood absence epilepsy develop at childhood and recover spontaneously during adolescence. The aberrant neural excitable network is pruned by a neural-maturing action. This study suggests the mechanism of acquired anti-epileptogenesis by levetiracetam treatment may be similar to spontaneous recovery of idiopathic generalized epilepsy during adolescence. |
Author | Mizuno, Takafumi Kikuyama, Hiroki Yoneda, Hiroshi Toyoda, Hirotaka Yoshida, Yasushi Kanazawa, Tetsufumi Hanaoka, Tadahito |
AuthorAffiliation | Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan |
AuthorAffiliation_xml | – name: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan |
Author_xml | – sequence: 1 givenname: Hiroki surname: Kikuyama fullname: Kikuyama, Hiroki organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan – sequence: 2 givenname: Tadahito surname: Hanaoka fullname: Hanaoka, Tadahito organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan – sequence: 3 givenname: Tetsufumi surname: Kanazawa fullname: Kanazawa, Tetsufumi organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan – sequence: 4 givenname: Yasushi surname: Yoshida fullname: Yoshida, Yasushi organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan – sequence: 5 givenname: Takafumi surname: Mizuno fullname: Mizuno, Takafumi organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan – sequence: 6 givenname: Hirotaka surname: Toyoda fullname: Toyoda, Hirotaka organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan – sequence: 7 givenname: Hiroshi surname: Yoneda fullname: Yoneda, Hiroshi organization: Department of Neuropsychiatry, Osaka Medical College, Osaka, Japan |
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CitedBy_id | crossref_primary_10_2196_49412 crossref_primary_10_1016_j_eplepsyres_2019_05_007 crossref_primary_10_1016_j_lfs_2021_119923 crossref_primary_10_3390_ijms25031690 crossref_primary_10_3389_fneur_2021_747372 crossref_primary_10_1016_j_yebeh_2019_02_012 |
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Keywords | Epileptogenesis Idiopathic generalized epilepsy Noda epileptic rat Apoptosis Levetiracetam |
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Title | The Mechanism of Anti-Epileptogenesis by Levetiracetam Treatment is Similar to the Spontaneous Recovery of Idiopathic Generalized Epilepsy during Adolescence |
URI | https://www.ncbi.nlm.nih.gov/pubmed/29209390 https://search.proquest.com/docview/1973452387 https://pubmed.ncbi.nlm.nih.gov/PMC5714728 https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002284660 |
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ispartofPNX | PSYCHIATRY INVESTIGATION, 2017, 14(6), , pp.844-850 |
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