Quantitative evaluation of central-type benzodiazepine receptors with [ 125I] Iomazenil in experimental epileptogenesis
This study aimed at quantitatively evaluating hippocampal central-type benzodiazepine receptors (BZRs) in the kainate model of temporal lobe epilepsy (TLE) by in vitro autoradiography (ARG) using [ 125I] Iomazenil (IMZ) specific ligand for central-type BZRs. Kainate (1 μg/0.5 μl) was injected into t...
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Published in | Epilepsy research Vol. 61; no. 1; pp. 105 - 112 |
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Main Authors | , , , , , , |
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Language | English |
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Abstract | This study aimed at quantitatively evaluating hippocampal central-type benzodiazepine receptors (BZRs) in the kainate model of temporal lobe epilepsy (TLE) by in vitro autoradiography (ARG) using [
125I] Iomazenil (IMZ) specific ligand for central-type BZRs. Kainate (1
μg/0.5
μl) was injected into the left amygdala to induce limbic status epilepticus. One, three, or six months after injection, in vitro ARG with [
125I] IMZ and cell counts were performed in the hippocampal CA1–4 regions and dentate gyrus ipsilateral to the kainate injection site, and were compared with the vehicle-injected control group. In all kainate-treated rats, clear pyramidal neuron loss was observed in left hippocampal areas CA1–4. Compared with the control group, progressive reduction of [
125I] IMZ binding was also observed. This resulted in a marked binding decrease paralleling pyramidal neuron loss in hippocampal areas CA1 (down to 83% of control), CA2 (76%), CA3 (75%), and CA4 (90%) at 6 months after kainate administration. Conversely, [
125I] IMZ binding significantly increased in the dentate gyrus (up to 106% of control) at 1 month, but returned to nearly normal at 3–6 months. These results suggest that central-type BZR neuroimaging is useful in detecting hippocampal sclerosis in the mesial TLE, though central BZR alterations differ depending on hippocampal subfields and post-seizure time-courses. |
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AbstractList | This study aimed at quantitatively evaluating hippocampal central-type benzodiazepine receptors (BZRs) in the kainate model of temporal lobe epilepsy (TLE) by in vitro autoradiography (ARG) using [
125I] Iomazenil (IMZ) specific ligand for central-type BZRs. Kainate (1
μg/0.5
μl) was injected into the left amygdala to induce limbic status epilepticus. One, three, or six months after injection, in vitro ARG with [
125I] IMZ and cell counts were performed in the hippocampal CA1–4 regions and dentate gyrus ipsilateral to the kainate injection site, and were compared with the vehicle-injected control group. In all kainate-treated rats, clear pyramidal neuron loss was observed in left hippocampal areas CA1–4. Compared with the control group, progressive reduction of [
125I] IMZ binding was also observed. This resulted in a marked binding decrease paralleling pyramidal neuron loss in hippocampal areas CA1 (down to 83% of control), CA2 (76%), CA3 (75%), and CA4 (90%) at 6 months after kainate administration. Conversely, [
125I] IMZ binding significantly increased in the dentate gyrus (up to 106% of control) at 1 month, but returned to nearly normal at 3–6 months. These results suggest that central-type BZR neuroimaging is useful in detecting hippocampal sclerosis in the mesial TLE, though central BZR alterations differ depending on hippocampal subfields and post-seizure time-courses. |
Author | Hirao, Toru Tamagami, Hiroshi Kakumoto, Miki Morimoto, Kiyoshi Watanabe, Takemi Ninomiya, Takashi Tanaka, Akihiro |
Author_xml | – sequence: 1 givenname: Hiroshi surname: Tamagami fullname: Tamagami, Hiroshi email: hiroshi_tamagami@nmp.co.jp organization: Research Center, Nihon Medi-Physics Co. Ltd., 3-1 Kitasode, Sodegaura City, Chiba Pref. 299-0266, Japan – sequence: 2 givenname: Kiyoshi surname: Morimoto fullname: Morimoto, Kiyoshi organization: Department of Neuropsychiatry, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan – sequence: 3 givenname: Takemi surname: Watanabe fullname: Watanabe, Takemi organization: Department of Neuropsychiatry, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan – sequence: 4 givenname: Takashi surname: Ninomiya fullname: Ninomiya, Takashi organization: Department of Neuropsychiatry, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan – sequence: 5 givenname: Toru surname: Hirao fullname: Hirao, Toru organization: Department of Neuropsychiatry, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa 761-0793, Japan – sequence: 6 givenname: Akihiro surname: Tanaka fullname: Tanaka, Akihiro organization: Research Center, Nihon Medi-Physics Co. Ltd., 3-1 Kitasode, Sodegaura City, Chiba Pref. 299-0266, Japan – sequence: 7 givenname: Miki surname: Kakumoto fullname: Kakumoto, Miki organization: Research Center, Nihon Medi-Physics Co. Ltd., 3-1 Kitasode, Sodegaura City, Chiba Pref. 299-0266, Japan |
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Keywords | Temporal lobe epilepsy Kainate model Benzodiazepine receptor Central-type Rat Iomazenil |
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