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Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure
Epilepsy is one of the most common and severe brain diseases. The exact cause of epilepsy is unclear. Epilepsy often occurs following brain damage, such as traumatic brain injury (TBI) and ischemia. Cerebrolysin is a porcine brain peptide that is a unique neurotropic and neuroprotective agent. Cereb...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596733/ https://www.ncbi.nlm.nih.gov/pubmed/33177978 http://dx.doi.org/10.3389/fnins.2020.568813 |
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author | Kang, Dong Hyeon Choi, Bo Young Lee, Song Hee Kho, A Ra Jeong, Jeong Hyun Hong, Dae Ki Kang, Beom Seok Park, Min Kyu Song, Hong Ki Choi, Hui Chul Lim, Man-Sup Suh, Sang Won |
author_facet | Kang, Dong Hyeon Choi, Bo Young Lee, Song Hee Kho, A Ra Jeong, Jeong Hyun Hong, Dae Ki Kang, Beom Seok Park, Min Kyu Song, Hong Ki Choi, Hui Chul Lim, Man-Sup Suh, Sang Won |
author_sort | Kang, Dong Hyeon |
collection | PubMed |
description | Epilepsy is one of the most common and severe brain diseases. The exact cause of epilepsy is unclear. Epilepsy often occurs following brain damage, such as traumatic brain injury (TBI) and ischemia. Cerebrolysin is a porcine brain peptide that is a unique neurotropic and neuroprotective agent. Cerebrolysin has been reported to increase neuroprotective effects after TBI, ischemia, and other CNS diseases. However, the effects of cerebrolysin on seizures are not known. Therefore, this study aimed to investigate the effects of neuropeptide cerebrolysin on neuronal death in the hippocampus after a seizure. To confirm the effects of cerebrolysin, we used a pilocarpine-induced seizure animal model. Cerebrolysin (2.5 ml/kg, i.p., once per day for 7 days) was immediately injected after a seizure induction. After 1 week, we obtained brain tissues and performed staining to histologically evaluate the potentially protective effects of cerebrolysin on seizure-induced neuronal death in the hippocampus. We found that cerebrolysin decreased hippocampal neuronal death after a seizure. In addition, an increase in brain-derived neurotrophic factor (BDNF) was confirmed through Western blot analysis to further support our hypothesis. Therefore, the present study suggests that the administration of cerebrolysin can be a useful therapeutic tool for preventing neuronal death after a seizure. |
format | Online Article Text |
id | pubmed-7596733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75967332020-11-10 Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure Kang, Dong Hyeon Choi, Bo Young Lee, Song Hee Kho, A Ra Jeong, Jeong Hyun Hong, Dae Ki Kang, Beom Seok Park, Min Kyu Song, Hong Ki Choi, Hui Chul Lim, Man-Sup Suh, Sang Won Front Neurosci Neuroscience Epilepsy is one of the most common and severe brain diseases. The exact cause of epilepsy is unclear. Epilepsy often occurs following brain damage, such as traumatic brain injury (TBI) and ischemia. Cerebrolysin is a porcine brain peptide that is a unique neurotropic and neuroprotective agent. Cerebrolysin has been reported to increase neuroprotective effects after TBI, ischemia, and other CNS diseases. However, the effects of cerebrolysin on seizures are not known. Therefore, this study aimed to investigate the effects of neuropeptide cerebrolysin on neuronal death in the hippocampus after a seizure. To confirm the effects of cerebrolysin, we used a pilocarpine-induced seizure animal model. Cerebrolysin (2.5 ml/kg, i.p., once per day for 7 days) was immediately injected after a seizure induction. After 1 week, we obtained brain tissues and performed staining to histologically evaluate the potentially protective effects of cerebrolysin on seizure-induced neuronal death in the hippocampus. We found that cerebrolysin decreased hippocampal neuronal death after a seizure. In addition, an increase in brain-derived neurotrophic factor (BDNF) was confirmed through Western blot analysis to further support our hypothesis. Therefore, the present study suggests that the administration of cerebrolysin can be a useful therapeutic tool for preventing neuronal death after a seizure. Frontiers Media S.A. 2020-10-16 /pmc/articles/PMC7596733/ /pubmed/33177978 http://dx.doi.org/10.3389/fnins.2020.568813 Text en Copyright © 2020 Kang, Choi, Lee, Kho, Jeong, Hong, Kang, Park, Song, Choi, Lim and Suh. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kang, Dong Hyeon Choi, Bo Young Lee, Song Hee Kho, A Ra Jeong, Jeong Hyun Hong, Dae Ki Kang, Beom Seok Park, Min Kyu Song, Hong Ki Choi, Hui Chul Lim, Man-Sup Suh, Sang Won Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure |
title | Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure |
title_full | Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure |
title_fullStr | Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure |
title_full_unstemmed | Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure |
title_short | Effects of Cerebrolysin on Hippocampal Neuronal Death After Pilocarpine-Induced Seizure |
title_sort | effects of cerebrolysin on hippocampal neuronal death after pilocarpine-induced seizure |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596733/ https://www.ncbi.nlm.nih.gov/pubmed/33177978 http://dx.doi.org/10.3389/fnins.2020.568813 |
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