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Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice

Status epilepticus (SE) is a frequent medical emergency that can lead to a variety of neurological disorders, including cognitive impairment and abnormal neurogenesis. The aim of the presented study was the in vitro evaluation of potential neuroprotective properties of a new pyrrolidine-2,5-dione de...

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Autores principales: Andres-Mach, Marta, Szewczyk, Aleksandra, Zagaja, Mirosław, Szala-Rycaj, Joanna, Lemieszek, Marta Kinga, Maj, Maciej, Abram, Michał, Kaminski, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004689/
https://www.ncbi.nlm.nih.gov/pubmed/33810180
http://dx.doi.org/10.3390/ijms22063240
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author Andres-Mach, Marta
Szewczyk, Aleksandra
Zagaja, Mirosław
Szala-Rycaj, Joanna
Lemieszek, Marta Kinga
Maj, Maciej
Abram, Michał
Kaminski, Krzysztof
author_facet Andres-Mach, Marta
Szewczyk, Aleksandra
Zagaja, Mirosław
Szala-Rycaj, Joanna
Lemieszek, Marta Kinga
Maj, Maciej
Abram, Michał
Kaminski, Krzysztof
author_sort Andres-Mach, Marta
collection PubMed
description Status epilepticus (SE) is a frequent medical emergency that can lead to a variety of neurological disorders, including cognitive impairment and abnormal neurogenesis. The aim of the presented study was the in vitro evaluation of potential neuroprotective properties of a new pyrrolidine-2,5-dione derivatives compound C11, as well as the in vivo assessment of the impact on the neurogenesis and cognitive functions of C11 and levetiracetam (LEV) after pilocarpine (PILO)-induced SE in mice. The in vitro results indicated a protective effect of C11 (500, 1000, and 2500 ng/mL) on astrocytes under trophic stress conditions in the MTT (3-[4,5-dimethylthiazole-2-yl]-2,5-diphenyltetrazolium bromide) test. The results obtained from the in vivo studies, where mice 72 h after PILO SE were treated with C11 (20 mg/kg) and LEV (10 mg/kg), indicated markedly beneficial effects of C11 on the improvement of the neurogenesis compared to the PILO control and PILO LEV mice. Moreover, this beneficial effect was reflected in the Morris Water Maze test evaluating the cognitive functions in mice. The in vitro confirmed protective effect of C11 on astrocytes, as well as the in vivo demonstrated beneficial impact on neurogenesis and cognitive functions, strongly indicate the need for further advanced molecular research on this compound to determine the exact neuroprotective mechanism of action of C11.
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spelling pubmed-80046892021-03-29 Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice Andres-Mach, Marta Szewczyk, Aleksandra Zagaja, Mirosław Szala-Rycaj, Joanna Lemieszek, Marta Kinga Maj, Maciej Abram, Michał Kaminski, Krzysztof Int J Mol Sci Article Status epilepticus (SE) is a frequent medical emergency that can lead to a variety of neurological disorders, including cognitive impairment and abnormal neurogenesis. The aim of the presented study was the in vitro evaluation of potential neuroprotective properties of a new pyrrolidine-2,5-dione derivatives compound C11, as well as the in vivo assessment of the impact on the neurogenesis and cognitive functions of C11 and levetiracetam (LEV) after pilocarpine (PILO)-induced SE in mice. The in vitro results indicated a protective effect of C11 (500, 1000, and 2500 ng/mL) on astrocytes under trophic stress conditions in the MTT (3-[4,5-dimethylthiazole-2-yl]-2,5-diphenyltetrazolium bromide) test. The results obtained from the in vivo studies, where mice 72 h after PILO SE were treated with C11 (20 mg/kg) and LEV (10 mg/kg), indicated markedly beneficial effects of C11 on the improvement of the neurogenesis compared to the PILO control and PILO LEV mice. Moreover, this beneficial effect was reflected in the Morris Water Maze test evaluating the cognitive functions in mice. The in vitro confirmed protective effect of C11 on astrocytes, as well as the in vivo demonstrated beneficial impact on neurogenesis and cognitive functions, strongly indicate the need for further advanced molecular research on this compound to determine the exact neuroprotective mechanism of action of C11. MDPI 2021-03-22 /pmc/articles/PMC8004689/ /pubmed/33810180 http://dx.doi.org/10.3390/ijms22063240 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Andres-Mach, Marta
Szewczyk, Aleksandra
Zagaja, Mirosław
Szala-Rycaj, Joanna
Lemieszek, Marta Kinga
Maj, Maciej
Abram, Michał
Kaminski, Krzysztof
Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice
title Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice
title_full Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice
title_fullStr Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice
title_full_unstemmed Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice
title_short Preclinical Assessment of a New Hybrid Compound C11 Efficacy on Neurogenesis and Cognitive Functions after Pilocarpine Induced Status Epilepticus in Mice
title_sort preclinical assessment of a new hybrid compound c11 efficacy on neurogenesis and cognitive functions after pilocarpine induced status epilepticus in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8004689/
https://www.ncbi.nlm.nih.gov/pubmed/33810180
http://dx.doi.org/10.3390/ijms22063240
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