Cargando…
Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling
Epilepsy is a complex neurological disorder with frequent psychiatric, cognitive, and social comorbidities in addition to recurrent seizures. Cognitive impairment, one of the most common comorbidities, has severe adverse effects on quality of life. Chronic intermittent hypobaric hypoxia (CIHH) has d...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874094/ https://www.ncbi.nlm.nih.gov/pubmed/33584201 http://dx.doi.org/10.3389/fnmol.2020.617143 |
_version_ | 1783649518224408576 |
---|---|
author | Sun, Can Fu, Jian Qu, Zhenzhen Jia, Lijing Li, Dongxiao Zhen, Junli Wang, Weiping |
author_facet | Sun, Can Fu, Jian Qu, Zhenzhen Jia, Lijing Li, Dongxiao Zhen, Junli Wang, Weiping |
author_sort | Sun, Can |
collection | PubMed |
description | Epilepsy is a complex neurological disorder with frequent psychiatric, cognitive, and social comorbidities in addition to recurrent seizures. Cognitive impairment, one of the most common comorbidities, has severe adverse effects on quality of life. Chronic intermittent hypobaric hypoxia (CIHH) has demonstrated neuroprotective efficacy in several neurological disease models. In the present study, we examined the effects of CIHH on cognition and hippocampal function in chronic epileptic rats. CIHH treatment rescued deficits in spatial and object memory, hippocampal neurogenesis, and synaptic plasticity in pilocarpine-treated epileptic rats. The Wnt/β-catenin pathway has been implicated in neural stem cell proliferation and synapse development, and Wnt/β-catenin pathway inhibition effectively blocked the neurogenic effects of CIHH. Our findings indicate that CIHH rescues cognitive deficits in epileptic rats via Wnt/β-catenin pathway activation. This study establishes CIHH and Wnt/β-catenin pathway regulators as potential treatments for epilepsy- induced cognitive impairments. |
format | Online Article Text |
id | pubmed-7874094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78740942021-02-11 Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling Sun, Can Fu, Jian Qu, Zhenzhen Jia, Lijing Li, Dongxiao Zhen, Junli Wang, Weiping Front Mol Neurosci Neuroscience Epilepsy is a complex neurological disorder with frequent psychiatric, cognitive, and social comorbidities in addition to recurrent seizures. Cognitive impairment, one of the most common comorbidities, has severe adverse effects on quality of life. Chronic intermittent hypobaric hypoxia (CIHH) has demonstrated neuroprotective efficacy in several neurological disease models. In the present study, we examined the effects of CIHH on cognition and hippocampal function in chronic epileptic rats. CIHH treatment rescued deficits in spatial and object memory, hippocampal neurogenesis, and synaptic plasticity in pilocarpine-treated epileptic rats. The Wnt/β-catenin pathway has been implicated in neural stem cell proliferation and synapse development, and Wnt/β-catenin pathway inhibition effectively blocked the neurogenic effects of CIHH. Our findings indicate that CIHH rescues cognitive deficits in epileptic rats via Wnt/β-catenin pathway activation. This study establishes CIHH and Wnt/β-catenin pathway regulators as potential treatments for epilepsy- induced cognitive impairments. Frontiers Media S.A. 2021-01-20 /pmc/articles/PMC7874094/ /pubmed/33584201 http://dx.doi.org/10.3389/fnmol.2020.617143 Text en Copyright © 2021 Sun, Fu, Qu, Jia, Li, Zhen and Wang. 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 Sun, Can Fu, Jian Qu, Zhenzhen Jia, Lijing Li, Dongxiao Zhen, Junli Wang, Weiping Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling |
title | Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling |
title_full | Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling |
title_fullStr | Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling |
title_full_unstemmed | Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling |
title_short | Chronic Intermittent Hypobaric Hypoxia Restores Hippocampus Function and Rescues Cognitive Impairments in Chronic Epileptic Rats via Wnt/β-catenin Signaling |
title_sort | chronic intermittent hypobaric hypoxia restores hippocampus function and rescues cognitive impairments in chronic epileptic rats via wnt/β-catenin signaling |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874094/ https://www.ncbi.nlm.nih.gov/pubmed/33584201 http://dx.doi.org/10.3389/fnmol.2020.617143 |
work_keys_str_mv | AT suncan chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling AT fujian chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling AT quzhenzhen chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling AT jialijing chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling AT lidongxiao chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling AT zhenjunli chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling AT wangweiping chronicintermittenthypobarichypoxiarestoreshippocampusfunctionandrescuescognitiveimpairmentsinchronicepilepticratsviawntbcateninsignaling |