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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Can, Fu, Jian, Qu, Zhenzhen, Jia, Lijing, Li, Dongxiao, Zhen, Junli, Wang, Weiping
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