Cargando…
The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice
Alcohol is a commonly used drug worldwide, and abuse of alcohol has become a serious public health problem. Alcohol consumption over time can cause cognitive deficits and memory impairment, which is thought to be associated with changes in the hippocampus. Given previously known effects of brain-der...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248118/ https://www.ncbi.nlm.nih.gov/pubmed/37303582 http://dx.doi.org/10.1016/j.heliyon.2023.e16660 |
_version_ | 1785055303169998848 |
---|---|
author | Ma, Jingyuan Xiong, Feng Li, Zhouru Dong, Guokai Sun, Xiaoming Yin, Wenjiang Cai, Hongxing |
author_facet | Ma, Jingyuan Xiong, Feng Li, Zhouru Dong, Guokai Sun, Xiaoming Yin, Wenjiang Cai, Hongxing |
author_sort | Ma, Jingyuan |
collection | PubMed |
description | Alcohol is a commonly used drug worldwide, and abuse of alcohol has become a serious public health problem. Alcohol consumption over time can cause cognitive deficits and memory impairment, which is thought to be associated with changes in the hippocampus. Given previously known effects of brain-derived neurotrophic factor (BDNF) in regulating synaptic plasticity and learning and memory, we investigated the effect of chronic alcohol consumption on spatial memory impairment in both sexes and changes in BDNF signaling in the hippocampus. After 4 weeks of intermittent access to 20% alcohol, memory impairment in both male and female mice was evaluated using the Morris water maze and the expression of BDNF, TrkB, phosphorylation of PLCγ1 (p-PLCγ1) and PLCγ1 in the hippocampus was examined using Western blot. As expected, females spent longer escape latencies during the training phase, and both sexes spent shorter time in the target quadrant. Furthermore, after 4 weeks 20% alcohol exposure, we found significantly decreased expression levels of BDNF in the hippocampus of female mice but increased levels in male mice. TrkB and PLCγ1 expression showed no significant change in the hippocampus of both sexes. These findings suggest that chronic alcohol exposure may induce spatial memory impairment in both sexes and opposite changes in expression of BDNF and p-PLCγ1 in the hippocampus of males and females. |
format | Online Article Text |
id | pubmed-10248118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102481182023-06-09 The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice Ma, Jingyuan Xiong, Feng Li, Zhouru Dong, Guokai Sun, Xiaoming Yin, Wenjiang Cai, Hongxing Heliyon Research Article Alcohol is a commonly used drug worldwide, and abuse of alcohol has become a serious public health problem. Alcohol consumption over time can cause cognitive deficits and memory impairment, which is thought to be associated with changes in the hippocampus. Given previously known effects of brain-derived neurotrophic factor (BDNF) in regulating synaptic plasticity and learning and memory, we investigated the effect of chronic alcohol consumption on spatial memory impairment in both sexes and changes in BDNF signaling in the hippocampus. After 4 weeks of intermittent access to 20% alcohol, memory impairment in both male and female mice was evaluated using the Morris water maze and the expression of BDNF, TrkB, phosphorylation of PLCγ1 (p-PLCγ1) and PLCγ1 in the hippocampus was examined using Western blot. As expected, females spent longer escape latencies during the training phase, and both sexes spent shorter time in the target quadrant. Furthermore, after 4 weeks 20% alcohol exposure, we found significantly decreased expression levels of BDNF in the hippocampus of female mice but increased levels in male mice. TrkB and PLCγ1 expression showed no significant change in the hippocampus of both sexes. These findings suggest that chronic alcohol exposure may induce spatial memory impairment in both sexes and opposite changes in expression of BDNF and p-PLCγ1 in the hippocampus of males and females. Elsevier 2023-05-30 /pmc/articles/PMC10248118/ /pubmed/37303582 http://dx.doi.org/10.1016/j.heliyon.2023.e16660 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Ma, Jingyuan Xiong, Feng Li, Zhouru Dong, Guokai Sun, Xiaoming Yin, Wenjiang Cai, Hongxing The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice |
title | The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice |
title_full | The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice |
title_fullStr | The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice |
title_full_unstemmed | The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice |
title_short | The effect of chronic alcohol exposure on spatial memory and BDNF–TrkB- PLCγ1 signaling in the hippocampus of male and female mice |
title_sort | effect of chronic alcohol exposure on spatial memory and bdnf–trkb- plcγ1 signaling in the hippocampus of male and female mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248118/ https://www.ncbi.nlm.nih.gov/pubmed/37303582 http://dx.doi.org/10.1016/j.heliyon.2023.e16660 |
work_keys_str_mv | AT majingyuan theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT xiongfeng theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT lizhouru theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT dongguokai theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT sunxiaoming theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT yinwenjiang theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT caihongxing theeffectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT majingyuan effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT xiongfeng effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT lizhouru effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT dongguokai effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT sunxiaoming effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT yinwenjiang effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice AT caihongxing effectofchronicalcoholexposureonspatialmemoryandbdnftrkbplcg1signalinginthehippocampusofmaleandfemalemice |