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Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats

The hypoglossal nerve controls tongue movements, and damages of it result in difficulty in mastication and food intake. Mastication has been reported to maintain hippocampus‐dependent cognitive function. This study was conducted to examine the effect of tongue motor loss on the hippocampus‐dependent...

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Autores principales: Kim, Doyun, Chung, Sena, Lee, Seung‐Hyun, Choi, Se‐Young, Kim, Soung‐Min, Koo, JaeHyung, Lee, Jong‐Ho, Jahng, Jeong Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706565/
https://www.ncbi.nlm.nih.gov/pubmed/28767193
http://dx.doi.org/10.1111/jcmm.13284
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author Kim, Doyun
Chung, Sena
Lee, Seung‐Hyun
Choi, Se‐Young
Kim, Soung‐Min
Koo, JaeHyung
Lee, Jong‐Ho
Jahng, Jeong Won
author_facet Kim, Doyun
Chung, Sena
Lee, Seung‐Hyun
Choi, Se‐Young
Kim, Soung‐Min
Koo, JaeHyung
Lee, Jong‐Ho
Jahng, Jeong Won
author_sort Kim, Doyun
collection PubMed
description The hypoglossal nerve controls tongue movements, and damages of it result in difficulty in mastication and food intake. Mastication has been reported to maintain hippocampus‐dependent cognitive function. This study was conducted to examine the effect of tongue motor loss on the hippocampus‐dependent cognitive function and its underlying mechanism. Male Sprague Dawley rats were subjected to the initial training of Morris water maze task before or after the bilateral transection of hypoglossal nerves (Hx). When the initial training was given before the surgery, the target quadrant dwelling time during the probe test performed at a week after the surgery was significantly reduced in Hx rats relative to sham‐operated controls. When the initial training was given after the surgery, Hx affected the initial and reversal trainings and probe tests. Brain‐derived neurotrophic factor (BDNF) expression, cell numbers and long‐term potentiation (LTP) were examined in the hippocampus on the 10(th) day, and BrdU and doublecortin staining on the 14(th) day, after the surgery. Hx decreased the hippocampal BDNF and cells in the CA1/CA3 regions and impaired LTP. BrdU and doublecortin staining was decreased in the dentate gyrus of Hx rats. Results suggest that tongue motor loss impairs hippocampus‐dependent cognitive function, and decreased BDNF expression in the hippocampus may be implicated in its underlying molecular mechanism in relation with decreased neurogenesis/proliferation and impaired LTP.
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spelling pubmed-57065652017-12-06 Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats Kim, Doyun Chung, Sena Lee, Seung‐Hyun Choi, Se‐Young Kim, Soung‐Min Koo, JaeHyung Lee, Jong‐Ho Jahng, Jeong Won J Cell Mol Med Original Articles The hypoglossal nerve controls tongue movements, and damages of it result in difficulty in mastication and food intake. Mastication has been reported to maintain hippocampus‐dependent cognitive function. This study was conducted to examine the effect of tongue motor loss on the hippocampus‐dependent cognitive function and its underlying mechanism. Male Sprague Dawley rats were subjected to the initial training of Morris water maze task before or after the bilateral transection of hypoglossal nerves (Hx). When the initial training was given before the surgery, the target quadrant dwelling time during the probe test performed at a week after the surgery was significantly reduced in Hx rats relative to sham‐operated controls. When the initial training was given after the surgery, Hx affected the initial and reversal trainings and probe tests. Brain‐derived neurotrophic factor (BDNF) expression, cell numbers and long‐term potentiation (LTP) were examined in the hippocampus on the 10(th) day, and BrdU and doublecortin staining on the 14(th) day, after the surgery. Hx decreased the hippocampal BDNF and cells in the CA1/CA3 regions and impaired LTP. BrdU and doublecortin staining was decreased in the dentate gyrus of Hx rats. Results suggest that tongue motor loss impairs hippocampus‐dependent cognitive function, and decreased BDNF expression in the hippocampus may be implicated in its underlying molecular mechanism in relation with decreased neurogenesis/proliferation and impaired LTP. John Wiley and Sons Inc. 2017-08-02 2017-12 /pmc/articles/PMC5706565/ /pubmed/28767193 http://dx.doi.org/10.1111/jcmm.13284 Text en © 2017 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kim, Doyun
Chung, Sena
Lee, Seung‐Hyun
Choi, Se‐Young
Kim, Soung‐Min
Koo, JaeHyung
Lee, Jong‐Ho
Jahng, Jeong Won
Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
title Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
title_full Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
title_fullStr Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
title_full_unstemmed Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
title_short Decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
title_sort decreased hippocampal brain‐derived neurotrophic factor and impaired cognitive function by hypoglossal nerve transection in rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706565/
https://www.ncbi.nlm.nih.gov/pubmed/28767193
http://dx.doi.org/10.1111/jcmm.13284
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