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Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration
Altered expression of neurotrophic factors as well as neuroinflammation is commonly associated with Major depressive disorder (MDD) and Alzheimer's disease (AD). To investigate whether or not reserpine-induced MDD affects the expression of AD-related proteins, the expression of γ-secretase comp...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389834/ https://www.ncbi.nlm.nih.gov/pubmed/22787484 http://dx.doi.org/10.5625/lar.2012.28.2.109 |
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author | Lee, Hye-Ryun Hwang, In-Sik Kim, Ji-Eun Choi, Sun-Il Lee, Young-Ju Goo, Jun-Seo Lee, Eon-Pil Choi, Hae-Wook Kim, Hong-Sung Lee, Jae-Ho Jung, Young-Jin Hwang, Dae-Youn |
author_facet | Lee, Hye-Ryun Hwang, In-Sik Kim, Ji-Eun Choi, Sun-Il Lee, Young-Ju Goo, Jun-Seo Lee, Eon-Pil Choi, Hae-Wook Kim, Hong-Sung Lee, Jae-Ho Jung, Young-Jin Hwang, Dae-Youn |
author_sort | Lee, Hye-Ryun |
collection | PubMed |
description | Altered expression of neurotrophic factors as well as neuroinflammation is commonly associated with Major depressive disorder (MDD) and Alzheimer's disease (AD). To investigate whether or not reserpine-induced MDD affects the expression of AD-related proteins, the expression of γ-secretase components and substrate were measured in brains of ICR mice following reserpine treatment for 15 days. In active avoidance test, total response time and peak slightly increased in the 2 mg/kg reserpine (RSP2)-treated group compared to vehicle-treated group (P<0.05). Expression and phosphorylation of MKP-1, which is a key factor in MDD pathology, were both higher in the RSP2-treated group than the vehicle- and 1 mg/kg reserpine (RSP1)-treated groups (P<0.02). Furthermore, full-length expression of amyloid precursor protein (APP) was enhanced in the RSP1 and RSP2-treated groups compared to the vehicle-treated group, whereas expression of γ-secretase components decreased (P<0.03). Among the three components of the γ-secretase complex, nicastrin protein underwent the largest decrease in expression, as detected by Western blotting (P<0.03). Therefore, the data presented here provide additional evidence about the pathological correlation between MDD and AD. |
format | Online Article Text |
id | pubmed-3389834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33898342012-07-11 Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration Lee, Hye-Ryun Hwang, In-Sik Kim, Ji-Eun Choi, Sun-Il Lee, Young-Ju Goo, Jun-Seo Lee, Eon-Pil Choi, Hae-Wook Kim, Hong-Sung Lee, Jae-Ho Jung, Young-Jin Hwang, Dae-Youn Lab Anim Res Original Article Altered expression of neurotrophic factors as well as neuroinflammation is commonly associated with Major depressive disorder (MDD) and Alzheimer's disease (AD). To investigate whether or not reserpine-induced MDD affects the expression of AD-related proteins, the expression of γ-secretase components and substrate were measured in brains of ICR mice following reserpine treatment for 15 days. In active avoidance test, total response time and peak slightly increased in the 2 mg/kg reserpine (RSP2)-treated group compared to vehicle-treated group (P<0.05). Expression and phosphorylation of MKP-1, which is a key factor in MDD pathology, were both higher in the RSP2-treated group than the vehicle- and 1 mg/kg reserpine (RSP1)-treated groups (P<0.02). Furthermore, full-length expression of amyloid precursor protein (APP) was enhanced in the RSP1 and RSP2-treated groups compared to the vehicle-treated group, whereas expression of γ-secretase components decreased (P<0.03). Among the three components of the γ-secretase complex, nicastrin protein underwent the largest decrease in expression, as detected by Western blotting (P<0.03). Therefore, the data presented here provide additional evidence about the pathological correlation between MDD and AD. Korean Association for Laboratory Animal Science 2012-06 2012-06-26 /pmc/articles/PMC3389834/ /pubmed/22787484 http://dx.doi.org/10.5625/lar.2012.28.2.109 Text en Copyright © 2012 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Hye-Ryun Hwang, In-Sik Kim, Ji-Eun Choi, Sun-Il Lee, Young-Ju Goo, Jun-Seo Lee, Eon-Pil Choi, Hae-Wook Kim, Hong-Sung Lee, Jae-Ho Jung, Young-Jin Hwang, Dae-Youn Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
title | Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
title_full | Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
title_fullStr | Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
title_full_unstemmed | Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
title_short | Altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
title_sort | altered expression of γ-secretase components in animal model of major depressive disorder induced by reserpine administration |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389834/ https://www.ncbi.nlm.nih.gov/pubmed/22787484 http://dx.doi.org/10.5625/lar.2012.28.2.109 |
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