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- PMID: 19537923
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Article: Quetiapine ameliorates anxiety-like behavior and cognitive impairments in stressed rats: Implications for the treatment of posttraumatic stress disorder
Title | Quetiapine ameliorates anxiety-like behavior and cognitive impairments in stressed rats: Implications for the treatment of posttraumatic stress disorder | ||||||
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Authors | |||||||
Keywords | Anxiety Cognitive impairment ERK PTSD Quetiapine | ||||||
Issue Date | 2010 | ||||||
Publisher | Akademie Ved Ceske Republiky, Fyziologicky Ustav. The Journal's web site is located at http://www.biomed.cas.cz/physiolres | ||||||
Citation | Physiological Research, 2010, v. 59 n. 2, p. 263-271 How to Cite? | ||||||
Abstract | The purpose of this study was to determine preventive and protective effects of chronic orally administration with quetiapine (QUE) against anxiety-like behavior and cognitive impairments in rats exposed to the enhanced single prolonged stress (ESPS), an animal model that is used to study post-traumatic stress disorder (PTSD), and to detect changes in the expression of cortical phosphorylated p44/42 extracellular-regulated protein kinase (pERK1/2). Before or after exposure to ESPS paradigm, consisting of 2-h constraint, 20-min forced swimming, etherinduced loss of consciousness, and an electric foot shock, rats were given orally QUE (10 mg/kg daily) for 14 days. Animals were then tested in the open field (OF), elevated plus-maze (EPM), and Morris water maze (MWM). Brains were removed for immunohistochemical staining of pERK1/2. ESPS exposure resulted in pronounced anxiety-like behavior compared to unexposed animals. ESPS-exposed animals also displayed marked learning and spatial memory impairments. However, QUE treatment (both before and after ESPS exposure) significantly ameliorated anxiety-like behavior, learning and spatial memory impairments. ESPS also markedly reduced the expression of pERK1/2 in the prefrontal cortex, medial amygdala nucleus, and cingulate gyrus. Both before and after ESPS exposure QUE treatments significantly elevated the reduced pERK1/2 expression in the three brain regions. QUE has preventive and protective effects against stress-associated symptoms and the changes in pERK1/2 functions may be associated with the pathophysiology of traumatic stress and the therapeutic efficacy of anti-PTSD therapy. © 2010 Institute of Physiology v.v.i., Academy of Sciences of the Czech Republic, Prague, Czech Republic. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/60792 | ||||||
ISSN | 2023 Impact Factor: 1.9 2023 SCImago Journal Rankings: 0.584 | ||||||
ISI Accession Number ID |
Funding Information: This work was supported by grants from the Natural Science Foundation of China (No. 30670758/30870886 to QR Tan, No. 30700259 to YC Chen, and No. 30670666 to BR Wang), and the 11th Five-Year Project of Military Medicine Foundations (06G096 to Dr. QR Tan). | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wang, HN | en_HK |
dc.contributor.author | Peng, Y | en_HK |
dc.contributor.author | Tan, QR | en_HK |
dc.contributor.author | Chen, YC | en_HK |
dc.contributor.author | Zhang, RG | en_HK |
dc.contributor.author | Qiao, YT | en_HK |
dc.contributor.author | Wang, HH | en_HK |
dc.contributor.author | Liu, L | en_HK |
dc.contributor.author | Kuang, F | en_HK |
dc.contributor.author | Wang, BR | en_HK |
dc.contributor.author | Zhang, ZJ | en_HK |
dc.date.accessioned | 2010-05-31T04:18:40Z | - |
dc.date.available | 2010-05-31T04:18:40Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Physiological Research, 2010, v. 59 n. 2, p. 263-271 | en_HK |
dc.identifier.issn | 0862-8408 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/60792 | - |
dc.description.abstract | The purpose of this study was to determine preventive and protective effects of chronic orally administration with quetiapine (QUE) against anxiety-like behavior and cognitive impairments in rats exposed to the enhanced single prolonged stress (ESPS), an animal model that is used to study post-traumatic stress disorder (PTSD), and to detect changes in the expression of cortical phosphorylated p44/42 extracellular-regulated protein kinase (pERK1/2). Before or after exposure to ESPS paradigm, consisting of 2-h constraint, 20-min forced swimming, etherinduced loss of consciousness, and an electric foot shock, rats were given orally QUE (10 mg/kg daily) for 14 days. Animals were then tested in the open field (OF), elevated plus-maze (EPM), and Morris water maze (MWM). Brains were removed for immunohistochemical staining of pERK1/2. ESPS exposure resulted in pronounced anxiety-like behavior compared to unexposed animals. ESPS-exposed animals also displayed marked learning and spatial memory impairments. However, QUE treatment (both before and after ESPS exposure) significantly ameliorated anxiety-like behavior, learning and spatial memory impairments. ESPS also markedly reduced the expression of pERK1/2 in the prefrontal cortex, medial amygdala nucleus, and cingulate gyrus. Both before and after ESPS exposure QUE treatments significantly elevated the reduced pERK1/2 expression in the three brain regions. QUE has preventive and protective effects against stress-associated symptoms and the changes in pERK1/2 functions may be associated with the pathophysiology of traumatic stress and the therapeutic efficacy of anti-PTSD therapy. © 2010 Institute of Physiology v.v.i., Academy of Sciences of the Czech Republic, Prague, Czech Republic. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Akademie Ved Ceske Republiky, Fyziologicky Ustav. The Journal's web site is located at http://www.biomed.cas.cz/physiolres | en_HK |
dc.relation.ispartof | Physiological Research | en_HK |
dc.subject | Anxiety | en_HK |
dc.subject | Cognitive impairment | en_HK |
dc.subject | ERK | en_HK |
dc.subject | PTSD | en_HK |
dc.subject | Quetiapine | en_HK |
dc.title | Quetiapine ameliorates anxiety-like behavior and cognitive impairments in stressed rats: Implications for the treatment of posttraumatic stress disorder | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Zhang, ZJ: zhangzj@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zhang, ZJ=rp01297 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.pmid | 19537923 | en_HK |
dc.identifier.scopus | eid_2-s2.0-77953932094 | en_HK |
dc.identifier.hkuros | 160162 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77953932094&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 59 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 263 | en_HK |
dc.identifier.epage | 271 | en_HK |
dc.identifier.isi | WOS:000278016200014 | - |
dc.publisher.place | Czech Republic | en_HK |
dc.identifier.scopusauthorid | Wang, HN=7501732342 | en_HK |
dc.identifier.scopusauthorid | Peng, Y=34870185600 | en_HK |
dc.identifier.scopusauthorid | Tan, QR=7102120177 | en_HK |
dc.identifier.scopusauthorid | Chen, YC=24775181700 | en_HK |
dc.identifier.scopusauthorid | Zhang, RG=7404864877 | en_HK |
dc.identifier.scopusauthorid | Qiao, YT=26650169400 | en_HK |
dc.identifier.scopusauthorid | Wang, HH=10144885500 | en_HK |
dc.identifier.scopusauthorid | Liu, L=35211019300 | en_HK |
dc.identifier.scopusauthorid | Kuang, F=6602241329 | en_HK |
dc.identifier.scopusauthorid | Wang, BR=7405917235 | en_HK |
dc.identifier.scopusauthorid | Zhang, ZJ=8061473900 | en_HK |
dc.identifier.issnl | 0862-8408 | - |