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Chronic fluoxetine treatment improves ischemia-induced spatial cognitive deficits through increasing hippocampal neurogenesis after stroke
Cognitive deficits, including spatial memory impairment, are very common after ischemic stroke. Neurogenesis in the dentate gyrus (DG) contributes to forming spatial memory in the ischemic brain. Fluoxetine, a selective serotonin reuptake inhibitor, can enhance neurogenesis in the hippocampus in phy...
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Published in: | Journal of neuroscience research 2009-01, Vol.87 (1), p.112-122 |
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container_title | Journal of neuroscience research |
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creator | Li, Wen-Lei Cai, Hui-Hui Wang, Bin Chen, Ling Zhou, Qi-Gang Luo, Chun-Xia Liu, Na Ding, Xin-Sheng Zhu, Dong-Ya |
description | Cognitive deficits, including spatial memory impairment, are very common after ischemic stroke. Neurogenesis in the dentate gyrus (DG) contributes to forming spatial memory in the ischemic brain. Fluoxetine, a selective serotonin reuptake inhibitor, can enhance neurogenesis in the hippocampus in physiological situations and some neurological diseases. However, whether it has effects on ischemia‐induced spatial cognitive impairment and hippocampal neurogenesis has not been determined. Here we report that fluoxetine treatment (10 mg kg−1, i.p.) for 4 weeks promoted the survival of newborn cells in the ischemic hippocampus and, consequently, attenuated spatial memory impairment of mice after focal cerebral ischemia. Disrupting hippocampal neurogenesis blocked the beneficial effect of fluoxetine on ischemia‐induced spatial cognitive impairment. These results suggest that chronic fluoxetine treatment benefits spatial cognitive function recovery following ischemic insult, and the improved cognitive function is associated with enhanced newborn cell survival in the hippocampus. Our results raise the possibility that fluoxetine can be used as a drug to treat poststroke spatial cognitive deficits. © 2008 Wiley‐Liss, Inc. |
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Neurogenesis in the dentate gyrus (DG) contributes to forming spatial memory in the ischemic brain. Fluoxetine, a selective serotonin reuptake inhibitor, can enhance neurogenesis in the hippocampus in physiological situations and some neurological diseases. However, whether it has effects on ischemia‐induced spatial cognitive impairment and hippocampal neurogenesis has not been determined. Here we report that fluoxetine treatment (10 mg kg−1, i.p.) for 4 weeks promoted the survival of newborn cells in the ischemic hippocampus and, consequently, attenuated spatial memory impairment of mice after focal cerebral ischemia. Disrupting hippocampal neurogenesis blocked the beneficial effect of fluoxetine on ischemia‐induced spatial cognitive impairment. These results suggest that chronic fluoxetine treatment benefits spatial cognitive function recovery following ischemic insult, and the improved cognitive function is associated with enhanced newborn cell survival in the hippocampus. Our results raise the possibility that fluoxetine can be used as a drug to treat poststroke spatial cognitive deficits. © 2008 Wiley‐Liss, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.21829</identifier><identifier>PMID: 18711744</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Analysis of Variance ; Animals ; Antimetabolites - pharmacology ; Bromodeoxyuridine - metabolism ; Cell Count - methods ; Cognition Disorders - diagnosis ; Cognition Disorders - drug therapy ; Cognition Disorders - pathology ; Disease Models, Animal ; fluoxetine ; Fluoxetine - therapeutic use ; focal cerebral ischemia ; hippocampus ; Infarction, Middle Cerebral Artery - complications ; Infarction, Middle Cerebral Artery - drug therapy ; Male ; Maze Learning - drug effects ; Mice ; Mice, Inbred C57BL ; neurogenesis ; Neurogenesis - drug effects ; Neurons - drug effects ; Neurons - physiology ; Psychomotor Performance - drug effects ; Reaction Time - drug effects ; sensorimotor function ; Serotonin Uptake Inhibitors - therapeutic use ; Severity of Illness Index ; Space Perception - drug effects ; spatial cognitive function ; Swimming ; Time Factors ; Zidovudine - pharmacology</subject><ispartof>Journal of neuroscience research, 2009-01, Vol.87 (1), p.112-122</ispartof><rights>Copyright © 2008 Wiley‐Liss, Inc.</rights><rights>2008 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4589-4a1235535f21d5848271f5931984effc07d94a71be9c0e10e44fbaf2974169d13</citedby><cites>FETCH-LOGICAL-c4589-4a1235535f21d5848271f5931984effc07d94a71be9c0e10e44fbaf2974169d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18711744$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Wen-Lei</creatorcontrib><creatorcontrib>Cai, Hui-Hui</creatorcontrib><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Chen, Ling</creatorcontrib><creatorcontrib>Zhou, Qi-Gang</creatorcontrib><creatorcontrib>Luo, Chun-Xia</creatorcontrib><creatorcontrib>Liu, Na</creatorcontrib><creatorcontrib>Ding, Xin-Sheng</creatorcontrib><creatorcontrib>Zhu, Dong-Ya</creatorcontrib><title>Chronic fluoxetine treatment improves ischemia-induced spatial cognitive deficits through increasing hippocampal neurogenesis after stroke</title><title>Journal of neuroscience research</title><addtitle>J. Neurosci. Res</addtitle><description>Cognitive deficits, including spatial memory impairment, are very common after ischemic stroke. Neurogenesis in the dentate gyrus (DG) contributes to forming spatial memory in the ischemic brain. Fluoxetine, a selective serotonin reuptake inhibitor, can enhance neurogenesis in the hippocampus in physiological situations and some neurological diseases. However, whether it has effects on ischemia‐induced spatial cognitive impairment and hippocampal neurogenesis has not been determined. Here we report that fluoxetine treatment (10 mg kg−1, i.p.) for 4 weeks promoted the survival of newborn cells in the ischemic hippocampus and, consequently, attenuated spatial memory impairment of mice after focal cerebral ischemia. Disrupting hippocampal neurogenesis blocked the beneficial effect of fluoxetine on ischemia‐induced spatial cognitive impairment. These results suggest that chronic fluoxetine treatment benefits spatial cognitive function recovery following ischemic insult, and the improved cognitive function is associated with enhanced newborn cell survival in the hippocampus. Our results raise the possibility that fluoxetine can be used as a drug to treat poststroke spatial cognitive deficits. © 2008 Wiley‐Liss, Inc.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Antimetabolites - pharmacology</subject><subject>Bromodeoxyuridine - metabolism</subject><subject>Cell Count - methods</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - drug therapy</subject><subject>Cognition Disorders - pathology</subject><subject>Disease Models, Animal</subject><subject>fluoxetine</subject><subject>Fluoxetine - therapeutic use</subject><subject>focal cerebral ischemia</subject><subject>hippocampus</subject><subject>Infarction, Middle Cerebral Artery - complications</subject><subject>Infarction, Middle Cerebral Artery - drug therapy</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>neurogenesis</subject><subject>Neurogenesis - drug effects</subject><subject>Neurons - drug effects</subject><subject>Neurons - physiology</subject><subject>Psychomotor Performance - drug effects</subject><subject>Reaction Time - drug effects</subject><subject>sensorimotor function</subject><subject>Serotonin Uptake Inhibitors - therapeutic use</subject><subject>Severity of Illness Index</subject><subject>Space Perception - drug effects</subject><subject>spatial cognitive function</subject><subject>Swimming</subject><subject>Time Factors</subject><subject>Zidovudine - pharmacology</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp1kM1u1DAURi0EotPCghdAXiGxSGsn9jheohEMoKpIiJ_uLI9zPXPbxA62U9pX6FOTMgOsWN3N-Y50DyEvODvljNVnVyGd1ryt9SOy4EyrSkihHpMFa5asEozXR-Q45yvGmNayeUqOeKs4V0IsyP1ql2JAR30_xVsoGICWBLYMEArFYUzxBjLF7HYwoK0wdJODjubRFrQ9dXEbsOAN0A48OiyZltk4bXcUg5tFGcOW7nAco7PDOC8CTCluIUDGTK0vkGguKV7DM_LE2z7D88M9IV_fvf2yel-df1p_WL05r5yQra6E5XUjZSN9zTvZirZW3EvdcN0K8N4x1WlhFd-Adgw4AyH8xvpaK8GXuuPNCXm1986__ZggFzPM70Hf2wBxyqZmUi6lfgBf70GXYs4JvBkTDjbdGc7MQ3gzhze_w8_sy4N02gzQ_SMPpWfgbA_8xB7u_m8yHy8-_1FW-wXmArd_FzZdm6VqlDTfL9bmUl1-42uljGh-Adjkn-M</recordid><startdate>200901</startdate><enddate>200901</enddate><creator>Li, Wen-Lei</creator><creator>Cai, Hui-Hui</creator><creator>Wang, Bin</creator><creator>Chen, Ling</creator><creator>Zhou, Qi-Gang</creator><creator>Luo, Chun-Xia</creator><creator>Liu, Na</creator><creator>Ding, Xin-Sheng</creator><creator>Zhu, Dong-Ya</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>200901</creationdate><title>Chronic fluoxetine treatment improves ischemia-induced spatial cognitive deficits through increasing hippocampal neurogenesis after stroke</title><author>Li, Wen-Lei ; Cai, Hui-Hui ; Wang, Bin ; Chen, Ling ; Zhou, Qi-Gang ; Luo, Chun-Xia ; Liu, Na ; Ding, Xin-Sheng ; Zhu, Dong-Ya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4589-4a1235535f21d5848271f5931984effc07d94a71be9c0e10e44fbaf2974169d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Antimetabolites - pharmacology</topic><topic>Bromodeoxyuridine - metabolism</topic><topic>Cell Count - methods</topic><topic>Cognition Disorders - diagnosis</topic><topic>Cognition Disorders - drug therapy</topic><topic>Cognition Disorders - pathology</topic><topic>Disease Models, Animal</topic><topic>fluoxetine</topic><topic>Fluoxetine - therapeutic use</topic><topic>focal cerebral ischemia</topic><topic>hippocampus</topic><topic>Infarction, Middle Cerebral Artery - complications</topic><topic>Infarction, Middle Cerebral Artery - drug therapy</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>neurogenesis</topic><topic>Neurogenesis - drug effects</topic><topic>Neurons - drug effects</topic><topic>Neurons - physiology</topic><topic>Psychomotor Performance - drug effects</topic><topic>Reaction Time - drug effects</topic><topic>sensorimotor function</topic><topic>Serotonin Uptake Inhibitors - therapeutic use</topic><topic>Severity of Illness Index</topic><topic>Space Perception - drug effects</topic><topic>spatial cognitive function</topic><topic>Swimming</topic><topic>Time Factors</topic><topic>Zidovudine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Wen-Lei</creatorcontrib><creatorcontrib>Cai, Hui-Hui</creatorcontrib><creatorcontrib>Wang, Bin</creatorcontrib><creatorcontrib>Chen, Ling</creatorcontrib><creatorcontrib>Zhou, Qi-Gang</creatorcontrib><creatorcontrib>Luo, Chun-Xia</creatorcontrib><creatorcontrib>Liu, Na</creatorcontrib><creatorcontrib>Ding, Xin-Sheng</creatorcontrib><creatorcontrib>Zhu, Dong-Ya</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Wen-Lei</au><au>Cai, Hui-Hui</au><au>Wang, Bin</au><au>Chen, Ling</au><au>Zhou, Qi-Gang</au><au>Luo, Chun-Xia</au><au>Liu, Na</au><au>Ding, Xin-Sheng</au><au>Zhu, Dong-Ya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic fluoxetine treatment improves ischemia-induced spatial cognitive deficits through increasing hippocampal neurogenesis after stroke</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>J. Neurosci. Res</addtitle><date>2009-01</date><risdate>2009</risdate><volume>87</volume><issue>1</issue><spage>112</spage><epage>122</epage><pages>112-122</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Cognitive deficits, including spatial memory impairment, are very common after ischemic stroke. Neurogenesis in the dentate gyrus (DG) contributes to forming spatial memory in the ischemic brain. Fluoxetine, a selective serotonin reuptake inhibitor, can enhance neurogenesis in the hippocampus in physiological situations and some neurological diseases. However, whether it has effects on ischemia‐induced spatial cognitive impairment and hippocampal neurogenesis has not been determined. Here we report that fluoxetine treatment (10 mg kg−1, i.p.) for 4 weeks promoted the survival of newborn cells in the ischemic hippocampus and, consequently, attenuated spatial memory impairment of mice after focal cerebral ischemia. Disrupting hippocampal neurogenesis blocked the beneficial effect of fluoxetine on ischemia‐induced spatial cognitive impairment. These results suggest that chronic fluoxetine treatment benefits spatial cognitive function recovery following ischemic insult, and the improved cognitive function is associated with enhanced newborn cell survival in the hippocampus. Our results raise the possibility that fluoxetine can be used as a drug to treat poststroke spatial cognitive deficits. © 2008 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18711744</pmid><doi>10.1002/jnr.21829</doi><tpages>11</tpages></addata></record> |
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subjects | Analysis of Variance Animals Antimetabolites - pharmacology Bromodeoxyuridine - metabolism Cell Count - methods Cognition Disorders - diagnosis Cognition Disorders - drug therapy Cognition Disorders - pathology Disease Models, Animal fluoxetine Fluoxetine - therapeutic use focal cerebral ischemia hippocampus Infarction, Middle Cerebral Artery - complications Infarction, Middle Cerebral Artery - drug therapy Male Maze Learning - drug effects Mice Mice, Inbred C57BL neurogenesis Neurogenesis - drug effects Neurons - drug effects Neurons - physiology Psychomotor Performance - drug effects Reaction Time - drug effects sensorimotor function Serotonin Uptake Inhibitors - therapeutic use Severity of Illness Index Space Perception - drug effects spatial cognitive function Swimming Time Factors Zidovudine - pharmacology |
title | Chronic fluoxetine treatment improves ischemia-induced spatial cognitive deficits through increasing hippocampal neurogenesis after stroke |
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