Effects of sub-acute and sub-chronic inhalation of 1-bromopropane on neurogenesis in adult rats

Abstract Purpose 1-Bromopropane (1-BP) intoxication is associated with depression and cognitive and memory deficits. The present study tested the hypothesis that 1-BP suppresses neurogenesis in the dentate gyrus, which is involved in higher cerebral function, in adult rats. Methods Four groups of 12...

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Veröffentlicht in:Toxicology (Amsterdam) 2013-02, Vol.304, p.76-82
Hauptverfasser: Zhang, Lingyi, Nagai, Taku, Yamada, Kiyofumi, Ibi, Daisuke, Ichihara, Sahoko, Subramanian, Kaviarasan, Huang, Zhenlie, Mohideen, Sahabudeen Sheik, Naito, Hisao, Ichihara, Gaku
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container_title Toxicology (Amsterdam)
container_volume 304
creator Zhang, Lingyi
Nagai, Taku
Yamada, Kiyofumi
Ibi, Daisuke
Ichihara, Sahoko
Subramanian, Kaviarasan
Huang, Zhenlie
Mohideen, Sahabudeen Sheik
Naito, Hisao
Ichihara, Gaku
description Abstract Purpose 1-Bromopropane (1-BP) intoxication is associated with depression and cognitive and memory deficits. The present study tested the hypothesis that 1-BP suppresses neurogenesis in the dentate gyrus, which is involved in higher cerebral function, in adult rats. Methods Four groups of 12 male Wistar rats were exposed to 0, 400, 800, 1000 ppm 1-BP, 8 h/day for 7 days. Another four groups of six rats each were exposed to 0, 400, 800 and 1000 ppm 1-BP for 2 weeks followed by 0, 200, 400 and 800 ppm for another 2 weeks, respectively. Another four groups of six rats each were exposed to 0, 200, 400 and 800 ppm 1-BP for 4 weeks. Rats were injected with 5-bromo-2′-deoxy-uridine ( BrdU ) after 4-week exposure at 1000/800 ppm to examine neurogenesis in the dentate gyrus by immunostaining. We measured factors known to affect neurogenesis, including monoamine levels, and mRNA expression levels of brain-derived neurotrophic factor (BDNF) and glucocorticoid receptor (GR), in different brain regions. Results BrdU-positive cells were significantly lower in the 800/1000 ppm-4-week group than the control. 1-Week exposure to 1-BP at 800 and 1000 ppm significantly reduced noradrenalin level in the striatum. Four-week exposure at 800 ppm significantly decreased noradrenalin levels in the hippocampus, prefrontal cortex and striatum. 1-BP also reduced hippocampal BDNF and GR mRNA levels. Conclusion Long-term exposure to 1-BP decreased neurogenesis in the dentate gyrus. Downregulation of BDNF and GR mRNA expression and low hippocampal norepinephrine levels might contribute, at least in part, to the reduced neurogenesis.
doi_str_mv 10.1016/j.tox.2012.12.009
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The present study tested the hypothesis that 1-BP suppresses neurogenesis in the dentate gyrus, which is involved in higher cerebral function, in adult rats. Methods Four groups of 12 male Wistar rats were exposed to 0, 400, 800, 1000 ppm 1-BP, 8 h/day for 7 days. Another four groups of six rats each were exposed to 0, 400, 800 and 1000 ppm 1-BP for 2 weeks followed by 0, 200, 400 and 800 ppm for another 2 weeks, respectively. Another four groups of six rats each were exposed to 0, 200, 400 and 800 ppm 1-BP for 4 weeks. Rats were injected with 5-bromo-2′-deoxy-uridine ( BrdU ) after 4-week exposure at 1000/800 ppm to examine neurogenesis in the dentate gyrus by immunostaining. We measured factors known to affect neurogenesis, including monoamine levels, and mRNA expression levels of brain-derived neurotrophic factor (BDNF) and glucocorticoid receptor (GR), in different brain regions. Results BrdU-positive cells were significantly lower in the 800/1000 ppm-4-week group than the control. 1-Week exposure to 1-BP at 800 and 1000 ppm significantly reduced noradrenalin level in the striatum. Four-week exposure at 800 ppm significantly decreased noradrenalin levels in the hippocampus, prefrontal cortex and striatum. 1-BP also reduced hippocampal BDNF and GR mRNA levels. Conclusion Long-term exposure to 1-BP decreased neurogenesis in the dentate gyrus. Downregulation of BDNF and GR mRNA expression and low hippocampal norepinephrine levels might contribute, at least in part, to the reduced neurogenesis.</description><identifier>ISSN: 0300-483X</identifier><identifier>EISSN: 1879-3185</identifier><identifier>DOI: 10.1016/j.tox.2012.12.009</identifier><identifier>PMID: 23266320</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>1-Bromopropane ; adults ; Animals ; Brain-Derived Neurotrophic Factor - genetics ; breathing ; chronic exposure ; cognition ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; cortex ; Dentate Gyrus - drug effects ; Dentate Gyrus - metabolism ; Depression ; Dose-Response Relationship, Drug ; Down-Regulation - drug effects ; Emergency ; gene expression ; glucocorticoid receptors ; hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Hydrocarbons, Brominated - administration &amp; dosage ; Hydrocarbons, Brominated - toxicity ; Inhalation Exposure ; Male ; memory ; messenger RNA ; Neurogenesis ; Neurogenesis - drug effects ; Neurotoxicity ; Neurotransmitters ; Norepinephrine ; Norepinephrine - metabolism ; poisoning ; Rats ; Rats, Wistar ; Receptors, Glucocorticoid - genetics ; RNA, Messenger - metabolism ; Solvents - administration &amp; dosage ; Solvents - toxicity ; Time Factors ; toxicology</subject><ispartof>Toxicology (Amsterdam), 2013-02, Vol.304, p.76-82</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2012 Elsevier Ireland Ltd</rights><rights>Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-6a5b4ba1bc16160f292c6f4fb64d7881f589365e4cdae017d47a0c50ba2572bd3</citedby><cites>FETCH-LOGICAL-c564t-6a5b4ba1bc16160f292c6f4fb64d7881f589365e4cdae017d47a0c50ba2572bd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0300483X12004283$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23266320$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Lingyi</creatorcontrib><creatorcontrib>Nagai, Taku</creatorcontrib><creatorcontrib>Yamada, Kiyofumi</creatorcontrib><creatorcontrib>Ibi, Daisuke</creatorcontrib><creatorcontrib>Ichihara, Sahoko</creatorcontrib><creatorcontrib>Subramanian, Kaviarasan</creatorcontrib><creatorcontrib>Huang, Zhenlie</creatorcontrib><creatorcontrib>Mohideen, Sahabudeen Sheik</creatorcontrib><creatorcontrib>Naito, Hisao</creatorcontrib><creatorcontrib>Ichihara, Gaku</creatorcontrib><title>Effects of sub-acute and sub-chronic inhalation of 1-bromopropane on neurogenesis in adult rats</title><title>Toxicology (Amsterdam)</title><addtitle>Toxicology</addtitle><description>Abstract Purpose 1-Bromopropane (1-BP) intoxication is associated with depression and cognitive and memory deficits. The present study tested the hypothesis that 1-BP suppresses neurogenesis in the dentate gyrus, which is involved in higher cerebral function, in adult rats. Methods Four groups of 12 male Wistar rats were exposed to 0, 400, 800, 1000 ppm 1-BP, 8 h/day for 7 days. Another four groups of six rats each were exposed to 0, 400, 800 and 1000 ppm 1-BP for 2 weeks followed by 0, 200, 400 and 800 ppm for another 2 weeks, respectively. Another four groups of six rats each were exposed to 0, 200, 400 and 800 ppm 1-BP for 4 weeks. Rats were injected with 5-bromo-2′-deoxy-uridine ( BrdU ) after 4-week exposure at 1000/800 ppm to examine neurogenesis in the dentate gyrus by immunostaining. We measured factors known to affect neurogenesis, including monoamine levels, and mRNA expression levels of brain-derived neurotrophic factor (BDNF) and glucocorticoid receptor (GR), in different brain regions. Results BrdU-positive cells were significantly lower in the 800/1000 ppm-4-week group than the control. 1-Week exposure to 1-BP at 800 and 1000 ppm significantly reduced noradrenalin level in the striatum. Four-week exposure at 800 ppm significantly decreased noradrenalin levels in the hippocampus, prefrontal cortex and striatum. 1-BP also reduced hippocampal BDNF and GR mRNA levels. Conclusion Long-term exposure to 1-BP decreased neurogenesis in the dentate gyrus. Downregulation of BDNF and GR mRNA expression and low hippocampal norepinephrine levels might contribute, at least in part, to the reduced neurogenesis.</description><subject>1-Bromopropane</subject><subject>adults</subject><subject>Animals</subject><subject>Brain-Derived Neurotrophic Factor - genetics</subject><subject>breathing</subject><subject>chronic exposure</subject><subject>cognition</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>cortex</subject><subject>Dentate Gyrus - drug effects</subject><subject>Dentate Gyrus - metabolism</subject><subject>Depression</subject><subject>Dose-Response Relationship, Drug</subject><subject>Down-Regulation - drug effects</subject><subject>Emergency</subject><subject>gene expression</subject><subject>glucocorticoid receptors</subject><subject>hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Hydrocarbons, Brominated - administration &amp; dosage</subject><subject>Hydrocarbons, Brominated - toxicity</subject><subject>Inhalation Exposure</subject><subject>Male</subject><subject>memory</subject><subject>messenger RNA</subject><subject>Neurogenesis</subject><subject>Neurogenesis - drug effects</subject><subject>Neurotoxicity</subject><subject>Neurotransmitters</subject><subject>Norepinephrine</subject><subject>Norepinephrine - metabolism</subject><subject>poisoning</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Glucocorticoid - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Solvents - administration &amp; dosage</subject><subject>Solvents - toxicity</subject><subject>Time Factors</subject><subject>toxicology</subject><issn>0300-483X</issn><issn>1879-3185</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk2LFDEQhoMo7rj6A7xoH730WJWk090IwrKsH7DgYV3wFtLpZDdjTzIm3eL-e6ud1YMHhYIi4XmLqnqLsecIWwRUr3fbOf3YckC-pQDoH7ANdm1fC-yah2wDAqCWnfhywp6UsgMALqR6zE644EoJDhumL7x3di5V8lVZhtrYZXaVieOvl73NKQZbhXhrJjOHFFcO6yGnfTrkdDDRVfQZ3ZLTjYuuhEJwZcZlmqts5vKUPfJmKu7ZfT5l1-8uPp9_qC8_vf94fnZZ20bJuVamGeRgcLCoUIHnPbfKSz8oObZdh77peqEaJ-1oHGA7ytaAbWAwvGn5MIpT9upYl7r6trgy630o1k0TdZiWolHJFhAa3v4fpe2pnvedIhSPqM2plOy8PuSwN_lOI-jVAr3TZIFeLdAUZAFpXtyXX4a9G_8ofu-cgJdHwJukzU0ORV9fUYUGACXQtES8ORKONvY9uKyLDS5aN4ZMZukxhX828PYvtZ0CuWimr-7OlV1aciQrNOpCAn21Xsl6JMgp806Inwm7tME</recordid><startdate>20130208</startdate><enddate>20130208</enddate><creator>Zhang, Lingyi</creator><creator>Nagai, Taku</creator><creator>Yamada, Kiyofumi</creator><creator>Ibi, Daisuke</creator><creator>Ichihara, Sahoko</creator><creator>Subramanian, Kaviarasan</creator><creator>Huang, Zhenlie</creator><creator>Mohideen, Sahabudeen Sheik</creator><creator>Naito, Hisao</creator><creator>Ichihara, Gaku</creator><general>Elsevier Ireland Ltd</general><scope>FBQ</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><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20130208</creationdate><title>Effects of sub-acute and sub-chronic inhalation of 1-bromopropane on neurogenesis in adult rats</title><author>Zhang, Lingyi ; Nagai, Taku ; Yamada, Kiyofumi ; Ibi, Daisuke ; Ichihara, Sahoko ; Subramanian, Kaviarasan ; Huang, Zhenlie ; Mohideen, Sahabudeen Sheik ; Naito, Hisao ; Ichihara, Gaku</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-6a5b4ba1bc16160f292c6f4fb64d7881f589365e4cdae017d47a0c50ba2572bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>1-Bromopropane</topic><topic>adults</topic><topic>Animals</topic><topic>Brain-Derived Neurotrophic Factor - genetics</topic><topic>breathing</topic><topic>chronic exposure</topic><topic>cognition</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>cortex</topic><topic>Dentate Gyrus - drug effects</topic><topic>Dentate Gyrus - metabolism</topic><topic>Depression</topic><topic>Dose-Response Relationship, Drug</topic><topic>Down-Regulation - drug effects</topic><topic>Emergency</topic><topic>gene expression</topic><topic>glucocorticoid receptors</topic><topic>hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Hydrocarbons, Brominated - administration &amp; dosage</topic><topic>Hydrocarbons, Brominated - toxicity</topic><topic>Inhalation Exposure</topic><topic>Male</topic><topic>memory</topic><topic>messenger RNA</topic><topic>Neurogenesis</topic><topic>Neurogenesis - drug effects</topic><topic>Neurotoxicity</topic><topic>Neurotransmitters</topic><topic>Norepinephrine</topic><topic>Norepinephrine - metabolism</topic><topic>poisoning</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Glucocorticoid - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Solvents - administration &amp; dosage</topic><topic>Solvents - toxicity</topic><topic>Time Factors</topic><topic>toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Lingyi</creatorcontrib><creatorcontrib>Nagai, Taku</creatorcontrib><creatorcontrib>Yamada, Kiyofumi</creatorcontrib><creatorcontrib>Ibi, Daisuke</creatorcontrib><creatorcontrib>Ichihara, Sahoko</creatorcontrib><creatorcontrib>Subramanian, Kaviarasan</creatorcontrib><creatorcontrib>Huang, Zhenlie</creatorcontrib><creatorcontrib>Mohideen, Sahabudeen Sheik</creatorcontrib><creatorcontrib>Naito, Hisao</creatorcontrib><creatorcontrib>Ichihara, Gaku</creatorcontrib><collection>AGRIS</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><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology (Amsterdam)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Lingyi</au><au>Nagai, Taku</au><au>Yamada, Kiyofumi</au><au>Ibi, Daisuke</au><au>Ichihara, Sahoko</au><au>Subramanian, Kaviarasan</au><au>Huang, Zhenlie</au><au>Mohideen, Sahabudeen Sheik</au><au>Naito, Hisao</au><au>Ichihara, Gaku</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of sub-acute and sub-chronic inhalation of 1-bromopropane on neurogenesis in adult rats</atitle><jtitle>Toxicology (Amsterdam)</jtitle><addtitle>Toxicology</addtitle><date>2013-02-08</date><risdate>2013</risdate><volume>304</volume><spage>76</spage><epage>82</epage><pages>76-82</pages><issn>0300-483X</issn><eissn>1879-3185</eissn><abstract>Abstract Purpose 1-Bromopropane (1-BP) intoxication is associated with depression and cognitive and memory deficits. The present study tested the hypothesis that 1-BP suppresses neurogenesis in the dentate gyrus, which is involved in higher cerebral function, in adult rats. Methods Four groups of 12 male Wistar rats were exposed to 0, 400, 800, 1000 ppm 1-BP, 8 h/day for 7 days. Another four groups of six rats each were exposed to 0, 400, 800 and 1000 ppm 1-BP for 2 weeks followed by 0, 200, 400 and 800 ppm for another 2 weeks, respectively. Another four groups of six rats each were exposed to 0, 200, 400 and 800 ppm 1-BP for 4 weeks. Rats were injected with 5-bromo-2′-deoxy-uridine ( BrdU ) after 4-week exposure at 1000/800 ppm to examine neurogenesis in the dentate gyrus by immunostaining. We measured factors known to affect neurogenesis, including monoamine levels, and mRNA expression levels of brain-derived neurotrophic factor (BDNF) and glucocorticoid receptor (GR), in different brain regions. Results BrdU-positive cells were significantly lower in the 800/1000 ppm-4-week group than the control. 1-Week exposure to 1-BP at 800 and 1000 ppm significantly reduced noradrenalin level in the striatum. Four-week exposure at 800 ppm significantly decreased noradrenalin levels in the hippocampus, prefrontal cortex and striatum. 1-BP also reduced hippocampal BDNF and GR mRNA levels. Conclusion Long-term exposure to 1-BP decreased neurogenesis in the dentate gyrus. Downregulation of BDNF and GR mRNA expression and low hippocampal norepinephrine levels might contribute, at least in part, to the reduced neurogenesis.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23266320</pmid><doi>10.1016/j.tox.2012.12.009</doi><tpages>7</tpages></addata></record>
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subjects 1-Bromopropane
adults
Animals
Brain-Derived Neurotrophic Factor - genetics
breathing
chronic exposure
cognition
Corpus Striatum - drug effects
Corpus Striatum - metabolism
cortex
Dentate Gyrus - drug effects
Dentate Gyrus - metabolism
Depression
Dose-Response Relationship, Drug
Down-Regulation - drug effects
Emergency
gene expression
glucocorticoid receptors
hippocampus
Hippocampus - drug effects
Hippocampus - metabolism
Hydrocarbons, Brominated - administration & dosage
Hydrocarbons, Brominated - toxicity
Inhalation Exposure
Male
memory
messenger RNA
Neurogenesis
Neurogenesis - drug effects
Neurotoxicity
Neurotransmitters
Norepinephrine
Norepinephrine - metabolism
poisoning
Rats
Rats, Wistar
Receptors, Glucocorticoid - genetics
RNA, Messenger - metabolism
Solvents - administration & dosage
Solvents - toxicity
Time Factors
toxicology
title Effects of sub-acute and sub-chronic inhalation of 1-bromopropane on neurogenesis in adult rats
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