The effect of methamphetamine on subventricular zone neurogenesis: Cell death, proliferation and differentiation
Methamphetamine (METH) is a potent and widely consumed psychostimulant which causes brain functional and structural abnormalities. However, little is known about the effect of METH on adult neurogenic niches and its consequences on the subventricular zone (SVZ). Thus, this work aims to disclose the...
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description | Methamphetamine (METH) is a potent and widely consumed psychostimulant which causes brain functional and structural abnormalities. However, little is known about the effect of METH on adult neurogenic niches and its consequences on the subventricular zone (SVZ). Thus, this work aims to disclose the effects of METH on SVZ neurogenesis. SVZ neurospheres were cultured from early postnatal mice and subjected to increasing concentrations of METH (1 μM to 500 μM). After 24 hours of exposure to METH cell death was triggered by both necrosis and apoptosis. METH exerted toxic effects on stem/progenitor cells expressing SOX2, but not on doublecortin-labeled neuroblasts. METH decreased BrdU incorporation in SVZ cell cultures. Furthermore, METH decreased the number of NeuN-positive neurons, as well as P-JNK-positive growing axons. Altogether, our data demonstrate that METH is toxic to SVZ cells and reduces neuronal differentiation and maturation at non toxic concentrations. |
doi_str_mv | 10.1109/ENBENG.2012.6331378 |
format | Conference Proceeding |
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R. ; Baptista, S. ; Malva, J. O. ; Silva, A. P. ; Agasse, F.</creator><creatorcontrib>Bento, A. R. ; Baptista, S. ; Malva, J. O. ; Silva, A. P. ; Agasse, F.</creatorcontrib><description>Methamphetamine (METH) is a potent and widely consumed psychostimulant which causes brain functional and structural abnormalities. However, little is known about the effect of METH on adult neurogenic niches and its consequences on the subventricular zone (SVZ). Thus, this work aims to disclose the effects of METH on SVZ neurogenesis. SVZ neurospheres were cultured from early postnatal mice and subjected to increasing concentrations of METH (1 μM to 500 μM). After 24 hours of exposure to METH cell death was triggered by both necrosis and apoptosis. METH exerted toxic effects on stem/progenitor cells expressing SOX2, but not on doublecortin-labeled neuroblasts. METH decreased BrdU incorporation in SVZ cell cultures. Furthermore, METH decreased the number of NeuN-positive neurons, as well as P-JNK-positive growing axons. Altogether, our data demonstrate that METH is toxic to SVZ cells and reduces neuronal differentiation and maturation at non toxic concentrations.</description><identifier>ISBN: 9781467345248</identifier><identifier>ISBN: 1467345245</identifier><identifier>EISBN: 1467345253</identifier><identifier>EISBN: 9781467345255</identifier><identifier>EISBN: 1467345261</identifier><identifier>EISBN: 9781467345262</identifier><identifier>DOI: 10.1109/ENBENG.2012.6331378</identifier><language>eng</language><publisher>IEEE</publisher><subject>apoptosis ; brain repair ; methamphetamine ; neural progenitors ; neurosciences ; subventricular zone</subject><ispartof>2012 IEEE 2nd Portuguese Meeting in Bioengineering (ENBENG), 2012, p.1-6</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://ieeexplore.ieee.org/document/6331378$$EHTML$$P50$$Gieee$$H</linktohtml><link.rule.ids>309,310,780,784,789,790,2058,27925,54920</link.rule.ids><linktorsrc>$$Uhttps://ieeexplore.ieee.org/document/6331378$$EView_record_in_IEEE$$FView_record_in_$$GIEEE</linktorsrc></links><search><creatorcontrib>Bento, A. 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METH exerted toxic effects on stem/progenitor cells expressing SOX2, but not on doublecortin-labeled neuroblasts. METH decreased BrdU incorporation in SVZ cell cultures. Furthermore, METH decreased the number of NeuN-positive neurons, as well as P-JNK-positive growing axons. Altogether, our data demonstrate that METH is toxic to SVZ cells and reduces neuronal differentiation and maturation at non toxic concentrations.</description><subject>apoptosis</subject><subject>brain repair</subject><subject>methamphetamine</subject><subject>neural progenitors</subject><subject>neurosciences</subject><subject>subventricular zone</subject><isbn>9781467345248</isbn><isbn>1467345245</isbn><isbn>1467345253</isbn><isbn>9781467345255</isbn><isbn>1467345261</isbn><isbn>9781467345262</isbn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>2012</creationdate><recordtype>conference_proceeding</recordtype><sourceid>6IE</sourceid><sourceid>RIE</sourceid><recordid>eNo1kN1KxDAQRiMiqGufYG_yALZ2kjRpvNOyrsKy3qzXS9pObKR_pKmgT2_RdW6GOfAdho-QNaQJQKrvNvvHzX6bsBRYIjkHrvIzcg1CKi4ylvFzEmmV_98ivyTRNH2ky-SgpIQrMh4apGgtVoEOlnYYGtONDQbTuR7p0NNpLj-xD95Vc2s8_R4W3OPsh3fscXLTPS2wbWmNJjS3dPRD6yx6E9ySNX1Na7fY_WJwv-yGXFjTThid9oq8PW0OxXO8e92-FA-72IHKQgy6BGatLEGlyFIhhKlVqYXSgjOWKwU2MzqD5XVhjcyAQ82kFrKqWCllzldk_ed1iHgcveuM_zqeSuI_9opcuw</recordid><startdate>201202</startdate><enddate>201202</enddate><creator>Bento, A. R.</creator><creator>Baptista, S.</creator><creator>Malva, J. O.</creator><creator>Silva, A. P.</creator><creator>Agasse, F.</creator><general>IEEE</general><scope>6IE</scope><scope>6IL</scope><scope>CBEJK</scope><scope>RIE</scope><scope>RIL</scope></search><sort><creationdate>201202</creationdate><title>The effect of methamphetamine on subventricular zone neurogenesis: Cell death, proliferation and differentiation</title><author>Bento, A. R. ; Baptista, S. ; Malva, J. O. ; Silva, A. 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P.</creatorcontrib><creatorcontrib>Agasse, F.</creatorcontrib><collection>IEEE Electronic Library (IEL) Conference Proceedings</collection><collection>IEEE Proceedings Order Plan All Online (POP All Online) 1998-present by volume</collection><collection>IEEE Xplore All Conference Proceedings</collection><collection>IEEE Electronic Library (IEL)</collection><collection>IEEE Proceedings Order Plans (POP All) 1998-Present</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Bento, A. R.</au><au>Baptista, S.</au><au>Malva, J. O.</au><au>Silva, A. P.</au><au>Agasse, F.</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>The effect of methamphetamine on subventricular zone neurogenesis: Cell death, proliferation and differentiation</atitle><btitle>2012 IEEE 2nd Portuguese Meeting in Bioengineering (ENBENG)</btitle><stitle>ENBENG</stitle><date>2012-02</date><risdate>2012</risdate><spage>1</spage><epage>6</epage><pages>1-6</pages><isbn>9781467345248</isbn><isbn>1467345245</isbn><eisbn>1467345253</eisbn><eisbn>9781467345255</eisbn><eisbn>1467345261</eisbn><eisbn>9781467345262</eisbn><abstract>Methamphetamine (METH) is a potent and widely consumed psychostimulant which causes brain functional and structural abnormalities. However, little is known about the effect of METH on adult neurogenic niches and its consequences on the subventricular zone (SVZ). Thus, this work aims to disclose the effects of METH on SVZ neurogenesis. SVZ neurospheres were cultured from early postnatal mice and subjected to increasing concentrations of METH (1 μM to 500 μM). After 24 hours of exposure to METH cell death was triggered by both necrosis and apoptosis. METH exerted toxic effects on stem/progenitor cells expressing SOX2, but not on doublecortin-labeled neuroblasts. METH decreased BrdU incorporation in SVZ cell cultures. Furthermore, METH decreased the number of NeuN-positive neurons, as well as P-JNK-positive growing axons. Altogether, our data demonstrate that METH is toxic to SVZ cells and reduces neuronal differentiation and maturation at non toxic concentrations.</abstract><pub>IEEE</pub><doi>10.1109/ENBENG.2012.6331378</doi><tpages>6</tpages></addata></record> |
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subjects | apoptosis brain repair methamphetamine neural progenitors neurosciences subventricular zone |
title | The effect of methamphetamine on subventricular zone neurogenesis: Cell death, proliferation and differentiation |
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