Effects of glutamate and nimodipine on survival rate of embryonic rat neuronal stem cells cultured in vitro
R74; BACKGROUND: At least three types of calcium ion channel (T, N, and L) have been recognized in nerve cells, but only the L type of channel is sensitive to drugs. Theoretically, nimodipine can lead to L-type channel inactivation and prevent calcium ion inflow, thereby exhibiting protective effect...
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description | R74; BACKGROUND: At least three types of calcium ion channel (T, N, and L) have been recognized in nerve cells, but only the L type of channel is sensitive to drugs. Theoretically, nimodipine can lead to L-type channel inactivation and prevent calcium ion inflow, thereby exhibiting protective effects on nerve cells.OBJECTIVE: To observe the protective effects of nimodipine on glutamate-induced injury to embryonic rat neural stem cells, and to make a comparison with MK-801, a nonselective glutamate receptor antagonist.DESIGN, TIME AND SETTING: The present in vitro experiment pertaining to neural stem cells was performed at the Department of Neurology, First Hospital, Jilin University between January 2005 and December 2006.MATERIALS: Glutamate was sourced from the Shanghai Biological Research Institute of the Chinese Academy of Sciences. Nimodipine was provided by Bayer Company, Germany. Brain tissue was taken from Wistar rats on day 15 of gestation for isolation and culture of neural stem cells.METHODS: Passage 2 neural stem cell spheres were taken for preparation of single cell suspension. The prepared single cell suspension was divided into 4 groups: (1) Normal control, normally cultured. (2)Glutamate, cultured with 50, 100, 200, 500, and 1000 μ mol/L glutamate. (3) Nimodipine, received a 30-minute nimodipine [1 ×(10-8-10-2) g/L] culture followed by a glutamate (200 μ mol/L) treatment step. (4)MK-801, given as 30- minute MK-801 (100 μ mol/L) culture, followed by a glutamate (200 μ mol/L)treatment step.MAIN OUTCOME MEASURES: Determination of glutamate-induced cell death by methyl thiazolyl tetrazolium (MTT) assay; calculation of neural stem cell survival rate following addition of nimodipine.RESULTS: The survival rate of neural stem cells was approximately 25.26% following 24 hour 50 μ mol/L glutamate culture and gradually decreased as the glutamate dose increased (P < 0.05 0.01). Only 9.27% of neural stem cells survived when the glutamate dose was 1 000 μ mol/L. The survival rate of neural stem cells was significantly higher, in a dose-dependent manner, in the nimodipine [1×(10-7-10-2) g/L] group than in the glutamate group. In addition, the MK-801 group exhibited a higher survival rate after 24 hour treatment than the glutamate group (P < 0.01).CONCLUSION: Glutamate (50-1 000 μ mol/L) induces injury to neural stem ceils dose-dependently.Nimodipine exhibits protective effects on injury to neural stem cells and presents the effects in a dose-dependent mann |
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Theoretically, nimodipine can lead to L-type channel inactivation and prevent calcium ion inflow, thereby exhibiting protective effects on nerve cells.OBJECTIVE: To observe the protective effects of nimodipine on glutamate-induced injury to embryonic rat neural stem cells, and to make a comparison with MK-801, a nonselective glutamate receptor antagonist.DESIGN, TIME AND SETTING: The present in vitro experiment pertaining to neural stem cells was performed at the Department of Neurology, First Hospital, Jilin University between January 2005 and December 2006.MATERIALS: Glutamate was sourced from the Shanghai Biological Research Institute of the Chinese Academy of Sciences. Nimodipine was provided by Bayer Company, Germany. Brain tissue was taken from Wistar rats on day 15 of gestation for isolation and culture of neural stem cells.METHODS: Passage 2 neural stem cell spheres were taken for preparation of single cell suspension. The prepared single cell suspension was divided into 4 groups: (1) Normal control, normally cultured. (2)Glutamate, cultured with 50, 100, 200, 500, and 1000 μ mol/L glutamate. (3) Nimodipine, received a 30-minute nimodipine [1 ×(10-8-10-2) g/L] culture followed by a glutamate (200 μ mol/L) treatment step. (4)MK-801, given as 30- minute MK-801 (100 μ mol/L) culture, followed by a glutamate (200 μ mol/L)treatment step.MAIN OUTCOME MEASURES: Determination of glutamate-induced cell death by methyl thiazolyl tetrazolium (MTT) assay; calculation of neural stem cell survival rate following addition of nimodipine.RESULTS: The survival rate of neural stem cells was approximately 25.26% following 24 hour 50 μ mol/L glutamate culture and gradually decreased as the glutamate dose increased (P < 0.05 0.01). Only 9.27% of neural stem cells survived when the glutamate dose was 1 000 μ mol/L. The survival rate of neural stem cells was significantly higher, in a dose-dependent manner, in the nimodipine [1×(10-7-10-2) g/L] group than in the glutamate group. In addition, the MK-801 group exhibited a higher survival rate after 24 hour treatment than the glutamate group (P < 0.01).CONCLUSION: Glutamate (50-1 000 μ mol/L) induces injury to neural stem ceils dose-dependently.Nimodipine exhibits protective effects on injury to neural stem cells and presents the effects in a dose-dependent manner at 1 ×( 107-10-2) g/L. Nimodipine displays neuroprotective effects equivalent to MK-801.</description><identifier>ISSN: 1673-5374</identifier><language>eng</language><publisher>Department of Neurology, First Hospital, Jinlin University, Changchun 1300021, Jilin Province, China</publisher><ispartof>中国神经再生研究(英文版), 2008-12, Vol.3 (12), p.1286-1289</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/zgsjzsyj-e/zgsjzsyj-e.jpg</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Xiaohong Lü</creatorcontrib><creatorcontrib>Hailong Fu</creatorcontrib><creatorcontrib>Qiang Sun</creatorcontrib><creatorcontrib>Li Cui</creatorcontrib><creatorcontrib>Dihui Ma</creatorcontrib><creatorcontrib>Weihong Lin</creatorcontrib><title>Effects of glutamate and nimodipine on survival rate of embryonic rat neuronal stem cells cultured in vitro</title><title>中国神经再生研究(英文版)</title><description>R74; BACKGROUND: At least three types of calcium ion channel (T, N, and L) have been recognized in nerve cells, but only the L type of channel is sensitive to drugs. Theoretically, nimodipine can lead to L-type channel inactivation and prevent calcium ion inflow, thereby exhibiting protective effects on nerve cells.OBJECTIVE: To observe the protective effects of nimodipine on glutamate-induced injury to embryonic rat neural stem cells, and to make a comparison with MK-801, a nonselective glutamate receptor antagonist.DESIGN, TIME AND SETTING: The present in vitro experiment pertaining to neural stem cells was performed at the Department of Neurology, First Hospital, Jilin University between January 2005 and December 2006.MATERIALS: Glutamate was sourced from the Shanghai Biological Research Institute of the Chinese Academy of Sciences. Nimodipine was provided by Bayer Company, Germany. Brain tissue was taken from Wistar rats on day 15 of gestation for isolation and culture of neural stem cells.METHODS: Passage 2 neural stem cell spheres were taken for preparation of single cell suspension. The prepared single cell suspension was divided into 4 groups: (1) Normal control, normally cultured. (2)Glutamate, cultured with 50, 100, 200, 500, and 1000 μ mol/L glutamate. (3) Nimodipine, received a 30-minute nimodipine [1 ×(10-8-10-2) g/L] culture followed by a glutamate (200 μ mol/L) treatment step. (4)MK-801, given as 30- minute MK-801 (100 μ mol/L) culture, followed by a glutamate (200 μ mol/L)treatment step.MAIN OUTCOME MEASURES: Determination of glutamate-induced cell death by methyl thiazolyl tetrazolium (MTT) assay; calculation of neural stem cell survival rate following addition of nimodipine.RESULTS: The survival rate of neural stem cells was approximately 25.26% following 24 hour 50 μ mol/L glutamate culture and gradually decreased as the glutamate dose increased (P < 0.05 0.01). Only 9.27% of neural stem cells survived when the glutamate dose was 1 000 μ mol/L. The survival rate of neural stem cells was significantly higher, in a dose-dependent manner, in the nimodipine [1×(10-7-10-2) g/L] group than in the glutamate group. In addition, the MK-801 group exhibited a higher survival rate after 24 hour treatment than the glutamate group (P < 0.01).CONCLUSION: Glutamate (50-1 000 μ mol/L) induces injury to neural stem ceils dose-dependently.Nimodipine exhibits protective effects on injury to neural stem cells and presents the effects in a dose-dependent manner at 1 ×( 107-10-2) g/L. Nimodipine displays neuroprotective effects equivalent to MK-801.</description><issn>1673-5374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNotjstqwzAURLVooWnaf9C-GPRybC1LSB8Q6CZdm2vrysi1pSLJLsnX16HdzMCcYZgbsuG7ShalrNQduU9pYKystZAb8nWwFrucaLC0H-cME2Sk4A31bgrGfTuPNHia5ri4BUYar3wt49TGc_CuuybU4xyDX3HKONEOxzHRbh7zHNFQ5-nicgwP5NbCmPDx37fk8-Vw2r8Vx4_X9_3zsUhc81wIsKDK0gKDFmStwHLNhEFltLaayVrgTmpuAC3WrWC2ZEpgpYSVYFYot-Tpb_cHvAXfN0OY43ouNZc-DZd0HhoUjNV8FSF_AZ2AWMo</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Xiaohong Lü</creator><creator>Hailong Fu</creator><creator>Qiang Sun</creator><creator>Li Cui</creator><creator>Dihui Ma</creator><creator>Weihong Lin</creator><general>Department of Neurology, First Hospital, Jinlin University, Changchun 1300021, Jilin Province, China</general><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20081201</creationdate><title>Effects of glutamate and nimodipine on survival rate of embryonic rat neuronal stem cells cultured in vitro</title><author>Xiaohong Lü ; Hailong Fu ; Qiang Sun ; Li Cui ; Dihui Ma ; Weihong Lin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s191t-2afa455fa0aba384af1902de4d99f90382e6391daefe8b20f5042e742f3ad82e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiaohong Lü</creatorcontrib><creatorcontrib>Hailong Fu</creatorcontrib><creatorcontrib>Qiang Sun</creatorcontrib><creatorcontrib>Li Cui</creatorcontrib><creatorcontrib>Dihui Ma</creatorcontrib><creatorcontrib>Weihong Lin</creatorcontrib><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>中国神经再生研究(英文版)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiaohong Lü</au><au>Hailong Fu</au><au>Qiang Sun</au><au>Li Cui</au><au>Dihui Ma</au><au>Weihong Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of glutamate and nimodipine on survival rate of embryonic rat neuronal stem cells cultured in vitro</atitle><jtitle>中国神经再生研究(英文版)</jtitle><date>2008-12-01</date><risdate>2008</risdate><volume>3</volume><issue>12</issue><spage>1286</spage><epage>1289</epage><pages>1286-1289</pages><issn>1673-5374</issn><abstract>R74; BACKGROUND: At least three types of calcium ion channel (T, N, and L) have been recognized in nerve cells, but only the L type of channel is sensitive to drugs. Theoretically, nimodipine can lead to L-type channel inactivation and prevent calcium ion inflow, thereby exhibiting protective effects on nerve cells.OBJECTIVE: To observe the protective effects of nimodipine on glutamate-induced injury to embryonic rat neural stem cells, and to make a comparison with MK-801, a nonselective glutamate receptor antagonist.DESIGN, TIME AND SETTING: The present in vitro experiment pertaining to neural stem cells was performed at the Department of Neurology, First Hospital, Jilin University between January 2005 and December 2006.MATERIALS: Glutamate was sourced from the Shanghai Biological Research Institute of the Chinese Academy of Sciences. Nimodipine was provided by Bayer Company, Germany. Brain tissue was taken from Wistar rats on day 15 of gestation for isolation and culture of neural stem cells.METHODS: Passage 2 neural stem cell spheres were taken for preparation of single cell suspension. The prepared single cell suspension was divided into 4 groups: (1) Normal control, normally cultured. (2)Glutamate, cultured with 50, 100, 200, 500, and 1000 μ mol/L glutamate. (3) Nimodipine, received a 30-minute nimodipine [1 ×(10-8-10-2) g/L] culture followed by a glutamate (200 μ mol/L) treatment step. (4)MK-801, given as 30- minute MK-801 (100 μ mol/L) culture, followed by a glutamate (200 μ mol/L)treatment step.MAIN OUTCOME MEASURES: Determination of glutamate-induced cell death by methyl thiazolyl tetrazolium (MTT) assay; calculation of neural stem cell survival rate following addition of nimodipine.RESULTS: The survival rate of neural stem cells was approximately 25.26% following 24 hour 50 μ mol/L glutamate culture and gradually decreased as the glutamate dose increased (P < 0.05 0.01). Only 9.27% of neural stem cells survived when the glutamate dose was 1 000 μ mol/L. The survival rate of neural stem cells was significantly higher, in a dose-dependent manner, in the nimodipine [1×(10-7-10-2) g/L] group than in the glutamate group. In addition, the MK-801 group exhibited a higher survival rate after 24 hour treatment than the glutamate group (P < 0.01).CONCLUSION: Glutamate (50-1 000 μ mol/L) induces injury to neural stem ceils dose-dependently.Nimodipine exhibits protective effects on injury to neural stem cells and presents the effects in a dose-dependent manner at 1 ×( 107-10-2) g/L. Nimodipine displays neuroprotective effects equivalent to MK-801.</abstract><pub>Department of Neurology, First Hospital, Jinlin University, Changchun 1300021, Jilin Province, China</pub><tpages>4</tpages></addata></record> |
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title | Effects of glutamate and nimodipine on survival rate of embryonic rat neuronal stem cells cultured in vitro |
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