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The in vitro genotoxic and cytotoxic effects of remeron on human peripheral blood lymphocytes
Remeron (Mirtazapine) is an antidepressant drug which exerts its action by blocking presynaptic α-2-adrenergic receptors and postsynaptic serotonin types 2 and 3 receptors. In this in vitro analysis, human peripheral blood lymphocytes was treated by remeron (10, 25, 40 and 55 μg/mL) for 24 hours and...
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Published in: | Drug and chemical toxicology (New York, N.Y. 1978) N.Y. 1978), 2015-07, Vol.38 (3), p.266-271 |
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creator | Norizadeh Tazehkand, Mostafa Topaktas, Mehmet |
description | Remeron (Mirtazapine) is an antidepressant drug which exerts its action by blocking presynaptic α-2-adrenergic receptors and postsynaptic serotonin types 2 and 3 receptors. In this in vitro analysis, human peripheral blood lymphocytes was treated by remeron (10, 25, 40 and 55 μg/mL) for 24 hours and 48 hours periods, then it was attempted to study of genotoxic and cytotoxic effects of the substance on human peripheral blood lymphocytes by some tests such as sister chromatid exchange (SCE), chromosomal abnormalities (CA) and micronucleus (MN) tests. Also proliferating effect of the substance was investigated. Remeron didn't significantly cause chromosomal abnormalities and sister chromatid exchange while caused micronucleus at 40 μg/mL concentration and 24 h periodic time and increased proliferation index of the both 24 and 48 hours treated cells was decreased in a concentration manner. Also, exposing to the remeron for 24 and 48 hours leaded to a decrease in mitotic index and nucleus division index in the cells by concentration dependent manner. These findings showed that remeron did not have significantly genotoxic effects on human peripheral blood lymphocytes while it showed cytotoxic effects on the cells, which is the first report on genotoxic and cytotoxic properties of remeron. |
doi_str_mv | 10.3109/01480545.2014.947425 |
format | article |
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In this in vitro analysis, human peripheral blood lymphocytes was treated by remeron (10, 25, 40 and 55 μg/mL) for 24 hours and 48 hours periods, then it was attempted to study of genotoxic and cytotoxic effects of the substance on human peripheral blood lymphocytes by some tests such as sister chromatid exchange (SCE), chromosomal abnormalities (CA) and micronucleus (MN) tests. Also proliferating effect of the substance was investigated. Remeron didn't significantly cause chromosomal abnormalities and sister chromatid exchange while caused micronucleus at 40 μg/mL concentration and 24 h periodic time and increased proliferation index of the both 24 and 48 hours treated cells was decreased in a concentration manner. Also, exposing to the remeron for 24 and 48 hours leaded to a decrease in mitotic index and nucleus division index in the cells by concentration dependent manner. These findings showed that remeron did not have significantly genotoxic effects on human peripheral blood lymphocytes while it showed cytotoxic effects on the cells, which is the first report on genotoxic and cytotoxic properties of remeron.</description><identifier>ISSN: 0148-0545</identifier><identifier>EISSN: 1525-6014</identifier><identifier>DOI: 10.3109/01480545.2014.947425</identifier><identifier>PMID: 25156279</identifier><language>eng</language><publisher>United States: Informa Healthcare</publisher><subject>Adrenergic alpha-Antagonists - toxicity ; Adult ; Cell Proliferation - drug effects ; Cells, Cultured ; Chromosome aberration ; cytotoxicity ; Dose-Response Relationship, Drug ; Female ; genotoxicity ; human lymphocytes ; Humans ; Lymphocytes - drug effects ; Lymphocytes - pathology ; Male ; Mianserin - analogs & derivatives ; Mianserin - toxicity ; Micronuclei, Chromosome-Defective - chemically induced ; micronucleus ; Micronucleus Tests ; Mirtazapine ; Mitosis - drug effects ; Mitotic Index ; remeron ; Risk Assessment ; Serotonin Antagonists - toxicity ; sister chromatid exchange ; Sister Chromatid Exchange - drug effects ; Time Factors ; Young Adult</subject><ispartof>Drug and chemical toxicology (New York, N.Y. 1978), 2015-07, Vol.38 (3), p.266-271</ispartof><rights>2014 Informa Healthcare USA, Inc. 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In this in vitro analysis, human peripheral blood lymphocytes was treated by remeron (10, 25, 40 and 55 μg/mL) for 24 hours and 48 hours periods, then it was attempted to study of genotoxic and cytotoxic effects of the substance on human peripheral blood lymphocytes by some tests such as sister chromatid exchange (SCE), chromosomal abnormalities (CA) and micronucleus (MN) tests. Also proliferating effect of the substance was investigated. Remeron didn't significantly cause chromosomal abnormalities and sister chromatid exchange while caused micronucleus at 40 μg/mL concentration and 24 h periodic time and increased proliferation index of the both 24 and 48 hours treated cells was decreased in a concentration manner. Also, exposing to the remeron for 24 and 48 hours leaded to a decrease in mitotic index and nucleus division index in the cells by concentration dependent manner. These findings showed that remeron did not have significantly genotoxic effects on human peripheral blood lymphocytes while it showed cytotoxic effects on the cells, which is the first report on genotoxic and cytotoxic properties of remeron.</description><subject>Adrenergic alpha-Antagonists - toxicity</subject><subject>Adult</subject><subject>Cell Proliferation - drug effects</subject><subject>Cells, Cultured</subject><subject>Chromosome aberration</subject><subject>cytotoxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>genotoxicity</subject><subject>human lymphocytes</subject><subject>Humans</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - pathology</subject><subject>Male</subject><subject>Mianserin - analogs & derivatives</subject><subject>Mianserin - toxicity</subject><subject>Micronuclei, Chromosome-Defective - chemically induced</subject><subject>micronucleus</subject><subject>Micronucleus Tests</subject><subject>Mirtazapine</subject><subject>Mitosis - drug effects</subject><subject>Mitotic Index</subject><subject>remeron</subject><subject>Risk Assessment</subject><subject>Serotonin Antagonists - toxicity</subject><subject>sister chromatid exchange</subject><subject>Sister Chromatid Exchange - drug effects</subject><subject>Time Factors</subject><subject>Young Adult</subject><issn>0148-0545</issn><issn>1525-6014</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kNtKxDAQhoMo7rr6BiJ5ga7NqW2uRBZPsODNeiklzcFG2qYkXbVvb0p3vZQZmAP_PwMfANcoXROU8tsU0SJllK1x7Nac5hSzE7BEDLMki6tTsJwkyaRZgIsQPtMUYc7IOVhghliGc74E77taQ9vBLzt4Bz905wb3YyUUnYJyHA6TNkbLIUBnoNet9q6DMet9KzrYa2_7WnvRwKpxTsFmbPvaRbMOl-DMiCboq0NdgbfHh93mOdm-Pr1s7reJJBkZEoMxUcgUWgjMOBUS0xgZNaxCnJgKK0RzIkWmeF7wAmlZqIKIDBFlch7bFaDzXeldCF6bsve2FX4sUVpOtMojrXKiVc60ou1mtvX7qtXqz3TEEwV3s8B2xvlWfDvfqHIQY-O88aKTNkzn_3nxC6A9ekk</recordid><startdate>20150703</startdate><enddate>20150703</enddate><creator>Norizadeh Tazehkand, Mostafa</creator><creator>Topaktas, Mehmet</creator><general>Informa Healthcare</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20150703</creationdate><title>The in vitro genotoxic and cytotoxic effects of remeron on human peripheral blood lymphocytes</title><author>Norizadeh Tazehkand, Mostafa ; Topaktas, Mehmet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-f223d1f8eaa2594ac2424264f5b193fb2d1473ca6d978981ec8d83a613df79d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adrenergic alpha-Antagonists - toxicity</topic><topic>Adult</topic><topic>Cell Proliferation - drug effects</topic><topic>Cells, Cultured</topic><topic>Chromosome aberration</topic><topic>cytotoxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>genotoxicity</topic><topic>human lymphocytes</topic><topic>Humans</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - pathology</topic><topic>Male</topic><topic>Mianserin - analogs & derivatives</topic><topic>Mianserin - toxicity</topic><topic>Micronuclei, Chromosome-Defective - chemically induced</topic><topic>micronucleus</topic><topic>Micronucleus Tests</topic><topic>Mirtazapine</topic><topic>Mitosis - drug effects</topic><topic>Mitotic Index</topic><topic>remeron</topic><topic>Risk Assessment</topic><topic>Serotonin Antagonists - toxicity</topic><topic>sister chromatid exchange</topic><topic>Sister Chromatid Exchange - drug effects</topic><topic>Time Factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Norizadeh Tazehkand, Mostafa</creatorcontrib><creatorcontrib>Topaktas, Mehmet</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Drug and chemical toxicology (New York, N.Y. 1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Norizadeh Tazehkand, Mostafa</au><au>Topaktas, Mehmet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The in vitro genotoxic and cytotoxic effects of remeron on human peripheral blood lymphocytes</atitle><jtitle>Drug and chemical toxicology (New York, N.Y. 1978)</jtitle><addtitle>Drug Chem Toxicol</addtitle><date>2015-07-03</date><risdate>2015</risdate><volume>38</volume><issue>3</issue><spage>266</spage><epage>271</epage><pages>266-271</pages><issn>0148-0545</issn><eissn>1525-6014</eissn><abstract>Remeron (Mirtazapine) is an antidepressant drug which exerts its action by blocking presynaptic α-2-adrenergic receptors and postsynaptic serotonin types 2 and 3 receptors. In this in vitro analysis, human peripheral blood lymphocytes was treated by remeron (10, 25, 40 and 55 μg/mL) for 24 hours and 48 hours periods, then it was attempted to study of genotoxic and cytotoxic effects of the substance on human peripheral blood lymphocytes by some tests such as sister chromatid exchange (SCE), chromosomal abnormalities (CA) and micronucleus (MN) tests. Also proliferating effect of the substance was investigated. Remeron didn't significantly cause chromosomal abnormalities and sister chromatid exchange while caused micronucleus at 40 μg/mL concentration and 24 h periodic time and increased proliferation index of the both 24 and 48 hours treated cells was decreased in a concentration manner. Also, exposing to the remeron for 24 and 48 hours leaded to a decrease in mitotic index and nucleus division index in the cells by concentration dependent manner. These findings showed that remeron did not have significantly genotoxic effects on human peripheral blood lymphocytes while it showed cytotoxic effects on the cells, which is the first report on genotoxic and cytotoxic properties of remeron.</abstract><cop>United States</cop><pub>Informa Healthcare</pub><pmid>25156279</pmid><doi>10.3109/01480545.2014.947425</doi><tpages>6</tpages></addata></record> |
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subjects | Adrenergic alpha-Antagonists - toxicity Adult Cell Proliferation - drug effects Cells, Cultured Chromosome aberration cytotoxicity Dose-Response Relationship, Drug Female genotoxicity human lymphocytes Humans Lymphocytes - drug effects Lymphocytes - pathology Male Mianserin - analogs & derivatives Mianserin - toxicity Micronuclei, Chromosome-Defective - chemically induced micronucleus Micronucleus Tests Mirtazapine Mitosis - drug effects Mitotic Index remeron Risk Assessment Serotonin Antagonists - toxicity sister chromatid exchange Sister Chromatid Exchange - drug effects Time Factors Young Adult |
title | The in vitro genotoxic and cytotoxic effects of remeron on human peripheral blood lymphocytes |
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