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Human myelotoxicity of two phycotoxins, okadaic acid and domoic acid. An in vitro study
Okadaic acid (OA), a diarrheic shellfish toxin and domoic acid (DA), an amnesic shellfish toxin are phycotoxins produced by various species of microalgaes. The aim of this study was to explore the effects of OA and DA on hematopoietic progenitors. For this purpose, three lineages of human hematopoie...
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Published in: | Toxicological and environmental chemistry 2008-01, Vol.90 (1), p.141-152 |
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creator | Batina, P. Hymery, N. Froquet, R. Sibiril, Y. Parent-Massin, D. |
description | Okadaic acid (OA), a diarrheic shellfish toxin and domoic acid (DA), an amnesic shellfish toxin are phycotoxins produced by various species of microalgaes. The aim of this study was to explore the effects of OA and DA on hematopoietic progenitors. For this purpose, three lineages of human hematopoietic progenitors, CFU-GM, BFU-E and CFU-MK optimized for toxicological studies were used. The effects of OA and DA on cell precursor proliferation and differentiation were investigated at concentration from 0.5 to 25 ng mL
−1
and from 0.1 to 100 µg mL
−1
, respectively. A study of concentration and effect relationship showed a cytotoxic effect of OA (25 ng mL
−1
) for human hematopoietic progenitors. Moreover, this phycotoxin inhibited erythroid progenitors proliferation and disturbed differentiation at concentrations of 5 ng mL
−1
and higher. OA IC
50
were determined at 7.5 ng mL
−1
, 7.54 ng mL
−1
and 1.19 ng mL
−1
for CFU-GM, BFU-E and CFU-MK, respectively. Cytotoxic effects of OA and DA were compared to those effect of trichothecenes (T-2 toxin and deoxynivalenol) described in previous studies. Results confirm that at low concentration (25 ng mL
−1
), OA is a potent myelotoxin for human hematopoietic progenitors, although platelets progenitors (CFU-MK) are most sensitive. DA did not exhibit any effect in the range of concentration tested. Taken together, these findings suggest that OA induced hematological abnormalities after chronic consumption similar to other food contaminants as trichothecenes. |
doi_str_mv | 10.1080/02772240701374948 |
format | article |
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−1
and from 0.1 to 100 µg mL
−1
, respectively. A study of concentration and effect relationship showed a cytotoxic effect of OA (25 ng mL
−1
) for human hematopoietic progenitors. Moreover, this phycotoxin inhibited erythroid progenitors proliferation and disturbed differentiation at concentrations of 5 ng mL
−1
and higher. OA IC
50
were determined at 7.5 ng mL
−1
, 7.54 ng mL
−1
and 1.19 ng mL
−1
for CFU-GM, BFU-E and CFU-MK, respectively. Cytotoxic effects of OA and DA were compared to those effect of trichothecenes (T-2 toxin and deoxynivalenol) described in previous studies. Results confirm that at low concentration (25 ng mL
−1
), OA is a potent myelotoxin for human hematopoietic progenitors, although platelets progenitors (CFU-MK) are most sensitive. DA did not exhibit any effect in the range of concentration tested. Taken together, these findings suggest that OA induced hematological abnormalities after chronic consumption similar to other food contaminants as trichothecenes.</description><identifier>ISSN: 0277-2248</identifier><identifier>EISSN: 1029-0486</identifier><identifier>DOI: 10.1080/02772240701374948</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><subject>domoic acid ; human hematopoietic progenitors ; Myelotoxicity ; okadaic acid ; phycotoxins</subject><ispartof>Toxicological and environmental chemistry, 2008-01, Vol.90 (1), p.141-152</ispartof><rights>Copyright Taylor & Francis Group, LLC 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-285b56e940668b25dc274d6bdaa70cc614b292b91355e7154214f159491df7103</citedby><cites>FETCH-LOGICAL-c354t-285b56e940668b25dc274d6bdaa70cc614b292b91355e7154214f159491df7103</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></links><search><creatorcontrib>Batina, P.</creatorcontrib><creatorcontrib>Hymery, N.</creatorcontrib><creatorcontrib>Froquet, R.</creatorcontrib><creatorcontrib>Sibiril, Y.</creatorcontrib><creatorcontrib>Parent-Massin, D.</creatorcontrib><title>Human myelotoxicity of two phycotoxins, okadaic acid and domoic acid. An in vitro study</title><title>Toxicological and environmental chemistry</title><description>Okadaic acid (OA), a diarrheic shellfish toxin and domoic acid (DA), an amnesic shellfish toxin are phycotoxins produced by various species of microalgaes. The aim of this study was to explore the effects of OA and DA on hematopoietic progenitors. For this purpose, three lineages of human hematopoietic progenitors, CFU-GM, BFU-E and CFU-MK optimized for toxicological studies were used. The effects of OA and DA on cell precursor proliferation and differentiation were investigated at concentration from 0.5 to 25 ng mL
−1
and from 0.1 to 100 µg mL
−1
, respectively. A study of concentration and effect relationship showed a cytotoxic effect of OA (25 ng mL
−1
) for human hematopoietic progenitors. Moreover, this phycotoxin inhibited erythroid progenitors proliferation and disturbed differentiation at concentrations of 5 ng mL
−1
and higher. OA IC
50
were determined at 7.5 ng mL
−1
, 7.54 ng mL
−1
and 1.19 ng mL
−1
for CFU-GM, BFU-E and CFU-MK, respectively. Cytotoxic effects of OA and DA were compared to those effect of trichothecenes (T-2 toxin and deoxynivalenol) described in previous studies. Results confirm that at low concentration (25 ng mL
−1
), OA is a potent myelotoxin for human hematopoietic progenitors, although platelets progenitors (CFU-MK) are most sensitive. DA did not exhibit any effect in the range of concentration tested. Taken together, these findings suggest that OA induced hematological abnormalities after chronic consumption similar to other food contaminants as trichothecenes.</description><subject>domoic acid</subject><subject>human hematopoietic progenitors</subject><subject>Myelotoxicity</subject><subject>okadaic acid</subject><subject>phycotoxins</subject><issn>0277-2248</issn><issn>1029-0486</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkU1LAzEQhoMoWKs_wFtOnlydfG_Ai4hfIHhRPC7ZZBeju5uapLb77622t4I9DTPzPMMLg9ApgQsCJVwCVYpSDgoIU1zzcg9NCFBdAC_lPpr87osVUB6io5Q-AKAUik_Q28O8NwPux6YLOSy99XnEocV5EfDsfbR_wyGd4_BpnPEWG-sdNoPDLvRh01_g6wH7AX_7HANOee7GY3TQmi41J5s6Ra93ty83D8XT8_3jzfVTYZnguaClqIVsNAcpy5oKZ6niTtbOGAXWSsJrqmmtCROiUURwSnhLhOaauFYRYFN0tr47i-Fr3qRc9T7ZpuvM0IR5qhhjIIHJnSAFKqlWbCdIeMm1XiWaIrIGbQwpxaatZtH3Jo4Vger3KdXWU1bO1drxQxtibxYhdq7KZuxCbKMZrF9F_k9XO_Utq8rLzH4AbdaimQ</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Batina, P.</creator><creator>Hymery, N.</creator><creator>Froquet, R.</creator><creator>Sibiril, Y.</creator><creator>Parent-Massin, D.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7T2</scope><scope>7TV</scope><scope>7U2</scope><scope>7U7</scope><scope>M7N</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20080101</creationdate><title>Human myelotoxicity of two phycotoxins, okadaic acid and domoic acid. An in vitro study</title><author>Batina, P. ; Hymery, N. ; Froquet, R. ; Sibiril, Y. ; Parent-Massin, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-285b56e940668b25dc274d6bdaa70cc614b292b91355e7154214f159491df7103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>domoic acid</topic><topic>human hematopoietic progenitors</topic><topic>Myelotoxicity</topic><topic>okadaic acid</topic><topic>phycotoxins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Batina, P.</creatorcontrib><creatorcontrib>Hymery, N.</creatorcontrib><creatorcontrib>Froquet, R.</creatorcontrib><creatorcontrib>Sibiril, Y.</creatorcontrib><creatorcontrib>Parent-Massin, D.</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Pollution Abstracts</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Toxicological and environmental chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Batina, P.</au><au>Hymery, N.</au><au>Froquet, R.</au><au>Sibiril, Y.</au><au>Parent-Massin, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human myelotoxicity of two phycotoxins, okadaic acid and domoic acid. An in vitro study</atitle><jtitle>Toxicological and environmental chemistry</jtitle><date>2008-01-01</date><risdate>2008</risdate><volume>90</volume><issue>1</issue><spage>141</spage><epage>152</epage><pages>141-152</pages><issn>0277-2248</issn><eissn>1029-0486</eissn><abstract>Okadaic acid (OA), a diarrheic shellfish toxin and domoic acid (DA), an amnesic shellfish toxin are phycotoxins produced by various species of microalgaes. The aim of this study was to explore the effects of OA and DA on hematopoietic progenitors. For this purpose, three lineages of human hematopoietic progenitors, CFU-GM, BFU-E and CFU-MK optimized for toxicological studies were used. The effects of OA and DA on cell precursor proliferation and differentiation were investigated at concentration from 0.5 to 25 ng mL
−1
and from 0.1 to 100 µg mL
−1
, respectively. A study of concentration and effect relationship showed a cytotoxic effect of OA (25 ng mL
−1
) for human hematopoietic progenitors. Moreover, this phycotoxin inhibited erythroid progenitors proliferation and disturbed differentiation at concentrations of 5 ng mL
−1
and higher. OA IC
50
were determined at 7.5 ng mL
−1
, 7.54 ng mL
−1
and 1.19 ng mL
−1
for CFU-GM, BFU-E and CFU-MK, respectively. Cytotoxic effects of OA and DA were compared to those effect of trichothecenes (T-2 toxin and deoxynivalenol) described in previous studies. Results confirm that at low concentration (25 ng mL
−1
), OA is a potent myelotoxin for human hematopoietic progenitors, although platelets progenitors (CFU-MK) are most sensitive. DA did not exhibit any effect in the range of concentration tested. Taken together, these findings suggest that OA induced hematological abnormalities after chronic consumption similar to other food contaminants as trichothecenes.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/02772240701374948</doi><tpages>12</tpages></addata></record> |
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subjects | domoic acid human hematopoietic progenitors Myelotoxicity okadaic acid phycotoxins |
title | Human myelotoxicity of two phycotoxins, okadaic acid and domoic acid. An in vitro study |
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