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Beta Androstenediol Mitigates the Damage of 1 GeV/n Fe Ion Particle Radiation to the Hematopoietic System

Identifieur interne : 000062 ( Pmc/Checkpoint ); précédent : 000061; suivant : 000063

Beta Androstenediol Mitigates the Damage of 1 GeV/n Fe Ion Particle Radiation to the Hematopoietic System

Auteurs : Roger Loria ; Mathew Beckman ; Daniel Contaifer ; Francisco Tamariz ; David Gibb ; Laura Thompson ; Peter Guida

Source :

RBID : PMC:3192055

Abstract

Abstract

Space exploration is associated with exposure to 1–3 Gy solar particle radiation and galactic cosmic radiation that could increase cancer rates. Effective nontoxic countermeasures to high linear energy transfer (LET) radiation exposure are highly desirable but currently not available. The aim was to determine whether a single subcutaneous injection of androstenediol (Δ5 androsten-3β, 17β-diol [AED]) could mitigate and restore the mouse hematopoetic system from the radiation-mediated injury of 3 Gy whole-body high LET 56Fe26+ exposure. The findings show that postradiation AED treatment has an overall positive and significant beneficial effect to restore the levels of hematopoeitic elements (p<0.001). Androstenediol treatment significantly increased monocyte levels at days 4, 7, and 14 and, similarly, increased red blood cell, hemoglobin, and platelet counts. Flow cytometry analysis 14 days after radiation and AED treatment demonstrated an increase (p<0.05) in bone marrow cells counts. Ex vivo osteoclastogenesis studies show that AED treatment is necessary and advantageous for the development and restoration of osteoclastogenesis after radiation exposure. These findings clearly show that androstenediol functions as a countermeasure to remedy hematopoeitic injury mediated by high LET iron ion radiation. Presently, no other agent has been shown to have such properties.


Url:
DOI: 10.1089/cbr.2010.0907
PubMed: 21790310
PubMed Central: 3192055


Affiliations:


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PMC:3192055

Le document en format XML

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<title xml:lang="en" level="a" type="main">Beta Androstenediol Mitigates the Damage of 1 GeV/n Fe Ion Particle Radiation to the Hematopoietic System</title>
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<name sortKey="Gibb, David" sort="Gibb, David" uniqKey="Gibb D" first="David" last="Gibb">David Gibb</name>
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<name sortKey="Thompson, Laura" sort="Thompson, Laura" uniqKey="Thompson L" first="Laura" last="Thompson">Laura Thompson</name>
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<name sortKey="Guida, Peter" sort="Guida, Peter" uniqKey="Guida P" first="Peter" last="Guida">Peter Guida</name>
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<series>
<title level="j">Cancer Biotherapy & Radiopharmaceuticals</title>
<idno type="ISSN">1084-9785</idno>
<idno type="eISSN">1557-8852</idno>
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<div type="abstract" xml:lang="en">
<title>Abstract</title>
<p>Space exploration is associated with exposure to 1–3 Gy solar particle radiation and galactic cosmic radiation that could increase cancer rates. Effective nontoxic countermeasures to high linear energy transfer (LET) radiation exposure are highly desirable but currently not available. The aim was to determine whether a single subcutaneous injection of androstenediol (Δ
<sup>5</sup>
androsten-3β, 17β-diol [AED]) could mitigate and restore the mouse hematopoetic system from the radiation-mediated injury of 3 Gy whole-body high LET
<sup>56</sup>
Fe
<sup>26+</sup>
exposure. The findings show that postradiation AED treatment has an overall positive and significant beneficial effect to restore the levels of hematopoeitic elements (
<italic>p</italic>
<0.001). Androstenediol treatment significantly increased monocyte levels at days 4, 7, and 14 and, similarly, increased red blood cell, hemoglobin, and platelet counts. Flow cytometry analysis 14 days after radiation and AED treatment demonstrated an increase (
<italic>p</italic>
<0.05) in bone marrow cells counts.
<italic>Ex vivo</italic>
osteoclastogenesis studies show that AED treatment is necessary and advantageous for the development and restoration of osteoclastogenesis after radiation exposure. These findings clearly show that androstenediol functions as a countermeasure to remedy hematopoeitic injury mediated by high LET iron ion radiation. Presently, no other agent has been shown to have such properties.</p>
</div>
</front>
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<pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
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<journal-id journal-id-type="nlm-ta">Cancer Biother Radiopharm</journal-id>
<journal-id journal-id-type="publisher-id">cbr</journal-id>
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<journal-title>Cancer Biotherapy & Radiopharmaceuticals</journal-title>
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<issn pub-type="ppub">1084-9785</issn>
<issn pub-type="epub">1557-8852</issn>
<publisher>
<publisher-name>Mary Ann Liebert, Inc.</publisher-name>
<publisher-loc>140 Huguenot Street, 3rd FloorNew Rochelle, NY 10801USA</publisher-loc>
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<subject>Original Articles</subject>
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</article-categories>
<title-group>
<article-title>Beta Androstenediol Mitigates the Damage of 1 GeV/n Fe Ion Particle Radiation to the Hematopoietic System</article-title>
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<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Loria</surname>
<given-names>Roger</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1,</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3,</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Beckman</surname>
<given-names>Mathew</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Contaifer</surname>
<given-names>Daniel</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3,</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tamariz</surname>
<given-names>Francisco</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gibb</surname>
<given-names>David</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Thompson</surname>
<given-names>Laura</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Guida</surname>
<given-names>Peter</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
</contrib>
<aff id="aff1">
<label>
<sup>1</sup>
</label>
Department of Microbiology, Immunology,
<institution>Virginia Commonwealth University</institution>
.</aff>
<aff id="aff2">
<label>
<sup>2</sup>
</label>
Department of Pharmacology and Toxicology,
<institution>Virginia Commonwealth University</institution>
.</aff>
<aff id="aff3">
<label>
<sup>3</sup>
</label>
Department of Emergency Medicine,
<institution>Virginia Commonwealth University</institution>
.</aff>
<aff id="aff4">
<label>
<sup>4</sup>
</label>
Department of Virginia Commonwealth University Reanimation Engineering Shock Center (VCURES),
<institution>Virginia Commonwealth University</institution>
.</aff>
<aff id="aff5">
<label>
<sup>5</sup>
</label>
Department of Medical,
<institution>Brookhaven National Laboratory</institution>
, Upton, New York.</aff>
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<author-notes>
<corresp>
<bold>
<italic>Address correspondence to: Roger Loria; Department of Microbiology, Immunology, Virginia Commonwealth University; 1101 E. Marshal Street, Richmond, VA 232980678. E-mail:</italic>
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<email xlink:href="mailto:loria@vcu.edu">
<bold>loria@vcu.edu</bold>
</email>
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</author-notes>
<pub-date pub-type="ppub">
<month>8</month>
<year>2011</year>
<pmc-comment>string-date: August 2011</pmc-comment>
</pub-date>
<volume>26</volume>
<issue>4</issue>
<fpage>453</fpage>
<lpage>459</lpage>
<permissions>
<copyright-statement>Copyright 2011, Mary Ann Liebert, Inc.</copyright-statement>
<copyright-year>2011</copyright-year>
</permissions>
<self-uri xlink:type="simple" xlink:href="cbr.2010.0907.pdf"></self-uri>
<abstract>
<title>Abstract</title>
<p>Space exploration is associated with exposure to 1–3 Gy solar particle radiation and galactic cosmic radiation that could increase cancer rates. Effective nontoxic countermeasures to high linear energy transfer (LET) radiation exposure are highly desirable but currently not available. The aim was to determine whether a single subcutaneous injection of androstenediol (Δ
<sup>5</sup>
androsten-3β, 17β-diol [AED]) could mitigate and restore the mouse hematopoetic system from the radiation-mediated injury of 3 Gy whole-body high LET
<sup>56</sup>
Fe
<sup>26+</sup>
exposure. The findings show that postradiation AED treatment has an overall positive and significant beneficial effect to restore the levels of hematopoeitic elements (
<italic>p</italic>
<0.001). Androstenediol treatment significantly increased monocyte levels at days 4, 7, and 14 and, similarly, increased red blood cell, hemoglobin, and platelet counts. Flow cytometry analysis 14 days after radiation and AED treatment demonstrated an increase (
<italic>p</italic>
<0.05) in bone marrow cells counts.
<italic>Ex vivo</italic>
osteoclastogenesis studies show that AED treatment is necessary and advantageous for the development and restoration of osteoclastogenesis after radiation exposure. These findings clearly show that androstenediol functions as a countermeasure to remedy hematopoeitic injury mediated by high LET iron ion radiation. Presently, no other agent has been shown to have such properties.</p>
</abstract>
<kwd-group kwd-group-type="author">
<title>Key words</title>
<kwd>androstenediol</kwd>
<kwd>bone marrow</kwd>
<kwd>high LET radiation</kwd>
<kwd>hematopoietic</kwd>
<kwd>osteoclastogenesis</kwd>
<kwd>radioprotector</kwd>
</kwd-group>
<counts>
<fig-count count="6"></fig-count>
<table-count count="1"></table-count>
<ref-count count="29"></ref-count>
<page-count count="7"></page-count>
</counts>
</article-meta>
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<list></list>
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<name sortKey="Beckman, Mathew" sort="Beckman, Mathew" uniqKey="Beckman M" first="Mathew" last="Beckman">Mathew Beckman</name>
<name sortKey="Contaifer, Daniel" sort="Contaifer, Daniel" uniqKey="Contaifer D" first="Daniel" last="Contaifer">Daniel Contaifer</name>
<name sortKey="Gibb, David" sort="Gibb, David" uniqKey="Gibb D" first="David" last="Gibb">David Gibb</name>
<name sortKey="Guida, Peter" sort="Guida, Peter" uniqKey="Guida P" first="Peter" last="Guida">Peter Guida</name>
<name sortKey="Loria, Roger" sort="Loria, Roger" uniqKey="Loria R" first="Roger" last="Loria">Roger Loria</name>
<name sortKey="Tamariz, Francisco" sort="Tamariz, Francisco" uniqKey="Tamariz F" first="Francisco" last="Tamariz">Francisco Tamariz</name>
<name sortKey="Thompson, Laura" sort="Thompson, Laura" uniqKey="Thompson L" first="Laura" last="Thompson">Laura Thompson</name>
</noCountry>
</tree>
</affiliations>
</record>

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