The Efficacies of 3,4,3-LIHOPO and DTPA for Enhancing the Excretion of Plutonium and Americium from the Rat: Comparison with Other Siderophore Analogues

With DTPA as a comparison, the siderophore analogue code named 3,4,3-LIHOPO has been tested for its ability to remove 238Pu and 241Am from rats after their inhalation or intravenous injection as nitrate. The most effective treatment regimen for inhaled Pu was the repeated administration of 30 µmol k...

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Veröffentlicht in:International journal of radiation biology 1992, Vol.62 (4), p.487-497
Hauptverfasser: Stradling, G.N., Gray, S.A., Ellender, M., Moody, J.C., Hodgson, A., Pearce, M., Wilson, I., Burgada, R., Bailly, T., Leroux, Y.G.P., El Manouni, D., Raymond, K.N., Durbin, P.W.
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container_end_page 497
container_issue 4
container_start_page 487
container_title International journal of radiation biology
container_volume 62
creator Stradling, G.N.
Gray, S.A.
Ellender, M.
Moody, J.C.
Hodgson, A.
Pearce, M.
Wilson, I.
Burgada, R.
Bailly, T.
Leroux, Y.G.P.
El Manouni, D.
Raymond, K.N.
Durbin, P.W.
description With DTPA as a comparison, the siderophore analogue code named 3,4,3-LIHOPO has been tested for its ability to remove 238Pu and 241Am from rats after their inhalation or intravenous injection as nitrate. The most effective treatment regimen for inhaled Pu was the repeated administration of 30 µmol kg−1 3,4,3-LIHOPO. By 7 days after exposure, the Pu contents of the lungs and total body were reduced respectively to 2 and 4% of those in untreated animals. These values were six and three times less than when DTPA was administered using the same protocol. For inhaled Am, 3,4,3-LIHOPO and DTPA were considered equally effective, the lung and total body contents being reduced respectively to 13 and 10% of those in controls. Some animals showed slight degenerative changes in the liver and proximal tubules of the kidneys after the repeated administration of 30 µmol kg−1 of 3,4,3-LIHOPO; however these changes were less marked than after DTPA treatment. After the intravenous injection of Pu, the most effective regimen was the single administration of 3 µmol kg−1 3,4,3-LIHOPO. The body content at 7 days was reduced to 7% controls compared with 19% after the repeated administration of 30 µmol kg−1 DTPA. At a dosage of 30 µmol kg−1, 3,4,3-LIHOPO was less effective owing to the higher retention of Pu in the liver. With repeated dosages of 30 µmol kg−1 3,4,3-LIHOPO was more effective than DTPA for the decorporation of Am; the body contents were 16 and 31% of those in controls respectively. Importantly, the body content was still reduced to 28% of control after a single administration of 3 µmol kg−1. The ligand 3,4,3-LIHOPO, which is also superior to other siderophore analogues, could represent a most significant development in the decorporation of Pu and Am.
doi_str_mv 10.1080/09553009214552381
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The most effective treatment regimen for inhaled Pu was the repeated administration of 30 µmol kg−1 3,4,3-LIHOPO. By 7 days after exposure, the Pu contents of the lungs and total body were reduced respectively to 2 and 4% of those in untreated animals. These values were six and three times less than when DTPA was administered using the same protocol. For inhaled Am, 3,4,3-LIHOPO and DTPA were considered equally effective, the lung and total body contents being reduced respectively to 13 and 10% of those in controls. Some animals showed slight degenerative changes in the liver and proximal tubules of the kidneys after the repeated administration of 30 µmol kg−1 of 3,4,3-LIHOPO; however these changes were less marked than after DTPA treatment. After the intravenous injection of Pu, the most effective regimen was the single administration of 3 µmol kg−1 3,4,3-LIHOPO. The body content at 7 days was reduced to 7% controls compared with 19% after the repeated administration of 30 µmol kg−1 DTPA. At a dosage of 30 µmol kg−1, 3,4,3-LIHOPO was less effective owing to the higher retention of Pu in the liver. With repeated dosages of 30 µmol kg−1 3,4,3-LIHOPO was more effective than DTPA for the decorporation of Am; the body contents were 16 and 31% of those in controls respectively. Importantly, the body content was still reduced to 28% of control after a single administration of 3 µmol kg−1. 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Psychology ; Injections, Intravenous ; Kidney - radiation effects ; Liver - metabolism ; Liver - radiation effects ; Pentetic Acid - pharmacology ; Plutonium - administration &amp; dosage ; Plutonium - pharmacokinetics ; Pyridones - pharmacology ; Radiocontamination ; Rats ; Tissues, organs and organisms biophysics</subject><ispartof>International journal of radiation biology, 1992, Vol.62 (4), p.487-497</ispartof><rights>1992 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1992</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-47da7808f8073c50e105170f71668d99e52be455fa4e862895086c648163d8f23</citedby><cites>FETCH-LOGICAL-c459t-47da7808f8073c50e105170f71668d99e52be455fa4e862895086c648163d8f23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/09553009214552381$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/09553009214552381$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,780,784,4021,27921,27922,27923,59645,59751,60434,60540,61219,61254,61400,61435</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4488657$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1357063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stradling, G.N.</creatorcontrib><creatorcontrib>Gray, S.A.</creatorcontrib><creatorcontrib>Ellender, M.</creatorcontrib><creatorcontrib>Moody, J.C.</creatorcontrib><creatorcontrib>Hodgson, A.</creatorcontrib><creatorcontrib>Pearce, M.</creatorcontrib><creatorcontrib>Wilson, I.</creatorcontrib><creatorcontrib>Burgada, R.</creatorcontrib><creatorcontrib>Bailly, T.</creatorcontrib><creatorcontrib>Leroux, Y.G.P.</creatorcontrib><creatorcontrib>El Manouni, D.</creatorcontrib><creatorcontrib>Raymond, K.N.</creatorcontrib><creatorcontrib>Durbin, P.W.</creatorcontrib><title>The Efficacies of 3,4,3-LIHOPO and DTPA for Enhancing the Excretion of Plutonium and Americium from the Rat: Comparison with Other Siderophore Analogues</title><title>International journal of radiation biology</title><addtitle>Int J Radiat Biol</addtitle><description>With DTPA as a comparison, the siderophore analogue code named 3,4,3-LIHOPO has been tested for its ability to remove 238Pu and 241Am from rats after their inhalation or intravenous injection as nitrate. 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The body content at 7 days was reduced to 7% controls compared with 19% after the repeated administration of 30 µmol kg−1 DTPA. At a dosage of 30 µmol kg−1, 3,4,3-LIHOPO was less effective owing to the higher retention of Pu in the liver. With repeated dosages of 30 µmol kg−1 3,4,3-LIHOPO was more effective than DTPA for the decorporation of Am; the body contents were 16 and 31% of those in controls respectively. Importantly, the body content was still reduced to 28% of control after a single administration of 3 µmol kg−1. 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Psychology</subject><subject>Injections, Intravenous</subject><subject>Kidney - radiation effects</subject><subject>Liver - metabolism</subject><subject>Liver - radiation effects</subject><subject>Pentetic Acid - pharmacology</subject><subject>Plutonium - administration &amp; dosage</subject><subject>Plutonium - pharmacokinetics</subject><subject>Pyridones - pharmacology</subject><subject>Radiocontamination</subject><subject>Rats</subject><subject>Tissues, organs and organisms biophysics</subject><issn>0955-3002</issn><issn>1362-3095</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFu1DAURS0EKkPhA1ggecGygec4dhzoZjQMtNJIM4JhHbmO3bhK4tFzotI_4XNxOgWEkLrys-491vMh5DWDdwwUvIdKCA5Q5awQIueKPSELxmWe8ZQ8JYs5TzPkz8mLGG8gTcDVCTlhXJQg-YL83LeWrp3zRhtvIw2O8rPijGeby4vtbkv10NBP-92SuoB0PbR6MH64puNM_TBoRx-GGdp10xgGP_X3xLK36M18cxj6-_ZXPX6gq9AfNPqYmFs_tnSbEqTffGMxHNqAli4H3YXrycaX5JnTXbSvHs5T8v3zer-6yDbbL5er5SYzhajGrCgbXSpQTkHJjQDLQLASXMmkVE1VWZFf2STH6cIqmatKgJJGFopJ3iiX81PCju8aDDGidfUBfa_xrmZQz5Lr_yQn5s2ROUxXvW3-EkerKX_7kOtodOdwthb_1IpCKSnKVDs_1vyQ7Pb6NmDX1KO-6wL-ZvhjW3z8B2-t7sbWaLT1TZgwiYyP_OEXYkynVw</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>Stradling, G.N.</creator><creator>Gray, S.A.</creator><creator>Ellender, M.</creator><creator>Moody, J.C.</creator><creator>Hodgson, A.</creator><creator>Pearce, M.</creator><creator>Wilson, I.</creator><creator>Burgada, R.</creator><creator>Bailly, T.</creator><creator>Leroux, Y.G.P.</creator><creator>El Manouni, D.</creator><creator>Raymond, K.N.</creator><creator>Durbin, P.W.</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><scope>IQODW</scope><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>1992</creationdate><title>The Efficacies of 3,4,3-LIHOPO and DTPA for Enhancing the Excretion of Plutonium and Americium from the Rat: Comparison with Other Siderophore Analogues</title><author>Stradling, G.N. ; Gray, S.A. ; Ellender, M. ; Moody, J.C. ; Hodgson, A. ; Pearce, M. ; Wilson, I. ; Burgada, R. ; Bailly, T. ; Leroux, Y.G.P. ; El Manouni, D. ; Raymond, K.N. ; Durbin, P.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-47da7808f8073c50e105170f71668d99e52be455fa4e862895086c648163d8f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Administration, Inhalation</topic><topic>Americium - administration &amp; dosage</topic><topic>Americium - pharmacokinetics</topic><topic>Amides - pharmacology</topic><topic>Animals</topic><topic>Aza Compounds - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Biological effects of radiation</topic><topic>Body Burden</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Injections, Intravenous</topic><topic>Kidney - radiation effects</topic><topic>Liver - metabolism</topic><topic>Liver - radiation effects</topic><topic>Pentetic Acid - pharmacology</topic><topic>Plutonium - administration &amp; dosage</topic><topic>Plutonium - pharmacokinetics</topic><topic>Pyridones - pharmacology</topic><topic>Radiocontamination</topic><topic>Rats</topic><topic>Tissues, organs and organisms biophysics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stradling, G.N.</creatorcontrib><creatorcontrib>Gray, S.A.</creatorcontrib><creatorcontrib>Ellender, M.</creatorcontrib><creatorcontrib>Moody, J.C.</creatorcontrib><creatorcontrib>Hodgson, A.</creatorcontrib><creatorcontrib>Pearce, M.</creatorcontrib><creatorcontrib>Wilson, I.</creatorcontrib><creatorcontrib>Burgada, R.</creatorcontrib><creatorcontrib>Bailly, T.</creatorcontrib><creatorcontrib>Leroux, Y.G.P.</creatorcontrib><creatorcontrib>El Manouni, D.</creatorcontrib><creatorcontrib>Raymond, K.N.</creatorcontrib><creatorcontrib>Durbin, P.W.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of radiation biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stradling, G.N.</au><au>Gray, S.A.</au><au>Ellender, M.</au><au>Moody, J.C.</au><au>Hodgson, A.</au><au>Pearce, M.</au><au>Wilson, I.</au><au>Burgada, R.</au><au>Bailly, T.</au><au>Leroux, Y.G.P.</au><au>El Manouni, D.</au><au>Raymond, K.N.</au><au>Durbin, P.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Efficacies of 3,4,3-LIHOPO and DTPA for Enhancing the Excretion of Plutonium and Americium from the Rat: Comparison with Other Siderophore Analogues</atitle><jtitle>International journal of radiation biology</jtitle><addtitle>Int J Radiat Biol</addtitle><date>1992</date><risdate>1992</risdate><volume>62</volume><issue>4</issue><spage>487</spage><epage>497</epage><pages>487-497</pages><issn>0955-3002</issn><eissn>1362-3095</eissn><abstract>With DTPA as a comparison, the siderophore analogue code named 3,4,3-LIHOPO has been tested for its ability to remove 238Pu and 241Am from rats after their inhalation or intravenous injection as nitrate. The most effective treatment regimen for inhaled Pu was the repeated administration of 30 µmol kg−1 3,4,3-LIHOPO. By 7 days after exposure, the Pu contents of the lungs and total body were reduced respectively to 2 and 4% of those in untreated animals. These values were six and three times less than when DTPA was administered using the same protocol. For inhaled Am, 3,4,3-LIHOPO and DTPA were considered equally effective, the lung and total body contents being reduced respectively to 13 and 10% of those in controls. Some animals showed slight degenerative changes in the liver and proximal tubules of the kidneys after the repeated administration of 30 µmol kg−1 of 3,4,3-LIHOPO; however these changes were less marked than after DTPA treatment. After the intravenous injection of Pu, the most effective regimen was the single administration of 3 µmol kg−1 3,4,3-LIHOPO. The body content at 7 days was reduced to 7% controls compared with 19% after the repeated administration of 30 µmol kg−1 DTPA. At a dosage of 30 µmol kg−1, 3,4,3-LIHOPO was less effective owing to the higher retention of Pu in the liver. With repeated dosages of 30 µmol kg−1 3,4,3-LIHOPO was more effective than DTPA for the decorporation of Am; the body contents were 16 and 31% of those in controls respectively. Importantly, the body content was still reduced to 28% of control after a single administration of 3 µmol kg−1. The ligand 3,4,3-LIHOPO, which is also superior to other siderophore analogues, could represent a most significant development in the decorporation of Pu and Am.</abstract><cop>London</cop><pub>Informa UK Ltd</pub><pmid>1357063</pmid><doi>10.1080/09553009214552381</doi><tpages>11</tpages></addata></record>
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ispartof International journal of radiation biology, 1992, Vol.62 (4), p.487-497
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source MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete
subjects Administration, Inhalation
Americium - administration & dosage
Americium - pharmacokinetics
Amides - pharmacology
Animals
Aza Compounds - pharmacology
Biological and medical sciences
Biological effects of radiation
Body Burden
Female
Fundamental and applied biological sciences. Psychology
Injections, Intravenous
Kidney - radiation effects
Liver - metabolism
Liver - radiation effects
Pentetic Acid - pharmacology
Plutonium - administration & dosage
Plutonium - pharmacokinetics
Pyridones - pharmacology
Radiocontamination
Rats
Tissues, organs and organisms biophysics
title The Efficacies of 3,4,3-LIHOPO and DTPA for Enhancing the Excretion of Plutonium and Americium from the Rat: Comparison with Other Siderophore Analogues
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