Evaluating the role of zinc in the occurrence of fibrosis of the skin: A preclinical study

Purpose To investigate the possible role of Zn as a trigger for NSF we were using a previously established preclinical model. The depletion of endogenous Zinc ions (Zn) caused by the administration of gadolinium‐based contrast agents (GBCAs) has been suggested as a possible pathomechanism for nephro...

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Veröffentlicht in:Journal of magnetic resonance imaging 2009-08, Vol.30 (2), p.374-383
Hauptverfasser: Pietsch, Hubertus, Pering, Christiane, Lengsfeld, Philipp, Walter, Jakob, Steger-Hartmann, Thomas, Golfier, Sven, Frenzel, Thomas, Hütter, Joachim, Weinmann, Hans-Joachim, Sieber, Martin A.
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container_end_page 383
container_issue 2
container_start_page 374
container_title Journal of magnetic resonance imaging
container_volume 30
creator Pietsch, Hubertus
Pering, Christiane
Lengsfeld, Philipp
Walter, Jakob
Steger-Hartmann, Thomas
Golfier, Sven
Frenzel, Thomas
Hütter, Joachim
Weinmann, Hans-Joachim
Sieber, Martin A.
description Purpose To investigate the possible role of Zn as a trigger for NSF we were using a previously established preclinical model. The depletion of endogenous Zinc ions (Zn) caused by the administration of gadolinium‐based contrast agents (GBCAs) has been suggested as a possible pathomechanism for nephrogenic systemic fibrosis (NSF). Materials and Methods In the Zn supplementation study, rats were injected with Gadodiamide, Omniscan, and Magnevist with or without Zn supplementation. In the Zn depletion study, animals were kept on a Zn‐deficient diet or a special control diet and received injections of Omniscan, OptiMARK, Magnevist, Gadovist, and Gd‐EDTA. Gd, Zn, and Cu concentrations in tissue were measured and histology of the skin was performed. Results As seen in earlier studies, a difference in Gd concentration in the skin was observed following treatment with the different GBCAs. High Gd concentration in the skin correlated with the occurrence of NSF‐like skin lesions. We observed no differences in the occurrence of skin lesions between the Zn supplementation and the Zn‐deficient groups compared to their respective control groups. Conclusion We found no significant effect of Zn on the initiation of NSF‐like skin lesions. The results further support data from previous studies highlighting the importance of complex stability of the investigated GBCAs. J. Magn. Reson. Imaging 2009;30:374–383. © 2009 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jmri.21845
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The depletion of endogenous Zinc ions (Zn) caused by the administration of gadolinium‐based contrast agents (GBCAs) has been suggested as a possible pathomechanism for nephrogenic systemic fibrosis (NSF). Materials and Methods In the Zn supplementation study, rats were injected with Gadodiamide, Omniscan, and Magnevist with or without Zn supplementation. In the Zn depletion study, animals were kept on a Zn‐deficient diet or a special control diet and received injections of Omniscan, OptiMARK, Magnevist, Gadovist, and Gd‐EDTA. Gd, Zn, and Cu concentrations in tissue were measured and histology of the skin was performed. Results As seen in earlier studies, a difference in Gd concentration in the skin was observed following treatment with the different GBCAs. High Gd concentration in the skin correlated with the occurrence of NSF‐like skin lesions. We observed no differences in the occurrence of skin lesions between the Zn supplementation and the Zn‐deficient groups compared to their respective control groups. Conclusion We found no significant effect of Zn on the initiation of NSF‐like skin lesions. The results further support data from previous studies highlighting the importance of complex stability of the investigated GBCAs. J. Magn. Reson. Imaging 2009;30:374–383. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 1053-1807</identifier><identifier>EISSN: 1522-2586</identifier><identifier>DOI: 10.1002/jmri.21845</identifier><identifier>PMID: 19629978</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; complex stability ; Contrast Media - pharmacokinetics ; Contrast Media - toxicity ; Copper - metabolism ; Edetic Acid - pharmacokinetics ; Edetic Acid - toxicity ; gadolinium ; gadolinium based contrast agents (GBCAs) ; Gadolinium DTPA - pharmacokinetics ; Gadolinium DTPA - toxicity ; Nephrogenic Fibrosing Dermopathy - chemically induced ; nephrogenic systemic fibrosis (NSF) ; Organometallic Compounds - pharmacokinetics ; Organometallic Compounds - toxicity ; Rats ; Rats, Wistar ; Skin - metabolism ; Zinc - metabolism ; Zinc - pharmacology</subject><ispartof>Journal of magnetic resonance imaging, 2009-08, Vol.30 (2), p.374-383</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><rights>(c) 2009 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4015-5cbc0eab8ed3d941fb178bbc51a83185b635ab68f0469d0244adf613487de6243</citedby><cites>FETCH-LOGICAL-c4015-5cbc0eab8ed3d941fb178bbc51a83185b635ab68f0469d0244adf613487de6243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmri.21845$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmri.21845$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27923,27924,45573,45574,46408,46832</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19629978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pietsch, Hubertus</creatorcontrib><creatorcontrib>Pering, Christiane</creatorcontrib><creatorcontrib>Lengsfeld, Philipp</creatorcontrib><creatorcontrib>Walter, Jakob</creatorcontrib><creatorcontrib>Steger-Hartmann, Thomas</creatorcontrib><creatorcontrib>Golfier, Sven</creatorcontrib><creatorcontrib>Frenzel, Thomas</creatorcontrib><creatorcontrib>Hütter, Joachim</creatorcontrib><creatorcontrib>Weinmann, Hans-Joachim</creatorcontrib><creatorcontrib>Sieber, Martin A.</creatorcontrib><title>Evaluating the role of zinc in the occurrence of fibrosis of the skin: A preclinical study</title><title>Journal of magnetic resonance imaging</title><addtitle>J. Magn. Reson. Imaging</addtitle><description>Purpose To investigate the possible role of Zn as a trigger for NSF we were using a previously established preclinical model. The depletion of endogenous Zinc ions (Zn) caused by the administration of gadolinium‐based contrast agents (GBCAs) has been suggested as a possible pathomechanism for nephrogenic systemic fibrosis (NSF). Materials and Methods In the Zn supplementation study, rats were injected with Gadodiamide, Omniscan, and Magnevist with or without Zn supplementation. In the Zn depletion study, animals were kept on a Zn‐deficient diet or a special control diet and received injections of Omniscan, OptiMARK, Magnevist, Gadovist, and Gd‐EDTA. Gd, Zn, and Cu concentrations in tissue were measured and histology of the skin was performed. Results As seen in earlier studies, a difference in Gd concentration in the skin was observed following treatment with the different GBCAs. High Gd concentration in the skin correlated with the occurrence of NSF‐like skin lesions. We observed no differences in the occurrence of skin lesions between the Zn supplementation and the Zn‐deficient groups compared to their respective control groups. Conclusion We found no significant effect of Zn on the initiation of NSF‐like skin lesions. The results further support data from previous studies highlighting the importance of complex stability of the investigated GBCAs. J. Magn. Reson. 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Pering, Christiane ; Lengsfeld, Philipp ; Walter, Jakob ; Steger-Hartmann, Thomas ; Golfier, Sven ; Frenzel, Thomas ; Hütter, Joachim ; Weinmann, Hans-Joachim ; Sieber, Martin A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4015-5cbc0eab8ed3d941fb178bbc51a83185b635ab68f0469d0244adf613487de6243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>complex stability</topic><topic>Contrast Media - pharmacokinetics</topic><topic>Contrast Media - toxicity</topic><topic>Copper - metabolism</topic><topic>Edetic Acid - pharmacokinetics</topic><topic>Edetic Acid - toxicity</topic><topic>gadolinium</topic><topic>gadolinium based contrast agents (GBCAs)</topic><topic>Gadolinium DTPA - pharmacokinetics</topic><topic>Gadolinium DTPA - toxicity</topic><topic>Nephrogenic Fibrosing Dermopathy - chemically induced</topic><topic>nephrogenic systemic fibrosis (NSF)</topic><topic>Organometallic Compounds - pharmacokinetics</topic><topic>Organometallic Compounds - toxicity</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Skin - metabolism</topic><topic>Zinc - metabolism</topic><topic>Zinc - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pietsch, Hubertus</creatorcontrib><creatorcontrib>Pering, Christiane</creatorcontrib><creatorcontrib>Lengsfeld, Philipp</creatorcontrib><creatorcontrib>Walter, Jakob</creatorcontrib><creatorcontrib>Steger-Hartmann, Thomas</creatorcontrib><creatorcontrib>Golfier, Sven</creatorcontrib><creatorcontrib>Frenzel, Thomas</creatorcontrib><creatorcontrib>Hütter, Joachim</creatorcontrib><creatorcontrib>Weinmann, Hans-Joachim</creatorcontrib><creatorcontrib>Sieber, Martin A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pietsch, Hubertus</au><au>Pering, Christiane</au><au>Lengsfeld, Philipp</au><au>Walter, Jakob</au><au>Steger-Hartmann, Thomas</au><au>Golfier, Sven</au><au>Frenzel, Thomas</au><au>Hütter, Joachim</au><au>Weinmann, Hans-Joachim</au><au>Sieber, Martin A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluating the role of zinc in the occurrence of fibrosis of the skin: A preclinical study</atitle><jtitle>Journal of magnetic resonance imaging</jtitle><addtitle>J. Magn. Reson. Imaging</addtitle><date>2009-08</date><risdate>2009</risdate><volume>30</volume><issue>2</issue><spage>374</spage><epage>383</epage><pages>374-383</pages><issn>1053-1807</issn><eissn>1522-2586</eissn><abstract>Purpose To investigate the possible role of Zn as a trigger for NSF we were using a previously established preclinical model. The depletion of endogenous Zinc ions (Zn) caused by the administration of gadolinium‐based contrast agents (GBCAs) has been suggested as a possible pathomechanism for nephrogenic systemic fibrosis (NSF). Materials and Methods In the Zn supplementation study, rats were injected with Gadodiamide, Omniscan, and Magnevist with or without Zn supplementation. In the Zn depletion study, animals were kept on a Zn‐deficient diet or a special control diet and received injections of Omniscan, OptiMARK, Magnevist, Gadovist, and Gd‐EDTA. Gd, Zn, and Cu concentrations in tissue were measured and histology of the skin was performed. Results As seen in earlier studies, a difference in Gd concentration in the skin was observed following treatment with the different GBCAs. High Gd concentration in the skin correlated with the occurrence of NSF‐like skin lesions. We observed no differences in the occurrence of skin lesions between the Zn supplementation and the Zn‐deficient groups compared to their respective control groups. Conclusion We found no significant effect of Zn on the initiation of NSF‐like skin lesions. The results further support data from previous studies highlighting the importance of complex stability of the investigated GBCAs. J. Magn. Reson. Imaging 2009;30:374–383. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19629978</pmid><doi>10.1002/jmri.21845</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
complex stability
Contrast Media - pharmacokinetics
Contrast Media - toxicity
Copper - metabolism
Edetic Acid - pharmacokinetics
Edetic Acid - toxicity
gadolinium
gadolinium based contrast agents (GBCAs)
Gadolinium DTPA - pharmacokinetics
Gadolinium DTPA - toxicity
Nephrogenic Fibrosing Dermopathy - chemically induced
nephrogenic systemic fibrosis (NSF)
Organometallic Compounds - pharmacokinetics
Organometallic Compounds - toxicity
Rats
Rats, Wistar
Skin - metabolism
Zinc - metabolism
Zinc - pharmacology
title Evaluating the role of zinc in the occurrence of fibrosis of the skin: A preclinical study
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