Cytotoxic effects of amiodarone and desethylamiodarone on human thyrocytes

Since recent in vivo evidence suggests that the benzofuran antiarrhythmic drug amiodarone has a direct toxic effect on the human thyroid gland, we have investigated the effects of both amiodarone and its metabolite desethylamiodarone on a novel immortalized functional human thyrocyte line (SGHTL-34...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochemical pharmacology 1989-12, Vol.38 (24), p.4397-4403
Hauptverfasser: Beddows, Simon A., Page, Simon R., Taylor, Anthony H., McNerney, Ruth, Whitley, Guy St J., Johnstone, Alan P., Nussey, Stephen S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4403
container_issue 24
container_start_page 4397
container_title Biochemical pharmacology
container_volume 38
creator Beddows, Simon A.
Page, Simon R.
Taylor, Anthony H.
McNerney, Ruth
Whitley, Guy St J.
Johnstone, Alan P.
Nussey, Stephen S.
description Since recent in vivo evidence suggests that the benzofuran antiarrhythmic drug amiodarone has a direct toxic effect on the human thyroid gland, we have investigated the effects of both amiodarone and its metabolite desethylamiodarone on a novel immortalized functional human thyrocyte line (SGHTL-34 cells). Desethylamiodarone markedly reduced cell number as assessed from both DNA and protein content. Few cells were left after 24 hr exposure to 12.5 μ/ml; the concentration producing death of 50% of cells ( ec 50) was 6.8 ± 1.1 μg/ml (mean ± SE, N = 15). Amiodarone was much less potent, producing a maximum decrease in cell number of approximately 25% at concentrations up to 50 μg/ml. The effect of desethylamiodarone was seen within 24 hr of culture. T 3 in concentrations up to 0.75 μg/ml had no effect on the action of amiodarone or desethylamiodarone on SGHTL-34 cells. Light microscopy demonstrated vacuolation of SGHTL-34 cells after 4-day culture with either the drug or its metabolite. Studies using primary cultures of human retroorbital fibroblasts demonstrated that the greater cytotoxicity of desethylamiodarone was not confined to thyrocytes. When SGHTL-34 cells were incubated with 2.5 μg/ml desethylamiodarone for 4 days, 71.7 ± 0.9% was taken up by the cells; there was no detectable conversion to amiodarone. Incubation of thyrocytes with 50 smg/ml amiodarone for 4 days resulted in the uptake of 80.1 ± 2.1% by the cells. In addition, 5.0 ± 0.1% of the amiodarone was converted to material with the same retention time as desethylamiodarone standard; of this material, 72.9 ± 2.8% was taken up by the cells. We conclude that desethylamiodarone, at concentrations near those found in the plasma of patients on long-term amiodarone therapy, exerts a direct cytotoxic effect on human thyroid cells in short-term culture. This effect may play a role in the aetiology of clinical thyroid disease during amiodarone therapy. We suggest that, since the effect is not restricted to thyrocytes, desethylamiodarone may play a role in the aetiology of amiodarone toxicity which occurs clinically in many tissues.
doi_str_mv 10.1016/0006-2952(89)90648-5
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_15805195</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0006295289906485</els_id><sourcerecordid>15805195</sourcerecordid><originalsourceid>FETCH-LOGICAL-c483t-17e72f7586f4de4f0615764a70c64038adf9e15268e2f96d0ecbe36602ea53c33</originalsourceid><addsrcrecordid>eNp9kE1LxDAQhoMoun78A4UeRPRQTdJ89SLI4ieCFz2HbDJhI22jSVfcf2_rLosnT8O888wwPAgdE3xJMBFXGGNR0prTc1Vf1FgwVfItNCFKVkMs1DaabJA9tJ_z-9gqQXbRLhWYSUYn6Gm67GMfv4MtwHuwfS6iL0wbojMpdlCYzhUOMvTzZfMnjl0xX7SmK4Y8RbvsIR-iHW-aDEfreoDe7m5fpw_l88v94_TmubRMVX1JJEjqJVfCMwfMY0G4FMxIbAXDlTLO10A4FQqor4XDYGdQCYEpGF7ZqjpAZ6u7Hyl-LiD3ug3ZQtOYDuIia8IV5qTmA8hWoE0x5wRef6TQmrTUBOtRoR6F6NGPVrX-VajHtZP1_cWsBbdZWjsb5qfrucnWND6Zzoa8wYSkTHIxYNcrDAYXXwGSzjZAZ8GFNHjWLob___gBG6CNAQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15805195</pqid></control><display><type>article</type><title>Cytotoxic effects of amiodarone and desethylamiodarone on human thyrocytes</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Beddows, Simon A. ; Page, Simon R. ; Taylor, Anthony H. ; McNerney, Ruth ; Whitley, Guy St J. ; Johnstone, Alan P. ; Nussey, Stephen S.</creator><creatorcontrib>Beddows, Simon A. ; Page, Simon R. ; Taylor, Anthony H. ; McNerney, Ruth ; Whitley, Guy St J. ; Johnstone, Alan P. ; Nussey, Stephen S.</creatorcontrib><description>Since recent in vivo evidence suggests that the benzofuran antiarrhythmic drug amiodarone has a direct toxic effect on the human thyroid gland, we have investigated the effects of both amiodarone and its metabolite desethylamiodarone on a novel immortalized functional human thyrocyte line (SGHTL-34 cells). Desethylamiodarone markedly reduced cell number as assessed from both DNA and protein content. Few cells were left after 24 hr exposure to 12.5 μ/ml; the concentration producing death of 50% of cells ( ec 50) was 6.8 ± 1.1 μg/ml (mean ± SE, N = 15). Amiodarone was much less potent, producing a maximum decrease in cell number of approximately 25% at concentrations up to 50 μg/ml. The effect of desethylamiodarone was seen within 24 hr of culture. T 3 in concentrations up to 0.75 μg/ml had no effect on the action of amiodarone or desethylamiodarone on SGHTL-34 cells. Light microscopy demonstrated vacuolation of SGHTL-34 cells after 4-day culture with either the drug or its metabolite. Studies using primary cultures of human retroorbital fibroblasts demonstrated that the greater cytotoxicity of desethylamiodarone was not confined to thyrocytes. When SGHTL-34 cells were incubated with 2.5 μg/ml desethylamiodarone for 4 days, 71.7 ± 0.9% was taken up by the cells; there was no detectable conversion to amiodarone. Incubation of thyrocytes with 50 smg/ml amiodarone for 4 days resulted in the uptake of 80.1 ± 2.1% by the cells. In addition, 5.0 ± 0.1% of the amiodarone was converted to material with the same retention time as desethylamiodarone standard; of this material, 72.9 ± 2.8% was taken up by the cells. We conclude that desethylamiodarone, at concentrations near those found in the plasma of patients on long-term amiodarone therapy, exerts a direct cytotoxic effect on human thyroid cells in short-term culture. This effect may play a role in the aetiology of clinical thyroid disease during amiodarone therapy. We suggest that, since the effect is not restricted to thyrocytes, desethylamiodarone may play a role in the aetiology of amiodarone toxicity which occurs clinically in many tissues.</description><identifier>ISSN: 0006-2952</identifier><identifier>EISSN: 1873-2968</identifier><identifier>DOI: 10.1016/0006-2952(89)90648-5</identifier><identifier>PMID: 2604742</identifier><identifier>CODEN: BCPCA6</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Amiodarone - analogs &amp; derivatives ; Amiodarone - metabolism ; Amiodarone - toxicity ; Biological and medical sciences ; Cells, Cultured ; Drug toxicity and drugs side effects treatment ; Fibroblasts - drug effects ; Humans ; Medical sciences ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Pharmacology. Drug treatments ; Thyroid Gland - cytology ; Thyroid Gland - drug effects ; Time Factors</subject><ispartof>Biochemical pharmacology, 1989-12, Vol.38 (24), p.4397-4403</ispartof><rights>1989</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-17e72f7586f4de4f0615764a70c64038adf9e15268e2f96d0ecbe36602ea53c33</citedby><cites>FETCH-LOGICAL-c483t-17e72f7586f4de4f0615764a70c64038adf9e15268e2f96d0ecbe36602ea53c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0006-2952(89)90648-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=6724756$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2604742$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beddows, Simon A.</creatorcontrib><creatorcontrib>Page, Simon R.</creatorcontrib><creatorcontrib>Taylor, Anthony H.</creatorcontrib><creatorcontrib>McNerney, Ruth</creatorcontrib><creatorcontrib>Whitley, Guy St J.</creatorcontrib><creatorcontrib>Johnstone, Alan P.</creatorcontrib><creatorcontrib>Nussey, Stephen S.</creatorcontrib><title>Cytotoxic effects of amiodarone and desethylamiodarone on human thyrocytes</title><title>Biochemical pharmacology</title><addtitle>Biochem Pharmacol</addtitle><description>Since recent in vivo evidence suggests that the benzofuran antiarrhythmic drug amiodarone has a direct toxic effect on the human thyroid gland, we have investigated the effects of both amiodarone and its metabolite desethylamiodarone on a novel immortalized functional human thyrocyte line (SGHTL-34 cells). Desethylamiodarone markedly reduced cell number as assessed from both DNA and protein content. Few cells were left after 24 hr exposure to 12.5 μ/ml; the concentration producing death of 50% of cells ( ec 50) was 6.8 ± 1.1 μg/ml (mean ± SE, N = 15). Amiodarone was much less potent, producing a maximum decrease in cell number of approximately 25% at concentrations up to 50 μg/ml. The effect of desethylamiodarone was seen within 24 hr of culture. T 3 in concentrations up to 0.75 μg/ml had no effect on the action of amiodarone or desethylamiodarone on SGHTL-34 cells. Light microscopy demonstrated vacuolation of SGHTL-34 cells after 4-day culture with either the drug or its metabolite. Studies using primary cultures of human retroorbital fibroblasts demonstrated that the greater cytotoxicity of desethylamiodarone was not confined to thyrocytes. When SGHTL-34 cells were incubated with 2.5 μg/ml desethylamiodarone for 4 days, 71.7 ± 0.9% was taken up by the cells; there was no detectable conversion to amiodarone. Incubation of thyrocytes with 50 smg/ml amiodarone for 4 days resulted in the uptake of 80.1 ± 2.1% by the cells. In addition, 5.0 ± 0.1% of the amiodarone was converted to material with the same retention time as desethylamiodarone standard; of this material, 72.9 ± 2.8% was taken up by the cells. We conclude that desethylamiodarone, at concentrations near those found in the plasma of patients on long-term amiodarone therapy, exerts a direct cytotoxic effect on human thyroid cells in short-term culture. This effect may play a role in the aetiology of clinical thyroid disease during amiodarone therapy. We suggest that, since the effect is not restricted to thyrocytes, desethylamiodarone may play a role in the aetiology of amiodarone toxicity which occurs clinically in many tissues.</description><subject>Amiodarone - analogs &amp; derivatives</subject><subject>Amiodarone - metabolism</subject><subject>Amiodarone - toxicity</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Fibroblasts - drug effects</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Pharmacology. Drug treatments</subject><subject>Thyroid Gland - cytology</subject><subject>Thyroid Gland - drug effects</subject><subject>Time Factors</subject><issn>0006-2952</issn><issn>1873-2968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMoun78A4UeRPRQTdJ89SLI4ieCFz2HbDJhI22jSVfcf2_rLosnT8O888wwPAgdE3xJMBFXGGNR0prTc1Vf1FgwVfItNCFKVkMs1DaabJA9tJ_z-9gqQXbRLhWYSUYn6Gm67GMfv4MtwHuwfS6iL0wbojMpdlCYzhUOMvTzZfMnjl0xX7SmK4Y8RbvsIR-iHW-aDEfreoDe7m5fpw_l88v94_TmubRMVX1JJEjqJVfCMwfMY0G4FMxIbAXDlTLO10A4FQqor4XDYGdQCYEpGF7ZqjpAZ6u7Hyl-LiD3ug3ZQtOYDuIia8IV5qTmA8hWoE0x5wRef6TQmrTUBOtRoR6F6NGPVrX-VajHtZP1_cWsBbdZWjsb5qfrucnWND6Zzoa8wYSkTHIxYNcrDAYXXwGSzjZAZ8GFNHjWLob___gBG6CNAQ</recordid><startdate>19891215</startdate><enddate>19891215</enddate><creator>Beddows, Simon A.</creator><creator>Page, Simon R.</creator><creator>Taylor, Anthony H.</creator><creator>McNerney, Ruth</creator><creator>Whitley, Guy St J.</creator><creator>Johnstone, Alan P.</creator><creator>Nussey, Stephen S.</creator><general>Elsevier Inc</general><general>Elsevier Science</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><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>19891215</creationdate><title>Cytotoxic effects of amiodarone and desethylamiodarone on human thyrocytes</title><author>Beddows, Simon A. ; Page, Simon R. ; Taylor, Anthony H. ; McNerney, Ruth ; Whitley, Guy St J. ; Johnstone, Alan P. ; Nussey, Stephen S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-17e72f7586f4de4f0615764a70c64038adf9e15268e2f96d0ecbe36602ea53c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Amiodarone - analogs &amp; derivatives</topic><topic>Amiodarone - metabolism</topic><topic>Amiodarone - toxicity</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Fibroblasts - drug effects</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Pharmacology. Drug treatments</topic><topic>Thyroid Gland - cytology</topic><topic>Thyroid Gland - drug effects</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beddows, Simon A.</creatorcontrib><creatorcontrib>Page, Simon R.</creatorcontrib><creatorcontrib>Taylor, Anthony H.</creatorcontrib><creatorcontrib>McNerney, Ruth</creatorcontrib><creatorcontrib>Whitley, Guy St J.</creatorcontrib><creatorcontrib>Johnstone, Alan P.</creatorcontrib><creatorcontrib>Nussey, Stephen S.</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><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Biochemical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beddows, Simon A.</au><au>Page, Simon R.</au><au>Taylor, Anthony H.</au><au>McNerney, Ruth</au><au>Whitley, Guy St J.</au><au>Johnstone, Alan P.</au><au>Nussey, Stephen S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytotoxic effects of amiodarone and desethylamiodarone on human thyrocytes</atitle><jtitle>Biochemical pharmacology</jtitle><addtitle>Biochem Pharmacol</addtitle><date>1989-12-15</date><risdate>1989</risdate><volume>38</volume><issue>24</issue><spage>4397</spage><epage>4403</epage><pages>4397-4403</pages><issn>0006-2952</issn><eissn>1873-2968</eissn><coden>BCPCA6</coden><abstract>Since recent in vivo evidence suggests that the benzofuran antiarrhythmic drug amiodarone has a direct toxic effect on the human thyroid gland, we have investigated the effects of both amiodarone and its metabolite desethylamiodarone on a novel immortalized functional human thyrocyte line (SGHTL-34 cells). Desethylamiodarone markedly reduced cell number as assessed from both DNA and protein content. Few cells were left after 24 hr exposure to 12.5 μ/ml; the concentration producing death of 50% of cells ( ec 50) was 6.8 ± 1.1 μg/ml (mean ± SE, N = 15). Amiodarone was much less potent, producing a maximum decrease in cell number of approximately 25% at concentrations up to 50 μg/ml. The effect of desethylamiodarone was seen within 24 hr of culture. T 3 in concentrations up to 0.75 μg/ml had no effect on the action of amiodarone or desethylamiodarone on SGHTL-34 cells. Light microscopy demonstrated vacuolation of SGHTL-34 cells after 4-day culture with either the drug or its metabolite. Studies using primary cultures of human retroorbital fibroblasts demonstrated that the greater cytotoxicity of desethylamiodarone was not confined to thyrocytes. When SGHTL-34 cells were incubated with 2.5 μg/ml desethylamiodarone for 4 days, 71.7 ± 0.9% was taken up by the cells; there was no detectable conversion to amiodarone. Incubation of thyrocytes with 50 smg/ml amiodarone for 4 days resulted in the uptake of 80.1 ± 2.1% by the cells. In addition, 5.0 ± 0.1% of the amiodarone was converted to material with the same retention time as desethylamiodarone standard; of this material, 72.9 ± 2.8% was taken up by the cells. We conclude that desethylamiodarone, at concentrations near those found in the plasma of patients on long-term amiodarone therapy, exerts a direct cytotoxic effect on human thyroid cells in short-term culture. This effect may play a role in the aetiology of clinical thyroid disease during amiodarone therapy. We suggest that, since the effect is not restricted to thyrocytes, desethylamiodarone may play a role in the aetiology of amiodarone toxicity which occurs clinically in many tissues.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>2604742</pmid><doi>10.1016/0006-2952(89)90648-5</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0006-2952
ispartof Biochemical pharmacology, 1989-12, Vol.38 (24), p.4397-4403
issn 0006-2952
1873-2968
language eng
recordid cdi_proquest_miscellaneous_15805195
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Amiodarone - analogs & derivatives
Amiodarone - metabolism
Amiodarone - toxicity
Biological and medical sciences
Cells, Cultured
Drug toxicity and drugs side effects treatment
Fibroblasts - drug effects
Humans
Medical sciences
Miscellaneous (drug allergy, mutagens, teratogens...)
Pharmacology. Drug treatments
Thyroid Gland - cytology
Thyroid Gland - drug effects
Time Factors
title Cytotoxic effects of amiodarone and desethylamiodarone on human thyrocytes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T18%3A52%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cytotoxic%20effects%20of%20amiodarone%20and%20desethylamiodarone%20on%20human%20thyrocytes&rft.jtitle=Biochemical%20pharmacology&rft.au=Beddows,%20Simon%20A.&rft.date=1989-12-15&rft.volume=38&rft.issue=24&rft.spage=4397&rft.epage=4403&rft.pages=4397-4403&rft.issn=0006-2952&rft.eissn=1873-2968&rft.coden=BCPCA6&rft_id=info:doi/10.1016/0006-2952(89)90648-5&rft_dat=%3Cproquest_cross%3E15805195%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=15805195&rft_id=info:pmid/2604742&rft_els_id=0006295289906485&rfr_iscdi=true