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THE PHARMACOKINETICS OF OCHRATOXIN A IN RATS
The absorption and tissue distribution of ochratoxin A (OCT A) following a single oral dose of OCT A were investigated in adult, male Wistar rats. In experiments concerning excretory patterns of OCT A, 14C-OCT A was used. A relatively large amount of OCT A was found in the circulating blood 48 hours...
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Published in: | Japanese journal of pharmacology 1977, Vol.27(5), pp.735-744 |
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container_title | Japanese journal of pharmacology |
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creator | SUZUKI, Shigetoshi SATOH, Tetsuo YAMAZAKI, Mikio |
description | The absorption and tissue distribution of ochratoxin A (OCT A) following a single oral dose of OCT A were investigated in adult, male Wistar rats. In experiments concerning excretory patterns of OCT A, 14C-OCT A was used. A relatively large amount of OCT A was found in the circulating blood 48 hours after dosing. The patterns of absorption, tissue distribution and excretion of OCT A were affected by acute catarrhal enteritis produced by OCT A and/or ochratoxin a (OCT a). Quantitative data show that OCT A is distributed mostly in the kidney and this finding is closely associated with the tissue specifity of OCT A-induced nephrotoxicity. OCT A was found to be hydrolyzed to its major metabolite, OCT a by addition of the homogenate of pancreas, duodenum and ileum. Approximately 56% of OCT A administered was excreted in both urine and feces as the unchanged toxin and OCT a during 120 hours following dosing. A relatively larger amount of OCT a was detected as compared with that of OCT A. |
doi_str_mv | 10.1254/jjp.27.735 |
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In experiments concerning excretory patterns of OCT A, 14C-OCT A was used. A relatively large amount of OCT A was found in the circulating blood 48 hours after dosing. The patterns of absorption, tissue distribution and excretion of OCT A were affected by acute catarrhal enteritis produced by OCT A and/or ochratoxin a (OCT a). Quantitative data show that OCT A is distributed mostly in the kidney and this finding is closely associated with the tissue specifity of OCT A-induced nephrotoxicity. OCT A was found to be hydrolyzed to its major metabolite, OCT a by addition of the homogenate of pancreas, duodenum and ileum. Approximately 56% of OCT A administered was excreted in both urine and feces as the unchanged toxin and OCT a during 120 hours following dosing. A relatively larger amount of OCT a was detected as compared with that of OCT A.</description><identifier>ISSN: 0021-5198</identifier><identifier>EISSN: 1347-3506</identifier><identifier>DOI: 10.1254/jjp.27.735</identifier><identifier>PMID: 592561</identifier><language>eng</language><publisher>Japan: The Japanese Pharmacological Society</publisher><subject>Animals ; Bile - analysis ; Digestive System - metabolism ; Enteritis - chemically induced ; Hydrolysis ; Kinetics ; Male ; Ochratoxins - metabolism ; Rats ; Tissue Distribution</subject><ispartof>The Japanese Journal of Pharmacology, 1977, Vol.27(5), pp.735-744</ispartof><rights>1977 Elsevier B.V.</rights><rights>The Japanese PharmacologicalSociety</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c546t-12b0bb152403bfd8055568c71ca49cd331ba4c34b21c7fc5bbbc7e485ea1dd2b3</citedby><cites>FETCH-LOGICAL-c546t-12b0bb152403bfd8055568c71ca49cd331ba4c34b21c7fc5bbbc7e485ea1dd2b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021519819606335$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/592561$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SUZUKI, Shigetoshi</creatorcontrib><creatorcontrib>SATOH, Tetsuo</creatorcontrib><creatorcontrib>YAMAZAKI, Mikio</creatorcontrib><title>THE PHARMACOKINETICS OF OCHRATOXIN A IN RATS</title><title>Japanese journal of pharmacology</title><addtitle>Jpn.J.Pharmacol.</addtitle><description>The absorption and tissue distribution of ochratoxin A (OCT A) following a single oral dose of OCT A were investigated in adult, male Wistar rats. 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A relatively larger amount of OCT a was detected as compared with that of OCT A.</description><subject>Animals</subject><subject>Bile - analysis</subject><subject>Digestive System - metabolism</subject><subject>Enteritis - chemically induced</subject><subject>Hydrolysis</subject><subject>Kinetics</subject><subject>Male</subject><subject>Ochratoxins - metabolism</subject><subject>Rats</subject><subject>Tissue Distribution</subject><issn>0021-5198</issn><issn>1347-3506</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><recordid>eNptj0tLw0AURgfxVasb1y6yFlPnmccyxNYEayNtBHfDzGRiE_oIM1Hw3zsl0pWbe7l8H4d7ALhFcIIwo49t201wOAkJOwEjRGjoEwaDUzCCECOfoTi6BFfWtu6MIKIX4JzFmAVoBB7KbOq9ZcnyNUmLl3wxLfN05RUzr0izZVIWH_nCSzw33LG6Bme12Fh987fH4H02LdPMnxfPeZrMfcVo0PsISyglYphCIusqgoyxIFIhUoLGqiIESUEVoRIjFdaKSSlVqGnEtEBVhSUZg_uBq8zeWqNr3plmK8wPR5AfhLkT5jjkTtiV74Zy9yW3ujpWB0MXPw1xa3vxqY-xMH2jNpq33dqimKEDjg3DUY-xWgvD9c5h6IDRzvu70YZb1eid0lVjtOp5tW_-e-4XP4B2Pg</recordid><startdate>19770101</startdate><enddate>19770101</enddate><creator>SUZUKI, Shigetoshi</creator><creator>SATOH, Tetsuo</creator><creator>YAMAZAKI, Mikio</creator><general>The Japanese Pharmacological Society</general><scope>6I.</scope><scope>AAFTH</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>19770101</creationdate><title>THE PHARMACOKINETICS OF OCHRATOXIN A IN RATS</title><author>SUZUKI, Shigetoshi ; SATOH, Tetsuo ; YAMAZAKI, Mikio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-12b0bb152403bfd8055568c71ca49cd331ba4c34b21c7fc5bbbc7e485ea1dd2b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>Animals</topic><topic>Bile - analysis</topic><topic>Digestive System - metabolism</topic><topic>Enteritis - chemically induced</topic><topic>Hydrolysis</topic><topic>Kinetics</topic><topic>Male</topic><topic>Ochratoxins - metabolism</topic><topic>Rats</topic><topic>Tissue Distribution</topic><toplevel>online_resources</toplevel><creatorcontrib>SUZUKI, Shigetoshi</creatorcontrib><creatorcontrib>SATOH, Tetsuo</creatorcontrib><creatorcontrib>YAMAZAKI, Mikio</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Japanese journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SUZUKI, Shigetoshi</au><au>SATOH, Tetsuo</au><au>YAMAZAKI, Mikio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>THE PHARMACOKINETICS OF OCHRATOXIN A IN RATS</atitle><jtitle>Japanese journal of pharmacology</jtitle><addtitle>Jpn.J.Pharmacol.</addtitle><date>1977-01-01</date><risdate>1977</risdate><volume>27</volume><issue>5</issue><spage>735</spage><epage>744</epage><pages>735-744</pages><issn>0021-5198</issn><eissn>1347-3506</eissn><abstract>The absorption and tissue distribution of ochratoxin A (OCT A) following a single oral dose of OCT A were investigated in adult, male Wistar rats. In experiments concerning excretory patterns of OCT A, 14C-OCT A was used. A relatively large amount of OCT A was found in the circulating blood 48 hours after dosing. The patterns of absorption, tissue distribution and excretion of OCT A were affected by acute catarrhal enteritis produced by OCT A and/or ochratoxin a (OCT a). Quantitative data show that OCT A is distributed mostly in the kidney and this finding is closely associated with the tissue specifity of OCT A-induced nephrotoxicity. OCT A was found to be hydrolyzed to its major metabolite, OCT a by addition of the homogenate of pancreas, duodenum and ileum. Approximately 56% of OCT A administered was excreted in both urine and feces as the unchanged toxin and OCT a during 120 hours following dosing. A relatively larger amount of OCT a was detected as compared with that of OCT A.</abstract><cop>Japan</cop><pub>The Japanese Pharmacological Society</pub><pmid>592561</pmid><doi>10.1254/jjp.27.735</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | ScienceDirect (Online service) |
subjects | Animals Bile - analysis Digestive System - metabolism Enteritis - chemically induced Hydrolysis Kinetics Male Ochratoxins - metabolism Rats Tissue Distribution |
title | THE PHARMACOKINETICS OF OCHRATOXIN A IN RATS |
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