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Testicular Mineralization in KK-Ay Mice Treated with an Oxovanadium Complex
Vanadium has potential for use in diabetes therapy. Many investigators have reported toxic effects of inorganic vanadium salts; however, there are few reports on toxic effects of oxovanadium(VO2+) complexes. Therefore, we studied VO2+ toxicity by examining histological changes and measuring the vana...
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Published in: | Journal of Toxicologic Pathology 2013, Vol.26(3), pp.329-333 |
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container_title | Journal of Toxicologic Pathology |
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creator | MOROKI, Takayasu YOSHIKAWA, Yutaka YOSHIZAWA, Katsuhiko TSUBURA, Airo YASUI, Hiroyuki |
description | Vanadium has potential for use in diabetes therapy. Many investigators have reported toxic effects of inorganic vanadium salts; however, there are few reports on toxic effects of oxovanadium(VO2+) complexes. Therefore, we studied VO2+ toxicity by examining histological changes and measuring the vanadium concentration in the testis after repeated oral administration of bis(1-oxy-2-pyridine-thiolato)oxovanadium(VO2+) (VO(opt)2) for 2 or 4 weeks in KK-Ay mice. Severe mineralization and degeneration/necrosis of the seminiferous tubules were detected after either 2 or 4 weeks of administration. Vacuolar changes in Sertoli cells and the seminiferous epithelia, and hyperplasia of Leydig cells were observed in the testes of some animals. Vanadium concentrations in the mineralized testis were much higher than those in the testis of untreated KK-Ay mice. These results represent the first report of the possibility for seminiferous tubules mineralization induced by VO(opt)2 administration. Therefore, our research provides important information about the potentially toxic effects of VO2+ complexes. |
doi_str_mv | 10.1293/tox.26.329 |
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Many investigators have reported toxic effects of inorganic vanadium salts; however, there are few reports on toxic effects of oxovanadium(VO2+) complexes. Therefore, we studied VO2+ toxicity by examining histological changes and measuring the vanadium concentration in the testis after repeated oral administration of bis(1-oxy-2-pyridine-thiolato)oxovanadium(VO2+) (VO(opt)2) for 2 or 4 weeks in KK-Ay mice. Severe mineralization and degeneration/necrosis of the seminiferous tubules were detected after either 2 or 4 weeks of administration. Vacuolar changes in Sertoli cells and the seminiferous epithelia, and hyperplasia of Leydig cells were observed in the testes of some animals. Vanadium concentrations in the mineralized testis were much higher than those in the testis of untreated KK-Ay mice. These results represent the first report of the possibility for seminiferous tubules mineralization induced by VO(opt)2 administration. Therefore, our research provides important information about the potentially toxic effects of VO2+ complexes.</description><identifier>ISSN: 0914-9198</identifier><identifier>EISSN: 1881-915X</identifier><identifier>EISSN: 1347-7404</identifier><identifier>DOI: 10.1293/tox.26.329</identifier><identifier>PMID: 24155568</identifier><language>eng</language><publisher>Tokyo: JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</publisher><subject>diabetes ; KK-Ay mice ; Leydig cell ; mineralization ; oxovanadium(VO2+) complex ; Short Communication ; testis</subject><ispartof>Journal of Toxicologic Pathology, 2013, Vol.26(3), pp.329-333</ispartof><rights>2013 The Japanese Society of Toxicologic Pathology</rights><rights>Copyright Japan Science and Technology Agency 2013</rights><rights>2013 The Japanese Society of Toxicologic Pathology 2013</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2433-c450ee88b43df25f2ef5d30b2e27f9336c49ab828f6f5f812179aea0fddce1523</citedby><cites>FETCH-LOGICAL-c2433-c450ee88b43df25f2ef5d30b2e27f9336c49ab828f6f5f812179aea0fddce1523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787613/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787613/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>MOROKI, Takayasu</creatorcontrib><creatorcontrib>YOSHIKAWA, Yutaka</creatorcontrib><creatorcontrib>YOSHIZAWA, Katsuhiko</creatorcontrib><creatorcontrib>TSUBURA, Airo</creatorcontrib><creatorcontrib>YASUI, Hiroyuki</creatorcontrib><title>Testicular Mineralization in KK-Ay Mice Treated with an Oxovanadium Complex</title><title>Journal of Toxicologic Pathology</title><addtitle>J Toxicol Pathol</addtitle><description>Vanadium has potential for use in diabetes therapy. Many investigators have reported toxic effects of inorganic vanadium salts; however, there are few reports on toxic effects of oxovanadium(VO2+) complexes. Therefore, we studied VO2+ toxicity by examining histological changes and measuring the vanadium concentration in the testis after repeated oral administration of bis(1-oxy-2-pyridine-thiolato)oxovanadium(VO2+) (VO(opt)2) for 2 or 4 weeks in KK-Ay mice. Severe mineralization and degeneration/necrosis of the seminiferous tubules were detected after either 2 or 4 weeks of administration. Vacuolar changes in Sertoli cells and the seminiferous epithelia, and hyperplasia of Leydig cells were observed in the testes of some animals. Vanadium concentrations in the mineralized testis were much higher than those in the testis of untreated KK-Ay mice. These results represent the first report of the possibility for seminiferous tubules mineralization induced by VO(opt)2 administration. Therefore, our research provides important information about the potentially toxic effects of VO2+ complexes.</description><subject>diabetes</subject><subject>KK-Ay mice</subject><subject>Leydig cell</subject><subject>mineralization</subject><subject>oxovanadium(VO2+) complex</subject><subject>Short Communication</subject><subject>testis</subject><issn>0914-9198</issn><issn>1881-915X</issn><issn>1347-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVkF1LwzAUhoMobk5v_AUF74TOfDRteiPI8ItNdjPBu5C2J1tGl8y0nZu_3oyNgTc54ZyH9xwehG4JHhKas4fWbYc0HTKan6E-EYLEOeFf56iPc5KEfy566KpplhjTDHN2iXo0IZzzVPTReAZNa8quVj76MBa8qs2vao2zkbHReBw_7UK_hGjmQbVQRT-mXUTKRtOt2yirKtOtopFbrWvYXqMLreoGbo51gD5fnmejt3gyfX0fPU3ikiaMxWXCMYAQRcIqTbmmoHnFcEGBZjpnLC2TXBWCCp1qrgWhJMsVKKyrqgTCKRugx0PuuitWEJq2DWfLtTcr5XfSKSP_T6xZyLnbSJaJLCUsBNwdA7z77oIAuXSdt-FmSZJMYMFSjgN1f6BK75rGgz5tIFjuxcsgXtJUBvEBHh3gZdOqOZxQ5YPdGk7o_qGYMIkx4adpuVBegmV_0tiNrA</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>MOROKI, Takayasu</creator><creator>YOSHIKAWA, Yutaka</creator><creator>YOSHIZAWA, Katsuhiko</creator><creator>TSUBURA, Airo</creator><creator>YASUI, Hiroyuki</creator><general>JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</general><general>Japan Science and Technology Agency</general><general>Japanese Society of Toxicologic Pathology</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>2013</creationdate><title>Testicular Mineralization in KK-Ay Mice Treated with an Oxovanadium Complex</title><author>MOROKI, Takayasu ; YOSHIKAWA, Yutaka ; YOSHIZAWA, Katsuhiko ; TSUBURA, Airo ; YASUI, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2433-c450ee88b43df25f2ef5d30b2e27f9336c49ab828f6f5f812179aea0fddce1523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>diabetes</topic><topic>KK-Ay mice</topic><topic>Leydig cell</topic><topic>mineralization</topic><topic>oxovanadium(VO2+) complex</topic><topic>Short Communication</topic><topic>testis</topic><toplevel>online_resources</toplevel><creatorcontrib>MOROKI, Takayasu</creatorcontrib><creatorcontrib>YOSHIKAWA, Yutaka</creatorcontrib><creatorcontrib>YOSHIZAWA, Katsuhiko</creatorcontrib><creatorcontrib>TSUBURA, Airo</creatorcontrib><creatorcontrib>YASUI, Hiroyuki</creatorcontrib><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Toxicologic Pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MOROKI, Takayasu</au><au>YOSHIKAWA, Yutaka</au><au>YOSHIZAWA, Katsuhiko</au><au>TSUBURA, Airo</au><au>YASUI, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Testicular Mineralization in KK-Ay Mice Treated with an Oxovanadium Complex</atitle><jtitle>Journal of Toxicologic Pathology</jtitle><addtitle>J Toxicol Pathol</addtitle><date>2013</date><risdate>2013</risdate><volume>26</volume><issue>3</issue><spage>329</spage><epage>333</epage><pages>329-333</pages><issn>0914-9198</issn><eissn>1881-915X</eissn><eissn>1347-7404</eissn><abstract>Vanadium has potential for use in diabetes therapy. Many investigators have reported toxic effects of inorganic vanadium salts; however, there are few reports on toxic effects of oxovanadium(VO2+) complexes. Therefore, we studied VO2+ toxicity by examining histological changes and measuring the vanadium concentration in the testis after repeated oral administration of bis(1-oxy-2-pyridine-thiolato)oxovanadium(VO2+) (VO(opt)2) for 2 or 4 weeks in KK-Ay mice. Severe mineralization and degeneration/necrosis of the seminiferous tubules were detected after either 2 or 4 weeks of administration. Vacuolar changes in Sertoli cells and the seminiferous epithelia, and hyperplasia of Leydig cells were observed in the testes of some animals. Vanadium concentrations in the mineralized testis were much higher than those in the testis of untreated KK-Ay mice. These results represent the first report of the possibility for seminiferous tubules mineralization induced by VO(opt)2 administration. Therefore, our research provides important information about the potentially toxic effects of VO2+ complexes.</abstract><cop>Tokyo</cop><pub>JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY</pub><pmid>24155568</pmid><doi>10.1293/tox.26.329</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | PubMed Central(OA) |
subjects | diabetes KK-Ay mice Leydig cell mineralization oxovanadium(VO2+) complex Short Communication testis |
title | Testicular Mineralization in KK-Ay Mice Treated with an Oxovanadium Complex |
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