Mechanism of cadmium induced crystal defects in developing rat tooth enamel
It is well known that exposure to environmental cadmium causes itai-itai (ouch-ouch) disease. However, the exact mechanism underlying this bone disease remains unresolved. By focusing on the calcification mechanism, we examined developing tooth enamel in rats exposed to cadmium to test the hypothesi...
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Veröffentlicht in: | Proceedings of the Japan Academy, Series B Series B, 2009, Vol.85(10), pp.500-507 |
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description | It is well known that exposure to environmental cadmium causes itai-itai (ouch-ouch) disease. However, the exact mechanism underlying this bone disease remains unresolved. By focusing on the calcification mechanism, we examined developing tooth enamel in rats exposed to cadmium to test the hypothesis that cadmium exposure may cause defects in crystal formation. Electron microscopy revealed the presence of perforated crystals in developing tooth enamel, indicating that the process of crystal nucleation may have been interrupted by cadmium exposure. Furthermore, biochemical analyses revealed that the catalytic activity of carbonic anhydrase in the immature enamel matrix declined remarkably despite the fact that quantitative reduction of this enzyme was insignificant, suggesting that the decline of catalytic activity may have resulted from the replacement of zinc with cadmium ions. Therefore, we concluded that the poor catalytic activity of cadmium-binding carbonic anhydrase might hinder the nucleation process, leading to an impairment in mineralization that causes itai-itai disease. (Communicated by Tatsuo SUDA, M.J.A.) |
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However, the exact mechanism underlying this bone disease remains unresolved. By focusing on the calcification mechanism, we examined developing tooth enamel in rats exposed to cadmium to test the hypothesis that cadmium exposure may cause defects in crystal formation. Electron microscopy revealed the presence of perforated crystals in developing tooth enamel, indicating that the process of crystal nucleation may have been interrupted by cadmium exposure. Furthermore, biochemical analyses revealed that the catalytic activity of carbonic anhydrase in the immature enamel matrix declined remarkably despite the fact that quantitative reduction of this enzyme was insignificant, suggesting that the decline of catalytic activity may have resulted from the replacement of zinc with cadmium ions. Therefore, we concluded that the poor catalytic activity of cadmium-binding carbonic anhydrase might hinder the nucleation process, leading to an impairment in mineralization that causes itai-itai disease. (Communicated by Tatsuo SUDA, M.J.A.)</description><identifier>ISSN: 0386-2208</identifier><identifier>EISSN: 1349-2896</identifier><identifier>DOI: 10.2183/pjab.85.500</identifier><identifier>PMID: 20009383</identifier><language>eng</language><publisher>Japan: The Japan Academy</publisher><subject>Animals ; Cadmium - toxicity ; cadmium binding carbonic anhydrase ; cadmium ions ; Carbonic Anhydrases - metabolism ; crystal defects ; Crystallization ; Dental Enamel - embryology ; Dental Enamel - enzymology ; Dental Enamel - pathology ; Dental Enamel - ultrastructure ; Dental Enamel Proteins - metabolism ; Electrophoresis, Polyacrylamide Gel ; Immunoblotting ; itai-itai (ouch-ouch) disease ; Male ; osteoporosis ; Rats ; Rats, Sprague-Dawley ; Tooth - embryology ; Tooth - enzymology ; Tooth - pathology ; Tooth - ultrastructure ; tooth enamel</subject><ispartof>Proceedings of the Japan Academy, Series B, 2009, Vol.85(10), pp.500-507</ispartof><rights>2009 The Japan Academy</rights><rights>2009 The Japan Academy 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c663t-bd45ba2faa1e1216315d5d358f8a32ce02005d55c573c1db2a8d1e4975c0e1d63</citedby><cites>FETCH-LOGICAL-c663t-bd45ba2faa1e1216315d5d358f8a32ce02005d55c573c1db2a8d1e4975c0e1d63</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/PMC3621555/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621555/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1876,4009,27902,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20009383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KAKEI, Mitsuo</creatorcontrib><creatorcontrib>SAKAE, Toshiro</creatorcontrib><creatorcontrib>YOSHIKAWA, Masayoshi</creatorcontrib><title>Mechanism of cadmium induced crystal defects in developing rat tooth enamel</title><title>Proceedings of the Japan Academy, Series B</title><addtitle>Proc. Jpn. Acad., Ser. B</addtitle><description>It is well known that exposure to environmental cadmium causes itai-itai (ouch-ouch) disease. However, the exact mechanism underlying this bone disease remains unresolved. By focusing on the calcification mechanism, we examined developing tooth enamel in rats exposed to cadmium to test the hypothesis that cadmium exposure may cause defects in crystal formation. Electron microscopy revealed the presence of perforated crystals in developing tooth enamel, indicating that the process of crystal nucleation may have been interrupted by cadmium exposure. Furthermore, biochemical analyses revealed that the catalytic activity of carbonic anhydrase in the immature enamel matrix declined remarkably despite the fact that quantitative reduction of this enzyme was insignificant, suggesting that the decline of catalytic activity may have resulted from the replacement of zinc with cadmium ions. Therefore, we concluded that the poor catalytic activity of cadmium-binding carbonic anhydrase might hinder the nucleation process, leading to an impairment in mineralization that causes itai-itai disease. (Communicated by Tatsuo SUDA, M.J.A.)</description><subject>Animals</subject><subject>Cadmium - toxicity</subject><subject>cadmium binding carbonic anhydrase</subject><subject>cadmium ions</subject><subject>Carbonic Anhydrases - metabolism</subject><subject>crystal defects</subject><subject>Crystallization</subject><subject>Dental Enamel - embryology</subject><subject>Dental Enamel - enzymology</subject><subject>Dental Enamel - pathology</subject><subject>Dental Enamel - ultrastructure</subject><subject>Dental Enamel Proteins - metabolism</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Immunoblotting</subject><subject>itai-itai (ouch-ouch) disease</subject><subject>Male</subject><subject>osteoporosis</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Tooth - embryology</subject><subject>Tooth - enzymology</subject><subject>Tooth - pathology</subject><subject>Tooth - ultrastructure</subject><subject>tooth enamel</subject><issn>0386-2208</issn><issn>1349-2896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkT1v2zAQhomiQeO4nboHmroEcvhhKvRSoDHaJEiCLu1MnMiTTUMSVZIy4H8fGk6EdCGJuwfPHV4S8pXRBWdKXA87qBdKLiSlH8iMieWq5GpVfSQzKlRVck7VObmIcUep4FKxT-ScU0pXQokZeXxGs4Xexa7wTWHAdm7sCtfb0aAtTDjEBG1hsUGTYq7n5x5bP7h-UwRIRfI-bQvsocP2MzlroI345fWek7-_fv5Z35dPv-8e1j-eSlNVIpW1XcoaeAPAkHFWCSattEKqRoHgBmneLlekkTfCMFtzUJbhcnUjDUVmKzEn30_eYaw7tAb7FKDVQ3AdhIP24PT_nd5t9cbvtag4k1JmwbdXQfD_RoxJdy4abFvo0Y9RcyYoo-oIXp1AE3yMAZtpCKP6GL4-hq-V1Dn8TF--32ti39LOwO0J2OVUNzgBEJIzLU6yLD-d2To18zcFjb14AUp2mYc</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>KAKEI, Mitsuo</creator><creator>SAKAE, Toshiro</creator><creator>YOSHIKAWA, Masayoshi</creator><general>The Japan Academy</general><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>7QP</scope><scope>5PM</scope></search><sort><creationdate>2009</creationdate><title>Mechanism of cadmium induced crystal defects in developing rat tooth enamel</title><author>KAKEI, Mitsuo ; SAKAE, Toshiro ; YOSHIKAWA, Masayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c663t-bd45ba2faa1e1216315d5d358f8a32ce02005d55c573c1db2a8d1e4975c0e1d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cadmium - toxicity</topic><topic>cadmium binding carbonic anhydrase</topic><topic>cadmium ions</topic><topic>Carbonic Anhydrases - metabolism</topic><topic>crystal defects</topic><topic>Crystallization</topic><topic>Dental Enamel - embryology</topic><topic>Dental Enamel - enzymology</topic><topic>Dental Enamel - pathology</topic><topic>Dental Enamel - ultrastructure</topic><topic>Dental Enamel Proteins - metabolism</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Immunoblotting</topic><topic>itai-itai (ouch-ouch) disease</topic><topic>Male</topic><topic>osteoporosis</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Tooth - embryology</topic><topic>Tooth - enzymology</topic><topic>Tooth - pathology</topic><topic>Tooth - ultrastructure</topic><topic>tooth enamel</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KAKEI, Mitsuo</creatorcontrib><creatorcontrib>SAKAE, Toshiro</creatorcontrib><creatorcontrib>YOSHIKAWA, Masayoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the Japan Academy, Series B</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KAKEI, Mitsuo</au><au>SAKAE, Toshiro</au><au>YOSHIKAWA, Masayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanism of cadmium induced crystal defects in developing rat tooth enamel</atitle><jtitle>Proceedings of the Japan Academy, Series B</jtitle><addtitle>Proc. Jpn. Acad., Ser. B</addtitle><date>2009</date><risdate>2009</risdate><volume>85</volume><issue>10</issue><spage>500</spage><epage>507</epage><pages>500-507</pages><issn>0386-2208</issn><eissn>1349-2896</eissn><abstract>It is well known that exposure to environmental cadmium causes itai-itai (ouch-ouch) disease. However, the exact mechanism underlying this bone disease remains unresolved. By focusing on the calcification mechanism, we examined developing tooth enamel in rats exposed to cadmium to test the hypothesis that cadmium exposure may cause defects in crystal formation. Electron microscopy revealed the presence of perforated crystals in developing tooth enamel, indicating that the process of crystal nucleation may have been interrupted by cadmium exposure. Furthermore, biochemical analyses revealed that the catalytic activity of carbonic anhydrase in the immature enamel matrix declined remarkably despite the fact that quantitative reduction of this enzyme was insignificant, suggesting that the decline of catalytic activity may have resulted from the replacement of zinc with cadmium ions. Therefore, we concluded that the poor catalytic activity of cadmium-binding carbonic anhydrase might hinder the nucleation process, leading to an impairment in mineralization that causes itai-itai disease. (Communicated by Tatsuo SUDA, M.J.A.)</abstract><cop>Japan</cop><pub>The Japan Academy</pub><pmid>20009383</pmid><doi>10.2183/pjab.85.500</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cadmium - toxicity cadmium binding carbonic anhydrase cadmium ions Carbonic Anhydrases - metabolism crystal defects Crystallization Dental Enamel - embryology Dental Enamel - enzymology Dental Enamel - pathology Dental Enamel - ultrastructure Dental Enamel Proteins - metabolism Electrophoresis, Polyacrylamide Gel Immunoblotting itai-itai (ouch-ouch) disease Male osteoporosis Rats Rats, Sprague-Dawley Tooth - embryology Tooth - enzymology Tooth - pathology Tooth - ultrastructure tooth enamel |
title | Mechanism of cadmium induced crystal defects in developing rat tooth enamel |
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