Myocardial ultrastructure in cardiac hypertrophy induced by thyroid hormone: an acute study in rats
The early responses of the myocardium ultrastructure under thyroid dysfunction conditions, hemodynamic parameters, cardiac hypertrophy and ultrastructural evaluations were performed in hypothyroid and hyperthyroid rats submitted to different doses [T4-25 and T4-100; 0.025 mg and 0.1 mg kg(-1) body w...
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description | The early responses of the myocardium ultrastructure under thyroid dysfunction conditions, hemodynamic parameters, cardiac hypertrophy and ultrastructural evaluations were performed in hypothyroid and hyperthyroid rats submitted to different doses [T4-25 and T4-100; 0.025 mg and 0.1 mg kg(-1) body weight (BW).per day, respectively)]. All groups were treated for 7 days. The animals were sacrificed, the hearts were excised and weighed and the left ventricle tissue samples were processed for transmission election microscopy. Systolic blood pressure (SBP) was not altered by administration of T4. An increased heart rate and ratio of heart weight to body weight (HW/BW) were found in the hyperthyroid rats. However, the SBP and HW/BW decreased significantly in hypothyroid rats. No significant ultrastructural alterations were detected when the hypothyroid and T4-25 groups were compared with the control group. Alterations of cardiomyocytes nuclei of these groups were also not detected. Notably, disorganization of intercellular junctions was observed in many cardiomyocytes of T4-100 group. The present results indicate that in the early stages of hyperthyroidism, the cardiac hypertrophy development was mainly due to direct effects of thyroid hormone. Despite cardiac hypertrophy development, there is no ultrastructural evidence of myocardial degeneration. |
doi_str_mv | 10.1007/s00428-004-1175-1 |
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All groups were treated for 7 days. The animals were sacrificed, the hearts were excised and weighed and the left ventricle tissue samples were processed for transmission election microscopy. Systolic blood pressure (SBP) was not altered by administration of T4. An increased heart rate and ratio of heart weight to body weight (HW/BW) were found in the hyperthyroid rats. However, the SBP and HW/BW decreased significantly in hypothyroid rats. No significant ultrastructural alterations were detected when the hypothyroid and T4-25 groups were compared with the control group. Alterations of cardiomyocytes nuclei of these groups were also not detected. Notably, disorganization of intercellular junctions was observed in many cardiomyocytes of T4-100 group. The present results indicate that in the early stages of hyperthyroidism, the cardiac hypertrophy development was mainly due to direct effects of thyroid hormone. Despite cardiac hypertrophy development, there is no ultrastructural evidence of myocardial degeneration.</description><identifier>ISSN: 0945-6317</identifier><identifier>EISSN: 1432-2307</identifier><identifier>DOI: 10.1007/s00428-004-1175-1</identifier><identifier>PMID: 15668802</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Biological and medical sciences ; Blood Pressure ; Body weight ; Cardiomegaly - etiology ; Cardiomegaly - pathology ; Cardiomyocytes ; Heart - drug effects ; Heart Rate ; Hyperthyroidism - complications ; Hyperthyroidism - pathology ; Hyperthyroidism - physiopathology ; Hypothyroidism - complications ; Hypothyroidism - pathology ; Hypothyroidism - physiopathology ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Microscopy, Electron, Transmission ; Myocardium - pathology ; Myocardium - ultrastructure ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Rats ; Rats, Wistar ; Rodents ; Thymectomy ; Thyroid ; Thyroid gland ; Thyroxine - pharmacology</subject><ispartof>Virchows Archiv : an international journal of pathology, 2005-03, Vol.446 (3), p.265-269</ispartof><rights>2005 INIST-CNRS</rights><rights>Springer-Verlag 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-c7df6939e27bd4f8ad43983e5f8bbd7d531d0909ad11ecde54a7d54c3e7e14e83</citedby><cites>FETCH-LOGICAL-c356t-c7df6939e27bd4f8ad43983e5f8bbd7d531d0909ad11ecde54a7d54c3e7e14e83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16661502$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15668802$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LI WEN HU</creatorcontrib><creatorcontrib>APARECIDO LIBERTI, Edson</creatorcontrib><creatorcontrib>MORAIS BARRETO-CHAVES, Maria Luiza</creatorcontrib><title>Myocardial ultrastructure in cardiac hypertrophy induced by thyroid hormone: an acute study in rats</title><title>Virchows Archiv : an international journal of pathology</title><addtitle>Virchows Arch</addtitle><description>The early responses of the myocardium ultrastructure under thyroid dysfunction conditions, hemodynamic parameters, cardiac hypertrophy and ultrastructural evaluations were performed in hypothyroid and hyperthyroid rats submitted to different doses [T4-25 and T4-100; 0.025 mg and 0.1 mg kg(-1) body weight (BW).per day, respectively)]. All groups were treated for 7 days. The animals were sacrificed, the hearts were excised and weighed and the left ventricle tissue samples were processed for transmission election microscopy. Systolic blood pressure (SBP) was not altered by administration of T4. An increased heart rate and ratio of heart weight to body weight (HW/BW) were found in the hyperthyroid rats. However, the SBP and HW/BW decreased significantly in hypothyroid rats. No significant ultrastructural alterations were detected when the hypothyroid and T4-25 groups were compared with the control group. Alterations of cardiomyocytes nuclei of these groups were also not detected. Notably, disorganization of intercellular junctions was observed in many cardiomyocytes of T4-100 group. The present results indicate that in the early stages of hyperthyroidism, the cardiac hypertrophy development was mainly due to direct effects of thyroid hormone. Despite cardiac hypertrophy development, there is no ultrastructural evidence of myocardial degeneration.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure</subject><subject>Body weight</subject><subject>Cardiomegaly - etiology</subject><subject>Cardiomegaly - pathology</subject><subject>Cardiomyocytes</subject><subject>Heart - drug effects</subject><subject>Heart Rate</subject><subject>Hyperthyroidism - complications</subject><subject>Hyperthyroidism - pathology</subject><subject>Hyperthyroidism - physiopathology</subject><subject>Hypothyroidism - complications</subject><subject>Hypothyroidism - pathology</subject><subject>Hypothyroidism - physiopathology</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Transmission</subject><subject>Myocardium - pathology</subject><subject>Myocardium - ultrastructure</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rodents</subject><subject>Thymectomy</subject><subject>Thyroid</subject><subject>Thyroid gland</subject><subject>Thyroxine - pharmacology</subject><issn>0945-6317</issn><issn>1432-2307</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpd0E1r3DAQBmARWppt2h-QSxGB9OZGY1kfzi2EpC2k5JKehSyNWQevtdXHwf8-WnYh0MsIRs8Mw0vIJbAfwJi6SYx1rW5qbQCUaOCMbKDjbdNypj6QDes70UgO6px8TumVsRY0yE_kHISUWrN2Q9yfNTgb_WRnWuYcbcqxuFwi0mmhxx9Ht-seY45hv11r2xeHng4rzds1hsnTbYi7sOAttQu1rmSkKRd_oDTanL6Qj6OdE349vRfk7-PDy_2v5un55-_7u6fGcSFz45QfZc97bNXgu1Fb3_FecxSjHgavvODgWc966wHQeRSdrc3OcVQIHWp-Qb4f9-5j-FcwZbObksN5tguGkoxUQnClZYVX_8HXUOJSbzO6ZYpDz9qK4IhcDClFHM0-TjsbVwPMHOI3x_hNreYQv4E68-20uAw79O8Tp7wruD4Bm5ydx2gXN6V3J6UEUd0bLnqOmA</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>LI WEN HU</creator><creator>APARECIDO LIBERTI, Edson</creator><creator>MORAIS BARRETO-CHAVES, Maria Luiza</creator><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20050301</creationdate><title>Myocardial ultrastructure in cardiac hypertrophy induced by thyroid hormone: an acute study in rats</title><author>LI WEN HU ; APARECIDO LIBERTI, Edson ; MORAIS BARRETO-CHAVES, Maria Luiza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-c7df6939e27bd4f8ad43983e5f8bbd7d531d0909ad11ecde54a7d54c3e7e14e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure</topic><topic>Body weight</topic><topic>Cardiomegaly - etiology</topic><topic>Cardiomegaly - pathology</topic><topic>Cardiomyocytes</topic><topic>Heart - drug effects</topic><topic>Heart Rate</topic><topic>Hyperthyroidism - complications</topic><topic>Hyperthyroidism - pathology</topic><topic>Hyperthyroidism - physiopathology</topic><topic>Hypothyroidism - complications</topic><topic>Hypothyroidism - pathology</topic><topic>Hypothyroidism - physiopathology</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Electron, Transmission</topic><topic>Myocardium - pathology</topic><topic>Myocardium - ultrastructure</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Rodents</topic><topic>Thymectomy</topic><topic>Thyroid</topic><topic>Thyroid gland</topic><topic>Thyroxine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LI WEN HU</creatorcontrib><creatorcontrib>APARECIDO LIBERTI, Edson</creatorcontrib><creatorcontrib>MORAIS BARRETO-CHAVES, Maria Luiza</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>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Virchows Archiv : an international journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LI WEN HU</au><au>APARECIDO LIBERTI, Edson</au><au>MORAIS BARRETO-CHAVES, Maria Luiza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myocardial ultrastructure in cardiac hypertrophy induced by thyroid hormone: an acute study in rats</atitle><jtitle>Virchows Archiv : an international journal of pathology</jtitle><addtitle>Virchows Arch</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>446</volume><issue>3</issue><spage>265</spage><epage>269</epage><pages>265-269</pages><issn>0945-6317</issn><eissn>1432-2307</eissn><abstract>The early responses of the myocardium ultrastructure under thyroid dysfunction conditions, hemodynamic parameters, cardiac hypertrophy and ultrastructural evaluations were performed in hypothyroid and hyperthyroid rats submitted to different doses [T4-25 and T4-100; 0.025 mg and 0.1 mg kg(-1) body weight (BW).per day, respectively)]. All groups were treated for 7 days. The animals were sacrificed, the hearts were excised and weighed and the left ventricle tissue samples were processed for transmission election microscopy. Systolic blood pressure (SBP) was not altered by administration of T4. An increased heart rate and ratio of heart weight to body weight (HW/BW) were found in the hyperthyroid rats. However, the SBP and HW/BW decreased significantly in hypothyroid rats. No significant ultrastructural alterations were detected when the hypothyroid and T4-25 groups were compared with the control group. Alterations of cardiomyocytes nuclei of these groups were also not detected. Notably, disorganization of intercellular junctions was observed in many cardiomyocytes of T4-100 group. The present results indicate that in the early stages of hyperthyroidism, the cardiac hypertrophy development was mainly due to direct effects of thyroid hormone. Despite cardiac hypertrophy development, there is no ultrastructural evidence of myocardial degeneration.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>15668802</pmid><doi>10.1007/s00428-004-1175-1</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Blood Pressure Body weight Cardiomegaly - etiology Cardiomegaly - pathology Cardiomyocytes Heart - drug effects Heart Rate Hyperthyroidism - complications Hyperthyroidism - pathology Hyperthyroidism - physiopathology Hypothyroidism - complications Hypothyroidism - pathology Hypothyroidism - physiopathology Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Microscopy, Electron, Transmission Myocardium - pathology Myocardium - ultrastructure Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Rats Rats, Wistar Rodents Thymectomy Thyroid Thyroid gland Thyroxine - pharmacology |
title | Myocardial ultrastructure in cardiac hypertrophy induced by thyroid hormone: an acute study in rats |
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