Coenzyme Q10 protect against ischemia/reperfusion induced biochemical and functional changes in rabbit urinary bladder
Purpose Ischemia, reperfusion, and free radical generation have been recently implicated in the progressive bladder dysfunction. Coenzyme Q10 (CoQ10) is a pro-vitamin like substance that appears to be efficient for treatment of neurodegenerative disorders and ischemic heart disease. Our goal was to...
Gespeichert in:
Veröffentlicht in: | Molecular and cellular biochemistry 2008-04, Vol.311 (1-2), p.73-80 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 80 |
---|---|
container_issue | 1-2 |
container_start_page | 73 |
container_title | Molecular and cellular biochemistry |
container_volume | 311 |
creator | Juan, Yung-Shun Hydery, Tasmina Mannikarottu, Anita Kogan, Barry Schuler, Catherine Leggett, Robert E Lin, Wei-Yu Huang, Chun-Hsiung Levin, Robert M |
description | Purpose Ischemia, reperfusion, and free radical generation have been recently implicated in the progressive bladder dysfunction. Coenzyme Q10 (CoQ10) is a pro-vitamin like substance that appears to be efficient for treatment of neurodegenerative disorders and ischemic heart disease. Our goal was to investigate the potential protective effect of CoQ10 in a rabbit model of in vivo bilateral ischemia and ischemia/reperfusion (I/R). Material and Methods Six groups of four male New Zealand White rabbits each were treated with CoQ10 (3 mg/kg body weight/day--dissolved in peanut oil) (groups 1-3) or vehicle (peanut oil) (groups 4-6). Groups 1 and 4 (ischemia-alone groups) had clamped bilateral vesical arteries for 2 h; in groups 2 and 5 (I/R groups), bilateral ischemia was similarly induced and the rabbits were allowed to recover for 2 weeks. Groups 3 and 6 were controls (shams) and were exposed to sham surgery. The effects on contractile responses to various stimulations and biochemical studies such as citrate synthase (CS), choline acetyltransferase (ChAT), superoxide dismutase (SOD), and catalase (CAT) were evaluated. The protein peroxidation indicator, carbonyl group, and nitrotyrosine contents were analyzed by Western blotting. Results Ischemia resulted in significant reductions in the contractile responses to all forms of stimulation in vehicle-fed rabbits, whereas there were no reductions in CoQ10-treated rabbits. Contractile responses were significantly reduced in vehicle-treated I/R groups, but significantly improved in CoQ10-treated rabbits. Protein carbonylation and nitration increased significantly in ischemia-alone and I/R bladders; CoQ10 treatment significantly attenuated protein carbonylation and nitration. CoQ10 up-regulated SOD and CAT activities in control animals; the few differences in CoQ10-treated animal in SOD and CAT after ischemia and in general increase CAT activities following I/R. Conclusions CoQ10 supplementation provides bladder protection against I/R injury. This protection effect improves mitochondrial function during I/R by repleting mitochondrial CoQ10 stores and potentiating their antioxidant properties. |
doi_str_mv | 10.1007/s11010-007-9696-y |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70419317</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1897593771</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-ce3f888fa40811e04f8b6373646e0675777ca8e42d0b437f84d59067501b52063</originalsourceid><addsrcrecordid>eNp9kU9v1DAQxS0EotvCB-ACFgduoTNxEttHtAKKVAkh6NlynPHWVf4sdoK0fHocshKIAyeP9X4zozePsRcIbxFAXidEQChyWehGN8XpEdthLUVRadSP2Q4EQKFQygt2mdIDZBgQn7ILVNjUGssd-7GfaPx5Goh_QeDHOM3kZm4PNoxp5iG5exqCvY50pOiXFKaRh7FbHHW8DdNv1dme27HjfhndnIH8dfd2PFDKKI-2bcPMlxhGG0-87W3XUXzGnnjbJ3p-fq_Y3Yf33_Y3xe3nj5_2724LJ7SYC0fCK6W8rUAhElRetY2QoqkagkbWUkpnFVVlB20lpFdVV-tVAGzrEhpxxd5sc7Oz7wul2QzZE_W9HWlakpFQoRYoM_j6H_BhWmL2kgxqWTd55wrhBrk4pRTJm2MMQ7ZlEMyaiNkSMWu5JmJOueflefDSDtT96ThHkIFyA1KW8tXiX5v_M_XV1uTtZOwhhmTuvpaAOXC1nqUUvwD8XKAV</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>197567367</pqid></control><display><type>article</type><title>Coenzyme Q10 protect against ischemia/reperfusion induced biochemical and functional changes in rabbit urinary bladder</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Juan, Yung-Shun ; Hydery, Tasmina ; Mannikarottu, Anita ; Kogan, Barry ; Schuler, Catherine ; Leggett, Robert E ; Lin, Wei-Yu ; Huang, Chun-Hsiung ; Levin, Robert M</creator><creatorcontrib>Juan, Yung-Shun ; Hydery, Tasmina ; Mannikarottu, Anita ; Kogan, Barry ; Schuler, Catherine ; Leggett, Robert E ; Lin, Wei-Yu ; Huang, Chun-Hsiung ; Levin, Robert M</creatorcontrib><description>Purpose Ischemia, reperfusion, and free radical generation have been recently implicated in the progressive bladder dysfunction. Coenzyme Q10 (CoQ10) is a pro-vitamin like substance that appears to be efficient for treatment of neurodegenerative disorders and ischemic heart disease. Our goal was to investigate the potential protective effect of CoQ10 in a rabbit model of in vivo bilateral ischemia and ischemia/reperfusion (I/R). Material and Methods Six groups of four male New Zealand White rabbits each were treated with CoQ10 (3 mg/kg body weight/day--dissolved in peanut oil) (groups 1-3) or vehicle (peanut oil) (groups 4-6). Groups 1 and 4 (ischemia-alone groups) had clamped bilateral vesical arteries for 2 h; in groups 2 and 5 (I/R groups), bilateral ischemia was similarly induced and the rabbits were allowed to recover for 2 weeks. Groups 3 and 6 were controls (shams) and were exposed to sham surgery. The effects on contractile responses to various stimulations and biochemical studies such as citrate synthase (CS), choline acetyltransferase (ChAT), superoxide dismutase (SOD), and catalase (CAT) were evaluated. The protein peroxidation indicator, carbonyl group, and nitrotyrosine contents were analyzed by Western blotting. Results Ischemia resulted in significant reductions in the contractile responses to all forms of stimulation in vehicle-fed rabbits, whereas there were no reductions in CoQ10-treated rabbits. Contractile responses were significantly reduced in vehicle-treated I/R groups, but significantly improved in CoQ10-treated rabbits. Protein carbonylation and nitration increased significantly in ischemia-alone and I/R bladders; CoQ10 treatment significantly attenuated protein carbonylation and nitration. CoQ10 up-regulated SOD and CAT activities in control animals; the few differences in CoQ10-treated animal in SOD and CAT after ischemia and in general increase CAT activities following I/R. Conclusions CoQ10 supplementation provides bladder protection against I/R injury. This protection effect improves mitochondrial function during I/R by repleting mitochondrial CoQ10 stores and potentiating their antioxidant properties.</description><identifier>ISSN: 0300-8177</identifier><identifier>EISSN: 1573-4919</identifier><identifier>DOI: 10.1007/s11010-007-9696-y</identifier><identifier>PMID: 18165912</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Animals ; Antioxidants - administration & dosage ; Antioxidants - pharmacology ; Biochemistry ; Biomedical and Life Sciences ; Bladder ; Body weight ; Carbonyl compounds ; Cardiology ; Cardiovascular diseases ; Catalase - metabolism ; Choline O-Acetyltransferase - metabolism ; Citrate (si)-Synthase - metabolism ; Dietary Supplements ; Enzymes ; Free radicals ; Ischemia ; Life Sciences ; Male ; Medical Biochemistry ; Mitochondria - metabolism ; Muscle Contraction - drug effects ; Oncology ; Peanut oil ; Peroxidation ; Rabbits ; Reperfusion Injury - drug therapy ; Reperfusion Injury - prevention & control ; Superoxide Dismutase - metabolism ; Ubiquinone - administration & dosage ; Ubiquinone - analogs & derivatives ; Ubiquinone - pharmacology ; Ubiquinone - therapeutic use ; Urinary bladder ; Urinary Bladder - drug effects ; Urinary Bladder - metabolism ; Urinary Bladder - pathology ; Urology</subject><ispartof>Molecular and cellular biochemistry, 2008-04, Vol.311 (1-2), p.73-80</ispartof><rights>Springer Science+Business Media, LLC. 2007</rights><rights>Springer Science+Business Media, LLC. 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-ce3f888fa40811e04f8b6373646e0675777ca8e42d0b437f84d59067501b52063</citedby><cites>FETCH-LOGICAL-c393t-ce3f888fa40811e04f8b6373646e0675777ca8e42d0b437f84d59067501b52063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11010-007-9696-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11010-007-9696-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18165912$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Juan, Yung-Shun</creatorcontrib><creatorcontrib>Hydery, Tasmina</creatorcontrib><creatorcontrib>Mannikarottu, Anita</creatorcontrib><creatorcontrib>Kogan, Barry</creatorcontrib><creatorcontrib>Schuler, Catherine</creatorcontrib><creatorcontrib>Leggett, Robert E</creatorcontrib><creatorcontrib>Lin, Wei-Yu</creatorcontrib><creatorcontrib>Huang, Chun-Hsiung</creatorcontrib><creatorcontrib>Levin, Robert M</creatorcontrib><title>Coenzyme Q10 protect against ischemia/reperfusion induced biochemical and functional changes in rabbit urinary bladder</title><title>Molecular and cellular biochemistry</title><addtitle>Mol Cell Biochem</addtitle><addtitle>Mol Cell Biochem</addtitle><description>Purpose Ischemia, reperfusion, and free radical generation have been recently implicated in the progressive bladder dysfunction. Coenzyme Q10 (CoQ10) is a pro-vitamin like substance that appears to be efficient for treatment of neurodegenerative disorders and ischemic heart disease. Our goal was to investigate the potential protective effect of CoQ10 in a rabbit model of in vivo bilateral ischemia and ischemia/reperfusion (I/R). Material and Methods Six groups of four male New Zealand White rabbits each were treated with CoQ10 (3 mg/kg body weight/day--dissolved in peanut oil) (groups 1-3) or vehicle (peanut oil) (groups 4-6). Groups 1 and 4 (ischemia-alone groups) had clamped bilateral vesical arteries for 2 h; in groups 2 and 5 (I/R groups), bilateral ischemia was similarly induced and the rabbits were allowed to recover for 2 weeks. Groups 3 and 6 were controls (shams) and were exposed to sham surgery. The effects on contractile responses to various stimulations and biochemical studies such as citrate synthase (CS), choline acetyltransferase (ChAT), superoxide dismutase (SOD), and catalase (CAT) were evaluated. The protein peroxidation indicator, carbonyl group, and nitrotyrosine contents were analyzed by Western blotting. Results Ischemia resulted in significant reductions in the contractile responses to all forms of stimulation in vehicle-fed rabbits, whereas there were no reductions in CoQ10-treated rabbits. Contractile responses were significantly reduced in vehicle-treated I/R groups, but significantly improved in CoQ10-treated rabbits. Protein carbonylation and nitration increased significantly in ischemia-alone and I/R bladders; CoQ10 treatment significantly attenuated protein carbonylation and nitration. CoQ10 up-regulated SOD and CAT activities in control animals; the few differences in CoQ10-treated animal in SOD and CAT after ischemia and in general increase CAT activities following I/R. Conclusions CoQ10 supplementation provides bladder protection against I/R injury. This protection effect improves mitochondrial function during I/R by repleting mitochondrial CoQ10 stores and potentiating their antioxidant properties.</description><subject>Animals</subject><subject>Antioxidants - administration & dosage</subject><subject>Antioxidants - pharmacology</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Bladder</subject><subject>Body weight</subject><subject>Carbonyl compounds</subject><subject>Cardiology</subject><subject>Cardiovascular diseases</subject><subject>Catalase - metabolism</subject><subject>Choline O-Acetyltransferase - metabolism</subject><subject>Citrate (si)-Synthase - metabolism</subject><subject>Dietary Supplements</subject><subject>Enzymes</subject><subject>Free radicals</subject><subject>Ischemia</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical Biochemistry</subject><subject>Mitochondria - metabolism</subject><subject>Muscle Contraction - drug effects</subject><subject>Oncology</subject><subject>Peanut oil</subject><subject>Peroxidation</subject><subject>Rabbits</subject><subject>Reperfusion Injury - drug therapy</subject><subject>Reperfusion Injury - prevention & control</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Ubiquinone - administration & dosage</subject><subject>Ubiquinone - analogs & derivatives</subject><subject>Ubiquinone - pharmacology</subject><subject>Ubiquinone - therapeutic use</subject><subject>Urinary bladder</subject><subject>Urinary Bladder - drug effects</subject><subject>Urinary Bladder - metabolism</subject><subject>Urinary Bladder - pathology</subject><subject>Urology</subject><issn>0300-8177</issn><issn>1573-4919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kU9v1DAQxS0EotvCB-ACFgduoTNxEttHtAKKVAkh6NlynPHWVf4sdoK0fHocshKIAyeP9X4zozePsRcIbxFAXidEQChyWehGN8XpEdthLUVRadSP2Q4EQKFQygt2mdIDZBgQn7ILVNjUGssd-7GfaPx5Goh_QeDHOM3kZm4PNoxp5iG5exqCvY50pOiXFKaRh7FbHHW8DdNv1dme27HjfhndnIH8dfd2PFDKKI-2bcPMlxhGG0-87W3XUXzGnnjbJ3p-fq_Y3Yf33_Y3xe3nj5_2724LJ7SYC0fCK6W8rUAhElRetY2QoqkagkbWUkpnFVVlB20lpFdVV-tVAGzrEhpxxd5sc7Oz7wul2QzZE_W9HWlakpFQoRYoM_j6H_BhWmL2kgxqWTd55wrhBrk4pRTJm2MMQ7ZlEMyaiNkSMWu5JmJOueflefDSDtT96ThHkIFyA1KW8tXiX5v_M_XV1uTtZOwhhmTuvpaAOXC1nqUUvwD8XKAV</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Juan, Yung-Shun</creator><creator>Hydery, Tasmina</creator><creator>Mannikarottu, Anita</creator><creator>Kogan, Barry</creator><creator>Schuler, Catherine</creator><creator>Leggett, Robert E</creator><creator>Lin, Wei-Yu</creator><creator>Huang, Chun-Hsiung</creator><creator>Levin, Robert M</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer Nature B.V</general><scope>FBQ</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>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</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>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20080401</creationdate><title>Coenzyme Q10 protect against ischemia/reperfusion induced biochemical and functional changes in rabbit urinary bladder</title><author>Juan, Yung-Shun ; Hydery, Tasmina ; Mannikarottu, Anita ; Kogan, Barry ; Schuler, Catherine ; Leggett, Robert E ; Lin, Wei-Yu ; Huang, Chun-Hsiung ; Levin, Robert M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-ce3f888fa40811e04f8b6373646e0675777ca8e42d0b437f84d59067501b52063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antioxidants - administration & dosage</topic><topic>Antioxidants - pharmacology</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Bladder</topic><topic>Body weight</topic><topic>Carbonyl compounds</topic><topic>Cardiology</topic><topic>Cardiovascular diseases</topic><topic>Catalase - metabolism</topic><topic>Choline O-Acetyltransferase - metabolism</topic><topic>Citrate (si)-Synthase - metabolism</topic><topic>Dietary Supplements</topic><topic>Enzymes</topic><topic>Free radicals</topic><topic>Ischemia</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical Biochemistry</topic><topic>Mitochondria - metabolism</topic><topic>Muscle Contraction - drug effects</topic><topic>Oncology</topic><topic>Peanut oil</topic><topic>Peroxidation</topic><topic>Rabbits</topic><topic>Reperfusion Injury - drug therapy</topic><topic>Reperfusion Injury - prevention & control</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Ubiquinone - administration & dosage</topic><topic>Ubiquinone - analogs & derivatives</topic><topic>Ubiquinone - pharmacology</topic><topic>Ubiquinone - therapeutic use</topic><topic>Urinary bladder</topic><topic>Urinary Bladder - drug effects</topic><topic>Urinary Bladder - metabolism</topic><topic>Urinary Bladder - pathology</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Juan, Yung-Shun</creatorcontrib><creatorcontrib>Hydery, Tasmina</creatorcontrib><creatorcontrib>Mannikarottu, Anita</creatorcontrib><creatorcontrib>Kogan, Barry</creatorcontrib><creatorcontrib>Schuler, Catherine</creatorcontrib><creatorcontrib>Leggett, Robert E</creatorcontrib><creatorcontrib>Lin, Wei-Yu</creatorcontrib><creatorcontrib>Huang, Chun-Hsiung</creatorcontrib><creatorcontrib>Levin, Robert M</creatorcontrib><collection>AGRIS</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science 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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</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 Korea</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>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</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>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Juan, Yung-Shun</au><au>Hydery, Tasmina</au><au>Mannikarottu, Anita</au><au>Kogan, Barry</au><au>Schuler, Catherine</au><au>Leggett, Robert E</au><au>Lin, Wei-Yu</au><au>Huang, Chun-Hsiung</au><au>Levin, Robert M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coenzyme Q10 protect against ischemia/reperfusion induced biochemical and functional changes in rabbit urinary bladder</atitle><jtitle>Molecular and cellular biochemistry</jtitle><stitle>Mol Cell Biochem</stitle><addtitle>Mol Cell Biochem</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>311</volume><issue>1-2</issue><spage>73</spage><epage>80</epage><pages>73-80</pages><issn>0300-8177</issn><eissn>1573-4919</eissn><abstract>Purpose Ischemia, reperfusion, and free radical generation have been recently implicated in the progressive bladder dysfunction. Coenzyme Q10 (CoQ10) is a pro-vitamin like substance that appears to be efficient for treatment of neurodegenerative disorders and ischemic heart disease. Our goal was to investigate the potential protective effect of CoQ10 in a rabbit model of in vivo bilateral ischemia and ischemia/reperfusion (I/R). Material and Methods Six groups of four male New Zealand White rabbits each were treated with CoQ10 (3 mg/kg body weight/day--dissolved in peanut oil) (groups 1-3) or vehicle (peanut oil) (groups 4-6). Groups 1 and 4 (ischemia-alone groups) had clamped bilateral vesical arteries for 2 h; in groups 2 and 5 (I/R groups), bilateral ischemia was similarly induced and the rabbits were allowed to recover for 2 weeks. Groups 3 and 6 were controls (shams) and were exposed to sham surgery. The effects on contractile responses to various stimulations and biochemical studies such as citrate synthase (CS), choline acetyltransferase (ChAT), superoxide dismutase (SOD), and catalase (CAT) were evaluated. The protein peroxidation indicator, carbonyl group, and nitrotyrosine contents were analyzed by Western blotting. Results Ischemia resulted in significant reductions in the contractile responses to all forms of stimulation in vehicle-fed rabbits, whereas there were no reductions in CoQ10-treated rabbits. Contractile responses were significantly reduced in vehicle-treated I/R groups, but significantly improved in CoQ10-treated rabbits. Protein carbonylation and nitration increased significantly in ischemia-alone and I/R bladders; CoQ10 treatment significantly attenuated protein carbonylation and nitration. CoQ10 up-regulated SOD and CAT activities in control animals; the few differences in CoQ10-treated animal in SOD and CAT after ischemia and in general increase CAT activities following I/R. Conclusions CoQ10 supplementation provides bladder protection against I/R injury. This protection effect improves mitochondrial function during I/R by repleting mitochondrial CoQ10 stores and potentiating their antioxidant properties.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>18165912</pmid><doi>10.1007/s11010-007-9696-y</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0300-8177 |
ispartof | Molecular and cellular biochemistry, 2008-04, Vol.311 (1-2), p.73-80 |
issn | 0300-8177 1573-4919 |
language | eng |
recordid | cdi_proquest_miscellaneous_70419317 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Animals Antioxidants - administration & dosage Antioxidants - pharmacology Biochemistry Biomedical and Life Sciences Bladder Body weight Carbonyl compounds Cardiology Cardiovascular diseases Catalase - metabolism Choline O-Acetyltransferase - metabolism Citrate (si)-Synthase - metabolism Dietary Supplements Enzymes Free radicals Ischemia Life Sciences Male Medical Biochemistry Mitochondria - metabolism Muscle Contraction - drug effects Oncology Peanut oil Peroxidation Rabbits Reperfusion Injury - drug therapy Reperfusion Injury - prevention & control Superoxide Dismutase - metabolism Ubiquinone - administration & dosage Ubiquinone - analogs & derivatives Ubiquinone - pharmacology Ubiquinone - therapeutic use Urinary bladder Urinary Bladder - drug effects Urinary Bladder - metabolism Urinary Bladder - pathology Urology |
title | Coenzyme Q10 protect against ischemia/reperfusion induced biochemical and functional changes in rabbit urinary bladder |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T20%3A46%3A52IST&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=Coenzyme%20Q10%20protect%20against%20ischemia/reperfusion%20induced%20biochemical%20and%20functional%20changes%20in%20rabbit%20urinary%20bladder&rft.jtitle=Molecular%20and%20cellular%20biochemistry&rft.au=Juan,%20Yung-Shun&rft.date=2008-04-01&rft.volume=311&rft.issue=1-2&rft.spage=73&rft.epage=80&rft.pages=73-80&rft.issn=0300-8177&rft.eissn=1573-4919&rft_id=info:doi/10.1007/s11010-007-9696-y&rft_dat=%3Cproquest_cross%3E1897593771%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=197567367&rft_id=info:pmid/18165912&rfr_iscdi=true |