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...

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Veröffentlicht in:Molecular and cellular biochemistry 2008-04, Vol.311 (1-2), p.73-80
Hauptverfasser: Juan, Yung-Shun, Hydery, Tasmina, Mannikarottu, Anita, Kogan, Barry, Schuler, Catherine, Leggett, Robert E, Lin, Wei-Yu, Huang, Chun-Hsiung, Levin, Robert M
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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
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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 &amp; 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 &amp; control ; Superoxide Dismutase - metabolism ; Ubiquinone - administration &amp; dosage ; Ubiquinone - analogs &amp; 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. 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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>
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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
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