Simvastatin decreased coenzyme Q in the left ventricle and skeletal muscle but not in the brain and liver in L-NAME-induced hypertension
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
    PubMed
          
           17824807
           
          
          
    DOI
          
           10.33549/physiolres.931397
           
          
          
      PII:  1397
  
    Knihovny.cz E-resources
    
  
              
      
- MeSH
- Time Factors MeSH
- Down-Regulation MeSH
- Hypertension chemically induced drug therapy metabolism MeSH
- Liver drug effects metabolism MeSH
- Coenzymes metabolism MeSH
- Muscle, Skeletal drug effects metabolism MeSH
- Rats MeSH
- Disease Models, Animal MeSH
- Brain drug effects metabolism MeSH
- NG-Nitroarginine Methyl Ester MeSH
- Nitric Oxide metabolism MeSH
- Rats, Wistar MeSH
- Simvastatin pharmacology therapeutic use MeSH
- Heart Ventricles drug effects metabolism MeSH
- Hydroxymethylglutaryl-CoA Reductase Inhibitors pharmacology therapeutic use MeSH
- Ubiquinone analogs & derivatives metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- coenzyme Q10 MeSH Browser
- Coenzymes MeSH
- NG-Nitroarginine Methyl Ester MeSH
- Nitric Oxide MeSH
- Simvastatin MeSH
- Hydroxymethylglutaryl-CoA Reductase Inhibitors MeSH
- Ubiquinone MeSH
- ubiquinone 9 MeSH Browser
Inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase (statins) have been proven to reduce effectively cholesterol level and morbidity and mortality in patients with coronary heart disease and/or dyslipoproteinemia. Statins inhibit synthesis of mevalonate, a precursor of both cholesterol and coenzyme Q (CoQ). Inhibited biosynthesis of CoQ may be involved in some undesirable actions of statins. We investigated the effect of simvastatin on tissue CoQ concentrations in the rat model of NO-deficient hypertension induced by chronic L-NAME administration. Male Wistar rats were treated daily for 6 weeks with L-NAME (40 mg/kg) or with simvastatin (10 mg/kg), another group received simultaneously L-NAME and simvastatin in the same doses. Coenzyme Q(9) and Q(10) concentrations were analyzed by high performance liquid chromatography. L-NAME and simvastatin alone had no effect on CoQ concentrations. However, simultaneous application of L-NAME and simvastatin significantly decreased concentrations of both CoQ homologues in the left ventricle and slightly decreased CoQ(9) concentration in the skeletal muscle. No effect was observed on CoQ level in the liver and brain. We conclude that the administration of simvastatin under the condition of NO-deficiency reduced the level of CoQ in the heart and skeletal muscle what may participate in adverse effect of statins under certain clinical conditions.
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