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Simvastatin treatment increases nitrite levels in obese women: Modulation by T−786C polymorphism of eNOS
•Obese women without comorbidities were treated by 45days with simvastatin.•Plasma MDA-TBARS levels diminished significantly after statin treatment.•Plasma nitrite levels increased significantly after simvastatin treatment.•Nitrite and MDA-TBARS were negatively correlated before and after treatment....
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Published in: | Nitric oxide 2013-09, Vol.33, p.83-87 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Obese women without comorbidities were treated by 45days with simvastatin.•Plasma MDA-TBARS levels diminished significantly after statin treatment.•Plasma nitrite levels increased significantly after simvastatin treatment.•Nitrite and MDA-TBARS were negatively correlated before and after treatment.•C-allele carrier women presented a higher raise in nitrite than T-allele carriers.
Evidence indicates an impairment of nitric oxide (NO) in obesity. Statins present pleiotropic effects independently of cholesterol-lowering, including increasing of eNOS expression and antioxidant effects. We evaluated the effects of simvastatin treatment at 45days on circulating nitrite (NO marker) and TBARS-MDA levels in obese women without comorbidities (hypertension, diabetes and dyslipidemia). Moreover, we verified whether obese women carrying the C variant of T−786C polymorphism located in eNOS may have increased levels of nitrite after treatment compared to TT genotype.
After simvastatin treatment, while the plasma nitrite levels increased 42% (P=0.0008), the TBARS-MDA levels reduced 58% (P=0.0069). We observed increased levels of nitrite in both groups of genotypes (TT vs. TC+CC); however, rise in C-allele carriers was 60% comparing with 44% in TT.
Our results demonstrated a restoration of nitrite levels in obese women treated with simvastatin, which is modulated by T−786C polymorphism. |
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ISSN: | 1089-8603 1089-8611 |
DOI: | 10.1016/j.niox.2013.07.005 |