Key result
Combining MitoQ10 and low-dose losartan significantly reduced systolic blood pressure to 167.1 mmHg compared to 206.6 mmHg in untreated controls and attenuated left ventricular hypertrophy.
Why the study?
Does the combination of MitoQ10 and low-dose losartan attenuate hypertension and left ventricular hypertrophy in stroke-prone spontaneously hypertensive rats?
Does the combination of MitoQ10 and low-dose losartan attenuate hypertension and left ventricular hypertrophy in stroke-prone spontaneously hypertensive rats?
Absolute Event Rate: 167.1% vs 206.6%
p-value: p=<0.001
The combination of a mitochondria-targeted antioxidant (MitoQ10) and a low-dose ARB (losartan) provides additive benefits in reducing blood pressure and attenuating left ventricular hypertrophy in a hypertensive rat model.
Does not support clinical use in hypertension; hypothesis-generating for MitoQ10-ARB synergy in future translational studies.
OBJECTIVE: Mitochondria-derived reactive oxygen species (ROS) play important roles in the development of cardiovascular disease highlighting the need for novel targeted therapies. This study assessed the potential therapeutic benefit of combining the mitochondria-specific antioxidant, MitoQ10, with the low-dose angiotensin receptor blocker (ARB), losartan, on attenuation of hypertension and left ventricular hypertrophy. In parallel, we investigated the impact of MitoQ10 on cardiac hypertrophy in a neonatal cardiomyocyte cell line. METHODS AND RESULTS: Eight-week-old male stroke-prone spontaneously hypertensive rats (SHRSPs, n=8-11) were treated with low-dose losartan (2.5 mg/kg per day); MitoQ10 (500 μmol/l); a combination of MitoQ10 and losartan (M+L); or vehicle for 8 weeks. Systolic pressure and pulse pressure were significantly lower in M+L rats (167.1 ± 2.9 mmHg; 50.2 ± 2.05 mmHg) than in untreated SHRSP (206.6 ± 9 mmHg, P<0.001; 63.7 ± 2.7 mmHg, P=0.001) and demonstrated greater improvement than MitoQ10 or low-dose losartan alone, as measured by radiotelemetry. Left ventricular mass index was significantly reduced from 22.8 ± 0.74 to 20.1 ± 0.61 mg/mm in the combination group (P<0.05). Picrosirius red staining showed significantly reduced cardiac fibrosis in M+L rats (0.82 ± 0.22 A.U.) compared with control (5.94 ± 1.35 A.U., P<0.01). In H9c2 neonatal rat cardiomyocytes, MitoQ10 significantly inhibited angiotensin II mediated hypertrophy in a dose-dependent manner (500 nmol/l MitoQ10 153.7 ± 3.1 microns vs. angiotensin II 200.1 ± 3.6 microns, P<0.001). CONCLUSION: Combining MitoQ10 and low-dose losartan provides additive therapeutic benefit, significantly attenuating development of hypertension and reducing left ventricular hypertrophy. In addition, MitoQ10 mediates a direct antihypertrophic effect on rat cardiomyocytes in vitro. MitoQ10 has potential as a novel therapeutic intervention in conjunction with current antihypertensive drugs.
No takes yet. Share an insight, caveat, or question.
McLachlan et al. (2013) studied Hypertension and left ventricular hypertrophy (n=38). MitoQ10 and losartan combination vs. Untreated control (vehicle) was evaluated on Systolic blood pressure (p=<0.001). Combining MitoQ10 and low-dose losartan significantly reduced systolic blood pressure to 167.1 mmHg compared to 206.6 mmHg in untreated controls and attenuated left ventricular hypertrophy.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: