Key result
Metoprolol (10 mg/kg/day) significantly attenuated cardiac pathological remodelling, lowered left ventricular mass, and reduced myocardial fibrosis in rats with experimental uremia.
Why the study?
Beta blockade prevents cardiac remodelling in heart failure, but whether it prevents cardiac pathological remodelling in chronic kidney disease remained untested.
Does metoprolol prevent cardiac pathological remodelling in Wistar rats with experimental uremia?
RCT
Randomly allocated
Does metoprolol prevent cardiac pathological remodelling in Wistar rats with experimental uremia?
In a rat model of uremia, metoprolol attenuated cardiac pathological remodeling and hypertrophic signaling, providing a scientific rationale for testing beta blockers in patients with chronic kidney disease.
Heart failure and chronic kidney disease (CKD) share several mediators of cardiac pathological remodelling. Akin to heart failure, this remodelling sets in motion a vicious cycle of progressive pathological hypertrophy and myocardial dysfunction in CKD. Several decades of heart failure research have shown that beta blockade is a powerful tool in preventing cardiac remodelling and breaking this vicious cycle. This phenomenon remains hitherto untested in CKD. Therefore, we set out to test the hypothesis that beta blockade prevents cardiac pathological remodelling in experimental uremia. Wistar rats had subtotal nephrectomy or sham surgery and were followed up for 10 weeks. The animals were randomly allocated to the beta blocker metoprolol (10 mg/kg/day) or vehicle. In vivo and in vitro cardiac assessments were performed. Cardiac tissue was extracted, and protein expression was quantified using immunoblotting. Histological analyses were performed to quantify myocardial fibrosis. Beta blockade attenuated cardiac pathological remodelling in nephrectomised animals. The echocardiographic left ventricular mass and the heart weight to tibial length ratio were significantly lower in nephrectomised animals treated with metoprolol. Furthermore, beta blockade attenuated myocardial fibrosis associated with subtotal nephrectomy. In addition, the Ca++- calmodulin-dependent kinase II (CAMKII) pathway was shown to be activated in uremia and attenuated by beta blockade, offering a potential mechanism of action. In conclusion, beta blockade attenuated hypertrophic signalling pathways and ameliorated cardiac pathological remodelling in experimental uremia. The study provides a strong scientific rationale for repurposing beta blockers, a tried and tested treatment in heart failure, for the benefit of patients with CKD.
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Chinnappa et al. (2023) conducted an RCT in Experimental uremia. Metoprolol vs. Vehicle was evaluated on Cardiac pathological remodelling (echocardiographic left ventricular mass, heart weight to tibial length ratio, and myocardial fibrosis). Metoprolol (10 mg/kg/day) significantly attenuated cardiac pathological remodelling, lowered left ventricular mass, and reduced myocardial fibrosis in rats with experimental uremia.
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