Key result
Ivabradine significantly lowered heart rate (174 vs 374 beats/min; p<0.001) and superior mesentery arterial flow in portal hypertensive rats compared to vehicle.
Why the study?
Does ivabradine improve hemodynamics in male Sprague-Dawley rats with portal hypertension?
RCT
randomly allocated
Does ivabradine improve hemodynamics in male Sprague-Dawley rats with portal hypertension?
Absolute Event Rate: 174% vs 374%
p-value: p=<0.001
In a rat model of portal hypertension, ivabradine reduced heart rate and splanchnic hyperemia without significantly affecting portal pressure.
Reduces HR and splanchnic flow without lowering portal pressure in rats; hypothesis-generating and leaves open clinical translation.
BACKGROUND: Ivabradine is a funny current inhibitor which is administered to patients with congestive heart failure to reduce their heart rate (HR) and attenuate oxidative stress. Chronic liver diseases are characterized by portal hypertension and hyperdynamic circulation with tachycardia. The present study aimed to investigate the effect of ivabradine on portal hypertension. METHODS: Male Sprague-Dawley rats received partial portal vein ligation (PVL) to induce portal hypertension. The PVL rats were randomly allocated to receive either vehicle or ivabradine treatment for 10 days. Then the hemodynamic data were collected. The levels of oxidative stress markers and the mRNA expression of nitric oxide synthase (NOS) were measured in the collateral vessel, the superior mesentery artery and the liver. In addition, the collateral vascular responsiveness to arginine vasopressin (AVP) was examined in the ivabradine-treated and vehicle-treated PVL rats. RESULTS: Treatment with ivabradine significantly lowered the HR (174 ± 20 vs. 374 ± 9 beats/min; p < 0.001) and the superior mesentery arterial flow (SMAf) (6.6 ± 0.3 vs. 9.1 ± 0.7 mL/min/100 g BW; p = 0.005) of the PVL rats compared with the control group. The mean arterial pressure, cardiac index, systemic vascular resistance, portal pressure and serum levels of oxidative stress markers were not significantly affected by ivabradine treatment. In addition, the NOS expression and collateral vascular responsiveness to AVP were not significantly influenced by ivabradine treatment, either. CONCLUSION: Ivabradine reduced the HR and SMAf in PVL rats, which alleviated the hyperdynamic circulatory state and splanchnic hyperemia of portal hypertension. However, whether these effects would help alleviate portal hypertension-related complications requires further clinical investigations.
No takes yet. Share an insight, caveat, or question.
Chang et al. (2018) conducted an RCT in portal hypertension. Ivabradine vs. vehicle was evaluated on Heart rate (HR) (p=<0.001). Ivabradine significantly lowered heart rate (174 vs 374 beats/min; p<0.001) and superior mesentery arterial flow in portal hypertensive rats compared to vehicle.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: