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Peer-reviewed veterinary case report

How tadalafil affects lung blood pressure in dogs with pulmonary

By Hori, Yasutomo et al.·Published in Veterinary journal (London, England : 1997)·2014·School of Veterinary Medicine, Japan·View original on PubMed

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Original publication title: Effect of the phosphodiesterase type 5 inhibitor tadalafil on pulmonary hemodynamics in a canine model of pulmonary hypertension.

Species:
dog

Plain-English summary

A group of healthy Beagle dogs was tested to see how well tadalafil, a medication used for pulmonary arterial hypertension (PAH), could lower high blood pressure in the lungs. After inducing PAH in these dogs, researchers found that both intravenous and oral doses of tadalafil significantly reduced the elevated pulmonary arterial pressure. The oral dose of 4.0 mg/kg was particularly effective, showing a decrease in pressure that lasted for up to six hours. This study suggests that tadalafil could be a promising new treatment option for dogs suffering from PAH.

People also search for: dog pulmonary hypertension treatment · Beagle high blood pressure in lungs · tadalafil for dogs with PAH

Abstract

Phosphodiesterase type 5 (PDE5) inhibitors are used for treating pulmonary arterial hypertension (PAH) in dogs. The long-acting PDE5 inhibitor tadalafil was recently approved for treatment of PAH in humans. Basic information related to the pharmacological and hemodynamic effects of tadalafil in dogs is scarce. In this study, the hemodynamic effects of tadalafil after intravenous (IV) and oral administration were investigated in a healthy vasoconstrictive PAH Beagle dog model induced by U46619, a thromboxane A2 mimetic. Six healthy Beagle dogs were anesthetized with propofol and maintained with isoflurane. Fluid-filled catheters were placed into the descending aorta to measure systemic arterial pressure and in the pulmonary artery to measure pulmonary arterial pressure (PAP). U46619 was infused via the cephalic vein to induce PAH. IV infusion of U46619 significantly elevated PAP from baseline in a dose-dependent manner. U46619-elevated PAP and pulmonary vascular resistance was significantly attenuated by the simultaneous infusion of tadalafil at 100 and 200 µg/kg/h. Likewise, oral administration of tadalafil at 1.0, 2.0, and 4.0 mg/kg significantly attenuated U46619-elevated PAP in a dose-dependent manner. U46619-elevated systolic and mean PAP decreased significantly 1 h after oral tadalafil administration at 4.0 mg/kg, and this effect was maintained for 6 h. In conclusion, tadalafil had a pharmacological effect in dogs and IV infusion of tadalafil induced pulmonary arterial relaxation, while oral administration of tadalafil decreased PAP. These results suggest that tadalafil may offer a new therapeutic option for treating dogs with PAH.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/25178687/