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Peer-reviewed veterinary case report

How pimobendan and SCH00013 affect heart function in dogs

By Hamabe, Lina et al.·Published in Journal of pharmacological sciences·2014·Department of Veterinary Surgery, Japan·View original on PubMed

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Original publication title: Comparative evaluation of calcium-sensitizing agents, pimobendan and SCH00013, on the myocardial function of canine pacing-induced model of heart failure.

Species:
dog

Plain-English summary

A group of 20 dogs with heart failure were treated with either pimobendan or a new drug called SCH00013 to see how well they improved. Over three weeks, the dogs receiving pimobendan showed better heart function without significant side effects, while those on the low dose of SCH00013 had some heart function improvement but also experienced thinning of the heart walls. The study suggests that pimobendan might be a more effective option for enhancing heart function in dogs with this condition.

People also search for: dog heart failure treatment · pimobendan for dogs · SCH00013 heart medication for dogs

Abstract

Pimobendan and SCH00013 are calcium sensitizers that possess dual action of calcium sensitization and phosphodiesterase-III inhibition. This study was conducted to comparatively evaluate the effect of these medications on the myocardial function of the canine pacing-induced heart failure model using echocardiography. Heart failure was induced in 20 dogs, to which pimobendan and two different doses of SCH00013 were administered orally to 15 dogs for 3 weeks, and the remaining 5 dogs served as the control. Cardiac evaluations were performed at baseline, week 1, week 2, and week 3. Significant thinning and dilation of the left ventricles, with systolic dysfunction, indicated by reduction of fractional shortening (FS) and strain values, were observed with a low dose of SCH00013. Whereas, although systolic dysfunction was observed with reduction of FS and radial strain, significant dilation and thinning of the left ventricles and reduction of circumferential strain were not observed with pimobendan. Pimobendan had a potent positive inotropic effect, with little effect on synchronicity, while low-dose SCH00013 had a weaker positive inotropic effect but was able to sustain synchronicity. Although, it failed to show significant statistical differences, the results of this study allow speculations that administration of pimobendan and SCH00013 may have differing effect on the myocardial function in the canine pacinginduced heart failure model.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/24599141/