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Effects of furosemide and the combination of furosemide and the labeled dosage of pimobendan on the circulating renin-angiotensin-aldosterone system in clinically normal dogs.

Authors :
Lantis, Andrea C.
Atkins, Clarke E.
DeFrancesco, Teresa C.
Keene, Bruce W.
Werre, Stephen R.
Source :
American Journal of Veterinary Research. Dec2011, Vol. 72 Issue 12, p1646-1651. 6p.
Publication Year :
2011

Abstract

Objective--To evaluate the effect of administration of the labeled dosage of pimobendan to dogs with furosemide-induced activation of the renin-angiotensin-aldosterone system (RAAS). Animals--12 healthy hound-type dogs. Procedures--Dogs were allocated into 2 groups (6 dogs/group). One group received furosemide (2 mg/kg, PO, q 12 h) for 10 days (days 1 to 10). The second group received a combination of furosemide (2 mg/kg, PO, q 12 h) and pimobendan (0.25 mg/kg, PO, q 12 h) for 10 days (days 1 to 10).To determine the effect of the medications on the RAAS, 2 urine samples/d were obtained for determination of the urinary aldosterone-to-creatinine ratio (A:C) on days 0 (baseline), 5, and 10. Results--Mean ± SD urinary A:C increased significantly after administration of furosemide (baseline, 0.37 ± 0.14 pg/g; day 5, 0.89 ± 0.23 µg/g) or the combination of furosemide and pimobendan (baseline, 0.36 ± 0.22 pg/g; day 5, 0.88 ± 0.55 pg/g). Mean urinary A:C on day 10 was 0.95 ± 0.63 pg/g for furosemide alone and 0.85 ± 0.21 pg/g for the combination of furosemide and pimobendan. Conclusions and Clinical Relevance--Furosemide-induced RAAS activation appeared to plateau by day 5. Administration of pimobendan at a standard dosage did not enhance or suppress furosemide-induced RAAS activation. These results in clinically normal dogs suggested that furosemide, administered with or without pimobendan, should be accompanied by RAAS-suppressive treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029645
Volume :
72
Issue :
12
Database :
Academic Search Index
Journal :
American Journal of Veterinary Research
Publication Type :
Academic Journal
Accession number :
67620199
Full Text :
https://doi.org/10.2460/ajvr.72.12.1646