Short-term treatment with cholestyramine increases long-acting anticoagulant rodenticide clearance from rabbits without affecting plasma vitamin K1 levels or blood coagulation

Author:

Muchiri Ruth N1,Rocha Jackie2,Tandon Ankit2,Chen Yongmei Luo3,Alemani Rebecca2,Ahmad Intakhar2ORCID,McDonald Zachary2,Lindeblad Matthew3,Rubinstein Israel45,van Breemen Richard B1ORCID,Feinstein Douglas L15ORCID

Affiliation:

1. Department of Pharmaceutical Sciences, Linus Pauling Institute, Oregon State University , Corvallis, Oregon 97331, USA

2. Department of Anesthesiology, University of Illinois , Chicago, Illinois 60612, USA

3. Department of Pharmacology, University of Illinois , Chicago, Illinois 60612, USA

4. Department of Medicine, University of Illinois , Chicago, Illinois 60612, USA

5. Research & Development Service, Jesse Brown VA Medical Center , Chicago, Illinois 60612, USA

Abstract

Abstract Administration of high-dose vitamin K1 (VK1) overcomes coagulopathy and bleeding elicited by acute poisoning with long-acting anticoagulant rodenticides (LAARs). However, long-term (months) treatment is required due to long LAAR biological half-lives that may lead to poor compliance and recurrent coagulopathy. The half-lives of LAARs are extended by slow metabolism, and similar to warfarin, are thought to undergo enterohepatic recirculation. We now show that treatment with the bile acid sequestrant cholestyramine (CSA) administered concomitantly with VK1 decreases plasma LAAR levels and increases LAAR fecal excretion. Daily CSA treatment for 14 days did not reduce plasma VK1 levels, or increase prothrombin time. Collectively, these data show that CSA accelerates LAAR clearance from rabbits without adverse effects on VK1 anticoagulation, and could provide an additional therapeutic option for treatment of LAAR poisoning.

Funder

NIH

Department of Veterans Affairs

Publisher

Oxford University Press (OUP)

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