Serum butyrylcholinesterase and paraoxonase 1 in a canine model of endotoxemia: Effects of choline administration


Tvarijonaviciute A., KOCATÜRK M., CANSEV M., Tecles F., Ceron J. J., YILMAZ Z.

RESEARCH IN VETERINARY SCIENCE, vol.93, no.2, pp.668-674, 2012 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 93 Issue: 2
  • Publication Date: 2012
  • Doi Number: 10.1016/j.rvsc.2011.09.010
  • Journal Name: RESEARCH IN VETERINARY SCIENCE
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.668-674
  • Keywords: BChE, Choline, Dog, Lipopolysaccharide, PON1, S1RS, CDP-CHOLINE, WHOLE-BLOOD, INVOLVEMENT, METABOLITES, INSULIN, SEPSIS, INHIBITION, RECEPTORS, DECREASE, RATS
  • Bursa Uludag University Affiliated: Yes

Abstract

Butyrylcholinesterase (BChE) and paraoxonase 1 (PON1) are two serum enzymes synthesized by the liver that are related with inflammation. The main objectives of this study were to determine changes in serum BChE and PON1 by using a canine model of endotoxemia, and to evaluate whether choline alters BChE and PON1 activities during inflammation. For this purpose, a total of 20 mongrel dogs were divided into four groups: control, choline (C), lipopolysaccharide (LPS), and LPS + C. Dogs in the control group were injected with 0.9% NaCl (0.2 ml/kg, i.v.). Dogs in C and LPS + C groups received choline chloride (20 mg/kg, i.v., three times with 4 h intervals). Endotoxin was injected (0.02 mg/kg, i.v., once) to the dogs of LPS and LPS + C groups. Statistically significant decreases in BChE and PON1 activities in LPS group were detected 24 and 48 h post injection, respectively. No statistically significant changes in BChE and PON1 activities at different times were detected in control, C, or LPS + C groups. In conclusion, the data obtained in present study revealed a decrease in serum BChE and PON1 activities in dogs during experimentally induced endotoxemia and that choline administration attenuates these changes. (C) 2011 Elsevier Ltd. All rights reserved.