1The Department of Clinical Sciences, College of Veterinary Medicine, Auburn University, AL, 36849, USA
Department of Anatomy, Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, AL, 36849, USA
*email: jack_kottwitz@hotmail.com
Online published on 28 January, 2019.
This study determined concentrations of thromboxane B2 (T×B2) and prostaglandin E2 (PGE2) and metabolites (PGEM) in alpacas utilising commercially available assays. Twenty healthy adult alpaca (11 castrated males and 9 females) participated in this study. Four ELISAs were utilised: two to quantitate T×B2 in serum as an indicator of in vitro cyclooxygenase-1 (COX-1) activity, one quantitated PGE2 and a fourth assay quantitated prostaglandin E2 and metabolites (PGEM) in plasma as indicators of in vitro cyclooxygenase-2 (COX-2) isoenzyme activity after leukocyte exposure to lipopolysaccharide. Known standards were utilised for confirmation of assay results. Alpaca serum T×B2 concentrations were substantially lower than reported in other species and those quantitated in four clinically normal horses using identical methods (alpaca=616±294, 95% CI [47, 753] pg/ml; horse=6087± 855, 95% CI [3964, 8210] pg/ml). Alpaca plasma mean PGEM concentration was 50±28, 95% CI [21, 111] pg/ml. Whole blood determination of T×B2 and PGE2 have been utilised in multiple species to evaluate COX isoenzymes for evaluating nonsteroidal anti-inflammatory drug (NSAID) COX inhibition. This study demonstrates that T×B2 as measured using these methods may not be an acceptable method for determination of COX-1 response to NSAIDs in alpaca. The low whole blood T×B2 levels identified by these assays may also indicate an intrinsic sensitivity to these drugs that warrants further investigation.
Alpaca, COX-1, COX-2, cyclooxygenase, prostaglandin E2, thromboxane