In vitro effects of nonsteroidal anti-inflammatory agents and prostaglandins I-2, E-2, and F-2 alpha on contractility of taenia of the large colon ofhorses
L. Van Hoogmoed et al., In vitro effects of nonsteroidal anti-inflammatory agents and prostaglandins I-2, E-2, and F-2 alpha on contractility of taenia of the large colon ofhorses, AM J VET RE, 60(8), 1999, pp. 1004-1009
Objectives-To determine the in vitro effect of various prostaglandins (PG)
and nonsteroidal anti-inflammatory drugs (NSAID) on contractile activity of
the large-colon taenia of horses.
Animals-14 healthy horses.
Procedure-The taenia was collected from the ventral colon, cut into strips
(2 x 10 mm), and mounted in a tissue bath system (20-ml capacity) that cont
ained oxygenated Krebs buffer solution warmed to 37.5 +/- 0.5 C. After equi
libration, incremental doses of PGE(2), PGF(2 alpha), PGl(2), flunixin megl
umine, carprofen, ketoprofen, and phenylbutazone were added to the baths, a
nd contractile activity was recorded. Magnitude of the response was calcula
ted by comparing contractile activity before and after administration of th
e PG or NSAID to the tissue baths.
Results-PGE(2) and PGF(2 alpha) caused a significant increase in contractil
e activity, whereas PGl(2) induced an inhibitory response. Activity of NSAI
D on contraction was predominantly inhibitory. At low concentrations, ketop
rofen induced an excitatory effect, which then became inhibitory at high co
ncentrations. Compared with the other NSAID, carprofen significantly reduce
d contractile activity at lower concentrations.
Conclusions-PGE(2) and PGF(2 alpha) appear to enhance contractility of larg
e-colon taenia of horses, whereas PGl(2) was inhibitory in the in vitro mod
el. Administration of NSAID also inhibited contractility, with carprofen ha
ving the most potent effect.
Clinical Relevance-Administration of NSAID in combination with liberation o
f endogenous PG may predispose horses to development of intestinal stasis a
nd subsequent impaction.