In vitro effects of erythromycin, lidocaine, and metoclopramide on smooth muscle from the pyloric antrum, proximal portion of the duodenum, and middle portion of the jejunum of horses
Je. Nieto et al., In vitro effects of erythromycin, lidocaine, and metoclopramide on smooth muscle from the pyloric antrum, proximal portion of the duodenum, and middle portion of the jejunum of horses, AM J VET RE, 61(4), 2000, pp. 413-419
Objective-To evaluate effects of erythromycin, lidocaine, and metoclopramid
e on smooth muscle of the pyloric antrum (PA), proximal portion of the duod
enum (PD), and middle portion of the jejunum (MJ) of horses.
Sample Population-Strips of smooth muscle from 7 horses.
Procedure-Isolated muscle strips were suspended in a bath and attached to i
sometric force transducers. Once stable spontaneous contractions were obser
ved, agents were added. Isometric stress responses were compared with the a
mplitude of spontaneous contractions.
Results-A single dose of erythromycin to the PA increased contractile ampli
tude (CA) for the longitudinal smooth muscle (mean +/- SEM, 76 +/- 16 g/cm(
2)) but decreased CA for circular smooth muscle (-79 +/- 23 g/cm(2)). The i
nhibitory effect was decreased by tetrodotoxin, N-G-nitro-L-arginine methyl
ester, and a vasoactive intestinal peptide antagonist. Erythromycin increa
sed CA for the MJ, which was maximal at 10(-4)M (171 +/- 36 g/cm(2)). Lidoc
aine increased CA for the PD, which was maximal at 10(-4)M (60 +/- 5 g/cm(2
)). Metoclopramide increased the CA, which was maximal at 10(-4)M for the P
A (75 +/- 26 g/cm(2)), PD (279 +/- 33 g/cm(2)), and MJ (456 +/- 59 g/cm(2))
.
Conclusions-Regional differences in responses to erythromycin, lidocaine, a
nd metoclopramide were evident in the gastrointestinal tract of horses. Met
oclopramide increased CA in all tissues used, whereas erythromycin inhibite
d CA in circular smooth muscle but stimulated CA in longitudinal smooth mus
cle from the PA. Inhibition is caused by stimulation of inhibitory nerves a
nd is mediated, in part, by nitric oxide and vasoactive intestinal peptide.