Djk. Lyster et al., REGULATION OF THE FREQUENCY OF MYOELECTRIC COMPLEXES IN THE ISOLATED MOUSE COLON, Journal of gastrointestinal motility, 5(3), 1993, pp. 143-151
Intracellular recordings were made from the circular muscle layer of t
he isolated mouse colon in the presence or absence of 2 muM nifedipine
at 37-degrees-C. Slow waves were recorded in about 35% of preparation
s and were up to 20 mV in amplitude when recorded from cells close to
the submucous plexus. Myoelectric complexes were also recorded and con
sisted of cholinergic (hyoscine sensitive) rapid oscillations (approxi
mately 2 Hz) superimposed on slow depolarizations (approximately 17 mV
) in membrane potential (resting membrane potential approximately 51 m
V) occurring every 80 to 410 seconds. In recordings made simultaneous
ly using 2 microelectrodes, aborally migrating complexes were observed
in all preparations whilst, in approximately half of these preparatio
ns, some complexes migrated orally or were stationary. The intervals b
etween complexes were increased by reducing the size of the preparatio
n and by the addition of 1 muM hyoscine. Pirenzipine (50 nM) also incr
eased the interval between complexes without affecting the cholinergic
rapid oscillations. The addition of 5-hydroxytryptamine (10 muM) init
iated a premature complex and decreased the intervals between complexe
s in the presence or absence of hyoscine. These studies have shown tha
t the intervals between myoelectric complexes recorded in vitro can be
increased or decreased by pharmacologically active substances, probab
ly by modifying neural control processes in the enteric nervous system
.