G. Dobreva et al., POSTSYNAPTIC AND PRESYNAPTIC EFFECTS OF NOREPINEPHRINE IN GUINEA-PIG COLONIC SUBMUCOUS PLEXUS, Neurogastroenterology and motility, 10(2), 1998, pp. 123-130
Intracellular recording techniques were used to investigate the effect
s of norepinephrine on submucous neurones in the guinea-pig distal col
on. In 81% of the neurones, pressure microejection of norepinephrine p
roduced a membrane hyperpolarization associated with a decrease in exc
itability and input resistance. Microejection of clonidine (1 mu M) mi
micked the norepinephrine-induced hyperpolarization, whereas both phen
tolamine (1 mu M) and yohimbine (1 mu M) reversibly suppressed it. Sup
erfusion of norepinephrine (1 nM - 10 mu M) hyperpolarized the cells i
n a concentration-dependent manner. Norepinephrine and clonidine (1 nM
- 10 mu M) caused a concentration-dependent presynaptic inhibition of
stimulus-evoked cholinergic fast excitatory postsynaptic potential. S
low inhibitory postsynaptic potentials (sISPSs) were induced by focal
electrical stimulation of the interganglionic fibre tracts in 43% of t
he neurones tested. Superfusion of both phentolamine (1 mu M) and yohi
mbine (1 mu M) reduced the sIPSPs while prazosin (1 mu M) had no signi
ficant effect. We concluded that norepinephrine acted post- and presyn
aptically via alpha(2)-adrenoreceptors to have an inhibitory effect on
the guinea-pig colonic submucous. In addition, our study strongly sup
ported the role of norepinephrine as a mediator of the sIPSPs. As a re
sult, norepinephrine would primarily suppress information transfer wit
hin the neuronal circuits in guinea-pig colonic submucosal plexus.