Cwr. Shuttleworth et al., Evidence that nitric oxide acts as an inhibitory neurotransmitter supplying taenia from the guinea-pig caecum, BR J PHARM, 127(6), 1999, pp. 1495-1501
1 Nitric oxide synthase-containing nerve fibres are abundant within taenia
of the guinea-pig caecum, but there is little previous evidence supporting
a direct role for nitric oxide (NO) in responses to enteric inhibitory nerv
e stimulation. In this study we have attempted to identify an NO-dependent
component of inhibitory transmission in isolated taenia coli.
2 Isometric tension was recorded in the presence of atropine and guanethidi
ne (both 1 mu M). Tone was raised with histamine (1 mu M), and intrinsic in
hibitory neurons stimulated using either a nicotinic agonist (1,1-dimethyl-
4-phenylpiperazinium iodide; DMPP) or electrical held stimulation (EFS).
3 DMPP (1-100 mu M) produced concentration-dependent biphasic relaxations,
comprising an initial peak relaxation followed by a sustained relaxation. R
esponses to DMPP were antagonized by tetrodotoxin (1 mu M) or apamin (0.3 m
u M) and abolished by hexamethonium (300 mu M). L-nitro-arginine (L-NOARG;
100 mu M) and oxyhaemoglobin (2%) both significantly reduced sustained rela
xations produced by DMPP.
4 EFS (5 Hz, 30s) also produced biphasic relaxations. Both L-NOARG and an i
nhibitor of soluble guanylate cyclase (ODQ, 1-10 mu M) reduced the sustaine
d component of EFS responses.
5 Two NO donors, sodium nitroprusside (SNP) and diethylenetriamine-nitric o
xide adduct (DENO), produced concentration-dependent relaxations. Responses
to SNP and DENO were antagonized by ODQ (l mu M) and by apamin (0.3 mu M).
6 These results suggest that NO contributes directly to a component of inhi
bitory transmission in guinea-pig taenia coli. The actions of NO appear to
be mediated via cyclic GMP synthesis, and may involve activation of small c
onductance calcium activated K+ channels. A role for NO is most evident dur
ing sustained relaxations evoked by longer stimulus trains or chemical stim
ulation of intrinsic neurons.