T. Takeuchi et al., NONADRENERGIC, NONCHOLINERGIC RELAXATION MEDIATED BY NITRIC-OXIDE WITH CONCOMITANT CHANGE IN CA2+ LEVEL IN RECTAL CIRCULAR MUSCLE OF RATS, European journal of pharmacology, 353(1), 1998, pp. 67-74
The mediators of nonadrenergic, noncholinergic (NANC) relaxation of th
e circular muscle of rat rectum were examined in vitro in the circular
muscle of rat rectum, N-G-nitro-L-arginine (L-NOARG) at 10 mu M did n
ot affect electrical field stimulation-induced relaxation but at 100 m
u M it inhibited electrical field stimulation-induced relaxation by ab
out 75% and 1-mM L-arginine reversed the inhibition. Exogenous nitric
oxide (NO) (1-10 mu M) concentration dependently relaxed the circular
muscle. Electrical field stimulation increased the cyclic GMP content
of the circular muscle to about twice its resting level. L-NOARG, even
at 10 mu M, completely inhibited the electrical field stimulation-ind
uced elevation of cyclic GMP content. However, L-arginine at 1 mM did
not reverse the inhibition in cyclic GMP content. Inhibitory junction
potentials (i.j.ps) induced by electrical field stimulation in the cir
cular muscle cells were not affected by L-NOARG, 100 mu M Apamin (less
than or equal to 1 mu M) did not affect the electrical field stimulat
ion-induced relaxation, but almost completely inhibited electrical fie
ld stimulation-induced i.j.ps. NO (0.3-10 mu M) induced relaxation of
the circular muscle with a concomitant decrease in intracellular Ca2level ([Ca2+](i)). Abundant immunoreactivity of NO synthase was found
in the circular muscle layer, in addition to myenteric and submucosal
plexus. The results suggest that NO induces NANC relaxation with a con
comitant change in [Ca2+](i) in the circular muscle of rat rectum. How
ever, the involvement of changes in cyclic GMP level and in membrane p
otentials in the mechanism was not shown in the present experimental c
onditions. (C) 1998 Elsevier Science B.V. All rights reserved.