1 The effect of NMDA on the motility of the rat portal vein was studied in
an isolated preparation. NMDA induced a concentration-dependent (10(-7) - 1
0(-4) M) increase of the contraction frequency (maximum increase, 148 +/- 6
% of control at NMDA 10(-4) M).
2 The NMDA-induced excitatory response was prevented by the competitive NMD
A receptor antagonists (+/-)-2-Amino-5-phosphonopentanoic acid (AP-5, 5 x 1
0(-4) M) or (RS)-3-(2-carboxypiperazine-4-yl) propyl-1-phosphonic acid (CPP
, 10(-4) M).
3 Tetrodotoxin (TTX, 10(-6) M) or atropine (10(-4) M) abolished the NMDA-in
duced increase of the portal vein motility and reversed the excitatory effe
ct to a concentration-dependent inhibition (maximum inhibition, 52+/-8 and
29+/-7% of controls, respectively, at NMDA 10(-3) M).
4 Removal of the endothelium abolished the NMDA-induced inhibitory response
. Sodium nitroprusside concentration-dependently (10(-7) - 10(-5) M) inhibi
ted the portal vein motility, while L-N-G-nitro-arginine methyl ester (L-NA
ME, 10(-4) M) reversed the inhibitory effect of NMDA (in the presence of TT
X), restoring the portal vein spontaneous activity to control values.
5 These results show that NMDA modulates the portal vein motility in a biph
asic manner: via indirect activation, through prejunctional NMDA receptors
presumably located on intrinsic excitatory neuronal afferences, or via dire
ct inhibition, through endothelial NMDA receptors activating the nitric oxi
de pathway. Overall these findings support the hypothesis of the existence
of a peripheral glutamatergic innervation modulating the contractile activi
ty of the rat portal vein.