The effects of quinolinic acid (QUIN) and quisqualate (QA) on the secr
etion of GnRH from MBH and LH and FSH from AP of 50 day old male rats
have been evaluated by means of an ''in vitro'' perifusion technique.
QUIN (100 mu M) is able to increase GnRH secretion with an action medi
ated by an NMDA receptor type, as shown by the inhibitory effect exert
ed by both a competitive (AP-5) and a non-competitive (MK-801) specifi
c antagonist. QA ''per se'' at the concentrations tested(1-100 mu M) d
oes not modify GnRH and gonadotropin secretion, but in the presence of
a specific KA/QA receptor antagonist (DNQX) exerts a stimulatory effe
ct at both levels. This observation might indicate that of the two QA
receptor subtypes (ionotropic and metabotropic), this agonist binds to
the metabotropic one with very low affinity: thus it is likely that a
higher dose is required in order to have any effect on gonadotropin s
ecretion. However, in the presence of DNQX, which binds to the ionotro
pic receptor, all the available QA can bind to the metabotropic one an
d can exert its action at MBH AP levels.