Journal of Neuroscience, Vol 14, 1358-1365, Copyright © 1994 by Society for Neuroscience
NMDA receptor antagonists decrease GABA outflow from the septum and increase acetylcholine outflow from the hippocampus: a microdialysis study
MG Giovannini, D Mutolo, L Bianchi, A Michelassi and G Pepeu
Department of Preclinical and Clinical Pharmacology, University of Florence, Italy.
The modulation of the septohippocampal cholinergic pathway by glutamatergic
or GABAergic inputs was studied by monitoring the outflow of ACh collected
via a transversal microdialysis probe implanted into the hippocampus and
other brain areas of freely moving rats. In one set of experiments a
transversal microdialysis membrane was inserted in the dorsal hippocampus,
drugs were administered intracerebroventricularly through a cannula
implanted in the lateral ventricle, and ACh outflow in the dialysate was
measured by an HPLC method with an electrochemical detector. The dialysis
membrane was usually perfused with Ringer's solution containing 7 microM
physostigmine sulfate. Intracerebroventricular injections of the NMDA
antagonists 3-((RS)-2- carboxypiperazin-4-yl)-propyl-1-phosphonic acid
(CPP; 1-50 nmol), MK801 (0.5-20 nmol), and
D(-)-2-amino-7-phosphonoheptanoic acid (100 nmol) brought about an increase
in hippocampal ACh outflow while the non-NMDA antagonist
6,7-dinitroquinoxaline-2,3-dione (0.25-20 nmol) was without effect. The
increase in ACh outflow following CPP administration was dose dependent and
reached a maximum of about 500%. It was abolished by TTX (0.5 microM)
delivered locally to the hippocampus via the dialysis membrane and
prevented by intracerebroventricular injection of the GABA agonist muscimol
(5 nmol). In a second set of experiments, one microdialysis membrane was
inserted in the dorsal hippocampus to detect ACh outflow and another in the
septum to administer drugs locally and at the same time detect septal GABA
outflow. The septal dialysis membrane was perfused with Ringer's solution
without physostigmine, and GABA levels in the dialysate were measured by an
HPLC method with a fluorescence detector. CPP (100 microM) perfused through
the septum resulted in a decrease in septal GABA outflow and a concomitant
increase in hippocampal ACh outflow. Muscimol (100 microM) administration
into the septum abolished the effect of CPP on hippocampal ACh outflow but
did not affect septal GABA outflow. These results demonstrate that in the
septum NMDA receptors tonically activate GABAergic neurons which in turn
inhibit the cholinergic septohippocampal neurons.