Volume 16, Number 12,
Issue of June 15, 1996
pp. 4041-4045
Copyright ©1996 Society for Neuroscience
Systemic NMDA Receptor Antagonist CGP-40116 Does Not Impair
Memory Acquisition but Protects against NMDA Neurotoxicity in Rhesus
Monkeys
Received Nov. 28, 1995; revised March 5, 1996; accepted March 21, 1996.
Sergei A. Gutnikov and
David Gaffan
Department of Experimental Psychology, Oxford University, Oxford
OX1 3UD, United Kingdom
A widely accepted hypothesis is that long-term potentiation (LTP)
is a synaptic mechanism of memory. NMDA receptors are critically
involved in induction but not maintenance of LTP; therefore, their
blockade should impair memory acquisition but not retrieval. In
Experiment 1, we investigated the effect of a systemic NMDA receptor
antagonist, CGP-40116 [D-isomer of CGP-37849:
(E)-2-amino-4-methyl-5-phosphono-3-pentenoic acid (6 mg/kg,
i.m.) 60 min before the testing session] on memory acquisition and
retrieval by monkeys in the ``object-in-place'' visual memory task,
an analog of human episodic memory. Only a small increase in error rate
was produced (<3%), and this increase was observed in both retention
and acquisition tests. This deficit is substantially smaller than the
previously reported deficit after fornix transection in the same task,
and is not specific to memory acquisition. In Experiment 2, we
investigated the neuroprotective effect of CGP-40116. NMDA (68 nmol)
was injected into the right hippocampus, then CGP-40116 (6 mg/kg) was
given intramuscularly, and then NMDA was injected into the left
hippocampus. The area of cell loss in CA1 and CA3 fields was smaller in
both hemispheres compared with unprotected monkeys (without CGP-40116).
Thus, CGP-40116 provides both retrograde and anterograde protection
against NMDA neurotoxicity. These data (1) demonstrate that acquisition
of episodic memories remains almost intact when an NMDA receptor
antagonist is given in a dose sufficient to block NMDA receptors in the
hippocampus, and (2) indirectly oppose the hypothesis that NMDA
receptor-dependent LTP plays the key role in memory.
Key words:
CGP-37849;
episodic memory;
excitatory amino acids;
glutamate receptor pharmacology;
NMDA receptor pharmacology;
competitive NMDA receptor antagonists;
excitotoxicity;
neuroprotection;
ischemic brain damage;
LTP;
primates