, Volume 181, Issue 2, pp 392–400

Inhibition of calcium-independent phospholipase A2 activity in rat hippocampus impairs acquisition of short- and long-term memory

Original Investigation

DOI: 10.1007/s00213-005-2256-9

Cite this article as:
Schaeffer, E.L. & Gattaz, W.F. Psychopharmacology (2005) 181: 392. doi:10.1007/s00213-005-2256-9



Phospholipase A2 (PLA2) is a family of enzymes that cleave membrane phospholipids generating important lipid mediators in signal transduction. In rat hippocampal slices, both intracellular cytosolic Ca2+-dependent PLA2 (cPLA2) and Ca2+-independent PLA2 (iPLA2) have been implicated in mechanisms of synaptic plasticity underlying memory processes. In mice, intraperitoneal injections of a selective iPLA2 inhibitor impaired spatial learning. Accordingly, reduced cPLA2 and iPLA2 activities were found in postmortem hippocampus of patients with Alzheimer’s disease.


This study investigates the effects of injections of PLA2 inhibitors directly into rat hippocampus on the acquisition of short-term (STM) and long-term memory (LTM) of a one-trial step-down inhibitory avoidance (IA) task.


Wistar rats were bilaterally implanted with cannulae in the CA1 region of the dorsal hippocampus. After surgery, the rats received bilateral injections of a vehicle, or of dual cPLA2 and iPLA2 inhibitors (MAFP or PACOCF3), or a selective iPLA2 inhibitor (bromoenol lactone) before training in IA. The animals were tested 1.5 h (for STM) and 24 h (for LTM) after training.


Significant inhibition of iPLA2 activity in rat hippocampus impaired acquisition of STM and LTM. Memory impairment did not result from neuronal death after iPLA2 inhibition. Moreover, IA training per se increased significantly hippocampal PLA2 activity.


The present results suggest a functional effect of hippocampal PLA2 on the neurochemistry of memory acquisition and support the hypothesis that reduced PLA2 activity may contribute to memory impairment in Alzheimer’s disease.


Phospholipase A2 Inhibition Rats Hippocampus Memory Inhibitory avoidance Alzheimer’s disease 

Copyright information

© Springer-Verlag 2005

Authors and Affiliations

  1. 1.Laboratory of Neuroscience (LIM-27), Department and Institute of Psychiatry, Faculty of MedicineUniversity of São PauloSão PauloBrazil

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