A new pyrrolidinone derivative, valproyl-2-pyrrolidinone (VP), was synthesized, followed by evaluation as a cognitive drug. VP gave rise to a significant protective effect against cerebral anoxia together with a potent prolongation of latency time for the reversal of scopolamine induced transient disruption of the memory of a passive avoidance response in rats. The quantitative experiment using HPLC demonstrated a significant reduction of hippocampal aspartate (Asp) and glutamate (Glu) following the intraperitoneal administration of VP at a dose of 300 mg/kg. © 1990, The Pharmaceutical Society of Japan. All rights reserved.
CITATION STYLE
Yamamoto, J., Matsuyama, K., & Ichikawa, M. (1990). Synthesis of Valproyl-2-Pyrrolidinone and its Evaluation as a Cognitive Drug with the Ability to Modulate Acidic Amino Acids in the Brain. Journal of Pharmacobio-Dynamics, 13(1), 70–75. https://doi.org/10.1248/bpb1978.13.70
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