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Inhibition of fatty acid amide hydrolase modulates anxiety-like behavior in PCP-treated rats.

Alexandre Seillier, Andrea Giuffrida

Pharmacology, Biochemistry, and Behavior June 2011 DOI: 10.1016/j.pbb.2011.03.010 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical animal study Peer reviewed
Population Rats treated with saline or sub-chronic PCP
Interventions PCP URB597 AM251
Measures Elevated-Plus-Maze
Topics Anxiety
Key points Sub-chronic PCP produced a CB(1)-dependent decrease in anxiety-like behavior in the Elevated-Plus-Maze, which URB597 reversed in a CB(1)-independent manner since AM251 did not block the reversal. The authors suggest PCP-treated rats have altered endocannabinoid transmission and that anxiety does not contribute to PCP-induced social withdrawal.

Abstract

Sub-chronic administration of PCP produces a social interaction deficit that is reversed by URB597, an inhibitor of the catabolic enzyme of the endocannabinoid anandamide. Since increased anxiety may contribute to social withdrawal and URB597 has been shown to have an anxiolytic action, we studied whether this drug affected saline- and PCP-treated rats' performance in the Elevated-Plus-Maze task, which has been used to assess anxiety-like effects. Sub-chronic PCP produced a CB(1)-dependent decrease in anxiety-like behavior that was reversed by URB597 in a CB(1)-independent fashion, as it was not blocked by the CB(1) antagonist AM251. These findings suggest that PCP-treated rats have altered endocannabinoid transmission and that anxiety does not contribute to the PCP-induced social withdrawal.

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