A selective cannabinoid CB2 agonist attenuates damage and improves memory retention following stroke in mice.

AIMS:

We have recently demonstrated that treatment with a cannabinoid CB2 agonist was protective in a mouse middle cerebral artery occlusion model of cerebral ischemia/reperfusion injury. The present study aimed to determine whether these protective effects of CB2 agonism would extend to a mouse photoinjury model of permanent ischemia and determine associated alterations in cognition and infarct size.

MAIN METHODS:

Mice received three injections of the CB2 selective agonist O-1966 or vehicle 1 h prior to and 2 and 5 days following induction of stroke. Infarct size was assessed at 1, 3, or 7 days post injury and learning and memory effects of injury and O-1966 treatment were assessed on days 6 and 7 using a novel object recognition task and an operant acquisition and retention procedure.

KEY FINDINGS:

O-1966 treated mice had significantly smaller infarct volumes compared with vehicle treated mice. Photoinjury was also associated with a significant memory impairment on day 7 post-injury, and this deficit was reversed with O-1966 treatment. Surprisingly, sham-operated mice receiving O-1966 treatment showed a significant learning deficit in both the recognition and operant tasks compared with vehicle treated sham mice.

SIGNIFICANCE:

We conclude that CB2 activation is protective against cognitive deficits and tissue damage following permanent ischemia, but may dysregulate glial or neuronal function of learning and memory circuits in the absence of injury and/or inflammation.
Copyright © 2015. Published by Elsevier Inc.