Abstract

Ischaemic insult results in short-term changes in cannabinoid-1 (CB1) receptor expression in the brain, but it is not known whether long-term changes occur, which could potentially mean a change in the intrinsic ability of the brain to withstand new ischaemic episodes. In this study, we have investigated the expression and functionality of CB1 receptors in coronal brain slices obtained from ovariectomised female rats 46days after middle cerebral artery occlusion (MCAO). The animals were treated with either 17ß-oestradiol or placebo pellets 6h after MCAO and thereafter housed either in isolated or enriched environments. [3H]CP55,940 autoradiography indicated no significant effect of 17ß-oestradiol treatment or housing environment upon CB1 receptor densities. There was, however, a modest but significant decrease in the CB1 receptor density on the ipsilateral side relative to the contralateral side in the frontal cortex, parietal cortex, CA1–CA3 regions of the hippocampus, thalamus and hypothalamus. CB1 receptor functionality was assessed by measurement of basal and CP55,940-stimulated [35S]GTPγS autoradiography. In the frontal cortex, parietal cortex, CA1–CA3 regions of the hippocampus and dentate gyrus, a robust stimulation, blocked by the CB1 receptor inverse agonist AM251, was seen. There were no significant changes in the response to CP55,940 with respect either to the 17ß-oestradiol treatment, housing environment or MCAO. Our results reveal that although there are modest long-term decreases in ipsilateral CB1 receptor densities following MCAO in female rats, these decreases do not result in a functional CB1 receptor deficit.

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