Figure 2From: Behavioural and morphological evidence for the involvement of glial cell activation in delta opioid receptor function: implications for the development of opioid toleranceThe antinociceptive effects of DLT (10 μg, i.t.) were assessed in the tail flick acute thermal pain test. Rats chronically treated with morphine exhibited enhanced δOR-mediated analgesia as compared with controls and this enhancement was blocked by chronic co-administration of morphine with the glial modulatory agent, propentofylline. All testing was performed 12 h following the final morphine injection. A) The latencies to respond with a brisk tail flick were measured prior to and at 10 minute intervals following DLT administration for 50 minutes. Three pre-drug latencies were averaged to obtain a baseline latency value for each rat. B) Mean tail flick latencies at 30 minutes post-DLT injection were converted to % M.P.E. values. Statistical analyses of thermal latencies were performed by two-way ANOVA followed by Bonferroni post-hoc while statistics for transformed % M.P.E. data were accomplished by one-way ANOVA followed by Tukey's post-hoc multiple comparison test. Data represent means ± s.e.m. for n = 5–6 rats per group. The asterisk denotes a significant difference from saline-treated rats. * = p < 0.05. 0: Baseline prior to drug administration; MS: morphine sulfate; PF: propentofylline.Back to article page