The Effects of Peptide and Lipid Endocannabinoids on Arthritic Pain at the Spinal Level

BACKGROUND: Hemopressin, a nonapeptide (PVNFKFLSH: HP) derived from the a chain of hemoglobin was shown to interact specifically with brain cannabinoid CB1 receptors. Therefore, it seems to be the only peptide structure with cannabinoid activities. Our goal in this study was to further characterize this peptide and to clarify the antinociceptive potency of the polyunsaturated fatty acid derivates, 2-arachidonoyl-glycerol (2-AG) and anandamide, by investigating their effects on mechanical allodynia at the spinal level. METHODS: HP was prepared on solid phase by in situ neutralization. After chronic intrathecal catheterization, mechanical hypersensitivity was produced in male Wistar rats by injection of carrageenan (300 mu g/30 mu L) into the tibiotarsal joint of one of the hind legs. Three hours after carrageenan administration, the ligands were administered intrathecally. The mechanical threshold was assessed using a dynamic aesthesiometer. RESULTS: 2-AG (1-200 mu g) and anandamide (10-200 mu g) decreased carrageenan-induced mechanical allodynia in a dose-dependent manner, whereas HP had no antinociceptive effect in a wide dose range (0.3-30 mu g). The effect of 2-AG was prevented by the CB, receptor antagonist AM 251, but not by the CB2 antagonist SSR144528-2. HP (3 and 30 mu g) also inhibited the effect of 2-AG. None of the ligands influenced the degree of edema. CONCLUSIONS: HP posttreatment had no effect on mechanical allodynia, whereas spinally injected 2-AG and anandamide were potent drugs. (Anesth Analg 2012;114:1346-52)