Inhibition of Fatty Acid Amide Hydrolase Improves Depressive-Like Behaviors Independent of Its Peripheral Antinociceptive Effects in a Rat Model of Neuropathic Pain

摘要

BACKGROUND: Neuropathic pain is often associated with depression. Enhancing endocannabinoids by fatty acid amide hydrolase (FAAH) inhibitors relieves neuropathic pain and stress-induced depressive-like behaviors in animal models. However, it is unclear whether FAAH inhibitor can relieve neuropathic pain-induced depression by or not by its antinociceptive effects. METHODS: Adult male Wistar rats with chronic constriction injury (CCI) to the sciatic nerve were treated with the systemic FAAH inhibitor URB597 (5.8 mg center dot kg(-1)center dot day(-1), intraperitoneally) or peripherally acting FAAH inhibitor URB937 (1.6 mg center dot kg(-1)center dot d(-1), intraperitoneally; n = 11-12). The treatment was applied from the 15th day after surgery and continued for 15 days. Mechanical withdrawal threshold was examined by Von Frey test before surgery and on the 28th day after CCI. Depressive-like behaviors were evaluated by forced swimming test (FST) and novelty-suppressed feeding (NSF) after 15-day treatment. The levels of anandamide and 2-arachidonoylglycerol in hippocampus were examined by liquid chromatography and mass spectrometry. Hippocampal neurogenesis including proliferation, differentiation, and survival of newborn cells was assessed by immunohistochemistry. RESULTS: After CCI injury, the rats developed significantly nociceptive and depressive-like behaviors, indicated by persistent mechanical hypersensitivity in Von Frey test, significantly prolonged immobility time in FST (sham: 84.2 +/- 13.4 seconds versus CCI: 137.9 +/- 18.8 seconds; P < .001), and protracted latency to feed in NSF (sham: 133.4 +/- 19.4 seconds versus CCI: 234.9 +/- 33.5 seconds; P < .001). For the CCI rats receiving treatment, compared to vehicle placebo group, pain threshold was increased by both URB597 (3.1 +/- 1.0 vs 11.2 +/- 1.2 g; P < .001) and URB937 (3.1 +/- 1.0 vs 12.1 +/- 1.3 g; P < .001). Immobility time of FST was reduced by URB597 (135.8 +/- 16.6 vs 85.3 +/- 17.2 seconds; P < .001) but not by URB937 (135.8 +/- 16.6 vs 129.6 +/- 17.8 seconds; P = .78). Latency to feed in NSF was also reduced by URB597 (235.9 +/- 30.5 vs 131.8 +/- 19.8 seconds; P < .001) but not by URB937 (235.9 +/- 30.5 vs 232.2 +/- 33.2 seconds; P = .72). Meanwhile, CCI decreased the number of proliferating cells and reduced survival of new mature neurons in hippocampus. URB597 but not URB937 treatment improved these cellular deficits. CONCLUSIONS: Inhibition of FAAH can improve depressive-like behaviors induced by neuropathic pain independent of its peripheral antinociceptive action. Enhanced neurogenesis in hippocampus might contribute to the antidepressive effects of URB597.