A CRF1, but not CRF2, receptor antagonist inhibits pain-related behavior in animals with arthritis but not in normal animals. A CRF1, but not CRF2, receptor.

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A CRF1, but not CRF2, receptor antagonist inhibits pain-related behavior in animals with arthritis but not in normal animals. A CRF1, but not CRF2, receptor antagonist inhibits pain-related behavior in animals with arthritis but not in normal animals. Audible (A, B) and ultrasonic (C, D) vocalizations and spinal withdrawal reflexes (E, F) were measured in two groups of animals: normal (left side in each graph) and arthritis (right side). In the normal group, behaviors were measured before (baseline) and during (15–20 min) drug application into the CeA by microdialysis. In the arthritis group, behaviors were measured before (baseline) and 6 h after arthritis induction and during (15–20 min) and after (30 min washout) drug application into the CeLC in the arthritis state. Vocalizations were evoked by brief (15 s) noxious (2000 g/30 mm2) stimulation of the knee with a calibrated forceps. Duration of vocalizations was measured as the arithmetic sum of the duration of each individual vocalization event during a 1 min period beginning with the onset of the mechanical stimulus as described previously (Han et al., 2005a; Neugebauer et al., 2007). A, NBI27914 (NBI, 50 μm, concentration in the microdialysis fiber) had no effect on audible vocalizations in normal animals (n = 5) but inhibited the increased vocalizations of arthritic rats significantly (n = 11, p < 0.001, Newman–Keuls multiple comparison test). B, Astressin-2B (50 μm, concentration in the microdialysis probe) did not affect audible vocalizations in normal rats (n = 6) and in arthritic rats (n = 6). C, NBI27914 had no significant effect on ultrasonic vocalizations of normal rats (n = 5) but inhibited the increased ultrasonic vocalizations of arthritic rats (n = 11, p < 0.01, Newman–Keuls multiple comparison test). D, Astressin-2B had no significant effect on ultrasonic vocalizations of normal rats (n = 6) and arthritic rats (n = 6). E, NBI27914 had no significant effect on hindlimb-withdrawal reflex thresholds in normal rats but increased the withdrawal thresholds of arthritic rats (n = 11, p < 0.01, Newman–Keuls multiple comparison test). F, Astressin-2B had no significant effect in arthritic animals (n = 6) and under normal conditions (n = 6). Hindlimb-withdrawal thresholds were measured by applying pressure of increasing force to the knee joint with a calibrated forceps. Bar histograms and error bars represent mean ± SE. **p < 0.01, ***p < 0.001. Yu Fu, and Volker Neugebauer J. Neurosci. 2008;28:3861-3876 ©2008 by Society for Neuroscience