Substance P (SP) and a calcitonin‐related gene alpha (αCGRP −/− ) are implicated in musculoskeletal pain perception and were shown to have different effects on the pathogenesis of osteoarthritis (OA). However, it has not been investigated, whether deficiency for SP or αCGRP impacts pain‐related behavior and well‐being as well as gait during development of experimental OA. We induced OA in the right knee of wild‐type (WT) mice and mice either deficient for SP (tachykinin 1, Tac‐1) or αCGRP (male, n = 8 per genotype) by destabilizing the medial meniscus (DMM). We monitored body weight and food and water intake as indicators of wellbeing, determined nest building and composite pain score, and performed CatWalk gait analysis over 12 weeks. Cartilage degeneration was determined by OARSI scoring. The 12‐week post‐DMM, cartilage degradation in the medial compartment was significantly reduced in Tac1 −/− mice compared to the WT and to αCGRP −/− mice, coinciding with highest unloading of the operated limb in Tac1 −/− . Behavioral and gait analysis revealed only minor differences between the genotypes. Paw print area was most prominently reduced in Tac1 −/− over the observation period; at 12 weeks, we found a significant reduction in normalized print area in Tac1 −/− compared to presurgery and to the WT at the same time‐point. Calculated weight bearing was significantly reduced only in Tac1 −/− . Overall, we observed minor impact of DMM on gait and behavior in the present study. The reduced cartilage damage in the absence of SP might be in part due to reduced loading, however, the mechanism is not clear yet.
