We investigated the
analgesic effects of
tramadol and the arthritic changes following
tramadol administration in the rat
hip osteoarthritis (OA) model using mono-iodoacetate (MIA). The right hip joints of male Sprague-Dawley rats (n = 5 rats/group) in the
Sham group were injected with 25 μl of sterile saline and 1% of
fluorogold (FG) retrograde neurotracer. In the MIA + Vehicle and MIA + Tramadol groups, FG and 25 μl of sterile saline with 0.5 mg of MIA were injected into the right hip joint. The MIA + Vehicle and MIA + Tramadol groups were administered daily for 4 weeks, either sterile saline (10 mg/kg, intraperitoneal [i.p.]) or
tramadol (10 mg/kg, i.p.). We assessed
hyperalgesia every week after MIA administration. Histopathological changes and immunoreactive neurons for
calcitonin gene-related peptide (CGRP) in dorsal root ganglia (DRG) were evaluated after 4 weeks of treatment. MIA injection into the hip joint led to
mechanical hyperalgesia (p < 0.01), which was significantly reduced by
tramadol administration (p < 0.01). Furthermore, daily i.p injection of
tramadol significantly suppressed CGRP expression in DRG (p < 0.0001). MIA + Vehicle and MIA + Tramadol groups showed significant cartilage reduction and degeneration compared to the
Sham group (p < 0.0001). Interestingly, OA changes significantly progressed in the MIA + Tramadol group compared to the MIA + Vehicle group (p < 0.0001).