Effects of risk factors on evoked pain patterns in rat models of experimental knee osteoarthritis.
Holly T PhilpottGarth BlacklerJoseph Daniel KlapakKyle K PitchersMadison TomlinsonNiall SmithJaclyn ViehwegerJoseph U UmohDavid W HoldsworthTristan MaerzChristopher Thomas AppletonPublished in: Journal of orthopaedic research : official publication of the Orthopaedic Research Society (2023)
Pain experiences in patients with knee osteoarthritis (OA) may be influenced differently by OA risk factors, reducing the translatability of preclinical research into the clinic. Our objective was to contrast evoked pain patterns after exposure to different OA risk factors including acute joint trauma, chronic instability, or obesity/metabolic syndrome using rat models of experimental knee OA. We tested longitudinal patterns of evoked pain behaviors (knee pressure pain threshold and hindpaw withdrawal threshold) in young male rats exposed to different OA-inducing risk factors including (1) nonsurgical joint trauma (impact-induced anterior cruciate ligament (ACL) rupture); (2) surgical joint destabilization (ACL + medial meniscotibial ligament transection); and (3) high fat/sucrose (HFS) diet-induced obesity. Histopathology for synovitis, cartilage damage, and subchondral bone morphology was performed. Pressure pain threshold was reduced (more pain) most, and earlier by joint trauma (Week 4-12) and HFS (Week 8-28) than by joint destabilization (Week 12). Hindpaw withdrawal threshold was reduced transiently after joint trauma (Week 4), with smaller and later reductions after joint destabilization (Week 12), but not with HFS. Synovial inflammation occurred at Week 4 after joint trauma and instability but only coincided with pain behaviors after joint trauma. Cartilage and bone histopathology were most severe after joint destabilization and least severe with HFS. The pattern, intensity, and timing of evoked pain behaviors varied due to OA risk factor exposure and were inconsistently associated with histopathological OA features. These findings may help to explain the challenges with translating preclinical OA pain research to multimorbid clinical OA contexts.
Keyphrases
- knee osteoarthritis
- chronic pain
- risk factors
- pain management
- neuropathic pain
- metabolic syndrome
- insulin resistance
- oxidative stress
- randomized controlled trial
- anterior cruciate ligament
- magnetic resonance
- cardiovascular disease
- clinical trial
- primary care
- magnetic resonance imaging
- study protocol
- early onset
- cross sectional
- soft tissue
- intensive care unit
- middle aged
- adipose tissue
- postmenopausal women
- total knee arthroplasty
- body mass index
- mental health
- physical activity
- bone loss