• Maral Tajerian, Peyman Sahbaie, Yuan Sun, David Leu, Hsun Yu Yang, Wenwu Li, Ting Ting Huang, Wade Kingery, and J David Clark.
• Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, United States; Department of Anesthesiology, Stanford University School of Medicine, Stanford, CA, United States; Palo Alto Institute of Research and Education, Palo Alto, CA, United States. Electronic address: maral@stanford.edu.
• Neurobiol Learn Mem. 2015 Sep 1; 123: 100-9.

AbstractComplex Regional Pain Syndrome (CRPS) is a major cause of chronic pain after surgery or trauma to the limbs. Despite evidence showing that the prevalence and severity of many forms of chronic pain, including CRPS, differ between males and females, laboratory studies on sex-related differences in animal models of CRPS are not available, and the impact of sex on the transition from acute to chronic CRPS pain and disability are unexplored. Here we make use of a tibia fracture/cast mouse model that recapitulates the nociceptive, functional, vascular, trophic, inflammatory and immune aspects of CRPS. Our aim is to describe the chronic time course of nociceptive, motor and memory changes associated with fracture/cast in male and female mice, in addition to exploring their underlying spinal mechanisms. Our behavioral data shows that, compared to males, female mice display lower nociceptive thresholds following fracture in the absence of any differences in ongoing or spontaneous pain. Furthermore, female mice show exaggerated signs of motor dysfunction, deficits in fear memory, and latent sensitization that manifests long after the normalization of nociceptive thresholds. Our biochemical data show differences in the spinal cord levels of the glutamate receptor NR2b, suggesting sex differences in mechanisms of central sensitization that could account for differences in duration and severity of CRPS symptoms between the two groups.Copyright © 2015 Elsevier Inc. All rights reserved.

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