A Fracture Pain Model in the Rat

Author:

Freeman Katie T.1,Koewler Nathan J.1,Jimenez-Andrade Juan M.2,Buus Ryan J.3,Herrera Monica B.4,Martin Carl D.1,Ghilardi Joseph R.5,Kuskowski Michael A.6,Mantyh Patrick W.7

Affiliation:

1. Junior Scientist, Neurosystems Center and Department of Diagnostic and Biological Sciences, University of Minnesota.

2. Research Associate, Neurosystems Center and Department of Diagnostic and Biological Sciences, University of Minnesota. Current Position: Assistant Professor, Department of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona.

3. Assistant Scientist.

4. Postdoctoral Associate, Neurosystems Center and Department of Diagnostic and Biological Sciences, University of Minnesota. Current Position: Research Associate, Department of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona.

5. Senior Scientist, Research Service, VA Medical Center, Minneapolis, Minnesota.

6. Senior Statistician, Geriatric Research, Education and Clinical Center, VA Medical Center, Minneapolis, Minnesota.

7. Professor, Neurosystems Center and Departments of Diagnostic and Biological Sciences, Psychiatry, Neuroscience, and Cancer Center, University of Minnesota. Current position: Professor, Department of Pharmacology, College of Medicine, University of Arizona, Tucson, Arizona.

Abstract

Background Because of the relative lack of understanding of the mechanisms that drive skeletal pain, the purpose of this study was to adapt a previously validated closed femur fracture model to quantitatively evaluate skeletal pain in female and male rats. Methods Three-month-old female and male Sprague-Dawley rats were anesthetized, and a stainless steel pin was inserted into the intramedullary space of the left femur. Three weeks later, the rats were reanesthetized, and left femoral diaphyses were fractured using a standardized impactor device. At 1-21 days after fracture, skeletal pain was measured by quantitatively assessing spontaneous guarding, spontaneous flinching, and weight bearing of the fractured hind limb. Results Females and males showed highly robust pain behaviors that were maximal at day 1 after fracture and returned gradually to normal nonfractured levels at days 14-21 after fracture. The magnitude of fracture pain was not significantly different at most time points between female and male rats. In both females and males, the pain-related behaviors were attenuated by subcutaneous morphine in a dose-dependent manner. Conclusions This model may help in developing a mechanism-based understanding of the factors that generate and maintain fracture pain in both females and males and in translating these findings into new therapies for treating fracture pain.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

Reference91 articles.

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