Effect of Sex on Motor Function, Lesion Size, and Neuropathic Pain after Contusion Spinal Cord Injury in Mice

Spinal cord injury (SCI) causes neurodegeneration, impairs locomotor function, and impacts the quality of life particularly in those individuals in whom neuropathic pain develops. Whether the time course of neurodegeneration, locomotor impairment, or neuropathic pain varies with sex, however, remain...

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Veröffentlicht in:Journal of neurotrauma 2020-09, Vol.37 (18), p.1983-1990
Hauptverfasser: McFarlane, Katelyn, Otto, Taylor E, Bailey, William M, Veldhorst, Amy K, Donahue, Renée R, Taylor, Bradley K, Gensel, John C
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container_end_page 1990
container_issue 18
container_start_page 1983
container_title Journal of neurotrauma
container_volume 37
creator McFarlane, Katelyn
Otto, Taylor E
Bailey, William M
Veldhorst, Amy K
Donahue, Renée R
Taylor, Bradley K
Gensel, John C
description Spinal cord injury (SCI) causes neurodegeneration, impairs locomotor function, and impacts the quality of life particularly in those individuals in whom neuropathic pain develops. Whether the time course of neurodegeneration, locomotor impairment, or neuropathic pain varies with sex, however, remains understudied. Therefore, the objective of this study in male and female C57BL/6 mice was to evaluate the following outcomes for six weeks after a 75-kdyn thoracic contusion SCI: locomotor function using the Basso Mouse Scale (BMS); spinal cord tissue sparing and rostral-caudal lesion length; and mechanical allodynia and heat hyperalgesia using hindpaw application of Von Frey filaments or radiant heat stimuli, respectively. Although motor function was largely similar between sexes, all of the males, but only half of the females, recovered plantar stepping. Rostral-caudal lesion length was shorter in females than in males. Mechanical allodynia and heat hyperalgesia after SCI developed in all animals, regardless of sex; there were no differences in pain outcomes between sexes. We conclude that contusion SCI yields subtle sex differences in mice depending on the outcome measure but no significant differences in behavioral signs of neuropathic pain.
doi_str_mv 10.1089/neu.2019.6931
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Whether the time course of neurodegeneration, locomotor impairment, or neuropathic pain varies with sex, however, remains understudied. Therefore, the objective of this study in male and female C57BL/6 mice was to evaluate the following outcomes for six weeks after a 75-kdyn thoracic contusion SCI: locomotor function using the Basso Mouse Scale (BMS); spinal cord tissue sparing and rostral-caudal lesion length; and mechanical allodynia and heat hyperalgesia using hindpaw application of Von Frey filaments or radiant heat stimuli, respectively. Although motor function was largely similar between sexes, all of the males, but only half of the females, recovered plantar stepping. Rostral-caudal lesion length was shorter in females than in males. Mechanical allodynia and heat hyperalgesia after SCI developed in all animals, regardless of sex; there were no differences in pain outcomes between sexes. 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identifier ISSN: 0897-7151
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subjects Antibiotics
Contusions
Drug withdrawal
Females
Filaments
Gender differences
Heat
Heat stimuli
Hyperalgesia
Lesions
Males
Neuralgia
Neurodegeneration
Nonsteroidal anti-inflammatory drugs
Original
Pain
Pain perception
Quality of life
Sex
Sex differences
Spinal cord injuries
Surgery
Surgical outcomes
Thorax
title Effect of Sex on Motor Function, Lesion Size, and Neuropathic Pain after Contusion Spinal Cord Injury in Mice
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