4.6 Article

Somatosensory behavioral alterations in a NGF-induced persistent low back pain model

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 418, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbr.2021.113617

Keywords

Nerve growth factor; Low back pain; Mechanical hypersensitivity; Mechanical hyperalgesia; Pain

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The study illustrates the time-dependent development of mechanical hypersensitivity in adult male rats in an NGF-induced LBP model, showing that mechanical sensitivity changes primarily locally in the ipsilateral trunk following NGF injections.
Low back pain (LBP) is a major global burden in part due to the underlying pathophysiological mechanisms being poorly understood. A LBP rat model involving two injections of nerve growth factor (NGF, an endogenous pain related neurotrophin) into trunk musculature was recently developed. Additional behavioral work in this NGFLBP rat model is required to better characterize local and remote somatosensory alterations related to NGFinduced peripheral and central sensitization. This work characterizes the time-dependent development of hypersensitivity to trunk and hindpaw cutaneous mechanical stimulation and deep muscle mechanical hyperalgesia in adult male Sprague-Dawley rats (n = 6/group). Behavioral assays were performed at baseline (Day 0, D0), D2, D5 (pre-and 4 h post-2nd NGF or control injection), D7, D10, and D14 in NGF and control groups. Trunk and hindpaw cutaneous mechanical hypersensitivity were tested using von Frey filaments. Deep trunk mechanical hyperalgesia was determined using a small animal algometer. NGF rats demonstrated increased cutaneous sensitivity to ipsilateral trunk mechanical stimuli at D7, D10, and D14. NGF rats also demonstrated ipsilateral deep mechanical hyperalgesia on D2, D5 + 4 h, D7, D10, and D14. Cutaneous hypersensitivity was delayed compared to deep hyperalgesia in NGF rats. No additional sensory changes were noted. Together, these results indicate that male mechanical somatosensory changes develop primarily locally in the ipsilateral trunk following unilateral NGF injections. These findings contrast with a previous report in female rats using this NGF-LBP model showing more widespread (bilateral) hyperalgesia and remote mechanical hypersensitivity. Future studies will examine potential sex-related pain behavioral differences in the NGF model.

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