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A Method to Enhance the Magnitude of Tactile Hypersensitivity Following Spinal Nerve Ligation in Rats

Overview
Specialty Neurology
Date 2014 Jun 15
PMID 24928434
Citations 2
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Abstract

Background: The rat L5/L6 spinal nerve ligation model (SNL) has been widely used to investigate putative analgesics. Pursuit of novel therapies in preclinical settings requires models with consistent and reproducible phenotypes.

New Method: We assessed the effects of repetitive stimulation of the hindpaws of SNL and Sham surgery rats during the 2 weeks immediately after surgery on the overall rate of achieving tactile hypersensitivity, as well as the magnitude of the hypersensitivity compared to unprimed rats. Beginning on day 2 post-surgery, and continuing on alternate days for a total of seven sessions, animals underwent light brushing/tapping (termed priming) of the hindpaws ipsilateral and contralateral to surgery.

Results: Priming the ipsilateral hindpaw enhanced the magnitude of tactile hypersensitivity such that the baseline withdrawal threshold (BWT) for primed SNL animals was significantly lower than unprimed SNL animals over post-surgical days 15-29. BWT was not different between primed and unprimed Sham rats. The percentage of SNL primed animals meeting the a priori criterion for tactile hypersensitivity of paw withdrawal threshold less than 2.0 grams was 98.9%±1.1%.

Comparison With Existing Method: SNL rats that did not receive stimulation (unprimed) showed significantly higher baseline hypersensitivity when evaluated on days 15-29, exemplified by only 34.5%±7.2% meeting the established <2.0g criterion.

Conclusion: Our data indicate that tactile priming during the 2 weeks immediately after SNL surgery enhances the magnitude of tactile hypersensitivity in the SNL model, and provide an optimized assay for evaluating putative analgesics.

Citing Articles

Core Outcome Measures in Preclinical Assessment of Candidate Analgesics.

Negus S Pharmacol Rev. 2019; 71(2):225-266.

PMID: 30898855 PMC: 6448246. DOI: 10.1124/pr.118.017210.


The α2,3-selective potentiator of GABA receptors, KRM-II-81, reduces nociceptive-associated behaviors induced by formalin and spinal nerve ligation in rats.

Witkin J, cerne R, Davis P, Freeman K, do Carmo J, Rowlett J Pharmacol Biochem Behav. 2019; 180:22-31.

PMID: 30825491 PMC: 6529285. DOI: 10.1016/j.pbb.2019.02.013.