» Articles » PMID: 29191755

Pharmacological Validation of Voluntary Gait and Mechanical Sensitivity Assays Associated with Inflammatory and Neuropathic Pain in Mice

Overview
Specialties Neurology
Pharmacology
Date 2017 Dec 2
PMID 29191755
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

The urgent need for more effective analgesic treatment options has prompted a re-evaluation of the behavioral tests used to assess pain in pre-clinical research, with an emphasis on inclusion of more voluntary, un-evoked behavioral assessments of pain. In order to validate voluntary gait analysis and a voluntary mechanical conflict-avoidance assay, we tested mouse models of neuropathy (spared nerve injury) and inflammation (complete Freund's adjuvant) alongside reflexive measures of mechanical and thermal hypersensitivity. To establish whether the observed changes in behavioral responses were pain-related, known analgesics (buprenorphine, gabapentin, carprofen) were also administered. Spared nerve injury persistently altered several gait indices, whereas complete Freund's adjuvant caused only transient changes. Furthermore, known analgesics could not reverse these gait changes, despite demonstrating their previously established efficacy in reflexive measures of mechanical and thermal hypersensitivity. In contrast, the mechanical conflict-avoidance assay demonstrated aversion in mice with neuropathy and inflammation-induced hypersensitivity, which could both be reversed by analgesics. We conclude that voluntary gait changes in rodent neuropathic and inflammatory pain models are not necessarily indicative of pain-related adaptations. On the other hand, mechanical conflict-avoidance represents a valid operant assay for quantifying pain-related behaviors in mice that can be reversed by known analgesics.

Citing Articles

Characterizing a new rat model of chronic pain after spine surgery.

Wu Q, Ford N, He S, Zhang C, Cui X, Liu J Bone Res. 2025; 13(1):34.

PMID: 40074742 PMC: 11904174. DOI: 10.1038/s41413-025-00408-1.


Tumor-infiltrating nerves functionally alter brain circuits and modulate behavior in a mouse model of head-and-neck cancer.

Barr J, Walz A, Restaino A, Amit M, Barclay S, Vichaya E Elife. 2024; 13.

PMID: 39302290 PMC: 11415076. DOI: 10.7554/eLife.97916.


Neuromuscular Polytrauma Pain is Resolved by Macrophage COX-2 Nanoimmunomodulation.

Cortez I, Gaffney C, Vichare R, Crelli C, Liu L, Lee E Int J Nanomedicine. 2024; 19:7253-7271.

PMID: 39050880 PMC: 11268785. DOI: 10.2147/IJN.S460418.


Quantification of stimulus-evoked tactile allodynia in free moving mice by the chainmail sensitivity test.

Ozdemir Y, Nakamoto K, Boivin B, Bullock D, Andrews N, Gonzalez-Cano R Front Pharmacol. 2024; 15:1352464.

PMID: 38464715 PMC: 10920263. DOI: 10.3389/fphar.2024.1352464.


Widespread latent hyperactivity of nociceptors outlasts enhanced avoidance behavior following incision injury.

Bavencoffe A, Lopez E, Johnson K, Tian J, Gorgun F, Shen B bioRxiv. 2024; .

PMID: 38352319 PMC: 10862851. DOI: 10.1101/2024.01.30.578108.


References
1.
Li G, Rhodes J, Girard I, Gammie S, Garland Jr T . Opioid-mediated pain sensitivity in mice bred for high voluntary wheel running. Physiol Behav. 2004; 83(3):515-24. DOI: 10.1016/j.physbeh.2004.09.003. View

2.
Huehnchen P, Boehmerle W, Endres M . Assessment of paclitaxel induced sensory polyneuropathy with "Catwalk" automated gait analysis in mice. PLoS One. 2013; 8(10):e76772. PMC: 3797113. DOI: 10.1371/journal.pone.0076772. View

3.
Rutten K, Robens A, Read S, Christoph T . Pharmacological validation of a refined burrowing paradigm for prediction of analgesic efficacy in a rat model of sub-chronic knee joint inflammation. Eur J Pain. 2013; 18(2):213-22. DOI: 10.1002/j.1532-2149.2013.00359.x. View

4.
Percie du Sert N, Rice A . Improving the translation of analgesic drugs to the clinic: animal models of neuropathic pain. Br J Pharmacol. 2014; 171(12):2951-63. PMC: 4055199. DOI: 10.1111/bph.12645. View

5.
Larson A, Brown D, Walser M . Pain threshold changes in adjuvant-induced inflammation: a possible model of chronic pain in the mouse. Pharmacol Biochem Behav. 1986; 24(1):49-53. DOI: 10.1016/0091-3057(86)90043-2. View