Published: Vol 7, Iss 16, Aug 20, 2017 DOI: 10.21769/BioProtoc.2506 Views: 14945
Reviewed by: Xi FengAdler R. DillmanAnonymous reviewer(s)
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Abstract
The Hargreaves test is specifically designed to assess thermal pain sensation in rodents such as rats and mice. This test has been used in experiments involving pain sensitization or recovery of thermal pain response following neural injury and regeneration. We present here a step-by-step protocol highlighted with important notes to guide first-time users through the learning process. Additionally, we have also included representative data from a rat model of sensory denervation showing how the data can be analysed to obtain meaningful results. We hope that this protocol can also assist potential users in deciding whether the Hargreaves test is a suitable test for their experiment.
Keywords: Thermal painBackground
The somatosensory system is responsible for processing sensory stimuli received from the environment. These sensory stimuli include pain, touch, pressure and vibration. To study how these stimuli are processed with the ultimate goal of repairing the system in the event of injury, neuroscientists have used a plethora of animal models and behavioral tests. Some of these experiments include administration of a noxious substance into the nervous system to investigate increased pain sensitivity (Zurowski et al., 2012), inducing a central or peripheral injury to the nervous system and then observing whether particular treatments promote neural regeneration (Andrews et al., 2009; Tan et al., 2012; Cheah et al., 2016), or developing in vivo neurodegenerative models with pathology in sensory neurons (Mellone et al., 2013). Whichever the case, having a suitable test to study the behavioral response of the animals is key.
Of all the sensations, pain is perhaps one of the most studied. Transmitted via different nociceptors, pain can be further categorized into different modalities such as thermal, mechanical and chemical. Depending on the experimental goal, all of these modalities can be assessed with a specific behavioral test. We present here our approach to the Hargreaves test which is a behavioral test designed for assessing response to thermal pain in rodents such as rats and mice (Hargreaves et al., 1988). Based on our experience, the Hargreaves test is relatively straight-forward and novel users can master it in a short period of time. With the aid of this step-by-step protocol, we hope to assist potential users in deciding if the Hargreaves test is a suitable test for them and also guide them through the learning process in an efficient manner.
Materials and Reagents
Equipment
Procedure
Note: All of the following animal procedures were conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act 1986. Please check with local/national regulations before starting the protocol.
Data analysis
The amount of time required to elicit a withdrawal response is termed as withdrawal latency which is measured in seconds. A longer withdrawal latency signifies a slower withdrawal response and vice versa. To obtain the average reaction time for an animal, calculate the mean from at least 3 trials. If 5 trials have been performed, the lowest and the highest values can be discounted as outlying values. To obtain a data point for a group of animals with one animal represents n = 1, calculate the mean of the average reaction time of the animals in the group. If the same set of animals is being tested repeatedly over different experimental conditions or timepoints, a paired or repeated measures statistical test should be used to determine the statistical significance. Usually, a P value of less than 0.05 is deemed to be statistically significant. Representative data are shown below (Figure 7).
Figure 7. Representative Hargreaves test data for adult Lewis rats which underwent a quadruple (C5-C8) dorsal root crush injury of the left forepaw or sham surgery. A baseline reading was recorded a week before surgery and experimental readings were recorded weekly during 1-8 weeks after surgery. As opposed to the sham control group, a longer time (in seconds) was required to elicit a withdrawal response from the injured group a week after surgery and this was sustained throughout the duration of the experiment signifying chronic thermal pain sensory deficit. The data were analyzed by repeated measures ANOVA and expressed as mean ± SEM, *P < 0.05 was statistically significant, n = 4.
Notes
Acknowledgments
M.R.A. is supported by a research grant from the Biotechnology and Biological Sciences Research Council (BBSRC). J.W.F. is supported by a grant from the European Union/Czech Ministry of Education–Operation Programme Research (CZ.02.1.01/0.0/0.0/15_003/0000419).
References
Article Information
Copyright
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
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Category
Neuroscience > Behavioral neuroscience > Animal model
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