2018
DOI: 10.21037/atm.2018.09.58
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Neuropathic pain models and outcome measures: a dual translational challenge

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Cited by 14 publications
(12 citation statements)
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“…This sort of pain is a functional derangement of the pain pathway 156 and can occur through alterations in any step of signal processing. Neurotransmitters, neuromodulators, and their respective receptors on neurons can be altered by neuroimmune mediators in presence, absence, or quantity, altering synaptic connectivity and leading to decreased modulation of the ascending pain signal and/or aberrant signaling by peripheral nociceptors.…”
Section: Neuroplasticitymentioning
confidence: 99%
“…This sort of pain is a functional derangement of the pain pathway 156 and can occur through alterations in any step of signal processing. Neurotransmitters, neuromodulators, and their respective receptors on neurons can be altered by neuroimmune mediators in presence, absence, or quantity, altering synaptic connectivity and leading to decreased modulation of the ascending pain signal and/or aberrant signaling by peripheral nociceptors.…”
Section: Neuroplasticitymentioning
confidence: 99%
“…Furthermore, preclinical models are limited for many reasons. For example, neuropathic pain that is induced does not consider the perceptive, emotional, or affective components of pain [124]. Additionally, nutritional treatments effective in mice may not translate to effective treatments in clinical models.…”
Section: Discussionmentioning
confidence: 99%
“… 1 It is not possible to directly measure pain in animals, as we do not have access to their subjective experiences, consequently many methods have been developed that quantify “nocifensive” behaviors, which are defined as behavioral responses to painful stimuli. Most nociception assays depend on a quick motor withdrawal reflex in response to a brief mechanical or thermal stimulation, and this simple movement is relatively easy to define and recognize, 2 5 but such assays lack similarity to clinical pain. In mice, these assays are genetically poorly correlated with more clinically relevant chronic pain assays 6 , 7 and are more closely associated with startle and reactivity traits.…”
Section: Introductionmentioning
confidence: 99%