Journal
EUROPEAN JOURNAL OF NEUROSCIENCE
Volume 54, Issue 2, Pages 4475-4496Publisher
WILEY
DOI: 10.1111/ejn.15266
Keywords
lateral spinothalamic tract; neuropathic pain; pain assessment; pain models; pain transmission
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This review discusses neuropathic pain development and handling. The first part describes the pathways of neuropathic pain and different in vivo models. The second part presents the knowledge about cellular and molecular mechanisms that may lead to neuropathic pain. Established animal models can simulate the diversity of neuropathic pain observed in clinics.
The International Association for the Study of Pain defines neuropathic pain as pain arising as a direct consequence of a lesion or disease affecting the somatosensory system. The associated changes can be observed in the peripheral as well as the central nervous system. The available literature discusses a wide variety of causes as predisposing for the development and amplification of neuropathic pain. Further, key interactions within sensory pathways have been discovered, but no common molecular mechanism leading to neuropathic pain has been identified until now. In the first part of this review, the pain mediating lateral spinothalamic tract is described. Different in vivo models are presented that allow studying trauma-, chemotherapy-, virus-, and diabetes-induced neuropathic pain in rodents. We furthermore discuss approaches to assess neuropathic pain in these models. Second, the current knowledge about cellular and molecular mechanisms suggested to underlie the development of neuropathic pain is presented and discussed. A summary of established therapies that are already applied in the clinic and novel, promising approaches closes the paper. In conclusion, the established animal models are able to emulate the diversity of neuropathic pain observed in the clinics. However, the assessment of neuropathic pain in the presented in vivo models should be improved. The determination of common molecular markers with suitable in vitro models would simplify the assessment of neuropathic pain in vivo. This would furthermore provide insights into common molecular mechanisms of the disease and establish a basis to search for satisfying therapeutic approaches.
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