Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Jul;54(2):4475-4496.
doi: 10.1111/ejn.15266. Epub 2021 May 26.

Neuropathic pain: Spotlighting anatomy, experimental models, mechanisms, and therapeutic aspects

Affiliations
Review

Neuropathic pain: Spotlighting anatomy, experimental models, mechanisms, and therapeutic aspects

Svenja Kankowski et al. Eur J Neurosci. 2021 Jul.

Abstract

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.

Keywords: lateral spinothalamic tract; neuropathic pain; pain assessment; pain models; pain transmission.

PubMed Disclaimer

References

REFERENCES

    1. Ahlgren S. C., & Levine J. D. (1993). Mechanical hyperalgesia in streptozotocin-diabetic rats. Neuroscience, 52(4), 1049-1055. http://dx.doi.org/10.1016/0306-4522(93)90551-p
    1. Ahmadi, S., Ebrahimi, S. S., Oryan, S., & Rafieenia, F. (2012). Blockades of ATP-sensitive potassium channels and L-type calcium channels improve analgesic effect of morphine in alloxan-induced diabetic mice. Pathophysiology, 19, 171-177. https://doi.org/10.1016/j.pathophys.2012.04.007
    1. Akintola, T., Raver, C., Studlack, P., Uddin, O., Masri, R., & Keller, A. (2017). The grimace scale reliably assesses chronic pain in a rodent model of trigeminal neuropathic pain. Neurobiology of Pain, 2, 13-17. https://doi.org/10.1016/j.ynpai.2017.10.001
    1. Alba-Delgado, C., Mico, J. A., Sánchez-Blázquez, P., & Berrocoso, E. (2012). Analgesic antidepressants promote the responsiveness of locus coeruleus neurons to noxious stimulation: Implications for neuropathic pain. Pain, 153. https://doi.org/10.1016/j.pain.2012.03.034
    1. Alles, S. R. A., Cain, S. M., & Snutch, T. P. (2020). Pregabalin as a pain therapeutic: Beyond calcium channels. Frontiers in Cellular Neuroscience, 14. https://doi.org/10.3389/fncel.2020.00083

LinkOut - more resources