AI Article Synopsis

  • Neuropathic pain is a chronic condition caused by nervous system injury, often worsening with time and poorly responding to typical treatments.
  • Naked mole-rats were studied to see if they have a different response to nerve injury compared to mice, especially regarding sensitivity to cold and mechanical stimuli.
  • The study found that while both species developed mechanical sensitivity after nerve injury, naked mole-rats showed no cold sensitivity, likely due to evolutionary adaptations not simply explained by receptor expression differences.

Article Abstract

Neuropathic pain is a chronic disease state resulting from injury to the nervous system. This type of pain often responds poorly to standard treatments and occasionally may get worse instead of better over time. Patients who experience neuropathic pain report sensitivity to cold and mechanical stimuli. Since the nociceptive system of African naked mole-rats contains unique adaptations that result in insensitivity to some pain types, we investigated whether naked mole-rats may be resilient to sensitivity following nerve injury. Using the spared nerve injury model of neuropathic pain, we showed that sensitivity to mechanical stimuli developed similarly in mice and naked mole-rats. However, naked mole-rats lacked sensitivity to mild cold stimulation after nerve injury, while mice developed robust cold sensitivity. We pursued this response deficit by testing behavior to activators of transient receptor potential (TRP) receptors involved in detecting cold in naïve animals. Following mustard oil, a TRPA1 activator, naked mole-rats responded similarly to mice. Conversely, icilin, a TRPM8 agonist, did not evoke pain behavior in naked mole-rats when compared with mice. Finally, we used RNAscope to probe for TRPA1 and TRPM8 messenger RNA expression in dorsal root ganglia of both species. We found increased TRPA1 messenger RNA, but decreased TRPM8 punctae in naked mole-rats when compared with mice. Our findings likely reflect species differences due to evolutionary environmental responses that are not easily explained by differences in receptor expression between the species.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475789PMC
http://dx.doi.org/10.1177/1744806920955103DOI Listing

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