Tolerance to Morphine-Induced Inhibition of TTX-R Sodium Channels in Dorsal Root Ganglia Neurons Is Modulated by Gut-Derived Mediators

• Published in: iScience Vol. 2; pp. 193 - 209
• Main Authors: Mischel, Ryan A., Dewey, William L., Akbarali, Hamid I.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 27.04.2018; Elsevier
• Subjects: Cellular Neuroscience; Microbiome; Neuroscience; Neuroscience; Cellular Neuroscience; Microbiome
• ISSN: 2589-0042; 2589-0042
• DOI: 10.1016/j.isci.2018.03.003

In the clinical setting, analgesic tolerance is a primary driver of diminished pain control and opioid dose escalations. Integral to this process are primary afferent sensory neurons, the first-order components of nociceptive sensation. Here, we characterize the factors modulating morphine action and tolerance in mouse small diameter dorsal root ganglia (DRG) neurons. We demonstrate that acute morphine inactivates tetrodotoxin-resistant (TTX-R) Na+ channels in these cells. Chronic exposure resulted in tolerance to this effect, which was prevented by treatment with oral vancomycin. Using colonic supernatants, we further show that mediators in the gut microenvironment of mice with chronic morphine exposure can induce tolerance and hyperexcitability in naive DRG neurons. Tolerance (but not hyperexcitability) in this paradigm was mitigated by oral vancomycin treatment. These findings collectively suggest that gastrointestinal microbiota modulate the development of morphine tolerance (but not hyperexcitability) in nociceptive primary afferent neurons, through a mechanism involving TTX-R Na+ channels. [Display omitted] •Gram-positive gut bacteria depletion prevents morphine antinociceptive tolerance•Tolerance develops to morphine inhibition of TTX-R Na+ channels in DRG neurons•Tolerance in isolated DRG neurons is mitigated by Gram-positive bacteria depletion•Morphine-induced gut mediators produce tolerance in DRG neurons Neuroscience; Cellular Neuroscience; Microbiome