Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain

Dedek, A.; Xu, J.; Lorenzo, L.-E.; Godin, A. G.; Kandegedara, C. M.; Glavina, G.; Landrigan, J. A.; Lombroso, P. J.; De Koninck, Y.; Tsai, E. C.; Hildebrand, M. E.

doi:10.1101/2021.06.15.447407

bioRxiv · 10.1101/2021.06.15.447407

Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain

Dedek, A.·Xu, J.·Lorenzo, L.-E.·Godin, A. G.·Kandegedara, C. M.·Glavina, G.·Landrigan, J. A.·Lombroso, P. J.·De Koninck, Y.·Tsai, E. C.·Hildebrand, M. E.

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Abstract

The prevalence and severity of many chronic pain syndromes differ across sex, and recent studies have identified differences in immune signalling within spinal nociceptive circuits as a potential mediator. Although it has been proposed that sex-specific pain mechanisms converge once they reach neurons within the superficial dorsal horn (SDH), direct investigations using rodent and human preclinical pain models have been lacking. Here, we discovered that in the Freunds Adjuvant in vivo model of inflammatory pain, where both male and female rats display tactile allodynia, a pathological coupling between KCC2-dependent disinhibition and NMDA receptor potentiation within SDH neurons was observed in male but not female rats. Unlike males, the neuroimmune mediator, BDNF, failed to downregulate inhibitory signalling elements (KCC2 and STEP61) and upregulate excitatory elements (pFyn, GluN2B, and pGluN2B) in female rats, resulting in no effect of ex vivo BDNF on synaptic NMDA receptor responses in female lamina I neurons. Importantly, this sex difference in spinal pain processing was conserved from rodents to humans. As in rodents, ex vivo spinal treatment with BDNF downregulated markers of disinhibition and upregulated markers of facilitated excitation in SDH neurons from male but not female human organ donors. Ovariectomy in female rats recapitulated the male pathological pain neuronal phenotype, with BDNF driving a coupling between disinhibition and NMDA receptor potentiation in adult lamina I neurons following the prepubescent elimination of sex hormones in females. This discovery of sexual dimorphism in a central neuronal mechanism of chronic pain across species provides a foundational step towards a better understanding and treatment for pain in both sexes.

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Dedek, A., Xu, J., Lorenzo, L.-E., Godin, A. G., Kandegedara, C. M., Glavina, G., Landrigan, J. A., Lombroso, P. J., De Koninck, Y., Tsai, E. C., Hildebrand, M. E.. 2021-06-16. Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain. https://doi.org/10.1101/2021.06.15.447407

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