Scaling Up Cortical Control Inhibits Pain

Jahrane Dale(New York University), Haocheng Zhou(Central South University), Qiaosheng Zhang(New York University), Erik Martinez(New York University), Sile Hu(New York University), Kevin Liu(New York University), Louise Urien(New York University), Zhe Chen(New York University), Jing Wang(New York University)
Cell Reports
May 1, 2018
Cited by 90Open Access
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Abstract

Acute pain evokes protective neural and behavioral responses. Chronic pain, however, disrupts normal nociceptive processing. The prefrontal cortex (PFC) is known to exert top-down regulation of sensory inputs; unfortunately, how individual PFC neurons respond to an acute pain signal is not well characterized. We found that neurons in the prelimbic region of the PFC increased firing rates of the neurons after noxious stimulations in free-moving rats. Chronic pain, however, suppressed both basal spontaneous and pain-evoked firing rates. Furthermore, we identified a linear correlation between basal and evoked firing rates of PFC neurons, whereby a decrease in basal firing leads to a nearly 2-fold reduction in pain-evoked response in chronic pain states. In contrast, enhancing basal PFC activity with low-frequency optogenetic stimulation scaled up prefrontal outputs to inhibit pain. These results demonstrate a cortical gain control system for nociceptive regulation and establish scaling up prefrontal outputs as an effective neuromodulation strategy to inhibit pain.


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