A neural circuit for alcohol withdrawal-induced hyperalgesia in a nondependent state

Abstract

Alcohol use disorder is highly prevalent worldwide, with characteristically severe pain sensitivity during withdrawal. Here, we established a mouse model of hyperalgesia during ethanol withdrawal (EW) before addiction to investigate the window for onset and underlying mechanisms. Viral tracing with in vivo microendoscopic and two-photon calcium imaging identified a circuit pathway from dorsal hippocampal CA1 glutamatergic neurons (dCA1 Glu ) to anterior cingulate cortex glutamatergic neurons (ACC Glu ) activated in EW mice with hyperalgesia. Chemogenetic inhibition of this pathway can alleviate hyperalgesia in EW mice, whereas artificial activation recapitulates EW-induced hyperalgesia in naïve mice. These findings demonstrate that the dCA1 Glu → ACC Glu neuronal pathway participates in driving EW-induced hyperalgesia before ethanol dependence in mice.

Neurotransmitters

• Dopamine
• Endorphins
• GABA (Gamma-Aminobutyric Acid)
• Glutamate
• Serotonin (5-HT)

Related

• Alcohol