Modulation of Pain Sensitivity by the Locus Coeruleus-Paraventricular Thalamic Nucleus-Anterior Cingulate Cortex Pathway in Mice.

Abstract

Noradrenergic projections from the locus coeruleus (LC) to the thalamus and anterior cingulate cortex (ACC) contribute to pain-like behaviors, yet their hierarchical organization remains unclear. This article examines how locus coeruleus-derived norepinephrine inputs to the paraventricular thalamic nucleus (PVA) and ACC differentially regulate nociceptive sensitization. In adult male and female mice, complete Freund's adjuvant was used to induce pain-like behaviors. To examine functional connectivity among locus coeruleus, PVA, and ACC, targeted recombination in active populations (Fos-TRAP), in vivo recordings, and viral tracing were combined. Then optogenetic and chemogenetic tools were used to selectively manipulate locus coeruleus projections and assess their impact on neural activity and pain behaviors. Complete Freund's adjuvant led to enhanced c-Fos expression in locus coeruleus, PVA, and ACC (cells per microscopic field; locus coeruleus: 13.60 ± 2.24 vs. 44.50 ± 7.72; PVA: 8.00 ± 1.58 vs. 66.40 ± 9.45; ACC: 12.80 ± 2.28 vs. 36.70 ± 2.59; P < 0.001), alongside increased γ-band activity and single-unit firing rates. Monosynaptic LC-ACC and polysynaptic LC-PVA-ACC circuits were identified. Notably, nociception-related locus coeruleus neurons preferentially projected to PVA, which subsequently targeted hyperactive ACC neurons. Under inflammatory pain conditions, activation of the LC-PVA-ACC circuits evoked greater ACC firing (Hz; LC-PVA-ACC vs. LC-ACC: 15.75 ± 2.88 vs. 9.72 ± 2.06; P < 0.001) and tactile stimulus-evoked responses (Hz; 22.98 ± 2.60 vs. 15.34 ± 1.86; P < 0.001) than direct LC-ACC activation. Consistently, optogenetic or chemogenetic manipulation of the LC-PVA-ACC circuit produced stronger modulation of mechanical and thermal pain sensitivity than direct LC-ACC stimulation. This study identified the LC-PVA-ACC pathway as a hierarchical noradrenergic circuit that modulates nociceptive sensitization via a thalamocortical relay, thereby revealing a circuit-specific mechanism by which the locus coeruleus-norepinephrine system regulates pain processing.