Activation of Parvalbumin Neurons in the Rostro-Dorsal Sector of the Thalamic Reticular Nucleus Promotes Sensitivity to Pain in Mice. (16th December 2017)

• Record Type: Journal Article
• Authors: Liu, Jing; Zhang, Meng-Qi; Wu, Xu; Lazarus, Michael; Cherasse, Yoan; Yuan, Mao-Yun; Huang, Zhi-Li; Li, Rui-Xi
• Is Part Of: Neuroscience. Volume 366(2017)
• Page Start: 113
• Page End: 123
• Publication Date: 2017-12-16
• Subjects: ABC avidin–biotin complex -- AD anterodorsal thalamic nucleus -- AM anteromedial thalamic nucleus -- AV anteroventral thalamic nucleus -- DREADD designer receptors exclusively activated by designer drugs -- EGTA ethylene glycol-bis(β-aminoethyl ether)-N, N, N′, N′-tetraacetic acid) -- HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid -- hrGFP humanized Renilla green fluorescent protein -- ic internal capsule -- LD laterodorsal thalamic nucleus -- LGP lateral globus pallidus -- MD mediodorsal thalamic nucleus -- PT paratenial thalamic nucleus -- PV parvalbumin -- TRN thalamic reticular nucleus -- TRNrd rostro-dorsal sector of TRN; thalamic reticular nucleus -- PV-Cre mouse -- pain regulation -- pharmacogenetics -- optogenetics; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2017.10.013
• Languages: English
• ISSNs: 0306-4522

Abstract

Highlights: Activation of PV neurons in the TRNrd promotes sensitivity to pain in mice. PV neurons in the TRNrd mainly projected to the AD, PT, AV, AM, MD, LD. PV neurons in the TRNrd inhibited neurons in the AD and PT by synaptic connection. Abstract: The calcium-binding protein, parvalbumin (PV), is highly expressed in thalamic reticular nucleus (TRN) GABAergic neurons, which receive input from the cerebral cortex and thalamus and send inhibitory output to the thalamic relay nucleus. Previous studies suggest that the TRN is involved in pain regulation as an important relay nucleus of the ascending pain pathway. However, little is known about its functional role in pain regulation and interconnectivity. In our study, the role of rostro-dorsal sector of TRN (TRNrd) PV-positive neurons in pain regulation was studied using chemogenetics based on designer receptors exclusively activated by designer drugs (DREADD). Then, projections from the TRNrd PV-positive neurons were explored using PV-Cre transgenic mice, conditional anterograde axonal tract tracing, and optogenetics, combined with immunohistochemistry and electrophysiology. The results showed that activation of PV-positive neurons in the TRNrd decreased the mechanical threshold and thermal latency of behaving mice during the light period when neuronal activity was low. Furthermore, the anterodorsal and paratenial thalamic nucleus received innervation from PV-positive neurons in the TRNrd. They were specifically inhibited by GABA, which is released from local axonal endings of PV neurons. These findings indicate that activation of PV neurons in the TRNrd increases pain sensitivity in PV-Cre transgenic mice.