Figure 7From: Metabotropic glutamate receptor 5 contributes to inflammatory tongue pain via extracellular signal-regulated kinase signaling in the trigeminal spinal subnucleus caudalis and upper cervical spinal cord Neuronal localization and expression of mGluR and effects of continuous i.t. administration of the mGluR5 antagonist, MPEP, on CFA-induced ERK phosphorylation. Photomicrographs of mGluR5 (A) and NeuN (B) staining in the Vc following noxious mechanical stimulation of the tongue on day 8 after CFA injection. (C) Overlay of the double imunofluoresence labeling, showing the neuronal nature of mGluR5-IR cells. Arrows indicate the double-labeled cells. (D, E, F) Photomicrographs of mGluR5 (D) and pERK (E) staining in the Vc on day 8 after CFA injection. (F) Overlay of the double imunofluoresence labeling, suggesting the colocalization of mGluR5 with pERK (arrows). (G) Normalized amount of mGluR5 protein in Vc and C1-C2 on day 8 after saline or CFA injection into the tongue. β-actin was used as a loading control. The mean number of noxious stimuli-triggered pERK-IR cells in the ipsilateral (H) and contralateral (I) Vc and C1-C2 on day 8 after CFA injection into the tongue with continuous i.t. administration of MPEP or saline. MPEP administration effectively decreased CFA-induced pERK upregulation. n = 4 in each group. Error bars indicate SEM.Back to article page