PMID- 17379421 OWN - NLM STAT- MEDLINE DCOM- 20070703 LR - 20220309 IS - 0306-4522 (Print) IS - 0306-4522 (Linking) VI - 146 IP - 3 DP - 2007 May 25 TI - Role of peripheral mu-opioid receptors in inflammatory orofacial muscle pain. PG - 1346-54 AB - The aims of this project were to investigate whether inflammation in the orofacial muscle alters mu opioid receptor (MOR) mRNA and protein expressions in trigeminal ganglia (TG), and to assess the contribution of peripheral MORs under acute and inflammatory muscle pain conditions. mRNA and protein levels for MOR were quantified by reverse-transcription-polymerase chain reaction (RT-PCR) and Western blot, respectively, from the TG of naive rats, and compared with those from the rats treated with complete Freund's adjuvant (CFA) in the masseter. TG was found to express mRNA and protein for MOR, and CFA significantly up-regulated both MOR mRNA and protein by 3 days following the inflammation. The MOR protein up-regulation persisted to day 7 and returned to the baseline level by day 14. We then investigated whether peripheral application of a MOR agonist, D-Ala2, N-Me-Phe4, Gly5-ol-enkephalin acetate salt (DAMGO), attenuates masseter nociception induced by masseteric infusion of hypertonic saline (HS) in lightly anesthetized rats. DAMGO (1, 5, 10 microg) or vehicle was administered directly into the masseter 5-10 min prior to the HS infusion. The DAMGO effects were assessed on mean peak counts (MPC) and overall magnitude as calculated by the area under the curve (AUC) of the HS-evoked behavioral responses. Under this condition, only the highest dose of DAMGO (10 microg) significantly reduced MPC, which was prevented when H-D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 (CTAP), a selective MOR antagonist, was co-administered. DAMGO pre-treatment in the contralateral masseter did not attenuate MPC. The same doses of DAMGO administered into CFA-inflamed rats, however, produced a greater attenuation of both MPC and AUC of HS-evoked nocifensive responses. These results demonstrated that activation of peripheral MOR provides greater anti-nociception in inflamed muscle, and that the enhanced MOR effect can be partly explained by significant up-regulation of MOR expression in TG. FAU - Nunez, S AU - Nunez S AD - Department of Biomedical Sciences, Program in Neuroscience, University of Maryland Baltimore School of Dentistry, 650 West Baltimore Street, Baltimore, MD 21201, USA. FAU - Lee, J-S AU - Lee JS FAU - Zhang, Y AU - Zhang Y FAU - Bai, G AU - Bai G FAU - Ro, J Y AU - Ro JY LA - eng PT - Journal Article DEP - 20070326 PL - United States TA - Neuroscience JT - Neuroscience JID - 7605074 RN - 0 (Analgesics, Opioid) RN - 0 (Receptors, Opioid, mu) RN - 100929-53-1 (Enkephalin, Ala(2)-MePhe(4)-Gly(5)-) RN - 9007-81-2 (Freund's Adjuvant) SB - IM MH - Analgesics, Opioid/pharmacology MH - Animals MH - Behavior, Animal/physiology MH - Blotting, Western MH - Dose-Response Relationship, Drug MH - Enkephalin, Ala(2)-MePhe(4)-Gly(5)-/pharmacology MH - Facial Pain/*physiopathology/psychology MH - Freund's Adjuvant MH - Functional Laterality/physiology MH - Inflammation/chemically induced/*physiopathology/psychology MH - Male MH - Masseter Muscle/metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, Opioid, mu/biosynthesis/genetics/*physiology MH - Reverse Transcriptase Polymerase Chain Reaction MH - Trigeminal Ganglion/metabolism EDAT- 2007/03/24 09:00 MHDA- 2007/07/04 09:00 CRDT- 2007/03/24 09:00 PHST- 2006/12/04 00:00 [received] PHST- 2007/02/07 00:00 [revised] PHST- 2007/02/09 00:00 [accepted] PHST- 2007/03/24 09:00 [pubmed] PHST- 2007/07/04 09:00 [medline] PHST- 2007/03/24 09:00 [entrez] AID - S0306-4522(07)00173-X [pii] AID - 10.1016/j.neuroscience.2007.02.024 [doi] PST - ppublish SO - Neuroscience. 2007 May 25;146(3):1346-54. doi: 10.1016/j.neuroscience.2007.02.024. Epub 2007 Mar 26.