Central Metabotropic Glutamate Receptors Differentially Participate in Interleukin-1β–Induced Mechanical Allodynia in the Orofacial Area of Conscious Rats
Abstract
The present study investigated the role of central metabotropic glutamate receptors (mGluRs) in interleukin-1β (IL-1β)–induced mechanical allodynia and mirror-image mechanical allodynia in the orofacial area. Experiments were carried out on male Sprague-Dawley rats weighing 230 to 280 g. After administration of 0.01, 0.1, 1, or 10 pg of IL-1β into a subcutaneous area of the vibrissa pad, we examined the withdrawal behavioral responses produced by 10 successive trials of an air-puff ramp pressure applied ipsilaterally or contralaterally to the IL-1β injection site. Subcutaneous injection of IL-1β produced mechanical allodynia and mirror-image mechanical allodynia in the orofacial area. Intracisternal administration of CPCCOEt, a mGluR1 antagonist, or MPEP, a mGluR5 antagonist, reduced IL-1β–induced mechanical allodynia and mirror-image mechanical allodynia. Intracisternal administration of APDC, a group II mGluR agonist, or L-AP4, a group III mGluR agonist, reduced both IL-1β–induced mechanical allodynia and mirror-image mechanical allodynia. The antiallodynic effect, induced by APDC or L-AP4, was blocked by intracisternal pretreatment with LY341495, a group II mGluR antagonist, or CPPG, a group III mGluR antagonist. These results suggest that groups I, II, and III mGluRs differentially modulated IL-1β–induced mechanical allodynia, as well as mirror-image mechanical allodynia, in the orofacial area.
Perspective
Central group I mGluR antagonists and groups II and III mGluR agonists modulate IL-1β–induced mechanical allodynia and mirror-image mechanical allodynia in the orofacial area. Therefore, the central application of group I mGluR antagonists or groups II and III mGluR agonists might be of therapeutic value in treating pain disorder.
Key words: Air puffs , IL-lβ , mechanical allodynia , metabotropic glutamate receptor , mirror-image allodynia , orofacial area
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Supported by Korea Research Foundation Grant (KRF-2005-042-E00147) and by Grants of Second-phase of Brain Korea 21 Project (Ministry of Education, Korea).
PII: S1526-5900(06)00687-0
doi:10.1016/j.jpain.2006.03.007
© 2006 American Pain Society. Published by Elsevier Inc. All rights reserved.
