The mGluR5 antagonist fenobam induces analgesic conditioned place preference in mice with spared nerve injury

• Published in: PloS one 2014-07, Vol.9 (7), p.e103524-e103524
• Main Authors: Lax, Neil C, George, David C, Ignatz, Christopher, Kolber, Benedict J
• Format: Article
• Language: English
• Subjects: Analgesics; Analgesics - pharmacology; Animals; Antagonism; Behavior; Biochemistry; Biology and Life Sciences; Chronic pain; Cognitive ability; Comparative analysis; Conditioning; Conditioning, Classical - drug effects; Consortia; Drug dosages; Excitatory Amino Acid Antagonists - pharmacology; Female; Gender differences; Glutamate; Glutamic acid receptors (metabotropic); Imidazoles - pharmacology; Injuries; Male; Medicine and Health Sciences; Mice; Mice, Inbred C57BL; Morphine; Morphine - pharmacology; Neurosciences; Pain; Peripheral Nerve Injuries - physiopathology; Place preference conditioning; Pyridines - pharmacology; Receptor, Metabotropic Glutamate 5 - antagonists & inhibitors; Receptors; Rodents; Spinal cord; Surgery
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0103524

Antagonists of metabotropic glutamate receptors (mGluRs) have the potential to act as analgesic drugs that may help alleviate chronic pain. This study was done to look at the possible rewarding properties of the mGluR5 antagonist, fenobam, in a cognitive assay. Analgesic conditioned place preference (aCPP) was used to examine the effects of fenobam (30 mg/kg) and the prototypical mGluR5 antagonist, MPEP, and these effects were compared to those of a drug with known analgesic properties, morphine (10 mg/kg). In each experiment, one group of mice received spared nerve injury (SNI) surgery to model chronic pain; the other group received a control sham surgery. Both fenobam and MPEP induced preference in the SNI mice, such that SNI mice spent significantly more time in the mGluR5 antagonist-paired chamber compared to a vehicle-paired chamber. No such preference developed for sham mice. Morphine induced preference in male and female mice in both the SNI and sham groups. The results showed that fenobam and MPEP likely reduced on-going distress in the SNI mice, causing them to prefer the chamber paired with the drug compared to the vehicle-paired chamber. Since sham animals did not prefer the drug-paired chamber, these data demonstrate that mGluR5 antagonism is non-rewarding in the absence of pain-like injury.