Skip to main content
Article
A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine-taking and cocaine-seeking behavior in rats
Addiction Biology
  • Thomas Keck, Rowan University
  • Mu-Fa Zou
  • Gui-Hua Bi
  • Hai-Ying Zhang
  • Xiao-Fei Wang
  • Hong-Ju Yang
  • Ratika Srivastava
  • Elliott L. Gardner
  • Zheng-Xiong Xi
  • Amy Hauck Newman
Document Type
Article
Version
Published Open Access
Publication Date
9-3-2013
DOI
http://dx.doi.org/10.1111/adb.12086
Abstract
Pre-clinical studies suggest that negative allosteric modulators (NAMs) of the metabotropic glutamate receptor subtype 5 (mGluR5), including 2-methyl-6-(phenylethynyl)pyridine (MPEP), 3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine (MTEP) and fenobam are highly effective in attenuating drug-taking and drug-seeking behaviors. However, both MPEP and MTEP have no translational potential for use in humans because of their off-target effects and short half-lives. Here, we report that 3-fluoro-5-[(6-methylpyridin-2-yl)ethynyl]benzonitrile (MFZ 10-7), a novel mGluR5 NAM, is more potent and selective than MPEP, MTEP and fenobam in both in vitro binding and functional assays. Similar to MTEP, intraperitoneal administration of MFZ 10-7 inhibited intravenous cocaine self-administration, cocaine-induced reinstatement of drug-seeking behavior and cocaine-associated cue-induced cocaine-seeking behavior in rats. Although MFZ 10-7 and MTEP lowered the rate of oral sucrose self-administration, they did not alter total sucrose intake. Further, MFZ 10-7 appeared to be more potent than MTEP in inducing downward shifts in the cocaine dose–response curve, but less effective than MTEP in attenuating sucrose-induced reinstatement of sucrose-seeking behavior. MFZ 10-7 and MTEP had no effect on basal locomotor behavior. These findings not only provide additional evidence supporting an important role for mGluR5 in cocaine reward and addiction, but also introduce a new tool for both in vitro and in vivo investigations with which to further characterize this role.
Comments

This article is a U.S. Government work and is in the public domain in the USA.

Published Citation
Keck, T. M., Zou, M., Bi, G., Zhang, H., Wang, X., Yang, H., . . . Newman, A. H. (2014). A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine-taking and cocaine-seeking behavior in rats: Novel mGluR5 antagonist MFZ 10-7 attenuates cocaine reward and relapse. Addiction Biology, 19(2), 195-209.
Citation Information
Thomas Keck, Mu-Fa Zou, Gui-Hua Bi, Hai-Ying Zhang, et al.. "A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine-taking and cocaine-seeking behavior in rats" Addiction Biology (2013)
Available at: http://works.bepress.com/thomas-keck/5/