6-methyl-2-(phenylethynyl)pyridine and Peripheral-Nerve-Injuries

6-methyl-2-(phenylethynyl)pyridine has been researched along with Peripheral-Nerve-Injuries* in 2 studies

Other Studies

2 other study(ies) available for 6-methyl-2-(phenylethynyl)pyridine and Peripheral-Nerve-Injuries

ArticleYear
Metabotropic Glutamate Receptor 5 and 8 Modulate the Ameliorative Effect of Ultramicronized Palmitoylethanolamide on Cognitive Decline Associated with Neuropathic Pain.
    International journal of molecular sciences, 2019, Apr-09, Volume: 20, Issue:7

    This study investigated whether metabotropic glutamate receptor (mGluR) 5 and 8 are involved in the effect of ultramicronizedpalmitoylethanolamide (um-PEA) on the cognitive behavior and long term potentiation (LTP) at entorhinal cortex (LEC)-dentate gyrus (DG) pathway in mice rendered neuropathic by the spare nerve injury (SNI). SNI reduced discriminative memory and LTP. Um-PEA treatment started after the development of neuropathic pain had no effects in sham mice, whereas it restored cognitive behavior and LTP in SNI mice. 2-Methyl-6-(phenylethynyl) pyridine (MPEP), a selective mGluR5 antagonist, improved cognition in SNI mice and produced a chemical long term depression of the field excitatory postsynaptic potentials (fEPSPs) in sham and SNI mice. After theta burst stimulation (TBS) MPEP restored LTP in SNI mice. In combination with PEA, MPEP antagonized the PEA effect on discriminative memory and decreased LTP in SNI mice. The (RS)-4-(1-amino-1-carboxyethyl)phthalic acid (MDCPG), a selective mGluR8 antagonist, did not affect discriminative memory, but it induced a chemical LTP and prevented the enhancement of fEPSPs after TBS in SNI mice which were treated or not treated with PEA. The effect of PEA on LTP and cognitive behavior was modulated by mGluR5 and mGluR8. In particular in the SNI conditions, the mGluR5 blockade facilitated memory and LTP, but prevented the beneficial effects of PEA on discriminative memory while the mGluR8 blockade, which was ineffective in itself, prevented the favorable action of the PEA on LTP. Thus, although their opposite roles (excitatory/inhibitory of the two receptor subtypes on the glutamatergic system), they appeared to be required for the neuroprotective effect of PEA in conditions of neuropathic pain.

    Topics: Amides; Animals; Dentate Gyrus; Disease Models, Animal; Ethanolamines; Excitatory Postsynaptic Potentials; Humans; Long-Term Potentiation; Male; Memory; Mice; Neuralgia; Olfactory Cortex; Palmitic Acids; Peripheral Nerve Injuries; Pyridines; Receptor, Metabotropic Glutamate 5; Receptors, Metabotropic Glutamate

2019
The mGluR5 antagonist fenobam induces analgesic conditioned place preference in mice with spared nerve injury.
    PloS one, 2014, Volume: 9, Issue:7

    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.

    Topics: Analgesics; Animals; Conditioning, Classical; Excitatory Amino Acid Antagonists; Female; Imidazoles; Male; Mice; Mice, Inbred C57BL; Morphine; Peripheral Nerve Injuries; Pyridines; Receptor, Metabotropic Glutamate 5

2014