%A Hussein,Rama Ashraf %A Ahmed,Marwa %A Breitinger,Hans-Georg %A Breitinger,Ulrike %D 2019 %J Frontiers in Molecular Neuroscience %C %F %G English %K Nociception,Glycinergic transmission,spinal α3 glycine receptors,glucose modulation,patch-clamp recording,Pain-related behaviour,tactile sensitivity,Hotplate assay,In vivo testing %Q %R 10.3389/fnmol.2019.00280 %W %L %M %P %7 %8 2019-November-22 %9 Brief Research Report %# %! Glycine receptors mediate glucose analgesia %* %< %T Modulation of Glycine Receptor-Mediated Pain Signaling in vitro and in vivo by Glucose %U https://www.frontiersin.org/articles/10.3389/fnmol.2019.00280 %V 12 %0 JOURNAL ARTICLE %@ 1662-5099 %X The inhibitory glycine receptor (GlyR) plays an important role in rapid synaptic inhibition in mammalian spinal cord, brainstem, higher brain centers, and is involved in transmission of nociceptive signals. Glucose and related mono- and disaccharides potentiate currents mediated by recombinant α1, α1-β, and α3 GlyRs. Here, we confirmed the specific potentiation of α3 GlyR signaling by glucose through: (i) patch-clamp electrophysiology on recombinant receptors; and (ii) by verifying in vitro data in a mouse model in vivo. Mice were intraperitoneally (IP) injected with glucose (2 g/kg) or vehicle, and then challenged with sublethal doses of strychnine (0.2 mg/kg and 0.5 mg/kg). Pain-related behavior was assessed using two established models: (i) touch sensitivity tests using von Frey filaments; and (ii) hotplate assay. We observed a reduction of pain sensitivity in glucose-treated mice relative to vehicle-treated control mice. Injection of strychnine resulted in an increased sensitivity to tactile and heat stimuli, which was reversed in the presence of glucose. Analgesic effects of glucose were more pronounced in von Frey experiments, consistent with the established use of this model for neuropathic pain. Overall, glucose showed mild analgesic effects and was able to compensate for strychnine-induced allodynia in mice. Since the action of strychnine is specific for GlyR, these experiments show for the first time an in vivo potentiation of GlyR activity by glucose and suggest a molecular mechanism for glucose-mediated analgesia.