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New Research, Sensory and Motor Systems

Group II metabotropic glutamate receptors modulate sound evoked and spontaneous activity in the mouse inferior colliculus

Inga Kristaponyte, Nichole L. Beebe, Jesse W. Young, Sharad J. Shanbhag, Brett R. Schofield and Alexander V. Galazyuk
eNeuro 17 December 2020, ENEURO.0328-20.2020; https://doi.org/10.1523/ENEURO.0328-20.2020
Inga Kristaponyte
1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA
2Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA, and Kent State University, Kent, Ohio 44240
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Nichole L. Beebe
1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA
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Jesse W. Young
1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA
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Sharad J. Shanbhag
1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA
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Brett R. Schofield
1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA
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Alexander V. Galazyuk
1Department of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH, USA
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Abstract

Little is known about the functions of group II metabotropic glutamate receptors (mGluRs2/3) in the inferior colliculus (IC)—a midbrain structure that is a major integration region of the central auditory system. We investigated how these receptors modulate sound-evoked and spontaneous firing in the mouse IC in vivo. We first performed immunostaining and tested hearing thresholds to validate VGAT-ChR2 transgenic mice on a mixed CBA/CaJ x C57BL/6J genetic background. Transgenic animals allowed for optogenetic cell type identification. Extracellular single neuron recordings were obtained before and after pharmacological mGluR2/3 activation. We observed increased sound-evoked firing—as assessed by the rate-level functions—in a subset of both GABAergic and non-GABAergic IC neurons following mGluR2/3 pharmacological activation. These neurons also displayed elevated spontaneous excitability and were distributed throughout the IC area tested, suggesting a widespread mGluR2/3 distribution in the mouse IC.

Significance Glutamate is the primary excitatory neurotransmitter in the brain. It binds to both ionotropic and metabotropic glutamate receptors. Fast ionotropic receptors generate rapid synaptic transmission, whereas slower metabotropic glutamate receptors (mGluRs) modulate this synaptic transmission. Here, we discovered that activation of group II mGluRs enhances sound-evoked and spontaneous neuronal firing in the inferior colliculus-the hub of the central auditory system. We used transgenic mice which allowed for identification of excitatory and inhibitory neurons and found that both these cell types are modulated by group II mGluRs. Our results provide better understanding of mGluR modulatory roles, which is crucial in opening avenues for using mGluR-targeting drugs to treat hearing disorders.

  • auditory
  • GABAergic
  • LY354740
  • mGluR2/3
  • neuromodulation
  • non-GABAergic

Footnotes

  • Authors report no conflict of interest.

  • HHS | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) [R01 DC016918]; HHS | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) [R01 DC004391]

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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Group II metabotropic glutamate receptors modulate sound evoked and spontaneous activity in the mouse inferior colliculus
Inga Kristaponyte, Nichole L. Beebe, Jesse W. Young, Sharad J. Shanbhag, Brett R. Schofield, Alexander V. Galazyuk
eNeuro 17 December 2020, ENEURO.0328-20.2020; DOI: 10.1523/ENEURO.0328-20.2020

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Group II metabotropic glutamate receptors modulate sound evoked and spontaneous activity in the mouse inferior colliculus
Inga Kristaponyte, Nichole L. Beebe, Jesse W. Young, Sharad J. Shanbhag, Brett R. Schofield, Alexander V. Galazyuk
eNeuro 17 December 2020, ENEURO.0328-20.2020; DOI: 10.1523/ENEURO.0328-20.2020
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Keywords

  • auditory
  • GABAergic
  • LY354740
  • mGluR2/3
  • neuromodulation
  • non-GABAergic

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