Submitted on August 18, 2006
Accepted on November 27, 2006
Endogenous mGluR Activity Suppresses GABAergic Transmission in Avian Cochlear Nucleus Magnocellularis Neurons
Yong Lu1*
1 Department of Neurobiology, Northeastern Ohio Universities College of Medicine (NEOUCOM), Rootstown, Ohio, United States
* To whom correspondence should be addressed. E-mail: ylu{at}neoucom.edu.
GABAergic transmission in the avian cochlear nucleus magnocellularis (NM) of the chick is subject to modulation by GABAB autoreceptors (Lu et al. 2005). Here, I investigated modulation of GABAergic transmission in NM by metabotropic glutamate receptors (mGluRs) with whole-cell recordings in brain slice preparations. I found that tACPD, a non-specific mGluR agonist, exerted dose-dependent suppression on evoked inhibitory postsynaptic currents (eIPSCs) in NM neurons. At concentrations of 100 or 200 µM, tACPD increased the failure rate of GABAergic transmission. Agonists for group I (3,5-DHPG, 200 µM), II (DCG-IV, 2 µM), and III (L-AP4, 10 µM) mGluRs produced a significant reduction in the amplitude of eIPSCs, and a significant increase in failure rate, indicating the involvement of multiple mGluRs in this modulation. The frequency, but not the amplitude, of miniature IPSCs (mIPSCs) was decreased significantly by 3,5-DHPG or DCG-IV. Neither frequency nor amplitude of mIPSCs was affected by L-AP4. mGluR antagonists LY341495 (20 µM) plus CPPG (10 µM) significantly increased the amplitude of eIPSCs, indicating that endogenous mGluR activity suppresses GABA release to NM neurons. Furthermore, blockage of mGluRs increased GABA-evoked discharges recorded under physiological Cl- concentrations, whereas tACPD (100 µM) eliminated them. The results indicate that mGluRs play important roles in achieving balanced excitation and inhibition in NM, and preserving fidelity of temporal information encoded by NM neurons.
