Glutamate co-transmission from developing medial nucleus of the trapezoid body--lateral superior olive synapses is cochlear dependent in kanamycin-treated rats

Biochem Biophys Res Commun. 2011 Feb 11;405(2):162-7. doi: 10.1016/j.bbrc.2010.12.129. Epub 2011 Jan 5.

Abstract

Cochlear dependency of glutamate co-transmission at the medial nucleus of the trapezoid body (MNTB)--the lateral superior olive (LSO) synapses was investigated using developing rats treated with high dose kanamycin. Rats were treated with kanamycin from postnatal day (P) 3 to P8. A scanning electron microscopic study on P9 demonstrated partial cochlear hair cell damage. A whole cell voltage clamp experiment demonstrated the increased glutamatergic portion of postsynaptic currents (PSCs) elicited by MNTB stimulation in P9-P11 kanamycin-treated rats. The enhanced VGLUT3 immunoreactivities (IRs) in kanamycin-treated rats and asymmetric VGLUT3 IRs in the LSO of unilaterally cochlear ablated rats supported the electrophysiologic data. Taken together, it is concluded that glutamate co-transmission is cochlear-dependent and enhanced glutamate co-transmission in kanamycin-treated rats is induced by partial cochlear damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cochlea / drug effects
  • Cochlea / growth & development*
  • Cochlea / metabolism
  • Female
  • Glutamic Acid / metabolism*
  • Hair Cells, Auditory / drug effects
  • Hair Cells, Auditory / metabolism*
  • Kanamycin / pharmacology
  • Olivary Nucleus / drug effects
  • Olivary Nucleus / growth & development*
  • Olivary Nucleus / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Glutamate / metabolism
  • Synapses / drug effects
  • Synapses / metabolism*
  • Vesicular Glutamate Transport Proteins / metabolism

Substances

  • Receptors, Glutamate
  • Slc17a8 protein, rat
  • Vesicular Glutamate Transport Proteins
  • Glutamic Acid
  • Kanamycin