Calcium Signaling in Mitral Cell Dendrites of Olfactory Bulbs of Neonatal Rats and Mice During Olfactory Nerve Stimulation and β-Adrenoceptor Activation

  1. Qi Yuan,
  2. Hiroki Mutoh,
  3. Franck Debarbieux, and
  4. Thomas Knöpfel1
  1. Laboratory for Neuronal Circuit Dynamics, Brain Science Institute, RIKEN, Wako-shi, Saitama, 351-0198, Japan

Abstract

Synapses formed by the olfactory nerve (ON) provide the source of excitatory synaptic input onto mitral cells (MC) in the olfactory bulb. These synapses, which relay odor-specific inputs, are confined to the distally tufted single primary dendrites of MCs, the first stage of central olfactory processing. β-adrenergic modulation of electrical and chemical signaling at these synapses may be involved in early odor preference learning. To investigate this possibility, we combined electrophysiological recordings with calcium imaging in olfactory bulb slices prepared from neonatal rats and mice. Activation of ON-MC synapses induced postsynaptic potentials, which were associated with large postsynaptic calcium transients. Neither electrical nor calcium responses were affected by β-adrenergic agonists or antagonist. Immunocytochemical analysis of MCs and their tufted dendrites revealed clear immunoreactivity with antibodies against α1A (Cav2.1, P/Q-type) and α1B (Cav2.2, N-type), but not against α1C (Cav1.2, L-type) or α1D (Cav1.3, L-type) calcium channel subunits. Moreover, nimodipine, a blocker of L-type calcium channels, had no effect on either electrical or calcium signaling at ON-MC synapses. In contrast to previous evidence, we concluded that in neonatal rats and mice (P5-P8), mitral cells do not express significant amounts of L-type calcium channels, the calcium channel type that is often targeted by β-adrenergic modulation. The absence of β-adrenergic modulation on either electrical or calcium signaling at ON-MC synapses of neonatal rats and mice excludes the involvement of this mechanism in early odor preference learning.

Footnotes

  • Article and publication are at http://www.learnmem.org/cgi/doi/10.1101/lm.75204.

    • Accepted June 3, 2004.
    • Received February 6, 2004.
| Table of Contents