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Neuron. 2010 Nov 4;68(3):500-11. doi: 10.1016/j.neuron.2010.09.026.

Dopaminergic modulation of axon initial segment calcium channels regulates action potential initiation.

Author information

1
Oregon Hearing Research Center, Oregon Health and Science University, Portland, OR 97239, USA. benderke@ohsu.edu

Abstract

Action potentials initiate in the axon initial segment (AIS), a specialized compartment enriched with Na(+) and K(+) channels. Recently, we found that T- and R-type Ca(2+) channels are concentrated in the AIS, where they contribute to local subthreshold membrane depolarization and thereby influence action potential initiation. While periods of high-frequency activity can alter availability of AIS voltage-gated channels, mechanisms for long-term modulation of AIS channel function remain unknown. Here, we examined the regulatory pathways that control AIS Ca(2+) channel activity in brainstem interneurons. T-type Ca(2+) channels were downregulated by dopamine receptor activation acting via protein kinase C, which in turn reduced neuronal output. These effects occurred without altering AIS Na(+) or somatodendritic T-type channel activity and could be mediated by endogenous dopamine sources present in the auditory brainstem. This pathway represents a new mechanism to inhibit neurons by specifically regulating Ca(2+) channels directly involved in action potential initiation.

PMID:
21040850
PMCID:
PMC2987607
DOI:
10.1016/j.neuron.2010.09.026
[Indexed for MEDLINE]
Free PMC Article

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