Ni(2+) affects dopamine uptake which limits suitability as inhibitor of T-type voltage-gated Ca(2+) channels

ACS Chem Neurosci. 2015 Jan 21;6(1):124-9. doi: 10.1021/cn500274g. Epub 2014 Dec 5.

Abstract

Neuronal T-type voltage-gated Ca(2+) channels are reported to have physiological roles that include regulation of burst firing, Ca(2+) oscillations, and neurotransmitter release. These roles are often exposed experimentally by blocking T-type channels with micromolar Ni(2+). We used Ni(2+) to explore the role of axonal T-type channels in dopamine (DA) release in mouse striatum, but identified significant off-target effects on DA uptake. Ni(2+) (100 μM) reversibly increased electrically evoked DA release and markedly extended its extracellular lifetime, detected using fast-scan cyclic voltammetry. Prior inhibition of the DA transporter (DAT) by cocaine (5 μM) occluded the facilitatory action of Ni(2+) on DA release and conversely, allowed Ni(2+) to inhibit release, presumably through T-channel inhibition. Ni(2+) further prolonged the timecourse of DA clearance suggesting further inhibition of DA uptake. In summary, Ni(2+) has major effects on DA transmission besides those due to T-channels that likely involve inhibition of the DAT.

Keywords: Dopamine; Ni2+; T-type VGCC; dopamine transporter; voltammetry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / metabolism
  • Action Potentials / drug effects
  • Analysis of Variance
  • Animals
  • Biophysics
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels, T-Type / metabolism*
  • Corpus Striatum / cytology*
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism
  • Dihydro-beta-Erythroidine / pharmacology
  • Dopamine / metabolism*
  • Dopamine Agents / pharmacology
  • Dose-Response Relationship, Drug
  • Electric Stimulation
  • Electrochemical Techniques
  • In Vitro Techniques
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neurons / drug effects*
  • Nickel / pharmacology*

Substances

  • Calcium Channel Blockers
  • Calcium Channels, T-Type
  • Dopamine Agents
  • Dihydro-beta-Erythroidine
  • nickel chloride
  • Nickel
  • Acetylcholine
  • Dopamine