SK channel modulation rescues striatal plasticity and control over habit in cannabinoid tolerance

Nat Neurosci. 2012 Jan 8;15(2):284-93. doi: 10.1038/nn.3022.

Abstract

Endocannabinoids (eCBs) regulate neuronal activity in the dorso-lateral striatum (DLS), a brain region that is involved in habitual behaviors. How synaptic eCB signaling contributes to habitual behaviors under physiological and pathological conditions remains unclear. Using a mouse model of cannabinoid tolerance, we found that persistent activation of the eCB pathway impaired eCB-mediated long-term depression (LTD) and synaptic depotentiation in the DLS. The loss of eCB LTD, occurring preferentially at cortical connections to striatopallidal neurons, was associated with a shift in behavioral control from goal-directed action to habitual responding. eCB LTD and behavioral alterations were rescued by in vivo modulation of small-conductance calcium activated potassium channel (SK channel) activity in the DLS, which potentiates eCB signaling. Our results reveal a direct relationship between drug tolerance and changes in control of instrumental performance by establishing a central role for eCB LTD in habit expression. In addition, SK channels emerge as molecular targets to fine tune the eCB pathway under pathological conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apamin / pharmacology
  • Benzamides / pharmacology
  • Biophysics
  • Cannabinoids / administration & dosage*
  • Cannabinoids / agonists
  • Cannabinoids / antagonists & inhibitors
  • Carbamates / pharmacology
  • Conditioning, Operant / drug effects
  • Corpus Striatum / cytology
  • Corpus Striatum / drug effects*
  • Cyclohexanols / pharmacokinetics
  • Dose-Response Relationship, Drug
  • Dronabinol / pharmacology
  • Drug Tolerance / physiology*
  • Electric Stimulation
  • Enzyme Inhibitors / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Guanosine 5'-O-(3-Thiotriphosphate) / pharmacokinetics
  • Habits*
  • Long-Term Synaptic Depression / drug effects
  • Long-Term Synaptic Depression / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Motor Activity / drug effects
  • Okadaic Acid / pharmacology
  • Patch-Clamp Techniques
  • Piperidines / pharmacology
  • Protein Binding / drug effects
  • Pyrazoles / pharmacology
  • Rimonabant
  • Small-Conductance Calcium-Activated Potassium Channels / metabolism*
  • Sodium Channel Blockers / pharmacology
  • Tritium / pharmacokinetics

Substances

  • Benzamides
  • Cannabinoids
  • Carbamates
  • Cyclohexanols
  • Enzyme Inhibitors
  • Piperidines
  • Pyrazoles
  • Small-Conductance Calcium-Activated Potassium Channels
  • Sodium Channel Blockers
  • cyclohexyl carbamic acid 3'-carbamoylbiphenyl-3-yl ester
  • Tritium
  • Okadaic Acid
  • Apamin
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • AM 251
  • Dronabinol
  • 3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol
  • Rimonabant