Circuit-dependent striatal PKA and ERK signaling underlies rapid behavioral shift in mating reaction of male mice

Proc Natl Acad Sci U S A. 2015 May 26;112(21):6718-23. doi: 10.1073/pnas.1507121112. Epub 2015 May 11.

Abstract

The selection of reward-seeking and aversive behaviors is controlled by two distinct D1 and D2 receptor-expressing striatal medium spiny neurons, namely the direct pathway MSNs (dMSNs) and the indirect pathway MSNs (iMSNs), but the dynamic modulation of signaling cascades of dMSNs and iMSNs in behaving animals remains largely elusive. We developed an in vivo methodology to monitor Förster resonance energy transfer (FRET) of the activities of PKA and ERK in either dMSNs or iMSNs by microendoscopy in freely moving mice. PKA and ERK were coordinately but oppositely regulated between dMSNs and iMSNs by rewarding cocaine administration and aversive electric shocks. Notably, the activities of PKA and ERK rapidly shifted when male mice became active or indifferent toward female mice during mating behavior. Importantly, manipulation of PKA cascades by the Designer Receptor recapitulated active and indifferent mating behaviors, indicating a causal linkage of a dynamic activity shift of PKA and ERK between dMSNs and iMSNs in action selection.

Keywords: action selection; dorsal striatum; in vivo FRET imaging; mating behavior; microendoscope.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cocaine / administration & dosage
  • Corpus Striatum / physiology*
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Electroshock
  • Female
  • Fluorescence Resonance Energy Transfer / instrumentation
  • Fluorescence Resonance Energy Transfer / methods
  • MAP Kinase Signaling System*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Receptors, Dopamine D1 / physiology
  • Receptors, Dopamine D2 / physiology
  • Reward
  • Sexual Behavior, Animal / physiology*

Substances

  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Cyclic AMP-Dependent Protein Kinases
  • Cocaine