Revisiting medial preoptic area plasticity induced in male mice by sexual experience

Arnaud Jean1, Pauline Bonnet1, Philippe Liere2

  • 1Sorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Neuroscience Paris - Seine; Institut de Biologie Paris Seine, 75005, Paris, France.

Scientific Reports
|December 21, 2017
PubMed

Insights

Male mice show lasting behavioral improvements after mating, linked to molecular changes in the medial preoptic area (mPOA). Sexual experience enhances neuronal plasticity and glial activation within the mPOA.

Area of Science:

  • Neuroscience
  • Behavioral Biology
  • Molecular Biology

Background:

  • Sexual experience enhances male sexual behavior efficiency in rodents.
  • Mechanisms underlying this improvement in mice are not well understood.
  • The medial preoptic area (mPOA) is crucial for integrating male sexual behavior.

Purpose of the Study:

  • To characterize molecular and morphological changes in the mouse mPOA following a single mating event.
  • To understand the neurobiological basis of enhanced sexual performance after initial experience.
  • To compare plasticity mechanisms in mice with those previously observed in rats.

Main Methods:

  • Analysis of molecular modifications in the mPOA of male mice after mating.
  • Assessment of behavioral improvements and morphological changes (dendritic spines, histone modifications).
  • Measurement of plasma and hypothalamic steroid levels, receptor levels, and protein expression (glutamate, calcium, NMDA receptor, microglial markers).

Main Results:

  • A single mating event induced long-lasting behavioral improvements and mPOA dendritic spine maturation.
  • Histone H3 acetylation and tri-methylation increased in the mPOA.
  • Levels of glutamate- and calcium-associated proteins (PSD-95, calbindin, GluN1) and the microglial marker Iba-1 were elevated in experienced mice.
  • Unlike rats, no changes were observed in the nitrergic system or sex steroid receptor levels.

Conclusions:

  • Sexual experience in male mice induces significant molecular and morphological plasticity in the mPOA.
  • These changes involve neuronal and glial elements, suggesting multicellular interactions.
  • Plasticity mechanisms differ between mice and rats but converge on mPOA network potentiation.

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