Presynaptic excitation via GABAB receptors in habenula cholinergic neurons regulates fear memory expression

• Juen Zhang ^[1] ; Lubin Tan ^[1] ; Yuqi Ren ^[2]
  1. [1] Tsinghua University

     Tsinghua University

     China

     
  2. [2] Peking University

     Peking University

     China

     
• Localización: Cell, ISSN 0092-8674, Vol. 166, Nº. 3, 2016, págs. 716-728
• Idioma: inglés
• Texto completo no disponible (Saber más ...)
• Resumen

  • Fear behaviors are regulated by adaptive mechanisms that dampen their expression in the absence of danger. By studying circuits and the molecular mechanisms underlying this adaptive response, we show that cholinergic neurons of the medial habenula reduce fear memory expression through GABAB presynaptic excitation. Ablating these neurons or inactivating their GABAB receptors impairs fear extinction in mice, whereas activating the neurons or their axonal GABAB receptors reduces conditioned fear. Although considered exclusively inhibitory, here, GABAB mediates excitation by amplifying presynaptic Ca2+ entry through Cav2.3 channels and potentiating co-release of glutamate, acetylcholine, and neurokinin B to excite interpeduncular neurons. Activating the receptors for these neurotransmitters or enhancing neurotransmission with a phosphodiesterase inhibitor reduces fear responses of both wild-type and GABAB mutant mice. We identify the role of an extra-amygdalar circuit and presynaptic GABAB receptors in fear control, suggesting that boosting neurotransmission in this pathway might ameliorate some fear disorders.