Midbrain dopaminergic inputs gate amygdala intercalated cell clusters by distinct and cooperative mechanisms in male mice. Aksoy-Aksel et al, (2021) Elife

24. Juni 2021 / Abt. Neurobiologie

Dopaminerge Signalübertragung im Gehirn spielt eine wichtige Rolle beim Lernen, aber die Mechanismen sind unvollständig verstanden. Wir fanden heraus, dass dopaminerge Eingänge auf Interkalierte Zellen in Amygdala, die für Furcht- und Extinktionslernen wichtig sind, diese Neurone durch die gemeinsame Freisetzung von zwei Transmittern, GABA und Dopamin, kontrollieren. Deren Effekt wird durch Extinktionslernen moduliert und kann die Aktivität der Interkalierten Zellen so beeinflussen, dass erlernte Furcht verringert wird.

 

Abstract

Dopaminergic signaling plays an important role in associative learning, including fear and extinction learning. Dopaminergic midbrain neurons encode prediction error-like signals when threats differ from expectations. Within the amygdala, GABAergic intercalated cell (ITC) clusters receive one of the densest dopaminergic projections, but their physiological consequences are incompletely understood. ITCs are important for fear extinction, a function thought to be supported by activation of ventromedial ITCs that inhibit central amygdala fear output. In mice, we reveal two distinct novel mechanisms by which mesencephalic dopaminergic afferents control ITCs. Firstly, they co-release GABA to mediate rapid, direct inhibition. Secondly, dopamine suppresses inhibitory interactions between distinct ITC clusters via presynaptic D1 receptors. Early extinction training augments both GABA co-release onto dorsomedial ITCs and dopamine-mediated suppression of dorso- to ventromedial inhibition between ITC clusters. These findings provide novel insights into dopaminergic mechanisms shaping the activity balance between distinct ITC clusters that could support their opposing roles in fear behavior.

Aksoy-Aksel A, Gall A, Seewald A, Ferraguti F, Ehrlich I. (2021) Midbrain dopaminergic inputs gate amygdala intercalated cell clusters by distinct and cooperative mechanisms in male mice.Elife. 2021 May 24;10:e63708. doi: 10.7554/eLife.63708.

Zum Seitenanfang