Acute-stress impairs cytoprotective mechanisms through neural inhibition of the insulin pathway

Abstract

Persistent activation of the "fight-or-flight" response accelerates aging and increases the susceptibility to disease. We show that repeated induction of the C. elegans flight response inhibits conserved cytoprotective mechanisms. This acute-stress response activates neurons that release tyramine, the invertebrate analog of adrenaline/noradrenaline. Tyramine stimulates the DAF-2/Insulin/IGF-1 pathway and precludes the nuclear translocation of the DAF-16/FOXO transcription factor through the activation of an adrenergic-like receptor TYRA-3 in the intestine. In contrast, environmental long-term stressors, such as heat or oxidative stress, reduce tyramine release allowing the induction of FOXO-dependent cytoprotective genes. These findings demonstrate how a neural stress-hormone signaling provides a statedependent neural switch between acute and long-term stress responses, and provide mechanistic insights how acute stress impairs cellular defensive systems. One Sentence Summary: The "fight-or-flight" response reduces resistance to environmental challenges.