Abstract

SummaryModel organisms subject to dietary restriction (DR) generally live longer. Accompanying this lifespan extension are improvements in overall health, based on multiple metrics. This indicates that pharmacological treatments that mimic the effects of DR could improve health in humans. To find new chemical structures that extend lifespan, we screened 30 000 synthetic, diverse drug‐like chemicals in Caenorhabditis elegans and identified several structurally related compounds that acted through DR mechanisms. The most potent of these NP1 impinges upon a food perception pathway by promoting glutamate signaling in the pharynx. This results in the overriding of a GPCR pathway involved in the perception of food and which normally acts to decrease glutamate signals. Our results describe the activation of a dietary restriction response through the pharmacological masking of a novel sensory pathway that signals the presence of food. This suggests that primary sensory pathways may represent novel targets for human pharmacology.

Highlights

  • Aging is profoundly influenced by environmental factors such as temperature, toxins, and nutrient availability

  • Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd

  • We identified over five hundred primary hits, of which one hundred and eighty were selected for re-testing

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Summary

Introduction

Aging is profoundly influenced by environmental factors such as temperature, toxins, and nutrient availability. Alterations in sensory neuron function can influence these processes in non-neuronal tissues. In the nematode Caenorhabditis elegans, the activity of the AFD neurons is required for the induction of heat-shock genes in multiple non-neuronal tissues, demonstrating that a stress response critical in promoting protein homeostasis (proteostasis) is under cell nonautonomous neuronal control (Prahlad et al, 2008). The unfolded protein response of the endoplasmic reticulum (UPRER) and the mitochondria (UPRmito) is influenced by neuronal function (Durieux et al, 2011; Sun et al, 2011; Singh & Aballay, 2012; Taylor & Dillin, 2013)

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