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Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response
Authors:Sunitha Rangaraju  Gregory M Solis  Sofia I Andersson  Rafael L Gomez‐Amaro  Rozina Kardakaris  Caroline D Broaddus  Alexander B Niculescu III  Michael Petrascheck
Institution:1. Department of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, USA;2. Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA, USA;3. Department of Molecular and Cellular Neuroscience, The Scripps Research Institute, La Jolla, CA, USA;4. Department of Psychiatry, Indiana University School of Medicine, Indianapolis, IN, USA
Abstract:Oxidative stress has long been associated with aging and has recently been linked to psychiatric disorders, including psychosis and depression. We identified multiple antipsychotics and antidepressants that extend Caenorhabditis elegans lifespan and protect the animal from oxidative stress. Here, we report that atypical antidepressants activate a neuronal mechanism that regulates the response to oxidative stress throughout the animal. While the activation of the oxidative stress response by atypical antidepressants depends on synaptic transmission, the activation by reactive oxygen species does not. Lifespan extension by atypical antidepressants depends on the neuronal oxidative stress response activation mechanism. Neuronal regulation of the oxidative stress response is likely to have evolved as a survival mechanism to protect the organism from oxidative stress, upon detection of adverse or dangerous conditions by the nervous system.
Keywords:antidepressant  anti‐aging  Caenorhabditis elegans  non‐cell‐autonomous  psychiatric disease  signal transduction  synaptic transmission  stress
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