Affiliation:
1. Department of Biomedical Sciences , University of North Dakota School of Medicine and Health Sciences , Grand Forks , ND , USA
2. Department of Physiology and Pharmacology , Drexel University School of Medicine , Philadelphia , PA , USA
Abstract
AbstractObjectivesOpioids including morphine and DAMGO activate mu-opioid receptors (MOR), increase intracellular reactive oxygen species (ROS) levels, and induce cell death. Ferrous iron (Fe2+) through Fenton-like chemistry increases ROS levels and endolysosomes are “master regulators of iron metabolism” and contain readily-releasable Fe2+stores. However, mechanisms underlying opioid-induced changes in endolysosome iron homeostasis and downstream-signaling events remain unclear.MethodsWe used SH-SY5Y neuroblastoma cells, flow cytometry, and confocal microscopy to measure Fe2+and ROS levels and cell death.ResultsMorphine and DAMGO de-acidified endolysosomes, decreased endolysosome Fe2+levels, increased cytosol and mitochondria Fe2+and ROS levels, depolarized mitochondrial membrane potential, and induced cell death; effects blocked by the nonselective MOR antagonist naloxone and the selective MOR antagonist β-funaltrexamine (β-FNA). Deferoxamine, an endolysosome-iron chelator, inhibited opioid agonist-induced increases in cytosolic and mitochondrial Fe2+and ROS. Opioid-induced efflux of endolysosome Fe2+and subsequent Fe2+accumulation in mitochondria were blocked by the endolysosome-resident two-pore channel inhibitor NED-19 and the mitochondrial permeability transition pore inhibitor TRO.ConclusionsOpioid agonist-induced increases in cytosolic and mitochondrial Fe2+and ROS as well as cell death appear downstream of endolysosome de-acidification and Fe2+efflux from the endolysosome iron pool that is sufficient to affect other organelles.
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6 articles.
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