| Literature DB >> 31398359 |
Nadia Peyravian1, Emre Dikici1, Sapna Deo1, Michal Toborek2, Sylvia Daunert3.
Abstract
Chronic use of prescription opioids exacerbates risk and severity of ischemic stroke. Annually, 6 million people die from stroke worldwide and there are no neuroprotective or neurorestorative agents to improve stroke outcomes and promote recovery. Prescribed opioids such as morphine have been shown to alter tight junction protein expression, resulting in the disruption of the blood brain barrier (BBB), ultimately leading to stroke pathogenesis. Consequently, protection of the BBB has been proposed as a therapeutic strategy for ischemic stroke. This perspective addresses the deficiency in stroke pharmacological options and examines a novel application and repurposing of FDA-approved opioid antagonists as a prospective neuroprotective therapeutic strategy to minimize BBB damage, reduce stroke severity, and promote neural recovery. Future directions discuss potential drug design and delivery methods to enhance these novel therapeutic targets.Entities:
Keywords: Blood brain barrier; Ischemic stroke; Naloxone; Naltrexone; Neuroprotection; Opioid antagonist
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Year: 2019 PMID: 31398359 PMCID: PMC6814577 DOI: 10.1016/j.pneurobio.2019.101679
Source DB: PubMed Journal: Prog Neurobiol ISSN: 0301-0082 Impact factor: 11.685