<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shekhar S</submitter><funding>NICHD NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>531-544</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6090562</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>833</volume><pubmed_abstract>Ischemic stroke is a devastating and debilitating medical condition with limited therapeutic options. However, accumulating evidence indicates a central role of inflammation in all aspects of stroke including its initiation, the progression of injury, and recovery or wound healing. A central target of inflammation is disruption of the blood brain barrier or neurovascular unit. Here we discuss recent developments in identifying potential molecular targets and immunomodulatory approaches to preserve or protect barrier function and limit infarct damage and functional impairment. These include blocking harmful inflammatory signaling in endothelial cells, microglia/macrophages, or Th17/?? T cells with biologics, third generation epoxyeicosatrienoic acid (EET) analogs with extended half-life, and miRNA antagomirs. Complementary beneficial pathways may be enhanced by miRNA mimetics or hyperbaric oxygenation. These immunomodulatory approaches could be used to greatly expand the therapeutic window for thrombolytic treatment with tissue plasminogen activator (t-PA). Moreover, nanoparticle technology allows for the selective targeting of endothelial cells for delivery of DNA/RNA oligonucleotides and neuroprotective drugs. In addition, although likely detrimental to the progression of ischemic stroke by inducing inflammation, oxidative stress, and neuronal cell death, 20-HETE may also reduce susceptibility of onset of ischemic stroke by maintaining autoregulation of cerebral blood flow. Although the interaction between inflammation and stroke is multifaceted, a better understanding of the mechanisms behind the pro-inflammatory state at all stages will hopefully help in developing novel immunomodulatory approaches to improve mortality and functional outcome of those inflicted with ischemic stroke.</pubmed_abstract><journal>European journal of pharmacology</journal><pubmed_title>Targeting vascular inflammation in ischemic stroke: Recent developments on novel immunomodulatory approaches.</pubmed_title><pmcid>PMC6090562</pmcid><funding_grant_id>R01 HL102042</funding_grant_id><funding_grant_id>R21 AG050049</funding_grant_id><funding_grant_id>P01 HL051971</funding_grant_id><funding_grant_id>R01 HL036279</funding_grant_id><funding_grant_id>F32 HL078147</funding_grant_id><funding_grant_id>R37 HL036279</funding_grant_id><funding_grant_id>R01 HD067541</funding_grant_id><funding_grant_id>P20 GM104357</funding_grant_id><funding_grant_id>R01 HL138685</funding_grant_id><funding_grant_id>T32 HL105324</funding_grant_id><funding_grant_id>R01 DK104184</funding_grant_id><pubmed_authors>Booz GW</pubmed_authors><pubmed_authors>Fan F</pubmed_authors><pubmed_authors>Cunningham MW</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Shekhar S</pubmed_authors><pubmed_authors>Pabbidi MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting vascular inflammation in ischemic stroke: Recent developments on novel immunomodulatory approaches.</name><description>Ischemic stroke is a devastating and debilitating medical condition with limited therapeutic options. However, accumulating evidence indicates a central role of inflammation in all aspects of stroke including its initiation, the progression of injury, and recovery or wound healing. A central target of inflammation is disruption of the blood brain barrier or neurovascular unit. Here we discuss recent developments in identifying potential molecular targets and immunomodulatory approaches to preserve or protect barrier function and limit infarct damage and functional impairment. These include blocking harmful inflammatory signaling in endothelial cells, microglia/macrophages, or Th17/?? T cells with biologics, third generation epoxyeicosatrienoic acid (EET) analogs with extended half-life, and miRNA antagomirs. Complementary beneficial pathways may be enhanced by miRNA mimetics or hyperbaric oxygenation. These immunomodulatory approaches could be used to greatly expand the therapeutic window for thrombolytic treatment with tissue plasminogen activator (t-PA). Moreover, nanoparticle technology allows for the selective targeting of endothelial cells for delivery of DNA/RNA oligonucleotides and neuroprotective drugs. In addition, although likely detrimental to the progression of ischemic stroke by inducing inflammation, oxidative stress, and neuronal cell death, 20-HETE may also reduce susceptibility of onset of ischemic stroke by maintaining autoregulation of cerebral blood flow. Although the interaction between inflammation and stroke is multifaceted, a better understanding of the mechanisms behind the pro-inflammatory state at all stages will hopefully help in developing novel immunomodulatory approaches to improve mortality and functional outcome of those inflicted with ischemic stroke.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2021-02-19T21:10:24Z</modification><creation>2019-03-26T23:51:39Z</creation></dates><accession>S-EPMC6090562</accession><cross_references><pubmed>29935175</pubmed><doi>10.1016/j.ejphar.2018.06.028</doi></cross_references></HashMap>