Cited by 92Neutrophil, Myeloperoxidase and Oxidative MechanismsNitric Oxide and Endothelin EffectsRedox biology and oxidative stress

Hypochlorous acid and chloramines increase endothelial permeability: possible involvement of cellular zinc

Tatsumi, T., Fliss, H.·1994·American Journal of Physiology-Heart and Circulatory Physiology

Abstract

The migration of neutrophils through the endothelium at sites of inflammation may be facilitated by oxidant-mediated disruption of cellular junctions. The present study examined the effects of noncytotoxic concentrations of the membrane-penetrating neutrophil oxidants hypochlorous acid (HOCI) and monochloramine (NH2Cl), or the membrane-impermeant taurine chloramine (taurine NCl), on cultured bovine aorta endothelial monolayers. HOCl (25 microM) or NH2Cl (10 microM), but not taurine NCl (100 microM), caused a reversible shortening of the cytoskeletal actin microfilaments, cell retraction, and increased permeability within 2 min. These effects were accompanied by an increase in intracellular zinc concentration as well as the oxidation of intracellular glutathione and protein sulfhydryls. The zinc ionophore pyrithione also increased permeability. HOCl or NH2Cl, but not taurine NCl, also rapidly increased microvascular permeability in isolated perfused rat lungs. The data suggest that HOCl and NH2Cl can increase endothelial permeability by causing very rapid cytoskeletal shortening and cell retraction, possibly as a result of the oxidation of intracellular sulfhydryls and mobilization of zinc.

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Crossref · 10.1152/ajpheart.1994.267.4.h1597

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  • Chloramines are membrane penetrating oxidants and react rapidly with sulphhydryl groups of proteins in the cytoskeleton and the extracellular matrix, causing disruption of tight junctions and an almost immediate increase in epithelial permeability.

    “Chloramines are membrane penetrating oxidants and react rapidly with sulphhydryl groups of proteins in the cytoskeleton and the extracellular matrix causing disruption of tight junctions and an almost immediate increase in epithelial permeability, as shown in in vitro studies [ (Tatsumi and Fliss 1994;Nakamura et al. 1995;Musch et al. 1999), as cited by Carbonnelle et al. (2002)].”

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Authors
Tatsumi, T., & Fliss, H.
Affiliations
University of Ottawa (CA)
Venue
American Journal of Physiology-Heart and Circulatory Physiology
Published
1994-10-01
Volume
267
Issue
4
Pages
H1597-H1607
ISSN
  • 0363-6135 (ISSN-L)
  • 1522-1539
OpenAlex
W2208875894
Cited by
92
References
0
Citations by year
2026: 1 · 2023: 2 · 2021: 2 · 2020: 4 · 2019: 3 · 2017: 3 · 2016: 3 · 2015: 1 · 2014: 2 · 2013: 2 · 2012: 3
FWCI
0.90
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Physiology-Heart and Circulatory Physiology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
Keywords
hypochlorous acid, monochloramine, taurine chloramine, endothelial permeability, neutrophil migration, cell retraction, intracellular zinc, glutathione oxidation, sulfhydryl oxidation, pyrithione, microvascular permeability, lung, inflammation
MeSH terms
Actins, Animals, Aorta, Cattle, Cell Membrane Permeability, Cell Survival, Cells, Cultured, Chloramines, Dose-Response Relationship, Drug, Endothelium, Vascular, Hypochlorous Acid, Lung, Male, Microcirculation, Actin Cytoskeleton, Perfusion, Pulmonary Circulation, Pyridines, Taurine, Thiones, Zinc, Rats, Sprague-Dawley, Rats, In Vitro Techniques

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