Literature DB >> 2982213

Protection against lethal hyperoxia by tracheal insufflation of erythrocytes: role of red cell glutathione.

B S van Asbeck, J Hoidal, G M Vercellotti, B A Schwartz, C F Moldow, H S Jacob.   

Abstract

Intact erythrocytes placed into the tracheobronchial tree of hyperoxic rats dramatically improved their chances for survival. Over 70 percent of the animals so treated survived more than 12 days during continuous exposure to 95 percent oxygen, whereas all of the control animals died within 96 hours. Lungs from erythrocyte-protected rats showed almost none of the morphologic damage suffered by untreated animals. Erythrocytes containing cyanomethemoglobin were as beneficial as normal erythrocytes, but cells in which glutathione was partially blocked were significantly less protective. Analogous results were obtained in vitro: 51Cr-labeled target cells released 70 to 90 percent of their label when exposed briefly to hydrogen peroxide or to toxic oxygen species generated by phorbol ester-stimulated neutrophils. Addition of intact erythrocytes decreased release by approximately 75 percent, but significantly less than this if red blood cell glutathione was partially blocked. These results suggest that insufflated erythrocytes, through their recyclable glutathione, protect rats from toxic oxygen species engendered by hyperoxia.

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Year:  1985        PMID: 2982213     DOI: 10.1126/science.2982213

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  21 in total

Review 1.  The pulmonary physician and critical care. 3. Pharmacotherapy in lung injury.

Authors:  M Messent; M J Griffiths
Journal:  Thorax       Date:  1992-08       Impact factor: 9.139

2.  Human red cells scavenge extracellular hydrogen peroxide and inhibit formation of hypochlorous acid and hydroxyl radical.

Authors:  C C Winterbourn; A Stern
Journal:  J Clin Invest       Date:  1987-11       Impact factor: 14.808

3.  Erythrocyte sialoglycoproteins engage Siglec-9 on neutrophils to suppress activation.

Authors:  Anel Lizcano; Ismael Secundino; Simon Döhrmann; Ross Corriden; Cristina Rohena; Sandra Diaz; Pradipta Ghosh; Lingquan Deng; Victor Nizet; Ajit Varki
Journal:  Blood       Date:  2017-04-17       Impact factor: 22.113

4.  Thermal injury, intravascular hemolysis, and toxic oxygen products.

Authors:  J R Hatherill; G O Till; L H Bruner; P A Ward
Journal:  J Clin Invest       Date:  1986-09       Impact factor: 14.808

5.  Directed targeting of immunoerythrocytes provides local protection of endothelial cells from damage by hydrogen peroxide.

Authors:  V R Muzykantov; D V Sakharov; S P Domogatsky; N V Goncharov; S M Danilov
Journal:  Am J Pathol       Date:  1987-08       Impact factor: 4.307

6.  Increased oxidative stress and altered levels of antioxidants in chronic obstructive pulmonary disease.

Authors:  Ahmed Nadeem; Hanumanthrao Guru Raj; Sunil Kumar Chhabra
Journal:  Inflammation       Date:  2005-02       Impact factor: 4.092

7.  Augmentation of glutathione in the fluid lining the epithelium of the lower respiratory tract by directly administering glutathione aerosol.

Authors:  R Buhl; C Vogelmeier; M Critenden; R C Hubbard; R F Hoyt; E M Wilson; A M Cantin; R G Crystal
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

8.  Antioxidant functions for the hemoglobin β93 cysteine residue in erythrocytes and in the vascular compartment in vivo.

Authors:  Dario A Vitturi; Chiao-Wang Sun; Victoria M Harper; Bessy Thrash-Williams; Nadiezhda Cantu-Medellin; Balu K Chacko; Ning Peng; Yanying Dai; J Michael Wyss; Tim Townes; Rakesh P Patel
Journal:  Free Radic Biol Med       Date:  2012-11-16       Impact factor: 7.376

9.  Cell-free hemoglobin: a novel mediator of acute lung injury.

Authors:  Ciara M Shaver; Cameron P Upchurch; David R Janz; Brandon S Grove; Nathan D Putz; Nancy E Wickersham; Sergey I Dikalov; Lorraine B Ware; Julie A Bastarache
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2016-01-15       Impact factor: 5.464

10.  Scavengers of reactive oxygen intermediates do not mediate the depression of macrophage hydrogen peroxide production caused by erythrocyte phagocytosis.

Authors:  M G Schwacha; D J Loegering; L M Commins; P W Gudewicz
Journal:  Inflammation       Date:  1991-12       Impact factor: 4.092

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