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Article type: Research Article
Authors: Saavedra, Arturo P.; | Warth, James A. | Burke, John F. | Norton, Kathryn J. | Gelfand, Jeffrey A.
Affiliations: Department of Dermatology, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA | Dana Farber Cancer Institute, Department of Cutaneous Oncology, Boston, MA, USA | Department of Medicine, Harvard Medical School, Brigham and Women's/Faulkner Hospitals, Boston, MA, USA | Department of Surgery, Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA | Department of Medicine, Tufts New England Medical Center, Boston, MA, USA | Department of Medicine, Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA
Note: [] Corresponding author: Dr. Arturo P. Saavedra, Department of Dermatology, Brigham and Women's Hospital, 221 Longwood Ave, Boston, MA 02115, USA. Tel.: +1 617 732 4918; Fax: +1 617 582 6060; E-mail: asoavedra@partners.org
Abstract: OBJECTIVE: We have studied dense erythrocytes separated on Arabinogalactan (Stractan) ultracentrifuged gradients in flame-burned patients and in normal individuals. In each case, the percentage of erythrocytes in the densest layers was increased when compared to age and sex matched controls. METHODS AND RESULTS: Using an in vitro system, we showed that as human whole blood is warmed to 48.6°C, the number of dense erythrocytes increases. In addition, the reduced glutathionine (GSH) content of the densest red blood cells is decreased compared to those in lighter fractions on the same gradient or to dense erythrocytes separated from blood incubated at room temperature. These dense red cells were largely composed of spherocytes and spheroechynocytes, two forms of erythrocytes which have been shown by others to have markedly abnormal flow characteristics in vitro. CONCLUSIONS: We have demonstrated that in vivo dense erythrocytes can be generated in the setting of flame burns. Thus, the underlying reason may be oxidant injury as represented by the reduced level of GSH that we found in association with the generation of dense erythrocytes.
DOI: 10.3233/CH-2012-1556
Journal: Clinical Hemorheology and Microcirculation, vol. 53, no. 4, pp. 349-356, 2013
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