21
Views
29
CrossRef citations to date
0
Altmetric
Original Article

Antioxidant Status and Susceptibility of Sickle Erythrocytes to Oxidative and Osmotic Stress

&
Pages 133-139 | Received 07 Nov 1995, Published online: 07 Jul 2009

References

  • Dacie J. The hereditary haemolytic anaemias. The Hemolytic Anaemias. Churchill Livingstone, Edinburgh 1988; vol. 2: 1–577
  • Francis R. B., Jr., Johnson C. S. Vascular occlusion in sickle cell disease: current concepts and unanswered questions. Blood 1991; 77: 1405–1414
  • Halliwell B., Gutteridge J. M.C. Free Radicals in Biology and Medicine. Clarendon Press, Oxford 1989; 1–543
  • Chow C. K. Cellular Antioxidant Defense Mechanisms. CRC Press, Boca Raton 1988; Vols. 1–3
  • McBrien D. C.H., Slater T. F. Free Radicals, Lipid Peroxidation and Cancer. Academic Press, London 1989; 1–447
  • Jain S. K. Vitamin E and membrane abnormalities in red cells of sickle cell disease patients and newborn. Annals New York Academy of Science 1989; 570: 461–463
  • Wali R. K., Jafe S., Kumar D., Sorgenete N., Kalra V. K. Increased adherence of oxidant treated human and bovine erythrocytes to cultured endothelial cells. Journal of Cell Physiology 1987; 113: 25–36
  • Chiu D., Lubin B. Oxidative hemoglobin denaturation and RBC destruction: The effect of heme on red cell membranes. Seminars in Hematology 1989; 26: 128–135
  • Chiu D., Lubin B. Abnormal vitamin E and glutathione peroxidase levels in sickle cell anemia. Journal of Laboratory and Clinical Medicine 1979; 94: 542–548
  • Jain S. K., Williams D. M. Reduced levels of plasma ascorbic acid (vitamin C) in sickle cell disease patients: its possible role in the oxidant damage to sickle cells in vivo. Clinica Chimica Acta 1985; 149: 257–261
  • Rice K.-Evans, Omorphos S. C., Baysal E. Sickle cell membranes and oxidative damage. Biochemical Journal 1986; 237: 265–269
  • Kuross S. A., Hebbel R. P. Nonheme iron in sickle erythrocyte membranes: association with phosphorus and potential role in lipid peroxidation. Blood 1988; 72: 1278–1285
  • van den Berg J. J.M., Kuypers F. A., Lubin B. H., Roelofsen B., den Kamp J. A.F.op. Direct and continuous measurement of hydroperoxide-induced oxidative stress on the membrane of intact erythrocytes. Free Radical Biology and Medicine 1990; 11: 255–261
  • Blumenfeld N., Zachowski A., Galacteros F., Beuzard Y., Devaux P. Transmembrane mobility of phospholipids in sickle erythrocytes: effect of deoxygena-tion on diffusion and asymmetry. Blood 1991; 77: 849–854
  • Sindel L. J., Baliga B. S., Bendich A., Mankad V. Nutritional deficiencies associated with vitamin E deficiency in sickle cell patients: the effect of vitamin supplementation. Nutrition Research 1990; 10: 267–273
  • Adelekan D. A., Thumham D. I., Adekile A. D. Reduced antioxidant capacity in pediatric patients with homozygous sickle cell disease. European Journal of Clinical Nutrition 1989; 43: 609–614
  • Jain S. K., Ross J. D., Duett J., Herbst J. J. Low plasma prealbumin and carotenoid levels in sickle cell disease patients. American Journal of Medical Science 1990; 299: 13–15
  • Schacter L. P., Del Villano B.C., Gordon E. M., Klein B. L. Red cell superoxide dismutase and sickle cell anemia symptom severity. American Journal of Hematology 1985; 19: 137–144
  • Das S. K., Hinds J. E., Hardy R. E., Collins J. C., Mukherjee S. Effects of physical stress on peroxide scavengers in normal and sickle cell trait erythrocytes. Free Radicals Biology & Medicine 1993; 14: 139–147
  • Das S. K., Nair C. R. Superoxide dismutase, glutathione peroxidase and catalase and lipid peroxidation of normal and sickled erythrocytes. British journal of Haematology 1980; 44: 87–92
  • Muskiet F. A., Muskiet F. D., Meiborg G., Schermer J. G. Supplementation of patients with homozygous sickle cell disease with zinc, alpha-tocopherol, vitamin C, soybean oil, and fish oil. American Journal of Clinical Nutrition 1991; 54: 736–744
  • Miki M., Tamai H., Mino M., Yamamoto Y., Niki E. Free-radical chain oxidation of rat blood cells by molecular oxygen and its inhibition by a-tocopherol. Archives of Biochemistry and Biophysics 1987; 258: 373–380
  • Yamamoto Y. Y., Niki E., Kamiya Y., Miki M., Tamai H., Mino M. Free radical chain oxidation and hemolysis of erythrocytes by molecular oxygen and their inhibition by vitamin E. Journal of Nutritional Science and Vitaminology 1986; 32: 475–479
  • Hatam L. J., Kayden H. J. A high performance liquid chromatographic method for the determination of tocopherol in plasma and cellular elements of the blood. Journal of Lipid Research 1979; 20: 639–645
  • Collins C. A., Chow C. K. Determination of vitamin A and vitamin A acetate by high performance liquid chromatography with fluorescence detection. Journal of Chromatography 1984; 317: 349–354
  • Tatum V. L., Changchit C., Chow C. K. Measurement of malondialdehyde by high performance liquid chromatography with fluorescence detection. Lipids 1990; 25: 226–229
  • Sedlack J., Lindsay R. H. Estimations of total protein-bound and non-protein sulfhydryl groups in tissues with Ellman's reagent. Analytical Biochemistry 1968; 25: 192–205
  • Recknagel R. O., Ghoshal A. K. Quantitative estimation of peroxidative degeneration of rat liver microsomal and mitochondrial lipids after carbon tetrachloride poisoning. Experimental and Molecular Pathology 1966; 5: 413–426
  • Omaye S. T., Tumbull J. D., Sauberlich H. E. Selected methods for the determination of ascorbic acid in animal cells, tissues, and fluids. Methods in Enzymology 1979; 62: 3–11
  • Chiang S. P., Gessert C. F., Lowry O. H. Colori-metric determination of extracted lipids. Air University School of Aviation Medicine, USAF, Texas. 1957; 56–113, Research Report
  • Riggs M. G., Ingram V. M. Differences in erythrocyte membrane proteins and glycoproteins in sickle cell disease. Biochemical and Biophysical Research Communications 1977; 74: 191–198
  • Hebbel R. The sickle erythrocyte in double jeopardy: autoxidation and iron decompartmentalization. Seminars in Hematology 1990; 27: 51–69
  • Haut A., Tudhope G. R., Cartwright G. E., Wintrobe M. M. Studies on osmotic fragility of incubated normal and abnormal erythrocytes. Journal of Clinical Investigations 1962; 41: 1766–1755
  • Mohandas N., Schrier S. L. Mechanisms of red blood cell destruction in hemolytic anemia. The Hereditary Hemolytic Anemia, W. C. Mentzer, G. M. Wagner. Churchill Livingstone, New York 1989; 391–430
  • Francis R. B., Jr., Johnson C. S. Vascular occlusion in sickle cell disease: current concepts and unanswered questions. Blood 1991; 77: 1405–1414, 1991

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.