Blood Elements Activation in Hemodialysis – Animal Model Studies
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 33122
Blood Elements Activation in Hemodialysis – Animal Model Studies

Authors: Karolina Grzeszczuk-Kuć, Jolanta Bujok, Tomasz Walski, Małgorzata Komorowska

Abstract:

Haemodialysis (HD) is a procedure saving patient lives around the world, unfortunately it brings numerous complications. Oxidative stress is one of the major factors which lead to erythrocytes destruction during extracorporeal circulation. Repeated HD procedures destroy blood elements and the organism is not able to keep up with their production. 30 HD procedures on healthy sheep were performed to evaluate effects of such treatment. Oxidative stress study was performed together with an analysis of basic blood parameters and empirical assessment of dialyzer condition after the procedure. A reversible decline in absolute leukocyte count, during first 30 min of HD, was observed. Blood clots were formed in the area of the blood inlet and outlet of the dialyzer. Our results are consistent with outcomes presented throughout the literature specifically with respect to the effects observed in humans and will provide a basis to evaluate methods for blood protection during haemodialysis.

Keywords: Animal model, blood components, haemodialysis, leukocytes, oxidative stress, sheep.

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1087992

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 2348

References:


[1] M. Nałęcz, Ed., Biocybernetyka i inŜynieria biomedyczna 2000 Tom 3 Sztuczne narządy, Warszawa: Akademicka Oficyna Wydawnicza EXIT, 2001, pp. 218-226,
[2] R. Tadeusiewicz Ed., P. Augustyniak Ed., Podstawy inŜynierii biomedycznej Tom II, Kraków: Wydawnictwa AGH, 2009, pp. 135-143,
[3] W. A. Nockher, J. Wiemer, J. E. Scherberich, Haemodialysis monocytopenia: differential sequestration kinetics of CD141CD161 and CD1411 blood monocyte subsets, Clin. Exp. Immunol., 123 (2001), pp. 49-55,
[4] K. Kose, P. Dogan, Z. Gunduz, R.Dusunsel, C. Z. Utas, Oxidative Stress in Hemodialyzed Patients and the Long-Term Effects of Dialyzer Reuse Practice, Clinical Biochemistry, Vol. 30, No. 8, 1997, pp. 601–606,
[5] S. Túri, I. Nemeth, I. Vargha, B. Matkovies, E. Dobos, Erythrocyte defense mechanisms against free oxygen radicals in hemodialyzed uremic children, Pediatr. Nephrol., 5 (1991), pp. 179–183,
[6] L. Chludzińska, E. Ananicz, A. Jarosławska, M. Komorowska, Near infrared radiation protects the red cell membrane against oxidation, Blood Cells, Molecules and Diseases, 35 (2005), pp. 74-79,
[7] R. L. Heath, L. Packer, Photoperoxidation in isolated chloroplasts. Kinetic and stoichiometry of fatty acid peroxidation, Arch. Biochem. Biophys. 125 (1968), pp. 189– 198,
[8] R. Hällgren, P. Venge, B. G. Danielson Neutrophil and eosinophil degranulation during hemodialysis are mediated by the dialysis membrane, Nephron, 32:1982, pp. 329–334,
[9] L. S. Kaplow, J. A. Goffinet, Profound neutropenia during the early phase of hemodialysis. J. Am. Med. Assoc. 203 (1968), pp. 1135-1137,
[10] P. R. Craddock, J. Ferh, A. P. Dalmasso et al., Hemodialysis leukopenia: pulmonary vascular leukostasis resulting from complement activation by dialyzer cellophane membranes. J. Clin. Invest., 59 (1977), pp. 879-888,
[11] A. T. Nguyen, C. Lethias, J. Zingraff, A. Herbelin, C. Naret, B. Descamps-Latscha, Hemodialysis membrane-induced activation of phagocyte oxidative metabolism detected in vivo and in vitro within microamounts of whole blood., Kidney Int., 28 (1985), pp. 158–167,
[12] E. Stoyanova, S. B. Sandoval, L. A. Zuniga, N. El-Yamani, E. Coll, S. Pastor, J. Reyes, E. Andre´s, J. Ballarin, N. Xamena, R. Marcos, Oxidative DNA damage in chronic renal failure patients. Nephrol. Dial. Transplant. 25 (2010), pp. 879 – 885,
[13] R. L. Levine, Carbonyl modified proteins in cellular regulations, aging, and disease. Free Radic. Biol. Med. 32(2002), pp. 790–796.