|
Sign In to gain access to subscriptions and/or personal tools.
|
New Features of Renal Lesion Induced by Stroma Free Hemoglobin
W.L. Chan
Department of Physiology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Nelson L.S. Tang
Department of Chemical Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Connie C.W. Yim
Department of Physiology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Fernand Mac-Moune Lai
Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Michael S.C. Tam
Department of Physiology, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
This study focused on the subacute renal lesions resulting from the infusion of stroma free hemoglobin (SFH), which remains under evaluation as a potential blood substitute despite limited renal toxicity observed in acute infusion. Four groups of rats received different doses of SFH (0.03, 0.48, 0.96, and 1.46 g, respectively) and were monitored, on alternate days, for their glomerular filtration rate over the course of 10 days. Another group of 6 rats receiving 0.96 g SFH was sacrificed at day 10 for examination of renal morphology. The low dose (0.03 g) of SFH infusion did not alter the creatinine clearance (Clcr) over 10 days. The Clcr decreased in rats receiving 0.48 g SFH but fully recovered at day 10. A persistent decrease in Clcr was observed in the groups of rats receiving 0.96 and 1.68 g of SFH. Tubular necrosis was the most prominent renal lesion distributed in the proximal tubules, especially in the convoluted segment of the juxtamedullary nephrons. Pearls' stained cytoplasmic granules and electron-dense lysosomal granules were found in surviving proximal tubules. Necrosis was the predominant mechanism of cell death. This study revealed for the first time proliferation of smooth endoplasmic reticulum in the proximal tubules after SFH treatment, where it appeared as nodular aggregates of tubulovesicular structures. The effect of SFH on the proximal tubule appeared to be a direct toxicity, and this toxicity was shown to be dose dependent. The presence of reversible toxicity indicated that a safety limit dosage for SFH infusion exists and that tolerance dose of SFH can be determined for clinical applications.
Key Words: Blood substitutes glomerular filtration rate proximal renal tubule acute tubular necrosis smooth endoplasmic reticulum
References
- Abassi Z., Kotob S., Pieruzzi F., Abouassali M., Keiser HR, Fratantoni JC, Alayash AI (1997). Effects of polymerization on the hypertensive action of diaspirin cross-linked hemoglobin in rats. J Lab Clin Med 129: 603-610.[CrossRef][Web of Science][Medline]
[Order article via Infotrieve]
- Aranow JS, Wang H., Zhuang J., Fink MP ( 1996). Effect of human hemoglobin on systemic and regional hemodynamics in a porcine model of endotoxemic shock. Crit Care Med 24: 807-814.[CrossRef][Web of Science][Medline]
[Order article via Infotrieve]
- Beeri R., Symon Z., Brezis M., Ben-Sasson SA, Baehr PH, Rosen S., Zager RA (1995). Rapid DNA fragmentation from hypoxia along the thick ascending limb of rat kidneys. Kidney Int 47: 1806-1810.[Web of Science][Medline]
[Order article via Infotrieve]
- Chang TM (1998). Modified hemoglobin-based blood substitutes: Cross-linked, recombinant and encapsulated hemoglobin. Vox Sang 74(suppl 2): 233-241.[Web of Science][Medline]
[Order article via Infotrieve]
- Dees JH, Masters Bss, Muller-Eberhard U., Johnson EF (1982). Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin and phenobarbital on the occurrence and distribution of four cytochrome P-450 isozymes in rabbit kidney, lung and liver. Cancer Res 42: 1423-1432.[Abstract/Free Full Text]
- Drabkin DL, Austin JH (1935). Spectrophotometric studies. II. Preparations from washed blood cells; nitric oxide hemoglobin and sulfhemoglobin. J Biol Chem 112: 51-65.[Free Full Text]
- Eldridge J., Russell R., Christenson R., Sakamoto R., Williams J., Parr M., Trump B., Delaney P., Mackenzie CF (1996). Liver function and morphology after resuscitation from severe hemorrhagic shock with hemoglobin solutions or autologous blood. Crit Care Med 24: 663-671.[CrossRef][Web of Science][Medline]
[Order article via Infotrieve]
- Fowler BA, Hook Ger, Lucier GC (1977). Tetrachlorodibenzo-p-dioxin induction of renal microsomal enzyme systems: Ultrastructural effects on Pars Recta (S3) proximal tubule cells of the rat kidney. J Pharmacol Exp Ther 203: 712-721.[Abstract/Free Full Text]
- Friedman HI, DeVenuto F. (1982). Morphological effects of transfusions with hemoglobin solutions. Crit Care Med 10: 288-293.[Web of Science][Medline]
[Order article via Infotrieve]
- Gibbs WW (1996). Artificial blood quickens. Several short-term substitutes approach final clinical trials. Sci Am 275: 44-48.[Medline]
[Order article via Infotrieve]
- Gonzalez P., Hackney AC, Jones S., Strayhorn D., Hoffman EB, Hughes G., Jacobs EE, Orringer EP (1997). A phase I/II study of polymerized bovine hemoglobin in adult patients with sickle cell disease not in crisis at the time of study. J Invest Med 45: 258-264.[Web of Science][Medline]
[Order article via Infotrieve]
- Gould SA, Moss GS ( 1996). Clinical development of human polymerized hemoglobin as a blood substitute. World J Surg 20: 1200-1207.[CrossRef][Web of Science][Medline]
[Order article via Infotrieve]
- Heyman SN, Fuchs S., Brezis M. (1995). The role of medullary ischemia in acute renal failure. New Horiz 3: 597-607.[Medline]
[Order article via Infotrieve]
- Heyman SN, Rosen S., Fuchs S., Epstein FH, Brezis M. (1996). Myoglobinuric acute renal failure in the rat: A role for medullary hypoperfusion. hypoxia, and tubular obstruction. J Am Soc Nephrol 7: 1066-1074.[Abstract]
- Jaffe R., Ariel I., Beeri R., Paltiel O., Hiss Y., Rosen S., Brezis M. (1997). Frequent apoptosis in human kidneys after acute renal hypoperfusion. Exp Nephrol 5: 399-403.[Web of Science][Medline]
[Order article via Infotrieve]
- Lieberthal W. (1995). Stroma-free hemoglobin: A potential blood substitute. J Lab Clin Med 126: 231-232.[Web of Science][Medline]
[Order article via Infotrieve]
- Nath KA, Balla G., Vercellotti GM (1992). Induction of heme oxygenase is a rapid protective response in rhabdomyolysis in rat. J Clin Invest 90: 267-270.[Web of Science][Medline]
[Order article via Infotrieve]
- Nath KA, Balla J., Croatt AJ, Vercellotti GM (1995). Heme protein-mediated renal injury: A protective role for 21-aminosteroids in vitro and in vivo. Kidney Int 47: 592-602.[Web of Science][Medline]
[Order article via Infotrieve]
- Paller MS (1988). Hemoglobin- and myoglobin-induced acute renal failure in rats: Role of iron in nephrotoxicity. Am J Physiol 255: F539-544.[Web of Science][Medline]
[Order article via Infotrieve]
- Pimstone NR, Engel P., Tenhunen R. (1971). Inducible hemo oxygenase in the kidney: A model for the homeostatic control of hemoglobin catabolism. J Clin Invest 50: 2042-2050.[Web of Science][Medline]
[Order article via Infotrieve]
- Rush GF, Maita K., Sleight SD (1983). Induction of rabbit renal mixed-function oxidases by phenobarbital: Cell specific ultrastructural changes in the proximal tubule. Proc Soc Exp Biol Med 172: 430-439.[CrossRef][Medline]
[Order article via Infotrieve]
- Scannon PJ (1982). Molecular modifications of hemoglobin. Crit Care Med 10: 261-265.[Web of Science][Medline]
[Order article via Infotrieve]
- Somers M., Piqueras AI, Strange K., Zeidel ML, Pfaller W., Gawryl M., Harris HW (1997). Interactions of ultrapure bovine hemoglobin with renal epithelial cells in vivo and in vitro. Am J Physiol 273: F38-52.[Web of Science][Medline]
[Order article via Infotrieve]
- Tam SC, Blumenstein J., Wong JT ( 1976). Soluble dextran-hemoglobin complex as a potential blood substitute. Proc Natl Acad Sci USA 73: 2128-2131.[Abstract/Free Full Text]
- Tam SC, Wong JT ( 1988). Impairment of renal function by stroma-free hemoglobin in rats. J Lab Clin Med 111: 189-193.[Web of Science][Medline]
[Order article via Infotrieve]
- Thompson A., McGarry AE, Valeri CR, Lieberthal W. (1994). Stroma-free hemoglobin increases blood pressure and GFR in the hypotensive rat: Role of nitric oxide. J Appl Physiol 77: 2348-2354.[Abstract/Free Full Text]
- Tyson GE, Bulger RE (1973). Vinblastine-induced aggregates of smooth endoplasmic reticulum in proximal tubular cells of rat kidney. Am J Anat 140: 201-212.[CrossRef][Web of Science]
- Urbaitis B., Lu YS, Fronticelli C., Bucci E. (1992). Renal excretion of pseudo-cross-linked human, porcine and bovine hemoglobins. Biochem Biophys Acta 1156: 50-56.[Medline]
[Order article via Infotrieve]
- Urbaitis BK, Razynska A., Corteza Q., Fronticelli C., Bucci E. (1991). Intravascular retention and renal handling of purified natural and intramolecular cross-linked hemoglobins. J Lab Clin Med 117: 115-121.[Web of Science][Medline]
[Order article via Infotrieve]
- Vogt BA, Alam J., Croatt AJ, Vercellotti GM, Nath KA ( 1995). Acquired resistance to acute oxidative stress. Possible role of heme oxygenase and ferritin. Lab Invest 72: 474-483.[Web of Science][Medline]
[Order article via Infotrieve]
- Zager RA (1996). Rhabdomyolysis and myohemoglobinuric acute renal failure. Kidney Int 49: 314-326.[Web of Science][Medline]
[Order article via Infotrieve]
- Zager RA, Gamelin LM (1989). Pathogenetic mechanisms in experimental hemoglobinuria acute renal failure. Am J Physiol 256: F446-455.[Web of Science][Medline]
[Order article via Infotrieve]
Toxicologic Pathology, Vol. 28, No. 5,
635-642 (2000)
DOI: 10.1177/019262330002800501

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati Twitter What's this?
|
|