The toxicities of native and modified hemoglobins
- PMID: 9034247
- DOI: 10.1016/s0891-5849(96)00499-6
The toxicities of native and modified hemoglobins
Abstract
Recent research on the potential use of hemoglobin derivatives as a blood substitute has revealed that the administration of large quantities of free hemoglobin into the circulation results in a variety of toxic side effects. Because it has been well established that hemoglobin, like myoglobin, has considerable pro-oxidant activity, a number of studies have appeared suggesting that the administered hemoglobins may catalyze various oxidative and peroxidative reactions, which in turn, would cause the observed pathologic conditions. This occurs as a result of the in vivo formation of highly oxidized forms of the native and modified hemoglobins. In addition, it has been proposed that considerable amounts of free hemin and iron may be generated as a result of the catabolism of the injected hemoglobin. Hemin is known to be very toxic when present in large amounts, and iron could catalyze the formation of hydroxyl radicals via Fenton-type reactions. Thus, the toxic activities of catabolic products of hemoglobin could also be involved in all or part of the observed side effects. The purpose of this review is to consider the conditions under which reactive species of hemoglobin may be formed in vivo, their potential reactivity, and whether their individual or combined oxidative activities could account for the biological damage that is observed in vivo following hemoglobin transfusions.
Similar articles
-
Hemoglobin induced apolipoprotein B crosslinking in low-density lipoprotein peroxidation.Arch Biochem Biophys. 1996 Feb 15;326(2):252-60. doi: 10.1006/abbi.1996.0073. Arch Biochem Biophys. 1996. PMID: 8611031
-
A novel hemoglobin-adenosine-glutathione based blood substitute: evaluation of its effects on human blood ex vivo.ASAIO J. 2000 Nov-Dec;46(6):679-92. doi: 10.1097/00002480-200011000-00007. ASAIO J. 2000. PMID: 11110264
-
Both hemoglobin and hemin cause damage to retinal pigment epithelium through the iron ion accumulation.J Pharmacol Sci. 2024 Jun;155(2):44-51. doi: 10.1016/j.jphs.2024.04.001. Epub 2024 Apr 2. J Pharmacol Sci. 2024. PMID: 38677785
-
Hemoglobin-based blood substitutes and the hazards of blood radicals.Free Radic Res. 2000 Oct;33(4):341-8. doi: 10.1080/10715760000300881. Free Radic Res. 2000. PMID: 11022843 Review.
-
Red cell substitutes from hemoglobin--do we start all over again?Curr Opin Chem Biol. 2010 Aug;14(4):538-43. doi: 10.1016/j.cbpa.2010.03.021. Epub 2010 Apr 12. Curr Opin Chem Biol. 2010. PMID: 20392662 Review.
Cited by
-
A product of heme catabolism modulates bacterial function and survival.PLoS Pathog. 2013;9(7):e1003507. doi: 10.1371/journal.ppat.1003507. Epub 2013 Jul 25. PLoS Pathog. 2013. PMID: 23935485 Free PMC article.
-
Is Hemopexin a Nephrotoxin or a Marker of Kidney Injury in Renal Ischemia-Reperfusion?Biomolecules. 2024 Nov 27;14(12):1522. doi: 10.3390/biom14121522. Biomolecules. 2024. PMID: 39766229 Free PMC article.
-
The GAS PefCD exporter is a MDR system that confers resistance to heme and structurally diverse compounds.BMC Microbiol. 2016 Apr 19;16:68. doi: 10.1186/s12866-016-0687-6. BMC Microbiol. 2016. PMID: 27095127 Free PMC article.
-
The heme sensing response regulator HssR in Staphylococcus aureus but not the homologous RR23 in Listeria monocytogenes modulates susceptibility to the antimicrobial peptide plectasin.BMC Microbiol. 2010 Dec 1;10:307. doi: 10.1186/1471-2180-10-307. BMC Microbiol. 2010. PMID: 21122114 Free PMC article.
-
Elevated red cell distribution width is associated with delayed postoperative recovery after correction of Tetralogy of Fallot.Ann Pediatr Cardiol. 2013 Jul;6(2):121-5. doi: 10.4103/0974-2069.115252. Ann Pediatr Cardiol. 2013. PMID: 24688227 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources