Journal
NEUROTOXICITY RESEARCH
Volume 4, Issue 7-8, Pages -Publisher
SPRINGER
DOI: 10.1080/1029842021000045624
Keywords
Apoptosis; Heme; Hemoglobin; Intracerebral hemorrhage
Categories
Funding
- National Parkinson Foundation, USA
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The exact pathogenesis of neuronal death following bleeding in brain parenchyma is still unknown. Hemoglobin (Hb) toxicity has been postulated to be one of the underlying mechanisms. The purpose of this study was to examine the possible contribution to neurotoxicity of each of the Hb compounds and to characterize the death pathway. Pheochromocytoma (PC12) and neuroblastoma (SH-SY5Y) cell lines were exposed to Hb, globin, hemin, protoporphyrin IX, and iron for 1.5-24 h. We found that Hb and hemin are highly toxic (LD50 of 8 and 20 mu mol/l, respectively) as compared to globin that was not toxic. In addition, protoporphyrin IX and iron, compounds of hemin, were less toxic than hemin itself (LD50 of 962 and 2070 mu mol/l, respectively). We also demonstrated that non-specific protein digestion with proteinase-K, markedly increased Hb toxicity. Hemin-treated cells caused a typical apoptotic cell-death pattern as indicated by DNA fragmentation, caspase activation and reduction in the mitochondrial membrane potential. Treatment with the antioxicant N-acetyl-l-cysteine or iron chelator, deferoxamine, diminished hemin-induced cell death, indicating a role of oxidative stress in this deleterious process. Thus, therapeutic strategies, based on antioxidant, iron chelator and anti-apoptotic agents may be effective in counteracting Hb neurotoxicity.
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