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Latunde-Dada, G.O., Vulpe, C.D., Anderson, G.J., Sim- pson, R.J. and McKie, A.T. (2004) Tissue-specific chan- ges in iron metabolism genes in mice following phenylhydrazine-induced haemolysis. Biochimica et Biophysica Acta, 1690(2), 169-176.

has been cited by the following article:

• TITLE: Effect of calcium and diltiazem on phenylhydrazine-induced oxidative injury in goat erythrocytes

  AUTHORS: Kaushik Das, Jharna Bhattacharyya

  KEYWORDS: Ca2+; Diltiazem; Erythrocyte; Free Radical; Lipid Peroxidation; Phenylhydrazine

  JOURNAL NAME: Health, Vol.2 No.10, October 26, 2010

  ABSTRACT: Lipid peroxidation, hemolysis and thiol contents were studied in intact goat erythrocytes exposed to phenylhydrazine. An increase in lipid peroxidation, hemolysis and thiol content was observed after phenylhydrazine treatment of erythrocyte. Extracellular Ca2+ potentiates the phenylhydrazine-induced lipid peroxidation and hemoly- sis of erythrocytes significantly. Ca2+ does not influence much the thiol content of phenylhydrazine treated erythrocytes. No effect of Ca2+ on control lipid peroxidation, hemolysis and thiol contents of erythrocytes was observed. Diltiazem and EDTA inhibited the increased responses of lipid peroxidation and hemolysis due to Ca2+. However the thiol content was not much influenced by either diltiazem or EDTA. The results suggest that oxidative damage of erythrocyte caused by phenyl hydrazine could be prevented by calcium channel antagonist, diltiazem, which may act as antioxidant also.