Literature DB >> 342457

Haemoglobin--a frustrated oxidase? Implications for red cell metabolism.

R W Carrell, C C Winterbourn, J K French.   

Abstract

The haem proteins can be considered, in one aspect of their function, as machines for activating oxygen. In the case of oxygen-carriers such as haemoglobin, the globin has evolved so that its conformation limits access to the haem group, with resultant reversible release of oxygen. However, distortion of the globin may allow either the discharge of oxygen as the activated product superoxide or, more threateningly, allow direct function of the haemoglobin as an oxidative enzyme. Support for this is shown by the reaction with acetylphenylhydrazine where haemoglobin functions as both an oxidase and oxygenase. An implication of oxidase activity is the potential to initiate free radical formation particularly with unsaturated lipids. Observations of the acetylphenylhydrazine reaction emphasize the role of glutathione as a free radical scavenger.

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Year:  1977        PMID: 342457     DOI: 10.3109/03630267709003909

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  2 in total

1.  The fatty acid composition of red cells deficient in glucose-6-phosphate dehydrogenase and their susceptibility to lipid peroxidation.

Authors:  M R Clemens; H Einsele; H D Waller
Journal:  Klin Wochenschr       Date:  1985-07-01

Review 2.  How Do Red Blood Cells Die?

Authors:  Perumal Thiagarajan; Charles J Parker; Josef T Prchal
Journal:  Front Physiol       Date:  2021-03-15       Impact factor: 4.566

  2 in total

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