Planta Med 1984; 50(2): 124-127
DOI: 10.1055/s-2007-969648
Research Articles

© Georg Thieme Verlag Stuttgart · New York

Photodynamic Hemolysis caused by α-Terthienyl

Etsuo Yamamoto1 , W. Donald MacRae1 , Federico J. Garcia2 , G. H. Neil Towers1
  • 1Department of Botany, University of British Columbia, Vancouver, B. C., V6T 2B1 Canada
  • 2Instituto de Quimica, Universidad Nacional Autonoma de Mexico, Mexico 20, D. F.
Further Information

Publication History

Publication Date:
26 February 2007 (online)

Abstract

The photohemolysis of human erythrocytes caused by α-terthienyl was partially inhibited by 10 mM sodium azide or 2,5-dimethylfuran, singlet oxygen scavengers, but not by 2,6,-di-t-butyl-4-methylphenol, a radical scavenger.

Lipid peroxidation was observed with erythrocyte ghosts. In contrast to the hemolysis of intact cells, 2,6,-di-t-butyl-4-methylphenol, completely inhibited lipid peroxidation, although azide partially protected the membrane. The results of the above two inhibitor experiments are in conflict and suggest that lipid peroxidation of the membrane is not the main cause of the photohemolysis.

Crosslinking of the membrane proteins, especially spectrins, was also observed, although radioactivity of 3H-α-terthienyl was not found in the crosslinked proteins.

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