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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/5440

Title: Oxidative damage induced by a novel porphyrin on rat brain mitochondria and its possible implications in therapy
Authors: CHATTERJEE, SR
KAMAT, JP
SHETTY, SJ
SRIVASTAVA, TS
DEVASAGAYAM, TPA
Keywords: gamma-linolenic acid
lipid-peroxidation
photodynamic therapy
cancer-therapy
photosensitization
photofrin
tumors
light
Issue Date: 1997
Publisher: CHURCHILL LIVINGSTONE
Citation: REDOX REPORT, 3(3), 183-188
Abstract: Free radical-induced oxidative damage is involved in several pathological disorders. On the other hand, selective induction of peroxidation in diseased tissue is a promising approach to the treatment of cancer by photodynamic therapy. In this study we have used rat brain mitochondria as a model to evaluate the ability of a new water soluble porphyrin, 5,10,15,20-tetrakis[4-(carboxymethyleneoxy)phenyl]porphyrin (T4CPP), to induce peroxidative damage during photosensitization. Peroxidation in mitochondria, one of the crucial targets of the photodynamic effect, was assessed from the formation of thiobarbituric acid reactive substances and lipid hydroperoxides. The effect on mitochondrial function was estimated from the loss of a mitochondrial marker enzyme, succinate dehydrogenase (SDH). The photodamage was observed to be time-and concentration-dependent of T4CPP. Inhibition studies suggested involvement of singlet oxygen (O-1(2)) and, to a lesser extent, of hydroxyl ((OH)-O-.), peroxyl (ROO.-) and superoxide radicals (O-2(.-)) in the photodamage. The addition of gamma-linolenic acid (a promoter of lipid peroxidation) to the system led to an enhancement of the T4CPP-induced peroxidative damage. Thus, our study indicated that the combination of gamma-linolenic acid and T4CPP could enhance the photodynamic effect and has potential applications in photodynamic therapy.
URI: http://dspace.library.iitb.ac.in/xmlui/handle/10054/5440
http://hdl.handle.net/10054/5440
ISSN: 1351-0002
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