Three-Way Effect of Cyanine Dye on the Structure and Function of Mitochondria
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- Yamashita Kikuji
- School of Dentistry, University of Tokushima
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- Ichikawa Tomokazu
- Institute for Genome Research, University of Tokushima Faculty of Pharmaceutical Sciences, University of Tokushima
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- Yamamoto Takenori
- Institute for Genome Research, University of Tokushima Faculty of Pharmaceutical Sciences, University of Tokushima
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- Kataoka Masatoshi
- School of Dentistry, University of Tokushima Institute for Genome Research, University of Tokushima
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- Nakagawa Yoshinori
- Drugs and Cosmetics Research Center, Hayashibara Biochemical Laboratories, Inc.
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- Terada Hiroshi
- Faculty of Pharmaceutical Sciences, Tokyo University of Science
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- Shinohara Yasuo
- Institute for Genome Research, University of Tokushima Faculty of Pharmaceutical Sciences, University of Tokushima Single-Molecule Bioanalysis Laboratory, National Institute of Advanced Industrial Science and Technology (AIST)
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Description
Previously, we found that the cationic cyanine dye tri-S-C4(5) uncoupled mitochondrial oxidative phosphorylation by acting as an inducer of the mitochondrial permeability transition (PT). In the present study, the actions of cyanine dyes such as tri-S-C4(5) and tri-S-C7(5) on the mitochondrial structures and functions were further characterized. In the presence of inorganic phosphate (Pi), cyanine dyes were found to accelerate mitochondrial oxygen consumption that was partially sensitive to the PT inhibitor cyclosporin A (CsA). However, not only the CsA-sensitive but also CsA-insensitive acceleration of mitochondrial respiration was induced by cyanine dyes; and both of them were found to be associated with the release of mitochondrial cytochrome c. On the contrary, in the absence of Pi, moderate acceleration of respiration was induced by cyanine dyes, but this respiratory effect was not associated with the induction of swelling or the release of mitochondrial cytochrome c. Thus, cyanine dyes were concluded to have 3 different effects on the mitochondrial functions depending on the Pi status.<br>
Journal
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- Journal of Health Science
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Journal of Health Science 49 (6), 448-453, 2003
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390001204497190400
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- NII Article ID
- 110003609103
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- NII Book ID
- AA11316464
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- ISSN
- 13475207
- 13449702
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- NDL BIB ID
- 6759256
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed