Cancer Research 09 AM Call for Abstracts
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 51, 3555-3558, July 1, 1991]
© 1991 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ogura, R.
Right arrow Articles by Hidaka, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ogura, R.
Right arrow Articles by Hidaka, T.

Electron Spin Resonance Studies on the Mechanism of Adriamycin-induced Heart Mitochondrial Damages

Ryohei Ogura1, Masayasu Sugiyama, Nobuya Haramaki and Toshihiro Hidaka

Department of Medical Biochemistry, Kurume University School of Medicine, 67 Asahi-machi, Kurume 830, Japan

Rats were given i.p. injections of Adriamycin (4 mg/kg body weight) for 6 consecutive days. Electron spin resonance spectrometry with spin labeling and a trapping technique was applied to heart mitochondria obtained from treated and control animals, in order to examine the physical response of heart mitochondrial membrane affected by Adriamycin.

The Adriamycin treatment resulted in a decrease of membrane fluidity (and an increase in order parameter S), with concomitant dysfunction of respiratory responses. The generation of hydroxyl radicals from mitochondria was enhanced in the Adriamycin-treated group. In addition, superoxide dismutase activity in the mitochondrial matrix was found to decrease. The heart mitochondria of Adriamycin-treated animals contained a large amount of lipid peroxide. These results suggest that the enhancement of hydroxyl radical formation in mitochondria affected by Adriamycin is one of the factors involved in Adriamycin-induced cardiotoxicity.

1 To whom requests for reprints should be addressed.

Received 7/20/90. Accepted 4/24/91.




This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
X. Yi, R. Bekeredjian, N. J. DeFilippis, Z. Siddiquee, E. Fernandez, and R. V. Shohet
Transcriptional analysis of doxorubicin-induced cardiotoxicity
Am J Physiol Heart Circ Physiol, March 1, 2006; 290(3): H1098 - H1102.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
Y. Teshima, M. Akao, S. P. Jones, and E. Marban
Uncoupling Protein-2 Overexpression Inhibits Mitochondrial Death Pathway in Cardiomyocytes
Circ. Res., August 8, 2003; 93(3): 192 - 200.
[Abstract] [Full Text] [PDF]


Home page
The OncologistHome page
T. Safra
Cardiac Safety of Liposomal Anthracyclines
Oncologist, August 1, 2003; 8(90002): 17 - 24.
[Abstract] [Full Text] [PDF]


Home page
Toxicol PatholHome page
T. Zima, V. Tesar, R. Sherwood, A. Sood, L.-C. Au, P. J. Richardson, and V. R. Preedy
Acute Dosage With Dexrazoxane, but not Doxorubicin, Is Associated With Increased Rates of Hepatic Protein Synthesis in vivo
Toxicol Pathol, October 1, 2001; 29(6): 591 - 599.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1991 by the American Association for Cancer Research.