Skip Navigation

Cardiovascular Research 2006 71(2):374-382; doi:10.1016/j.cardiores.2006.05.014
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Heinzel, F. R.
Right arrow Articles by Heusch, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Heinzel, F. R.
Right arrow Articles by Heusch, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Copyright © 2006, European Society of Cardiology

Formation of reactive oxygen species at increased contraction frequency in rat cardiomyocytes

Frank R. Heinzela, Yukun Luoa, Giuliano Dodonia, Kerstin Boenglera, Frank Petratb, Fabio Di Lisac, Herbert de Grootb, Rainer Schulza and Gerd Heuscha,*

aInstitut für Pathophysiologie, Universitätsklinikum Essen, Hufelandstraße 55, 45122 Essen, Germany
bInstitut für Physiologische Chemie, Universitätsklinikum Essen, Germany
cDipartimento di Chimica Biologica (F.D.L.), Università di Padova, Italy

* Corresponding author. Email address: gerd.heusch{at}uni-essen.de

Objective Reactive oxygen species (ROS) play an ambivalent role in cardiomyocytes: low concentrations are involved in cellular signaling, while higher concentrations contribute to cellular injury. We studied ROS formation during increases in contraction frequency in isolated cardiomyocytes.

Methods Rat ventricular cardiomyocytes were loaded with dichlorodihydrofluorescein and electrically stimulated (37 °C). ROS formation was assessed by the rate of oxidation-dependent fluorescence increase (OxR). Oxygen consumption (VO2) and NAD(P)H autofluorescence were measured in parallel experiments.

Results Increases in contraction frequency were accompanied by an increase in VO2 and a decrease in NAD(P)H fluorescence. OxR increased to 124±4%, 146±8%, 204±25% and 256±29% of OxR at baseline during 1, 2, 3 and 4 Hz stimulation, and subsequently returned to baseline values with 0.2 Hz. The OxR increase was dose-dependently inhibited by the antioxidant NAC (10 and 100 mM), but unaffected by the NO synthase inhibitor L-NAME (200 µM and 10 mM). The OxR increase was attenuated when myosin ATPase activity was inhibited by butanedione monoxime (BDM; 5 mM).

Conclusion Increased contraction frequency induces ROS formation in rat cardiomyocytes.

KEYWORDS Myocytes; Oxygen radicals; Redox signaling; Contractile function


Time for primary review 20 days


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.