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Am J Physiol Heart Circ Physiol 283: H1720-H1728, 2002. First published June 20, 2002; doi:10.1152/ajpheart.00347.2002
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Vol. 283, Issue 4, H1720-H1728, October 2002

SPECIAL COMMUNICATIONS
Validation of formamide as a detubulation agent in isolated rat cardiac cells

Fabien Brette, Kimiaki Komukai, and Clive H. Orchard

School of Biomedical Sciences, University of Leeds, Leeds LS2 9NQ, United Kingdom

Kawai M, Hussain M, and Orchard CH. Am J Heart Circ Physiol 277: H603-H609, 1999 developed a technique to detubulate rat ventricular myocytes using formamide and showed that detubulation results in a decrease in cell capacitance, Ca2+ current density, and Ca2+ transient amplitude. We have investigated the mechanism of this detubulation and possible direct effects of formamide. Staining ventricular cells with di-8-ANEPPS showed that the t tubule membranes remain inside the cell after detubulation; trapping of FITC-labeled dextran within the t tubules showed that detubulation occurs during formamide washout and that the t tubules appear to reseal within the cell. Detubulation had no effect on the microtubule network but resulted in loss of synchronous Ca2+ release on electrical stimulation. In contrast, formamide treatment of atrial cells did not significantly change cell capacitance, Ca2+ current amplitude, action potential configuration, the Ca2+ transient or the response of the Ca2+ transient to isoprenaline. We conclude that formamide washout induces detubulation of single rat ventricular myocytes, leaving the t tubules within the cell, but without direct effects on cell proteins that might alter cell function.

transverse tubules; rat ventricular cell; di-8-ANEPPS; rat atrial cell; Ca2+ current; Ca2+ transient


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