Abstract

Purkinje fibers of the sheep heart were exposed to (a) 0.1mm dihydro-ouabain (DHO), followed by (b) 0.1mm DHO in Na-free solution or to (c) 1mm dinitrophenol (DNP). The degree of electrical decoupling was characterized in terms of the inside longitudinal resistancer i as measured with a 3-microelectrode voltage-clamp technique. Procedurea increasedr i by a factor of 3.7±1.1 (mean±sd),b by a factor of 9.8±2.2, whereas inc incomplete voltage control indicated nearly complete uncoupling. Intracellular calcium activity (aCa i ) was monitored with a microelectrode system. At control conditionsaCa i was below 0.1 μm. The procedures listed above increasedaCa i to (a) 4±1.5 μm, (b) 8±2 μm, and (c) 36±12 μm. The increase ofaCa i was in good correlation with the changes in core resistance. Effects on nexus ultrastructure, investigated with freeze-fracture techniques, are shown in histograms. At control conditions, the particle diameter distributed around a single peak (8.3±0.5 nm). Proceduresb andc induced a second population at 10.8 nm; increased decoupling reduced the control population in favor of the 10.8 nm population. Decoupling enlarged the width of the nexus gap by a factor of 1.6; again, the control population decreased in favor of a new population. In the decoupled state the height of the particle was smaller. Pits on the E-face displayed a more regular array and a nearly unchanged center-to-center spacing. Separation into several peaks was not possible due to scatter of the data. We interpret the findings to mean that elevatedaCa i induces a conformational change of the nexus subunits which corresponds to a transition from an open to a closed state. The conformational change can be formally described by a particle contraction which disrupts the continuity with the particle of the adjacent membrane. Purkinje fibers exposed to DNP for 1 hr showed thinned (7.7±0.5 mm) and elongated particles. We suggest that this is a secondary event and not a precursor of functional uncoupling.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.