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. 2017 Jun 1;68(4):387–413. doi: 10.1007/s12576-017-0541-0

Fig. 1.

Fig. 1

Scheme of a single cell in the EO model. a Scheme of the ionic dynamics for a single-cell model. Simulated ionic currents (i x) involved in the AP generation are shown: i Na fast Na+ current, i pNa persistent Na+ current, i bNa background Na+ current, i NaCa Na+/Ca2+ exchange (NCX) current, i CaL Ca2+ current via L-type Ca2+ channels, i bCa background Ca2+ current, i to transient outward K+ current, i Kr, i Ks rapid and slow components of delayed K+ current, i K1 rectifier K+ current, i NaK Na+/K+ pump current, DS dyadic space, TC terminal cisterns, LR longitudinal reticulum, i rel Ca2+ release flow from the sarcoplasmic reticulum (SR), i up SERCA pump flow from cytosol to the SR, i tr Ca2+ diffusion between the LR and the TC, CaS Ca2+ complexes with calsequestrin, CaTnC Ca2+ complexes with TnC, B 1, B 2 Ca2+ complexes with fast and slow buffer ligands. b Rheological scheme for a single cell model, where a contractile element (CE) is connected to an in-series and parallel passive elastic element (SE, XSE, PE), and a viscous element (VS) is inserted in parallel to the PE. Variables l, l 1 and l ex define deformations of PE, CE and XSE, respectively, relative to their slack lengths (see text for details)