932
Views
2
CrossRef citations to date
0
Altmetric
Original Article

Influence of NO and [Ca2+]o on [Ca2+]i homeostasis in rat ventricular cardiomyocytes

, , , , , & show all
Pages 1338-1343 | Received 13 Nov 2017, Accepted 11 Jun 2018, Published online: 26 Jul 2018

References

  • Benitah JP, Alvarez JL, Gomez AM. L-type Ca(2+) current in ventricular cardiomyocytes. J Mol Cell Cardiol. 2010;48:26–36.
  • Tandan S, Wang Y, Wang TT, et al. Physical and functional interaction between calcineurin and the cardiac L-type Ca2+ channel. Circ Res. 2009;105:51–60.
  • Heineke J, Auger-Messier M, Correll RN, et al. CIB1 is a regulator of pathological cardiac hypertrophy. Nat Med. 2010;16:872–879.
  • Frank D, Frey N. Cardiac z-disc signaling network. J Biol Chem. 2011;286:9897–9904.
  • Shim AL, Mitrokhin VM, Kazanski V, et al. Discrete stretch eliminates electrophysiological dose-dependent effects of nitric oxide donor SNAP in rat atrium. Bull Exp Biol Med. 2017;163:705–709.
  • Shim AL, Mitrokhin VM, Gorbacheva LR, et al. Kinetics of mechanical stretch-induced nitric oxide production in rat ventricular cardiac myocytes. Bull Exp Biol Med. 2017;163:583–585.
  • Kazanski EV, Kamkin GA, Makarenko YE, et al. Role of nitric oxide in the regulation of mechanosensitive ionic channels in cardiomyocytes: Contribution of NO-synthases. Bull Exp Biol Med. 2010;150:263–267.
  • Gallo MP, Ghigo D, Bosia A, et al. Modulation of guinea-pig cardiac L-type calcium current by nitric oxidesynthase inhibitors. J Physiol. 1998;506:639–651.
  • Gallo MP, Malan D, Bedendi I, et al. Regulation of cardiac calcium current by NO and cGMP-modulating agents. Pflugers Arch. 2001;441:621–628.
  • Abi-Gerges N, Fischmeister R, Méry PF. G protein-mediated inhibitory effect of a nitric oxide donor on the L-type Ca2+ current in rat ventricular myocytes. J Physiol. 2001;531:117–130.
  • Han S, Schiefer A, Isenberg G. Ca2+ load of guinea-pig ventricular myocytes determines efficacy of brief Ca2+ currents as trigger for Ca2+ release. J Physiol. 1994;480:411–421.
  • Han ZY, Chen M, Wen P, et al. 8%-9% and 12%-13% hypoxic gas induced free radicals generation in rat's left and right myocardium. Sheng Li Xue Bao. 1995;47:453–462.
  • Han J, Kim E, Ho WK, et al. Effects of volatile anesthetic isoflurane on ATP-sensitive K+ channels in rabbit ventricular myocytes. Biochem Biophys Res Commun. 1996;229(3):852–856.
  • Kazanski V, Mitrokhin VM, Mladenov MI, et al. Cytokine effects on mechano-induced electrical activity in atrial myocardium. Immunol Invest. 2017;46:22–37.
  • Kirstein M, Rivet-Bastide M, Hatem S, et al. Nitric oxide regulates the calcium current in isolated human atrial myocytes. J Clin Invest. 1995;95:794–802.
  • Campbell DL, Stamler JS, Strauss HC. Redox modulation of L-type calcium channels in ferret ventricular myocytes. Dual mechanism regulation by nitric oxide and S-nitrosothiols. J Gen Physiol. 1996;108:277–293.
  • Wahler GM, Dollinger SJ. Nitric oxide donor SIN-1 inhibits mammalian cardiac calcium current through cGMP-dependent protein kinase. Am J Physiol. 1995;268:45–54.
  • Aksyonov A, Mitrokhin VM, Mladenov MI. Effects of interleukin-2 on bioelectric activity of rat atrial myocardium under normal conditions and during gradual stretching. Immunol Lett. 2015;167:23–28.
  • Mitrokhin VM, Mladenov MI, Kamkin AG. Effects of interleukin-6 on the bio-electric activity of rat atrial tissue under normal conditions and during gradual stretching. Immunobiology. 2015;220:1107–1112.
  • Ovchinnikov RS, Mitrokhin VM, Mladenov MI. Effects of interleukin-17A on the bio-electric activity of rat atrial myocardium under normal conditions and during gradual stretching. Cytokine. 2015;76:561–565.
  • Mitrokhin V, Kazanski V, Kalsin V, et al. Interleukin-6 induced activation of a non-selective outward cation conductance in human cardiac fibroblasts. Cytokine. 2017;97:117–122.
  • Rickover O, Zinman T, Kaplan D, et al. Exogenous nitric oxide triggers classic ischemic preconditioning by preventing intracellular Ca2+ overload in cardiomyocytes. Cell Calcium. 2008;43:324–333.
  • Franzini-Armstrong C, Protasi F, Ramesh V. Shape, size, and distribution of Ca(2+) release units and couplons in skeletal and cardiac muscles. Biophys J. 1999;77:1528–1539.
  • Kass SR, Sanguinetti CM. Inactivation of calcium channel current in the Calf cardiac purkinje fiber; evidence for voltage and calcium-mediated mechanisms. J Gen Physiol. 1984;84:705–726.
  • Lipp P, Huser J, Pott L, et al. Spatially non-uniform Ca2+ signals induced by the reduction of transverse tubules in citrate-loaded guinea-pig ventricular myocytes in culture J Physiol (Lond). 1996;497:589–597.
  • Matsuoka S, Nicoll DA, Hryshko LV, et al. Regulation of the cardiac Na(+)-Ca2+ exchanger by Ca2+. Mutational analysis of the Ca(2+)-binding domain. J Gen Physiol. 1995;105:403–420.
  • Fujioka Y, Hiroe K, Matsuoka S. Regulation kinetics of Na+-Ca2+ exchange current in guinea-pig ventricular myocytes. J Physiol (Lond). 2000;529:611–623.
  • Brette F, Salle L, Orchard CH. Differential modulation of L-type Ca2+ current by SR Ca2+ release at the T-tubules and surface membrane of rat ventricular myocytes. Circ Res. 2004;95:1–7.
  • Diaz ME, O’Neill SC, Eisner DA. Sarcoplasmic reticulum calcium content fluctuation is the key to cardiac alternans. Circ Res. 2004;94:650–656.
  • Louch WE, Bito V, Heinzel FR, et al. Reduced synchrony of Ca2+ release with loss of T-tubules a comparison to Ca2+ release in human failing cardiomyocytes. Cardiovasc Res. 2004;62:63–73.