VI. Synaptic Fuel Cell Reactions in Vascular-Interstitial-Neuromuscular Closed Circuit: Theory of Neuromuscular Activation

References

• Hodgkin A. L., Huxley A. F. A Quantitative Description of Membrane Current and Its Application to Conduction and Excitation in Nerve. J. Physiol. (Lond.) 1952; 117: 500
   Google Scholar
• Katz B. Nerve, Muscle and Synapse. McGraw-Hill, New York 1966
   Google Scholar
• Nordenström B. E. W. Biologically Closed Electric Circuits: Clinical, Experimental and Theoretical Evidence for an Additional Circulatory System. Nordic Medical Publications, Stockholm 1983
   Google Scholar
• Nordenström B. E. W. An Additional Circulatory System: Vascular-Interstitial Closed Electric Circuits (VICC). J. Biol. Phys. 1987; 15: 43–55
   Google Scholar
• Nordenström B. E. W. I. Neuromuscular Activation Requires Conduction Through Vessels. Physiol. Chem. Phys. Med. NMR 1989; 21: 249–256
   PubMed Web of Science ®Google Scholar
• Nordenström B. E. W. Vascular-Interstitial Neuromuscular Circuits in Neuromuscular Activation: Differences in Femoral and Sciatic Nerves in the Rat. J. Bioelectricity 1989; 8: 109–117
   Google Scholar
• Nordenström B. E. W., Larsson H. II. Slow and Rapid Electrical Pulses in the Caval Vein at Pain-Evoked Leg Contraction in the Rat. Physiol. Chem. Phys. Med. NMR 1989; 21: 257–264
   PubMed Web of Science ®Google Scholar
• Nordenström B. E. W. IV. Electrical Pulses Appear in the Inferior Vena Cava and Abdominal Aorta at Contraction of Leg Muscles. Physiol. Chem. Phys. Med. NMR 1992; 24: 147–152
   PubMed Web of Science ®Google Scholar
• Nordenström B. E. W., Larsson H., Lindqvist M. V. Potential Differences in the Inferior Vena Cava and Between Cava and Extravascular Electrode Accompanying Leg Contraction in Man. Physiol. Chem. Phys. Med. NMR 1992; 24: 153–158
   PubMed Web of Science ®Google Scholar
• Nordenström B. E. W. III. The Action Potential; an Effect of Fuel Cell Reactions in the Synapse. Physiol. Chem. Phys. Med. NMR 1989; 21: 265–278
   PubMed Web of Science ®Google Scholar
• Elfvin L.-G. The Ultrastructure of Neuronal Contacts. Prog. Neurobiol. 1976; 8: 45–79
   Web of Science ®Google Scholar
• Alberts B., Bray D., Lewis J., Raff M., Roberts K., Watson J. D. Molecular Biology of the Cell. Garland, New York, London 1983
   Google Scholar
• Heuser J. E., et al. Synaptic Vesicle Exocytosis Captured by Quick Freezing and Correlated with Quantal Transmitter Release. J. Cell Biol. 1979; 81: 275–300
   PubMed Web of Science ®Google Scholar
• Szent-Györgyi A. Bioelectronics. Academic Press, New York 1968; 79
   Google Scholar
• Cope F. W. Solid-state Physics of Electron and Ion Transport in Biology. Adv. Biol. Med. Phys. 1970; 13: 1
   PubMedGoogle Scholar
• Keilin D. On Cytochrome, a Respiratory Pigment, Common in High Plants. Proc. Roy. Soc. 1925; B98: 312–339
   Google Scholar
• Keilin D. Cytochrome and Respiratory Enzymes. Proc. Roy. Soc. s.B Lond. 1929; 104: 206–251
   Google Scholar
• Warburg O. Chemische Konstitution von Fermenten. Erg. Enzymforsch. 1939; 7: 210
   Google Scholar
• Mitchell P. Chemiosmotic Coupling and Phosphorylation. Glynn Research, Bodmin, CornwallEngland 1966
   Google Scholar
• Mitchell P. Coupling of Phosphorylation to Electron and Hydrogen Transfer by a Chemi-osmotic Type of Mechanism. Nature 1961; 191: 144–148
   PubMed Web of Science ®Google Scholar
• Pethig R. Ionic, Electron and Proton Transport in Membranes. A Review of the Physical Processes Involved, in Modern Bioelectrochemistry, F. Gutmann, H. Keyser. Plenum Press, New York 1986
   Google Scholar
• Blankenship R. E., Parson W. W. The Photochemical Electron Transfer Reactions of Photosynthetic Bacteria and Plants. Annu. Rev. Biochem. 1978; 47: 635–653
   PubMed Web of Science ®Google Scholar
• Eley D. D. Semiconductivity in Biological Molecules. Horizons in Biochemistry, M. Kosha, B. Pullman. Academic Press, New York, London 1962
   Google Scholar
• Ernster L., Schatz G. Mitochondria: A Historical Review. J. Cell Biol. 1981; 91: 227–255
   PubMed Web of Science ®Google Scholar
• Capaldi R. A. Membrane Proteins in Energy Transduction. Marcel Dekker, New York 1979
   Google Scholar
• Hackenbrock C. R. Lateral Diffusion and Electron Transfer in the Mitochondrial Inner Membrane. Trends Biochem. Sci. 1981; 6: 151–154
   Web of Science ®Google Scholar
• Thornber J. P., Markwell J. P. Photosynthetic Pigment-Protein Complexes in Plant and Bacterial Membranes. Trends Biochem. Sci. 1981; 6: 122–125
   Web of Science ®Google Scholar
• Konings W. N., Michels P. A. M. Electron-Transfer-Driven Solute Trans-location Across Bacterial Membranes. Diversity of Bacterial Respiratory Systems, C. J. Knowles. CRC Press, Boca Raton, FL 1980; Vol. 1: 33–86
   Google Scholar
• Gray E. G. The Synapse. Sci. J. 1967; 3: 66
   Google Scholar
• Hanzon V., Toschi G. Electron Microscopy on Microsomal Fractions from Rat Brain. Exp. Cell Res. 1959; 16: 256
   PubMed Web of Science ®Google Scholar
• Cummins J., Hyden H. Adenosine Triphosphate Levels and Adenosine Triphosphatase in Neurons Glia and Neuronal Membranes of the Vestibular Nucleus. Biochim. Biophys. Acta 1962; 60: 271
   PubMed Web of Science ®Google Scholar
• Rosenberg T. On Accumulation and Active Transport in Biological Systems. I. Thermodynamical Considerations. Acta Chem. Scand. 1948; 2: 14
   Google Scholar
• Nordenström B. E. W. Vesicles, Basement Membranes, and the Endothelial Fibrin Film as Possible Products of Biological Electrode Reactions. Electropharmacology, G. M. Eckert, F. Gutmann, H. Keyzer. CRC Press, Boca Raton, FL 1990; 189–203, Chapter 8
   Google Scholar
• Bockris J. O'M., Drazic D. M. Electrochemical Science. Taylor and Francis, London 1972
   Google Scholar
• Skou J. C. The Relationship of a (M²⁺ + Na⁺)-Activated K⁺ Stimulated Enzyme or Enzyme System to the Active Linked Transport of Na⁺ and K⁺ Across the Cell Membrane, in Membrane Transport and Metabolism, A. Kleinzeller, A. Kotyk. Academic Press, New York 1961; 228
   Google Scholar
• Baker P. F. The Relationship Between Phosphorus Metabolism and the Sodium Pump in Intact Nerve. Biochim. Biophys. Acta 1963; 75: 287
   PubMed Web of Science ®Google Scholar
• Bonting S. L., Caravaggio L. L. Sodium-Potassium-Activated Adenosine Triphosphatase in the Squid Giant Axon. Nature 1962; 194: 1180
   PubMed Web of Science ®Google Scholar
• Caldwell P. C., Keynes R. D. The Utilization of Phosphate Bond Energy for Sodium Extrusion from Giant Axons. J. Physiol. (Lond.) 1957; 137: 12
   Google Scholar
• Dunham E. T. Linkage of Active Cations Transport to ATP Utilization. Physiologist 1957; 1: 23
   Google Scholar
• Autidore J. V., Murray L. Cardiac (Microsomal) Na + K Adenosinetri-phosphatase and Its Possible Relationship to the Active Na + K Transport System. Arch. Biochem. Biophys. 1962; 99: 372
   PubMed Web of Science ®Google Scholar
• Portius H. J., Repke K. Versuche zur Charakterisierung einer Transport-ATPase fur Na und K in der Zellmembran des Herzmuskels. Arch. Exp. Pathol. Pharmakol. 1963; 245: 62
   Google Scholar
• Skou J. C. Preparation from Mammalian Brain and Kidney of the Enzyme System Involved in Active Transport of Na' and K +. Biochim. Biophys. Acta 1962; 58: 314
   PubMed Web of Science ®Google Scholar