Cell Membrane Changes After in Vivo Acute Na⁺ Load in Normotensive and Spontaneously Hypertensive Rats

References

• Imaizumi T., Takeshita A., Ashihara T., Nakamura M. Salt loading augments vascular responses to indomethacin in stroke-prone SHR. Am J Physiol 1982; 243: H360–H364
   PubMed Web of Science ®Google Scholar
• Chrysant S. G., Walsh G. M., Kem D. C., Frohlich E. D. Hemodynamic and metabolic evidence of salt sensitivity in spontaneously hypertensive rats. Circulation 1976; 86: 53–54
   Google Scholar
• Louis W. J., Tabei R., Spector A. S., Sjoerdsma A. Studies on the spontaneously hypertensive rat. Genealogy, effects of varying salt intake and kinetics of catecholamine metabolism. Circ Res 1969; 24–25((suppl I))93–102
   Google Scholar
• Dietz R., Schomig A., Rascher W., Strasser R., Kubler W. Sodium and its hypertension accelerating effect on stroke-prone spontaneously hypertensive rats: volume retention versus enhanced vasopressor activity. Salt & Hypertension, JI. Iwai. Igaku Shoin. 1982; 243–257
   Google Scholar
• Dietz R., Schomig A., Haebara H., Mann J. F. E, Rascher W., Grunherz N., Gross R. Studies on the pathogenesis of spontaneous hypertension of rats. Circ Res 1978; 43: I96–I108
   Google Scholar
• Jones A. W. Altered transport in large and small arteries from spontaneously hypertensive rats and the influence of calcium. Circ Res 1974; 34: I117–I122
   Web of Science ®Google Scholar
• Postnov Y. V., Orlov S. N., Gulak R. V. Altered permeability of the erythrocyte membrane for sodium and potassium ions in spontaneously hypertensive rats. Pflügers Arch 1976; 365: 257–263
   PubMed Web of Science ®Google Scholar
• Altman J., Garay R. P., Papadimitriou A., Worcel M. Alterations in22Na fluxes of arterial smooth muscles of spontaneously hypertensive rats. Proc Drit Pharmacol Soc 1977; 496P
   Google Scholar
• Wiley J. S., Hutchinson J. S., Mendelsohn F. A. O, Doyle A. E. Increased sodium permeability of erythrocytes in spontaneously hypertensive rats. Clin Exp Pharmacol Physiol 1980; 7: 527–530
   PubMed Web of Science ®Google Scholar
• Friedman S. M., Nakashima M., MacIndoe A., Friedman C. L. Increased erythrocyte permeability to Li and Na in the spontaneously hypertensive rats. Experientia 1976; 32: 476–478
   PubMedGoogle Scholar
• Friedman S. M. Evidence for enhanced sodium transport in the tail artery of the spontaneously hypertensive rat. Hypertension 1976; 1: 572–582
   Google Scholar
• Yamori Y., Nara Y., Horie R., Ohtaka M. Ion permeability of erythrocyte membrane in spontaneously hypertensive rat. Jap Heart J 1977; 18: 604–605
   PubMedGoogle Scholar
• Montenay-Garestier T., Aragon I., Devynck M. A., Meyer P., Helene C. Evidence for structural changes in erythrocyte membranes of spontaneously hypertensive rats. A fluorescence polarization study. Biochem Biophys Res Comm 1981; 100: 660–665
   PubMed Web of Science ®Google Scholar
• de Mendonca M., Knorr A., Grichois M. L., Ben-Ishay D., Garay R. P., Meyer P. Erythrocytic sodium transport systems in primary and secondary hypertension of the rat. Kidney Intern 1982; 21(suppl. II)S69–S75
   Google Scholar
• Postnov Y. V., Orlov S., Podukin N. N. Decrease in calcium binding by the red blood cell membrane in spontaneously hypertensive rats and in essential hypertension. Pflügers Arch 1979; 379: 191–195
   PubMed Web of Science ®Google Scholar
• Devynck M. A., Pernollet M. G., Nunez A. M., Meyer P. Analysis of calcium handling in erythrocyte membranes of genetically hypertensive rats. Hypertension 1981; 3: 397–403
   PubMed Web of Science ®Google Scholar
• Boriskina G. M., Gulak P. V., Postnov Y. V. Phosphoinositide content in the erythrocyte membranes of rats with spontaneous hypertension. Experientia 1978; 34: 744
   PubMedGoogle Scholar
• Koutouzov S., Marche P., Girard A., Meyer P. Altered turnover of polyphosphoinositides in the erythrocyte membrane of the spontaneously hypertensive rat. Hypertension 1983; 5: 409–414
   PubMed Web of Science ®Google Scholar
• Gonick H. C., Kramer HH, Paul W., Lu E. Circulating inhibitor of sodium-potassium activated adenosine triphosphate after expansion of extracellular fluid volume in rats. Clin Sci Mol Med 1977; 53: 329–334
   PubMedGoogle Scholar
• de Wardener H. E., Clarkson E. M., Bitensky L., MacGregor G. A., Alagband-Zadeh J., Chayen J. Effect of sodium intake on ability of human plasma to inhibit renal Na+K+adenosine triphosphatase in vitro. Lancet 1981; i: 411–412
   Google Scholar
• Haddy F. J., Overbeck H. W. The role of humoral agents in volume-expanded hypertension. Life Sci 1976; 19: 935–948
   PubMed Web of Science ®Google Scholar
• Nathan I., Fleischer G., Dvilansky A., Livne A., Parola A. H. Membrane dynamic alterations associated with activation of human platelets by thrombin. Biochim Biophys Acta 1980; 598: 417–421
   PubMed Web of Science ®Google Scholar
• Aragon I., Montenay-Garestier T., Devynck M. A., Pernollet M. G., Nunez A. M., Ben-Ishay D., Meyer P., Helene C. Diffuse structural abnormalities in cell membranes from genetically hypertensive rats. Clin Sci Mol Med 1982; 63: 37s–39s
   Google Scholar
• Shinitzky M., Barenholz Y. Fluidity parameters of lipid regions determined by fluorescence polarization. Biochim Biophys Acta 1978; 515: 367–394
   PubMed Web of Science ®Google Scholar
• Van Kampen E. S., Zijlstra W. G. Standardization of hemoglobinometry. II. The hemoglobincyanide method. Clin Chim Acta 1961; 6: 538
   PubMed Web of Science ®Google Scholar
• Garay R. P., Garrahan P. S. The interaction of sodium and potassium with the sodium pump in red cells. J Physiol 1973; 231: 297–325
   PubMed Web of Science ®Google Scholar
• Hatzinikolaou P., Gavras H., Brunner H. R., Gavras I. Role of vasopressin, catecholamines and plasma volume in hypertonic saline-induced hypertension. Am J Physiol 1981; 240: H827–H831
   PubMed Web of Science ®Google Scholar
• de Mendonca M., Garay R. P., Ben-Ishay D., Meyer P. Abnormal erythrocyte cation transport in primary hypertension. Hypertension 1981; 31: 179–181
   Google Scholar
• Ellory J. C., Flatman P. W., Stewart G. W. Inhibition of human red cell sodium and potassium transport by divalent cations. J Physiol 1983; 340: 1–18
   PubMed Web of Science ®Google Scholar
• Wieth J. O. Effects of monovalent cations on sodium permeability of human red cells. Acta Physiol Scand 1970; 79: 76–87
   PubMedGoogle Scholar
• Kimelberg H. K. Alterations in phospholipid-dependent Na+K+-ATPase activity due to lipid fluidity. Effect of cholesterol and Mg²⁺. Biochim Biophys Acta 1975; 413: 143–146
   Web of Science ®Google Scholar
• Dahl L. K. Effect of chronic excess salt feeding. Elevation of plasma cholesterol in rats and dogs. J Exp Med 1960; 112: 363–373
   Google Scholar
• Cooper R. H. Anemia with spur cells: a red cell defect acquired in serum and modified in the circulation. J Clin Invest 1969; 48: 1820–1827
   PubMed Web of Science ®Google Scholar
• Giraud F., Claret M., Garay R. P. Interactions of cholesterol with the Na+pump in red blood cells. Nature 1976; 264: 646–648
   PubMed Web of Science ®Google Scholar
• Yeagle P. L. Cholesterol modulation of Na+K+-ATPase hydrolyzing activity in the human erythrocyte. Biochim Biophys Acta 1983; 727: 39–45
   PubMed Web of Science ®Google Scholar
• Haddy F. J., Pamnani M. B., Clough D. L. Humoral factors and the sodium-potassium pump in volume-expanded hypertension. New Trends in Arterial Hypertension, M. Worcel, JP Bonvalet, SZ Langer, J. Menard, J. Sassard. Elsevier/North Holland. 1981; 189–199
   Google Scholar
• Yamori Y., Igawa T., Kanbe T., Kihara M., Nara Y., Horie R. Intracellular electrolyte balance in genetic hypertension. 8th International Congress of Nephrology. University Studio Athens. 1981; 337
   Google Scholar