Effect of SH-Group Reagents on Net Water Transport in Frog Urinary Bladder

References

• Bentley P. J. The effects of neurohypophyseal extracts on water transfer across the wall of the isolated bladder of the toad Bufo marinus. J. Endocrinol. 1958; 17: 201–209
   PubMed Web of Science ®Google Scholar
• Bentley P. J. Physiological properties of the isolated frog bladder in hyperosmotic solutions. Comp. Biochem. Physiol. 1964; 12: 233–239
   Google Scholar
• Bourguet J. Influence de la temperature sur la cinetique de l'augmentation de permeabilite a l'eau de la vessie de grenouille sous Taction de l'ocytocine. J. Physiol. (Paris). 1966; 58: 476
   Google Scholar
• Bourguet J., Chevalier J., Hugon J. S. Alterations in membrane associated particles distribution during antidiuretic challenge in frog urinary bladder epithelium. Biophys. J. 1976; 16: 627–639
   Google Scholar
• Bourguet J., Jard S. Un dispositif automatique de measure et d'enregistrement du flux net d'eau a travers la peau et la vessie des amphibians. Biochim. Biophys. Acta. 1964; 88: 442–444
   PubMed Web of Science ®Google Scholar
• Brown P. A., Feinstein M. B., Sha'afi R. I. Membrane proteins related to water transport in human erythrocytes. Nature (Lond). 1975; 254: 523–525
   PubMed Web of Science ®Google Scholar
• Cecil R., McPhee J. R. Sulfur chemistry of proteins. Adv. Prot. Chem. 1959; 14: 255–389
   PubMedGoogle Scholar
• Chevalier J., Adragna N., Bourguet J., Gobin R. Fine structure of intra‐membranous particle aggregates in ADH‐treated frog urinary bladder and skin: influence of glutaraldehyde and N‐ethyl maleimide. Cell Tissue Res. 1981; 218: 595–606
   Google Scholar
• Chevalier J., Bourguet J., Hugon J. S. Membrane associated particles. Distribution in frog urinary bladder epithelium at rest and after oxytocin treatment. Cell Tissue Res. 1974; 152: 129–140
   Google Scholar
• Frenkel A., Ekblad E. B. M., Edelman I. S. Effects of sulfhydryl reagents on basal and vasopressin‐stimulated Na+ transport in the toad bladder. Biomembranes, H. Eisenberg, E. Katchalski‐Katzir, L. A. Manson. Plenum Press, New‐York 1975; Vol. 7: 61–80
   Google Scholar
• Hays R. M., Chevalier J., Gobin R., Bourguet J. Fusion images and intramembrane particle aggregates during the action of antidiuretic hormone. A rapid‐freeze study. Cell Tissue Res. 1985; 240: 433–439
   Google Scholar
• Humbert F., Montesano R., Grosso A., DeSousa R. C., Orci L. Particle aggregates in plasma and intracellular membranes of toad bladder (granular cell). Experientia. 1977; 33: 1364–1367
   Google Scholar
• Kachadorian W. A., Levine S. D., Wade J. B., di Scala V. A., Hays R. M. Relationship of aggregated intramembranous particles to water permeability in vasopressin treated toad urinary bladder. J. Clin. Invest. 1977; 59: 576–581
   Google Scholar
• Kachadorian W. A., Wade J. B., di Scala V. A. Vasopressin induced structural changes in toad bladder luminal membrane. Science 1975; 190: 67–69
   Google Scholar
• Leaf A. Some actions of neurohypophyseal hormones on a living membrane. J. Gen. Physiol. 1960; 43: 175–189
   PubMedGoogle Scholar
• Muller J., Kachadorian W. A., di Scala V. A. Evidence that ADH‐stimulated intramembranous particle aggregates are transferred from cytoplasmic to luminal membranes in toad bladder epithelial cells. J. Cell Biol. 1980; 85: 83–95
   PubMed Web of Science ®Google Scholar
• Parisi M., Pisam M., Merot J., Chevalier J., Bourguet J. The role of microtubules and microfilaments in the hydrosmotic response to antidiuretic hormone. Biochim. Biophys. Acta. 1985; 817: 333–342
   Google Scholar
• Pratz J., Ripoche P., Corman B. Evidence for proteic water pathways in the luminal membrane of kidney proximal tubule. Biochim. Biophys. Acta. 1986; 856: 259–266
   Google Scholar
• Rasmussen H., Schwartz I. L., Schoessler M. A., Hochster G. Studies on the mechanisms of action of vasopressin. Proc. Natl. Acad. Sci. U.S.A. 1960; 46: 1278–1287
   Google Scholar
• Ripoche P., Bourguet J., Parisi M. The effect of hypertonic media on water permeability of frog urinary bladder. Inhibition by catecholamines and prostaglandin E. J. Gen. Physiol. 1973; 61: 110–124
   Google Scholar
• Sawyer W. H., Schissgall R. M. Increased permeability of the frog bladder to water response to dehydration and neurohypophyseal extracts. Am. J. Physiol. 1956; 187: 312–314
   Google Scholar
• Wade J. B. Membrane structural specialization of the toad urinary bladder revealed by the freeze‐fracture technique. III. Location, structure and vasopressin dependence of intramembranous particle arrays. J. Membr. Biol. Special Issue. 1978; 40: 281–296
   Google Scholar