99
Views
70
CrossRef citations to date
0
Altmetric
Review Article

Lacrimal fluid and electrolyte secretion: A review

Pages 607-617 | Received 26 Sep 1988, Accepted 13 Mar 1989, Published online: 02 Jul 2009

References

  • Holly F., Lemp M. A. Tear physiology and dry eyes. Surv. Ophthalmol. 1977; 22: 69–87
  • Sjogren H., Bloch K. J. Keratocon-junctivitis sicca and the Sjogren syndrome. Surv. Ophthalmol. 1971; 16: 145–159
  • Maudgal P. C., Missotten L. The dry eye syndrome. Superficial Keratitis, P. C. Maugdal, L. Missotten. Dr. W. bv Junk, The HagueNetherlands 1981; 151–157
  • Weil B. A. The dry eye. The Lacrimal System, B. Milder, B. A. Weil. Appleton-Century-Crofts, Norwalk, CTUSA 1983; 117–124
  • Thaysen J. H. The lacrimal gland. Physiology of Membrane Disorders, T. E. Andreoli, J. F. Hoffman, D. D. Fanestil. Plenum, New York, NYUSA 1978; 415–433
  • Botelho S. Y., Martinez E. V. Electrolytes in lacrimal gland fluid and in tears at various flow rates in the rabbit. Am. J. Physiol. 1973; 225: 606–609
  • Whitwell J. Denervation of the lacrimal gland. Brit. J. Ophthal. 1958; 42: 518–525
  • Botelho S. Y., Hisada M., Fuenmayor N. Functional innervation of the lacrimal gland in the cat. Arch. Ophthalmol. 1966; 76: 581–588
  • de Haas E. B.H. Lacrimal gland response to parasympathicomimetics after parasympathetic denervation. Arch. Ophthalmol. 1960; 64: 34–43
  • Goldstein A. M., de Palau A., Botelho S. Y. Inhibition and facilitation of pilocarpine-induced lacrimal flow by norepinephrine. Invest. Ophthalmol. 1967; 6: 498–511
  • Alexander J. H., van Lennep E. W., Young J. A. Water and electrolyte secretion by the exorbital lacrimal gland of the rat studied by micropunctiure and catheterization techniques. Pflugers Arch. 1972; 337: 299–309
  • Botelho S. Y., Martinez E. V., Pholpramool C., van Prooyen H. C., Janssem J. T., de Palau A. Modification of stimulated lacrimal gland flow by sympathetic nerve impulses in rabbit. Am. J. Physiol. 1976; 230: 80–84
  • Kikkawa T., Akagi Y. Sympathetic innervation and its physiological function in rabbit lacrimal gland. Recent Advances on the Lacrimal System, M. Yamaguchi. Asahi Evening News, KyotoJapan 1978; 11–20
  • Tangkrisanavinont V. Stimulation of lacrimal secretion by sympathetic nerve impulses in the rabbit. Life Sci. 1984; 34: 2365–2371
  • Emmelin N. G., Stromblad B. C.R. Sensitization of the lachrymal gland by treatment with a parasympathicolytic agent. Acta Physiol. Scand. 1956; 36: 171–174
  • Botelho S. Y., Goldstein A. M., Martinez E. V. Norepinephrine-responsive beta-adrenergic receptors in rabbit lacrimal gland. Am. J. Physiol 1973; 224: 1119–1122
  • Gilbard J. P., Dartt D. A. Changes in lacrimal gland fluid osmolarity with flow rate. Invest. Ophthalmol. Vis. Sci. 1982; 23: 804–806
  • Hisada M., Botelho S. Y. Membrane potentials of in situ lacrimal gland in cat. Am. J. Physiol. 1968; 214: 1262–1267
  • Silva P., Stoff J., Field M., Fine L., Forrest J. N., Epstein F. H. Mechanism of active chloride secretion by shark rectal gland: Role of Na,K-ATPase in chloride transport. Am. J. Physiol. 1977; 233: F298–F306
  • Botelho S. Y., Fuenmayor N., Hisada M. Flow and potentials during perfusion of lacrimal gland with electrolyte solutions. Am. J. Physiol. 1978; 235: C8–C12
  • Dartt D. A., Moller M., Poulsen J. H. Lacrimal gland electrolyte and water secretion in the rabbit: Localization and role of (Na++K+)-activated ATPase. J. Physiol. 1981; 321: 557–569
  • Petersen O. H., Maruyama Y. Calcium-activated potassium channels and their role in secretion. Nature 1984; 307: 693–696
  • Petersen O. H. Calcium-activated potassium channels and fluid secretion by exocrine glands. Am. J. Physiol. 1986; 251: G1–G13
  • Petersen O. H. Potassium channels and fluid secretion. News Physiol. Sci. 1986; 1: 92–95
  • Petersen O. H., Finlay I., Suzuki K., Dunne M. J. Messenger-mediated control of potassium channels in secretory cells. J. Exp. Biol. 1986; 124: 33–52
  • Burgen A. S.V. The secretion of potassium in saliva. J. Physiol. 1956; 132: 20–39
  • Kikkawa T. Secretory potentials in the lacrimal gland of the rabbit. Jap. J. Ophthalmol. 1970; 14: 25–40
  • Botelho S. Y., Dartt D. A. Effect of calcium antagonism or chelation on rabbit lacrimal gland secretion and membrane potentials. J. Physiol. 1980; 304: 397–403
  • Iwatsuki N., Petersen O. H. Mem-Membrane potential, resistence, and intercellular communication in the lacrimal gland: Effects of acetylcholine and adrenaline. J. Physiol. 1978; 278: 507–520
  • Iwatsuki N., Petersen O. H. intracellular Ca2+ injection causes membrane hyperpolarization and conductance increase in lacrimal acinar cells. Pflugers Arch. 1978; 377: 185–187
  • Parod R. J., Putney J. W. The role of calcium in the receptor mediated control of potassium permeability in the rat lacrimal gland. J. Physiol. 1978; 281: 371–381
  • Findlay I. A patch-clamp study of potassium channels and whole-cell currents in acinar cells of the mouse lacrimal gland. J. Physiol. 1984; 350: 179–195
  • Marty A., Tan Y. P., Trautmann A. Three types of calcium-dependent channel in rat lacrimal glands. J. Physiol. 1984; 357: 293–325
  • Trautmann A., Marty A. Activation of Ca-dependent K channels by carbamylcholine in rat lacrimal glands, Proc. Natl. Acad. Sci. USA 1984; 81: 611–615
  • Marty A. Ca2+ -dependent K+ channels with large unitary conductance. Trends Neurosci. 1983; 6: 262–265
  • LechlFiter J., Dartt D., Brehm P. Vasoactive intestinal peptide activates Ca2+ -dependent K+ channels through a cAMP pathway in mouse lacrimal cells. Neuron. 1988; 1: 227–237
  • Frizzell R. A., Halm D. R., Rechkemmer G., Shoemaker R. L. Chloride channel regulation in secretory epithelia. Fed. Proc. 1986; 45: 2727–2731
  • Welsh M. J. An apical-membrane chloride channel in human tracheal epithelium. Science 1986; 232: 1648–1650
  • Mandel K. G., Dharmsathaphorn K., McRoberts J. A. Characterization of a cyclic AMP-activated C1− transport pathway in the apical membrane of a human colonic epithelial cell line. J. Biol. Chem. 1986; 261: 704–712
  • Evans M. G., Marty A., Tan Y. P., Trautmann A. Blockage of Ca-activated C1 conductance by furosemide in rat lacrimal glands. Pflugers Arch. 1986; 406: 65–68
  • Findlay I., Petersen O. H. Acetylcholine stimulates a Ca+2-dependent C1−-conductance in mouse lacrimal acinar cells. Pflugers Arch. 1985; 403: 328–330
  • Saito Y., Ozawa T., Hayashi H., Nishiyama A. Acetylcholine-induced change in intracellular C1 activity of the mouse lacrimal acinar cells. Pflugers Arch. 1985; 405: 108–111
  • Suzuki K., Petersen O. H. The effect of Na+ and C1 removal and of loop diuretics on acetylcholine-evoked membrane potential changes in mouse lacrimal acinar cells. Q.J. Exp. Biol. 1985; 70: 437–445
  • Greger R., Schlatter E., Gogelein H. C1-channels in the apical cell membrane of the rectal gland “induced” by cAMP. Pflugers Arch. 1985; 403: 446–668
  • Welsh M. J., Smith P. L., Frizzell R. A. Intracellular chloride activities in the isolated perfused shark rectal gland. Am. J. Physiol 1983; 245: F640–F644
  • Welsh M. J. Intracellular chloride activities in canine tracheal epithelium, J. Clin, Invest 1983; 71: 1392–1401
  • Musch M. U., Orellana S. A., Kimberg L. S., Field M., Halm D., Krpny E. J., Frizzell R. A. Na+ -K+ -C1 co-transport in the intestine of a marine teleost. Nature 1982; 300: 351–353
  • McRoberts J. A., Erlinger S., Rindler M. J., Saier M. H. Furosemide-sensitive salt transport in the Madin-Darby canine kidney cell line. J. Biol, Chem 1982; 257: 2260–2266
  • Hopfer U., Liedtke C. M. Proton and bicarbonate transport mechanisms in the intestine. Ann, Rev, Physiol 1987; 49: 51–67
  • Reuss L., Stoddard J. S. Role of H+ and HCO3 in salt transport in gallbladder epithelium. Ann, Rev, Physiol 1987; 69: 35–49
  • Parod R. J., Leslie B. A., Putney J. M. Muscarinic and a-adrenergic stimulation of Na and Ca uptake by dispersed lacrimal cells. Am. J. Physiol 1980; 239: G99–G105
  • Parod R. J., Putney J. W. Stimuluspermeability coupling in rat lacrimal gland. Am. J. Physiol 1980; 239: G106–G113
  • Saito Y., Ozawa T., Nishiyama A. Acetylcholine-induced Na+ influx in the mouse lacrimal gland acinar cells: Demonstratration of multiple Na+ transport mechanisms by intracellular Na+ activity measurements. J. Membrane Biol 1987; 98: 135–144
  • Mircheff A. K., Ingham C. E., Lambert R. W., Hales K. L., Yiu S. C. Na/H anti-porter in lacrimal acinar basal-lateral membranes. Invest. Ophthalmol. Vis. Sci. 1987; 28: 1726–1729
  • Peters C. L., Bradley M. E., Yiu S. C., Mircheff A. K. Muscarinic receptors in cell surface and intracellular membranes of rat exorbital lacrimal gland. Invest. Ophthalmol. Vis. Sci. 1986; 27(suppl.)26
  • Mircheff A. K., Bradley M. E., Yiu S. C., Lambert R. W. Rapid stimulation-associated changes in exocrine Na,K-ATPase subcellular distribution. The Cellular and Molecular Biology of Cell Sodium, S. G. Schultz. Academic Press, New YorkUSA 1988, In press
  • Saito Y., Ozawa T., Suzuki S., Nishiyama A. Intracellular pH regulation in the mouse lacrimal gland acinar cells. J. Membrane Biol. 1988; 101: 73–81
  • Lambert R. W., Yiu S. C., Mircheff A. K. Sodium/proton and chloride/bicarbonate antiport activities in intact isolated lacrimal acini. Invest. Ophthalmol. 1988; 29(suppl)56
  • Sajto Y., Ozgwa T., Nishiyama A. Na+ -H+ and C1 -HCO3 antiporters in the mouse lacrimal gland acinar cells. Exocrine Secretion, P. Y.D. Wong, J. A. Young. Hong Kong University Press, Hong Kong 1988; 161–163
  • Lambert R. W., Bradley M. E., Mircheff A. K. C1/HCO3 antiporters in rat lacrimal gland. Am. J. Physiol. 1988; 255: G367–G373
  • Putney J. W., Van De Walle C. M. Effect of carbachol on ouabain-sensitive uptake of 86Rb by dispersed lacrimal gland cells. Life Sci. 1979; 24: 1119–1124
  • Mircheff A. K., Lu C. C., Conteas C. N. Resolution of apical and basal-lateral membrane populations from rat exorbital lacrimal gland. Am. J. Physiol. 1983; 245: G661–G667
  • Mircheff A. K., Lu C. A map of membrane populations isolated from rat exorbital gland. Am. J. Physiol. 1984; 247: G651–G661
  • Wood R. L., Mircheff A. K. Apical and basal-lateral Na,K-ATPase in rat lacrimal acinar cells. Invest. Ophthalmol. Vis. Sci. 1986; 27: 1293–1296
  • Wood R. L., Mircheff A. K. Immunolocalization of Na,K-ATPase in rat exorbital lacrimal gland acinar cells. Invest. Ophthalmol. Vis. Sci. 1986; 27(suppl.)26
  • Lewis S. A., Wills N. K. Apical membrane permeability and kinetic properties of the sodium pump in mammalian urinary bladder epithelium. J. Physiol 1983; 341: 169–184
  • Yiu S. C., Lambert R. W., Bradley M. E., Ingham C. E., Hales K. L., Wood R. L., Mircheff A. K. Stimulation-associated redistribution of Na,K-ATPase in rat lacrimal gland. J. Membrane Biol. 1988; 102: 185–194

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.