cGMP modulates transport across the ciliary epithelium

• Published in: The Journal of membrane biology Vol. 146; no. 3; pp. 293 - 305
• Main Authors: Carré, D A, Civan, M M
• Format: Journal Article
• Language: English
• Published: United States 01-08-1995
• Subjects: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology; Animals; Barium - pharmacology; Bumetanide - pharmacology; Cats; Cells, Cultured; Chloride Channels - metabolism; Chlorides - pharmacology; Ciliary Body - drug effects; Ciliary Body - metabolism; Colforsin - pharmacology; Cyclic AMP - physiology; Cyclic GMP - pharmacology; Cyclic GMP - physiology; Epithelium - drug effects; Epithelium - metabolism; Humans; Male; Models, Biological; Patch-Clamp Techniques; Potassium Channels - drug effects; Potassium Channels - metabolism; Rabbits; Second Messenger Systems - physiology; Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors; Sodium-Potassium-Exchanging ATPase - metabolism; Species Specificity; Strophanthidin - pharmacology
• ISSN: 0022-2631; 1432-1424
• DOI: 10.1007/BF00233949

cGMP reduced the short-circuit current (ISC) when applied to the aqueous surface of isolated rabbit and cat ciliary epithelia. cGMP either stimulated (in the rabbit) or had no effect (in the cat) on ISC when applied to the stromal surface. Addition of the cGMP-mediated hormone atrial natriuretic peptide (ANP) to the stromal (but not the aqueous) surface, or the nitrovasodilator sodium nitroprusside to the stromal surface, inhibited ISC across rabbit ciliary epithelium. The response to stromal cGMP was partly mediated by K+ channels at the stromal surface of the rabbit pigmented epithelial (PE) cells, since the effect was inhibited by stromal Ba2+, and was unaffected by Cl- replacement, by bumetanide, or by DIDS. In contrast, the response to aqueous cGMP was not likely mediated by changing either K+ or Cl- channels, based on transepithelial measurements of rabbit ciliary epithelium and complementary whole-cell patch clamping of cultured human nonpigmented ciliary epithelial (NPE) cells. The possibility of interacting effects between cGMP and cAMP in targeting the Na+, K(+)-exchange pump was also considered. Strophanthidin blocked the responses to either aqueous or stromal cGAMP. Applying 10 microns forskolin to generate endogenous cAMP enhanced the subsequent response to aqueous cGMP by approximately equal to 80%. We conclude that cGMP has at least two actions on the ciliary epithelium. The major effect may be to reverse cAMP-mediated inhibition of the NPE Na+ pumps at the aqueous surface of both rabbit and cat ciliary epithelia. The second effect is likely mediated by increasing K(+)-channel and pump activity of the rabbit PE cells at the stromal surface.