OSMO-DEPENDENT CL- CURRENTS ACTIVATED BY CYCLIC-AMP IN FOLLICLE-ENCLOSED XENOPUS-OOCYTES

Citation
Ro. Arellano et R. Miledi, OSMO-DEPENDENT CL- CURRENTS ACTIVATED BY CYCLIC-AMP IN FOLLICLE-ENCLOSED XENOPUS-OOCYTES, Proceedings - Royal Society. Biological Sciences, 258(1353), 1994, pp. 229-235
Citations number
24
Categorie Soggetti
Biology
ISSN journal
09628452
Volume
258
Issue
1353
Year of publication
1994
Pages
229 - 235
Database
ISI
SICI code
0962-8452(1994)258:1353<229:OCCABC>2.0.ZU;2-1
Abstract
The role of adenosine 3',5'-cyclic monophosphate (cAMP) in generating the osmo-dependent slow inward membrane currents (S-in) elicited by ac tivation of follicle stimulating hormone (FSH) or acetylcholine (ACh) receptors was studied in voltage-clamped, follicle-enclosed oocytes of Xenopus laevis (follicles). Forskolin (FSK) also generated S-in curre nts, and in low concentrations it potentiated the S-in currents elicit ed by FSH but not those elicited by ACh. Moreover, intra-oocyte inject ions of cAMP elicited similar slow inward currents (cAMP-S-in) that: ( i) were carried mainly by chloride ions; (ii) were abolished by defoll iculating the oocytes; and (iii) were dependent on the osmolarity of t he external medium. Compared with the Ca2+-dependent chloride channels that are located in the oocyte membrane; the cAMP-activated S-in chan nels were less permeable to I- and Br-, and their current-voltage rela tion did not rectify strongly at negative potentials. Generation of cA MP-S-in desensitized the FSH-S-in currents, but did not have effects o n both the S-in and the fast chloride current (F-in) specifically elic ited by ACh. Furthermore, follicular phospholipase C activation throug h stimulation of angiotensin II (AII) receptors failed to generate the current responses elicited by ACh. We conclude that cAMP acts as a po tent second messenger in generating the osmo-dependent Cl- currents el icited by FSH but not those elicited by ACh. The mechanisms underlying the ACh responses remain unknown. The osmo-dependent chloride channel s activated by cAMP may play a role in the control of volume of the fo llicular cells-oocyte complex.