Membrane Potential in Luteal Cells from Cyclic Rats: Relationship to Steroidogenic Capacity.
- Author:
lnkyo KIM
1
;
Hye Soo PARK
;
Bon Sook KOO
Author Information
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords: Membrane potential; steroidogenesis; luteal cells
- MeSH: Animal; Corpus Luteum/*metabolism; Estrus/metabolism; Female; Ions; Luteal Cells/*metabolism; Membrane Potentials; Rats; Rats, Inbred Strains; Steroids/*biosynthesis; Support, Non-U.S. Gov't
- From:Yonsei Medical Journal 1988;29(1):29-36
- CountryRepublic of Korea
- Language:English
- Abstract: To examine the electrophysiological properties of luteal cells and the relationship between membrane potential and luteal steroidogenic capacity, the membrane potential of luteal cells and the luteal steroidogenesis were measured under different ionic conditions following treatment with various drugs and gonadotropins. The membrane potential of luteal cells did not vary throughout the estrous cycle and was -55 +/- 1 mV. The membrane potential was highly dependent upon the external K+ concentration and was depolarized by the deprivation of external Ca2+, however) there seemed to be a lower K+ permeability in luteal membranes as the presence of 10-9 M valinomycin, a K+ ionophore Caused hyperpolarization from -55 to -91 mV. Luteal progestin production was increased in a high K+ solution but not m a Ca2+-free solution indicating that Ca2+ may be essential for steroid synthesis and/or secretion by luteal cells. Gonadotropins and ouabain induced a depolarization of the membrane potential and stimulated luteal steroidogenesis; however; prostaglandin F2alpha stimulated only steroidogenesis without any changes in membrane potential. These results suggest that the relationship between steroidogenesis and the changes in membrane potential by drugs and gonadotropins is still obscure and remains to be eluridated. The relationship between membrane potential and steroidogenesis in the luteal cell may be dependent upon the availability of intracelluar Ca2+.
