Arachidonic acid release from rat Leydig cells: The involvement of G protein, phospholipase A2 and regulation of cAMP production
Author
dc.contributor.author
Ronco Macchiavello, Ana María
Author
dc.contributor.author
Moraga,
Author
dc.contributor.author
Llanos Silva, Miguel
Admission date
dc.date.accessioned
2019-01-29T17:51:01Z
Available date
dc.date.available
2019-01-29T17:51:01Z
Publication date
dc.date.issued
2002
Cita de ítem
dc.identifier.citation
Journal of Endocrinology, Volumen 172, Issue 1, 2018, Pages 95-104
Identifier
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00220795
Identifier
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10.1677/joe.0.1720095
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/163483
Abstract
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We have previously demonstrated that the release of arachidonic acid (AA) from human chorionic gonadotropin (hCG)-stimulated Leydig cells occurs in a dose- and time-dependent manner. In addition, the amount of AA released was dependent on the hormone-receptor interaction and the concentration of LH-hCG binding sites on the cell surface. The present study was conducted to evaluate the involvement of phospholipase A2 (PLA2) and G proteins in AA release from hormonally stimulated rat Leydig cells, and the possible role of this fatty acid in cAMP production. Cells were first prelabelled with [14C]AA to incorporate the fatty acid into cell phospholipids, and then treated in different ways to evaluate AA release. hCG (25 mIU) increased the release of AA to 180 ± 12% when compared with AA released from control cells, arbitrarily set as 100%. Mepacrine and parabromophenacyl bromide (pBpB), two PLA2 inhibitors, decreased the hormone-stimulated AA release to 85 ± 9 and 70 ± 24% respectively. Con