A Przylipiak, T Rabe, L Kiesel, J Przylipiak, K Klinga, B Runnebaum
Index: Gynecol. Endocrinol. 10(2) , 95-100, (1996)
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Leukotriene C4, at doses of 0.01 and 0.1 nmol/l added to superfused cells in pulse of 4-min duration, evoked follicle-stimulating hormone (FSH) release up to 12- to 26-fold of basal secretion. Higher and lower concentrations of leukotriene C4 were not able to induce FSH secretion. Gonadotropin-releasing hormone (GnRH)-induced FSH release was reduced by 38-57% by the leukotriene receptor antagonist FPL 55712 (10 mumol/l). Moreover, we have shown that FSH release occurs parallel to leukotriene C4 synthesis in rat anterior pituitary cells. Mellitin (100 nmol/l), an activator of phospholipase A2, induced FSH and radioactivity secretion in rat anterior pituitary cells previously preincubated for 24 h with [3H]arachidonic acid (AA).
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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FPL 55712
CAS:40786-08-1 |
C27H29NaO9 |
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Strategies in the design of peptidoleukotriene antagonists.
1993-01-01 [J. Lipid Mediat. 6(1-3) , 265-73, (1993)] |
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Leukotriene receptor blockade in experimental heart failure.
1997-01-01 [Res. Exp. Med. (Berl.) 197(4) , 177-87, (1997)] |
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Leukotriene cysLT1 (LTD4) receptor antagonism of H1-antihist...
1997-03-01 [Inflamm. Res. 46 Suppl 1 , S93-4, (1997)] |
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Effects of atropine, acetylsalicylic acid, FPL 55712, and ph...
1989-06-01 [Eur. Respir. J. 2(6) , 517-21, (1989)] |
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In vitro effect of DP-1904, a novel anti-asthma agent, again...
1998-08-01 [Pharmacol. Res. 38(2) , 141-7, (1998)] |
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