Calcium influx similarly stimulates the release of chorionic gonadotrophin and placental lactogen from human placental explants

Placenta ◽  
1992 ◽  
Vol 13 ◽  
pp. 189-198
Author(s):  
B. Polliotti ◽  
S. Meuris ◽  
P. Lebrun ◽  
C. Robyn
1981 ◽  
Vol 240 (5) ◽  
pp. E550-E555
Author(s):  
S. Handwerger ◽  
P. M. Conn ◽  
J. Barrett ◽  
S. Barry ◽  
A. Golander

To study the effects of calcium on the release of human placental lactogen (hPL), placental explants were exposed to media containing lower or higher concentrations of calcium than normally available to the placenta. Explants exposed for 2 h to calcium-poor medium or medium containing either 2 mM EDTA or 2 mM EGTA released 160, 248, and 253% more hPL, respectively, than control explants. In contrast, explants exposed to medium containing higher than normal calcium concentrations released the same amounts of hPL as the control explants. At lower than normal extracellular calcium concentrations, the increased hPL release was inversely proportional to the calcium concentration. The increased release in calcium-poor medium was inhibited by subsequent exposure of the explants to medium containing calcium and was prevented by either barium or magnesium. Changes in barium or magnesium concentrations, however, had no effects on hPL release in the presence of normal extracellular calcium concentrations. Methoxyverapamil (D 600), an inhibitor of calcium flux, stimulated hPL release. Because low extracellular calcium and methoxyverapamil both inhibit calcium influx, these experiments suggest that calcium influx inhibits hPL release. The role of calcium in the regulation of hPL release therefore appears to be different from that reported in other release systems.


Abstracts ◽  
1977 ◽  
pp. 295
Author(s):  
Irving Boime ◽  
Melody Boime ◽  
Sophie Boguslawski ◽  
Tom Landefeld ◽  
Diana McWilliams ◽  
...  

1982 ◽  
Vol 99 (2) ◽  
pp. 288-294 ◽  
Author(s):  
Marco Tabarelli ◽  
R. Kofler ◽  
S. Schwarz ◽  
G. Wick

Abstract. Rat placental extracts (rPE) were investigated in bioassays for their possible content of rat placental lactogen (rPL) and rat chorionic gonadotrophin (rCG). Luteotrophic and lactogenic activity of rPL was assessed by substitution of rats depleted of endogenous prolactin (Prl) by means of bromoergocryptine (BEC) in early pregnancy and the period of lactation, respectively. The abortifacient effect of a single dose of BEC on day 6 of pregnancy was abolished by rPE equivalent to 1 g rat placenta corresponding to 5 IU bovine Prl (NIH-P-B 2). Substitution was necessary until the evening of day 7 indicating that rPL does not take over the function of Prl before day 8. During lactation rPE reversed the lactation inhibiting effect of daily BEC treatment. In this assay rPL activity corresponded to 1.25–2.5 IU bPrl/g placenta. In order to test for the possible existence of rCG the gonadotrophic activity of rPE was assessed in immature female mice. No gonadotrophic activity was found when rPE equivalent to 1 g rat placenta was administered, whereas equivalents of 3 mg human placenta and 12 mg rat pituitary entailed a dose-dependent response. In this system 0.12 IU human chorionic gonadotrophin (hCG), which served as standard, was the minimal dose (MD) resulting in increased uterine weight. In addition rPE was tested in the immature female rat, where the limit of detection was found to be 0.5 IU hCG. Again no gonadotrophic activity was found in rPE. As the effects of rCG might have been restricted to its presumed target, the corpus luteum of pregnancy, rPE was also tested in pregnant rats depleted of endogenous luteinizing hormone (LH) by a single injection of anti-LH antibodies on day 10 of pregnancy. A MDof 0.5 IU hCG, which served as standard, prevented resorption of foetuses in all animals tested. rPE equivalent to 3.5 g rat placenta, rat pregnancy serum of day 18 and placental transplants could not substitute for endogenous LH.


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