INCREASED LH RECEPTOR MESSENGER-RNA AND EXTENDED CORPUS-LUTEUM FUNCTION INDUCED BY PROLACTIN AND INDOMETHACIN TREATMENT IN-VIVO IN HYSTERECTOMIZED PSEUDOPREGNANT RATS
E. Bjurulf et al., INCREASED LH RECEPTOR MESSENGER-RNA AND EXTENDED CORPUS-LUTEUM FUNCTION INDUCED BY PROLACTIN AND INDOMETHACIN TREATMENT IN-VIVO IN HYSTERECTOMIZED PSEUDOPREGNANT RATS, Journal of Reproduction and Fertility, 102(1), 1994, pp. 139-145
To assess the effects of prostaglandins and prolactin on corpus luteum
function and regression, sterile-mated adult pseudopregnant rats hyst
erectomized on day 5 after mating were injected with indomethacin or p
rolactin. Daily samples of blood were collected via the tail, from day
12 to day 21, and assayed for serum concentrations of progesterone, 2
0 alpha-dihydroprogesterone and LH, whereafter corpora lutea and the r
emainder of ovaries were separated and the tissue content of PGF(2 alp
ha), PGE(2) and LH receptor mRNA were measured. Injections of prolacti
n (8 iu) s.c. or a low dose of indomethacin (200 mu g kg(-1)) s.c. wer
e administered twice a day, beginning on day 13 after mating. Both ind
omethacin and prolactin significantly increased serum progesterone con
centrations (P < 0.05; n = 8), and extended the period of functional c
orpora lutea when compared with controls. Indomethacin, but not prolac
tin, lowered the concentration of serum 20 alpha-dihydroprogesterone.
In the corpora lutea of indomethacin-treated animals, collected on day
21, both prostaglandins measured were reduced in concentration by 50%
or more, compared with controls (P < 0.05; n = 8), whereas prolactin
had no effect. Both prolactin and indomethacin treatment caused a subs
tantial (tenfold) increase in the concentration of LH receptor mRNA, c
onfined solely to the luteal compartment. These findings in vivo provi
de further evidence for a luteolytic role of locally synthesized prost
aglandins in the rat ovary. Furthermore, prolactin can sustain corpus
luteum function by exerting a luteotrophic effect during the late lute
al phase, as judged by the stimulation of progesterone synthesis and t
he expression of LH receptors.