1988
DOI: 10.1016/0090-6980(88)90276-6
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Prostaglandin E2 opunteracts the effects of PGF2α in indomethacin treated cycling gilts

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Cited by 57 publications
(30 citation statements)
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“…The role of PGE2 in corpus luteum function during early preg¬ nancy of pigs is unknown. However, PGE2 can counteract the luteolytic effect of PGF2a, since chronic intrauterine infusions of PGE2 from day 7 in cyclic gilts (Akinlosotu et al, 1986(Akinlosotu et al, , 1988, and day 9 in cows (Giménez & Henricks, 1981) and ewes (Pratt et ai, 1979), inhibits luteolysis, main¬ tains luteal progesterone production and prolongs the oestrous cycle. Shelton et al (1990) Our studies also demonstrated that LH and prostaglandins F2a and E2 interact to inhibit progesterone production by pig luteal cells.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The role of PGE2 in corpus luteum function during early preg¬ nancy of pigs is unknown. However, PGE2 can counteract the luteolytic effect of PGF2a, since chronic intrauterine infusions of PGE2 from day 7 in cyclic gilts (Akinlosotu et al, 1986(Akinlosotu et al, , 1988, and day 9 in cows (Giménez & Henricks, 1981) and ewes (Pratt et ai, 1979), inhibits luteolysis, main¬ tains luteal progesterone production and prolongs the oestrous cycle. Shelton et al (1990) Our studies also demonstrated that LH and prostaglandins F2a and E2 interact to inhibit progesterone production by pig luteal cells.…”
Section: Discussionmentioning
confidence: 99%
“…Other prostaglandins, such as E2, I2 and D2 are also produced by luteal tissue and prolong the lifespan of the corpus luteum in ewes (Huecksteadt & Weems, 1978), cows (Milvae & Hansel, 1983;Alila et al, 1988) and humans (Bennegard et al, 1990). Prostaglandin E2 (PGE2) also counteracts the effects of PGF2a in indomethacin-treated cyclic gilts (Akinlosotu et al, 1986(Akinlosotu et al, , 1988, but the mechanism of action of prostaglandins on luteal function in pigs is still unknown.…”
Section: Introductionmentioning
confidence: 99%
“…Einspannier et al [10] [12]. The presence of the blastocyst probably also acts to alter the final product such that the primary prostaglandin released is PGE 2 rather than PGF Za [1,28]. As a matter of fact, PGE 2 neutralised the luteolytic effect of simultaneously infused PGFZa in indomethacin-treated gilts [1] with fewer PGF Za secretion spikes, and with a lower amplitude than has been reported for pregnant, as compared to cyclic gilts [28].…”
mentioning
confidence: 96%
“…Oxytocin, acting through oxytocin receptors (OTR) in the endometrium and myometrium, is involved in the control of prostaglandin F2α (PGF2α) and prostaglandin E2 (PGE2) secretion in pigs [3][4][5][6][7][8]. Prostaglandin F2α is responsible for luteal regression in non-pregnant pigs [1,9], while prostaglandin E2 acts as a luteotrophic and antiluteolytic factor that promotes maintenance of the corpus luteum during early pregnancy in pigs [10,11].Alteration of PG secretion by OT is implicated in maternal recognition of pregnancy in pigs [12][13][14]. Moreover, OT stimulates myometrial secretion of PGF2α and PGE2 as well as the contractile activity of the porcine myometrium during early pregnancy [8,15,16].…”
mentioning
confidence: 99%
“…Oxytocin, acting through oxytocin receptors (OTR) in the endometrium and myometrium, is involved in the control of prostaglandin F2α (PGF2α) and prostaglandin E2 (PGE2) secretion in pigs [3][4][5][6][7][8]. Prostaglandin F2α is responsible for luteal regression in non-pregnant pigs [1,9], while prostaglandin E2 acts as a luteotrophic and antiluteolytic factor that promotes maintenance of the corpus luteum during early pregnancy in pigs [10,11].…”
mentioning
confidence: 99%