MACROPHAGE INFILTRATION INTO THE PORCINE CORPUS-LUTEUM DURING PROSTAGLANDIN F-2-ALPHA-INDUCED LUTEOLYSIS

Citation
Ke. Hehnke et al., MACROPHAGE INFILTRATION INTO THE PORCINE CORPUS-LUTEUM DURING PROSTAGLANDIN F-2-ALPHA-INDUCED LUTEOLYSIS, Biology of reproduction, 50(1), 1994, pp. 10-15
Citations number
25
Categorie Soggetti
Reproductive Biology
Journal title
ISSN journal
00063363
Volume
50
Issue
1
Year of publication
1994
Pages
10 - 15
Database
ISI
SICI code
0006-3363(1994)50:1<10:MIITPC>2.0.ZU;2-U
Abstract
Although it has been reported that the number of macrophages increases in the pig CL at the time of luteolysis, the temporal association bet ween this infiltration and the sequence of events involved in luteolys is has not been established. In the current study, single CL on an ova ry of estrogen-treated pseudopregnant gilts were induced to undergo lu teolysis after the introduction of prostaglandin F-2alpha (PGF)-impreg nated silastic implants on Day 13 (Day 0 = first day of estrus). Other CL on the same ovary were treated with implant material only (vehicle -implanted) or left unimplanted. At 6, 12, and 24 h after implant plac ement, CL were removed and progesterone concentrations as well as the number and location of macrophages within each CL were determined. Pro gesterone concentrations declined significantly (p < 0.05) by 12 and 2 4 h postimplantation in PGF-treated CL but not in vehicle-implanted or unimplanted CL. There was a significant influx (p < 0.05) of macropha ges at 6 h in all implanted CL (PGF or vehicle-implanted) as compared with unimplanted CL. In PGF-treated CL, macrophage numbers progressive ly increased through 24 h. In contrast, although a macrophage influx a lso occurred in vehicle-implanted CL at 6 h, macrophage numbers progre ssively declined through 24 h. The simplest explanation for these data is that the initial rise in macrophage numbers at 6 h after Ct implan tation is a result of the implantation procedure itself. Further, the observation that most of the influx of macrophages occurred after the decrease in progesterone concentration in PGF-treated CL is consistent with their role in phagocytosis of cellular debris.