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Regular Article |
and Prolactin on Intercellular Adhesion Molecule-1 Expression and Monocyte/Macrophage Accumulation in the Rat Corpus Luteum1
a Department of Animal and Nutritional Sciences, University of New Hampshire, Durham, New Hampshire 03824-3590
b Department of Animal Science, University of Wisconsin, Madison, Wisconsin 53706-1284
ABSTRACT
Expression of intercellular adhesion molecule-1 (ICAM-1) and the accumulation of monocytes/macrophages are inflammatory events that occur during PRL (PRL)-induced regression of the rat corpus luteum. Here we have compared the ability of prostaglandin F2
(PGF) and PRL to induce, in rat corpora lutea, inflammatory events thought to perpetuate luteal regression. Immature rats were ovulated with eCG-hCG and then hypophysectomized (Day 0), which resulted in a single cohort of persistent, functional corpora lutea. On Days 911, the rats received twice daily injections of saline, PGF (Lutalyse, 250 µg/injection), or PRL (312 µg/injection) to induce luteal regression. Surprisingly, luteal weight and plasma progestin concentrations (progesterone and 20
-dihydroprogesterone) did not differ between PGF-treated rats and controls; whereas both luteal weight and plasma progestins declined significantly in PRL-treated rats. Furthermore, corpora lutea of PGF-treated rats and controls contained relatively minimal ICAM-1 staining and few monocytes/macrophages. In contrast, but as expected, corpora lutea of PRL-treated rats stained intensely for ICAM-1 and contained numerous monocytes/macrophages. In an additional experiment, there was no indication that luteal prostaglandin F2
receptor mRNA diminished as a result of hypophysectomy. These findings suggest that prolactin, not PGF, induces the inflammatory events that accompany regression of the rat corpus luteum.
First decision: 25 August 2000.
1 Supported by U.S. Department of Agriculture grant 9835208-6654 and by funds from the University of New Hampshire Vice President for Research. This manuscript is scientific contribution number 2059 from the New Hampshire Agricultural Experiment Station.
2 Correspondence: D.H. Townson, Department of Animal and Nutritional Sciences, Kendall Hall, 128 Main St., University of New Hampshire, Durham, NH 03824-3590. FAX: 603 862 3758; dave.townson{at}unh.edu
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