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Effect of oxytocin on expression of cytosolic phospholipase A2 mRNA and protein in ovine endometrial tissue in vivo

  • P. D. Burns
  • , G. A. Graf
  • , S. H. Hayes
  • , W. J. Silvia

Producción científica: Article › revisión exhaustiva

11 Citas (Scopus)

Resumen

The induction of endometrial prostaglandin (PG) F2α synthesis by oxytocin is dependent upon activation of phospholipase (PL) A2 and mobilization of arachidonic acid. The objective of this study was to determine if oxytocin stimulates PGF2α synthesis by inducing synthesis of cytosolic PLA2 (cPLA2). In Experiment 1, 15 ovariectomized ewes were given progesterone and estradiol to simulate an estrous cycle. Ewes were then given an injection of oxytocin on Day 14 of the simulated estrous cycle. Jugular blood samples were collected and assayed for 13,14-dihydro-15-keto-prostaglandin F2α (PGFM). Uteri were collected at 0, 7.5, 25, 90, or 240 min postinjection (n = 3 ewes/time point). Total RNA was isolated from caruncular endometrium and subjected to dot-blot analysis. Oxytocin induced a rapid and transient increase in serum PGFM (P < 0.01). However, endometrial concentrations of cPLA2 mRNA did not change following oxytocin administration (P > 0.10). In Experiment 2, 11 ovary-intact ewes were given oxytocin (n = 5) or saline (n = 6) on Day 15 after estrus. Jugular blood samples were collected and assayed for serum concentrations of PGFM. Uteri were collected at 15 min postinjection. Homogenates were prepared from caruncular endometrium and subjected to Western blot analysis. Concentrations of PGFM were higher in oxytocin treated ewes compared to saline treated ewes at 15 min postinjection (P < 0.01). Endometrial concentrations of cPLA2 protein were greater in the cytosolic than in the microsomal fraction (P < 0.01). Oxytocin did not affect the amount of cPLA2 protein in either fraction (P > 0.10). In conclusion, oxytocin did not effect expression of either cPLA2 mRNA or protein in ovine endometrium. Oxytocin may stimulate PGF2α synthesis by activating cPLA2 protein that is already present in an inactive form.

Idioma originalEnglish
Páginas (desde-hasta)237-246
Número de páginas10
PublicaciónDomestic Animal Endocrinology
Volumen19
N.º4
DOI
EstadoPublished - 2000

Nota bibliográfica

Funding Information:
The authors wish to thank Doug Yelton and Brent Broaddus for their extensive efforts in these experiments and to Dr. Phillip Chapman for helping with the statistical analyses. This research was supported in part by grants from the Kentucky Agricultural Station and USDA (96-35203-3495) to P.D.B. This report is published with the approval of the Kentucky Agricultural Experiment Station (Publication No. 99-07-125).

Financiación

The authors wish to thank Doug Yelton and Brent Broaddus for their extensive efforts in these experiments and to Dr. Phillip Chapman for helping with the statistical analyses. This research was supported in part by grants from the Kentucky Agricultural Station and USDA (96-35203-3495) to P.D.B. This report is published with the approval of the Kentucky Agricultural Experiment Station (Publication No. 99-07-125).

FinanciadoresNúmero del financiador
Kentucky Agricultural Experiment Station
U.S. Department of Agriculture96-35203-3495

    ASJC Scopus subject areas

    • Food Animals
    • Animal Science and Zoology
    • Endocrinology

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