At present, the mechanism of zona escape in vivo is poorly understood, as are the factors contributing to in vitro """"""""hatching"""""""" from the zona pellucida. The overall goal of the present study is to obtain an understanding of the contributing factors of in vivo zona escape by studying the presence of enzyme activity in flushates that are coincident with the zona escape time window (Gonzales and Bavister, 1995) in both pregnant and pseudopregnant hamsters. Collections of embryos and flushates from the uterus during the zona escape time window will be used to compare the morphology of eggs/embryos, their location in the reproductive tract, and the presence of enzymatic activity in pregnant, pseudopregnant, and non- pregnant uteri of hamsters. Therefore, the objectives of this proposed study are: 1) to determine if there is a uterine enzyme activity that is potentially responsible for zona lysis in vivo that is coincident with the zona escape time window in both pregnant and pseudopregnant hamsters, 2) to test the hypothesis that there is no zona lytic activity in non-pregnant cycling hamster females and 3) to determine if zona lytic activity is different in vitro than the zona lytic activity in vivo. In this study the contribution of each participants involved in zona escape (the zona pellucida, the embryo and the uterine epithelium) is examined to achieve a more complete understanding of the mechanism of zona loss in utero. This study will also provide a foundation for further research to elucidate 1) regulatory effect of uterine enzyme activity associated with the critical preimplantation period, and 2) possible embryo-maternal dialogue.

Project Start
1999-09-30
Project End
1999-12-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
17
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Colorado State University-Pueblo
Department
Type
DUNS #
City
Pueblo
State
CO
Country
United States
Zip Code
81001
Unis, Dave; Osborne, Cassandra; Diawara, Moussa M (2009) Arsenite exposure compromises early embryonic development in the Golden hamster. Reprod Toxicol 28:329-34
Kulkosky, Paul J; Wise, Valarie J; Brandt, Sara S et al. (2004) Interaction of TRH and CCK in the satiation of alcohol intake. Physiol Behav 82:53-6
Gonzales, D S; Bavister, B D; Mese, S A (2001) In utero and in vitro proteinase activity during the Mesocricetus auratus embryo zona escape time window. Biol Reprod 64:222-30
Kulkosky, P J; Allison, C T; Mattson, B J (2000) Thyrotropin releasing hormone decreases alcohol intake and preference in rats. Alcohol 20:87-91
Kulkosky, P J; Allison, C T; Allison, T G et al. (1998) Interaction of CCK and 8-OH-DPAT in the satiation of alcohol intake. Alcohol 16:305-9
Kulkosky, P J; Allison, T G; Carr, B A (1996) Angiotensin II reduces alcohol intake and choice in water- or food-restricted rats. Alcohol 13:359-63
Kulkosky, P J; Carr, B A; Flores, R K et al. (1995) Conditioned taste aversions induced by alcohol and lithium in rats selectively bred for ethanol neurosensitivity. Alcohol Clin Exp Res 19:945-50
Schnur, P; Espinoza, M; Flores, R (1994) Context-specific sensitization to naloxone-precipitated withdrawal in hamsters: effect of pimozide. Pharmacol Biochem Behav 48:791-7
Schnur, P; Espinoza, M; Flores, R (1992) Effects of diurnal phase and pimozide on cholecystokinin-elicited hypoactivity in the hamster. Pharmacol Biochem Behav 43:979-84
Schnur, P; Espinoza, M; Flores, R et al. (1992) Blocking naloxone-precipitated withdrawal in rats and hamsters. Pharmacol Biochem Behav 43:1093-8