Effects of Exogenous Oxytocin on Embryonic Survival in Cows

Yildiz A. , Z. Eris i r: Effects of Exogenous Oxytocin on Embryonic Survival in Cows. Acta Vet Brno 2006, 75: 73-78. The aim of this study was to evaluate the effect of oxytocin on embryonic survival in dairy cows. Pregnancy was verified using the early pregnancy factor (EPF) activity on Day 4 after artificial insemination (AI). Pregnant cows were randomly allotted to two groups: treated (n = 8) and control (n = 8). Oxytocin (100 IU, 5 ml, DIF Turkey) was administered twice daily by intravenous injections to treated cows and sterile saline (5 ml) to control cows immediately before milking on days 4 to 7 after AI. Blood samples were taken via jugular vein every day from day 4 to 8 and every other day until Day 20 following insemination to evaluate the effect of oxytocin on embryonic survival. The embryonic loss was diagnosed in 3 of the 8 cows treated with oxytocin, and embryonic survival rate was 62.5% in this group versus 87.5% in controls. Short cycles occurred in 37.5% of oxytocin-treated cows. At the same time their serum progesterone concentrations rose more slowly than in controls. It was concluded that cows administered oxytocin on days 4 to 7 after insemination are at a higher risk of pregnancy loss. Conception rate, embryonic mortality, short cycle, progesterone Reproductive performance in the cattle industry is arguably lower than desired. Early embryonic mortality is one of the major problems in animal breeding. Conception rates among cattle have been reported to be as high as 90%, yet calving rates are in the range of 50 to 60% (Sreenan and Diskin 1983) or lower, and much of this decline can be attributed to embryonic mortality. Progesterone synthesis by the corpus luteum (CL) is necessary for maintenance of early pregnancy in the cow (Stewart 1990). Premature regression of the CL and the subsequent reduction in progesterone secretion results in loss of pregnancy (Thatcher et al. 1994). Exogenous oxytocin is often used by dairies to increase milk letdown (Farin and Est i l l 1993; Lemaster et al. 1999). Oxytocin leads to luteal regression by driving the release of prostaglandin F2α (PGF2α) from the endometrium (Balaguer 1999). It may induce release of PGF2α in pregnant cows and ewes (Burgess et al. 1990) albeit at a level much lower than that observed in cycling animals (La France and Goff 1985). Several researchers have demonstrated an increased release of PGF2α after injections of oxytocin, which resulted in shortened luteal phases in cows (Newcomb et al. 1977; Milvae and Hansel 1980; Fuchs et al. 1996). Regression of the corpus luteum leads to a decline in circulating progesterone and deprivation of the fetus of nutrient support. This may result in abortion. Some studies reported that oxytocin influenced progesterone production from corpus luteum (Lemaster et al. 1999; Tan et al. 1982). However, other authors (Mares and Casida 1963; Richardson and Masson 1985) have not observed an effect of oxytocin on progesterone production. To our knowledge, the effect of oxytocin on embryonic loss has not been studied yet. Therefore, the objective of this work was to evaluate the effect of oxytocin on embryonic survival in dairy cows. Materials and Methods Holstein cows aged 3 5 years were used in this experiment. All animals were clinically healthy. The estrus of cows was synchronized with two intramuscular injections of 526 μg Cloprostenol (Estrumate, DIF Turkey) eleven ACTA VET. BRNO 2006, 75: 73–78 Address for correspondence: Yrd. Doç. Dr. Atilla YILDIZ Firat Üniversitesi, Sivrice Meslek Yüksekokulu Süt Hayvanciligi Programi, Elazig, Turkey Phone: +90 424 237 00 00/4131 Fax: +90 424 236 08 46 E-mail: [email protected] http://www.vfu.cz/acta-vet/actavet.htm days apart (Day 0). All cows were artificially inseminated (AI) with semen from a single Holstein bull of known high fertility at 12 h past detection of estrus. The experiment was conducted in accordance with the guidelines on animal welfare under the protocol approved by Ethical Committee of Veterinary Faculty of Firat University, Turkey. The Early Conception Factor (ECF) is a glycoprotein and occurs in blood 48 h after conception. Early pregnancy factor (EPF) is a protein called specific gamma interferon and a secreted substance with growth regulatory and immunomodulatory properties that is required for successful establishment of pregnancy. EPF has important characteristics that render it a superior applicant for an early chemical signal between the embryo and mother (Morton 1998). The detection of EPF in pregnant animals has thus important implications for the study of embryonic-maternal signaling in mammals (Cruz et al. 2001). EPF is needed for survival of the embryo during the pre and peri-implantation stages of pregnancy (Igarashi 1987; Athanasas et al. 1989; Athanasas-Plats is et al. 1991, 2000). It is detectable in maternal serum within 24 h of fertilization in all species studied so far (Morton 1998). Its values are higher in pregnant than in non-pregnant cows 2 days after AI (Ko 1998). Although it is not a certain indicator of pregnancy, EPF activity can be used as a method for early pregnancy diagnosis in cattle (Sakonju et al. 1993). In our experiment, serum EPF activity for confirmation of pregnancy on Day 4 following insemination was used. Non-pregnant cows were removed from the trial. Pregnant cows were randomly allotted to two groups as treated (n = 8) and control (n = 8). Oxytocin (100 IU,5 ml, DIF Turkey) was given twice daily by IV injections to treated group and sterile saline (5 ml) to control group immediately before milking on days 4 7 after AI. Serum EPF activity was repeatedly used to confirm whether pregnancy was sustained throughout the study along with progesterone to evaluate the effect of oxytocin. Rectal palpation was also performed in cows not seen in estrus on day 45 after AI to confirm pregnancy. Blood samples were taken via jugular vein every day from day 4 to 8 and every other day until Day 20 post insemination. Blood samples were allowed to clot; the serum was removed, incubated at 56 °C for 30 minutes, and then stored at -20 °C until assayed. Serum was assayed for progesterone by radioimmunoassay (A commercial assay kit, Coat-a-Count; Diagnostic Products Corporation, Los Angeles, CA) as described in detail by Yildiz (1999). The interand intra-assay coefficients of variation were 10.8 and 9.5%, respectively. The sensitivity of the assay was 15 pg/tube. Serum EPF activity was assayed using the rosette inhibition test (RIT). The test is well documented (Morton et al. 1974, 1976; Rolfe et al. 1984; Cavanagh and Morton 1996). This test is based on the capacity of lymphocytes, in the presence of guinea-pig serum as a source of complement, to bind heterologous erythrocytes to their cell surface (rosette formation) (Bach and Antoine 1968). The rosette inhibition test does not give a 100% reliable result but it is so far the only applicable method to detect the presence of EPF at concentrations at which it normally appears in vivo (Morton 1998). The assay was carried out as described by Sakonju et al. (1993) and Yildiz (1999). In summary, the lymphocyte suspension (0.1 ml), previously incubated with diluted test serum, was incubated at 37 °C for 90 min with absorbed diluted guinea-pig complement (0.05 ml) and anti-lymphocyte serum, serially double-diluted over a range of 1 in 128 × 103. Rosettes were formed by adding a suspension (0.1 ml) of sheep red blood cells, centrifuging the mixture at 120 g for 5 min, and re-suspending it gently by rotation and pipetting. The suspension was then spread on a Rosenthal counting chamber and the numbers of rosettes in all divisions were counted. The rosette inhibition titer (RIT) was defined as the highest dilution of anti-lymphocyte serum causing a reduction of at least 25% in the rosette number compared to the proportion of rosettes in the two tubes without antiserum. This titer was multiplied by 1/500 and recorded as the logarithm to base 2. Data analysis Females were declared non-pregnant when serum RIT was < 5 (Yildiz and Deveci 2000). Verification of short cycle was determined by progesterone concentration (P4 < 1.0 ng/ml). At each stage after AI, data were analyzed by T-test (SPSS 1999).