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The aim of this study was to assessed the differences in embryos quality between the natural estrus and two systems of estrus synchronization in multiparous sows and prepuberal gilts. In this experiment, multiparous sows (n = 63) and prepuberal gilts (n = 42) were used. The subgroups of these animals were treated with PMSG (1500 U.I.) + hCG (500 U.I.) or PG-600 synchronization systems. These animals were inseminated twice, 24 and 36 h after hCG injection. The control gilts (n = 20) were from the third subgroup and were inseminated two times at 12 h intervals during their natural estrus cycles. A statistically significant increased number of corpora lutea (CL) and embryos was observed between natural estrus and both synchronization systems in multiparous sows (p < 0.001). There were no differences found in the number of degenerative embryos isolated from both ovaries between PMSG + hCG, PG-600, and natural estrus groups in multiparous sows (p = 0.484), (p = 0.279), (p = 0.213), (p = 0.138), respectively. However, an increased number of unfertilized oocytes in multiparous sows after treatment with PMSG + hCG as compared to control animals (p = 0.041) was observed. A statistically higher number of embryos after treatment with PMSG + hCG was also observed in the separate groups of multiparous sows and prepuberal gilts as compared to PG-600 treated animals. No differences were found, however, in the number of degenerative embryos between those two separate groups of animals after treatment with PMSG + hCG and PG-600 of both ovaries: (p = 0.175), (p = 0.344), (p = 0.122), and (p = 0.055), respectively. It can be suggested that the differences in the number of embryos isolated from both ovaries after these two treatments systems in prepuberal gilts and multiparous sows may be a result of age-dependent different response to gonadotropins and the reproductive competence of these females.
The aims of this study were to compare two methods of estrus synchronization and to evaluate the effectiveness of the PMSG treatment combined with P4 application. Fifty non-lactating seasonal anestrus fat-tailed ewes were randomly assigned into five groups. The controlled internal drug release devices (CIDR) were applied during day 14 in group I and in group II. Progesterone impregnated sponges were applied during day 14 in group III and in group IV. And then 500 IU PMSG was injected in group I and III i.m. intravaginal devices removed. Ewes in group V served as controls. There was no difference between the groups in the peak value of LH and LH surge. Although LH surge was seen in the control groups 5 sheep, none of the control ewes expressed estrus. Different progestagen treatments have no different results when they are evaluated in terms of the success of the estrus synchronization. PMSG application, after P4 treatment, increased the success of the synchronization.
The aim of this study was to determine the short-, mid- and long-term effects of cloprostenol (a synthetic analogue of prostoglandin F2α, PG) and equine chorionic gonadotropin (E) administration on reproductive organs (uterine tissue and ovaries) in female rats. Three different groups, PG, E, and control (C), were created, as well as six subgroups of the PG and E groups. After the treatment procedure, reproductive organs were removed surgically 7, 14, and 21 days after the last injection. Morphometric and histopathological changes in tissues were evaluated. It was shown that PG and E had a moderate proliferative effect on epithelial cells and endometrial glands, especially in the mid-term. It was also observed that, regardless of the time of application, some pathological changes can result from hormone administration.
The study was carried out during April and May 2006, on thirty-eight 15 - 23-month-old Holstein heifers with inactive ovaries, which were selected from a private dairy herd with 300 heifers. The heifers were randomly distributed into two groups: norgestomet group (n=29), and a control group (n=9). In the norgestomet group, silicone ear implants containing 6 mg of norgestomet were implanted, and a solution containing 3 mg of norgestomet and 5 mg of oestradiol valerate was injected intramuscularly. The silicone implants were removed 11 d later, and the heifers were continuously observed for signs of oestrus for three days. The heifers were inseminated 48 and 78 h after the removal of the implants, and after the first insemination they were treated with 50 µg of GnRH analogue. The rate of the induced oestrus was 86.2% (25/29) and 0% (0/9) in norgestomet and control groups, respectively. The pregnancy rate was 48.2% (14/29) and 0% (0/9) in norgestomet and control groups, respectively. Our results showed that fertile oestrus can be stimulated successfully in post-pubertal heifers with inactive ovaries by a norgestomet treatment, and-successful pregnancy rate can be obtained by a fixed-time insemination during this oestrus.
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