The aim of this study was to investigate the influence of short-term treatment of highenergy diet after ovulation on ovarian function and metabolic status in ewe. Cycling ewes Ossimi were divided into treatment group (TG; n = 6) and control group (CG; n = 6). After ultrasonographic detection of ovulation (day 0), a high-energy diet (12.55 MJ DE/kg diet; 125% of maintenance) was fed to TG from day 1 to day 4 after ovulation (4 days). The highenergy diet consisted of 850 g concentrate mixture and 150 g alfalfa hay, plus ad libitum access to wheat straw. The CG was offered as maintenance diet (10 MJ DE/kg diet) throughout the experiment. Follicular development was observed ultrasonographically every other day while blood samples were collected daily throughout the experiment for the analysis of glucose, total cholesterol, urea, triglycerides, total proteins, aspartate aminotransferase (AST), alanine transaminase (ALT) and glutamate oxaloacetate transaminase (GOT). Transient feeding of high-energy ration during early luteal phase of estrous cycle significantly influenced the concentration of glucose and some metabolic profiles. Total proteins were greater at first, third and fourth day after ovulation (ovulation is day 0) in TG when compared to CG ewes. Blood glucose concentration was greater in TG than that of CG at days 1, 2, 3 and 4 postovulation. The average number of small follicles (2–2.9 mm) of the first follicular wave after ovulation was greater in TG ewes (23.3 follicles) than that of CG (2.2). There was no difference in the number of medium (3–5 mm) and large sized follicles (>5 mm) between CG and TG ewes. Moreover, the maximum size of large follicles did not differ between CG (5.6 mm) and TG ewes (5.9 mm). In conclusion, high-energy diet may improve number of small follicles and alter energy metabolite during early luteal phase in cycling ewe

The aim of this study was to investigate the influence of short-term treatment of highenergy diet after ovulation on ovarian function and metabolic status in ewe. Cycling ewes Ossimi were divided into treatment group (TG; n = 6) and control group (CG; n = 6). After ultrasonographic detection of ovulation (day 0), a high-energy diet (12.55 MJ DE/kg diet; 125% of maintenance) was fed to TG from day 1 to day 4 after ovulation (4 days). The highenergy diet consisted of 850 g concentrate mixture and 150 g alfalfa hay, plus ad libitum access to wheat straw. The CG was offered as maintenance diet (10 MJ DE/kg diet) throughout the experiment. Follicular development was observed ultrasonographically every other day while blood samples were collected daily throughout the experiment for the analysis of glucose, total cholesterol, urea, triglycerides, total proteins, aspartate aminotransferase (AST), alanine transaminase (ALT) and glutamate oxaloacetate transaminase (GOT). Transient feeding of high-energy ration during early luteal phase of estrous cycle significantly influenced the concentration of glucose and some metabolic profiles. Total proteins were greater at first, third and fourth day after ovulation (ovulation is day 0) in TG when compared to CG ewes. Blood glucose concentration was greater in TG than that of CG at days 1, 2, 3 and 4 postovulation. The average number of small follicles (2–2.9 mm) of the first follicular wave after ovulation was greater in TG ewes (23.3 follicles) than that of CG (2.2). There was no difference in the number of medium (3–5 mm) and large sized follicles (>5 mm) between CG and TG ewes. Moreover, the maximum size of large follicles did not differ between CG (5.6 mm) and TG ewes (5.9 mm). In conclusion, high-energy diet may improve number of small follicles and alter energy metabolite during early luteal phase in cycling ewe

In this study we compared the effect of dinoprost and cloprostenol on changes of corpus luteum blood flow during luteolysis. Ten nonlactating cyclic ewes were synchronized with double PGF2α injections 11 days apart. At Day 10, the animals were classified into 2 groups and received the third dose of PGF2α after confirmation of the presence of a mature CL. The first group received (12.5 mg/im) dinoprost and the second group received (250 μg/im) cloprostenol. A color Doppler ultrasound scan was performed by the same operator according to the following timeline: 0, 0.5, 1, 2, 4, 6, 12, and 24 hours, then every 24 hours until Day 4). The size, morphology, and blood flow of the CL was evaluated during the regression. The results showed that regression of the CL did not differ between the dinoprost and cloprostenol groups. There was no significant effect on diameter of the CL in both groups, though the size of the CL decreased gradually and slowly. Pretreatment progesterone concentration did not differ between groups. The results showed that the nitric oxide level was significantly increased within half an hour after the dinoprost treatment, and was significantly decreased in the cloprostenol group after half an hour. The blood velocity was increased significantly half an hour after the dinoprost treatment and it was decreased in the cloprostenol-treated group. In conclusion, both cloprostenol and dinoprost affect CL by controlling the nitric oxide level and blood supply of the CL via different mechanisms to induce luteolysis.

In this study we compared the effect of dinoprost and cloprostenol on changes of corpus luteum blood flow during luteolysis. Ten nonlactating cyclic ewes were synchronized with double PGF2α injections 11 days apart. At Day 10, the animals were classified into 2 groups and received the third dose of PGF2α after confirmation of the presence of a mature CL. The first group received (12.5 mg/im) dinoprost and the second group received (250 μg/im) cloprostenol. A color Doppler ultrasound scan was performed by the same operator according to the following timeline: 0, 0.5, 1, 2, 4, 6, 12, and 24 hours, then every 24 hours until Day 4). The size, morphology, and blood flow of the CL was evaluated during the regression. The results showed that regression of the CL did not differ between the dinoprost and cloprostenol groups. There was no significant effect on diameter of the CL in both groups, though the size of the CL decreased gradually and slowly. Pretreatment progesterone concentration did not differ between groups. The results showed that the nitric oxide level was significantly increased within half an hour after the dinoprost treatment, and was significantly decreased in the cloprostenol group after half an hour. The blood velocity was increased significantly half an hour after the dinoprost treatment and it was decreased in the cloprostenol-treated group. In conclusion, both cloprostenol and dinoprost affect CL by controlling the nitric oxide level and blood supply of the CL via different mechanisms to induce luteolysis.