No abstract

Recent studies have shown that adiponectin, an adipokine predominantly produced by adipose tissue, regulates several reproductive processes. However, the mechanisms of action of adiponectin on the maturation of goat oocytes remain to be determined. The aim of this study was to investigate whether (a) adiponectin influences the meiotic maturation of goat oocytes; (b) MAPK MEK 1/2 mediates the effects of adiponectin; and 3) adiponectin differentially affects mRNA relative abundance of genes relevant for adiponectin signal transduction in goat oocytes. The addition of adiponectin (5 μg/ml) during the maturation of goat oocytes resulted in a higher percentage of successful nuclear maturation compared to those of the group without adiponectin (p < 0.05). Adiponectin-stimulated nuclear oocyte maturation was significantly impaired by a mitogen-activated protein kinase MEK 1/2 inhibitor, U0126 (p < 0.05). There was no evidence of any adiponectin-induced difference in the relative transcript abundances of AdipoR1, AdipoR2, AMPKα1, AMPKα2, PPARα and PPARγ genes. In conclusion, these results indicate that adiponectin has a positive effect on the meiotic maturation of goat oocytes through the MAPK MEK 1/2 pathway. Furthermore, the adiponectin does not affect the relative abundance of genes relevant for adiponectin signal transduction in goat oocytes.

Ten pluriparous mares were used as donors to supply embryos which were transferred into 103 recipients, 31 of which were nulliparous, 34 were pluriparous and lactating, and 38 were pluriparous and non-lactating. The embryos were recovered eight days after ovulation and pregnancy was confirmed by ultrasound six days after the transfer; the length of the embryos was measured ultrasonographically on days 12, 14, 16, 18, 20, 25 and 30 after the embryo transfer. One hundred and fifteen of 200 flushes provided embryos, 12 being degenerate and 103 being viable embryos. From the 103 embryo transfers carried out, 51 pregnancies were confirmed by ultrasound within 30 days; 16 of the 31 nulliparous recipients became pregnant, 16 of the 34 pluriparous lactating recipients and 19 of the 38 pluriparous non-lactating recipients. There were no significant differences between the groups of mares in the mean (sd) rate of growth of their embryos between 12 and 30 days of gestation.

No abstract

Technologies for automating animal management and monitoring tasks can improve efficiency and productivity of livestock production. We developed the e-Synch system for automated control and monitoring the estrous cycle of cattle through intravaginal hormone delivery and sensing. Thus, our objective was to evaluate luteinizing hormone (LH) concentrations after intravaginal instillation of the Gonadotropin-releasing hormone (GnRH) analogue Gonadorelin with the e-Synch system. This system consists of an intravaginal electronically controlled automated hormone delivery and sensing device integrated with an IoT platform. Lactating Holstein cows with their estrous cycle synchronized were used in two experiments (Exp). In Exp 1, at 48 h after induction of luteolysis, cows (n=5-6 per group) were randomized to receive 100 µg of Gonadorelin through intramuscular (i.m.) injection, 100 µg of Gonadorelin in a 2 mL solution delivered with e-Synch, and an empty e-Synch device. In Exp 2, at 48 h after induction of luteolysis cows (n=6-7 per group) were randomized to receive 100 µg of Gonadorelin i.m., or an intravaginal treatment with e-Synch consisting of 100 or 1,000 µg of Gonadorelin in 2 or 10 mL of solution containing 10% citric acid as absorption enhancer. Circulating concentrations of LH were analyzed with linear mixed models with or without repeated measurements. In Exp 1, cows in the i.m. Gonadorelin treatment had a surge of LH whereas cows in the other two treatments did not have a surge of LH for up to 8 h after treatment. In Exp 2, the 1,000 µg dose of Gonadorelin elicited more LH release than the 100 µg dose, regardless of solution quantity. The overall LH response as determined by area under the curve, mean, and maximum LH concentrations was similar between cows receiving 1,000 µg of Gonadorelin delivered with e-Synch and 100 μg of Gonadorelin i.m. Increasing volume of solution for delivering the same dose of Gonadorelin partially increased LH release only for the 100 µg dose. We conclude that the e-Synch system could be used to automatically release Gonadorelin in a dose and volume that induces a surge of LH of similar magnitude than after i.m. injection of 100 μg of Gonadorelin. Also, the dose of Gonadorelin delivered by e-Synch is more critical than the volume of solution used.

abstract:The experiment was conduct to assess the follicular dynamics, time and synchrony of ovulation in nuliparous Murrah buffaloes (Bubalus bubalis) treated with an ovsynch protocol associated with progesterone. Eight nuliparous cycling buffaloes received an intravaginal CIDR device containing 1.9 g of progesterone and 100 mg of a GnRH analogue i.m. (Gonadorelin, Profertil  ) without regard to the stage of the estrous cycle (day of treatment, day 0) followed by 500 UI eCG (eCG, Novormon  ) 7 days later and 0.150 mg of PGF 2α i.m. (d-Cloprostenol, Prolise  ) 8 days later at the time of CIDR device removal. A second-treatment of the same GnRH analogue (100 mg, i.m.) was given 48 h after PGF 2α . All buffaloes presented a BSC of 3,5 (scale 1 to 5, 1 = very thin and 5 = fat) Follicular dynamics was monitored by transrectal ultrasound (Pie Medical, linear transducer of 7.5 MHz ). Only one female ovulated after first GnRH application. The diameter of the ovulatory follicle at the day of device removal was 7.5 ± 1.0 mm and at the day of second GnRH injection was 10.5 ± 1.2 mm. The interval between device removal and ovulation was 67.0 ± 6.0 hours and ovulation rate was 75% (6/8).

No abstract

The objective of this study was to test the €œmale effect€ on the reproductive performance of Anglo Nubian does (n = 180), aged between 24 and 60 months, under different male-to-female ratios (1:20 €“ T20, 1:30 €“ T30, and 1:40 €“ T40) and climatic conditions (dry season €“ DS, and rainy season €“ RS). Does were randomly distributed into three groups (T20, T30, and T40) and were isolated from bucks at a distance of 300 m for 60 days before the start of the experiments. The first manifestation of estrous during the DS occurred 6.83 ± 4.54 (T20), 6.72 ± 4.56 (T30) and 7.05 ± 5.23 (T40) days following the onset of the breeding season (P>0.05). In the RS, onset of estrous was observed 6.60 ± 4.74 (T20), 6.70 ± 4.43 (T30) and 7.46 ± 4.54 (T40) days after the beginning of the breeding season (P>0.05). Estrous induction in females during the DS occurred in 95% (T20), 80% (T30), and 75.5% (T40) of all females. During the RS, estrous detection reached 100% (T20), 100% (T30), and 97.5% (T40) of all females, with no difference between all RS and DS groups. Estrous synchronization during the DS occurred in 35.00% (T20), 36.66% (T30), and 32.50% (T40) of all females, for an average occurrence of 34.72%. During the RS, synchronization occurred in 65% (T20), 70% (T30) and 62.25% (T40) of all females, for an average occurrence of 65.75%; no difference was detected between the RS and the DS. Pregnancy rates in the DS groups were 65.0% (T20), 70.0% (T30), and 62.5% (T40), while pregnancy rates in the RS were 90.0% (T20), 86.6% (T30), and 95.0% (T40). No difference was observed for conception rates between any of the RS and DS groups. Prolificacy during the DS was 1.30 (T20), 1.30 (T30) and 1.35 (T40), while in the RS prolificacy was 1.29 (T20), 1.25 (T30) and 1.30 (T40). Thus, the male effect can be used effectively for goats under 1:20€“1:40 male-to-female ratios in a 45-day mating season under varying climatic conditions.