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The effect of L-165041 (PPARδ-agonist) on decreasing apoptosis and intracellular lipid content was assessed in fresh and vitrified-warmed in vitro -produced bovine embryos. It was hypothesised that the addition of L-165041 to the culture medium enhances development and cryopreservation. Oocytes were allocated to one of two treatments: control-standard culture medium, or L-165041 added to the medium on day1 with no media change. Ultrastructure, cleavage, and blastocyst rates were evaluated in fresh, and in post-vitrification cultured embryos by optical and electronic microscopy. A subset of fresh embryos were fixed for TUNEL assay and for Sudan-Black-B histochemical staining. Vitrified-warmed embryos were assessed using MALDI-MS technique. Cleavage and blastocyst rates (control 49.4±5.2, L-165041 51.8±4.3) were not influenced by L-165041. The proportion of inner cell mass cells (ICM) was higher in fresh embryos, and the rate of total and ICM apoptosis was lower in L-165041. In warmed-embryos, total and ICM apoptosis was lower in L-165041. The overall hatching rate was higher in L-165041 (66.62±2.83% vs 53.19±2.90%). There was less lipid accumulation in fresh L-165041-embryos. In conclusion, the use of L-165041 is recommended to improve the viability of in vitro -derived bovine embryos.

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This study was conducted to assess effects of different doses of pFSH on follicular recruitment, superovulatory response, ova/embryo recovery, and embryo yield in lactating ewes. Ewes (n = 24) had a superovulation treatment regimen imposed. All ewes were implanted with a progesterone intravaginal device for 9 d, and administered either 100 (G-100) or 200 (G-200) mg pFSH, proportioned into six doses administered at 12-h intervals, starting 60 h before device removal. At 7 days subsequent to progesterone device removal, there were non-surgical embryo recoveries (NSER) from ewes having three or more corpora lutea. At the time of the first pFSH injection, number of antral follicles were similar (P < 0.05) between ewes in the G-100 and G-200 group, however, there were more 3.1-4.0 mm follicles in ewes of the G-200 than G-100 group at the time of the second pFSH administration. Estrous response and CL number were less (P < 0.05) in ewes of the G-100 (66.7 % and 2.6 ±â€¯0.7) than G-200 (91.7 % and 11.6 ±â€¯1.2) group. There were embryo collections from 100 % and 90.9 % of ewes in the G-100 and G-200 groups, respectively (P > 0.05). Viable embryo numbers and ova/embryo recovery rate were greater (P < 0.05) in ewes of the G-200 (6.9 ±â€¯1.1 and 67.8 %) than G-100 (1.0 ±â€¯0.5 and 27.6 %) group. A dose of 200 mg pFSH was more effective in inducing a superovulatory response and embryo yield after NSER in ewes, however, the 100 mg dose was insufficient for these purposes.

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This study assessed the cervical ultrasonography mapping as a tool to select donor ewes for non-surgical embryo recovery (NSER). Lacaune ewes had their cervix evaluated by ultrasonography 12 hr after induced oestrus onset (Trial 1, n = 24) or 30 min before NSER (Trial 2, n = 17). Cervical rings were longitudinally evaluated and classified by their degree of misalignment on ultrasonography (DMUS) into: DMUS-1-cervix rectilinear, DMUS-2-intermediate and DMUS-3-highly asymmetrical. For predicting cervical transposing, only DMUS-1 and DMUS-2 were considered suitable. Similar ranking was attributed to degree of misalignment on the cervical map (DMCM 1-3), established immediately before NSER, which was performed at days 6 to 7 after oestrus. In Trial 1, cervical retraction for NSER was not possible only in three ewes classified as DMUS-3 (3/14, 21.4%). No difference (p > .05) was observed in the cervical transposing rates between ewes with different DMUS (ranged from 80% to 100%). In Trial 2, DMUS-1 and DMUS-2 reached 100% of transposing, and the only DMUS-3 ewe has not been transposed. In Trial 1, the prediction performance for successful cervical transposing showed low sensitivity (45%) and no specificity due to a high incidence of false negatives (52%). However, in Trial 2, sensitivity and specificity were both 100%. The DMCM and DMUS were uncorrelated, probably due to cervical stretching required to perform NSER. In conclusion, cervical ultrasound assessment immediately before NSER was more efficient to predict the cervical transposing than at induced oestrus, allowing the classification and selection of ewes eligible for NSER.

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This study assessed the effect of progestogen treatment length on ovarian parameters and embryo yield in superovulated Lacaune ewes collected by nonsurgical embryo recovery. Twenty-three lactating ewes were superovulated 30 d apart using a cross-over design. All ewes received 60 mg of MAP intravaginal sponges for 6 (G-6 group) or 9 (G-9 group) d. A total dose of 133 mg pFSH was given in six decreasing doses (twice a day) starting at 60 h before device removal. Ultrasound examination of the ovaries was performed at the first pFSH injection and one day before embryo recovery, which was performed 6-7 d after the onset of estrus. Embryo recovery was conducted only in ewes that expressed estrus and were mated. There was no difference (P > 0.05) in the total number of follicles between G-6 (15.7 ± 1.0) and G-9 (15.6 ± 0.8) at the time of the first pFSH treatment. The percentage of responding donors with ≥3 corpora lutea (CL; 78.2% [18/23] vs 69.5% [16/23]), mean (±SEM) CL number (7.0 ± 1.2 vs 8.1 ± 1.6), transcervical passage rate (94.4% [17/18] vs 83.3% [15/18], and ova/embryo recovery rate (54.5% [60/110] vs 68.0% [83/122]) were not different (P > 0.05) between the G-6 and G-9 groups. However, the mean number of viable embryos was lower (P < 0.05) in the G-6 group (1.8 ± 0.7) than in the G-9 group. (3.5 ± 1.1). In conclusion, treatment with an intravaginal MAP sponge for 9 d during a superovulation protocol is beneficial for viable embryo yield in Lacaune ewes out of the breeding season.

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The objective of this study was to assess the effect of the duration of progesterone-based estrus induction protocols on preovulatory follicular dynamics, ovulatory response, and embryo yield after non-surgical embryo recovery (NSER) in Lacaune ewes. Females received acetate medroxyprogesterone intravaginal sponges for six (G-6; n = 14) or nine (G-9; n = 14) days plus d-cloprostenol and eCG 24 h before sponge removal (Day 0). Preovulatory follicular dynamics and the luteal characteristics are evaluated by B-mode and Color-Doppler ultrasonography. NSER was performed five to six days after ovulation. The estrous behavior rate was 85.7% for both groups, and the percentage of ewes that ovulated was 92.9% in G-6 and 100% in G-9. The day of wave emergence (relative to Day 0) did not differ (P > 0.05) between G-6 (-3.0 ±â€¯0.5) and G-9 (-4.2 ±â€¯0.5). The number of follicles of size 4.1-5.0 mm was higher (P < 0.05) in G-9 (1.4 ±â€¯0.2) compared to G-6 (0.8 ±â€¯0.2) during the Days -4 to 0. At NSER, the transcervical penetration rate was 95.2% (20/21) and its duration time was lower (P < 0.05) in G-9 (3.4 ±â€¯0.6 min) than in G-6 (7.2 ±â€¯1.3 min). The number of ovulations and viable embryos was higher (P < 0.05) in G-9 (2.9 ±â€¯0.3 and 1.3 ±â€¯0.4, respectively) than in G-6 (1.9 ±â€¯0.3 and 0.4 ±â€¯0.2, respectively). In conclusion, the 9-day protocol promoted higher ovulation rate and embryo yield; moreover, the cervical dilation treatment allowed NSER in a high percentage of Lacaune ewes.

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This study investigated the feasibility of applying fixed-time (cryopreserved) embryo transfer in ewes. Embryos (n = 106) were non-surgically recovered from superovulated donors (n = 39) on day 6-7 after oestrus. Straws containing one or two embryos (morulae and/or blastocysts) subjected to either slow freezing (SF, n = 62) or vitrification (VT, n = 44) were randomly used within fixed-time embryo transfer on Day 8.5. Recipient ewes were nulliparous (n = 58) bearing corpora lutea after synchronous oestrous induction protocol. The pregnancy rate was higher (p = .03) in SF (39.4%) than VT (16.9%) and survival rate tended (p = .08) to be higher in SF than in VT (25.8% vs. 15.9%). Lambing rates were similar (p = .13) between SF (20.9%) and VT (15.9%). Embryos recovered by non-surgical route after cervical dilation treatment and later cryopreserved by either slow freezing or vitrification produced reasonable pregnancy rates after FTET.

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To evaluate the effects of moderate dietary restriction and lipid supplementation on ovarian follicular development, hormonal and metabolic profile, thirty-five prepuberal ewe lambs were blocked by body weight and randomly assigned to treatments: ALUS (control) - unsupplemented-diet ad libitum (3.5% ether extract, n = 9); R-US - intake restricted to 85% of the ALUS diet (n = 9); AL-LS - lipid-supplemented-diet ad libitum (9.8% ether extract, n = 8); R-LS - intake restricted to 85% of the ALLS diet (n = 9), from 95 ± 8 days of age until estrus or 7 months of age. Lipid supplementation did not reduce dry matter intake. Daily weight gain was greater in lambs fed ad libitum. Plasma glucose was greater in the RLS treatment group, while serum insulin was less with lipid supplementation. There was a treatment by age interaction on total cholesterol, HDL cholesterol and triglyceride serum concentrations. Estrus was detected in 43% of the animals and the overall ovulation rate was 60%. The number of follicles, diameter of the largest follicle, body weight, age and serum progesterone at puberty did not differ among treatment groups. The mean diameter of the largest follicle was greater in lambs having than in those not having ovulations and increased with age in both groups. There was an interaction between the effects of occurrence of ovulation and age on the number of follicles between 3 and 5 mm and > 5 mm. Lipid supplementation and dietary restriction altered the metabolic profile in ewe lambs with no concomitant changes in values for reproductive variables.

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Males and females, including purebred Santa Inês lamb (SI) and crosses between Santa Inês dams and Texel (TxSI), Ile de France (IFxSI) and Bergamasca (BxSI) sires were feedlot finished and slaughtered at 15, 25, 35 and 45kg live weight. After slaughter, the following non- carcass components were weighed and calculated the allometric growth. Lungs of BxSI males grew faster than those of SI and TxSI. Trachea/esophagus in SI and TxSI males grew slower than IFxSI and BxSI. Kidneys BxSI males grew faster than TxSI and IFxSI. Livers of female TxSI lamb grew more rapidly than those of females in the other genetic groups. In both males and females, the rumen/reticulum grew faster in the TxSI group than SI and BxSI groups.

Machos e fêmeas, Santa Inês puros (SI) e cruzados de matrizes Santa Inês com reprodutores das raças Texel (TxSI), Ile de France (IFxSI) e Bergamácia (BxSI), terminados em confinamento e abatidos aos 15, 25, 35 e 45kg de peso vivo. Após o abate, foram tomados os pesos das vísceras e analisado o crescimento alométrico. O pulmão dos machos BxSI cresceu em taxas mais elevadas que SI e TxSI. A tráqueia/esôfago dos machos SI e TxSI cresceu mais lentamente que dos IFxSI e BxSI. Os rins dos machos BxSI cresceram mais rápido comparado aos dos TxSI e IFxSI. O fígado das fêmeas TxSI cresceu em taxas mais elevadas quando comparadas às fêmeas dos outros grupos genéticos. Os machos e fêmeas do grupo TxSI apresentaram taxas de crescimento maiores para rúmen/retículo, respectivamente, comparado aos grupos SI e BxSI.

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The estrus behavior was evaluated during an induced and natural subsequent estrus in twelve Guzera breed cows, in the winter and summer seasons in two consecutive years. The proportion of cows that responded to estrus synchronization was 84.8 percent. The effect of the interaction season x year of experiment on estrous cycle length was observed. Pro-estrus was longer in the summer (57.69±4.72h) and in the natural estrus (74.23±4.41h) than in the winter (38.95±4.02h) and in the induced estrus (22.40±4.36h). Estrus length was similar in the winter (11.48±0.70h) and in the summer seasons (13.40±0.82h) as well as among cows with induced (12.47±0.75h) and natural estrus (12.41±0.76h). The number of mounts accepted during estrus and the number of mounts accepted/ hour in estrus were similar in winter (29.17±2.86 and 2.59±0.22, respectively) and summer (31.45±3.36 and 2.42±0.26, respectively) as well as between induced (30.23±3.10 and 2.54±0.24, respectively) and natural estrus (30.40±3.14 and 2.47±0.24, respectively). The length and intensity of estrus were not influenced by synchronization or season of the year. Longer period of pro-estrus in summer may favor the identification of sexually active animals in this season.

A manifestação do comportamento estral foi avaliada durante um estro induzido e o estro subseqüente, em 12 vacas da raça Guzerá, no inverno e no verão em dois anos consecutivos. A proporção de vacas que respondeu à sincronização de estros foi de 84,8 por cento. Observou-se efeito de interação entre estação e ano sobre a duração do ciclo estral. O proestro foi maior no verão (57,69±4,72h) e no estro natural (74,23±4,41h), que no inverno (38,95±4,02h) e no estro induzido (22,40±4,36h). A duração do estro foi similar no inverno (11,48±0,70h) e no verão (13,40±0,82h), assim como entre as vacas com estro induzido (12,47±0,75h) e natural (12,41±0,76h). O número de montas recebidas durante o estro e o número de montas recebidas/hora em estro foram similares no inverno (29,17±2,86 e 2,59±0,22, respectivamente) e no verão (31,45±3,36 e 2,42±0,26, respectivamente), assim como entre o estro induzido (30,23±3,10 e 2,54±0,24, respectivamente) e o natural (30,40±3,14 e 2,47±0,24, respectivamente). A duração e a intensidade do estro não foram influenciadas pela sincronização ou pela estação do ano. O maior período de proestro no verão pode favorecer a identificação dos animais sexualmente ativos.