Ovulation Interval Research Articles

Prostaglandin F2α treatment does not hasten ovulation in weaned sows

This study evaluated the efficiency of prostaglandin F2α (PGF) to hasten ovulation in weaned sows. In experiment I, weaned sows detected in estrus (0 h) received: no hormone (Control; n = 56); 0.5 mg PGF IM at 0 h and 2 h (PGF0; n = 56); or 0.5 mg PGF IM at 24 h and 26 h (PGF24; n = 55). In experiment II, weaned sows that did not express estrus signs until 72 h after weaning (0 h) were assigned to: no hormone (Control; n = 45); 10 µg buserelin acetate IM at 0 h (Buserelin; n = 43); 0.5 mg PGF IM at 34 h and 36 h (PGF; n = 44); or 10 µg buserelin acetate IM at 0 h plus 0.5 mg PGF IM at 34 h and 36 h (Buserelin + PGF; n = 45). In experiment I, no effect of PGF on the interval treatment onset to ovulation was observed (P > 0.05), and no treatment effect was observed on the relative or cumulative proportion of females that ovulated post-treatment onset (P > 0.05). In experiment II, treatment onset to ovulation interval was shorter for Buserelin group than for PGF group (P < 0.05), and a higher cumulative percentage of Buserelin treated sows ovulated up to 48 h compared to PGF and Control groups (P < 0.01), with no differences from Buserelin + PGF. Treatments did not affect total number of piglets born in both experiments (P > 0.05). In conclusion, PGF did not hasten ovulation timing or affect litter size in weaned sows.

Estrous, ovulation and reproductive responses of ewes synchronized with a long interval prostaglandin–based protocol for timed AI

The aim was to characterize and assess the reproductive performance of a long interval prostaglandin (PG)–based protocol for timed AI (TAI) at different times. During breeding season three experiments were done involving 622 Merino ewes, 11 rams, and five androgenized wethers per 100 ewes. All ewes were estrus synchronized with two PG injections 15–day apart (PG15): Day −15 and 0 (Hour 0). Estrous distribution respect to Hour 0, estrous response and synchrony after Hour 0, and interval from Hour 0 to estrus detection (PG–estrus) was evaluated (Experiment I; n = 105 ewes). Interval from estrus detection to ovulation (estrus–ovulation) and from Hour 0 to ovulation (PG–ovulation) was determined (Experiment II; n = 12 ewes). Visual–physical score of cervical mucus at TAI, non–return to service to Day 23 (NRR23), fertility, prolificacy, and fecundity to Day 60 in four cervical fresh semen TAI groups was evaluated (Experiment III; n = 505 ewes; 107 nulliparous-398 multiparous). Three groups with single service at 56 (Control), 44 or 68, and one with double service at 44 and 68 ± 1.5 h after Hour 0 (PG15–56, PG15–44, PG15–68, and PG15–44/68 groups, respectively) were tested. Ninety-eight-point one percent of the ewes showed estrus from Hour −48 up to 84 respects to Hour 0. Twenty percent of them showed estrus from Hour −48 up to 0, and 78.1 % from Hour 12 up to 84 (Experiment I). The largest proportion of ewes in estrus was observed between Hour 36 and 60 (80.5 %). PG–estrus interval was 54.1 ± 10 h (means ± SD). Estrus–ovulation interval was 32.4 ± 5.8 h, and PG–ovulation interval was 77.0 ± 16.6 h (Experiment II). Ewe parity did not affect any of the reproductive variables (P > 0.05; Experiment III). There were no significant differences (P > 0.05) between Control and different groups in mucus score (2.18 ± 0.08, 2.02 ± 0.07, 2.14 ± 0.09, 2.25 ± 0.10), NRR23 (76.0, 71.9, 78.6, 79.4 %) or fertility (66.4, 64.1, 66.7, 73.8 %; PG15–56, PG15–44, PG15–68 or PG15–44/68 groups, respectively). Prolificacy in PG15-44 group was lower (1.07 ± 0.03; P < 0.05) than other groups (1.27 ± 0.05, 1.23 ± 0.05, 1.20 ± 0.04), and fecundity than PG15–44/68 group (0.84, 0.69, 0.82, 0.89), without differences among other groups (PG15–56, PG15–44, PG15–68 or PG15–44/68 groups, respectively). We concluded that any time between 56 and 68 h after PG15 protocol could be used to perform cervical TAI using fresh semen, without benefits of a double TAI service at 44 and 68 h.

Effect of cloprostenol on luteolysis in jennies

An intensive farm system has progressively emerged with the rapid development of the donkey industry. One of the primary challenges impeding the development of the donkey industry and the preservation of endangered donkey species is the low reproductive efficiency of jennies (Feng Yang et.al. Equine Veterinary Journal 2021, 53: 1218-1226). In donkeys, luteolysis occurs between days 15 and 17 after ovulation (Carluccio A. et.al. Theriogenology, 2007, 68(6): 914-919). To shorten the estrus cycle, a new estrus cycle may start after luteolysis is induced by the PGF2α analog (Duccio P. et.al. Theriogenology, 2018, 121: 175-180). Treatment of mares and cattle with PGF2α analogs from the fifth day after ovulation induces luteolysis (Bergfelt DR. et.al. Theriogenology, 2006, 65(8): 1605-1619). However, information regarding luteolysis in jennies is limited. In this study, we aimed to investigate the effect of cloprostenol on luteolysis in jennies. The PGF2α analog used in the experiment was cloprostenol (0.2 mg/2 ml, Ningbo Second Hormone Factory, Zhejiang, China). To study the effects of different cloprostenol doses on the estrus cycle, jennies were treated with 0.2 mg (n=30), 0.4 mg (n=30), or 0.6 mg (n=30)cloprostenol (PGF2α), respectively. The time of luteolysis, ovulation interval, follicular size at ovulation, and ovulation rates were compared between the groups. The results showed that luteolysis rates in the jennies within 72 h of treatment were higher than 90% in the three treatment groups. The time required for luteolysis was not statistically different among the three groups. In addition, the estrus interval, ovulation interval, ovulation diameter, and ovulation rate did not differ among the three groups. To examine the timing effect of cloprostenol treatment on the estrus cycle, jennies were treated with 0.4 mg cloprostenol on the third (D 3, n=30), fifth (D 5, n=30), or seventh (D 7, n=30) day following ovulation, respectively. The results showed that the luteal phase of the D 3 treatment group was shorter than that of the D 5 and D 7 treatment groups, and in the D 5 treatment group was shorter than that of the D 7 group (P < 0.05). In can be concluded that treatment with 0.4 mg cloprostenol on the third day following ovulation shortens the length of the luteal phase and estrus cycle considerably.

Effect of cloprostenol on luteolysis and comparison of different estrus synchronization protocols in jennies

Estrus synchronization is necessary for intensive donkey farming. Studies on estrus synchronization in jennies are, however, scarce. We aimed to investigate the susceptibility of the donkey corpus luteum to cloprostenol and design a successful estrus synchronization protocol. Firstly, the effects of different cloprostenol doses and the timing effect of cloprostenol treatment on estrous cycle was investigated. The time from treatment to luteolysis, the ovulation interval, pre-ovulatory diameter, and ovulation rates were compared between groups. Secondly, to identify the best protocol, eight estrus synchronization protocols from three categories were examined. In the first category, jennies in groups A (n = 55) and B (n = 30) received a progesterone releasing intra-vaginal device (JVID®) and cloprostenol treatment. In the second category (group C to F), jennies were pretreated with deslorelin, and then treated with JVID and cloprostenol, including groups C (n = 50), D (n = 50), E (n = 70), and F (n = 65). In the third category, jennies were treated with deslorelin and cloprostenol, including groups G (n = 40) and H (n = 40). Comparisons were made among groups regarding the degree of synchronization, ovulation, and pregnancy rates. Treatment with 0.4 mg cloprostenol on the third day following ovulation minimized the length of the luteal phase and estrous cycle. Synchronization rate varied from 60.0% to 88.6% among groups and was highest in group E. Pregnancy rates did not differ among the eight protocols. In conclusion, cloprostenol effectively induced luteolysis in jennies and a treatment protocol combining deslorelin, cloprostenol, and JVID is efficient for estrus synchronization in donkeys.

Adaptive immune response ranking is associated with reproductive phenotypes in grazing dairy cows divergent in genetic merit for fertility traits

A strong adaptive immune response has been reported to have positive effects on fertility; therefore, we investigated antibody- and cell-mediated adaptive immune responses (AMIR and CMIR, respectively) and their associations with reproductive phenotypes using a population of animals that differed in their estimated genetic merit for fertility traits (fertility breeding value; FertBV). Holstein-Friesian heifers (n = 528) grazed on pasture in 4 herds based on age. These herds included 277 heifers of positive (POS) FertBV and 251 of negative (NEG) FertBV. The adaptive immune response (IR) was evaluated before puberty at 7.5 mo of age and used to rank animals as high, average, or low for AMIR, CMIR, and overall IR (combined CMIR and AMIR). The animals were studied from 12 wk of age through to the end of their second lactation to measure growth, puberty, and timing and success of fertility phenotypes, including those related to ovulation and pregnancy. Initial analysis indicated no difference in fertility outcomes between cows ranked as high or average for AMIR (n = 55, n = 407, respectively), CMIR (n = 87, n = 354, respectively), and IR (n = 29, n = 470, respectively), so these groups were pooled as HiAv-IR. Proportions of heifers of POS FertBV were similar within HiAv and low categories across AMIR (0.52 and 0.58, respectively), CMIR (0.51 and 0.59, respectively), and IR (0.53 and 0.48, respectively). Heifers with HiAv-IR had a greater average daily weight gain from 13 to 52 wk of age (661 g, 95% confidence interval 652, 669 vs. 619 g, 95% confidence interval 591, 647) and tended to be younger at puberty (371 d, 95% confidence interval 366, 377 vs. 385 d, 95% confidence interval 369, 401) than low-IR heifers. Low-CMIR cows of a NEG FertBV had a >40 d longer calving to first ovulation interval during their first lactation compared with HiAv-CMIR NEG FertBV cows. Low-CMIR cows also had decreased pregnancy rates at both 3 wk (25% ± 7% vs. 42% ± 3%; least squares means ± standard error) and 6 wk (33% ± 7% vs. 54% ± 3%; least squares means ± standard error) into the seasonal breeding period during their first lactation, compared with HiAv-CMIR cows. In summary, although the number of POS and NEG FertBV cows was similar in each immune group; interaction effects between FertBV and immune ranking on reproductive phenotypes are evident when cows were ranked by the overall IR. There were also associations between dairy cows' CMIR ranking and ability to return to estrus and become pregnant early in the breeding period, which will have benefits in seasonal breeding systems.

Effect of Artificial Lighting Duration on Egg Production and Egg Quality of Local Chickens

Low egg production and long ovulation interval among chickens are the problems faced by farmers. Thus, an appropriate technology for increasing egg production is necessary. This study aims to analyze the effect of artificial light duration on egg production and egg quality of local chickens. This experiment, which has a completely randomized design, was conducted in the city of Palu, between December 2017 and September 2018. The hens were divided into G0 (control; 12 h lighting), G1 (13 h lighting), G2 (14 h lighting), and G3 (16 h lighting). Research variables were follicle-stimulating hormone (FSH) and luteinizing hormone (LH) concentration, egg production, clutch, and egg quality. Egg production was significantly influenced by the addition of light but not the quality of local-chicken eggs (egg weight, egg yolk index, egg white index, air sack diameter, yolk color, and shell thickness). Nonetheless, artificial light in G2 (12 h natural day light + 2 h artificial light) significantly influenced the increase of both FSH and LH concentrations at approximately 235.57 pg/ml (range, 162.15–397.72 pg/ml) and 1,021.98 pg/ml (range, 2,521.08–3,543.06 pg/ml), respectively. Chickens raised under a 14-hour artificial light achieved an increase in egg production without affecting egg quality. Keywords : Artificial light, Egg Production, Quality of Egg, Local-chicken DOI : 10.7176/JBAH/12-8-03 Publication date : April 30th 2022

Hormonal Management for the Induction of Luteolysis and Ovulation in Andalusian Jennies: Effect on Reproductive Performance, Embryo Quality and Recovery Rate

Simple SummaryEmbryo transfer is of utmost importance in endangered species such as donkeys. To maximize the number of embryos obtained and, thus, the number of foals born, the manipulation of cycles (shortening of interval between cycles and timely ovulation induction) is crucial. Therefore, the aim of this study was to compare two prostaglandins (luprostiol, LUP, and dinoprost, DIN) and two ovulation-inducing agents (human Chorionic Gonadotropin, hCG, and deslorelin, DES) in 26 fertile embryo donor jennies. In Experiment 1, jennies were randomly treated with either LUP or DIN after recovering the embryos. In Experiment 2, the jennies were treated with either hCG or DES to synchronize ovulation and breeding. Both prostaglandins shortened the cycles similarly and did not affect the embryos recovered. Although the ovulation inductors reported similar results, DES induced ovulation more rapidly. Interestingly, the embryo quality was lower when the uterus showed high edema at the time of insemination.Two prostanglandins (luprostiol, LUP, and dinoprost, DIN) and two ovulation-inducing agents (human Chorionic Gonadotropin, hCG, and deslorelin, DES) were evaluated for luteolysis and estrus induction, and for ovulation induction, respectively, in embryo donor jennies. Twenty-six fertile Andalusian jennies were used. In Experiment 1, jennies (n = 112 cycles) were randomly treated with either LUP or DIN after embryo flushing. In Experiment 2, donors (n = 84 cycles) were randomly treated with either hCG or DES to induce ovulation. No differences were found between prostaglandins for all variables studied (prostaglandin–ovulation interval (POI), interovulatory interval (IOI), embryo recovery rate (ERR), positive flushing rate (PFR) and embryo grade (EG)). The ovulation rate was similar for hCG and DES (60.9% vs. 78.7%). However, the interval to ovulation (ITO) was affected (62.61 ± 7.20 vs. 48.79 ± 2.69 h). None of the other variables studied (ERR, PFR and EG) were affected (p > 0.05), except for embryo quality (p = 0.009). In short, both prostaglandins evaluated are adequate to induce luteolysis and estrus. Both ovulation-inducing agents hastened ovulation, but DES seems to be more effective than hCG. Follicular diameter affected the interval from treatment to ovulation, and high uterine edema was related to low embryo quality.

Positive genetic merit for fertility traits is associated with superior reproductive performance in pasture-based dairy cows with seasonal calving

New Zealand's Fertility Breeding Value (FertBV) is reported as the percentage of a sire's daughters that calve in the first 42 d of the seasonal calving period and is an estimate of genetic merit for fertility for dairy cattle. Reproductive physiology, milk production, and changes in body weight and body condition score of 2 groups of cows divergent in FertBV (+5.0%: POS; -5.1%: NEG) were characterized during their first 2 lactations. Cows grazed fresh pasture and were managed in a seasonal calving system; they were bred by artificial insemination on observed estrus for the entire breeding period (98 d in lactation 1 and 76 d in lactation 2). During lactation 1, all animals were primiparous and were randomly allocated to 1 of 2 herds, ensuring each herd was balanced for FertBV and expected calving date. During lactation 2, cows that became pregnant during lactation 1 were managed as 1 herd. Cows not inseminated in the first 42 d of the breeding season were examined for the presence of a corpus luteum and treated with an anestrus program. On average, the interval from calving to ovulation was 19 d longer in lactation 1 and 10 d longer in lactation 2 for NEG FertBV cows. The percent of cows submitted for artificial insemination after 21 d (i.e., submission rate) was 38 and 25 percentage points greater in the POS FertBV cows during lactations 1 and 2, respectively. Pregnancy rate from 42 d of breeding was 33 and 30 percentage points greater, respectively. There was no effect of FertBV on vaginal discharge score postcalving; however, POS FertBV cows had a 50% lower risk of having subclinical endometritis (polymorphonuclear leukocytes >7%) 42 d postcalving. Interactions between FertBV and month relative to calving identified that NEG FertBV cows were fatter (greater body condition score) in the month before calving, but thinner between 3 and 5 mo postcalving. There was no effect of FertBV on lactation length, estimated 270-d milk yields, or daily milk, fat, or protein yields, and only small effects on milk fat and protein percentage across the lactations. In summary, the POS FertBV cows had superior uterine health, a shorter calving to ovulation interval, a greater submission rate, and a greater pregnancy rate earlier in the breeding season when compared with the NEG FertBV cohort. Based on these results, these may be useful phenotypes to include in genetic selection indices.

Evaluation and characterization of estrus alerts and behavioral parameters generated by an ear-attached accelerometer-based system for automated detection of estrus

Our objectives were to evaluate the performance of an ear-attached automated estrus detection (AED) system (Smartbow; Zoetis) that monitored physical activity and rumination time, and to characterize AED system estrus alert features (i.e., timing and duration). Lactating Holstein cows (n = 216) commenced a protocol for the synchronization of estrus at 50 ± 3 DIM or 18 ± 3 d after artificial insemination. For 7 d after induction of luteolysis with PGF2α (d 0), we used visual observation of estrous behavior (30 min, 2 times per day) and data from an automated mounting behavior monitoring system based on a pressure-activated tail-head sensor (HeatWatch; Cowchips LLC) as a reference test (RTE) to detect behavioral estrus. Concomitantly, estrus alerts and their features were collected from the AED system. Progesterone levels confirmed luteal regression, and transrectal ultrasonography confirmed the occurrence and timing of ovulation. Performance metrics for the AED system were estimated with PROC FREQ in SAS, using the RTE or ovulation only as a reference. Performance was also estimated after the removal of cows with a discrepancy between the RTE and ovulation. Continuous outcomes with or without repeated measurements were evaluated by ANOVA using PROC MIXED in SAS. Based on the RTE, 86.6% (n = 187) of the cows presented estrus and ovulated; 1.4% (n = 3) presented estrus and did not ovulate; 6.4% (n = 14) did not present estrus but ovulated; and 5.6% (n = 12) did not present estrus or ovulation. We found no difference in the proportion of cows detected in estrus and with ovulation for the AED system (83.4%) and the RTE (86.6%). Compared with estrus events as detected by the RTE, sensitivity for the AED was 91.6% (95% CI: 87.6-95.5) and specificity was 69.2% (95% CI: 51.5-87.0). Using ovulation as reference, sensitivity was 89.6% (95% CI: 85.3-93.8) and specificity was 86.7% (95% CI 69.5-100). For all cows with agreement between the RTE and ovulation, sensitivity was 92.5% (95% CI: 88.7-96.3) and specificity was 91.7% (95% CI: 76.0-100). The mean (±SD) interval from induction of luteolysis to estrus alerts, estrus alert duration, and the onset of estrus alerts to ovulation interval were 72.2 ± 18.1, 13.5 ± 3.8, and 23.8 ± 7.1 h, respectively. We concluded that an ear-attached AED system that monitored physical activity and rumination time was effective at detecting cows in estrus and generated few false positive alerts when accounting for ovulation, cow physiological limitations, and the limitations of the RTE.

212 Ovarian ultrasound of sows by parity and season to determine effects of induced ovulation and single PCAI on farrowing rate and litter size

Abstract Increasing the distribution of semen from genetically superior sires accelerates the rate of improvement of economically important traits. Using a single fixed time post-cervical AI (SFTI) with ovulation control, the number of inseminations per ejaculate can be doubled. The objective of the study was to determine whether ovarian ultrasound could help identify parity (P1, 2, 3-6, ≥ 7) and seasonal (May-Jun, Jul-Aug, Sep-Oct) effects on fertility following induced ovulation and SFTI. Sows received OvuGel® (n = 914) on Days 3-5 after weaning and a SFTI 24 h later. Control sows (n = 881) that expressed estrus on Days 3-6 received a post-cervical AI on each day standing. Ovaries of a sub-population of sows (n = 436) were scanned by ultrasound to assess follicle size and insemination to ovulation interval. Interval from insemination to ovulation &gt; 24 h tended (P = 0.09) to reduce farrowing rate (FR, 74.1 ± 2.8%) compared to inseminations £ 24 h (83.4 ± 2.8%), regardless of treatment. In addition, sows that ovulated by Day 6 after weaning had greater (P = 0.03) total born (TB, 12.9 ± 0.5) than those ovulating ≥ 7 d (11.5 ± 0.5). Follicle number (16.3 ± 0.7) and size (7.0 ± 0.5 mm) on Day 4 did not differ between treatments. OvuGel increased (P = 0.002) the proportion of sows ovulating (88.9%) versus Controls (78.6%), but for both treatments, fewer P1 sows ovulated (75.0%) when compared to P3-6 (90.4%). Treatments did not differ in FR (78.5%), but seasonal interactions were observed (P = 0.05), most notably in Sep-Oct. Parity affected FR (P = 0.02), and was lower in P1 (66.1%) compared to 3 P2 (82.2%). Also, OvuGel and Control did not differ in TB (13.0) but parity ≥ 7 had the lowest TB (11.8) compared to younger parity females. In summary, OvuGel increased the proportion of sows ovulating by 10.3%, resulting in similar FR and TB compared to Control sows inseminated multiple times based on estrus.

Principal Component Analysis of Factors Affecting Ovulation Interval of Selected Women

Principal Component Analysis of Factors Affecting Ovulation Interval of Selected Women

Evaluation of embryo collection and transfer days on the pregnancy rate of Mangalarga Marchador mares during the breeding season

Background: Proper timing for embryo collection and transfer in horses -which is critical for the success of this biotechnology- is still debated. Additionally, there is little information on this technology under tropical conditions. Objective: To determine the best day for collection and transfer of embryos in Mangalarga Marchador mares under Brazilian northeast’s conditions. Methods: Donors (n= 30) and recipients (n= 76) in diestrus phase were selected based on both clinical and gynecology examinations. Estrus was induced on both donor and recipient mares by intramuscular injection of 5 mg Dinoprost, aiming to obtain an ovulation interval of -1 to +3 between recipient and donor. Ovulation was induced with buserelin acetate when the largest follicle reached at least 35 mm in diameter. At this time, mares were subjected to artificial insemination at 48-hour intervals until ovulation. The embryos were collected on days 7, 8, and 9 after ovulation. Results: The embryo collection on day 8 was more efficient (p 0.05) than day 9, which presented the same efficiency (p>0.05) as day 7. From a total of 76 embryos transferred to the recipients, that were between days 4 and 9 after ovulation, there was no influence (p>0.05) of the day of transfer on pregnancy rate. Conclusions: The embryo collection must be performed on day 8 after ovulation, and transfer can be performed on any day of that interval (4-9) without affecting the pregnancy rate.

Polymorphisms in the anti-oxidant paraoxonase-1 (PON1) gene associated with fertility of postpartum dairy cows

Paraoxonase 1 (PON1) is a negative acute phase plasma protein synthesized by the liver that has anti-oxidant activity. The aim of this study was to evaluate the association of single nucleotide polymorphisms (SNPs) in the PON1 promoter region with plasma PON1 activity and fertility in Holstein dairy cows. Sixty-eighty Holstein cows were used in this initial investigative study. Blood samples were collected weekly beginning 28 days prior to expected calving, twice weekly in week 1 and 2 postpartum, and then once weekly through 6 weeks postpartum for plasma PON1 activity analysis. Cows were synchronized for ovulation and timed AI at 63–70 DIM using an Ovsynch program. Pregnancy diagnosis was confirmed by rectal palpation and reproductive performance data was recorded until 210 DIM. DNA was extracted from blood of each cow and a fragment of proximal PON1 gene promoter was sequenced. Seven single nucleotide polymorphisms (SNPs) were identified in the promoter region of the PON1 gene at positions −22, −105, −176, −221, −392, −611 and −676, six of which were significantly associated with plasma PON1 activity level. The SNPs −221 and −392 were significantly associated with both plasma PON1 activity and the calving to conception interval (P < 0.05) with no significant effect on calving to first ovulation interval. In conclusion, the genotypes associated with higher plasma PON1 activity in SNP locations −221 and −392 were also associated with a reduced calving to conception interval in this study set of cows. These SNPs may provide novel genetic markers for improved fertility in future larger studies in dairy cows.

Effects of parity on productive, reproductive, metabolic and hormonal responses of Holstein cows

The objective of this study was to determine the effects that parity may have on production, reproduction and the metabolic status of Holstein cows managed in a production system based on total mixed ration and pasture. Primiparous (n = 22) and multiparous (n = 24) cows from a dairy farm research station in Uruguay were used in a completely randomized design. Body weight (BW), body condition score (BCS) and backfat thickness (BFT) were recorded weekly from −30 to 70 days postpartum. Milk production was measured daily, and milk composition was determined weekly. Resumption of postpartum ovarian activity and progesterone profiles were measured three times a week based on milk progesterone. Blood was collected to determine the levels of glucose, insulin-like growth factor I (IGF-1), insulin, non-esterified fatty acids (NEFA), β-hydroxybutyrate (BHB), albumin, total protein and cholesterol. Milk production and components were lower for primiparous cows (p < 0.01) than multiparous cows. Body weights were also lower in primiparous cows than in multiparous cows (p < 0.05); however, BCS and BFT were greater (p < 0.01) in primiparous cows than in multiparous cows. Primiparous cows had greater levels of glucose, insulin and IGF-1 and lower concentrations of NEFA and BHB (p < 0.01) than multiparous cows. The intervals from calving to first ovulation were not affected by parity; however, primiparous cows showed less abnormal cycles (27.2%) than multiparous cows (50.0%) (p < 0.01). The present study found that a feeding system based on TMR and pasture was sufficient to produce over 25 L of milk per day without extending their calving to first ovulation interval in primiparous and multiparous cows. However, multiparous cows showed a greater imbalance in metabolic and hormonal profiles than primiparous cows, causing abnormal ovarian activity.

Effects of estrus synchronization using Matrix® followed by treatment with the GnRH agonist triptorelin to control ovulation in mature gilts

Estrus and ovulation responses in Matrix-treated gilts may affect ovulation synchrony in response to triptorelin. In experiment 1, estrus and ovulation measures at 12h intervals after last Matrix feeding (LMF) were analyzed. For the 398 gilts that displayed estrus, 87.4% were detected on Days 6–8 after LMF. Duration of estrus was 24–60h for 85.6% of gilts and negatively correlated with interval from LMF to estrus (r=−0.53, P<0.0001). The estrus to ovulation interval was positively correlated with duration of estrus (r=0.61, P<0.0001). In experiment 2, gilts (n=96) received intravaginal treatment with 2mL of gel containing placebo (Control) at 96h, 200μg of triptorelin at 96h (TRP96), 120h (TRP120) or 144h (TRP144) after LMF. Estrus measures did not differ (P>0.10) among treatments. The proportion of gilts ovulating 32–56h after treatment was greater for TRP120 and TRP144 (P<0.01) compared to other treatments. The treatment to ovulation intervals for all triptorelin treatments were shorter (P<0.001) than Control. In experiment 3, gilts (n=86) received placebo (Control), 100μg (TRP100), 200μg (TRP200), or 400μg (TRP400) of triptorelin at 120h after LMF. There was no effect of treatment (P>0.10) on estrus or on interval from LMF to estrus. The proportion of gilts ovulating by 40, 48 and 56h after treatment increased (P<0.05) with triptorelin compared to Control. Our results indicate that gilts receiving 100–400μg of triptorelin at 120h after LMF had the greatest ovulation synchrony 24–48h following treatment. These studies provide important information for developing a procedure for a single insemination in synchronized gilts.

Effects of a single 20\xa0mg dose of letrozole on ovarian function post dominant follicle selection: an exploratory randomized controlled trial

BackgroundOur objective was to explore the impact of a single dose of an aromatase inhibitor (letrozole) administered at defined times of the follicular phase or immediately after ovulation on dominant follicle development, luteogenesis and new follicle wave emergence.MethodsA prospective pilot study using a randomized complete block, controlled, open label design was conducted at an academic clinical research center. Forty-five healthy, female volunteers (25.5 ± 0.9 years, BMI 25.0 ± 0.6 kg/m2) who had not taken hormonal contraceptives for a minimum of 2 months were recruited. A 20 mg dose of Letrozole was administered once orally in each of 3 groups when the dominant follicle reached a diameter of 1) 12 mm, 2) 18 mm, 3) the first day following ovulation (post-ovulation), or 4) treatment was withheld (control). Serial ultrasonography and phlebotomy began on day 4 of the menstrual cycle and continued for 1.5 menstrual cycles. Participants recorded menses and daily events in a life events calendar for the duration of the study. Demographic and single point measurements were compared among groups by ANOVA. Changes in hormone concentrations over time were compared among groups by repeated measures ANOVA. Kruskal-Wallis tests were used for non-normally distributed data.ResultsThe dominant follicle in all treatment groups ovulated. There were no differences among experimental groups in peak follicle diameter, follicular growth rate, endometrial thickness at ovulation or inter-ovulatory interval. Plasma concentrations of estradiol dropped, while FSH and LH concentrations rose following treatment in all treatment groups. Plasma FSH and LH concentrations were higher in the 18 mm group compared to the 12 mm and post-ovulation groups (P < 0.02).ConclusionAdministration of a single 20 mg dose of Letrozole at the times of the menstrual cycle we examined did not induce dominant follicle regression or failure of corpus luteum formation. Letrozole-induced suppression of estradiol synthesis by the dominant follicle was not detrimental to follicle growth or ovulation following follicle selection, likely due to increased circulating concentrations of FSH and LH resulting from a lack of estradiol-induced suppression of the hypothalamic-pituitary-ovarian axis.Trials registration numberClinical trials registration number NCT01046578.

Automated activity monitoring and visual observation of estrus in a herd of loose housed Hereford cattle: Diagnostic accuracy and time to ovulation

A prospective cohort study was performed in the purebred Hereford herd at Götala Beef and Lamb Research Centre, Sweden. The study's first objective was to assess the ability of an automatic activity monitoring system (AAMS) to detect estrus in beef suckler cows, and its second objective was to estimate the time from estrus to ovulation. The study sample (n = 38) consisted of 14 Hereford heifers and 24 Hereford cows. Standardized visual observation of estrus was performed for 20 minutes thrice daily, and animal activity was recorded with an AAMS system, Heatime (SCR Engineers Ltd., Israel). Cows in estrus underwent transrectal ultrasonography every 8 hours, to estimate the time of ovulation. Blood samples for progesterone analysis were collected thrice weekly throughout the study period. A cutoff value of 1-ng progesterone/mL of serum was used to define luteal activity. The AAMS had a 90% (95% confidence interval [CI] 77%–97%) sensitivity and 100% specificity (95% CI 94%–100%), and visual detection of estrus had a 77% sensitivity (95% CI 62%–88%) and a 89% specificity (95% CI 79%–95%) for identifying estrus when compared to the gold standard defined by temporal pattern of serum progesterone concentration. When both methods were used in parallel, the sensitivity increased to 96% (95% CI 86%–99%), and the specificity increased to 90% (95% CI 80%–96%). The time of ovulation after estrus was determined on 50 occasions. The median estrus (AAMS detected) to ovulation interval was 25 hours for heifers and 23 hours for cows (interquartile range 11–29 hours and 19–25 hours, respectively). The median estrus (visually detected) to ovulation interval was 28 hours for heifers and 21 hours for cows (interquartile range 13–29 hours for both categories). In conclusion, the AAMS had both a higher sensitivity and specificity for estrus detection than thrice-daily visual observation. The time from detection of estrus to ovulation observed in this study indicates that reproductive performance might be improved if Hereford cattle are inseminated sooner after detection of estrus than is currently recommended.

The effect of permanent or temporary contact with the lamb and contact with males on the lambing to first ovulation interval in Saint Croix sheep

The effect of suckling and presence of the lamb, or ram, on the lambing to first ovulation interval in Saint Croix sheep was determined. Ten days after lambing 50 ewes and their lambs were assigned to three different suckling treatments: continuous suckling (CS), restricted suckling (RS), restricted lamb presence (RP). Ewes from each treatment were allocated to groups that had contact with a ram (TR) or remained isolated from rams (IR). Therefore, overall, there were six groups with 2 factors: CS-IR (n=7) CS-TR (n=7); RS-IR (n=11); RS-TR (n=11); RP-IR (n=7), and RP-TR (n=7). The presence of the ram (P=0.01) and restricted suckling (P=0.05) reduced the interval from lambing to first ovulation, while no interaction was found (P>0.05) between these two factors. An effect of treatment and its interaction influenced significantly the number of vocalizations and growth rate in lambs. At the day of weaning RP vocalized more than RS (P<0.01), which in turn vocalized more than CS (P<0.01), followed by a general decline to pre-weaning levels 48h later. Lambs in RP had greater growth rate during first 3 d after weaning compared with RS (P<0.05), which displayed greater growth rate that CS (P<0.05). In addition, an effect of treatment (P=0.05) was found in cortisol concentration. Our results indicate that Saint Croix ewes respond to the ram effect in early postpartum, shortening the resumption of postpartum ovarian activity. When this technique is combined with restricted suckling, additional benefits are achieved for lambs with reduced weaning stress.

The PGF2α agonists luprostiol and d-cloprostenol reliably induce luteolysis in luteal phase mares without evoking clinical side effects or a stress response

In the present study we have evaluated a possible stress reaction in response to two different PGF2α analogs—luprostiol and d-cloprostenol—and their effects on estrous cycle characteristics. In a cross-over-design eight mares received in alternating order either luprostiol (Treatment LUP; 3.75mg im), d-cloprostenol (Treatment CLO; 22.5μg im) or saline (Treatment CON; NaCl 0.9% 0.5ml im) on day 8 after ovulation. Injection of either LUP or CLO, but not of CON resulted in a significant decline of progesterone concentration in plasma to baseline concentrations within two days (time: p<0.001, treatment: p<0.01, time×treatment: p<0.05). The treatment to ovulation interval was significantly shorter in LUP and CLO than in CON cycles (LUP: 9.4±0.4 d; CLO: 9.4±1.3 d; CON: 16.1±0.8 d; p<0.001). Injection of either LUP or CLO, but not of CON significantly increased salivary cortisol concentration (immediately before injection: CON 1.3±0.2, LUP 1.4±0.3, CLO 1.4±0.3ng/ml; 60min after injection: CON 1.0±0.3, LUP 8.0±1.4, CLO 4.2±0.7ng/ml; time: p<0.01, treatment: p<0.001, time×treatment: p<0.001). Heart rate decreased over time (p<0.05) independent of treatment and no changes in heart rate variability were detected. Injection of the PGF2α analogs CLO and LUP reliably induced luteolysis and apart from a transient increase in salivary cortisol concentration no signs of a physiological stress response or apparent side effects occurred.

Reduction of liver function delays resumption of postpartum ovarian activity and alters the synthesis of acute phase proteins in dairy cows

The aim of this study was to evaluate the concentration of acute phase proteins, milk production, and resumption of postpartum ovarian activity of clinically healthy dairy cows in a semi-extensive system with different Liver Functionality Index (LFI) values. The animals were divided into two groups: Low LFI (LLFI: −7 to −12; n: 10) and High LFI (HLFI: −7 to −4; n: 10). Animals with LLFI had lower paraoxonase activity and lower albumin concentration in the pre- and postpartum periods (P<0.05), higher non-esterified fatty acids prepartum (P<0.005), and higher haptoglobin concentration postpartum (P<0.01). The LLFI group showed lower resumption of ovarian activity until 44days postpartum (29%; P<0.05) than HLFI (86%). Milk production did not differ between groups. Therefore, this study suggests that the LFI is an important biomarker of synthesis of acute phase proteins and the first ovulation interval, and it can be used to improve the production and reproductive performance.