In cattle, elevated concentrations of circulating progesterone (P4) in the immediate postconception period are associated with advanced conceptus development, while low P4 is implicated as a causative factor in low pregnancy rates observed in dairy cows. This study aimed to: 1) describe the transcriptional changes that occur in the bovine endometrium during the estrous cycle, 2) determine how elevated P4 affects these changes, 3) identify if low P4 alters the expression of these genes, and 4) assess the impact that low P4 has on conceptus development. Relatively few differences occurred in endometrial gene expression during the early luteal phase of the estrous cycle (Day 5 vs. 7), but comparison of endometria from more distant stages of the luteal phase (Day 7 vs. 13) revealed large transcriptional changes, which were significantly altered by exogenous supplementation of P4. Induction of low circulating P4 altered the normal temporal changes in gene expression, and these changes were coordinate with a delay in the down-regulation of the PGR from the LE and GE. Altered endometrial gene expression induced by low P4 was associated with a reduced capacity of the uterus to support conceptus development after embryo transfer on Day 7. In conclusion, the present study provides clear evidence that the temporal changes in the transcriptome of the endometrium of cyclic heifers are sensitive to circulating P4 concentrations in the first few days after estrus. Under low P4 conditions, a suboptimal uterine environment with reduced ability to support conceptus elongation is observed.

The postovulatory rise in circulating progesterone (P4) concentrations is associated with increased pregnancy success in beef and dairy cattle. Our study objective was to determine how elevated P4 alters endometrial gene expression to advance conceptus development. Synchronized heifers were inseminated (Day 0) and randomly assigned to pregnant high P4 or to pregnant normal P4. All high P4 groups received a P4-release intravaginal device on Day 3 after insemination that increased P4 concentrations up to Day 7 (P < 0.05). Tissue was collected on Day 5, 7, 13, or 16 of pregnancy, and endometrial gene expression was analyzed using the bovine Affymetrix (Santa Clara, CA) microarrays. Microarray analyses demonstrated that the largest number of P4-regulated genes coincided with the day when the P4 profiles were different for the longest period. Genes with the largest fold change increase (such as DGAT2 and MSTN [also known as GDF8]) were associated with triglyceride synthesis and glucose transport, which can be utilized as an energy source for the developing embryo. Temporal changes occurred at different stages of early pregnancy, with the greatest difference occurring between well-separated stages of conceptus development. Validation of a number of genes by quantitative real-time PCR indicated that P4 supplementation advances endometrial gene expression by altering the time (FABP, DGAT2, and MSTN) or duration (CRYGS) of expression pattern for genes that contribute to the composition of histotroph.

Higher systemic progesterone in the immediate post-conception period is associated with an increase in embryonic growth rate, interferon-tau production and pregnancy rate in cattle. The objective of this study was to examine the effect of increasing progesterone concentration on Day 3 on subsequent embryo survival and development. Oestrus (Day 0) was synchronised in beef-cross heifers (n=210) and approximately two-thirds of the heifers were inseminated with semen from a proven sire, while the remainder were not inseminated. In order to produce animals with divergent progesterone concentrations, half of the animals received a progesterone-releasing intravaginal device (PRID) on Day 3 of the oestrous cycle, which was left in situ until slaughter. The four treatment groups were: (i) pregnant, high progesterone; (ii) pregnant, normal progesterone; (iii) non-pregnant, high progesterone; and (iv) non-pregnant, normal progesterone. Animals were blood-sampled twice daily from Days 0 to 8 and once daily thereafter until slaughter on Days 5, 7, 13 or 16, corresponding to the 16-cell stage, the blastocyst stage, the beginning of elongation and the day of maternal recognition of pregnancy, respectively. Embryos were recovered by flushing the tract with phosphate-buffered saline and characterised by stage of development and, in the case of Days 13 and 16, measured. Data were analysed by mixed models ANOVA, Chi-square analysis and Student's t-test where appropriate. Insertion of a PRID on Day 3 increased (P<0.05) progesterone concentrations from Day 3.5 onwards. There was no difference between treatments in the proportion of embryos at the expected stage of development on Days 5 or 7 (P>0.05). While not significantly different, the proportion of viable embryos recovered was numerically greater in the high progesterone group on both Day 13 (58 v. 43%) and Day 16 (90 v. 50%). Elevation of progesterone significantly increased embryonic length on Day 13 (2.24+/-0.51 mm v. 1.15+/-0.16 mm, P=0.034) and Day 16 (14.06+/-1.18 cm v. 5.97+/-1.18 cm, P=0.012). In conclusion, insertion of a PRID on Day 3 of the oestrous cycle increased serum progesterone concentrations on subsequent days, which, while having no phenotypic effect on embryonic development on Days 5 or 7, was associated with an increase in embryonic size on Days 13 and 16.

This study examined the correlation between measurement of follicle growth by ultrasound,

No abstract

To determine the effects of the anti-inflammatory ketoprofen, alone or with local anesthesia (LA) during castration on cortisol, immune, and acute phase responses, 40 Friesian calves (215 +/- 3.5 kg) were assigned as follows: 1) control, 2) surgical castration (SURG), 3) SURG following ketoprofen (3 mg/kg BW i.v.; SURG + K), 4) SURG following LA (9 mL of 2% lidocaine hydrochloride to each testis; SURG + LA), or 5) SURG following LA and K (SURG + LA + K). Total cortisol response was greater (P< 0.05) in SURG, SURG + LA, and SURG + K + LA calves than in control calves and was not different between control and SURG + K calves. The interval to peak cortisol was longer (P < 0.05) for SURG + K + LA calves than for either SURG or SURG + K calves. On d 3, KLH-induced interferon-gamma production was lower (P < 0.05) in SURG calves than in control calves, whereas concanavalin A-induced interferon-gamma production was lower (P < 0.05) in all castration groups than in control. On d 1 after surgery, fibrinogen was higher (P < 0.05) in SURG and SURG + LA calves than in control calves, whereas SURG + LA + K calves had lower (P < 0.05) fibrinogen than did SURG calves. Haptoglobin was higher (P < 0.05) in SURG calves on d 1, 3, and 7 than in control calves. On d 1 after surgery, SURG + K and SURG + LA + K calves had lower (P < 0.05) haptoglobin concentrations than SURG calves, whereas SURG + K calves had lower (P < 0.05) levels than SURG calves on d 3. In conclusion, surgical castration induced a significant elevation in cortisol secretion; the rise in cortisol was reduced to control levels by the administration of ketoprofen but not local anaesthetic. Thus, systemic analgesia using ketoprofen is more effective than local anesthesia during castration to alleviate the associated stress response.

There is a variable anoestrous period following parturition in the cow. Follicular growth generally resumes within 7-10 days in the majority of cows associated with a transient follicle-stimulating hormone (FSH) rise that occurs within 3-5 days of parturition. Dairy cows that are not nutritionally stressed generally ovulate their first post-partum dominant follicle (approximately 15 days), whereas beef suckler cows in good body condition normally have a mean of 3.2 +/- 0.2 dominant follicles (approximately 30 days) to first ovulation; and beef cows in poor body condition have a mean of 10.6 +/- 1.2 dominant follicles (approximately 70-100 days) to first ovulation. The lack of ovulation of dominant follicles during the post-partum period is associated with infrequent luteinizing hormone (LH) pulses, with both suckling and low level of nutrition being implicated in the prolonged suppression of LH pulses in the absence of progesterone. In dairy cows, the normal pattern of early resumption of ovulation may be delayed in high-yielding Holstein-type cows generally because of the effects of severe negative energy balance, dystocia, retained placental membranes and uterine infections. First ovulation in both dairy and beef cows is generally silent (i.e., no behavioural oestrus) and is generally (>70%) followed by a short cycle. The key to optimizing resumption of ovulation in both beef and dairy cows is appropriate pre-calving nutrition and management so that cows calve down in optimal body condition (body condition score; BCS; 2.75-3.0) with post-partum body condition loss restricted to <0.5 BCS units.

To determine the effects of castration of calves, with or without local anesthesia, on plasma cortisol, scrotal circumference, ADG, and ADFI, 56 Friesian bulls (5.5 mo of age; mean +/- SE BW = 173 +/- 2 kg) were randomly assigned to each of seven treatments: 1) control (CON); 2) s.c. injection of .1 mg of a human serum albumin-GnRH conjugate with DEAE-dextran adjuvant (HSA-GnRH); 3) burdizzo castration without local anesthetic (BURD); 4) burdizzo castration following local anesthetic administration (BURD + LA); 5) surgical castration without local anesthetic (SURG); 6) surgical castration following local anesthetic administration (SURG + LA); and 7) local anesthetic administration alone (LAA). Blood samples for cortisol analyses were taken via jugular catheter from -2 to 10 h and at 24, 48, and 72 h relative to treatment. Average daily feed intakes were recorded for 5-d periods and calves weighed at 7-d intervals before and after treatment. Local anesthetic alone had no effect (P > .10) on any variable. The HSA-GnRH calves had elevated (P < .05) plasma cortisol from 2 to 6 h compared with CON calves. Peak plasma cortisol was elevated (P < .01) in BURD, BURD + LA, SURG, and SURG + LA compared with CON calves. The SURG calves (46.0 ng/mL) had higher (P < .03) peak cortisol than BURD (31.4 ng/mL) and SURG + LA (35.4 ng/mL) calves. There was no difference in peak cortisol between BURD and BURD + LA (26.5 ng/mL) calves. The ADG from d 0 to 7 was reduced (P < .05) in calves in BURD + LA, SURG, and SURG + LA treatments (-.01, -.83 and -.24 kg, respectively) compared with CON calves (.54 kg). The ADFI were reduced (P < .05) in BURD and BURD + LA calves during d 1 to 5 and in BURD + LA, SURG, and SURG + LA calves during d 6 to 10 compared with CON calves. The scrotal circumferences of BURD and BURD + LA calves were greater (P < .05) than those of CON calves for 7- and 35-d periods post-castration, respectively. Castration induced increases in cortisol and decreases in ADG and ADFI. Surgical castration induced a greater plasma cortisol response than burdizzo castration, and the administration of local anesthetic reduced the cortisol response of surgical castrates but was less effective for burdizzo castrates.