Dynamics In Heifers Research Articles

Intraovarianism. Local mechanisms that affect follicle and luteal dynamics in heifers and women†.

Intraovarianism is represented by greater follicle activity in right ovary (RO) than left ovary (LO) during the two or three follicular waves per interovulatory interval in heifers and the ovulatory wave in women. In each species, selection between the dominant follicle (DF or F1) and future largest subordinate follicle (F2) is manifested by diameter deviation. The RO has more ≥6mm predeviation follicles in heifers, more 2-10mm predeviation follicles in women, and greater frequency of ovulation in each species. The RO propensity for ovulation likely develops before birth or at least before sexual maturity as indicated by (1) heavier RO with more follicles in recently born calves and heavier right fetal gonad with more DNA content in humans and (2) greater RO frequency for largest follicle of a wave in sexually immature heifers and for first ovulation of puberty. In heifers, intraovarianism is also expressed by (1) two-way enhancement effect between DF and corpus luteum (CL) when in same ovary, (2) regression of predeviation follicles when adjacent to the regressing CL, (3) more frequent location of F2 during predeviation in ovary that contains F1, (4) greater diameter increase during recovery of subordinate follicles when in RO with the future DF, and (5) effect of an intraovarian pattern on the pattern in the next wave. The nature of these forms of intraovarianism is not known but may be physical rather than from local passage of factors between structures. Intraovarianism should be considered when studying systemic hormonal effects on ovarian dynamics.

Coxiella burnetii antibody dynamics in heifers born to vaccinated versus non-vaccinated dams in a chronically infected dairy herd.

This study was designed to compare Coxiella burnetii antibody dynamics in heifers born to vaccinated or non-vaccinated dams in a single high-producing dairy herd chronically infected with the bacterium. Antibody dynamics were examined from birth to the postpartum period in replacement heifers (n = 14) born to non-vaccinated dams (n = 7) or to dams that had been vaccinated on gestation days 171-177 (n = 7) and 192-198. Samples of blood, milk, faeces, vaginal fluid, colostrum and cotyledons (the latter two only at parturition) were obtained in the dams over the period from gestation days 171-177 to postpartum days 91-97. Blood samples were used to detect antibodies against C. burnetii and remaining samples for PCR identification of the bacterium. In their calves/heifers, blood samples for antibody determinations were collected from birth to postpartum at the time points 1-7 and 22-28 days and 3, 6 and 12 months of age; 90-96 and 210-216 days of gestation; and 22-28 days postpartum. All calves were born seronegative for C. burnetii. Irrespective of the shedding status of their mothers (7 were C. burnetii shedders), seroconversion occurred after colostrum intake in all calves born to seropositive cows (n = 9) and in two of three vaccinated seronegative dams. Thereafter antibody titres gradually declined and by 6 months of age all calves were seronegative. Seronegativity persisted until their first postpartum period. These findings indicate that cows vaccinated during advanced pregnancy transfer immunity to their calves via the colostrum. Maternal C. burnetii antibodies in calves persisted for three months in calves born both to seronegative vaccinated and seropositive dams.

Effects of propylene glycol drenching before and after luteolysis on blood glucose, ovarian steroids and follicular dynamics in heifers

The effect of propylene glycol drenching on ovarian and hormonal dynamics was studied in heifers. Five cycling heifers were used twice (as control and treatment) with crossover design. After the confirmation of ovulation (day 0), the heifers in the treatment group received propylene glycol on days 6, 7 and 8 as an oral drench (250 ml of 90% propylene glycol). On day 10, prostaglandin F2α (PGF2α), 15 mg per head of dinoprost, was administered intramuscularly to induce luteal regression followed by the follicular phase and then propylene glycol was again administered twice daily (500 ml/day) on days 10, 11 and 12. Palpation per rectum and ovarian ultrasonography were performed every other day from days 0 to 10, and daily after PGF2α administration until the subsequent ovulation (second ovulation) for analysis of follicular and luteal dynamics. Blood samples were also collected every other day from days 0 to 10, and then at 6 h intervals after PGF2α administration until the second ovulation. For the samples taken at 6-h intervals after PGF2α administration, the concentrations of glucose showed clear daily fluctuations in both groups. Changes in the plasma concentration of glucose in the treatment group were significantly (P < 0.05) higher than those of the control groups during the period between 0 and 72 h after PGF2α administration. No significant difference was detected in the growth of dominant follicles, maximum diameter of the ovulatory follicles and the changes in oestradiol and progesterone during the follicular phase between treatment and control groups. This study showed the clear daily fluctuations and stimulatory changes in the blood glucose concentrations at 24-h intervals during the short-term treatment of propylene glycol drenching in heifers. However, no significant changes in ovarian and hormonal dynamics were found under such metabolic conditions.

A comparison of the follicular dynamics in heifers of the Czech Fleckvieh and Holstein breeds

Differences in follicular development and repeatability of follicular growth pattern among Czech Fleckvieh (n = 20) and Holstein (n = 23) heifers were investigated. Follicular dynamics was evaluated by daily sonographic scanning during three interovulatory intervals. The mean duration of the interovulatory interval was 20.66 &amp;plusmn; 0.32 days, no differences between breeds were observed. The proportion of the non-alterna-ting pattern was nearly the same as that of the alternating pattern (54% and 46%, respectively). The majority of IOIs &amp;le; 21 days were of the 2-wave pattern (71%) whereas only 29% of them were of the 3-wave pattern. Conversely, the majority of IOIs &amp;ge; 22 days were of the 3-wave pattern (84%), whereas only 16% were of the 2-wave pattern. Differences could be observed in the Czech Fleckvieh heifers. Comparing 2- and 3-wave interovulatory intervals, 44.2% of the heifers exhibited 3 waves and 55.8% of the heifers exhibited 2 waves of follicular growth. The ratio of 3- to 2-wave heifers was about the same in the Holstein breed; in Czech Fleckvieh 2-wave cycles slightly dominated (11/12, 8/12; respectively). In Holstein heifers, the first follicular wave occurred 0.92 &amp;plusmn; 0.15 days after ovulation in 2-wave interovulatory intervals, and the emergence of the first wave in 2-wave Czech Fleckvieh heifers appeared later (P &amp;lt; 0.05), 1.83 &amp;plusmn; 0.3 days after ovulation. The maximal size reached by the dominant follicles in all animals and in the Czech Fleckvieh differed in the first and in the second wave of 2-wave cycles (P &amp;lt; 0.05). In 3-wave interovulatory intervals the dominant follicles in the second wave differed (P &amp;lt; 0.05) from the mean diameters of the first and the third wave in the Czech Fleckvieh. The ovulatory follicles were significantly (P &amp;lt; 0.05) smaller in 2-wave than in 3-wave interovulatory intervals among all animals and between the Holstein and Czech Fleckvieh heifers. In conclusion, we found a similar pattern of ovarian follicular dynamics in Czech Fleckvieh and Holstein heifers kept under identical nutritional and environmental conditions. Whether the significant difference in the emergence of the 1st fol-licular wave in 2-wave IOIs between C and H heifers is of real biological significance is ambiguous.

27 FOLLICULAR RESPONSE TO DIFFERENT eCG DOSES IN AN OVSYNCH + PROGESTERONE PROTOCOL IN BEEF HEIFERS

An experiment was designed to evaluate the effect of different doses of eCG on ovarian follicular dynamics in heifers treated with a Ovsynch plus progesterone protocol. Twenty-five cyclic yearling Black Angus heifers (373.0 ± 35.7 kg), in 2 replicates, received an injection of 100 μg of GnRH (Ovurelin, Bomac Laboratories Ltd., Auckland, New Zealand) i.m. and an intravaginal progesterone device (1.38 g of progesterone; Eazi-Breed CIDR, Pfizer Animal Health, New Zealand) on Day 0 (beginning of the experiment), followed by 500 μg of cloprostenol (PGF, Estrumate, Intervet/Schering-Plough Animal Health, Auckland, New Zealand) i.m. on Day 7, and a second 100 μg of GnRH injection given i.m. on Day 9 (56 h after PGF). At the time of PGF treatment, heifers were randomly assigned to 5 treatment groups to receive 0, 300, 500, 700, or 1000 IU of eCG (Folligon, Intervet/Schering-Plough Animal Health) i.m. Heifers were monitored by ultrasonography (Aloka 900-SSD equipped with a 7.5-MHz linear-array transducer; Aloka, Tokyo, Japan) daily from Day 0 to 9 (GnRH), and then every 12 h until ovulation. Data were analyzed by one-way ANOVA or Kruskall-Wallis test, and means or ranks were compared with LSD or Wilcoxon rank sum tests, respectively. Because a replicate effect was observed (P &lt; 0.05) in the size of the dominant follicle at the second GnRH and prior to ovulation, replicate effect was included in the analysis. The luteal area at PGF treatment was significantly greater (P &lt; 0.01) in heifers that ovulated (750.0 ± 97 mm2) in response to the first GnRH treatment than in those that did not (301.6 ± 42.7 mm2). The diameter of the dominant follicle at the time of PGF treatment was also greater (P &lt; 0.05) in ovulating (11.2 ± 0.4 mm) than in nonovulating (9.7 ± 0.5 mm) heifers. The interval from the first GnRH treatment to the emergence of the next follicular wave was longer (P = 0.50) and more variable in heifers that did not ovulate (2.9 ± 0.4 d; n = 27) than in those that ovulated (1.9 ± 0.2 d; n = 23). There was no effect (P &lt; 0.37) of eCG on the interval from PGF to ovulation (86 ± 1.9 h). The number of ovulations after the second GnRH was higher (P = 0.01) in the group of heifers treated with 1000 IU of eCG (1.8 ± 0.4) than in the other groups (1.0 ± 0.0; 1.1 ± 0.1; 1.2 ± 0.1; 1.0 ± 0.1). There was an effect of day of follicular wave emergence on the number of ovulations (P &lt; 0.01). Heifers with a wave emerging 1 to 3 days after the first GnRH (n = 37), had one ovulation (1.0 ± 0.0), whereas heifers with a wave emerging on Day 4 (3 out of 4 heifers) and Days 5 to 7 (n = 9), ovulated 2 or more follicles. In summary, the multiple ovulation effect occurred when eCG was given to heifers with a follicular wave emerging on or after Day 4, and was potentiated when heifers received 1000 IU of eCG. Although the dose of eCG given at the time of PGF treatment in an Ovsynch program has a significant effect on follicular development, the time of emergence of the dominant follicle appeared to be more important in the ovulation of preovulatory follicle/s after the eCG and the second GnRH treatment.

Follicular Dynamics in Heifers during Pre‐pubertal and Pubertal Period Kept under Two Levels of Dietary Energy Intake

The objective of this study was to characterize follicular dynamics in pre-pubertal, pubertal and post-pubertal periods, as well as the effect of high-energy intake on follicular development and age at puberty in heifers. Thirty-one Nelore (Bos indicus) heifers, 6 months old, were randomly assigned to receive two different diets: one of low (GI) and other of high dietary energy intake (GII). Animals were evaluated in relation to body weight gain by being weighed every 21 days. Heifers were evaluated every other day by real-time linear ultrasonography to characterize ovarian structures development from weaning to post-pubertal period. Blood samples were collected to determine plasmatic concentrations of progesterone by RIA method. The ovulation was determined when progesterone concentrations were >1 ng/mL in three consecutive samples, and by ultrasound images of corpus luteum; and oestrous behaviour in some animals. Age at puberty differed among heifers of GII (17.00 +/- 0.46 months) compared with heifers of GI (19.87 +/- 0.47 months; p < or = 0.05). Maximum size of the dominant follicles at pre-pubertal period was greater in GII heifers than in GI (10.52 +/- 0.33 and 9.76 +/- 0.15 mm, respectively; p < or = 0.05). As heifers approached first ovulation time, size of dominant follicle increased (11.75 +/- 0.37 mm for GI and 12.52 +/- 0.91 mm for GII; p < or = 0.05). Body weight at puberty was not different in both groups (302.33 +/- 27.31 kg for GI and 326.19 +/- 27.78 kg for GII heifers; p > 0.05). We conclude that animals receiving high dietary energy intake attained the puberty earlier and the development of follicles were different than in low dietary energy intake.

The effect of estradiol benzoate on synchrony of estrus and fertility in cattle after removal of a progesterone-releasing intravaginal device

The aim was to determine the effect of estradiol benzoate (EDB) given after removal of a progesterone-releasing intravaginal device (PRID) at either emergence or dominance of a follicle wave, on the interval to estrus, variation in its onset and pregnancy rate in heifers. Heifers (n=186) were assigned randomly to four treatments in a 2 × 2 factorial design; emergence or dominance of a follicle wave at PRID removal, with or without 0.5 mg EDB 24 h after PRID removal. Ovarian ultrasonography was performed to confirm follicular status; data from heifers of undeterminable follicular status were excluded (n=36). Mean size of the largest follicle of the new wave at PRID removal was smaller (P < 0.01) in heifers given EDB at emergence (6.3 ± 0.09 mm) compared with those given it at dominance (10.9 ± 0.30 mm). The onset of estrus was earlier (P < 0.01) in heifers given EDB at dominance (median 42 h, range 13 h) compared with those not given EDB at dominance (median 43 h, range 42 h). The median interval to estrus was decreased (P < 0.01) in heifers given EDB at emergence (median 48 h, range 73 h) compared with those not given EDB at emergence (median 66 h, range 45 h). Variation in onset of estrus was reduced (P < 0.05) in heifers given EDB compared with those not given EDB. The pregnancy rate was not affected when EDB was given at dominance, however, it was decreased (P < 0.05) when given at emergence (23 of 40 vs 26 of 32, respectively). To determine the effect of EDB on follicular dynamics in heifers treated with EDB at emergence, heifers (n=37) were assigned to two treatments: at emergence with or without EDB and their ovaries were examined daily using ultrasonography. Follicular dynamics were not different (P > 0.05) in EDB-heifers compared with untreated controls. Mean serum estradiol was greater (P < 0.01) in EDB-treated heifers compared with controls. In conclusion, 0.5 mg EDB given 24 h after PRID removal to heifers decreased the interval to estrous onset at emergence or dominance, decreased variation in onset of estrus and decreased pregnancy rates when given at emergence of a follicle wave.

Effect of LH or GnRH on the dominant follicle of the first follicular wave in beef heifers.

A study was designed to characterise ovarian follicular dynamics in heifers treated with porcine luteinizing hormone (pLH) or gonadotropin releasing hormone (GnRH) on days 3, 6 or 9 (ovulation = day 0), corresponding to the growing, early-static, and late-static phases of the first follicular wave. Following ovulation, 65 beef heifers were assigned, by replicate, to the following seven treatment groups: 25 mg im of pLH on days 3, 6 or 9 (n = 9 per group); 100 microg im of GnRH on days 3, 6 or 9 (n = 9 per group); or controls (no treatment; n = 11). Ovulation occurred within 36 h in 67%, 100% and 67% of heifers treated with pLH and in 89%, 56% and 22% of heifers treated with GnRH on days 3, 6 or 9, respectively (treatment-by-day interaction, P < 0.09). Combined for all treatment days, ovulation rates were 78% and 56% in pLH- and GnRH-treated groups, respectively (P < 0.09). Overall, mean day (+/- SD) of emergence of the second follicular wave in heifers that ovulated was different from that in controls or in heifers that did not ovulate (P < 0.05). Mean (+/- SD) day of emergence of the second wave occurred earlier (day 5.6+/-1.2; P < 0.05) in heifers that ovulated after treatment on day 3 (n = 14) than in controls (day 8.7+/-1.6; n = 11); however, wave emergence in all heifers treated on day 6 (day 8.1+/-0.5; n = 18) did not differ from controls, regardless of whether or not ovulation occurred. In the heifers that ovulated in response to treatment on day 9 (n = 8), the emergence of the second follicular wave was delayed (day 10.9+/-0.4; P < 0.05). The day of emergence of the second wave in the 14 treated heifers that failed to ovulate, irrespective of the day of treatment (day 8.9+/-1.4) did not differ from control heifers. The emergence of the second wave was more synchronous in day 6 heifers (regardless of whether they ovulated) and in day 9 heifers that ovulated compared to control heifers (P < 0.05). Results did not support the hypothesis that the administration of pLH or GnRH at known stages of the follicular wave in cycling heifers would consistently induce ovulation or atresia and, thereby, induce emergence of a new follicular wave at a predictable interval. New wave emergence was induced consistently (1.3 days post-treatment) only in those animals that ovulated in response to treatment. However, 22% of LH-treated heifers and 44% of GnRH-treated heifers failed to ovulate. Treatments did not induce atresia of the dominant follicle or alter the interval to new wave emergence in animals that did not ovulate in response to treatment.

Sequential changes in ovarian follicular dynamics in Bos indicus heifers before and after nutritional anoestrus.

This study examined the effects of live mass on ovarian follicular dynamics in heifers before and after the onset of nutritional anoestrus. The effects of decreased live mass on secretion of progesterone, LH and FSH were also investigated. Ovarian characteristics were monitored in 16 postpubertal Brahman heifers using daily transrectal ultrasonography. After two normal oestrous cycles, 11 heifers (treatment group) were allocated to a restricted diet, until the cessation of their oestrous cycles, that resulted in a decrease in live mass of 0.8 kg day-1. Heifers were then fed an ad libitum diet, resulting in increasing live mass until resumption of oestrous cycles. Five heifers (control group) were fed an unrestricted diet throughout the experimental period. The concentrations of progesterone in plasma were monitored twice a week and the concentrations of LH and FSH were determined on day 6 after ovulation, before initiation of dietary restriction, after a 17% decrease in live mass and after the onset of anoestrus in the treatment group. Onset of anoestrus was preceded by linear decreases in the size of ovarian follicles and corpora lutea, and in the persistence of the first dominant follicles of oestrous cycles. These changes were proportional to the decrease in live mass (P < 0.001). The frequency of pulses of LH or mean concentration of FSH on day 6 of the oestrous cycle were not changed after a 17% decrease in live mass, and did not increase following the onset of anoestrus, although concentrations of progesterone were < 0.2 ng ml-1, suggesting that release of LH was suppressed at this time.(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of Induced Suprabasal Progesterone Concentrations on Follicular Dynamics in Heifers

Effect of Induced Suprabasal Progesterone Concentrations on Follicular Dynamics in Heifers

Follicular dynamics in heifers after injection of PGF 2α during the first wave of follicular development

Follicular dynamics in heifers after injection of PGF 2α during the first wave of follicular development

Ovarian follicular dynamics in heifers during early pregnancy.

Daily ultrasonic monitoring of individual follicles was used to compare follicular wave characteristics of nonbred (n = 6) and pregnant heifers (n = 6). The dominant follicle of the first wave (Wave 1) did not differ significantly between reproductive statuses for any endpoint. The dominant follicle of Wave 2 was the ovulatory follicle in all nonbred heifers. The maximum diameter of the dominant follicle of Wave 2 was greater (p less than 0.05) for the nonbred heifers (14.8 mm) than for the pregnant heifers (13.0 mm). The dominant follicle of Wave 3 was detected later (p less than 0.003; Day 19.7 vs. Day 17.3) and reached a greater diameter (p less than 0.05; 16.6 mm vs. 12.0 mm) in the nonbred than in the pregnant heifers. On the mean day of onset of luteolysis (Day 15.2) in the nonbred heifers, the dominant follicle was similar in diameter for the two groups. Within a few days, the follicle began to regress in the pregnant heifers but maintained or increased in diameter in the nonbred heifers so that a greater maximum diameter was attained. During Days 0 70 of pregnancy, the interval from emergence of a wave to the emergence of the next wave was constant (not significantly different; mean intervals, 8.5 9.8 days). The mean maximum diameter attained by the dominant follicles differed significantly among the first 6 follicular waves; diameter was greatest for Wave 1 (15.7 mm), smallest for Waves 2 (13.1 mm) and 3 (12.6 mm), and intermediate for Waves 4 (14.0 mm), 5 (13.7 mm), and 6 (14.5 mm).(ABSTRACT TRUNCATED AT 250 WORDS)

Ovarian follicular dynamics in heifers: Test of two-wave hypothesis by ultrasonically monitoring individual follicles

The two-wave hypothesis for follicular development during the bovine estrous cycle was tested by ultrasonically monitoring individual follicles in 10 heifers during an interovulatory interval. A dominant follicle was defined as one that reached a diameter of at least 11 mm. Subordinate follicles were defined as those that appeared to originate from the same follicular pool as a dominant follicle. A dominant follicle and its cohorts were defined as a wave. Two waves during an interovulatory interval were identified in 9 of 10 heifers. The first wave was first identified, retrospectively, on a mean of Day 0.2 ± 0.1 (ovulation = Day 0) and gave origin to a dominant anovulatory follicle and a mean of 1.4 ± 0.3 identified subordinates. The dominant follicle reached maximum diameter (mean, 15.8 ± 0.8 mm) on an average of Day 7 and then decreased (P<.04) by Day 11. The subordinate follicles increased in diameter for a few days and then regressed. The second wave was first identified on a mean of Day 10.0 ± 0.4 and gave origin to the ovulatory follicle and a mean of 0.9 ± 0.3 subordinates. One of the 10 heifers had 3 waves of follicular activity characterized by an anovulatory wave emerging on Day 0, another anovulatory wave emerging on Day 10, and an ovulatory wave emerging on Day 16. Results strongly supported the two-wave hypothesis but also indicated that a minority of interovulatory intervals in this heifer population may have 3 waves of follicular activity.