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PubMed2001

Uptake of beta-carotene by ovarian and uterine tissues and effects on steroidogenesis during the estrous cycle in cats.

OBJECTIVES: To determine uptake of beta-carotene by ovarian and uterine tissues and influence of dietary beta-carotene on steroidogenesis and production of uterine protein during the estrous cycle in cats. ANIMALS: 56 female cats. PROCEDURE: Cats were fed diets containing 0, 0.4, 2, or 10 mg of beta-carotene daily for 8 weeks prior to detection of estrus. At time of observed estrus, all cats were manually induced to ovulate. Blood samples were obtained at estrus and every 2 days until day 14 after ovulation. On that day, cats underment laparotomy, and the ovaries and uterus were removed. Uterine contents were flushed, and luteal and endometrial tissues were obtained. RESULTS: Concentrations of beta-carotene in plasma and luteal and endometrial tissues increased in a dose-dependent manner. Concentrations of plasma progesterone were higher between days 6 and 10 after ovulation in cats fed diets containing beta-carotene and continued to increase through day 14 after ovulation in cats fed a diet containing 10 mg of beta-carotene. Plasma concentration of estradiol-17beta also was higher between days 0 and 4 after ovulation in cats fed diets containing beta-carotene. Cats fed a diet containing 10 mg of beta-carotene had the highest plasma estradiol concentration. Total uterine protein concentration was higher in cats fed beta-carotene, compared with values for cats fed an unsupplemented diet. CONCLUSION AND CLINICAL RELEVANCE: Cats readily absorb beta-carotene. Increased concentrations of progesterone, estradiol, and uterine protein may provide more optimal ovarian function or a better uterine environment for embryonic survival and development.

Animals↗
PubMed2001

Characteristics and management practices associated with milk production in dairy herds in Ohio enrolled in official Dairy Herd Improvement Association programs.

OBJECTIVE: To determine herd characteristics and management practices associated with milk production in dairy herds enrolled in official Dairy Herd Improvement Association (DHIA) programs in Ohio. SAMPLE POPULATION: 186 dairy farms in Ohio. PROCEDURE: All herds in official DHIA programs in 9 counties were invited to participate. Information regarding herd characteristics and management practices was obtained, using a standardized questionnaire. Bulk-tank milk samples were obtained for bacteriologic culture. Official DHIA test-day records were obtained, and associations were identified, using multivariable ANOVA procedures. RESULTS: Of 479 eligible producers, 186 (39%) participated, and consecutive bulk-tank milk samples were available for culture from 172 (36%). Streptococcus agalactiae and Mycoplasma spp were not recovered from bulk-tank milk samples, but Staphylococcus aureus was recovered from 64 (37%) herds. Mean (+/- SD) number of lactating cows in participating herds was 97+/-66, with 123 (66%) herds milking < 100 cows. The RHA was significantly associated with number of cows in milk, estimated percentage of herd detected in estrus, reported annual percentage of heifer calves born alive that died before 8 weeks old, percentage days in milk, use of bovine somatotropin during the preceding 2 years, and sex of the person completing the questionnaire. CONCLUSIONS AND CLINICAL RELEVANCE: In this study, the strongest indicator of milk production was number of cows in milk. However, merely adding cows to a herd should not be considered to guarantee increased milk production, because other management traits could be confounded with increased number of cows in a herd.

Animal Husbandry↗
PubMed1990

Effect of selection for growth traits on age and weight at puberty in bovine females.

This 20-yr study, using 584 beef heifers born in the spring of 1984 or 1985, was conducted to determine whether selection for growth traits affected age and weight at puberty. Heifers were from three Hereford lines selected for weaning weight, final weight, and final weight plus muscling score, a control line and a line of Angus cattle. In addition, heifers from reciprocal crosses among the selection lines, control and Angus groups were evaluated. Intact bulls and androgenized heifers fitted with marking harnesses were used to aid in detection of estrus for heifers born in 1984 and 1985, respectively. The time of puberty was identified by the first behavioral estrus. During both years, heifers were weighed at 56-d intervals; these weights were used to calculate weight at puberty. Mean age at puberty was determined using survival analysis; percentages of heifers that were pubertal by the end of the study were transformed to logits for analysis. Heifers born in 1985 were heavier (P less than .05) at puberty than those born in 1984. Heifers in lines selected for growth traits were younger at puberty (P less than .05; 20 d) than were heifers in the control line because of combined direct and maternal genetic effects. Heifers from the final weight, control (P less than .05) and weaning weight lines (P less than .10) weighed less at puberty than Angus heifers; selection line x Angus crossbred heifers were heavier at puberty (P less than .05) than their respective pureline or purebred contemporaries due to heterotic effects. Selection for weaning weight, final weight or final weight plus muscling score did not have a detrimental effect on age at puberty in heifers.

Age Factors↗
PubMed1992

Influence of biostimulation on reproduction in postpartum beef cows.

Three experiments were conducted to evaluate the effects of biostimulation (exposure to bulls or androgenized females) on various reproductive variables in suckled beef cows. Bulls or testosterone-treated cows (TTC) were introduced to cows, randomly allotted to one of four groups, within 72 h postpartum. In Exp. 1, Groups 1 and 3 were exposed to bulls and Groups 2 and 4 were exposed to TTC. In Exp. 2, Groups 1 and 3 were exposed to bulls and Groups 2 and 4 served as controls (isolated from biostimulation). In Exp. 3, Groups 1 and 3 were exposed to TTC and Groups 2 and 4 served as controls. Mean postpartum intervals to estrus were not different between cows exposed to either bulls or TTC in Exp. 1 (P greater than .10). However, in Exp. 2 and 3, cows exposed to either bulls or TTC had reduced postpartum intervals to estrus (44 and 41 d, respectively) compared with control cows (52 d; P less than .05). Fewer control cows were in estrus at either 40 d (P less than .05; Exp. 2 and 3) or 60 d (P less than .05; Exp. 3) postpartum than were cows exposed to bulls or TTC. No differences were observed between groups in any experiment for postpartum intervals to pregnancy (P greater than .10). These data indicate that cows exposed to biostimulation from either bulls or TTC immediately after calving return to estrus earlier than do cows isolated from biostimulation.

Animals↗
PubMed1999

Strategies for managing reproduction in the heat-stressed dairy cow.

Establishment and maintenance of pregnancy is difficult in lactating dairy cows exposed to heat stress because of reductions in estrous detection rate and the proportion of inseminated cows that maintain pregnancy. The most common approach to ameliorate heat stress in developed countries has been to alter the cow's environment through provision of shade, fans, sprinklers, and so on. Nonetheless, seasonal variation in reproductive function persists. Increased understanding of bovine reproductive function and its alteration by heat stress has led to additional strategies for reducing deleterious consequences of heat stress on reproduction. These include hormonally induced timed artificial insemination, which can reduce losses in reproductive efficiency caused by poor detection of estrus, and embryo transfer, which can increase pregnancy rate by allowing embryos to bypass the period when they are most sensitive to elevated temperature (i.e., in the first 1 to 2 d after breeding). Other efforts are directed toward developing methods to protect the embryo from harmful actions of elevated temperature. Approaches being studied include manipulation of embryonic synthesis of heat shock proteins and use of antioxidants to reduce free radical damage associated with heat stress. It may also be possible to reduce the magnitude of hyperthermia caused by heat stress. This might be possible physiologically, for example by feeding of agents that affect thermoregulatory systems, or genetically by selecting for specific traits conferring thermal resistance. Finally, the development of bovine somatotropin as a lactational promotant means that it may be possible to extend lactations beyond 305 d and voluntarily discontinue inseminations during periods of heat stress.

Animals↗
PubMed1998

Estimation of genetic parameters for scrotal circumference, age at puberty in heifers, and hip height in Brahman cattle.

Genetic parameters were estimated for scrotal circumference (SC; n=287), age at puberty in heifers (AP; n=292), and hip height in both sexes (HH; n=684) for Brahman cattle born from 1984 to 1994 at the Subtropical Agricultural Research Station, Brooksville, Florida. Age at puberty was defined as the age (days) at first detected ovulatory estrus. Measurements of SC and HH were taken at 18 mo of age. Fixed effects considered in the SC model were year of birth (YOB), age of dam (AOD), and age at measurement (AGE) as a linear covariate. Fixed effects fitted to the AP model were YOB and AOD. Fixed effects in the HH model were YOB, sex, AOD, and AGE as a linear covariate. Variances and covariances were estimated using REML with a derivative-free algorithm and fitting a multiple trait animal model. Estimates of heritability for SC, AP, and HH were .28, .42, and .65, respectively. Estimates of genetic correlations between SC and AP, SC and HH, and AP and HH were -.32, .19, and .25, respectively. Estimates of environmental correlations were .19 between SC and HH, and -.13 between AP and HH. Estimates of genetic parameters indicate a favorable genetic relationship between SC in Brahman bulls and AP in Brahman heifers under subtropical conditions. There was also evidence that selecting Brahman bulls for HH would not adversely affect SC but would have some detrimental effect on AP in female progeny.

Age Factors↗
PubMed2001

Synchronization of ovulation using GnRH or hCG with the CO-Synch protocol in suckled beef cows.

The objectives of this study were to evaluate replacing GnRH with hCG and the effects of 48-h calf removal (CR) on pregnancy rates of cows synchronized with the CO-Synch protocol. Suckled beef cows (n = 467) at two locations were assigned to treatment by breed, age, and calving date. Treatment included either GnRH with (n = 121) or without CR (n = 117) or hCG with (n = 115) or without CR (n = 114) using the CO-Synch protocol. On d 0 and 9, cows received either hCG (2,500 IU, i.m.) or GnRH (100 microg, i.m.), and on d 7 all cows received PGF2alpha (25 mg). At one location, blood samples were collected from all cows (n = 203) on d -14, -7, 0, 7, 9, and 16. Calves were removed on d 7 and returned on d 9 (48 h) from approximately half of the cows that received GnRH or hCG. Cows that were detected in estrus between d 6 and 9 were bred approximately 12 h later and received no further injections. Cows not observed in estrus by d 9 received a second injection of either GnRH or hCG and were timed-inseminated. The AI pregnancy rates for GnRH-treated cows with or without CR and hCG-treated cows with or without CR were 46, 49, 35, and 34%, respectively (P = 0.44). Pregnancy rates of cows differed by treatment x age interaction (P = 0.07), hormone (P = 0.09), and hormone x age (P = 0.01) but not by CR (P = 0.66) or CR x age (P = 0.33). Among 2-yr-olds, pregnancy rates were higher for cows treated with hCG without CR than for cows that received GnRH with calf removal, whereas cows treated with hCG with CR and GnRH without CR were intermediate. In addition hCG-treated 2-yr-olds had higher pregnancy rates than GnRH-treated 2-yr-olds regardless of calf presence, but the reverse was true for older cows. Overall, GnRH-treated cows (48%) had a higher (P = 0.09) pregnancy rate than hCG-treated cows (34%). Among anestrous cows, GnRH and hCG were similar (P = 0.40) in their ability to induce ovulation and corpus luteum formation after the first and second injections of GnRH (31 and 76%, respectively) or hCG (39 and 61%, respectively). More (P = 0.001) hCG-treated cows exhibited short estrous cycles following timed AI. We conclude that hCG is not a suitable replacement for GnRH to synchronize ovulation with the CO-Synch protocol in multiparous cows, although further evaluation among primiparous cows is warranted using hCG with the CO-Synch protocol.

Age Factors↗
PubMed2001

Administration of p.g. 600 to sows at weaning and the time of ovulation as determined by transrectal ultrasound.

This study determined whether the interval from estrus to ovulation was altered by giving P.G. 600 to sows at weaning. Mixed-parity sows received P.G. 600 i.m. (n = 72) or no treatment (n = 65) at weaning (d 0). Beginning on d 0, sows were observed for estrus twice daily. At the onset of estrus and thereafter, ultrasound was performed twice daily to determine the average size of the largest follicles and time of ovulation. Weaning age (20.1+/-0.4 d) did not differ (P > 0.10) between treatments. More P.G. 600 sows expressed estrus within 8 d (P < 0.01) than controls (94.4% vs 78.4%, respectively). Parity was associated with expression of estrus (P < 0.02), with 78% of first-parity and 93% of later-parity sows exhibiting estrus. However, no treatment x parity effect was observed (P > 0.10). The interval from weaning to estrus was reduced (P < 0.0001) by P.G. 600 compared with controls (3.8+/-0.1 d vs 4.9+/-0.1 d). Follicle size at estrus was not affected by treatment (P > 0.10). The percentage of sows that ovulated did not differ (P > 0.10) for P.G. 600 and control sows (90.3% vs 81.5%, respectively). Time of ovulation after estrus was not affected by treatment and averaged 44.8 h. However, univariate analysis indicated that the interval from weaning to estrus influenced the interval from estrus to ovulation (r = 0.43, P < 0.0001). Further, multivariate analysis showed an effect of treatment on the intervals from weaning to estrus, weaning to ovulation (P < 0.0001), and estrus to ovulation (P < 0.04). Within 4 d after weaning, 81% of the P.G. 600 sows had expressed estrus compared with 33% of controls. However, this trend reversed for ovulation, with only 35% of P.G. 600 sows ovulating by 36 h after estrus compared with 40% of controls. The estrus-to-ovulation interval was also longer for control and P.G. 600 sows expressing estrus < or = 3 d of weaning (45 h and 58 h, respectively) than for sows expressing estrus after 5 d (39 h and 32 h, respectively). Farrowing rate and litter size were not influenced by treatment. However, the interval from last insemination to ovulation (P < 0.02) indicated that more sows farrowed (80%) when the last insemination occurred at < or = 23 to > or = 0 h before ovulation compared with insemination > or = 24 h before ovulation (55%). In summary, P.G. 600 enhanced the expression of estrus and ovulation in weaned sows but, breeding protocols may need to be optimized for time of ovulation based on the interval from weaning to estrus.

Animals↗
PubMed2002

Seasonal effects on estrous behavior and time of ovulation in nonlactating beef cows.

Estrous behavior and time of ovulation relative to the onset of estrus were determined in mature Angus x Hereford cows (n = 17 to 21 each season) during summer, winter, and spring for 2 yr. Estrous behavior was evaluated during the first of two consecutive estrous periods, and time of ovulation was determined during the second estrus. Concentrations of progesterone were quantified in twice weekly blood samples to ensure all cows had normal estrous cycles. The HeatWatch system was used to measure the duration of estrus, number of mounts received per estrus, and duration of the longest interval between mounts received. Commencing 16 h after the onset of the second estrus, transrectal ultrasonography was performed every 4 h until the dominant follicle was no longer present on the ovary, and time of ovulation was defined as 2 h preceding the absence of the dominant follicle. There was a seasonal effect on the duration of estrus; cows were estrus longer in summer (17.6 +/- 0.8 h) than in winter (15.5 +/- 0.8 h; P = 0.07) or spring (13.9 +/- 0.9 h; P < 0.05). Cows were mounted more times per estrus (P < 0.05) in winter (59.0 +/- 5.3) than in summer (43.6 +/- 5.3) or spring (38.2 +/- 5.8). Intervals between mounts of estrous cows were longer (P < 0.05) in summer (4.1 +/- 0.4 h) than in spring or winter (2.7 +/- 0.4 h). During all seasons, cows were mounted more times (P < 0.01) between 0600 to 1200 (3.2 +/- 0.2 mounts received/h of estrus) than during other times of the day (2.1 +/- 0.2 mounts received/h of estrus). Cows ovulated 31.1 +/- 0.6 h after the onset of estrus, and time of ovulation was not influenced by season. We conclude that season influences estrous behavior of beef cows; cows are mounted more times per estrus in winter than in summer or spring. Time of ovulation relative to the onset of estrus is constant during all seasons and averages 31.1 h.

Animals↗
PubMed2006

Stimulation of estrous behavior in grazing female goats by continuous or discontinuous exposure to males.

Two experiments were conducted during the anestrous period to determine: (1) whether males rendered sexually active by exposure to artificial long days stimulate estrous activity of female goats under grazed conditions (Exp. 1); and (2) whether continuous presence of the buck is necessary to stimulate this estrous activity (Exp. 2). In Exp. 1, 2 groups of females (n = 20/group), one in confinement and another under grazing conditions, were exposed to 4 bucks subjected to natural photoperiod (2 males/group). Two other groups of females (n = 20/group), in confinement or grazing, were exposed to 4 males treated with artificial long days (2 males/group). All groups were exposed to males for 15 d. The percentage of does detected in estrus during these 15 d was greater (P < 0.001) in the 2 groups exposed to males sexually prepared by long days (confined, 95%; grazed, 90%) than in groups exposed to males in natural photoperiod (confined, 15%; grazed, 45%). Does in Exp. 2 were allowed to graze and were exposed continuously (n = 26) or discontinuously (from 1700 to 0900; n = 26) for 18 d to males that had been stimulated to enter the breeding season by exposure to long days. The proportion of does that displayed estrous behavior in 18 d did not differ (P = 0.55) between groups (96.2 and 92.3% for continuous and discontinuous groups, respectively). The results indicate that anestrous goats managed under grazing conditions can be stimulated to express estrus by joining with males previously exposed to artificial long days. Continuous presence of the male is not necessary for this male effect.

Animal Husbandry↗
PubMed2007

Influence of body condition and bovine somatotropin on estrous behavior, reproductive performance, and concentrations of serum somatotropin and plasma fatty acids in postpartum Brahman-influenced cows.

Ninety-nine multiparous Brahman-influenced (1/4 to 3/8 Brahman) cows were managed to achieve low (BCS = 4.3 +/- 0.1; n = 50) or moderate (BCS = 6.1 +/- 0.1; n = 49) body condition (BC) to determine the influence of bovine somatotropin (bST) on estrous characteristics, reproductive performance, and concentrations of serum GH and plasma NEFA. Beginning 32 d postpartum, cows within each BC were assigned randomly to treatment with or without bST. Non-bST-treated cows received no treatment, and treated cows were administered bST (Posilac, 500 mg s.c.) on d -35, -21, and -7 before initiation of the breeding season. On d -7, all cows received an intravaginal, controlled internal drug-releasing (CIDR) device. On d 0 (initiation of the 70-d breeding season), the CIDR were removed and cows received prostaglandin F2alpha (PGF2alpha). Blood samples were collected from the median caudal vein of the cows at each bST treatment and at d -28 and 0. Estrous behavior was monitored by radiotelemetry during the first 30 d of the breeding season. Growth hormone was increased (P < 0.05) in low and moderate BC cows treated with bST. The percentage of cows detected in estrus during the first 30 d of the breeding season was decreased (P = 0.05) for low BC (64%) compared with moderate BC (82%) cows. The interval to first estrus tended (P = 0.07) to be shorter in low BC-bST-treated cows (3.7 +/- 1.9 d) than in moderate BC-bST-treated cows (9.6 +/- 1.8 d). During the first 30 d of the breeding season, cows in low BC had a decreased (P = 0.02) number of mounts received and increased (P = 0.001) quiescence between mounts compared with cows in moderate BC. The number of mounts received was reduced (P = 0.04) in bST-treated cows. More (P = 0.02) cows treated with bST became pregnant during the first 3 d of the breeding season compared with non-bST-treated cows. The cumulative first-service conception rate tended (P = 0.07) to be greater for bST-low BC cows than non-bST-treated cows in low or moderate BC. On d 0, NEFA were greater (P < 0.05) in bST-treated vs. non-bST-treated cows. Low BC and bST reduced the intensity of behavioral estrus in postpartum Brahman-influenced cows. However, bST increased the first-service conception rate during the first 30 d of breeding and pregnancy rates during the first 3 d of breeding in postpartum Brahman-influenced cows.

Animal Husbandry↗
PubMed1987

Influence of biostimulation by mature bulls on occurrence of puberty in beef heifers.

The objective of this study was to determine if biostimulation of prepuberal beef heifers by mature bulls would alter proportions of heifers exhibiting puberty, or age or weight at puberty. Angus (A), A X Hereford (H) and Tarentaise X HA heifers (n = 103) were stratified by age and weight within breed-type and location of birth and allotted randomly to the following treatments: 1) heifers exposed to mature bulls (T1; n = 52) or 2) heifers isolated from bulls (T2; n = 51). At the start of the experiment, heifers in T1 and T2 were 287 +/- 2 and 286 +/- 2 d of age, respectively. Male-to-female ratio for T1 was 1:26. Heifers in T1 and T2 were maintained in drylots separated by .5 km. Heifers were observed for estrus twice daily for 152 d. Puberty was characterized by the following criteria: 1) behavioral estrus, 2) presence of a palpable corpus luteum (d 9; estrus = d 0) and 3) a rise in serum progesterone above 1 ng/ml (d 9). Proportions of heifers reaching puberty by 11, 12, 13, 14 and 15 mo of age did not differ (P greater than .10) between treatments. Percentages of heifers reaching puberty by the end of the experiment were 84 and 89% for T1 and T2, respectively. Age and weight at puberty did not differ (P greater than .10) between treatments and averaged 370 +/- 7 d and 293 +/- 4 kg, respectively. Results from this experiment indicated that presence of mature bulls did not alter proportions of beef heifers reaching puberty, or age and weight at puberty.

Animals↗
PubMed1987

Genotype x environment interactions involving proportion of Brahman breeding and season of birth. II. Postweaning growth, sexual development and reproductive performance of heifers.

Postweaning growth, sexual development and reproductive traits were evaluated over a 3-yr period on 201 spring-born and 180 fall-born crossbred heifers with 0, 1/4 or 1/2 Brahman breeding. The proportion of Brahman breeding X season of birth interaction was significant for five traits (average daily gain weaning to yearling, yearling condition score, percentage of heifers detected in estrus, prebreeding condition score and percentage of heifers that became pregnant) and was not significant for six traits (yearling weight, hip height and conformation score, age and weight at puberty and prebreeding weight. Among spring-born heifers, 1/4 and 1/2 Brahman heifers outgained (P less than .05) 0 Brahman heifers from weaning to yearling by 50 and 66 g/d, respectively; among fall-born heifers, 1/4 and 1/2 Brahman heifers outgained (P less than .05) 0 Brahman heifers by 41 and 104 g/d, respectively. Yearling weight of 1/2 Brahman heifers was 13 and 10 kg heavier (P less than .05), respectively, than 0 and 1/4 Brahman heifers. Yearling hip height of 1/4 and 1/2 Brahman heifers were 1.9 and 5.7 cm taller (P less than .05), respectively, than 0 Brahman heifers. Weight prior to the start of the breeding season were similar among crossbred heifer groups and spring-born heifers were 66 kg heavier (P less than .05) than fall-born heifers. The percentage of heifers that became pregnant was similar among spring-born crossbred heifer groups, whereas among fall-born heifer groups 1/4 and 1/2 Brahman heifers were 25.2 and 49.4 percentage points lower (P less than .05), respectively, than 0 Brahman heifers.

Animals↗
PubMed1988

Effects of litter size and light regimen imposed during lactation on ovarian follicular population at weaning in third-parity sows.

Sixteen third-parity sows maintained under two photoperiod treatments (16 h light: 8 h dark [16 h] or 4 h light: 20 h dark [4 h]) were assigned to be unilaterally ovariectomized (left ovary) at weaning on d 28 after farrowing a small litter (12 or fewer piglets; S) or a large litter (more than 12 piglets; L). Antral follicles were classified as atretic or nonatretic and divided into six size classes. The right ovary was obtained at slaughter, 16 d after estrus was detected. Number of antral follicles in the left ovary was greater (P less than .05) for L sows (540) than for S sows (427). Sows exposed to 16 h of light with large litters had a higher number of atretic follicles than all other groups (litter size x photoperiod interaction, P less than .05). Number of nonatretic follicles were similar between groups. However, when nonatretic follicles were classed by size (1 = smallest; 6 = largest), their distribution differed. In Class 1, L sows had more follicles than S sows (P less than .05). For Classes 3 and 4, photoperiod interacted with litter size to decrease the number of follicles in L 16 h sows (litter size x photoperiod interaction, P less than .05). These lower numbers of nonatretic follicles were related to a higher rate of follicular atresia in L 16 h sows. In Classes 2, 3 and 4, L 16 h sows had more atretic follicles than any other group (litter size x photoperiod interaction, P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗