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Biomedical subjects

R D Randel

Publications and source records attributed to R D Randel.

At least 55 records · Page 3Linked to original sources

Effect of dietary phenolic amines on testicular function and luteinizing hormone secretion in male angora goats.

To test the effect of dietary phenolic amines on pituitary-gonadal functions, 24 postpubertal male Angora goats were assigned during the breeding season to a control diet or to graze on a pasture dominated by phenolic amine-containing vegetation (PA). Compared with control bucks, bucks grazing PA had decreased (P < .001) serum concentrations of testosterone, increased (P < .001) triiodothyronine (T3) and thyroxine (T4), greater (P < .001) reduction in scrotal circumference (SC), lower (P < .001) body weight gains, and reduced (P < .01) semen volume. Sperm concentration and progressive motility were not affected by treatment. On d 75 of treatment, endogenous and GnRH-stimulated LH secretion were greater (P < .01), but endogenous and stimulated testosterone secretion tended (P < .10) to be reduced in the PA bucks relative to the controls. Endogenous serum concentrations of LH and testosterone were positively correlated in the controls, whereas no correlation was detected in the PA males. We conclude that during the breeding season, increased consumption of plants with a high concentration of phenolic amines can affect the reproductive competence of male goats in a manner that suggests a premature ending of the active reproductive phase. The concurrent influence of dietary phenolic amines on serum T3 and T4, and the relationship of these hormones with expression of seasonal reproduction in domestic and wild ruminants, warrants further analysis of the relationship between dietary phenolic amines, thyroid function, and reproduction in these species.

Acacia↗

Genotypic effects on norepinephrine-induced changes in thermogenesis, metabolic hormones, and metabolites in newborn calves.

Heat production was measured in newborn Angus-, Brahman-, and Tuli-sired calves born to Angus (n = 20) and Brahman (n = 26) dams, before (thermoneutral metabolic rate, TMR) and after norepinephrine (NE) infusion (peak metabolic rate, PMR), to assess genotypic effects on nonshivering thermogenesis in brown adipose tissue. Calves were fed pooled colostrum, fitted with jugular catheters, and placed in a temperature-controlled (37 degrees C) water immersion system. Heat production, determined by indirect calorimetry, and tympanic temperature were measured continuously in calves from approximately 3 to 6 h of age. Blood samples were collected at birth and at 0, 5, 20, 40, 60, 80, 100, and 120 min relative to NE infusion (35 micrograms.min-1.kg BW-1 for 4 min), and plasma was analyzed for metabolites (glucose, NEFA, and urea nitrogen [PUN]) and hormones (cortisol, triiodothyronine [T3] and thyroxine [T4]). Weight-specific TMR (cal.min-1.kg-1) was not affected by breed of sire or dam, although weight-specific PMR (cal.min-1.kg-1) was lower (P < .01) in Brahman-sired calves than in Angus- or Tuli-sired calves and was lower (P < .001) in calves born to Brahman rather than Angus dams. The reduction in weight-specific PMR due to the maternal Brahman influence was sire-breed dependent, and the reduction was largest (P < .01) for Tuli-sired (34.3%), intermediate (P < .05) for Brahman-sired (15.1%), and lowest (P > .25) for Angus-sired calves (4.1%). The PMR:TMR ratio was 1.80 and 2.21 +/- .06 in calves born to Brahman and Angus dams, respectively. Peak tympanic temperature was .6 degree C lower (P < .01) in calves born to Brahman rather than Angus dams. At birth, plasma NEFA concentrations were higher (P < .001) and glucose tended (P = .13) to be higher in calves born to Brahman rather than Angus dams. Cortisol, T3, and T4 concentrations at birth were higher in calves born to Brahman dams than in those born to Angus dams. These results suggest that calves born to Brahman dams may have less thermogenically active brown adipose tissue than calves born to Angus dams, which may contribute to the relative cold intolerance of calves with Bos indicus inheritance.

Adipose Tissue, Brown↗

Body temperature and endocrine interactions before and after calving in beef cows.

Multiparous beef cows (n = 7) were used to evaluate peripartum changes and interactions among body temperature (BT) and circulating progesterone (P4), estradiol-17beta (E2), triiodothyronine (T3), cortisol, thyroxine (T4), and 13,14-dihydro-15-keto-prostaglandin F2alpha (PGFM) concentrations. Electronic temperature monitors were placed under the obliquus abdominis internus muscle of the left flank, and BT was measured using radiotelemetry every 3 min for 10-s periods from 144 h before to 24 h after calving. Environmental temperatures (ET) were recorded hourly. Body and environmental temperatures were averaged, separately, within 8-h periods. Blood samples were collected every 8 h, and hormone concentrations were measured. Time of day affected BT (P < .01), at 0300 cows had the lowest BT, at 1900 the highest, and at 1100 values were intermediate. Body temperature remained relatively constant (P > .10) from 144 to 56 h before calving and from 8 to 24 h after calving but decreased (P < .01) from 48 to 8 h before calving. Precalving BT was affected (P < .01) by ET, but hour-before-calving (time) had the greatest effect on BT during the 48 to 8 h immediately preceding parturition (b' = .41, P < .01) and was independent of ET effects. Before the BT decrease, cows gestating heifers had lower (P < .01) BT than cows gestating bulls. Plasma E2, PGFM, T3, and T4 concentrations before the precalving decrease in body temperature were greater (P < .03) in cows gestating bull rather than heifer calves. Approximately 30% of the variation (R2) during the temperature decrease was explained by plasma hormone concentrations; PGFM (b' = -.30, P < .05) and T3 (b' = -.22, P < .10) had the most significant effects. In conclusion, BT of the cow before the precalving decrease was affected by ET and sex of calf. However, the prepartum BT decrease was independent of these variables, and seemed partially endocrine-induced.

Animals↗

Artificial insemination, hybridization and pregnancy detection in sika deer (Cervus nippon ).

Artificial insemination (AI) was performed on sika hinds (Cervus nippon ) receiving various dosages of pregnant mare serum gonadotropin (PMSG; Year 1: 0, 50 and 100 IU; Year 2: 100 and 150 IU) and using semen collected from elk and 1 2 elk x 1 2 sika stags. The time from synchronization device removal (CIDR vs norgestomet) to estrus was determined through observations of mounting activity. Methods for pregnancy detection, serum progesterone (P4), estrone sulfate (E1S), pregnancy-specific protein B (PSPB) and ultrasonography, following AI (Year 1: AI, Days 28 and 48 after AI; Year 2: AI, Days 42, 53 and 100 after AI) and a 90-d natural breeding season were investigated. From available production data, body weights were compared among sika and 1 4 elk x 3 4 sika hybrids relative to age. Pregnancy rates tended (P < 0.10) to differ relative to PMSG treatment and sire; administration of 0 IU PMSG resulted in fewer hinds becoming pregnant to AI than 50 or 100 IU of PMSG. Hinds receiving 100 IU of PMSG had higher (P < 0.05) pregnancy rates than hinds receiving 150 IU PMSG. Time to standing estrus did not differ (P > 0.10) between the CIDR and norgestomet groups. Pregnancy rates 50 d after a 90-d breeding season were similar (P > 0.10) between ultrasound (70.9%) and PSPB (61.6%). Serum P4 after 90 d in breeding groups and 50 d after stag removal were higher (P < 0.05) for pregnant than open hinds. Pregnancy rates (Year 1) 48 d after AI were similar (P > 0.10) between ultrasound (49.0%) and PSPB (37.3%). Serum P4 28 and 48 d after AI were higher (P < 0.05) for pregnant than open hinds. Serum E1S was higher (P < 0.01) for pregnant than open hinds 48 d after AI. Pregnancy rates (Year 2) 100 d after AI did not differ (P > 0.10) between ultrasound and PSPB (66.7%). Serum P4 was higher (P < 0.03) in pregnant than open hinds at 42, 53 and 100 d after AI. At 100 d after AI, pregnant hinds had higher (P < 0.002) serum E1S than open hinds. At 6 to 8 and 11 to 13 mo of age, 1 4 elk x 3 4 sika males tended (P < 0.08) to be heavier than sika males, while 1 4 elk x 3 4 sika females were heavier (P < 0.05) than sika females at all ages. In summary, this study documents the use of AI and methods for pregnancy detection in sika hinds as well as preliminary information regarding the production of elk-x-sika hybrids.

Journal Article↗

Effects of diets containing free gossypol on follicular development, embryo recovery and corpus luteum function in Brangus heifers treated with bFSH.

Thirty 2 yr old Brangus heifers were randomly assigned to 1 of 3 dietary treatments: Control, 0 g of free gossypol (FG) per head per day (FGHD) from corn and soybean meal (SBM); 5 g of FGHD from cottonseed meal (CSM); and 15 g of FGHD from whole cottonseed (WCS). Blood samples were collected weekly for serum progesterone (P(4)) and later quantified by RIA. Whole blood was collected on Days 1, 28, 42, 56 and 70 for erythrocyte fragility (EF) analysis. Following 65 d on dietary treatments and estrus detection, the heifers received bovine-FSH (bFSH) once daily on Days 10, 11 and 12 postestrus, and PGF(2alpha) on Day 12 postestrus. Fifteen of the thirty heifers were randomly selected, and 12 h following PGF(2alpha), the ovaries were removed and follicular diameters, ovarian weight and stromal weights were recorded. Follicular fluid was analyzed for steroid content by RIA. The remaining fifteen heifers were artificially inseminated. Embryos were recovered non-surgically on Day 7 postestrus and graded, and the recovery efficiencies were calculated. Following embryo collection, both ovaries were removed, the number of CLs was recorded, and CL P(4) content was determined by RIA. By Day 42 of treatment, heifers receiving CSM had elevated (P < 0.04) EF compared with the Controls, and remained elevated above that of Controls throughout the study. At Day 70, the CSM heifers tended to have higher (P < 0.07) EF than the WCS group, which in turn tended to be higher (P < 0.06) than the Controls. The Control and CSM heifers gained weight during the 70 d treatment period, while heifers consuming WCS lost weight (P < 0.05). Ovarian and stromal weights did not differ (P > 0.10) among treatment groups. Heifers receiving CSM had fewer (P < 0.05) follicles > 5 mm than WCS or Control heifers. Follicular fluid weights and steroid content did not differ (P > 0.10) among treatments. Both CL weight and the number of CLs per heifer were similar (P > 0.10) among treatments. Heifers receiving CSM or WCS had a higher (P < 0.003) CL P(4) content per gram of CL tissue than the Controls. Progesterone content per CL was greater in WCS heifers (P < 0.003) than in CSM heifers, while both the CSM and WCS heifers had a higher CL P(4) content than the Control heifers. Weekly and Day 7 postestrus serum concentrations of P(4) were similar (P > 0.10) among treatments. The number of embryos recovered, number of degenerated embryos, embryo grades and recovery efficiencies were not affected (P > 0.10) by dietary treatments. To standardize heifers relative to the number of degenerated embryos, the percentage of degenerated embryos recovered was calculated and tended to be greater (P < 0.06) in heifers consuming CSM than in either the Control or WCS groups. While most ovarian, follicular and embryo characteristics were not affected by dietary free gossypol, these results suggest that differences in the availability of free gossypol and/or dietary components between CSM and WCS may influence weight gain, CL P(4) content and embryo viability.

Journal Article↗

Testicular and epididymal function during the peripuberal period in Brahman bulls receiving various amounts of protein degradable in the rumen.

Thirty-nine Brahman bulls with an initial age and weight of 301.7 +/- 4.1 d and 202.7 +/- 4.7 kg, respectively, were randomly allocated to 1 of 2 dietary treatment groups within age, weight and sire in order to study the influence of source of protein and stage of peripuberal period on testicular and epididymal function. In the soybean meal treatment the amount of protein undegradable in the rumen averaged 47%, while it was 72% in the fish meal treatment. The supplements were isocaloric and isonitrogenous. Bulls were electroejaculated, and castrations were performed randomly in a predetermined order when the first ejaculate with the first motile sperm cells (Stage 1), 10 to 25 million (Stage 2), and 50 million or more sperm cells (Stage 3 - puberty) was obtained. Testicular and epididymal traits were analyzed for a single testicle and epididymis. Daily sperm production, daily sperm production per gram of testicular parenchyma, testicular weight and testicular parenchyma weight were not affected by treatment. Bulls receiving fish meal had heavier (P < 0.01) epididymis than soybean meal-fed bulls (6.6 +/- 1.0 vs 3.9 +/- 0.6 g) but similar (P > 0.05) epididymal sperm reserves. Daily sperm production (1 testicle) was 115.2 +/- 0.1, 447.4 +/- 0.1, 792.7 +/- 0.1 million sperm cells, and daily sperm production per gram of testicular parenchyma was 1.5 +/- 0.5, 3.2 +/- 0.6 and 6.4 +/- 0.6 million sperm cells for bulls at Stage 1, 2 and 3, respectively. Sire and amount of undegradable intake protein had significant (P < 0.05) affects on the distribution of epididymal sperm reserves, with soybean meal-fed bulls having the higher proportions of epididymal sperm reserves in the cauda epididymis.

Journal Article↗

Exogenous PGF(2)alpha enhanced GnRH-induced LH release in postpartum cows.

This study evaluated the effect of exogenous PGF(2)alpha on circulating LH concentrations in postpartum multiparous (n = 32) and primiparous (n = 46) Brahman cows. The cows were randomly allotted within parity and calving date to receive 0, 1, 2 or 3 mg im PGF(2)alpha (alfaprostol)/100 kg body weight (BW), with or without GnRH on Day 30 after calving. Blood samples were collected at weekly intervals from calving through treatment. Serum progesterone concentrations were determined using RIA procedures to assure that only anestrous cows were treated. Sterile marker bulls were maintained with cows on Coastal bermudagrass pastures until the first estrus was detected. Multiparous cows had a shorter (P < 0.05) interval from calving to estrus than did primiparous cows. Serum LH was affected by time (P < 0.0001), PGF(2)alpha dose (P < 0.0002), GnRH (P < 0.0001), parity by PGF(2)alpha dose (P < 0.0003), PGF(2)alpha dose by GnRH (P < 0.0009), parity by GnRH (P < 0.0008), and by parity by PGF(2)alpha dose by GnRH (P < 0.0005). Multiparous cows not receiving GnRH had higher mean serum LH (P < 0.02), LH peak pulse height (P < 0.03), and area under the LH release curve (P < 0.03) compared with primiparous cows. The number of LH pulses/6 h was greater (P < 0.06) in multiparous than primiparous cows, and was greater (P < 0.02) in multiparous cows receiving 3 mg/100 kg BW than in cows receiving 2 mg/100 kg BW, but not in the controls or in cows receiving 1 mg/100 kg BW. Exogenous GnRH resulted in increased (P < 0.0001) serum LH concentrations in all cows, and LH was enhanced (P < 0.0009) by simultaneous treatment with PGF(2)alpha. Primiparous cows had a greater response (P < 0.0005) to PGF(2)alpha and GnRH compared with multiparous cows. Pituitary release of LH in response to GnRH was enhanced by simultaneous exposure to PGF(2)alpha in Day 30 postpartum cows.

Journal Article↗

Sire breed of calf influences peripartum endocrine profiles and postpartum anestrus in Brahman cows.

The literature indicates that sire breed of calf influences beef calf performance. However, there is little information concerning sire breed of calf effects on reproduction in beef cows. In this experiment, Angus (A), Brahman (B), or Tuli (T) bulls were bred to 136 Brahman (B) cows to examine sire breed of calf influence on peripartum hormone profiles and the length of postpartum anestrus. Cows were bled from 7 d prepartum to 28 d postpartum to determine peripartum hormone concentrations. Cows carrying AB calves had greater (P < 0.05) prepartum estradiol-17 beta concentrations than did cows carrying BB and TB calves. Prepartum and postpartum progesterone concentrations did not differ between cows with AB, BB, and TB calves. Cows with TB calves had lower (P < 0.01) 13,14-dihydro-15-keto-prostaglandin F2 alpha (PGFM) concentrations than did cows with AB and BB calves during the early postpartum period. Adjusting for birth weight removed the sire breed of calf effect on postpartum PGFM concentrations, but not prepartum estradiol-17 beta. Postpartum anestrus was shorter (P < 0.05) for cows nursing BB calves (84 +/- 6 d) than for cows nursing AB (101 +/- 6 d) or TB calves (110 +/- 7 d). Adjustment for estradiol or PGFM concentrations did not reduce sire breed of calf effects on the length of postpartum anestrus. Further work is heeded to determine how calf genotype may modulate the postpartum reproductive function of the dam.

Anestrus↗

Oxytocin induces prostaglandin F2 alpha release in pregnant cows: influence of gestational age and oxytocin receptor concentrations.

Brahman cows with known breeding dates received i.v. injections of either 10 or 100 IU oxytocin (OT) on Days 50, 150, 250, or 280 of gestation (n = 6 for each stage). Concentrations of the prostaglandin (PG) F2 alpha metabolite, 13,14-dihydro-15-keto-prostaglandin (PGFM), and OT were measured in samples of peripheral plasma collected at 15-min intervals for 1 h before and 1 h after treatment and then at 30-min intervals for 3 h. Plasma progesterone was measured daily for 14 days after OT injections on Days 50 and 250 of gestation. The increase in plasma OT after injection was dose-dependent (p = 0.001) but not affected by stage of gestation. Plasma PGFM increased after OT in a dose- and stage-dependent manner (p = 0.0001). At Day 280, the increase in plasma PGFM after 100 IU OT was sevenfold greater than at Day 50. Plasma progesterone declined significantly during the 7th to 12th days postinjection and returned to normal pregnancy values by the 14th day (4.4 +/- 0.3 ng/ml) except in two cows treated on Day 50 of gestation that later aborted. In these, plasma progesterone was significantly lower, 2.6 +/- 0.1 ng/ml. In a second experiment, the concentration of OT receptors was determined in endometrium collected from purebred Angus or Hereford cows slaughtered on Days 50, 150, 250, and 280 of gestation (n = 3 or 4 at each stage). Endometrial concentrations of OT receptor changed as a function of gestational age, increasing sixfold from Day 50 to Day 280, which was parallel to the increase by OT of plasma PGFM. Thus, endometrial OT receptors are functionally coupled to PGF2 alpha release during pregnancy, and their concentration determines the magnitude of OT-induced PGF2 alpha release during gestation. Consequently, endogenous OT is a factor in the regulation of PGF2 alpha release from the bovine uterus during pregnancy and parturition.

Animals↗

Heat tolerance in two tropically adapted Bos taurus breeds, Senepol and Romosinuano, compared with Brahman, Angus, and Hereford cattle in Florida.

Two trials were conducted with heifers to determine heat tolerance among temperate Bos taurus (Angus, Hereford), Bos indicus (Brahman), tropical Bos taurus (Senepol, Romosinuano), and the reciprocal crosses of Hereford and Senepol. Differences among breeds in temperament score, circulating concentrations of cortisol, and blood packed cell volume were also investigated. Trial 1 used 43 Angus, 28 Brahman, 12 Hereford, 23 Romosinuano, 16 Senepol, 5 Hereford x Senepol (H x S), and 5 Senepol x Hereford (S x H) heifers. Trial 2 used 36 Angus, 31 Brahman, 9 Hereford, 14 Senepol, 19 H x S, and 10 S x H heifers. On the hottest summer date in Trial 1, rectal temperature of Angus was greater (P < .001) than that of Brahman, Senepol, or Romosinuano. Rectal temperature and plasma cortisol were significantly less in Senepol than in Brahman, suggesting that the differences in rectal temperature between these breeds may be due to differences in stress response possibly related to differences in temperament. Reciprocal crosses of Hereford and Senepol had rectal temperatures nearly as low as that of Senepol and displayed substantial heterosis (-9.4%, P < .05) in log10 rectal temperature on the hottest summer date. On both the hottest and coolest dates in Trial 1, Angus heifers had significantly faster respiration rates than Brahman, Romosinuano, or Senepol heifers, and Brahman had significantly slower respiration rates than Romosinuano or Senepol. On the hottest summer date in Trial 2, rectal temperature in Angus heifers was greater (P < .001) than in Brahman or Senepol had rectal temperatures similar to that of Senepol, or heterosis for log10 rectal temperature was similar to that in Trial 1 (-9.8%, P < .05). Considering rank order among breeds, Brahman always had the slowest respiration rate and greatest packed cell volume. Brahman had significantly greater temperament scores and plasma cortisol concentrations than Angus or Senepol, except that plasma cortisol was not different between Brahman and Senepol on the hottest summer date. On this date, rectal temperature did not differ between Brahman and Senepol, which supports the hypothesis that there is a relationship between response to stress and rectal temperature that helps explain differences in rectal temperature between Brahman and Senepol. The results of these trials demonstrate heat tolerance of the Senepol and Romosinuano, two Bos taurus breeds. Furthermore, the results suggest a substantial level of dominance of the Senepol's ability to maintain constant body temperature in a hot environment as measured by rectal temperature in crosses with a non-adapted breed.

Adaptation, Physiological↗

Adrenocorticotropic hormone dose response and some physiological effects of transportation on pregnant Brahman cattle.

The appropriate dose and the ability of exogenous ACTH to mimic the physiological effects of a real stressor need to be determined. In Exp. 1, 25 pregnant Brahman heifers were injected i.v. with either 0 (saline), .125, .25, .5, or 1 i.u. of ACTH/kg BW. Plasma cortisol was determined in blood samples collected during a 5-h period, and an integrated cortisol response was calculated for each cow. The greater the dose of ACTH, the greater was the integrated cortisol response (P < .001). However, peak plasma cortisol in response to the four doses of ACTH did not differ (P > .6). The plasma cortisol concentrations returned to baseline more slowly in those cows receiving the greater doses of ACTH, making their integrated areas of response greater. In Exp. 2, pregnant Brahman cows were either transported 48 km (n = 28), injected with 1 i.u. of ACTH/kg BW (n = 21), or served as shams (n = 28). Each treatment was repeated at 60, 80, 100, 120, and 140 d of gestation. Shrink was greater for the transported cows than for either the ACTH-treated or sham cows, 14.3, 6.0, and 5.2 kg (P < .001). Shrink also decreased in response to each subsequent application of treatment for all three treatment groups (P < .001). Transported cows had lower plasma cortisol concentrations after the first two applications of treatments (P < .006). The range of doses of ACTH caused a similar peak cortisol release; however, it took cortisol longer to return to baseline as ACTH dose increased. Repeated administration of exogenous ACTH did not cause the same amount of shrinkage as transportation, and the resultant cortisol concentrations remained consistent for each administration. There was no apparent carryover effect of repeated administration of ACTH at 20-d intervals. Maximal plasma cortisol concentrations in Brahman cattle can be obtained with doses of ACTH much smaller than those traditionally injected. However, larger doses of ACTH maintained plasma cortisol concentrations for a longer duration. Repeated transportation caused a decrease in cortisol release and shrinkage indicative of psychological habituation. Injections of ACTH did not cause the same physiological response as transportation.

Adrenocorticotropic Hormone↗

Effects of dietary fat and season on steroid hormonal profiles before parturition and on hormonal, cholesterol, triglycerides, follicular patterns, and postpartum reproduction in Brahman cows.

Spring-calving Brahman cows (S) artificially inseminated to Brahman, Angus, or Tuli sires and fall-calving Brahman cows (F) naturally bred to Brahman were allotted randomly to receive 3.74% (LF; n = 9 S and 6 F), 5.20% (MF; n = 8 S and 6 F), or 6.55% dietary fat (HF; n = 8 S). Diets were formulated to contain differing fatty acid concentrations and to be isocaloric and isonitrogenous. Cows were bled and fed twice daily from 2 wk before expected calving date through d 21 after calving. Ultrasonography was performed on d 14 and 21 after calving. From d 21 to 90 after calving a sterile bull equipped with a chin-ball marker was placed with the cows to aid in estrus detection. In both seasons progesterone decreased (P < .01) and estradiol-17 beta increased (P < .01) as parturition approached. Cows receiving MF and HF had increased (P < .01) total numbers of follicles compared to LF cows, and cows receiving MF had larger (P < .01) follicles. During the spring, cows receiving HF and cows bred to Brahman or Tuli sires had longer (P < .01) gestation lengths. Progesterone concentrations before calving were affected (P < .01) by treatment x sire and estradiol-17 beta by a time x treatment interaction (P < .01). Cholesterol after calving was higher (P < .01) in HF cows than in LF or MF cows. In the fall, LF cows had heavier (P < .01) calves than cows receiving MF. Birth weight was also affected (P < .01) by treatment x sex of calf. Progesterone was affected (P < .01) by treatment x sex of calf. Estradiol-17 beta was affected (P < .01) by sex of calf and treatment x sex of calf. Across seasons, by d 90 after calving, 9 of 15 (60%) LF and 11 of 15 (73.3%) MF cows showed estrual behavior. Cows in the spring had increased (P < .01) numbers and larger follicles compared to the fall. In conclusion, dietary fat may influence steroid hormone concentrations before calving, calf birth weight and postpartum follicular populations; furthermore, follicular populations may also be influenced by season.

Animals↗

Effect of histone-H2A (H-H2A), platelet activating factor (PAF) and pregnancy specific protein B (PSPB) on secretion of prostaglandins E and F2 alpha (PGE; PGF2 alpha) by bovine endometrium and H-H2A on basal secretion of luteinizing hormone (LH) by bovine pituitary cells in vitro.

Effects of H-H2A, PSPB or PAF on day 16 bovine endometrial secretion of PGE and PGF2 alpha and H-H2A on basal secretion of LH by bovine pituitary cells in vitro were examined in two experiments. PAF (P < or = 0.08) and H-H2a + PAF (P < or = 0.10) treatment for two hours in an in vitro perfusion system tended to increase secretion of PGF2 alpha expressed as a proportion of the prechallenge concentrations of PGF2 alpha by day 16 bovine caruncular endometrium, which occurred during the two-hour period after treatment removal. PGF2 alpha was increased (P < or = 0.02) in the two hour period after the treatment was removed in both control and H-H2A-treated endometrium. H-H2A (P < or = 0.07) and PSPB (P < or = 0.08) tended to increase PGE, while H-H2A + PSPB (P < or = 0.05) and H-H2A + PAF (P < or = 0.03) increased secretion of PGE expressed as a proportion of the prechallenge concentrations of PGE by day 16 bovine caruncular endometrium during the challenge and postchallenge treatment periods, but did not differ (P < or = 0.05) between the two-hour challenge period and the two-hour postchallenge period after removal of the treatment. In experiment two, H-H2A decreased (P < or = 0.05) basal secretion of LH by bovine pituitary cells in vitro. These data suggest that H-H2A and PSPB preferentially stimulate secretion of PGE by bovine endometrial tissue and may play a role in maternal recognition of pregnancy, while PAF increased PGF2 alpha secretion. In addition, H-H2A may play a role in regulating secretion of LH by the pituitary. Key words: Pregnancy Specific Protein B, Histone-H2A, Prostaglandin E and F2 alpha, Platelet Activating Factor, Endometrium, Cow.

Animals↗

Regulation of adrenocorticotropin secretion in vitro by anterior pituitary corticotrophs from fallow deer (Dama dama).

The actions of corticotropin-releasing hormone (CRH), vasopressin (VP), the synthetic glucocorticoid dexamethasone (DEX), and mifepristone (RU 486), a glucocorticoid antagonist, on the secretion of adrenocorticotropin (ACTH) by cultured fallow deer corticotrophs were studied in vitro. On Day 5 of primary culture, corticotrophs were challenged for up to 4 hr with medium alone (Control), CRH, VP, DEX, forskolin (FSK), phorbol ester (TPA), cyclic AMP (cAMP), and/or RU 486 at various concentrations and combinations. CRH, VP, FSK and TPA each stimulated (P < 0.01) the secretion of ACTH in dose- and time-related manners. Relative to Control, CRH at 0.001 and 0.1 microM and VP at 0.01 and 1 microM increased (P < 0.01) medium concentration of ACTH by 7.3-, 13.5-, 3.7- and 9.0-fold, respectively. There was a treatment x incubation time interaction (P < 0.01) such that at 30-min posttreatment, CRH-induced ACTH secretion tended (P < 0.10) to be less than that obtained via VP treatment, whereas at 1, 3, and 4 hr posttreatment, medium concentration of ACTH from cells treated with 0.1 microM CRH was greater (P < 0.05) than that in cells treated with 1 microM VP. At equimolar doses of 0.01 and 0.1 microM, CRH was 3.4- and 3.0-fold more potent (treatment x dose, P < 0.05) than VP. Cotreatment with 1 microM DEX reduced (P < 0.001) the stimulatory effects of CRH (0.1 microM), VP (1 microM), FSK (10 microMs), TPA (0.1 microM), and cAMP (0.001 M). However, the coaddition of RU 486 (1 microM) to the CRH plus DEX- and the FSK plus DEX-treated wells partially negated the inhibitory effects of DEX. RU 486 completely negated the inhibitory effects of DEX on the VP-, TPA-, and cAMP-stimulated secretion of ACTH. These data indicate that CRH is a more potent stimulator of ACTH secretion than is VP in primary culture of fallow deer pituitary cells. This study also demonstrates the utility of an in vitro culture system to investigate stress-related hormonal interactions in cervids.

Adrenocorticotropic Hormone↗

Influence of calf genotype on colostral immunoglobulins in Bos taurus and Bos indicus cows and serum immunoglobulins in their calves.

Purebred Bos indicus calves are documented to have lower survival rates than Bos taurus calves. Thus, this study was designed to investigate the possibility that this decreased survival rate may be attributed to dam colostral immunoglobulin (Ig) concentrations and subsequent calf serum Ig concentrations. The specific objective was to determine the effect of breed type of calf on colostrum production, immunoglobulin concentrations in colostrum and calf serum, and availability and absorption efficiency of Ig. Brahman (B) and Angus (A) cattle were reciprocally mated to produce calves of the following types: A x A (n = 8), A x B (n = 9), B x B (n = 11), and B x A (n = 11). At birth, calves were separated from their dams and a blood sample was collected before feeding pooled colostrum (30 mL/kg birth weight) at 1 and 6 h of age. From 6 to 12 h of age, each calf was placed in a box that allowed interaction with the dam but prevented suckling. At 12 h of age, each calf was fed its dam's colostrum and placed with the dam. Additional blood samples were collected at 12, 24, and 48 h after birth. Serum and colostrum samples were analyzed for IgG, IgG1, IgG2, IgM, and IgA using single radial immunodiffusion (RID) assay techniques. The cows were hand-milked after induction of milk letdown with oxytocin at 1 and 12 h after calving. Colostrum volume was recorded, and samples were collected. Brahman cows produced more (P < .001) colostrum at 1 and 12 h than A cows. Total Ig concentrations were obtained by summing IgG, IgG1, IgG2, IgM, and IgA concentrations. Total Ig (P < .02), IgG (P < .005), and IgA (P < .01) concentrations in colostrum were greater in cows producing crossbred calves. Total Ig (P < .006), IgG (P < .02), IgG1 (P < .004), and IgG2 (P < .02) available in colostrum were affected by B x B and A x B breed types of calf. Brahman cows had more Ig available at 1 and 12 h than A cows due to increased production of colostrum. Breed type influenced colostral Ig in cattle. Serum concentrations of total Ig, IgG, IgG1, IgG2, IgM, and IgA in the calf and efficiency of absorption at 6 and 12 h were not affected by breed type, sex of calf, or any interaction.

Animals↗

Influence of undegraded intake protein supplementation on milk production, weight gain, and reproductive performance in postpartum Brahman cows.

Eighty first-calf Brahman heifers and 51 mature Brahman cows were allotted to one of three diets based on parity, sex of calf, and breed of calf sire (Angus, Brahman, or Tuli) to evaluate rumen undegraded intake protein's (UIP) influence on production characteristics and reproductive performance. Supplements contained either 38.1% (low), 56.3% (medium), or 75.6% (high) UIP. Supplements were given from d 7 to 119 after calving to dams grazing rye-ryegrass overseeded Coastal bermudagrass pastures and with access to Coastal bermudagrass hay. Dam and calf BW and dam body condition score were recorded on d 7, 35, 63, 91, and 119 after calving. Four-hour milk production was recorded on the above days for low (n = 18), medium (n = 19), and high (n = 18) UIP animals and on d 7 and 35 for the entire group. Blood for progesterone RIA was drawn weekly and on d 6, 8, 10, and 12 after an observed estrus. Medium UIP heifers produced more (P < .02) milk (1.18 +/- .07 kg/4 h) than high UIP heifers (.94 +/- .07 kg/4 h), but milk production in mature cows was not influenced by diet. Low UIP dams had lower (P < .04) first-service conception rates (29.2%) than medium (57.6%) and tended (P < .10) to have lower rates than high UIP dams (54.6%). Overall pregnancy rates tended (P < .10) to be higher in medium (61.5%) and high (56.4%) UIP groups than in the low (43.2%) UIP group. Supplementing UIP at the medium rate improved first-service conception rates and tended to improve pregnancy rates.

Animal Feed↗

Breed affects thermoregulation and epithelial morphology in imported and native cattle subjected to heat stress.

The objective of this study conducted in tropical Brazil was to characterize some physiological responses to heat stress in imported Bos taurus, native Bos taurus, and native Bos indicus cattle. Imported Simmental (n = 107) native Simmental (n = 99), and native Bos indicus cattle (n = 121) (42 to 80 mo of age) were evaluated. Animals were walked 7 km at 37 degrees C and 60 to 65% relative humidity during midday. Rectal temperatures and respiration rates were taken before and after the walk. A .01-cm2 sample of cutaneous tissue from the lateral cervical region was obtained from each animal. Slices were stained with hematoxylin-eosin solution, and the epithelial strata were counted. Perimeter of the sweat glands was also calculated. Rectal temperatures before the walk were greater (P < .001) in imported Simmental (40.52 +/- .04 degrees C) than in native Simmental (38.92 +/- .04 degrees C) or Bos indicus (38.90 +/- .04 degrees C). Rectal temperatures after the walk were greater (P < .001) in native Simmental (39.87 +/- .05 degrees C) than in Bos indicus (39.46 +/- .05 degrees C). Because of the heat, imported Simmental were not capable of finishing the drive, and rectal temperatures could not be taken. Respiration rates before and after the walk were greater (P < .001) in imported Simmental (64.3 +/- .6; 95.8 +/- .8) than in native Simmental (35.0 +/- .6; 56.8 +/- .8) or Bos indicus (15.0 +/- .2; 33.2 +/- .8). Sweat gland perimeter was greater (P < .001) in Bos indicus (540.5 +/- 19.1 mm) than in native Simmental (382.0 +/- 27.6 micrograms) or imported Simmental 497.2 +/- 17.4 micrograms). Native Bos indicus were environmentally adapted, native Simmental had elevated body temperatures and respiration rates, and imported Simmental had dramatically increased body temperatures and respiration rates. Native Bos indicus cattle were environmentally adapted and differed in skin histology, sweat gland histometry, and number of epithelial strata.

Animals↗