The effect of beta-carotene on thyroxine and cholesterol levels in pregnant heifers before and after parturition

Thyroxine (T4) and cholesterol concentrations and their dynamic changes and differences were studied in 20 pregnant heifers 10 days before calving until 56 days after calving. Ten control heifers were fed the feed ration for pregnant heifers according to Czechoslovak Standard CSN 46 7070. The feed ration given to another ten (experimental) heifers was fortified with 300 mg of synthetic beta-carotene per head/day within the period of five months before insemination, during pregnancy and till the 56th day after parturition. As suggested by the regression function of straight line, no obvious differences were recorded in the dynamic changes of T4 before parturition and during the first days after parturition. T4 concentrations had a generally descending tendency in both groups, the lowest values being recorded in the 48th hour in the experimental group and the 24th hour in the control. A marked increase of T4 concentrations with the values significantly higher in the control group than in the experimental group was observed between the 21st and 35th day after calving. A medium increase of cholesterol concentrations was found in the heifers given rations fortified with beta-carotene. No significant differences in cholesterol concentrations were observed between the two groups, except in the 72nd hour and the seventh day. Significant T4: cholesterol correlations were recorded in the experimental animals in the first and second hours, on the 42nd day (P less than 0.05), and in the 72nd hour (P less than 0.001); in the control group these observations were made the seventh day before calving and in the sixth hour and on the 14th, 21st and 56th days (P less than 0.05) after calving. It is inferred from the results that beta-carotene interferes with the activity of the thyroid gland and the production of its hormones, and that the increases or decreases of the activity of this gland, caused by beta-carotene, influence the metabolism of cholesterol in the body.     

Effect of large dietary doses of beta-carotene on plasma retinoid and beta-carotene levels and on progesterone production in the granulosa cells of Japanese quail

An experiment was conducted to study the effect of large-dose beta-carotene supplementation on blood retinoid and beta-carotene levels as well as on the progesterone secretion of the granulosa cells in Japanese quail. Laying quails were assigned to three dietary groups. The control group (Group C) received the basal diet (laying feed containing 9000 IU vitamin A/kg). In the treated groups (Groups BC1 and BC2) the basal diet was supplemented with 10(2) and 10(3) mg/kg beta-carotene (BC), respectively. At the end of the two-week feeding period, 10 birds from each group were euthanised. Blood samples were analysed for retinol, retinyl palmitate and beta-carotene concentrations. Granulosa cells were isolated from ovarian follicles (F1 and F2), and PMSG-induced in vitro progesterone (P4) secretion was measured. Similar retinol concentrations were found in both beta-carotene supplemented groups, indicating saturation of the retinol-transporting system. beta-carotene supplementation was accompanied by hypercarotenaemia, but did not increase the retinyl palmitate levels in the blood. PMSG-induced P4 production of the granulosa cells decreased significantly in Groups BC1 and BC2 in a dose-dependent manner.     

The effect of phenothiazine on plasma prolactin levels in non-pregnant mares

Sixteen non-pregnant pony mares were divided into four groups of similar age and bodyweight (bwt). Groups were randomly assigned to one of four treatments consisting of oral administration of perphenazine (0.5 and 1.0 mg/kg bwt, phenothiazine (10 mg/kg bwt) and a control group. Blood samples were taken by jugular venepuncture and plasma prolactin concentrations measured using an homologous assay for equine prolactin. Analysis of variance was conducted on data designed as a split plot over time. Perphenazine given orally (0.5 and 1.0 mg/kg bwt) increased plasma prolactin concentrations when measured 3 and 6 h following feeding (P less than 0.05). Prolactin concentrations returned to normal by 11 h post drug administration. There was no response in plasma prolactin concentrations following oral phenothiazine treatment (10 mg/kg bwt). Perphenazine at the 1.0 mg/kg bwt level was discontinued after two days due to two mares exhibiting signs of hyperesthesia.     

Composition of milk from pony mares fed various levels of digestible energy

Twenty-two pony mares were fed one of three diets that provided 93.0, 74.8 or 57.2 kcal of digestible energy (DE) per kg body weight per day. Milk samples were taken at 14 day intervals. A total of five samples were taken from each mare. The samples were analyzed for total solids, crude protein, lactose, total lipids, ash, calcium and phosphorus. Gross energy was calculated from composition data. Increases in energy intake decreased the concentration of total solids, protein, fat and gross energy of mare's milk. Energy intake had a greater influence on the mare's body condition than on milk energy production. It was concluded the objective of a feeding program for a lactating mare should be to keep the mare in a desirable body condition rather than to influence milk composition or production.     

Morphological structure of the mucous membrane and submucosa of rumen in calves receiving synthetic or natural beta-carotene and vitamins AD3E.

In an experiment conducted on 20 calves from 1 day to 12 weeks old, supplements of beta-carotene were fed in the form of Rovimix beta-carotene 10%, artificially dehydrated carrot or vitamins AD3E. Postmortem examination carried out at 12 weeks showed that supplementation of beta-carotene or vitamins AD3E resulted in a better structural development of the ruminal papillae as compared to the control group. In addition, beta-carotene reduced the keratinization of the stratified squamous epithelial cell layer of the rumen and increased the glycosaminoglycan level of that organ wall.     

Control of cyathostome infections in mares treated at parturition with ivermectin

Six mares were treated on the day of parturition with an intramuscular injection of 0.2 mg kg-1 ivermectin and placed in a pasture free of equine parasites as soon as possible after foaling. The mares and their foals were compared with a similar group of untreated mares and foals on an adjoining pasture. The experimental data was derived from mare and foal fecal egg counts, foal necropsies and pasture larval counts. Ivermectin administered to mares on the day of parturition, when combined with movement to parasite-free pastures, significantly lowered the cyathostome (small strongyle) egg production for 4 months. This reduced cyathostome exposure was reflected in lower worm-burdens in their foals for 5 months. The results indicate that ivermectin will effectively control equine strongyles when mares and their foals are moved to parasite-free pastures.     

Effect of seminal plasma on uterine inflammation, contractility and pregnancy rates in mares

REASONS FOR PERFORMING STUDY: There is conflicting evidence over the role seminal plasma plays in sperm transport and inflammation within the uterus of mares. In in vitro studies, seminal plasma has been shown to reduce polymorphonuclear neutrophil (PMN) function, but the opposite effect on uterine inflammation has been reported in vivo. OBJECTIVES: To study the effect of seminal plasma on uterine contractility, inflammation and pregnancy rates by inseminating mares with low doses of sperm free from seminal plasma (Group 1) and containing seminal plasma (Group 2). METHODS: Synchronised mares were inseminated with 50 x 10(6) sperm in either skim milk extender or seminal plasma. Uterine lavage was performed 6 h after insemination to assess the inflammatory response. The contraction frequency of the uterus was measured over a 4 min period 10 mins and 6 h after insemination, using B-mode ultrasonography. Pregnancy rates were assessed 16 days after insemination. RESULTS: Uterine contractions were less frequent in Group 1 mares inseminated with seminal plasma and significantly more PMNs were found in the lavage fluid of those mares. Pregnancy rates were identical in both groups (62%). CONCLUSIONS: This study provides evidence that seminal plasma decreases uterine contractility and increases the inflammatory response of the uterus to semen. No effect of seminal plasma on pregnancy rates was demonstrated. POTENTIAL RELEVANCE: Mares that develop persistent mating-induced endometritis may have inherently poor uterine contractility and impaired uterine clearance. The presence of seminal plasma during breeding may not be desirable in these mares. The role of seminal plasma in problem mares warrants additional study.     

Induction of parturition in mares: effect on passive transfer of immunity to foals

Parturition was induced in 11 mares, using a synthetic prostaglandin. Eight mares, not treated, were used as controls. There was no significant difference between the serum immunoglobulin G (IgG) concentrations of the treated and control mares. The concentration of IgG in the colostrum of treated mares compared favorably with that reported for naturally foaling mares. Four foals from treated mares died or were euthanatized because of weakness during the 1st 24 hours after birth. The mean IgG concentration in the surviving foals from treated mares at 24 to 36 hours of age was 1,561 mg/100 ml, which was significantly (P less than 0.01) lower than the mean concentration of 2,731 mg/100 ml in foals from control mares. The mean serum IgG concentration in foals from control mares was significantly (P less than 0.01) greater than that of their dams, whereas the mean serum IgG concentration of the foals from treated mares was significantly (P less than 0.01) lower than that of their dams.     

Plasma prolactin concentrations in mares and their neonates after oxytocin induction of parturition

Studies were undertaken to investigate the effects of oxytocin induction on prolactin release in term (Group II) and preterm (Group III) mares and to compare these effects to spontaneously foaling mares (Group I). Since physiological concentrations of prolactin in blood have not been measured in the neonatal foal, experiments were designed to monitor prolactin in the cord artery and jugular blood of the foals from all groups of mares. Although prolactin levels varied in term mares (Group I and II) during the last 11 days of pregnancy, an increase was observed between Day -6 and Day 0 (2.7 and 11.9 ng/ml respectively; P less than 0.1). The average concentration of prolactin over the last 4 days (Days -3 to 0) had increased by 40% when compared to the average concentration on Days -6, -5, and -4. These findings indicate a rising trend which appears to occur concomitantly with changes in concentrations of 2 mammary components tested, sodium and potassium. Prolactin concentrations did not significantly increase in term mares after oxytocin treatment or in spontaneously foaling mares. However, the preterm induced mares had higher prolactin concentrations during the first stage of labor (19.3 +/- 7.2 ng/ml) than prior to treatment with oxytocin (4.7 +/- 2.0 ng/ml; P less than 0.01). Levels of prolactin in all groups significantly declined by 20-min post-placental expulsion. For the first 30 min after birth, prolactin concentrations in foals from oxytocin-induced mares appeared to be 2-fold higher than those from spontaneously foaling mares. Thereafter, prolactin values declined to baseline values by 48 hrs. When comparing cord arterial plasma with cord venous plasma in each group, prolactin concentrations were similar. However, the average prolactin levels in both the cord artery and vein appeared higher (ave: 1.1 ng/ml) in Group II and III than in Group I (less than 0.5 ng/ml). From these results, the authors suggest that 1) prolactin may have a role in regulating mammary secretory products in mares just prior to parturition; 2) oxytocin may increase prolactin secretion in preterm induced mares; 3) oxytocin induction may have a short term effect to increase circulatory prolactin concentrations in neonates in utero regardless whether their dams were treated preterm or term.     

Simultaneous fluorometric determination of vitamins A and E in serum

A simple fluorometric method suitable for serial determinations is reported for simultaneous determination of vitamins A and E in serum. The solvents are pretreated chemically and by distillation. After shaking with ascorbic acid in ethanol, the vitamins are extracted from the serum samples with petroleum ether. The extract is used for the determination. The sensitivity of the method is 20 micrograms/100 ml for vitamin A and 0.04 micrograms/ml for vitamin E. Recovery rates are between 87 and 106%. The method was tested on a total of 160 serum samples of healthy animals belonging to 8 different species. The results showed good agreement with the so-called reference values published in the literature.     

Effect of photoperiod on reproductive activity and hair in mares.

The effects of photoperiod on reproductive activity and hair changes in pony mares were studied in 2 experiments. In experiment I, the effect of a fixed daily photoperiod on the onset of the breeding season was studied in 36 mares from Nov 13, 1973, to June 13, 1974. The 4 treatment groups were as follows: daily photoperiod equivalent to the normal day length (control group); constant light 24 hours a day with no dark (L24:D0 group); 16-hour daily photoperiod with 8 hours of dark (L16:D8 group); and 9-hour daily photoperiod with 15 hours of dark (L9:D15 group). The intervals from beginning of experiment to 1st ovulation of breeding season, to shedding of hair in tufts, and to appearance of a smooth coat were shorter (P less than 0.05) for L16:D8 group (107.1 +/- 11.1, 56.0 +/- 0, and 145.8 +/- 4.0 days, respectively) than for control, L24:D0, and L9:D15 groups and were shorter (P less than 0.05) for L24:D0 group (less than 156.1 +/- 12.2, 99.5 +/- 9.5, and 173.9 +/- 9.9 days, respectively) than for control group (192.1 +/- 3.3, 134.9 +/- 8.9, and 205.0 +/- 0 days, respectively) or L9:D15 group (less than 200.3 +/- 5,8, 150.6 +/- 12.9, and 201.7 +/- 3.3 days, respectively). These intervals were not significantly different between the control group and the L9:D15 group, but fewer (P less than 0.05) mares in the L9:D15 group had at least 1 ovulation by termination of the project. In experiment II, the effect of photoperiod on onset of anestrus was studied in 3 groups of 7 mares each. Mares in group A, as part of a previous experiment, were induced to enter the breeding season earlier than normal by a gradual increase in daily photoperiod beginning on Oct 13, 1972. From Feb 16, 1973, to June 22, 1973, group A mares were maintained at a fixed daily photoperiod of 15 hours 23 minutes. Mares in group B, as part of a previous experiment, were kept under environmental conditions simulating normal conditions in southern Wisconsin. On June 22, 1973 (beginning of the present experiment), the following treatments began: groups A and B were exposed to natural day length. In addition, 7 mares (group C) were allotted from a band of mares that had been exposed to natural day length and were exposed to 15-hour 23-minute daily photoperiod from the beginning of the present experiment (June 22, 1973) to the end (June 22, 1974). The interval to onset of anestrus was longer (P less than 0.05) for group C mares (234.6 +/- 35 days) than for group B mares (133.6 +/- 16.5 days). Significant difference did not exist between group A (144.0 +/- 45.9 days) and group B. A fixed daily photoperiod of 16 or 24 hours induced early onset of the breeding season and early shedding of hair, with development of a smooth coat. A photoperiod of 9 hours retarded the onset of the breeding season. Mares induced to begin the breeding season earlier than normal did not become anestrous earlier than normal. Mares kept on a long daily photoperiod in the fall became anestrous later than normal.     

Estrone concentration in sow milk during and after parturition

Colostrum and milk samples were obtained from five Yorkshire gilts through manual expression of glands at the onset of parturition; at 1, 2, 4 and 8 h after birth of the first piglet and at 8-h intervals thereafter until 96 h. Oxytocin (30 units) was used to stimulate milk ejection for all samples except during parturition. Samples were frozen until subjected to a validated radioimmunoassay for estrone (E1). In a preliminary study no differences existed in concentrations of E1 among various glands. Therefore, mean of values obtained from three randomly selected glands was used for analysis in the main trial. Concentration of E1 at birth averaged 13.6 +/- 1.78 ng/ml (X +/- SE), and decreased to 6.05 +/- .80, 3.12 +/- .60, 1.42 +/- .30, .69 +/- .20 and .33 +/- .92 ng/ml at 4, 8, 16, 32 and 96 h, respectively. The postpartum decrease in the concentration of E1 in the milk is most likely due to the loss of the placental source.