Effects of biotechnical management procedures on blood parameters in gilts. 3. Lipids

Suisynchron treatment was applied to platform-kept gilts over 20 days. The dosage was 100 mg per animal and die. This was followed by 1,000 I.U. PMS and 250 I.U. HCG. Artificial insemination was applied five days after the first hormone administration and followed by one Gravigonan injection after another twelve to 15 days. Blood samples were drawn from those animals as well as from 20 gilts synchronised in the above way and another 20 untreated gilts from a production unit during the various phases of treatment and cycle. Those samples were used for assessment of cholesterol, lipoid-P, free fatty acids, triglyceride, and beta-lipoproteids. The levels of free and total cholesterol went up along with Suisynchron feeding, whereas lipoid-P and beta-lipoproteids declined. Free fatty acid levels went down with significance (P less than 0.01), and triglycerides increased (P less than 0.05). Cholesterol levels were not altered by PMS/HCG administration. The levels of lipoid-P, free fatty acids, and beta-lipoproteids rose to their magnitudes prior to Suisynchron treatment. Tirglycerides rose by 50 per cent. At the time of full oestrus triglyceride levels doubled (P less than 0.01). Unimportant rises were recorded also for cholesterol, beta-lipoproteids, free fatty acids, and lipoid-P. In animals with spontaneous oestrus all lipid parameters were ligher than in sows with full oestrus after synchronisation.     

Effects of biotechnical management procedures on blood parameters in gilts. 2. Protein-bound iodine and copper

Two groups of twelve gilts each kept on platforms were synchronised in two passes over 20 days, using 100 mg Suisynchron per animal and die followed by PMS treatment (1,000 I.U. Intergonan) and HCG treatment (250 I.U.). Complement fixation occurred five days after the first hormone application and was followed twelve to 15 days later by another phase of treatment, using Gravigonan (250 I.U. follicle-stimulating hormone (FSH), 500 I.U. HCG, 1 mg oestradiol benzoate in 10 ml serum of swine). Blood samples were continuously drawn during the various phases of treatment and cycle from the above animals as well as from 20 gilts synchronised in the above way and from another 20 untreated gilts. Protein-fixed iodine and copper levels were assessed from those samples. The protein-fixed iodine and copper levels of the blood were significantly reduced (P less than 0.01) by synchronisation, using Suisynchron. None of the two parameters was particularly affected by PMS and HCG treatments. Blood-borne protein-fixed iodine and copper was increased by administration of gonabione. Both parameters went up further during full oestrus at which date they were higher in untreated animals than in synchronised. (Protein-fixed iodine: 3.50/226micrograms/100 ml; P less than 0.01; copper: 0.283/0.234 mg/100 ml; P less than 0.01).     

Effect of anticoagulants on the change of blood parameters in diestric gilts

The above problem was studied by furnishing four groups of six gilts each with ear catheters for the following intravenous catheter treatment: 2,500 IU heparin per die over ten days, supported by two daily oral applications of 1 g Falithrom, or 2,500 IU heparin plus two daily applications of 1 g Falithrom, all intravenously. The last group remained untreated for control. One day of the dioestrus was chosen for catheter bleeding of all animals at 6 a.m., 8 a.m., noon, and 4 p.m. and subsequent determination from the plasma of free fatty acids, copper, inorganic phosphorus, total protein, albumin, globulin, chloride, urea, cholesterol, alkaline phosphatase, blood sugar, and beta-lipoproteides. Significant differences regarding these parameters between the various groups were not even established, if alpha = 0.25. The anticoagulants used in the study may be used without any reservation for catheter rinsing and clearing and will not cause any significant change in the levels of the blood parameters.     

Acid and alkaline phosphatase in bovine antral follicles

Acid and alkaline phosphatases were measured in the follicular fluid of 766 individual follicles from 96 cows. Follicles were obtained by bilateral ovariectomy or at slaughter from animals at various stages of the estrous cycle and pregnancy. Mean follicle size varied with the physiological state of the cow (P less than .0001). Acid phosphatase activity (U/microliters) varied inversely with follicle size (P less than .001) but not with stage of the estrous cycle or gestation. Total acid phosphatase activity per follicle increased with follicle size (P less than .05). Neither acid phosphatase nor alkaline phosphatase concentration was associated with atresia. Alkaline phosphatase activity (U/microliters) was greater in the smallest follicles (less than 50 microliters) than in other size groups (P less than .0001). Alkaline phosphatase activity (U/microliters) was greater (P less than .05) during the preovulatory phase of the estrous cycle than during other phases. A high concentration of follicular fluid phosphatases cannot be used as a marker for atresia but is characteristic of healthy small antral follicles.     

Effect of various injection times in ovulation stimulation in gilts following previous biotechnical puberty induction

A conclusion derived from the slaughter of 69 gilts was that no role was played by the time intervals tested between puberty induction, using 500 IU of PMS and 250 IU HCG, and subsequent action to stimulate ovulation. Very good follicle maturation and follicle formation as well as the usual uterus and ovary weights were observed, no matter whether 500 IU of HCG were injected to stimulate ovulation 54, 72 or 78 hours after puberty had been induced. Ovulation was very efficiently synchronised by 500 IU of HCG in all three groups in which the ovulation figures relative to follicle formation 120 hours from puberty induction were 92.6, 94.6 or 92.7 per cent.     

Effect of L-carnitine supplementation on performance parameters in gilts and sows

The effect of L-carnitine supplementation during pregnancy and lactation on performance parameters of sows was studied. The trial comprised a total of 127 sows (40 gilts, 87 mature sows) which were divided into a control and a treatment group. All animals were fed individually and received basic feed mixtures for pregnancy and lactation with low carnitine concentrations (gestation diet: 4.7 mg/kg feed, lactation diet: 12.5 mg/kg feed). The rations of the sows in the treated group were supplemented with 125 mg L -carnitine per head and day during pregnancy and 250 mg L -carnitine per head and day during lactation. The animals of the control group received identical feed mixtures in identical amounts, but without the L -carnitine supplement. L -carnitine supplementation resulted in higher sow liveweight gains between day 1 and day 85 of pregnancy. The number of piglets per litter and the number born alive did not differ between the control sows and those treated with L -carnitine. However, the L -carnitine-supplemented sows produced only half as many non-viable piglets as the control animals. Moreover, litter weight and mean birth weight of piglets from L -carnitine-treated sows were higher than in the control sows. This effect was more marked in gilts (+8% higher litter weight, +9% higher piglet weight) than in sows (+7% and +6%, respectively). Piglets from sows whose ration was supplemented with L -carnitine showed higher liveweight gains during the suckling period (+12% for gilts, +4% for sows), which is why litter weights post weaning were also higher among the sows treated with L -carnitine than in the control sows (+14% for gilts, +10% for sows). Overall, the study shows that dietary supplementation with L -carnitine during pregnancy and lactation improves the reproductive performance of sows.     

Effect of colostrum ingestion on gamma-glutamyltransferase and alkaline phosphatase activities in neonatal pups.

Analysis of hepatic enzyme activities in serum samples from 1- to 3-day-old pups revealed alkaline phosphatase (ALP) activities that were 30 times higher and gamma-glutamyltransferase (GGT) activities that were 100 times higher than activities in clinically normal adult dogs. A study was conducted to investigate high enzyme activity in pups and to determine whether there is any association between serum enzyme activity and colostrum ingestion, passive transfer of maternal serum enzyme (in colostrum or in utero), or excessive renal or hepatic tissue enzymes. Serum enzyme activity was quantified in 15 neonatal pups before and after ingestion of colostrum and in 3 colostrum-deprived neonates fed a milk substitute. Serum samples were collected on postpartum days 0, 1, 10, 15, and 30. Enzyme activity was also quantified in serum from pregnant and lactating bitches (collected on days -2, 0, 1, 10, 30), hepatic and renal tissue from clinically normal adult dogs and 1-day-old pups, colostrum, milk (collected on days 10 and 30), and milk replacer. Significant (P less than 0.01) differences in serum GGT and ALP activities between colostrum-deprived and suckling pups did not exist before initial feeding. Significant (P less than 0.001) increases in serum GGT and ALP activities developed within 24 hours in suckling pups, but not in the colostrum-deprived pups. At 10 and 30 days after birth, serum GGT and ALP activities were less than values before suckling in all pups. Enzyme activities in bitches' serum remained within the normal range for adult dogs throughout whelping and lactation.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effect of various doses HCG on ovulation stimulation in gilts following previous biotechnical puberty induction

The effects of various doses of human chorionic gonadetropine (HCG) to stimulate ovulation in 86 gilts in which puberty had been induced by administration of 500 IU of pregnant mare serum (PMS) and 250 IU of HCG were established by slaughter. Only 26.9 per cent of the group without HCG had completed ovulation 120 hours from puberty induction, but 93.5 per cent had done so in the group which had received additional 500 IU or HCG 78 hours after the PMS/HCG injection. Ovulation was completed by 71.4 per cent of those sows which had been stimulated, using 250 IU of HCG. More accurate timing of ovulation in animals of one and the same group can be helpful in better insemination timing.     

Effect of estradiol-17 beta treatment of gilts on blood mononuclear cell functions in vitro.

Porcine blood mononuclear cells (BMC) were exposed to prepartum concentration of estrogen in gilts before acquisition (in vivo), and their subsequent reactivity (in vitro) was explored. In a cross-over experimental designed study, 6 ovariectomized gilts were injected once with 3.75 mg of estradiol-17 beta benzoate in arachidic oil or with arachidic oil only during 2 experiments. The ability of their BMC to proliferate in response to stimulation with phytohemagglutinin, concanavalin A, and pokeweed mitrogen was assayed in cultures of blood and in cultures of purified BMC. After 2 days of mitogen stimulation, activity of accessible interleukin 2 was quantified in supernatants obtained from cultures of purified BMC and supernatants of blood cultures stimulated with pokeweed mitogen. Also, production of immunoglobulins by purified BMC in response to polyclonal stimuli was measured. Three days after treatment with estradiol, the proliferative response was suppressed in blood cultures stimulated with concanavalin A (P less than 0.05) and phytohemagglutinin (P less than 0.07). Effects of estradiol treatment were not found in any of the assays performed with purified BMC. We, therefore, assumed that in vivo exposure to estradiol can affect the function of porcine BMC; however, this was only evident when the in vitro assays were performed on blood cultures.     

Alkaline phosphatase and alkaline phosphatase isoenzymes in the cat

Feline alkaline phosphatase and alkaline phosphatase isoenzymes have been studied in tissue and serum. Alkaline phosphatase from various organs was quantitated and then subjected to cellulose acetate electrophoresis. The effects of bile duct ligation, prednisolone treatment and phenobarbital treatment on serum alkaline phosphatase was measured. The diagnostic importance of feline serum alkaline phosphatase levels is discussed in light of the results of this and other studies.     

Origin of serum alkaline phosphatase in the dog.

The origin of canine serum alkaline phosphatase (ALP) was investigated by various means. On the basis of electrophoretic migration, neuraminidase treatment, thermal denaturation, and chromatographic fractionation, canine serum was found to contain ALP principally of hepatic origin. There was evidence of only a minor portion of ALP being of osseous origin. Intestinal ALP was not detected in canine serum when monitored by immunochemical technique, L-phenylalanine inhibition, and thermal denaturation.     

Isoenzymes of alkaline phosphatase in serum of lambs and ewes.

Electrophoresis in polyacrylamide gels was used to identify isoenzymes of serum alkaline phosphatase in sheep. Skeletal isoenzyme predominated in the serum of lambs and liver, skeletal and intestinal isoenzymes were found in the serum of adult ewes. In r ewes (R-r-i blood group system) intestinal isoenzyme activity was 67 per cent of total serum activity; in R ewes intestinal activity was only 36 per cent of total activity. Relative activities of the three isoenzymes differed greatly within individual ewes and between individual ewes during pregnancy and lactation.     

后备母猪的引进与管理

对于一个需要进行连续繁殖生产的猪场来说,引进后备母猪是一项必不可少的工作。本人曾在《当代畜禽养殖业》2003年第11期上发表了“引进种猪的方法”一文,主要对引进种猪的注意事项进行了简单总结。根据目前刚刚开始从事养猪业的个体饲养场(户)比较多(猪价低谷时投资)的特点,以     

小母猪的选留和育肥期的饲养管理

小母猪的选育和育肥期的饲养管理对其终生繁殖性能有着至关重要的作用，做好小母猪的前期选育和育肥期的饲养管理，可以在很大程度上提高小母猪的生产、繁殖性能及延长使用年限。１小母猪的选留 在后备母猪转入育肥群进行育肥阶段，作为养猪生产者必须做好对后备猪的选留。当仔猪达到２８或３５日龄，体重达７．５ｋｇ以上时进行第一次筛选。首先参考其父母代生产成绩，无遗传缺陷，同胞数不少于７头，有效乳头至少６对以上发育良好且对称或均匀，不少于３对在脐部之前的，无瞎奶和赘生小乳头，阴户端正，体躯匀称，肢蹄健壮，前胸和后臀丰…     

The influence of fasting on blood glucose,triglycerides, cholesterol,and alkaline phosphatase in rats

Serum concentrations of glucose, cholesterol, triglycerides, and serum alkaline phosphatase activity were measured over different periods of time of food deprivation in male rats. Thirty percent of non-fasted rat's sera was found to be lipemic. At 16 hours of fasting, glucose levels dropped by 30% compared to the level of the non-fasting control group, and remained at a relatively constant level for up to 48 hours of fasting. Triglyceride concentrations decreased at 16 hours after fasting. Serum cholesterol levels were not changed at any of the fasting periods compared to the non-fasted control group. Alkaline phosphatase activity was decreased at 8 hours of fasting, with further declines in activity of the serum enzyme seen at 16, 24, and 48 hours of fasting. It was concluded that at 16 to 18 hours fasting, a non-absorptive state had been reached in male rats.