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1.
Kinetic properties and substrate specificity of the lysine transport system in porcine mammary gland were studied using mammary tissue explants from nine lactating sows. Sodium dependence of lysine uptake was determined by replacing sodium in the medium with choline. Kinetic parameters of lysine uptake were determined using lysine concentrations from 5 microM to 5.12 mM. Competition of lysine uptake by other amino acids was determined using the cationic amino acids, arginine and ornithine, and using other essential amino acids. Transport of lysine was time-dependent and was unaffected by replacing sodium with choline. Lysine uptake occurred by a transport mechanism with a Km of approximately 1.4 mM and a Vmax of 7.9 mmol x kg cell water(-1) x 30 min(-1). Lysine uptake was inhibited by arginine and ornithine and by high concentrations of L-alanine, L-methionine, L-leucine, cycloleucine, and D-lysine, but not by 2-(methylamino)-isobutyric acid. This transport mechanism is the primary system responsible for uptake of cationic amino acids in lactating sow mammary tissue. The relatively high Km, compared with physiological blood concentrations of lysine, indicates that the kinetic properties of the lysine transport system should not be limiting to milk protein synthesis. Transmembrane transport of lysine by lactating sow mammary tissue should be a direct function of plasma concentrations. However, interactions of other amino acids with the uptake system may affect lysine uptake.  相似文献   

2.
Recent advances in swine protein nutrition are characterized by the development of functional amino acids (AA) in regulating fetal and postnatal survival, growth and development. These AA include arginine, glutamine, glutamate, proline, leucine, cysteine and tryptophan. Due to limited knowledge on AA nutrition, pork producers have traditionally paid little attention to supplementing the arginine family of AA to swine diets. Results of recent studies indicate that functional AA serve important regulatory functions in nutrient metabolism, protein turnover, and immune function, therefore enhancing efficiency of feed utilization by pigs. The underlying mechanisms include activation of nitric oxide, mammalian target of rapamycin, gaseous signaling, and AMP-activated protein kinase pathways, as well as anti-oxidative function. Dietary supplementation with arginine, glutamine, proline or leucine to weanling piglets enhances their growth performance. Arginine or glutamine is also effective in increasing milk production by lactating sows. Furthermore, supplementing arginine to the diet of pregnant gilts between days 30 and 114 of gestation increases the number of live-born piglets and litter birth-weight. Availability of feed-grade functional AA holds great promise for improving animal health and nutrient utilization in pig production worldwide. Additionally, feedstuffs of animal origin [e.g., blood meal (ring dried), feather meal (hydrolyzed), meat and bone meal, porcine protein meal, and poultry by-product meal (both feed- and petfood-grades)] are excellent and cost-effective sources of both essential and functional AA for formulating balanced swine diets. New knowledge on AA nutrition provides a much needed scientific basis for revising the next edition of swine nutrient requirements.  相似文献   

3.
The cellular uptake of branched-chain amino acids in mammary tissue is important for understanding their role in milk synthesis in the sow. This study characterized the kinetic properties and substrate specificity of the valine uptake system in the porcine mammary gland. Mammary tissue was collected from lactating sows at slaughter and tissue explants were incubated in media containing isosmotic salt and amino acids of interest, plus [3H]valine tracer. Valine uptake was time-dependent and was dependent on the presence of sodium, as indicated by a reduction in uptake when sodium in the medium was replaced by choline. The valine transport system in porcine mammary tissue had a Km of 0.64 mM, a Vmax of 1.84 mmol-kg cell water(-1) 30 min(-l), and a Kd (diffusion constant) of 1.16 L x kg cell water(-1) x 30 min(-1). Valine uptake was inhibited by leucine and alpha-aminoisobutyric acid and by high concentrations of L-alanine, L-lysine, cycloleucine, L-glutamine, and L-methionine, but not by 2-(methyl-amino)-isobutyric acid. This transport system is the primary system responsible for uptake of valine, and probably other branched-chain amino acids, in lactating sow mammary tissue. Physiological concentrations of valine in the blood are below the Km of the specific valine transport system and well below the diffusion uptake capabilities. The kinetic parameters of this valine transport system should not be limiting to valine uptake for milk protein synthesis. However, competition of valine uptake with branched-chain amino acids, as well as with other amino acids, may affect valine uptake in lactating tissue.  相似文献   

4.
Postnatal changes of plasma amino acids in suckling pigs   总被引:9,自引:0,他引:9  
Amino acids, ammonia, urea, orotate, and nitrate plus nitrite (stable oxidation products of nitric oxide) were determined in plasma of 1- to 21-d-old suckling pigs. Jugular venous blood samples were obtained from pigs at 1, 3, 7, 14, and 21 d of age for analysis of plasma amino acids and metabolites by HPLC and enzymatic methods. Plasma concentrations of arginine and its immediate precursors (citrulline and ornithine) decreased (P < 0.01) progressively (20 to 41%) with increasing age from 3 to 14 d. Plasma concentrations of glutamine declined (P < 0.01) progressively (10 to 31%) during the 1st wk of life. Plasma concentrations of branched-chain amino acids, threonine, and alanine decreased (P < 0.01) (5 to 12%) in 14- and 21-d-old pigs, compared with 1- and 3-d-old pigs. There were no postnatal changes (P > 0.05) in plasma concentrations of other amino acids. Plasma concentrations of ammonia increased (P < 0.01) by 18 and 46%, whereas those of nitrate plus nitrite decreased (P < 0.01) by 16 and 29%, in 7- and 14-d-old pigs, respectively, compared with 1- to 3-d-old pigs. Because arginine plays a crucial role in ammonia detoxification via the hepatic urea cycle and is the physiological substrate for nitric oxide synthesis, our results of the decreased plasma concentrations of arginine and nitrate plus nitrite, as well as the increased plasma ammonia concentration, indicate a hitherto unrecognized deficiency of arginine in 7- to 21-d-old suckling pigs. Arginine is an essential amino acid for piglets and has a great potential to enhance neonatal growth; therefore, further studies are necessary to elucidate the mechanism responsible for arginine deficiency in sow-reared piglets and to identify hormonal and metabolic means for improving neonatal arginine nutrition and growth.  相似文献   

5.
王若梦  董宽虎 《草地学报》2012,20(4):705-710
以苦马豆(Swainsonia salsula Taub.)为试验材料,通过8个不同浓度(0(CK),80,160,240,320,400,480和560 mmol·L-1 )NaCl胁迫,对苦马豆苗期脯氨酸(Pro)含量及吡咯啉-5-羧酸合成酶(P5CS)、鸟氨酸δ-氨基转移酶(δ-OAT)和脯氨酸脱氢酶(ProDH)活性进行测定,探讨苦马豆对NaCl胁迫的耐受程度和脯氨酸代谢与其耐盐性的关系,以期揭示苦马豆苗期脯氨酸代谢规律,为进一步研究其耐盐性奠定基础。结果表明:在NaCl胁迫下,苦马豆植株根冠比呈现先升高后降低的趋势,苦马豆中脯氨酸含量随NaCl浓度的升高而增大(P<0.05),在400 mmol·L-1 NaCl胁迫时,脯氨酸代谢最为旺盛;400 mmol·L-1 NaCl浓度为苦马豆耐盐阈值。随NaCl浓度的不断升高,苦马豆苗期脯氨酸合成由以鸟氨酸途径为主逐渐转变为以谷氨酸途径为主,鸟氨酸途径为辅的协同合成。  相似文献   

6.
Background: Persistent lactation,as the result of mammary cellular anabolism and secreting function,is dependent on substantial mobilization or catabolism of body reserves under nutritional deficiency.However,little is known about the biochemical mechanisms for nutrition-restricted lactating animals to simultaneously maintain the anabolism of mammary cells while catabolism of body reserves.In present study,lactating sows with restricted feed allowance(RFA)(n = 6),24% feed restriction compared with the control(CON) group(n = 6),were used as the nutrition-restricted model.Microdialysis and mammary venous cannulas methods were used to monitor postprandial dynamic changes of metabolites in adipose and mammary tissues.Results: At lactation d 28,the RFA group showed higher(P 0.05) loss of body weight and backfat than the CON group.Compared with the CON group,the adipose tissue of the RFA group had higher(P 0.05) extracellular glutamate and insulin levels,increased(P 0.05) lipolysis related genes(HSL and ATGL) expression,and decreased(P 0.05) glucose transport and metabolism related genes(VAMP8,PKLR and LDHB) expression.These results indicated that under nutritional restriction,reduced insulin-mediated glucose uptake and metabolism and increased lipolysis in adipose tissues was related to extracellular high glutamate concentration.As for mammary glands,compared with the CON group,the RFA group had up-regulated(P 0.05) expression of Notch signaling ligand(DLL3) and receptors(NOTCH2 and NOTCH4),higher(P 0.05) extracellular glutamate concentration,while expression of cell proliferation related genes and concentrations of most metabolites in mammary veins were not different(P 0.05) between groups.Accordingly,piglet performance and milk yield did not differ(P 0.05) between groups.It would appear that activation of Notch signaling and adequate supply of glutamate might assist mammogenesis.Conclusions: Mammary cell proliferation and catabolism of adipose tissues in nutrition-restricted lactating sows were associated with extracellular high glutamate levels.  相似文献   

7.
Introduction Proline is widely found in all types of mammalian tissue, and accounts for about 20% of the amino acids that constitute collagen (A dams 1970). Proline is nutritionally nonessential but biologically it is an important amino acid and consequently mammalian organisms synthesize the required amounts of proline even in the absence of sufficient proline consumption via food. The metabolism of higher animals is unique, and amino acid metabolism differs from one tissue to the next. Some organs are capable of synthesizing nonessential amino acids for use throughout the body. For example, arginine is primarily synthesized in the kidney and then released and distributed throughout the body. Pyrroline-5-carboxylate reductase is the enzyme responsible for the final stage of proline synthesis, and its activity has been confirmed in many important organs and tissue such as the cartilage, liver, small intestine, kidney and thymus gland (H erzfeld et al. 1977; S mith and P hang 1978). However, the different levels of pyrroline-5-carboxylate reductase activity among these organs has led to the belief that different amounts of proline are synthesized in these organs. In order to ascertain biological responses to dietary proline deficiency, it is important to identify the organs that release and distribute proline throughout the body when insufficient proline is consumed through the diet, thus reducing the blood proline concentration. Few studies have investigated this issue, but when ascertaining biological responses to dietary proline deficiency, it is more important to elucidate the effect of dietary proline deficiency on the metabolism of proline and other amino acids that are closely related metabolically to proline, in proline synthesizing organs. One of the most effective ways to assess amino acid metabolism in a target tissue of higher animals is to measure the difference between the arterial and venous concentrations of amino acids. I shikawa (1974) measured arteriovenous differences in order to examine the release of proline from the kidney and small intestine of fasted rats and the uptake of proline by the liver. In a previous study, it was found that when the plasma proline concentration was reduced to the fasting level by the consumption of a proline-deficient diet, proline was released from the kidney (W atanabe et al. 1995, 1997). In the present study, to ensure the induction of dietary proline deficiency, a completely purified diet containing all amino acids except for proline was prepared and fed to rats under experimental conditions. To investigate the role of the small intestine and liver in supplying and ingesting proline when the uptake of proline through food is restricted, the release and uptake of amino acids in the small intestine and liver were assessed by measuring carotid artery–portal vein and portal–hepatic vein differences in proline in rats.  相似文献   

8.
Recent advances in swine protein nutrition are characterized by the development of functional amino acids(AA)in regulating fetal and postnatal survival,growth and development. These AA include arginine,glutamine,glutamate,proline,leucine, cysteine and tryptophan. Due to limited knowledge on AA nutrition,pork producers have traditionally paid little attention to supplementing the arginine family of AA to swine diets. Results of recent studies indicate that functional AA serve important regulatory functions in nutrient metabolism,protein turnover, and immune function,therefore enhancing efficiency of feed utilization by pigs. The underlying mechanisms include activation of nitric oxide,mammalian target of rapamycin,gaseous signaling,and AMP-activated protein kinase pathways, as well as anti-oxidative function. Dietary supplementation with arginine,glutamine, proline or leucine to weanling piglets enhances their growth performance. Arginine or glutamine is also effective in increasing milk production by lactating sows. Furthermore,supplementing arginine to the diet of pregnant gilts between days 30 and 114 of gestation increases the number of live-born piglets and litter birth-weight. Availability of feed-grade functional AA holds great promise for improving animal health and nutrient utilization in pig production worldwide. Additionally, feedstuffs of animal origin[e. g. , blood meal (ring dried),feather meal(hydrolyzed),meat and bone meal, porcine protein meal,and poultry by-product meal(both feed- and petfood-grades )]are excellent and cost-effective sources of both essential and functional AA for formulating balanced swine diets.New knowledge on AA nutrition provides a much needed scientific basis for revising the next edition of swine nutrient requirements.  相似文献   

9.
Sixteen Hereford and 16 Holstein heifers were used to study the relationship of milk production potential to mammary development and differentiation. Heifers were slaughtered 150, 180, and 260 days of first gestation and at 49 days of first lactation. Prolactin binding capacity of mammary tissue was 2.5 fold higher in dairy than beef heifers at day 260 of gestation (27.2 vs 11.0 fmols/mg protein). In both breeds, maximal growth hormone binding in liver coincided with the beginning of the rapid phase of mammary growth at 180 days. Mammary tissue from dairy heifers released more casein and alpha-lactalbumin during in vitro incubations than tissue from beef heifers. No differences were observed between breeds with respect to incorporation of [14C]acetate into lipids. Mass of dairy mammary tissue at 49 days of lactation was 3.3 times greater (16.4 vs 4.9 kg) and produced 5.7 times more milk (20.3 vs 3.5 kg/day) than its beef counterpart. The total DNA content and the RNA/DNA ratio of lactating dairy mammary tissue was approximately twice that of lactating beef mammary tissue. The data suggested that the higher milk production observed in dairy cattle is a result of a greater number of secretory cells and greater activity per cell.  相似文献   

10.
Mastitis is inflammation of mammary gland affecting all the species of domestic animals. Fragments of the mitochondrial genome released from dying cells are considered surrogate markers of mitochondrial injury. We hypothesized that bovine mastitis would be associated with increased cell free mitochondrial DNA (mtDNA) content in serum and milk. Milk and serum samples were collected from sub-clinical mastitic and normal animals. Mastitis was confirmed by California mastitis test and bacterial isolation. Oxidative stress, nitric oxide and inflammatory cytokines were also estimated. Real time polymerase chain reaction was conducted in serum and milk from sub-clinical mastitic animals and compared with healthy animals targeting the mtDNA genes cytochrome b. Mastitis animals showed higher oxidative stress markers and nitric oxide along with higher level of inflammatory cytokines. Cell free mtDNA was significantly higher in serum and milk of mastitic animals comparing to that of healthy control. The higher cell free relative mtDNA content in mastitis animals indicates injury to the mammary epithelial cells and thereby releasing the mtDNA in the milk and blood. This mtDNA may be a bio-marker of oxidative stress and tissue injury in bovine mastitis.  相似文献   

11.
Two experiments were conducted with young pigs to determine the efficacy of ornithine (Orn) or citrulline (Cit) as precursors of arginine (Arg). In Exp. 1, pigs were individually fed an Arg-deficient, semipurified diet (.18% Arg) supplemented with .3% Arg or an equimolar quantity of Orn or Cit. Supplemental Arg or Cit increased rate and efficiency of weight gain, but Orn addition was without effect. Free Arg in plasma 3 h post-prandial was increased by addition of either Arg or Cit to the basal diet. Liver Arg was elevated by dietary addition of Arg, Orn or Cit; kidney Arg and Orn were elevated only in pigs receiving supplemental Cit. Arginine or Cit addition to the diet increased Arg concentration in muscle tissue, but muscle Orn was unresponsive to any of the supplements fed. In Exp. 2, pigs were again fed the Arg-deficient, semipurified diet supplemented with .3% Arg or four times an isomolar quantity of ornithine. Arginine addition to the diet increased weight gain and feed efficiency, while Orn supplementation was without effect. Plasma Orn was increased by excess Orn, while plasma Cit was unaffected by supplemental Arg or Orn. Moreover, excess Orn increased free Orn and proline (Pro) in liver, kidney and muscle. Free Cit, however, increased only in liver from feeding excess Orn. In addition, excess Orn decreased both plasma ammonia and free glutamine (Gln) concentration in brain. Arginase activity was roughly 10, 40 and 100 times greater in hepatic tissue than in renal cortex, renal medulla or intestinal mucosa, respectively, while hepatic ornithine transcarbamoylase (OTC) activity was about 15 times greater than the activity present in mucosa tissue. Renal OTC activity was too low to be accurately measured.  相似文献   

12.
The effects of long-term administration of recombinant bovine somatotropin (rbST) on glucose turnover and the utilization of glucose in the mammary gland using a continuous infusion of [3-3H]glucose and [U-14C]glucose in lactating crossbred Holstein Friesian(HF) cattle were investigated. Glucose turnover of rbST-treated animals was significantly higher than those of control animals ( P  < 0.05) in mid lactation, while plasma glucose concentrations were not affected. The utilization of glucose of non-mammary tissues of rbST-treated animals significantly increased ( P  < 0.05) as lactation advanced. The glucose taken up by the mammary gland in early lactation increased flux through the lactose synthesis and the pentose cycle pathway with significant increases in NADPH formation for fatty acid synthesis during rbST administration. The utilization of glucose carbon incorporation into milk appeared to increase in milk citrate and milk triacylglycerol but not for milk lactose as lactation advances in rbST-treated animals. The stimulant effect for milk yield by rbST treatment was transiently and significantly increased in early lactation and was decreased in late lactation even though there was a high level of udder blood flow. These findings demonstrate that the regulation of biosynthetic capacity within the mammary gland would be influenced more by local than by systemic factors. The proportion of glucose would be metabolized less for lactose synthesis, but metabolized more via the Embden-Meyerhof pathway and the tricarboxylic acid cycle as lactation advances.  相似文献   

13.
本试验旨在研究妊娠早期饲粮中添加N-氨甲酰谷氨酸(NCG)对母羊胚胎存活及相关血液指标的影响,并对其作用机制进行初步探讨。选择发情正常、健康状况良好的湖羊50只,随机分为2组(对照组和NCG试验组),每组25只母羊,自配种当天开始给母羊分别饲喂基础饲粮(对照组)和基础饲粮+0.11%NCG(NCG组),饲喂期38 d。测定妊娠第19和38天母羊血浆游离氨基酸、总一氧化氮合酶(TNOS)、内皮型一氧化氮合酶(eNOS)、诱导型一氧化氮合酶(iNOS)、一氧化氮(NO)、雌二醇、孕酮的浓度;38 d时每组各屠宰7只妊娠母羊,测定妊娠母羊的黄体数和活胎儿数等指标。结果显示,与对照组相比,妊娠第38天时,NCG组每只母羊总胎儿数增加了79.72%(P<0.05),活胎儿数增加了79.72%(P<0.05),胎儿形成指数增加了0.26(P<0.05),胎水体积增加了72.89%(P<0.05),活胎儿总重提高了71.13% (P<0.05);NCG组妊娠第19天的甘氨酸、蛋氨酸、赖氨酸、精氨酸、NO、iNOS、eNOS和孕酮的浓度显著高于对照组(P<0.05),NCG组妊娠第19天的瓜氨酸和脯氨酸极显著高于对照组(P<0.01);NCG组妊娠第38天的精氨酸、脯氨酸和NO显著高于对照组(P<0.05),NCG组妊娠第38天的iNOS和eNOS的浓度极显著高于对照组(P<0.01)。由此,妊娠早期饲粮中添加NCG提高了胚胎和胎儿的存活,增加了妊娠母羊第38天的总胎儿数和活胎儿数,改善了母羊的繁殖性能,其作用机制可能是NCG促进了母羊内源性精氨酸的合成,提高了母羊血浆精氨酸、NO和孕酮含量,改善了子宫内环境和营养供给,使之有利于胚胎着床和妊娠维持。  相似文献   

14.
The mouse whey acidic protein (WAP) gene was introduced into the genome of pigs and its expression was analyzed in the mammary gland. Mouse WAP was detected in milk of lactating females from five lines at levels between .5 and 1.5 g/liter, thereby representing as much as 2% of the total milk proteins. The corresponding mRNA was expressed in mammary tissue at levels similar to those of pig beta-lactoglobulin and beta-casein. The pattern of WAP secretion in three pigs over a period of 6 wk was quantitatively similar to that of pig beta-lactoglobulin. From the eight transgenic pigs analyzed, three successfully completed one lactational period, but five pigs stopped lactating a few days after parturition. Our results show that it is possible to produce large quantities of a foreign protein in milk of pigs over a full lactational period. However, expression of WAP can compromise the mammary gland and render it nonfunctional.  相似文献   

15.
Effects of exposure to hot environment on urea metabolism were studied in lactating Holstein cows. Four cows were fed ad libitum a total mixed ration and housed in a temperature‐controlled chamber at constant moderate (18°C) or high (28°C) ambient temperatures in a cross‐over design. Urea nitrogen (N) kinetics was measured by determining urea isotopomer in urine after single injection of [15N2]urea into the jugular vein. Both dry matter intake and milk yield were decreased under high ambient temperature. Intakes of total N and digestible N were decreased under high ambient temperature but urinary urea‐N excretion was increased. The ratio of urea‐N production to digestible N was increased, whereas the proportion of gut urea‐N entry to urea‐N production tended to be decreased under high ambient temperature. Neither return to the ornithine cycle, anabolic use nor fecal excretion of urea‐N recycled to the gut was affected by ambient temperature. Under high ambient temperature, renal clearance of plasma urea was not affected but the gut clearance was decreased. Increase of urea‐N production and reduction of gut urea‐N entry, in relative terms, were associated with increased urinary urea‐N excretion of lactating dairy cows in higher thermal environments.  相似文献   

16.
为探讨脾源性酪氨酸激酶(spleen tyrosine kinase,SYK)的表达与奶牛乳腺发育和泌乳功能之间的关系,试验采用Western blotting和激光共聚焦显微技术对泌乳期高乳品质、低乳品质及干乳期的中国荷斯坦奶牛乳腺组织中SYK的表达含量和表达部位的变化进行研究。结果表明,干乳期奶牛乳腺组织中SYK的表达显著高于泌乳期奶牛乳腺组织(P<0.05),泌乳期高乳品质、低乳品质奶牛乳腺组织中SYK的表达差异不显著(P>0.05);在干乳期SYK主要在乳腺导管上皮细胞的胞质中表达,而在泌乳期SYK在腺泡上皮细胞中表达。结果提示SYK是乳腺上皮细胞增殖与分化的调节因子,主要参与干乳期乳腺组织的重建过程。  相似文献   

17.
The aim of this study was to compare the ability of milk macrophages and macrophages from the mammary gland secretions during the mid-dry period for their interaction with the mastitis-causing Streptococcus uberis. We also aimed to determine if S. uberis induced the release of the cytokine tumour necrosis alpha (TNF-alpha) and the bactericidal moiety nitric oxide (NO) from milk macrophages of lactating cows and macrophages from the mammary gland secretions at the mid-dry period. Macrophages were isolated from the mammary gland secretions of cows during the mid-lactation or mid-dry period, and compared with blood monocytes for their interaction with the important mastitis-causing pathogen S. uberis. When infected in vitro with S. uberis, milk macrophages from lactating cows with S. uberis released modest amounts of the cytokine tumour necrosis factor alpha (TNF-alpha) (139 pg/ml) and the bactericidal moiety nitric oxide (NO) (3-4 microM of nitrite). Blood monocytes from lactating cows released significantly higher amounts of TNF-alpha (345 +/- 143 pg/ml) and NO (7 +/- 2 microM of nitrite) after interaction with S. uberis, compared to milk macrophages (P < 0.01 for both TNF-alpha and NO). Stimulation of blood monocytes with the cytokine interferon-gamma (IFN-gamma) enhanced significantly the release of NO and TNF-alpha, but IFN-gamma did not significantly enhance the production of NO and TNF-alpha by milk macrophages from lactating cows. Milk macrophages from all lactating cows failed to kill S. uberis efficiently, and this lack of killing was unaffected by prior treatment with gamma interferon (IFN-gamma) (P > 0.05). Rather, S. uberis multiplied significantly inside infected milk macrophages from lactating cows, with a two-fold increase in bacterial numbers at 2 h post-infection. Milk macrophages from lactating cows were able however, to kill a significant proportion (50-60%, P < 0.01) of phagocytosed Staphylococcus aureus. Blood monocytes from all cows were found to exert significant bactericidal activity against S. uberis. There were no significant differences in the bactericidal activity of milk macrophages obtained from lactating cows with low somatic cell counts (SCC; < 10(5) ml(-1)) compared with those with a mildly elevated SCC (> 10(5) ml(-1)) (P > 0.05). In contrast, mammary gland secretion macrophages isolated from the same cows in the mid-dry period killed a significant proportion of phagocytosed S. uberis (50-65% of ingested S. uberis killed, P < 0.01) although cytokine production in response to in vitro bacterial infection was low. We conclude that the bactericidal activity of mammary gland secretion macrophages against a virulent strain of S. uberis is low during the lactation period. In addition, our data indicate that S. uberis is not a strong inducer of NO and TNF-alpha in macrophages from the milk or mammary gland secretions of cows during the drying off period. Finally, IFN-gamma does not activate milk macrophages or macrophages from cows during the lactating period or mammary gland secretions during the drying off period.  相似文献   

18.
In a previous study, ornithine addition to an arginine-deficient diet did not improve whole-body arginine status in enterally-fed piglets; however, the metabolic fates of the supplemental ornithine were not studied. This experiment determined the metabolic fates of the supplemental ornithine and whether ornithine metabolism was affected by the addition of -ketoglutarate. Male piglets (n = 20, 1.8 kg), fitted with gastric catheters for diet and isotope infusion, portal vein catheters for isotope infusion and femoral vein catheters for blood sampling (d 0), received 2 d of a complete diet, followed by 5 d of 1 of 4 test diets: the arginine-deficient diet (basal), or the basal diet with either -ketoglutarate [ +  - KG; 4.6 mmol/(kg d)], ornithine [ + Orn; 9.2 mmol/(kg d)] or both [ +  - KG/ + Orn; 4.6 mmol/(kg d)  - ketoglutarate + 9.2 mmol/(kg d) ornithine]. Piglets received primed, constant infusions of [1-14C]ornithine infused intragastrically (either d 5 and d 7) to determine ornithine kinetics, and [guanido-14C]arginine intragastrically to measure arginine flux (d 6). Piglets receiving the ornithine-containing diets had a higher intragastric ornithine flux (P < 0.0001) and ornithine oxidation (P < 0.05). Ornithine supplementation did not increase arginine synthesis, although the ornithine supplemented piglets had a greater conversion of ornithine to proline (P < 0.0001). The fates of supplemental ornithine in piglets fed an arginine-deficient diet appear to be oxidation and proline synthesis; this was not affected by the presence of -ketoglutarate.  相似文献   

19.
Effects of increased ammonia and/or arginine absorption across the portal-drained viscera (PDV) on net splanchnic (PDV and liver) metabolism of nitrogenous compounds and urinary N excretion were investigated in six catheterized Hereford x Angus steers (501 +/- 1 kg BW) fed a 75% alfalfa:25% (as-fed basis) corn-soybean meal diet (0.523 MJ of ME/[kg BW(0.75).d]) every 2 h without (27.0 g of N/kg of dietary DM) and with 20 g of urea/kg of dietary DM (35.7 g of N/kg of dietary DM) in a split-plot design. Net splanchnic flux measurements were obtained immediately before beginning and ending a 72-h mesenteric vein infusion of L-arginine (15 mmol/h). For 3 d before and during arginine infusion, daily urine voided was measured and analyzed for N composition. Feeding urea increased PDV absorption (P < 0.01) and hepatic removal (P < 0.01) of ammonia N, accounting for 80% of increased hepatic urea N output (P < 0.01). Numerical increases in net hepatic removal of AA N could account for the remaining portion of increased hepatic urea N output. Arginine infusion increased hepatic arginine removal (P < 0.01) and hepatic urea N output (P < 0.03) and switched hepatic ornithine flux from net uptake to net output (P < 0.01), but numerical changes in net hepatic removal of ammonia and AA N could not account fully for the increase in hepatic urea N output. Increases in urine N excretion equaled quantities of N fed as urea or infused as arginine. Estimated salivary urea N excretion was not changed by either treatment. Urea cycle regulation occurs via a complex interaction of mechanisms and requires N sources other than ammonia, but the effect of increased ammonia absorption on hepatic catabolism of individual AA in the present study was not significant.  相似文献   

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