Reducing effect of dietary anacardic acid on body fat pads in rats

We have previously shown that anacardic acid has an uncoupling effect on oxidative phosphorylation in rat liver mitochondria using succinate as a substrate (Toyomizu et al. 2000). In the present study, in order to clarify whether or not anacardic acid could be used advantageously as a special feed/food supplement to reduce fat deposition through the uncoupling action, two sets of experiments were conducted to determine quantitatively the effect of dietary anacardic acid (0.1% w/w) supplementation. More specifically, effects on growth, feed efficiency, fattening, and levels of several constituents of blood serum in rats fed normal and low protein–high carbohydrate (CHO) diets were examined. There were no significant differences in bodyweight gain, feed consumption and feed efficiency among the experimental groups. For the total fat pad content, including inguinal and epididymal fat, significant interaction was shown between both treatments: dietary anacardic acid at 0.1% w/w significantly decreased the total fat pad content in rats fed the CHO diet, but not in rats fed the normal diet. Weights of heart, spleen and brown adipose tissue were not affected by either the dietary treatment or anacardic acid, while both liver and kidney weights decreased with feeding of anacardic acid at 0.1% w/w, but were not affected by the CHO diet. Anacardic acid supplementation in the diet had no effect on serum glutamic oxaloacetic transaminase, alkaline phosphatase or lactate dehydrogenase levels, suggesting that the dysfunction of liver or kidney may not be induced by dietary anacardic acid. The results of the present study reveal a unique function of anacardic acid in that, for dietary conditions enhancing body fat deposition, that is consumption of a diet high in carbohydrates, dietary anacardic acid has the potential to decrease body fat deposition. A possible mechanism for differences observed in anacardic acid‐induced regulation of body fat pad content between rats fed the normal and CHO diets, based on uncoupling action of anacardic acid on the mitochondrial oxidative phosphorylation, is discussed.     

无氮饲粮中铬添加水平对大鼠器官指数、肠道黏膜形态及血清指标的影响

本试验旨在研究无氮饲粮中添加不同水平丙酸铬(Cr Pro)对Sprague Dawley(SD)大鼠器官指数、肠道黏膜形态及血清指标的影响。试验选用36只体重均一的断奶雌性SD大鼠,分为3个处理,每个处理6个重复,每个重复2只鼠。各处理分别饲喂无氮基础饲粮(对照组,含铬0.08 mg/kg)及在基础饲粮上分别添加0.2和1.0 mg/kg Cr(以Cr Pro形式)的试验饲粮,试验期21 d。结果显示:1)饲粮添加0.2 mg/kg的Cr显著提高了大鼠脾脏指数(P0.05)。2)饲粮添加1.0 mg/kg的Cr显著提高了大鼠空肠绒毛高度与隐窝深度的比值(P0.05)。3)与对照组相比,饲粮添加1.0 mg/kg的Cr显著提高了血清白蛋白和尿酸含量(P0.05),饲粮添加0.2 mg/kg Cr显著提高了血清尿酸含量(P0.05)。由此可见,无氮饲粮中补充适量铬对改善大鼠机体免疫器官指数、肠黏膜形态及血清蛋白质代谢有一定的作用。     

吡啶甲酸铬对吉富罗非鱼生长、饲料利用和非特异性免疫功能的影响

本试验研究饲料不同水平吡啶甲酸铬对其生长、饲料利用,体成分、血液生化指标和非特异性免疫功能的影响。600尾吉富罗非鱼分为5个处理组,每个处理各设4个重复,每重复30尾鱼。每个处理铬添加量分别为0、0.4、0.8、1.2 mg/kg和10.0 mg/kg,在0.38 m3玻璃纤维钢桶中用开放式流水养殖,饲养8周。结果表明,饲料中添加吡啶甲酸铬对吉富罗非鱼的增重率、特异生长率、饲料系数、蛋白效率及蛋白质沉积率均有显著影响(P<0.05)。当铬添加量为0～0.8 mg/kg时,随着添加量增加,可显著提高吉富罗非鱼增重率、特定生长率、蛋白质效率和蛋白质沉积率(P<0.05),显著降低饲料系数(P<0.05),但对成活率和肝体比无显著影响(P>0.05);当饲料中添加为1.2 mg/kg～10.0 mg/kg时并未能进一步提高罗非鱼的生长和饲料利用。同时,铬添加水平为0～0.8 mg/kg,随着添加水平增加,显著提高吉富罗非鱼全鱼的蛋白质和磷含量(P<0.05),显著降低全鱼水分、脂肪和灰分含量(P<0.05),并显著提高吉富罗非鱼血清总蛋白含量以及肝胰脏AKP、ACP和LZM的活性(P<0.05),显著降低血清葡萄糖含量(P<0.05),但对血清胆固醇和甘油三酯含量及肝胰脏T-SOD活性无显著影响(P>0.05)。当饲料中添加铬1.2 mg/kg和10.0 mg/kg,除了显著降低肝胰脏AKP活性外(P<0.05),对血清生化指标和肝胰脏非特异性免疫酶活性无显著影响(P>0.05)。综合生长、饲料利用、体组成成分、血液生化指标和肝胰脏非特异性免疫酶活性的影响结果表明,对于0.91～4.93 g吉富罗非鱼,饲料中以吡啶甲酸铬的形式添加0.8～1.2 mg/kg铬为宜。     

有机铬对热应激蛋鸡生产性能和血液生化指标的影响

试验选用91周龄新罗曼商品蛋鸡480只,按2×2双因子试验设计随机分为5组,对照组饲喂不添加铬的玉米-豆粕型基础日粮,4个试验组饲喂在基础日粮中分别添加了以吡啶羧酸铬或酵母铬来源的0.2mg/kg或0.4mg/kg的日粮,试验30d,以研究有机铬对热应激蛋鸡生产性能和血液生化指标的影响。试验结果显示:①有机铬能在一定程度上促进热应激蛋鸡的蛋白质利用,提高热应激蛋鸡的生产性能;②铬水平对血清尿素氮有极显著的影响(P<0.01),添加0.4mg/kg铬组均极显著地低于对照组(P<0.01),说明了补铬能够抑制由高温引起的蛋白质分解过程,从而起到缓解高温应激的作用;③吡啶羧酸铬和酵母铬在作用效果上无显著的差异;从经济效益方面考虑,0.4mg/kg铬水平的酵母铬和吡啶羧酸铬经济效益较高。     

L-肉碱对肉鸡脂质代谢的影响

160只1日龄艾维茵肉仔鸡随机分为4组,每组40只,分别饲喂添加0、30、50和100m gk/gL-肉碱的玉米-豆粕型日粮,以研究L-肉碱对肉鸡脂质代谢的影响。经7周试验,结果表明:L-肉碱显著影响了肉鸡血清中甘油三酯、胆固醇、游离脂肪酸、高密度脂蛋白胆固醇的含量和肉鸡腹脂率(P<0.05或0.01),但对肉鸡的生长性能未产生显著影响P(>0.05)。综合各项指标的变化,似100mg k/g L-肉碱对肉鸡的脂肪和胆固醇代谢有较明显的影响。     

Dietary L-carnitine increases plasma insulin-like growth factor-I concentration in chicks fed a diet with adequate dietary protein level

1. The effect of L-carnitine supplemented into experimental diets with varying dietary protein concentrations (50, 200 and 400 g/kg) on body weight gain and plasma insulin-like growth factor-I (IGF-I) concentration in chicks was examined. 2. Dietary L-carnitine supplementation provided 0, 200, 500 and 1000 mg/kg. Chicks were given the diet ad libitum for 10 d. 3. When L-carnitine was provided as 500 or 1000 mg/kg, body weight gain was significantly improved in birds receiving the 200 and 400 g protein/kg diets. 4. There was an interaction between dietary L-carnitine and protein content on plasma IGF-I concentration. L-carnitine supplementation had little influence on plasma IGF-I concentrations in birds receiving the low protein (50 g/kg) diet. When dietary L-carnitine concentrations were increased from 0 to 1000 mg/kg in the adequate protein (200 g/kg) diet, plasma IGF-I concentrations were also increased. However, when dietary L-carnitine content was more than 500 mg/kg in the 400 g/kg protein group, plasma IGF-I concentration decreased with increasing dietary L-carnitine content. 5. Body weight change correlated significantly with the alteration in plasma IGF-I concentrations in chicks given diets with adequate dietary protein. 6. In conclusion, the improvement in body weight gain caused by dietary L-carnitine supplementation was achieved when chicks were given their dietary protein requirement, which may be partially explained by an increase in plasma IGF-I concentration.     

Food intake and abdominal adipose tissue in White Leghorn hens fed diets of different protein and energy concentrations

1. Single Comb White Leghorn hens of 2 ages (44 and 80 weeks) were fed diets of different energy (10.88, 12.13 or 13.39 MJ ME and 140 g protein/kg) or protein (120, 140, 160 or 180 g and 12.13 MJ ME/kg) concentration over an 8-week period. 2. Food intake did not change with increasing concentrations of dietary protein. Protein intake was directly correlated with dietary protein concentration. 3. Energy intake increased with dietary energy concentration but, generally, failed to match the increases in dietary energy concentration. Energy, rather than protein, concentration was the major determinant of food intake. 4. Efficiency of energy utilisation decreased and mean adipocyte size increased with higher energy intake. 5. A bimodal adipocyte size distribution, consisting of a primary large size and a secondary small size population, was present in the abdominal fat pad of birds of both ages. There was no significant difference in the numbers of large adipocytes between the hens of the two ages. 6. The greater mean fat pad weight in the older hens was associated with increased mean cell volume in the population of large adipocytes.     

Effects of L-carnitine fed during gestation and lactation on sow and litter performance

Multiparous sows (n = 307) were used to evaluate the effects of added dietary L-carnitine, 100 mg/d during gestation and 50 ppm during lactation, on sow and litter performance. Treatments were arranged as a 2 (gestation or lactation) x2 (with or without L-carnitine) factorial. Control sows were fed 1.81 kg/d of a gestation diet containing .65% total lysine. Treated sows were fed 1.59 kg/d of the control diet with a .23 kg/d topdressing of the control diet that provided 100 mg/d of added L-carnitine. Lactation diets were formulated to contain 1.0% total lysine with or without 50 ppm of added L-carnitine. Sows fed 100 mg/d of added L-carnitine had increased IGF-I concentration on d 60 (71.3 vs. 38.0 ng/mL, P<.01) and 90 of gestation (33.0 vs. 25.0 ng/mL, P = .04). Sows fed added L-carnitine had increased BW gain (55.3 vs 46.3 kg; P<.01) and last rib fat depth gain (2.6 vs. 1.6 mm; P = .04) during gestation. Feeding 100 mg/d of added L-carnitine in gestation increased both total litter (15.5 vs. 14.6 kg; P = .04) and pig (1.53 vs 1.49 kg; P<.01) birth weight. No differences were observed in pig birth weight variation. Added L-carnitine fed during gestation increased litter weaning weight (45.0 vs. 41.3 kg, P = .02); however, no effect of feeding L-carnitine during lactation was observed. No differences were observed in subsequent days to estrus or farrowing rate. Compared to the control diet, feeding added L-carnitine in either gestation, lactation, or both, increased (P<.05) the subsequent number of pigs born alive, but not total born. In conclusion, feeding L-carnitine throughout gestation increased sow body weight and last rib fat depth gain and increased litter weights at birth and weaning.     

Effects of L-carnitine administration on growth performance, carcass traits, blood serum parameters and abdominal fatty acid composition of ducks.

Effects of L-carnitine administration via drinking water on growth performance, carcass traits, blood serum parameters and abdominal fatty acid composition of ducks was examined. One hundred day-old Turkish native duck chicks were divided into two groups, each with five replicates and given the same diets with 0 and 200 mg/l carnitine chlorhydrate via drinking water. The study lasted 8 weeks, with the first 4 weeks as a starter and the last 4 weeks as grower period. At the end of the study five ducks were randomly selected from each subgroup for slaughter. Growth performance parameters of ducks were not affected significantly by L-carnitine administration. Live weight, daily weight gain, cumulative feed consumption and average feed conversion efficiency were found to be 1490 and 1621 g, 26.0 and 28.1 g, 5386 and 5662 g, 3.75 and 3.54 kg/kg in the control and in the carnitine groups respectively. L-carnitine administration did not effect carcass traits and serum cholesterol, total lipid, triglyceride and glucose levels. Total saturated fatty acid content of abdominal fat significantly decreased, mono- and polyunsaturated fatty acid content were not affected by L-carnitine administration. In conclusion, L-carnitine administration by drinking water did not affect growth performance, carcass traits and blood parameters in ducks.     

Development of divergent lines of lean and fat broilers using plasma very low density lipoprotein concentration as selection criterion; results over the fourth generation and lack of effect of dietary fat on performance and carcase fat content

Comparisons were made of the performance and carcase composition of lean and fat broilers from the 4th generation of a breeding experiment which were fed diets containing 25 or 80 g fat/kg. Selection over the 4th generation resulted in continued divergence in the selection trait and the correlated responses of total body lipid and protein contents and the efficiencies of conversion of food and dietary protein. In both lines body weight, efficiency of food utilisation and total body lipid and protein contents were unaffected by dietary fat content. Tissue fatty acid composition was influenced by dietary and genetic factors: dietary fat increased the proportions of linoleic and oleic acids at the expense of palmitic, palmitoleic and stearic acids whilst greater body fatness increased the proportion of palmitoleic at the expense of linoleic acid.     

Effects of dietary supplementation with L-carnitine and fat on blood acid-base responses to handling in slaughter weight pigs

Blood acid-base responses to handling were evaluated in slaughter weight pigs fed diets supplemented with l-carnitine and fat. The study was carried out as a randomized block design with a 2 x 2 factorial arrangement of treatments: 1) dietary L-carnitine supplementation (0 vs. 150 ppm, as-fed basis); and 2) dietary fat supplementation (0 vs. 5%, as-fed basis). Sixty pigs (91.1 +/- 5.14 kg BW) were housed in mixed-gender groups of five and had ad libitum access to test diets (0.68% true ileal digestible lysine, 3,340 kcal of ME/kg, as-fed basis) for 3 wk. At the end of the feeding period (110.3 +/- 7.52 kg BW), pigs were subjected to a standard handling procedure, which consisted of moving individual animals through a facility (12.2 m long x 0.91 m wide) for eight laps (up and down the facility), using electric prods (two times per lap). There was no interaction between dietary L-carnitine and fat supplementation for any measurement. Pigs fed 150 ppm of supplemental L-carnitine had lower baseline blood glucose (P < 0.05) and higher baseline blood lactate (P < 0.05) concentrations than the nonsupplemented pigs. After handling, pigs fed L-carnitine-supplemented diets had a higher (P < 0.05) blood pH and showed a smaller (P < 0.05) decrease in blood pH and base excess than those fed the nonsupplemental diets. Baseline plasma FFA concentrations were higher (P < 0.01) in pigs fed the 5% fat diet. After the handling procedure, blood glucose, lactate, and plasma FFA were higher (P < 0.05) in pigs fed the 5 vs. 0% fat diets, but blood pH, bicarbonate, and base excess were not affected by dietary fat. The handling procedure decreased (P < 0.01) blood pH, bicarbonate, base excess, and total carbon dioxide and increased (P < 0.01) blood lactate, partial pressure of oxygen, and glucose, and also increased (P < 0.01) rectal temperature. Free fatty acid concentrations were increased by handling in pigs fed both 0 and 5% fat and 150 ppm L-carnitine. In conclusion, dietary L-carnitine supplementation at the level and for the feeding period evaluated in the current study had a relatively small but positive effect on decreasing blood pH changes in finishing pigs submitted to handling stress; however, dietary fat supplementation had little effect on blood acid-base balance.     

Influence of chromium tripicolinate on growth and glucose metabolism in yearling horses

Thoroughbred and Quarter Horse yearlings (n = 24; 335+/-7 d of age) were used in a 112-d feeding trial to determine whether chromium (Cr) supplementation would alter growth, development, and energy metabolism of growing horses on high-concentrate diets. The horses were assigned at random within breed and gender subgroups to one of four treatment groups: A) basal concentrate; B) basal plus 175 microg of Cr/kg concentrate; C) basal plus 350 microg of Cr/kg concentrate; and D) basal plus 700 microg of Cr/kg concentrate. Chromium was provided via Cr tripicolinate (Prince Agri Products, Quincy, IL). The horses were weighed, measured for withers and hip height, heart girth, and body length and underwent ultrasound evaluation for croup fat thickness. The concentrate was fed for ad libitum consumption for two, 1.5-hr feeding periods daily. Coastal bermudagrass (Cynodon dactylon) hay was group-fed (six animals/group) at 1% of BW daily. Feed intake was 60% concentrate and 40% hay, resulting in a supplemental Cr intake of 0, 105, 210, and 420 microg/kg diet for groups A, B, C, and D, respectively. Colts consumed more concentrate and total feed than did fillies (P < .05), but no dietary effect on feed intake was detected. Colts weighed more than fillies at the completion of the experiment (P = .0754), but no dietary effects on weight, body measurements, or croup fat were detected. An i.v. glucose tolerance test (.2 g of glucose/kg BW) and an i.v. insulin sensitivity test (.1 IU of insulin/kg BW) were conducted on each animal during the third 28-d period of the experiment. Plasma glucose peaked immediately following injection and decreased more rapidly in animals consuming the high-Cr diet than in those consuming the control diet (P < .01). Mean glucose fractional turnover rate values increased (P = .0369) and mean half-life of glucose decreased (P = .0634) in response to the high Cr supplementation. Plasma glucose depletions in animals fed the other two diets were between and not different from (P > .10) the depletions in control animals or in those fed high-Cr diets. No difference in insulin sensitivity was detected (P > .10). Results indicate that Cr tripicolinate supplementation of yearling horses increases the rate at which glucose is metabolized and may lower the plasma glucose concentration. No effect of Cr supplementation on development of the animals was detected.     

Effect of microbial phytase on energy availability,and lipid and protein deposition in growing swine

Two experiments were conducted to determine the effect of phytase on energy availability in pigs. In Exp. 1, barrows (initial and final BW of 26 and 52 kg) were allotted to four treatments in a 2 x 2 factorial arrangement. Corn-soybean meal (C-SBM) diets were fed at two energy levels (2.9 and 3.2 x maintenance [M]) with and without the addition of 500 phytase units/kg of diet. The diets contained 115% of the requirement for Ca, available P (aP), and total lysine, and Ca and aP were decreased by 0.10% in diets with added phytase. Pigs were penned individually and fed daily at 0600 and 1700, and water was available constantly. Eight pigs were killed and ground to determine initial body composition. At the end of Exp. 1, all 48 pigs were killed for determination of carcass traits and protein and fat content by total-body electrical conductivity (TOBEC) analysis. Six pigs per treatment were ground for chemical composition. In Exp. 2, 64 barrows and gilts (initial and final BW of 23 and 47 kg) were allotted to two treatments (C-SBM with 10% defatted rice bran or that diet with reduced Ca and aP and 500 phytase units/kg of diet), with five replicate pens of barrows and three replicate pens of gilts (four pigs per pen). In Exp. 1, ADG was increased (P < 0.01) in pigs fed at 3.2 x M. Based on chemical analyses, fat deposition, kilograms of fat, retained energy (RE) in the carcass and in the carcass + viscera, fat deposition in the organs, and kilograms of protein in the carcass were increased (P < 0.10) in pigs fed the diets at 3.2 vs. 2.9 x M. Based on TOBEC analysis, fat deposition, percentage of fat increase, and RE were increased (P < 0.09) in pigs fed at 3.2 x M. Plasma urea N concentrations were increased in pigs fed at 3.2 x M with no added phytase but were not affected when phytase was added to the diet (phytase x energy, P < 0.06). Fasting plasma glucose measured on d 28, ultrasound longissimus muscle area (LMA), and 10th-rib fat depth were increased (P < 0.08) in pigs fed phytase, but many other response variables were numerically affected by phytase addition. In Exp. 2, phytase had no effect (P > 0.10) on ADG, ADFI, gain:feed, LMA, or 10th-rib fat depth. These results suggest that phytase had small, mostly nonsignificant effects on energy availability in diets for growing pigs; however, given that phytase increased most of the response variables measured, further research on its possible effects on energy availability seems warranted.     

Clenbuterol-induced desensitization in murine adipocytes: relationship to in vivo effectiveness

In vitro lipolytic response of isolated murine fat cells to epinephrine (EPI) or clenbuterol (CB) was used to evaluate the potential for the beta 2-adrenergic agonist, CB, to induce cellular resistance to further beta-adrenergic stimulation. Feeding CB (20 mg/kg diet) to mice for 1, 3 or 6 wk decreased adipocyte sensitivity to EPI or CB by 35-45%, with no differences in magnitude of this desensitization across time. Basal and maximal rates of lipolysis were similar for control- and clenbuterol-fed mice. In agreement with the feeding studies, a 2 hr preincubation of control-fat tissue with either 10 microM EPI or 100 microM CB, followed by adipocyte isolation and restimulation with EPI, reduced adipocyte sensitivity by 50%. In addition, maximal rates of lipolysis were decreased 24% and 34% for EPI and CB treated tissue, respectively. The similar adaptive responses of the adipocytes to CB exposure in vivo or in vitro suggest that CB interacts directly with fat cells in vivo and can induce tolerance. Mice fed CB for 12 wk had 33% smaller epididymal fat pads compared to controls, but pad weight differences were only 10% if feeding of CB was discontinued 1 wk before the 12 wk analysis. The reversal in fat pad gain with a 1 wk removal of CB from the diet indicates at least partial effectiveness of CB through 12 wk. The modest beta-adrenergic desensitization established by wk 1 was similar on wk 6 suggesting that CB-induced adipocyte resistance is of little consequence to the fat-reducing properties of CB administration.     

羊、鸡抗鼠脂肪细胞膜抗血清对大鼠体脂与生长性能的影响

应用提取的鼠脂肪细胞膜分别免疫羊和鸡 ,所产生的抗血清用于 Wistar大鼠被动免疫。实验 1: 组腹腔注射羊正常血清 , 组腹腔注射羊抗鼠脂肪细胞膜抗血清 ,剂量均为 1m L /只 ,连续注射 4 d。结果表明 ,羊抗鼠脂肪细胞膜抗血清免疫促进了大鼠体增重 ,降低了体脂沉积 ,与对照组相比 ,7周末体重增加 6 .35 % (P<0 .0 5 ) ,饲料摄入增加6 .85 % (P<0 .0 1) ,料重比 (F/G)提高 4 5 .0 0 % (P<0 .0 5 ) ;肾周、附睾、网膜脂肪垫重量分别降低 2 3.92 % (P<0 .0 5 )、34.4 5 % (P<0 .0 5 )、0 .98% ,脂肪总量降低 2 0 .92 %。实验 2 :1组腹腔注射鸡正常血清 ,2组腹腔注射鸡抗鼠脂肪细胞膜抗血清 ,剂量均为 1m L/只 ,连续注射 4 d。结果表明 ,鸡抗鼠脂肪细胞膜抗血清免疫对大鼠的生长发育产生了不利影响 ,7周末 ,免疫大鼠平均体重较对照组减少 4 0 g(P<0 .0 5 ) ,饲料摄入显著降低 (P<0 .0 1) ;对体脂的沉积和血液中 TG和 FFA的影响没有规律 ,且无统计学意义     

饲料中铬源及铬添加水平对凡纳滨对虾幼虾生长性能、血清生化指标及非特异性免疫酶活性的影响

本试验旨在研究饲料中铬源及铬添加水平对凡纳滨对虾幼虾生长性能、血清生化指标及非特异性免疫酶活性的影响,探讨3种铬源在饲料中的最适添加水平。采用双因素试验设计,铬源分别为氯化铬(Cr Cl3)、吡啶甲酸铬(Cr-Pic)和蛋氨酸铬(Cr-Met),铬添加水平分别为0、0.3、0.6、0.9、1.2和2.0 mg/kg,配制成16种试验饲料,投喂凡纳滨对虾幼虾8周。挑选初始体重为(0.897±0.001)g的凡纳滨对虾幼虾1 920尾,随机分为16组,每组3个重复,每个重复40尾。结果表明:铬源、铬添加水平及两者的交互作用对凡纳滨对虾的终末体重、增重率、饲料系数和蛋白质效率有显著影响(P0.05)。铬添加水平为0.3~2.0 mg/kg的各组幼虾的终末体重、增重率显著高于未添加铬组(P0.05),以Cr-Met形式添加0.9 mg/kg铬时上述指标达到最大值。Cr Cl3和Cr-Met组在铬添加水平为0.9 mg/kg时饲料系数最低,但与铬添加水平为1.2 mg/kg时差异不显著(P0.05);Cr-Pic组在铬添加水平为1.2 mg/kg时饲料系数最低。3种铬源下,蛋白质效率均在铬添加水平为0.9 mg/kg时达最大值,但与铬添加水平为1.2mg/kg时差异不显著(P0.05)。铬源、铬添加水平及两者的交互作用对全虾粗脂肪和粗灰分含量有显著影响(P0.05),但对全虾粗蛋白质和水分含量无显著影响(P0.05)。铬源、铬添加水平及两者的交互作用对血清总蛋白、葡萄糖、胆固醇和甘油三酯含量均有显著影响(P0.05),以Cr-M et形式添加0.9 mg/kg铬时呈现出最高的血清总蛋白含量和最低的血清葡萄糖含量。铬源、铬添加水平及两者的交互作用对血清碱性磷酸酶、酸性磷酸酶、酚氧化物酶及总超氧化物歧化酶活性有显著影响(P0.05),以Cr-Met形式添加0.9 mg/kg铬时血清酚氧化物酶和总超氧化物歧化酶活性最高。以增重率为评价指标,以Cr Cl3、Cr-Pic和Cr-Met为铬源时,经折线模型得出饲料中铬的适宜添加水平分别为1.33、1.27、1.04 mg/kg。通过比较可知,Cr-Met的相对生物利用率最高,Cr-Pic次之,Cr Cl3最低。     

Effect of L-carnitine supplementation on utilisation of energy and protein in broiler chicken fed different dietary fat levels.

Effects of a supplementation of 80 mg L-carnitine per kg diet were studied in broiler chicken at two dietary levels of fat (4 and 8%) and different feeding levels (ad libitum in a growth trial, 95 and 85% of ad libitum in a balance trial). A low-carnitine basal diet adequate in amino acid concentration was used. In the growth trial, each diet was fed to 9 groups of 10 birds each for 16 days from day 5 of live onwards. Growth and feed intake were determined. At the end of the trial, birds were killed and homogenised for subsequent empty body analysis. Accretion of protein and energy was determined using a representative blank group killed at the beginning of the trial. In the balance trial, 8 individual birds were used per treatment. Birds were offered the feed at approximately 85 and 95% of ad libitum intake, which was determined with separate birds for both fat levels. Excreta were quantitatively collected three times daily for 8 consecutive days beginning on day 17 individually for each bird. Supplemented L-carnitine did not significantly affect any response criterion. However, growth and feed conversion tended to be improved by about 5% in the carnitine supplemented diets when fed ad libitum. An interaction between carnitine and fat level occurred with regard to feed conversion, indicating that carnitine had a positive effect at the high fat level, but not at the low fat level. L-carnitine did not positively affect the metabolisability of energy (ME/GE) and the efficiency of energy utilisation (RE/GE or RE/ME). Similarly, no significant carnitine effect was determined with regard to N accretion and the efficiency of utilisation of dietary protein in both trials. It is concluded that endogenous carnitine synthesis is not the limiting factor for energy utilisation in broiler chicken, even at high dietary fat concentration. Occasionally reported positive effects of supplemental carnitine were likewise caused by reasons other than improved energy or protein utilisation. Further studies on amino acid utilisation and catabolism should consider marginal amino acid supply.     

Evaluation of xylanase in low-energy broiler diets

The objective of the current study was to evaluate the effect of feeding a thermo-tolerant xylanase in low-energy broiler diets on performance and processing parameters. Evaluation criteria included average broiler BW, FCR, livability, carcass yield, and fat pad yields. The experimental design consisted of 3 nutrient profiles: positive control, negative control 1 (−66 kcal/kg), and negative control 2 (−132 kcal/kg). Two xylanase inclusion programs were included in the negative control 1 and 2 diets; 60 g/t was included in the starter and grower diets with either 60 or 100 g/t in the finisher and withdrawal diets, yielding a total of 7 treatment groups with 8 replicate pens per treatment each containing 42-d-old straight-run chicks per treatment (2,352 total broilers). Broilers were reared in floor pens through 45 d of age. The dietary program consisted of 5 dietary phases: starter (1–15 d), grower 1 (16–23 d), grower 2 (24–31 d), finisher (32–38 d), and withdrawal (39–45 d). Body weights and feed consumption were determined on days of dietary changes, including d 15, 23, 31, 38, and 45. On d 45, 4 male and 4 female broilers per replicate (448 total) were subjected to an 8-h feed withdrawal period and processed to obtain carcass and fat pad weights. Reducing the dietary energy level increased FCR and decreased the fat pad weight of broilers in the negative control 2 treatment compared with the positive control. Inclusion of xylanase during the starter phase increased d 15 BW and reduced FCR. The inclusion of xylanase continued to reduce FCR throughout the trial, as compared with diets without xylanase inclusion. Within this study, we have demonstrated the effectiveness of xylanase inclusion in reduced-energy diets (−66 and −132 kcal/kg) to improve FCR of broilers to that of broilers fed energy-adequate diets.     

日粮铬水平对肉鸡生长性能、免疫机能及胴体脂肪含量的影响

选用３００只１日龄艾维茵肉仔鸡,研究了日粮中添加不同水平的吡啶羧酸铬对肉鸡的生长性能、免疫机能及胴体品质的影响。日粮添加的吡啶羧酸铬水平分别为０、２００、４００和６００μｇ／ｋｇ。试验期为８周。试验结果表明,０～８周日粮添加６００μｇ／ｋｇ的吡啶羧酸铬时肉鸡生长速度最快,显著高于对照组（Ｐ＜０．０５）。添加吡啶羧酸铬２００～６００μｇ／ｋｇ,对３周龄肉鸡的脾脏、胸腺和法氏囊的发育没有显著影响,对肉鸡血清抗体滴度没有显著影响。吡啶羧酸铬可以降低肉鸡腹脂和肝脂率,对改善胴体品质有益。     

Effect of dietary L-carnitine supplementation on growth performance of piglets from control sows or sows treated with L-carnitine during pregnancy and lactation

Previous studies showed that supplementation of sows' diets with L-carnitine increases body weights of their piglets at birth. This study was performed to investigate whether piglets of sows treated with L-carnitine differ in their growth potential from that of piglets of untreated control sows after weaning. It was also investigated whether supplementation of piglets' diets with L-carnitine improves their growth after weaning. In two trials, piglets of the first litters of primiparous sows (trial 1) and the second litters of the same sows (trial 2) were divided into four groups: group 1, piglets of control sows, fed a control diet; group 2, piglets of control sows fed a diet supplemented with 30 mg L-carnitine/kg; group 3, piglets of L-carnitine-treated sows, fed a control diet; group 4, piglets of L-carnitine-treated sows fed a diet supplemented with 30 mg L-carnitine/kg. Mean initial body weights of the piglets of the four groups were identical. They were 8.5 kg in trial 1 and 12.5 kg in trial 2. Diets were fed ad libitum over a period of 35 days. Piglets from sows treated with L-carnitine did not differ in body weight gains, feed intake and gain : feed ratio from those of control sows. In trial 1, piglets supplemented with L-carnitine had higher body weight gains (p < 0.005) and showed a tendency towards a higher gain : feed ratio (p = 0.09) than piglets fed the control diets. In trial 2, no significant difference in these parameters emerged between piglets fed the diet supplemented with L-carnitine and those fed the control diet. In conclusion, this study shows that dietary L-carnitine treatment of sows does not improve the growth potential of their piglets after weaning under the conditions of equal initial body weights. The study also shows that L-carnitine supplementation of their diets improves the growth performance in light piglets of primiparous sows.