M144 The mechanisms of lipid deposition in dexamethasoneexposed broiler ch<strong>ic</strong>kens (Gallus gallus domest<strong>ic</strong>us) in the late growingstage. Y. L. Cai* 1,2 , Z. G Song 2 , X. H. Zhang 2 , X. J. Wang 2 , H. C. Jiao 2 , andH. Lin 2 , 1 College of Biolog<strong>ic</strong>al Science, Jinan, Shandong, China, 2 College ofAnimal Science, Taian, Shandong , China.Male Arbor Acres ch<strong>ic</strong>kens (35 d of age, n = 30) were injected with dexamethasone(DEX) or saline for 3 d, and a pair-fed group was included. DEX administrationresulted in enhanced lipid deposition in cerv<strong>ic</strong>al fat; abdominal fat and thighfat also had an increased trend. DEX injection increased plasma triglyceride(TG), very-low-density lipoprotein (VLDL) and insulin concentration not onlyin fasted status but also in fed status. DEX administration led to higher postheparinlipoprotein lipase (LPL) activity and plasma glucose level in fastedstatus. In fasted status, DEX administration resulted in increased ME activityin liver, liver FAS activity tended to increase in DEX-injected ch<strong>ic</strong>ken. Butthe FAS and ME activity in DEX ch<strong>ic</strong>kens had no signif<strong>ic</strong>ant change in fedstatus. DEX injection resulted in enhanced ACC and FAS mRNA levels inliver in fasted status. Compared to pair-fed, ME mRNA level in liver tendedto increase in DEX ch<strong>ic</strong>kens in fasted status. In fed status, DEX administrationled to enhanced liver ACC and ME mRNA expressions compared to pairfedch<strong>ic</strong>kens. DEX administration up-regulated FAS mRNA expression inabdominal fat in fasted status, but the ME and FAS mRNA levels of abdominalfat in fed status were not altered by DEX injection. DEX injection resultedin LPL mRNA expression of abdominal fat in fed status, and in fasted statusLPL mRNA level trended to increase by DEX injection. We also measured themRNA levels of PPARγ and ATGL in abdominal fat in fasted and fed status.Neither of these two genes' mRNA expression was altered by DEX injection.The results suggested that the increased hepat<strong>ic</strong> de novo lipogenesis and in turn,the increased circulating lipid flux contributes to the augmented fat depositionin adipose tissues in DEX-challenged ch<strong>ic</strong>kens. Up-regulation of LPL mRNAlevel in abdominal fat and increased plasma LPL activity also contribute tothe enhanced fat deposits. The results ind<strong>ic</strong>ated that glucocort<strong>ic</strong>oids togetherwith the induced hyperinsulinemia should be responsible for the up-regulatedhepat<strong>ic</strong> lipogenesis.Key Words: dexamethasone, fat deposition, de novo lipogenesisM145 Effect of RRR-α-tocopherol succinate on immunityand meat quality in broilers. Z. Xuhui*, Z. Xiang, Z. Yanmin, and W. Tian,Nanjing Agr<strong>ic</strong>ultural University, Nanjing, Jiangsu, China.The objective of this study was to compare the effect of two esters ofα-tocopherol, all-rac-α-tocopherol acetate (DL-α-TOA) and RRR-αtocopherolsuccinate (D-α-TOS) on immunity and meat quality in broilerch<strong>ic</strong>ks. Three-hundred-twenty day-old Arbor Acres broiler were randomlydistributed to 4 treatments, each of wh<strong>ic</strong>h had 8 pens of 10 ch<strong>ic</strong>ks per pen.Birds in the control group were fed with the diets supplemented with 30 mg/kgDL-α-TOA (control), or basal diet with D-α-TOS supplementation of 10, 30,50 mg/kg (TOS1, TOS2, and TOS3 group), respectively for 42 d. The resultsshowed that, signif<strong>ic</strong>ant positive correlations were observed between dietarysupplemental α-TOS levels and plasma (R 2 = 0.9831, P = 0.2097) or hepat<strong>ic</strong> (R 2= 0.9336, P = 0.3503) α-tocopherol concentrations, and a negative correlationwith plasma (R 2 = –0.9511, P = 0.0207) or hepat<strong>ic</strong> (R 2 = –0.9903, P = 0.0135)MDA levels. The concentrations of IgA for TOS3 (21 d) or IgG for TOS2 (42d) were signif<strong>ic</strong>antly increased (P < 0.05) by 25.15% and 30.77%, or 18.49%and 19.15%, respectively, as compared with the control and TOS2. Markedenhancement of splen<strong>ic</strong> T and B lymphocyte proliferation occurred in TOS3as compared to the other groups. Furthermore, 30–50 mg/kg dietary α-TOSsupplementation resulted in an increase in the activities of serum T-SOD, GSH-Px, T-AOC and hepat<strong>ic</strong> T-SOD, T-AOC (P < 0.05 or P < 0.01). Furthermore,hepat<strong>ic</strong> ROS levels were decreased signif<strong>ic</strong>antly (P < 0.05). As for the meatquality, 48-h drip loss and shear force of breast and leg muscle was signif<strong>ic</strong>antlydecreased in broilers of 30–50 mg/kg dietary α-TOS supplementation group,and also the cooking loss of leg muscle. These results ind<strong>ic</strong>ated that, 30–50mg/kg dietary D-α-TOS could enhance the immune functions and antioxidantcapacity of broilers, and further the water holding capacity and tenderness,wh<strong>ic</strong>h might result from increased retention of serum and hepat<strong>ic</strong> α-tocopheroland reduction in lipid peroxidation, as evidenced by the decrease in MDA andROS.M146 Effect of different selenium sources on anti-oxidationfunction in geese. B. W. Wang*, N. Wang, X. X. Jiang, P. Sun, and B. Yue,High Quality Waterfowl Research Institute, Qingdao Agr<strong>ic</strong>ultural University,Qingdao, Shandong Province, China.To explore the effect of selenium yeast on anti-oxidation function in geese, 96one-day-old geese of similar body weight were selected and randomly dividedinto four groups, with three repl<strong>ic</strong>ates in each group and eight in each repl<strong>ic</strong>ate(half male, half female). The proportion of selenium in the same basal dietswas 0.30 mg/kg respectively. Group 1 was treated as control and to the dietof the other three groups was added sodium selenite (SS), Se-enr<strong>ic</strong>hed yeast(SY) and Nano-Se respectively. The whole experiment lasted 9 wk and after9 wk all geese underwent blood and liver sampling. The main results wereas follows: the activity of GSH-PX, T-SOD and T-AOC among three formsof selenium sources both at 4 and 9 w serum and liver were signif<strong>ic</strong>antlyhigher than the control group (P < 0.05); the content of MDA and H 2O 2wasreduced signif<strong>ic</strong>antly (P < 0.05) both in 4 and 9 w serum and liver. There wasno difference in the activity of GSH-Px among three forms of selenium sourcesin both 4 w serum and liver (P > 0.05). SY had more signif<strong>ic</strong>ant ability toincrease GSH-Px than SS in both 4 w serum and liver (P < 0.05). SY had moresignif<strong>ic</strong>ant ability to increase T-SOD than SS in both 4 and 9 w serum and liver(P < 0.05). SY had more signif<strong>ic</strong>ant ability to increase T-AOC than SS in 4 and9 w serum and 4 w liver (P < 0.05). Nano-Se had more signif<strong>ic</strong>ant ability toincrease T-AOC than SS in 9 w liver (P < 0.05). SY had more signif<strong>ic</strong>ant abilityto reduce the content of MDA than SS in both 4 and 9 w serum and liver (P< 0.05). There was no difference in the content of H 2O 2among three forms ofselenium sources in both 4 and 9 w serum and liver (P > 0.05). The main resultsshowed that under the conditions of the experiment, three forms of seleniumcan promote the anti-oxidation function and SY was a better source of seleniumfor geese.Key Words: goose, different selenium sources, anti-oxidation functionM147 Effect of different selenium yeast addition level onanti-oxidation function and fatty-liver production of liver-breeding geese.P. Sun, B. W. Wang*, Z. G. Liu, B. Yue, X. X. Jiang, and N. Wang, High QualityWaterfowl Research Institute, Qingdao Agr<strong>ic</strong>ultural University, Qingdao,Shandong Province, China.To explore the effect of different selenium yeast addition level on anti-oxidationfunction and fatty-liver production of liver-breeding geese, one hundred 13-wkoldliver-breeding geese were selected and divided into four groups randomly,25 in each group. The first, second and third group were test group and thefourth group was control group. The addition level of selenium yeast in the dietwas 0.25, 0.15, 0.05, 0.0 mg/kg respectively. The trial lasted 35 d and whenthe trial was ended, the anti-oxidation ind<strong>ic</strong>ators were measured. The resultsshowed that when 0.25 mg/kg selenium yeast was added, the T-AOC in serumwas signif<strong>ic</strong>antly higher than that of the control group(P < 0.01); the T-SODactivity in serum and liver was higher than that of the 0.05 mg/kg group(P
M148 Effect of the hydrolyzed wheat gluten on growthperformance, digestive enzyme activity, and intestinal morphology ofweaning piglets. Y. Feng 1 , X. Wang* 1 , G. Shu 1 , Q. Jiang 1 , J. Yang 1 , and Z.Zhang 2 , 1 College of Animal Science, South China Agr<strong>ic</strong>ultural University,Guangzhou, Guangdong Province, PR China, 2 Zhengzhou Newwill NutritionTechnology Co., LTD, Zhengzhou, Henan Province, PR China.A total of 120 weaning piglets (Large White × Landrace) at an average initialbody weight of 9.9 kg were used in a 10-day growth trial to investigate theeffect of the hydrolyzed wheat gluten on growth performance, activity ofdigestive enzymes, and intestinal morphology of weaning piglets. The pigletswere randomly allocated to 3 treatments, each of wh<strong>ic</strong>h had 4 pens of 10piglets per pen. The dietary treatments were: (1) basal diet, (2) basal diet +3% hydrolyzed wheat gluten, and (3) basal diet + 0.25% Glycyl-Glutamine(0.25%Gly-Gln). Eight randomly selected pigs from each treatment (two pigs/pen) were slaughtered to determine the activity of digestive enzymes, intestinalmorphology and gene expression at the end of the experiment. All data wereanalyzed with SAS (SAS Institute, Cary, NC, USA) using ANOVA. Theresult showed that the supplement of hydrolyzed wheat gluten in bas<strong>ic</strong> dietscan improved growth performance, increased the ADFI (P < 0.05), and ADG,decreased diarrhea occurrence and CD 4+/CD 8+ratio. The villus height wasincreased, and the crypt depth decreased in duodenum as compared with thecontrol group. The supplement of 0.25%Gly-Gln in bas<strong>ic</strong> diets also increasedADG and ADFI, decreased diarrhea occurrence. The supplement of 3%hydrolyzed wheat gluten or 0.25%Gly-Gln to the diet improved the activitiesof amylase, lipase, and trypsinase in duodenum digesta. The supplement of3% hydrolyzed wheat gluten or 0.25%Gly-Gln to the diet up-regulated mRNAexpression of PEPT1 and ASCT2 in duodenum and jejunum. These resultssuggested that hydrolyzed wheat gluten may stimulate the growth performanceby up-regulating gene mRNA expression, increasing the digestive enzymeactivities, and improving the intestinal morphology.The work was supported by NSFC(30671519); The Joint Funds of theNational Natural Science Foundation of China(U0731004); NationalScience & Technology Pillar Program During the 11th Five-year Plan ofChina(2006BAD12B06); and the Major Program of Guangdong Science andTechnology(2009A080303009).Key Words: hydrolyzed wheat gluten, weaning piglets, growth performanceM149 Effect of iron on the antioxidant system and bloodbiochem<strong>ic</strong>al indexes of piglet. D. Xiaowei*, W. Pengpeng, W. Ping, Z. Ruiyu,C. Juan, and Y. Qingqiang, College of Animal Science and Veterinary Med<strong>ic</strong>ine,Henan Agr<strong>ic</strong>ultural University, Zhengzhou, Ahenau, China.In order to investigate the effect of different doses of iron on the antioxidantsystem and blood biochem<strong>ic</strong>al indexes of piglets, iron dextran (150 mg/ml) wasused by injection to induce iron-overloaded and iron-def<strong>ic</strong>ient. Fifteen 0-d-oldpiglets with the same body weight were randomly assigned to three groups.The piglets in the iron-overloaded, iron-def<strong>ic</strong>ient and the control groups wereinjected with 3 mL iron dextran at 450 mg/kg body weight, 3 mL iron dextranat 150 mg/kg body weight, and 3 mL sterile saline solution at the ages of 3and 7 d, respectively. At the age of 7 d, the piglets were killed. The serum,liver and spleen were collected for biochem<strong>ic</strong>al analysis. Iron contents in serumand tissues of liver and spleen were analyzed by Z-2000 atom absorptionspectrometer. The contents of CHO, TG, HDL-C, TB, CB, TP, ALB, Glu, SUN,ALT and AKP were determined by HITACHI 7020 automat<strong>ic</strong> biochem<strong>ic</strong>alanalyzer (Hitachi Ltd., Tokyo, Japan). The levels of MDA, GSH-Px, CAT, POD,SDH, XOD and SOD were measured by UNIC 7200 spectrophotometer (UNICApparatus Co., Ltd., Shanghai, China) using commercial reagents (NanjingJiancheng Biotechnology Institute, Nanjing, China). The results showed thatdifferent doses of iron signif<strong>ic</strong>antly affected the antioxidant system and bloodbiochem<strong>ic</strong>al indexes of piglets. Compared with control group, the iron levelsin organs and serum were increased (P < 0.05) in the iron-overloaded group,while decreased (P < 0.05) in the iron-def<strong>ic</strong>ient group. The contents of TP, TB,HDL-C, MDA, GSH-Px and POD in serum were obviously increased (P < 0.05)in the iron-overloaded group, and decreased (P < 0.05) in the iron-def<strong>ic</strong>ientgroup. The levels of AKP and TG were decreased (P < 0.05), compared withthe control group. The result also ind<strong>ic</strong>ated that iron had an effect on lipidperoxidation reaction in piglet.Key Words: piglet, iron, antioxidant systemM150 Effects of different antioxidants on retention rateof vitamin A and vitamin E in piglet premix. Z. B. Yang* 1 , W. R. Yang 1 ,S. Z. Jiang 1 , L. Li 1 , and H. Cao 2 , 1 Shandong Agr<strong>ic</strong>ultural University, Taian,Shandong, PRC, 2 Novus International, Inc., St. Louis, MO, USA.Two experiments were conducted to evaluate retention rate of vitamin A andvitamin E in high Zn and Cu piglet premixes with or without addition ofantioxidants. In Experiment 1, A typ<strong>ic</strong>al piglet premix was used, containing355,000 IU/kg vitamin A, 433 IU/kg vitamin E, 5200 mg/kg Cu, 4420 mg/kgZn. The premix was kept in a commercial farm for 54 d without any antioxidantsupplementation in winter in North China, and HPLC was used to detect thecontent of vitamins A and E every 9 d. The results showed that the contentsof vitamins A and E in the premix decreased linearly (P < 0.01) as increasedstorage time. The content of vitamins A and E in the premix was only 53.86%and 36.19% left respectively at d 54. In Experiment 2, two kinds of antioxidants,SQ Max and M6 (Novus International, Inc., St. Charles, MO, USA) were usedin the same typ<strong>ic</strong>al piglet premix as Experiment 1. The treatments were: 1)the control diet (without addition of any antioxidant); 2) the control diet withaddition of SQ M6 (1200 mg/kg); 3) the control diet with addition of SQMax (2000 mg/kg). The premix of all three treatments was packed in blackaluminium foil bags, and kept in an oven at 40°C for 70 d to imitate summerweather conditions North China. The same testing method was used to detectthe content of vitamins A and E every 7 d. The results showed that vitamins Aand E contents in the premix of the three treatments were decreased linearly (P< 0.01) with increased storage time. Compared with the control, the retentionrate of vitamin A and vitamin E in the premix with SQ M6 and SQ Maxsupplementation had signif<strong>ic</strong>antly improved (Table 1). In conclusion, vitaminsA and E in the premix can be oxidized rapidly with increased storage time, andaddition of single (SQ M6) or complex (SQ Max) antioxidants is benef<strong>ic</strong>ial inprotection of oxidation of vitamin A and vitamin E in the premix.Table 1. Retention rate of vitamins A and E in premix with differentantioxidants at 40°C (%) 1Vitamin AVitamin EWeek CTR SQMax M6 CTR SQMax M60 100 100 100 100 100 1001 97.8 97.1 98.4 78.6 83.9 84.12 95.1 91.7 99 79.7 86.0 86.13 92.3 90.7 99.8 66.1 79.8 79.94 91.3 89.8 93.7 57.1 71.6 71.65 81.7 87.8 87.7 62.7 63.8 63.86 65.8 84.0 79.2 63.8 56.5 56.57 71.1 80.6 84.9 54.0 54.6 49.28 76.4 87.3 90.6 41.5 45.2 42.19 69.7 73.9 77.9 33.9 39.5 41.510 49.3 60.5 67.1 32.0 42.3 43.01Retention rate (%) = the detection value at certain days/the initial content ×100Key Words: antioxidant, premix, retention rate of vitamin A and EM151 Effect of different levels of xylo-oligosaccharidessupplementation on growth performance and nutrients utilization ofpiglets. H. S. Huang 1 , S. Zhou* 1 , Z. B. Yang 2 , W. R. Yang 2 , L. Xiao 3 , andX. A. Zhang 3 , 1 Qinghai University, Xining, PRC, 2 Shandong Agr<strong>ic</strong>ulturalUniversity, Taian, Shandong, PRC, 3 Shandong Longlive Bio-technology Co.,Ltd, Qingdao,Shandong, PRC.Two experiments were conducted to assess the effects of xylo-oligosaccharides(XOS) on nutrients utilization and growth performance of piglets. In Experiment1, a total of four hundred 28-d-old postweaning pigs were randomly assignedto one of 5 dietary treatments with 8 repl<strong>ic</strong>ates of 10 piglets each. Treatmentsincluded: 1) basal diet (BD, control); 2) BD + 50 mg/kg XOS; 3) BD + 100mg/kg XOS; 4) BD + 200 mg/kg XOS; 5) BD + 100 mg/kg aureomycin(chloroteracycline). The control diet was formulated to meet all nutritionalrequirements based on NRC (1998). Pigs were fed a control diet for 7 d and thenfed the test diets for 35 d. Body weights and feed intakes were measured everyweek to determine the ADG, ADFI and feed:gain ratio (F:G). Mortalities andhealth status were visually observed and recorded daily throughout the entireexperimental period. All the piglets had the similar ADG, ADFI and F:G (P >37
- Page 1 and 2: Inaugural ASAS-CAAVAsia Pacif ic Ri
- Page 3 and 4: Scientific ProgramTable of Contents
- Page 5 and 6: 1 Advanced needle-free injection te
- Page 7 and 8: 9 Pig personality, meat quality, an
- Page 9 and 10: 17 The contamination and distributi
- Page 11 and 12: 25 Genetic evaluations for measures
- Page 13 and 14: of control and the lowest of SDAP g
- Page 15 and 16: 39 Effects of bacterial protein and
- Page 17 and 18: Advances in Digestive Physiology Me
- Page 19 and 20: L-arginine increased (P < 0.05) the
- Page 21 and 22: average final weight (AFW) and aver
- Page 23 and 24: 71 Building a foundation: Cells, st
- Page 25 and 26: 78 Effect of the level of vitamin A
- Page 27 and 28: 86 Evaluation of phosphorus excreti
- Page 29 and 30: 94 Responses of dairy cows to suppl
- Page 31 and 32: 102 Construction and analysis of a
- Page 33 and 34: M132 Study on the effects of pectin
- Page 35: M140 Effect of Mintrex Zn on perfor
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- Page 41 and 42: M163 The main fatty acid contents i
- Page 43 and 44: M170 Zinc requirements of yellow br
- Page 45 and 46: M178 Influences of dietary riboflav
- Page 47 and 48: M185 Application of an advanced syn
- Page 49 and 50: M193 Studies on the effects of oreg
- Page 51 and 52: M202 Plasma leucine turnover rate,
- Page 53 and 54: 103 Use of natural antimicrobials t
- Page 55 and 56: 111 The somatotropic axis in growth
- Page 57 and 58: Environmental Impacts of Cattle, Sw
- Page 59 and 60: 128 Opportunities for international
- Page 61 and 62: Animal Health PostersT211 Locoweed
- Page 63 and 64: T219 Stabilization of roxarsone and
- Page 65 and 66: Beef Species PostersUrinary purine
- Page 67 and 68: T233 The effects of sire and breed
- Page 69 and 70: T242 Ultrastructure of oocyte and e
- Page 71 and 72: T249 Effect of different combinatio
- Page 73 and 74: Forages and Pastures PostersIn vitr
- Page 75 and 76: T263 Effects of leaf meal of Brouss
- Page 77 and 78: T271 The effects of feeding expandi
- Page 79 and 80: Lactation Biology PostersT278 Effec
- Page 81 and 82: Physiology and Endocrinology Poster
- Page 83 and 84: T288 Effect of Aspergillus meal pre
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T301 Observation of the feeding man
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T307 Effect of levels of Yucca schi
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T313 Study of lysine requirement of
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energy, 5, 26energy and nutrient di
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protein digestive enzyme, 44protein
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HHai, Y., T222, T248Hai-Ying, Z., T
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Song, X., T223Song, Z. G, M144, T20
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102NOTES