实验兔新品系(WHBE兔)蛋白质需要特点及相关机理研究
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摘要
WHBE兔是由日本大耳白兔突变产生的实验兔新品系,以其白色被毛(White hair)和黑色眼睛(Black eye)的特征而得名,具有能产生高效价抗体的特性。目前对WHBE兔遗传特性的研究较多,而有关营养需要方面的研究几乎空白。由于蛋白质营养与动物的免疫功能密切相关,本文通过饲养试验,氮代谢试验、免疫功能测定等一系列试验,研究了生长期和育成期的WHBE兔对日粮粗蛋白的营养需要特点,并从消化层面(盲肠微生态变化情况)和代谢层面(相关功能基因表达)探讨WHBE兔对蛋白质最佳需要量的产生机理。最后,对WHBE兔日粮中限制性氨基酸的适宜比例作了初步研究。
     1.日粮粗蛋白水平对生长期WHBE兔生长性能、氮代谢、免疫功能、盲肠发酵参数及肝脏功能基因表达的影响
     选用40日龄WHBE断奶仔兔60只,进行为期6周的饲养试验。将仔兔随机分为5组(Ⅰ,Ⅱ,Ⅲ,Ⅳ和V组),分别饲以粗蛋白水平为12%,14%,16%,18%和20%的等消化能(10.0MJ/kg)、等粗纤维(12%)日粮,通过测定动物生长性能、血清生化指标和免疫学指标、盲肠发酵参数及相关激素和酶的基因表达峰度,观察日粮粗蛋白水平对兔生长性能和免疫功能影响,确定生长期WHBE兔对粗蛋白的生长需要和免疫需要,并探讨相关机理。另外选取30只WHBE幼兔,并随机分为5组,分别饲喂5种不同粗蛋白水平(12,14,16,18和20%)的等消化能和等粗纤维日粮,进行氮代谢试验,估算生长期WHBE兔的维持氮需要量及净蛋白利用率。
     试验结果表明:仔兔日增重与粗蛋白水平间存在回归关系(Y=-0.2325X2+7.6371X-40.335,R2=0.6237),经分析,当日粮粗蛋白水平为16.4%时,动物生长性能最佳。日粮粗蛋白水平对动物的采食量无显著影响,但对料重比影响显著。血清碱性磷酸酶的活力以16%粗蛋白组最高,但组间差异不显著;而血清胰岛素样生长因子-Ⅰ(IGF-Ⅰ)的含量以Ⅲ、Ⅳ组为高,与Ⅰ、Ⅱ、Ⅴ组差异显著(P<0.01,P<0.05)。Ⅱ-Ⅳ组的血清总蛋白的含量明显高于Ⅰ组(P<0.05),各组尿素氮含量随蛋白水平提高而显著上升(P<0.01,P<0.05)。在免疫学指标上,随日粮粗蛋白水平提高,各组仔兔的自然杀伤细胞活力、脾脏指数和胸腺指数呈上升趋势,均以V组最高,V组的自然杀伤细胞活力、脾脏指数分别比Ⅰ组提高36%和31%(P<0.05),而V组的胸腺指数比Ⅱ组提高41%(P<0.05)。脂多糖诱导淋巴细胞增殖的刺激指数(LPS SI)以Ⅳ组最高,分别与Ⅰ、Ⅱ组差异显著(P<0.01,P<0.05),而与Ⅲ、Ⅴ组无显著差异。而刀豆素蛋白刺激指数(ConA SI)以Ⅲ组最高,Ⅳ、Ⅴ组次之,Ⅲ-Ⅴ组间无显著差异,但Ⅲ-Ⅴ组分别与Ⅰ、Ⅱ组差异显著(P<0.01,P<0.05)。白介素-1β(IL-1β)的浓度以Ⅳ组最高,显著高于Ⅰ组(P<0.05),免疫球蛋白含量也以Ⅲ、Ⅳ组为高,但各组间差异不显著(P>0.05)。血清NO含量和SOD活性以Ⅲ、Ⅳ组为高,与Ⅰ组差异显著(P<0.01,P<0.05),而MDA含量变化则与SOD活性的变化趋势相反。从盲肠发酵参数看,氨态氮和微生物蛋白的浓度也以16%粗蛋白组最高,且Ⅲ组微生物蛋白浓度显著高于其他4组(P<0.01)。肝脏IGF-1 mRNA的表达峰度以Ⅲ、Ⅳ组最高,与Ⅰ组差异显著。PEPCK mRNA则在16%粗蛋白水平下的表达量最大,并显著高于12%粗蛋白组。从氮代谢试验结果分析可得:生长期WHBE兔平均净蛋白利用率为445g/kg,维持氮需要量为491mg/kg BW0.75。
     2.日粮粗蛋白水平对育成期WHBE兔生长性能、氮代谢、免疫功能、盲肠微生物环境及肝脏功能基因表达的影响
     选用90日龄WHBE兔60只,进行为期6周育成期饲养试验。动物分组和采食日粮与生长期试验相同。除测定了生长期饲养试验的相关指标外,育成期试验还进行了抗卵清白蛋白抗体生成实验,以及盲肠微生物区系的DGGE分析。另取30只成年WHBE兔,进行与生长期动物相同的氮代谢试验,随后选用20只16周龄WHBE兔进行无氮日粮代谢试验,即将试兔随机分为5组,分别按55,45,35,25和0g/d饲喂无氮日粮。
     结果表明:14%-20%粗蛋白水平下,兔子的日增重均显著高于12%粗蛋白水平组(P<0.01),日增重与粗蛋白水平间存在回归关系(y=-0.1147x2+4.1556x-13.154,R2=0.5851),当粗蛋白水平达到18.1%时,动物生长性能最佳。日粮粗蛋白水平对动物的采食量无显著影响。各组兔碱性磷酸酶的活力均低于相应的生长期动物,但IGF-Ⅰ的浓度则高于生长期动物,且IGF-Ⅰ浓度以16%粗蛋白组最高,与12%粗蛋白组差异显著。育成兔的其他各项生化指标的变化趋势基本与生长兔相同。在免疫学指标上,各项免疫学参数随粗蛋白水平的升高均有先上升后下降的趋势,其中,自然杀伤细胞活力、LPS SI、和IL-1β等指标以16%粗蛋白组最高,12%,14%粗蛋白组为低。脾脏指数和胸腺指数都以18%粗蛋白水平组最高,与12%,14%粗蛋白组差异显著(P<0.05),16%和18%粗蛋白组的ConA SI显著高于14%和20%粗蛋白组(P<0.05)。免疫球蛋白含量以16%粗蛋白水平组为高,但各组间差异不显著(P>0.05)。抗卵清白蛋白的抗体生成率也以16%粗蛋白水平组最高,且与12%粗蛋白组差异显著(P<0.05)。血清NO含量和SOD活性的变化趋势与免疫指标的变化一致。从盲肠发酵参数看,18%粗蛋白水平下,氨态氮和微生物蛋白和总挥发性脂肪酸浓度最高,而pH值最低,且盲肠微生物DGGE分析结果显示,在该蛋白水平下,动物盲肠微生物多样性程度最大。WHBE兔在育成期的肝脏IGF-ⅠmRNA和PEPCKmRNA的表达特点与生长期一致。氮代谢试验结果表明,育成期WHBE兔平均净蛋白利用率(NPU)为496g/kg,比生长期增高12%;维持氮需要量则为480 mg/kgBW0.75/d,此结果与通过无氮日粮代谢试验估算结果(486 mg/kgBW0.75/d)基本一致。证实了氮代谢试验结果的准确性。试验结果同时发现,无氮日粮采食量越少,氮排泄量越多,提示当WHBE兔采食氮很低时,可能会通过体蛋白分解代谢来满足机体维持氮的需要。3.成年WHBE兔日粮适宜粗蛋白与限制性氨基酸组合的研究
     选用100日龄WHBE兔36只,将日粮粗蛋白水平(12%和16%)和限制性氨基酸按满足NRC标准的百分比(80%,100%和120%)不同随机分为6组(12-80、12-100、12-120、16-80、16-100和16-120),分别喂以6种不同粗蛋白和氨基酸组合的日粮,其中前3组日粮粗蛋白水平为12%,赖氨酸含量分别为0.72%,0.9%和1.08%,含硫氨基酸含量分别为0.52%,0.65%和0.78%;后3组日粮粗蛋白水平为16%,赖氨酸与含硫氨基酸组成分别与相应的前3组相同。通过饲养试验、氮代谢试验和免疫功能的测定,观察这6种粗蛋白和氨基酸组合日粮对WHBE兔的氮代谢和免疫功能的影响。试验结果表明,动物的日增重和氮利用率以12-120、16-80组最高,12-80、16-120组最低,12-120、16-80组分别与12-80、16-120差异显著(P<0.01),但12-120组的总氮排泄量明显低于16-80组(P<0.01)。12-120、16-80组动物的脾脏指数和胸腺指数也都高于其他4组,16-80组动物的脾脏指数分别与12-80、12-100、16-100和16-120组差异显著(P<0.01)。抗卵清白蛋白抗体阳性的动物数以12-120组最多,分别与12-100、16-100和16-120组差异显著(P<0.05)。血清总蛋白含量随日粮氨基酸水平提高有上升趋势,血清尿素氮含量以12-100和12-120组最高,与其他各组差异显著(P<0.01,P<0.05)。以上结果表明,12-120组和16-80组的日粮粗蛋白和氨基酸组合比较适宜,考虑到16-80组氮排放量较高,故以12-120组最佳。
     综上所述,生长期和育成期WHBE兔的维持氮需要量为分别为491和480mg/kg BW0.75 /d,而净蛋白利用率分别为445和496g/kg;生长期WHBE兔适宜生长的日粮粗蛋白水平为16.4%,14%-20%日粮粗蛋白水平均能满足育成期WHBE兔最大生长需要,其最佳点在18.1%。保证生长期和育成期WHBE兔处于最佳免疫状态的日粮粗蛋白水平均在16-18%之间。在这一范围,机体抗氧化能力最强,盲肠微生物数量和种类最多,发酵作用也最强,且肝脏IGF-ⅠmRNA和PEPCKmRNA的最高表达峰度也处于这一适宜水平。此外,适当增加合成氨基酸的比例可降低日粮粗蛋白水平,不仅不影响WHBE兔的生长和免疫,而且可减少氮的排放。
A new strain of laboratory rabbit (WHBE rabbit), originated from Japanese White rabbit but characterized by its black eye and higher antibody titer, was used in this study to assess the characteristics of protein requirement. The crude protein requirements for maintenance, growth and maintaing maximal immune function during growing and developing periods were evaluated via feeding trial, nitrogen (N) balance trial and immune function test, and some mechanisms were explained in terms of digestive (ceacal fermentation and bacterial community) and metabolism (functional gene expression)facets. Furthermore, the optimal proportions of limited amino acids in diets were also studied.
     1. Effects of dietary crude levels on growth performance, N metabolism, immune function, ceacal fermentation, and hepatic functional gene expression in growing WHBE rabbits
     Sixty weaned WHBE rabbits, at the age of 40 days, were divided into 5 groups (Ⅰ,Ⅱ,Ⅲ,ⅣandⅤ) according to dietary crude protein levels(12%,14%,16%,18% and 20%, respectively). Five diets had similar the digestible energy (10.0MJ/kg) and crude fibre(12%) contents. Feed intake and growth performance were measure during the six-week feeding trial and the blood biochemical indices, immunological parameters, ceacal fermentation, and expression abundant of hepatic IGF-ⅠmRNA and PEPCK-C mRNA were determined when the trial was finished. After feeding trial, another 30 young WHBE rabbits at the age of 10 weeks were used in a N balance trial.The rabbits were divided into five equal groups and fed the same diets as feeding trial, correspondingly. The net protein utilization and the N requirements for maintenance were estimated from the relationship between the N retention and intake.
     All animals had similar feed intake. Protein levels had significant effects on daily gain (P< 0.05), and the relationship between dairy gain (Y) and dietary protein level (X) was calculated as Y=-0.2325X2+7.6371X-40.335(R2=0.6084), from which the optimal diary gain can be estimated to be at 16.4% CP level.Serum total protein and albumin in 14-20% CP groups were higher than group I. The contents of Urea-N were increased with the increasing dietary protein level, but it was suitable in the third group. The activity of alkaline phosphatase (ALP) was the highest in groupⅢ, but no significant difference was found. At 16 or 18% CP level, The circulation IGF-Ⅰconcentrations were higher than that of at 12,14 and 20%, respectively (P<0.01, P<0.05). The natural killer (NK) cell activity, spleen indices and thymus indices had a trend to increase with the increasing levels of CP, being highest at 20% CP level. The above three indices (NK cell activity, spleen and thymus indices) in group V were significantly increased by 36,31 and 41%, compared with that in groupⅠ,ⅠandⅡ, correspondingly. The lymphocyte proliferation assay showed that the stimulation indices (SI) induced by both T-cell mitogen concanavalin A (ConA) and B-cell mitogen lipopolysaccharides (LPS) were higher in groupⅢ,ⅣandⅤthan that in groupⅠandⅡ, while no significant difference was found among groupⅢ,ⅣandⅤ. The concentration of IL-1βwas highest in groupⅣ, and had significant difference, compared with groupⅠ(P<0.05). The contents of immune globulin A, M and G (IgA, IgM and IgG) had the same trend as the change of IL-1β, but no significant difference was found. The activity of superoxide dismutase (SOD) and concentration of nitric oxide (NO) in groupⅢandⅣwere significantly higher than that of in groupⅠ.However, the change of maleic dialdehyde (MDA) concentration was contrary to that of SOD. The CP levels had significant effects on caecal fermentation, with highest concentrations of ammonia N (NH3-N) and microbial protein in groupⅢ. Expression of hepatic IGF-I was consistent with that of circulating IGF-Ⅰ.Expression abundant of hepatic PEPCK-C mRNA was also highest at 16% CP level.The result of N balance trial showed that average net protein utilization was 445g/kg, and the estimated N requirement for maintenance was 491 mg/kg BW0.75 per day in growing WHBE rabbits.
     2. Effects of dietary crude levels on growth performance, N metabolism, immune function, ceacal fermentation and bacterial community, and hepatic functional gene expression in developing WHBE rabbits
     Sixty 90-day WHBE rabbits were carried out in a six-week feeding trial to observe the effects of dietary crude protein levels on performance of developing WHBE rabbits. The experimental design and diets were the same as that of growing rabbits described above. Besides all parameters detected in growing period, antibody response to ovalbumin was tested and the ceacal bacterial community was analized by DGGE technology in this trial.After feeding trial,another 30 adult WHBE rabbit were used in N balance trial as described above. And then, twenty rabbits at the age of 16 weeks were fed a N-free ration to estimate the requirements of N for maintenance. The rabbits were divided into five groups and offered the N-free ration at levels of 55,45,35,25 and 0 g per day, respectively.
     Daily gain in groupⅡ-Ⅴwere all higher than in group I (P<0.01),the optimal protein level (18.1%) can be obtained from the regression equation (y=-0.1147x2+4.1556x-13.154, R2=0.5851).The changes of some biochemical indices in developing period had the similar trend with that of in growing period. Compared with growing period, the ALP activity in developing period sharply decreased, while the circulation IGF-Ⅰconcentrations increased, with highest IGF-Ⅰconcentrations at 16%CP level in developing period. The NK cell activity, SI induced by LPS, and IL-1βcontents were also highest at 16% CP level, but spleen and thymus indices had a maximam value at 18% CP level, differed significantly with groupⅠorⅡ. SI induced by ConA was higher at 16 and 18% CP level than that at 14 and 20%(P<0.05). The changes of IgA, IgM and IgG were the same as growing period. The positive rate of antibody response to ovalbumin was also highest in groupⅢ, differed significantly from group I (P<0.05). The change with different protein levels in the parameters of SOD, NO and MDA were consistent with that of immune status. The protein levels had strong effects on caecal fermentation and microbial community, with highest concentrations of NH3-N and microbial protein, VFA contents and variety of microbial community in groupⅣ. Expression of hepatic IGF-I and PEPCK-C mRNA were also consistent with that of growing period. Average net protein utilization during developing period was 496g/kg, higher by 12% compared with growing period. The estimated N requirement for maintenance in N balance trial was 480 mg/kg BW0.75 per day, in agreement with the result from the trial in the N-free ration (486 mg/kgBW0.75 per day). The lower intake of N-free ration resulted in more N excretion, suggesting that protein catabolism may occur in the body of rabbit to meet maintenance requirements for N when the dietary N intake was very low.
     3. Optimal combinations of crude protein and amino acids in developing WHBE rabbits
     The effects of diets with different combinations of crude protein and amino acids on immune function and nitrogen metabolism were studied by nitrogen metabolism trial and immune function test. Thirty six adult WHBE rabbits(100 d old) were randomly divided into 6 groups(12-80, 12-100,12-120,16-80,16-100 and 16-120) according to 6 diets with different combination of CP-AA. The crude protein level in groups 12-80,12-100,12-120 was 12%, while that in group 16-80,16-100 and 16-120 was 16%. From group 12-80 to 12-120 or group 16-80 to 16-120, contents of lysine were 0.72,0.9 and 1.08%, and contents of methionine plus cystine were 0.52, 0.65 and 0.78%, respectively. Both daily weight gain and total N utilization were significant higher in group 12-120 and 16-80 than those in group 12-80 or 16-80 (P<0.01).While compared with the group 16-80, the content of total N excretion in group 12-120 significantly decreased from 2.10 to 1.59 g/d (P< 0.01).Combinations of crude protein and amino acids had significant effects on immune function, with the highest level of antibody response to ovalbumin in group 12-120, which was significant higher than that in group 12-100,16-100 and 16-120 (P<0.05). Both indices of spleen and thymus in group 12-80 and 160-100 were higher than those in the other 4 groups, although there were no significant differences among them except the spleen index in group 16-80.The serum total protein was increased with the increasing amino acids content. The blood urea N was highest in groups 16-100 and 16-120 (5.1mmol/l), which should significant differences from the other 4 groups (P<0.01,P<0.05).The suitable combinations of crude protein and amino acids were the diets in group 12-120 and 16-80, but as the total N excretion concerned, group 12-120 was optimal.
     In summary, the requirements of N for maintenance are 491 and 480 mg/kg BW0.75 for growing and developing WHBE rabbits, respectively. The net protein utilization during developing period (496g/kg) is higer than that during growing period (445g/kg). The optimal CP levels to assure the maximal growth performance of WHBE rabbit are 16.4 and 18.1% in growing and developing periods, respectively, while the range of 16-18% CP level are suitable to satisfy the need for immune response in either growing or developing periods. The optimal ceacal environment, the maximal antioxidant capacity, and the highest expression of hepatic IGF-ⅠmRNA and PEPCK-C mRNA may be obtained at the suitable CP levels. However, reducing CP level but increasing amino acids contents is effective to enhance immune function and lessen environment pollution in rabbit feeding procedure.
引文
Abbott EM, Pakins JJ, and Holmes PH.1988.Influence of dietary protein on the pathophysiology of haemonchosis in lambs given continuous infections. Research in veterinary science,45:41-49.
    Abecia L, Fondevila M, Balcells J, et al.2005.Molecular profiling of bacterial species in the rabbit caecum. FEMS.Microbiology Letter.244(1):111-115.
    Agca C,Greenfield RB,Hartwell JR, Donkin SS.2002.Cloning and characterization of bovine cytosolic and mitochondrial PEPCK during transition to lactation. Physiol.Genomics,11:53-63.
    Ahmed F, Quadri SS.1985.Effect of supplementation of essential amino acid on immune response in protein-deficient rats. Nutr. Rep. Int,31:711.
    Amalia EY.2004. The laboratory rabbit:an animal model of atherosclerosis research. Lab Animals,38:246-256.
    Apgar GA, Kornegay ET, Lindemann MD, and Notter DR.1995.Evaluation of copper sulfate and a copper lysine complex as growth promoters for weanling swine J. Anim. Sci,73,2640-2646.
    Aschkenasy A.1979. Prevention of immunodepressive effects of excess dietary leucine by isoleucine and valine in the rat. J. Nutr,109:1214.
    Asherson GL, Zembala M, Perera MA, Mayhew B, Thomas WR.1977.Production of immunity and unresponsiveness in the mouse by feeding contact sensitizing agents and the role of suppressor cells in the peyer's patches, mesenteric lymph nodes and other lymphoid tissues.Cell Immunol,33(1):145-155.
    Association of Official Analytical Chemist,1990.Official Methods of analysis,15th Edition. AOAC,Arlington, VA,69-90.
    Austic RE, Dietert RR, Sung YJ, and Taylor R L.1991.Amino acids in immune function. In:Proc.Cornell Nutr. Conf. Oct.8-10.109. Rochester, NY.
    Bailey M, Haverson K, Inman C,Harris C,Jones P, Corfield G, Miller B,and Stokes C.2005.The development of the mucosal immune system pre-and post-weaning: balancing regulatory and effector function. Proceeding of the Nutrition Soeciety, 64:451-457.
    Barta O,Shaffer LM, Huang LJ.1984.Separations of lymphocytes, monocytes and neutrophils.In:Barta,O.(Ed.),Laboratory Techniques of Veterinary Clinical Immunology. Charles C.Thomas, Springfield, IL, USA, pp.31-42.
    Baum Jamie I, Layman Donald K, Freund Gregory G, et al.2006.A reduced carbohydrate, increased protein diet stabilizes glycemic control and minimizes adipose tissue glucose disposal in rats.J. Nutr,136:1855-1861.
    Bell R and Hoffman-Goetz L.1983.Effect of protein deficiency on endogenous pyrogen-mediated acute phase proteinresponses. Can. J. Physiol.Pharmacol,61: 376-380.
    Bell RG, Hazell LA and Price P.1976.Influence of dietary protein restriction on immune competence Ⅱ.Efecct of lympoid tissue. Clin. Exp.Immunol, 26:314-326.
    Bennegadi N, Gidenne T, Licois L.2001.Impact of fiber deficiency and sanitary status on non-specific enteropathy of growing rabbit. Anim.Res,50:401-403.
    Berg RD,1996.The indigenous gastrointestinal microflora. Trend Microbiol, 4:430-435.
    Berger Alvin, Bruce German J, Chiang Bor-Luen, et al.1993.Influence of feeding unsaturated fats on growth and immune status of mice. J.Nutr,123:225-233.
    Bhargava K K, Hanson RP, and Sunde ML.1971.Effects of threonine on growth and antibody production in chicks infected with Newcastle disease virus. Poultry Sci, 50:710-713.
    Bhaskara P and Sivakumar B.1986. Interleukin-1 in malnutrition. Arch. Dis. Child, 61:182-185.
    Boulahrouf A, Fonty G, Gouet P.1991.Establishment counts and identification of the fibrolytic bacteria in the digestive tract of rabbit. Influence of feed cellulose content. Curr. Microbiol,22:1-25.
    Bounous G and Kongshavn PAL.1982.Influence of dietary protein on the immune system of mice.J.Nutr,115:1403.
    Bounous G, Kongshavn PA.1978.The effect of dietary amino acid on immune reactivity. Immunology,35(2):257-266.
    Bradley SF and Kauffman CA.1988.Protein malnutrition and the febrile response in the fischer rat. J.Leukocyte Biol,43:36-40.
    Brewer Nathan R.2006.Biology of the rabbit. Journal of animal association for laboratory animal science,43(1):8-24.
    Butcher GD, Miles RD.2002.Interrelationship of nutrition and immunity. Available at http://edis. ifas.ufl.edu.1-10.
    Calder Phlip C.2001.Nutrition and immunity function.Nutrition Clinique et Metabolism,15(4):286-297.
    Cann IKO, Kocherginskaya SA, A WB.1996.Denaturing gradient gel electrophoresis analysis of polymerase chain-reaction amplified genes coding for 16S rRNAs from ruminal fibrolytic bacteria. Proc Jap Soc Rumen Metabol Physiol,7:10-18.
    Carlos Munoz, Liana Schlesinger and Jean-Marc Cavaillon.1995.Interaction between cytokines, nutrition and infection. Nutrition Research,15(12) 1815-1844.
    Colette Spach and Alexander Aschkenasy.1979.Effects of a protein-free diet on the changes in Cyclic AMP and cyclic GMP levels induced by immunization in splenic T and B lymphocytes in the Rat. J.Nutr,109:1265-1273.
    Collier J and Vallance P.1989.Second messenger role for NO widens nervous and immune systems.Trends Pharmacol.Sci,10:427-432.
    Cook M and Miller CC.1991.Amino acids can influence immune response of animals.Feedstuffs,63(24):12.
    Cook ME.1991.Nutrition and the immune response of the domestic fowl.Crit. Rev. Poultry Biol,3:167-189.
    Cooper WC, Good RA, and Maritin T.1974.Effects of protein insufficient on immune responsiveness.Am.J.Clin.Nutr,27:647.
    Cunningham-Rundles S.Lin Deborah HO.1998.Nutrition and immune system of the gut. Nutrition,14:573-579.
    Cunningham-Rundles S.Malnutrition and gut immune function.1994.Cuur Opin Gastroenterol,10:664.
    Dabbert CB,Lochmiller RL, Waldroup PW, Teeter RG.1996.Examination of the
    dietary methionine requirements of breeding northern bobwhite, Colinus virginianus.Poultry Science,75(8):991-997.
    DE Blas C, Wiseman J (Editors).1998.The nutrition of rabbit. Wallingford UK, CAB International.
    De Blas JC,Maria J, and Rodriguez JM.1985.Units for feed evaluation and requirements for commercially grown rabbits. J.Anim Sci,60:1021-1028.
    De Blas JC,Perez MJ, Fraga E, Rodriguez JM and Galvez JF.1981.Effect of diet on feed intake and growth of rabbits from weaning to slaughter at different ages and weights. J.Anim.Sci,52:1225.
    DE Blas JC, Taboada E, Nicodemus N, Campos R, Piquer J and Mendez J.1996.The response of highly productive rabbits to dietary Threonine content for reproduction and growth. In Lebas F.(editor) Proceeding of the 6th World Rabbit Congress, Toulouse, Vol.1.Association Francaise de Cunculture, Lempdes.
    Demirel R, Caliskaner S.1999.A research on utilization of urea by New Zealand
    White, California rabbits, Turkish Journal of Agriculture & forestry,23(1):75-81.
    DeOme GC, Leffer EC.1972.Effect of cecotomy on digestive processes in the rabbit.J Amin. Sci,35:215.
    Doherty J F, Golden MH, Remick DG and Griffin GE.1994.Production of interleukin-6 and tumor necrosis factor-alpha in vitro is reduced in whole blood of severely malnourished children. Clin.Sci.(Lond.),86:347-351.
    Dorn AR, Moriarty CS, Osborne JP, et al.1986.A new system for mononuclear cell separation. Am.Clin.Prod. Rev,5:26-33.
    Durmic Z,Pethick DW,Pluske JR, Hampson DJ.1998.Changes in bacterial populations in the colon of pigs fed different sources of dietary fibre, and the development of swine dysentery after experimental infection. J Appl Microbiol, 85:574-582.
    Efron DT and Barbul A.1998.Modulation of inflammation and immunity by arginine supplements. Curr. Opin. Clin. Nutr. Metab. Care,1:531-538.
    Esparza M Luisa, Larralde Jesus and Alfredo Martinez J.1996.Development-related nutritional utilization and immune function in mice fed on two different protein
    sources.Nutrition research,16(5):829-839.
    Evoy D, Lieberman MD, Fahey TJ, Daly JM.1998.Immunonutrition:the role of arginine. Nutrition,14:611-617.
    Fernandez C and Fraga MJ.1996. Effect of fat inclusion in diets for rabbit on the efficiency of digestible energy and protein utilization.World rabbit science, 4:19-23.
    Fortun-Lamothe L, Boullier S.2006. A review on the interactions between gut microflora and digestive mucosal immunity. Possible ways to improve the health of rabbits, Livestock Science, doi:10.1016/j.livsci.2006.09.005.
    Fraga MJ, de Bias JC, Perez E, Rodriguez JM, Perez CJ and Galvez JF.1983.Effect of diet on chemical composition of rabbits slaughtered at fixed body weights. J.Anim.Sci,56:1097.
    Freeman BA and Crapo JD.1982.Biology of disease free radicals and tissue injury. Lab.Invest,47:412-426.
    Fukada H, Ozaki Y, Pierce AL, Adachi S,Yamauchi K, Hara A, Swanson P, Dickhoff WW.2004.Salmon growth hormone receptor:molecular cloning, ligand specificity, and response to fasting. Gen Comp Endocrinol,139:61-71.
    Gibson TE.1983.The influence of nutrition on the relationship between gastro-intestinal parasites and their host. Proceeding of nutrition society, 22:15-20.
    Gidenne T, Pinheriro V, Falcao-e-Cunba L.2000.A Comprehensive approach of the rabbit digestion:consequences of a reduction of in dietary fiber supply. Livest. Prod. Sci,64:225-237.
    Girard J, Ferre'P, Pe'gorier JP, Due'e PH.1992.Adaptions of glucose and fatty acid metabolism during perinatal period and suckling-weaning transition. Physiol Rev, 72:507-562.
    Gouet P, Fonty G.1979.Change in the digestive microflora of holoxenic rabbit from birth until adulthood. Ann.Biol.Anim. Bioch. Biophys,19:553-566.
    Greenfield RB,Cecava MJ,Donkin SS.2000.Changes in mRNA expression for gluconeogenic enzymes in liver of dairy cattle during the transition to lactation. J
    Dairy Sci,83:1228-1236.
    Guarner F, Malagelada JR.2003.Gut flora in health and disease. Lancet,360: 512-519.
    Hall ER,1952.Investigation on microbiology of cellulose utilization in domestic rabbits.J.Gen. Microbiol,7:350-357.
    Hane BG, Jager K, Drexler H.1993.The Pearsons product-moment correlation coefficient is better suited for identification of DNA fingerprint profiles than band matching algorithms. Electrophoresis,14:967-972.
    Hanson RW, Reshef L.1997.Regulation of phosphoenolpyruvate carboxykinase (GTP) gene expression. Annu Rev Biochem,66:581-611.
    Hesketh JE, Vasconcelos MH, Bermano G.1998.Regulatory signals in messenger RNA:determinants of nutrient-gene interaction and metabolic compartmentation. Br J Nutr,80:307-321.
    Higuchi R, Dollinger G, Fockler C,Watson R,1993.Kinetic PCR analysis:real-time monitoring of DNA amplification reactions. Bio/Technology,1.1:1026-1030.
    Hoffman-Goetz L and Kluger MJ.1979.Protein deficiency:its effects on body temperature in health and diseasestates.Am. J.Clin. Nutr,32:1423-1427.
    Hoffman-Goetz L and Marcon T.1983.Effect of in vitro amino acid supplementation of endogenous pyrogen fever. Nutr. Res,3:237-241.
    Hoover WH, Heitmann RN.1975.Cercal nitrogen metabolism and amino acid absorption in the rabbit. J.Nutr,105:245-252.
    Host A, Jacobsen HP, Halken S,Holmenlund D.1995.The natural history of cow's milk protein allergy/intolerance Eur J.Clin. Nutr,49(suppl):13-18.
    Houdijk Jos GM, Jessop Neil S,Knox David P and Kyriazakis Ilias.2005.Secondary infection of Nippostrongylus brasiliensis in lactating rats is sensitive to dietary protein content. British Journal of nutrition,93:493-499.
    Jecsai J, Teleki M, Juhasz B.1985.Effect of caecotrophy on protein and amino acid metabolism of Angro rabbits.Acta Veterinaria,33(1/2):51-57.
    Jose DG, and Good RA.1973.Quantitative effects of nutritional essential amino acid deficiencies upon immune responses to tumor in mice.J.Exp.Med,137:1.
    Kanamoto R, Yokota T and Hayashi Shin-Ichi.1994. Expression of c-mys and Insulin-like factor-Ⅰ in the liver of growing rat vary reciprocally in response to change in dietary protein. J.Nutr,'124:2329-2334.
    Kaqnoff MF.1978.Effects of antigen-feeding on intestinal and systemic immune responses.Ⅲ.Antigen-specific serum-mediated suppression of humoral antibody responses after antigen feeding. Cell Immunol,40(1):186-203.
    Kauffman CA, Jones PG and Kluger MJ.1986.Fever and malnutrition:endogenous pyrogen/interleukin-1 in mal nourished patients.Am.J.Clin. Nutr,44:449-452.
    Kelley Darshan S,Nelson Gary J, Serrato Claire M, et al.1988.Effect of type of dietary fat on induces of immune status of rabbit.J.Nutr,18:1376-1384.
    Kenney Mary Alice, Magee Joan Linder and Piedad-Pascual Felicitas.1970.Dietary Amino Acids and Immune Response in Rats.J.Nutr,300:1063-1072.
    Keshavarz-Valian Hossein, Alger Nelda E and Boissonneault Gilbert A.1985.Effects of p-aminobenzoicacid, methionine, threonine and protein levels on susceptibility of mice to plasmodium berghei.Journal of Nutrition,115(12): 1613-1620.
    Keusch Gerald T.2003.The History of Nutrition:Malnutrition, Infection and Immunity.J. Nutr,133:336S-340S,
    Keusch GT.1993.Malnutrition and the thymus gland. In:Nutrient Modulation of the Immune Response.(Cunningham-Run-dles S.,ed.)pp.283-299. Marcel Dekker, Inc.,New York, NY.
    Kew Samantha, Wells Sharon M, Parveen Yaqoob, et al.1999.Dietary glutamine enhances murine T-lymphocyte responsiveness.Journal of Nutrition, 129:1524-1531.
    Kirchner Se'verine, Kaushik Sadasivam and Ste'phane Panserat,2003.Low Protein Intake Is Associated with Reduced Hepatic Gluconeogenic Enzyme Expression in Rainbow Trout (Oncorhynchus Mykiss) J.Nutr,133:2561-2564.
    Klasing KC,Leshchinsky TV.2000.Interactions between nutrition and immunity. Lessons from animal agriculture. In:Nutrition and immunology:Principles and practice. Editors:Gershwin JB, Germanand Keen CL.Elsevier:Amsterdan. P. 363-373.
    Klasing KC.1988.Nutritional aspects of leukeytic cytokine.J.Nutr,118:1436-1446.
    Klasing, KC and Barnes DM.1988.Decreased amino acid requirements of growing chicks due to immunologic stress.J.Nutr,118:1158.
    Kleinman RE.1991.Immune consequences of dietary proteins in infancy. Carnation nutrition education series,2:109-120.
    Kleinman RE.1992.Immune response to dietary antigens and the development of hypoallergenic formulas. Nutrition research,12(1):151-160.
    Kocherginskaya SA, Aminov R, White BA.2001.Analysis of the rumen bacterial diversity under two different diet conditions using denaturing gradient gel electrophoresis, random sequencing, and statistical ecology approaches Anaerobe, 7:119-134.
    Kornegay ET, Lindemann MD and Ravindran V.1993.Effects of dietary lysine levels on performance and immune response of weanling pigs housed at two floor space allowances.J Anim Sci,71:552-556.
    Korzeiewski C, Callewaert DM.1983.An enzyme-release assay for nature cytotoxicity. J Immunol Methods,64:313-20.
    Kwark H, Austic RE and Dietert RR.1999.Influence of dietary arginine concentration on lymphoid organ growth in chickens, Poultry Science,78: 1536-1541.
    Lebas F, Gidenne T, Perez JM and Licois D.1998.Nutrition and pathology.In:De Blas C and Wiseman J.(eds.).The nutrition of the rabbit. CAB publishing, Wallingford, UK,197.
    Lebas F.1998.Nutrition requirement of rabbits, J Appl.Rabbit Ret,(1):14-16.
    Lebas, F, Coudert P, Rouvier R and De Rochambeau H.1984.Le Lapin:Elevage et pathology, FAO (ed.)
    Lelkes, L.1986.Mucoid enteritis-overeating and microbial inbalance in the development of mucoid enteropathy in rabbits. J.Appl.Rabbit Res,9:148-151.
    Lemaigre FP, Rousseau GG.1994.Transcriptional control of genes that regulate glycolysis and gluconeogenesis in adult liver. Biochem J.,303:1-14.
    Lemonzy S,Pucilowska JB,Underwood LE.1994.Reduction of IGF-I in protein restricted rats is as-sociated with differential regulation of IGF-binding protein messenger ribonucleic acids in liver and kidney, and peptides in liver and serum. Endocrinology,135(2):617-623.
    Lippard V, Schloss O and Johnson P.1936.Immune reactions induced in infants by intestinal absorption of incompletely digested cow milk protein. Am. J.Dis. Health,51:562-574.
    Lyoumi S, Tamion F, Petit J, et al.1998.Induction and modulation of acute-phase response by Protein malnutrition in rats:comparative effect of systemic and localized Inflammation on Interleukin-6 and acute-phase protein synthesis, J. Nutr,128:166-174.
    Maerten L, Luzi F, and De Groote G.1997.Effect of dietary protein and amino acids on the performance, carcass composition and N-excretion of growing rabbits. Ann. Zootech,46:255.
    Maerten, L.1992.Rabbit nutrition and feeding:A review of some developments.J. Appl.Rabbit Res,15:889.
    Maertens Luc,2003.Feeding rabbits, in:Richard O.K. and Church DC (editors), Livestock feeds and feeding,5th Edition. Englewood Cliffs, New Jersey: Prentice Hall Inc,482.
    Marie C and Gelato.1993.Growth hormone-insulin-like growth factor Ⅰ and immune function,TEM,4:106-110.
    Marounek M, Vovk SJ, and Skrivanova V.1995.Distribution of activity of hydrolytic enzymes in the digestive tract of rabbits.Br. J.Nutr,73:463.
    McDonald P, Edwards RA, Greenhalgh JFD.2001.Animal Nutrition,6th Edition. Longman/Wiley, New York.
    McMurtry JP, Frands GL, Upton Z.1997.Insilin-like growth factors in poultry. Domest.Anim.Endocrinol,14:199-229.
    Miller BG, Newby TJ, Stokes CR, Brown PJ, Bourne FJ.1984.The importance of dietary antigen in the cause of postweaning diarrhea in pigs. Am J Vet Res, 45(9):1730-1733.
    Milner JA, Wakerling AE, and Visek WJ.1974.Effect of arginine deficiency on growth and intermediary metabolism in rats.J. Nutr,104:1681-1689.
    Miura Y, Kato H, Hoguchi T.1992.Effect of dietry protein on IGF-I messenger ribonucleic acid content in rat liver. Bri J Nutri,67:257-265.
    Miyasaki N, Takizawa K, Hirata T, Ueno K, Kadowaki M, Ishibashi T.1997.Effects of age on amino acid requirement for maintenance of broilers. Hokuriku J.Zootech. Sci,74,56-59.
    Mocncada S,Palmer RM and Higgs EA,1991.Nitric oxide:physiology, pathophyology, and pharmacology. Pharmacol.Rev,43:109-142.
    Motta Ferreira W, Fraga MJ, and Carabano R.1996.1nclusion of grape pomace in substitution for luceme hay in diets for growing rabbit. Animal Science, 63:167-174.
    Muyzer G, De Waal EC,Uitterlinen AG.1993.Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16SrRNA.Appl Eviron Microbiol,59: 695-700.
    National Research Council (NRC).1977.Nutritional Requirements of Rabbits 2nd Edition. National Academy of Science. Washington. DC.USA.1-30.
    Padilha MTS,Licois D,Gidenne T, Carre B.1999.Caecal microflora and fermentation pattern in exclusively milk-fed young rabbits.Reprod.Nutr.Dev, 39:223-230.
    Parker NT, Goodrum KJA.1990.Comparison of casein, lactalbumin, and soy protein effect on the immune response to a T-dependent antigen. Nutrition research, 10(7):781-792
    Partridge GG, Garthwaite PH, Findlay M.1989. Protein and energy retention by growing rabbits offered diets with increasing proportion of fibre.Journal of Agricultural Science,112:171-178.
    Pedroso FL, de Jesus-Ayson EGT, Cortado HH, Hyodo S,Ayson FG.2006.Changes in mRNA expression of grouper (Epinephelus coioides) growth hormone and insulin-like growth factor I in response to nutritional status. Gen. Comp. Endocrinol,145:237-246.
    Peeters JE.1987.Etiology and pathology of diarrhoea in weanling rabbits.In Auxilia T(Ed.),Rabbit Production Systems including Welfare.Commission of the European Communities,127-137.
    Pilkis SJ, Granner DK.1992.Molecular physiology of the regulation of hepatic gluconeogenesis and glycolysis. Annu Rev Physiol,54:885-909.
    Popovic Petar J, Zeh Herbert J.and Ochoa Juan B.2007.Arginine and immunity. J. Nutr,137:1681S-1686S.
    Regensbogenova M, Pristas P, Javorsky P, Moon-van der Staay SY, van der staay GWM, Hackstein JHP, Newbold CJ, McEwan NR.2004.Assessment of ciliates in the sheep rumen by DGGE. Lett Appl Microbiol,39:144-147.
    Reinhardt KLC, and Steward KLW.1979. Antibody affinity and clearance function studies in high and low antibody affinity mice:The effect of protein deficiency. Immunology,38:735-739.
    Salimonu LS.1993.Natural killer activity in protein-calorie malnutrition. In:Nutrient modulation of the immune response. (S.Cunningham-Rundles, ed.)pp.359-368. Marcel Dekker, Inc.,New York, NY.
    SAS.1997. Changes and enhancements through Release 6.12.Cary, NC USA:SAS Inst.
    Schreiber RA, Walker WA.1989.Food allergy:facts and fiction. Mayo Clin Proc, 64(11):1381-1391.
    Schultize WH,Moughan P J, Smith WC.1988.Amino acid requirements of growing meat rabbit. The amino acid composition of rabbit whole-body issue a theoretical estimate of ideal amino acid. Animal Production,47(2):297-301.
    Searle L.1984.The berthelot or indophenol reaction and its use in the analytical chemistry of nitrogen:a review. Analyst,109:549-568.
    Shigeru Konashi, Kazuaki Takahashi and Yukio Akiba.2000.Effects of dietary essential amino acid deficiencies on immunological variables in broiler chickens.British Journal of Nutrition,83:449-456
    Simpson JM, Ccrackwnv J, White BA.1999.Application of denaturing gradient
    elelectrophores is for the analysis of theporcineg astrointestinal microbiota. J Micro Methods,36:167-179.
    Slade LM and Hintz HF.1969.Comparison of digestion in horses,ponies, rabbits and guinea pig. J.Anita. Sci,28:842-843.
    Slade, LM, Robinson DW.1970.Nitrogen metabolism in rabbits and guinea pigs. J. Anim.Sci,30:1044.
    Snedecor GW, Cochran WG.1989.Statistical Methods,8th edition. Iowa state University Press, Ames, IA.
    Stocks CR, Miller BG, Bailey M, Wilson AD, Bourne FJ.1987.The immune response to dietary antigens and its influence on disease susceptibility in farm animals. Vet Immunol Immunopathol,17(1-4):413-423.
    Stokes C R, Newby TJ and Bourne F J.1983.The influence of oral immunization on local and systemic immune responses to heterologous antigens.Clin Exp Immunol,52(2):399-406.
    Straus DS,Takemoto CD.1990.Effect of dietary protein deprivation on insulin-like growth factor IGF-Ⅰ and Ⅱ,IGF binding protein 2 and serum albumin gene expression in rat. Endocrinology,127:1849-1860.
    Suarez Butler MF, Bobbi LH, Kelli A, et al.2005.Arginine supplementation enhances mitogen-induced splenocyte proliferation but does not affect in vivo indicators of antigen-specific immunity in mice.J.Nutr,135:1146-1150.
    Susanna CR, Deborah HL.1998.Nutrition and the immune system of the gut. Nutrition,14:573-579.
    Swarbrick ET, Stokes CR, Soothill JF.1979.Absorption of antigens after oral immunisation and the simultaneous induction of specific systemic tolerance.Gut, 20:121-125.
    Taboada E, Mendez J and DE Blas JC.1996.The response of highly productive rabbits to dietary sulphur amino acid content for reproduction and growth. Reproduction, Nutrition and Development,36:191-203.
    Takahashi S, Kajikawa M, Umezawa T, Kato H, et al.1990.Effect of dietary proteins on the plasma immunoreactive insulin-like growth factor-1/somatomedin C concentration in the rat. Br. J. Nutr,63:521-534.
    Thomas MP and Bhattacharjee JK.1981.Effect of dietary essential amino acid limitations upon the susceptibility to salmonella typhimurium and the effect upon humoral and cellular immune responses in mice. Infection and immunity,32(1): 251-259.
    Tsiagbe VK, Cook ME, Harper AE and Sunde ML.1987a. Efficacy of cysteine in replacing methionine in the immune responses of broiler chicks. Poultry Sci, 66:1138-1146.
    Tsiagbe VK, Cook ME, Harper AE, and Sunde ML.1987b. Enhanced immune responses in broiler chicks fed methionine-supplemented diets. Poultry Sci, 66:1147-1154.
    Uehara A, Gottschall PE, Dahl RR and Arimura A.1987.Stimulation of ACTH release by human interleukin-β, but not by interleukin-a, in conscious, freely-moving rats. Biochem. Biophys.Res. Commun,146:1286-1290.
    Uma Srivastava, Colette Spach, and Alexander Aschkenasy.1975.Cyclic AMP metabolism and nucleic acid content in thelymphocytes of the thymus, spleen, and lymph Nodes of protein-deficient rats.J.Nutr,105:924-938.
    van Buul-Offers SC and Kooijman R.1998.The role of grow hormone and insulin-like growth factors in the immune system.CMLS Cellular and Molecular Life Sciences,54:1083-1094.
    van Heugten E, Spears JW, Coffey MT, Kegley EB and Qureshi MA.1994a. The effect of methionine and aflatoxin on immune function in weanling pigs.J.Anim. Sci.72:658-664
    van Heugten E, Spears JW and Coffey MT.1994b.The effect of dietary protein on performance and immune response in weanling pig subjected to an inflammatory challenge.J.Anim.Sci,72:2661-2669.
    .Van Soest PJ, Robertson Lewis BA.1991.Methods for dietary fiber, neutral detergent fiber, and non starch polysaccharides in relation to animal nutrition. J. Dairy. Sci.74:3583-3597.
    Vande Haar MJ, Moats-Staats BM, Davenport ML, et al.1991.Reduced serum concentrations of insulin-like growth factor-I (IGF-Ⅰ) in protein-restricted growing rats are accompanied by reduced IGF-I mRNA levels in liver and skeletal muscle.J.Endocrinol.130:305-312.
    Varela-Alvarez H.1991.Feeding rabbits, in:Church DC (ed). Livestock feeds and feeding,3th Edition.Englewood Cliffs, New Jersey:Prentice Hall Inc,454.
    Wang HF, Zhu WY, Yao W, et al.2007.DGGE and 16S rDNA sequencing analysis of bacterial communities in colon content and feces of pig fed whole crop rice. Anaerobe,13:127-133.
    Wang Ying, Eleswarapu Satyanarayana, Beal WE, et al.,2003.Reduced serum insulin-like growth factor (IGF)'I is associated with reduced liver IGF-Ⅰ mRNA and liver growth hormone receptor mRNA in food-deprive cattle,J.Nutr,133:2555-2566.
    Wilson M, Seymour R and Henderson B.1998.Bacterial perturbation of cytokine networks.Infect. Immun,66:2401-2409.
    Woloski B M RNJ,Smith ET, Meyer WJ, Fuller GM and Blalock JE.1985. Corticotropin-releasing activity of monokines. Science,230:1035-1037.
    Woodward BD, Woods JW and Crouch DA.1992.Direct evidence that primary acquired cell-mediated immunity is less resistant than is primary thymus-dependent humoral immunity to the depressive influence of wasting protein-energy malnutrition in weanling mice. American Journal of Clinical Nutrition,55,1180-1185.
    Wu R, Coleman N, Stanley M.1996.Different susceptibility of cervical keratinocytes containing human papillomavirus to cell mediated cytotoxicity. Chin Med J, 109(11):854-8.
    Xiccato G.1998.Fat Digestion. In:DE Blas C,Wiseman J(Editors).The nutrition of rabbit. CAB International publishing. Wallingford UK.55-68.
    Zhu WY, Williams BA, Konstantinov SR Tamminga S, De Vos W M, Akkermans AD. 2003.Analysis of 16S rDNA reveals bacterial shift during in vitro fermentation of fermentable carbohydrate using piglet faeces as inoculum.Anaerobe,9: 175-180.
    Zinn RA, Owens FN.1986.A rapid procedure for purine measurement and its use for estimating net ruminal protein synthesis. Can Anim Sci,66:157-166.
    Zoetendal EG, Akkermans AD, De Vos W.1998."Temperature gradient gel electrophoresis analysis of 16S rRNA from human fecal samples reveals stable and host-specific communities of active bacteria. Appl Environ Microbiol,64: 3854-3859.
    白云峰,谷子林,霍贵成.,2004.日粮蛋白水平对獭兔泌乳、增重及被毛密度的影响.中国畜牧杂志,40(5):23-25。
    蔡春芳,吴康,潘新法等.2001.蛋白质营养对异育银鲫生长和免疫力的影响.水生生物学报,25(6):590-596.
    陈民利,蔡月琴,陶涛等.2008.微卫星标记对WHBE兔封闭群、日本大耳白兔和新西兰兔的遗传分析.中国比较医学杂志,18(9):21-27.
    陈民利,赵伟春,应华忠等.2005.WHBE兔遗传特异性的RAPD分析.浙江大学学报-农业与生命科学版,31(4),493-495。
    陈伟健.2008.蛋白能量平衡对反刍动物饲料组合效应的影响及其机理研究,浙江大学博士学位论文.
    冯宗慈,高民.1993.通过比色测定瘤胃液氨氮含量方法的改进.内蒙古畜牧科学,(4):40-41.
    付琳林,李海星,曹郁生.2004.利用变性梯度凝胶电泳分析微生物多样性.生物技术通报,2,39-40.
    高启禹,吴襟,徐光翠等.2006.寡糖对SPF大鼠肠道微生物多样性影响的研究.生物技术,16(5):28-30.
    杭苏琴,毛胜勇,黄瑞华等.2006.断奶仔猪饲喂甘露寡糖后粪样菌群的变化.农业生物技术学报,14(5):701-705.
    侯永清,呙于民,周毓平.2000.蛋白质、氨基酸营养与动物机体免疫.饲料工业,21(8):5-7.
    侯永清,呙于明,周毓平等.2001.日粮蛋白质、赖氨酸、蛋氨酸及苏氨酸水平对早期断奶仔猪免疫机能的影响.中国畜牧杂志,37(4):18-20.
    胡晓武,张向民,吴清朗等.1996.血清碱性磷酸酶降低的临床意义.上海医学 检验杂志.11(2):81.
    科研条件发展“九五”计划和2010年远景目标纲要,原国家科委,1997.
    雷秋霞,李福昌,吴洪涛.2003.不同蛋白水平对生长肉兔生长性能及血液生化指标的影响.中国养兔杂志,2:21-23.
    李成文.1990.现代免疫化学技术.上海:上海科学技术出版社,8.
    李宏,魏云霞.2002.家兔日粮营养水平的综合评价及家兔的饲养标准.中国草食动物,2:38-41.
    李在连,冯永堂主编.2001.《临床免疫学》.科学出版社.
    李振,李平.2002.蛋白质营养与家禽免疫.中国饲料,18:22-23.
    刘世明,张力,魏春梅,常城,卢月香,彭大惠.1991.德系安哥拉兔蛋白质维持需要量及可消化粗蛋白利用率的研究.畜牧兽医学报,22(4):323-326.
    刘艳芬,马建升,黄银姬,黄晓亮,廖建才,2006.谷氨酰胺对肉仔鸡免疫器官发育及免疫功能的影响.中国兽医学报,26(5):567-569.
    任家玲.1995.生长肥育兔营养水平的研究.中国养兔杂志,1:18-19。
    施新猷,1989.《医学实验动物学》.西安:陕西科学技术出版社,48-49.
    唐良美,刘曼丽.1987.日粮的能量及蛋白质水平对肥育兔生产性能的影响.中国养兔杂志,6:21-23。
    汪海峰.2006.脆茎水稻营养学评价及其对猪生产性能和肠道微生物区系的影响,浙江大学博士学位论文.
    汪平,简文素.2003.不同营养水平对獭兔生长毛皮品质影响的研究.四川草原,2:29-31.
    王士长,陈金茂.1999.不同营养水平对肉兔生产性能的影响.中国养兔杂志,6:20-23.
    谢晓红,刘曼丽.1994.齐卡生长兔日粮适宜能量、蛋白水平的研究.中国养兔杂志,4:16-21.
    谢晓红,唐良美.1990.粗蛋白和粗纤维水平对肉兔日粮消化率的影响.中国养兔
    杂志,3:16-18.
    杨凤主编.2003.动物营养学,第二版,北京:中国农业出版社.160-175.
    杨俊涛综述.1997.谷氨酰胺与免疫细胞.国外医学.创伤与外科基本问题分册,18:3-7.
    姚文,朱伟云,韩正康,Akkermans ADL,Williams B,Tamminga S.2004.应用变性梯度凝胶电泳和16S rDNA序列分析对山羊瘤胃细菌多样性的研究.中国农业科学,37:1374-1378.
    张永翠,李福昌.2008.日粮添加不同水平蛋氨酸对2~3月龄肉兔生长发育、免疫性能及血液生化指标的影响.西南农业学报,21(2):472-475.
    赵国成.1996.粗纤维对家兔的营养作用.毛皮动物饲养,3:11-13.
    赵国先,王余丁,朱慧中等,1997.肉兔日粮氨基酸水平与氮沉积.中国饲料,18:12-13.
    中华人民共和国质量技术监督检验检疫总局.2001.中华人民共和国国家标准,实验动物—兔配合饲料GB14924.4-2001.北京:中国标准出版社.
    祝素珍,李福昌.2004.2~3月龄肉兔日粮消化能水平对消化代谢和产肉性能影响的研究.动物营养学报,16(4):51-57.

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