n-3PUFA抑制NFκB活化与骨骼肌生长的关系研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
本试验的目的是研究日粮中持续添加亚麻籽(富含n-3 PUFA)对生长肥育期猪肌肉生长的影响,并在细胞水平探讨了n-3 PUFA影响肌肉生长的分子机制。
     课题的研究内容由两部分组成,第一部分为动物试验,研究日粮中持续添加亚麻籽(富含n-3 PUFA)对生长肥育期猪肌肉块重量的影响,并在机体水平研究了基因表达与肌肉块重之间的关系;第二部分为细胞培养试验,是针对日粮中持续添加亚麻籽(富含n-3 PUFA)对生长肥育期猪肌肉生长的调控效果,在细胞水平探讨了n-3 PUFA调控肌肉生长的分子机制。
     第一部分,动物试验。试验采用单因子完全随机设计,选择80±4d健康去势公猪24头,按体重随机分为4组,每组6重复栏,单栏饲养。设计生长期(80-140d)及肥育期(140-170d)两种日粮,其中对照日粮由玉米、豆粕和脂肪粉等主要原料构成;试验日粮中加入10%的亚麻籽而不用脂肪粉,两种日粮等能等氮。4组猪随机接受日粮处理,其中第1组饲喂对照日粮(C组),其余3组猪分别在屠宰前30d,60d和90d饲喂试验日粮(分别为T1,T2和T3组),而其他时间饲喂对照日粮,试验期共90d。度量了各处理组胴体性状和肉质性状;以及背最长肌、后肢肌肉块重量(股四头肌、股二头肌、瓣膜肌、半腱肌、股薄肌和腰肌)的影响;采用气相色谱方法分析了饲料、肌肉以及脂肪组织中脂肪酸组成。并利用半定量RT-PCR法测定超氧化物酶体增殖激活受体(peroxisomeproliferators-activated receptor,PPARγ)及肿瘤坏死因子α(tumor necrosis factor,TNFα)在脾脏、肌肉组织和脂肪组织中的mRNA丰度,在试验结束时用ELISA试剂盒测定血清中TNFα浓度。主要研究结果如下:
     1.猪生长肥育期添加亚麻籽对组织中n-3PUFA富集量和肌肉块重量的影响。在生长肥育猪170日龄屠宰时,尽管各处理组背膘厚、瘦肉率、眼肌面积均没有显著影响(P>0.05)。各处理组股二头肌重、瓣膜肌、半腱肌和腰肌重差异不显著(P>0.05)。背最长肌、股四头肌和股薄肌重随亚麻籽添加时间的延长呈线性上升(P<0.05)。背最长肌,皮下脂肪组织中LNA含量随亚麻籽添加时间的延长呈极显著线性上升(P<0.01)。背最长肌和皮下脂肪组织中二十碳五烯酸(eicosapentenoic acid,EPA)和二十二碳五烯酸(Docosapentaenoic Acid,DPA)含量随添加时间的延长呈极显著线性上升(P<0.01)。此外,肌肉组织中二十二碳六烯酸(Docosahexaenoic Acid,DHA)含量随添加时间的延长呈极显著二次曲线上升(P<0.01)。回归分析发现背最长肌重随肌肉中n-3PUFA(R~2=0.89,P<0.01),尤其是α-亚麻酸(α-Linolenic acid,LNA)(R~2=0.86,P<0.01)含量的增加而呈显著的二次曲线上升。这些结果表明在生长肥育猪屠宰前30d-90d添加亚麻籽,通过提高组织中n-3PUFA富集量,促进了背最长肌、半腱肌和股薄肌的生长,提高肌肉重。
     2.为进一步在机体水平研究基因表达与肌肉块重之间的关系,试验分析了猪生长肥育期添加亚麻籽对PPARγ、TNFα基因表达和肌肉块重量的影响。脾脏中PPARγ的表达随亚麻籽添加时间增加呈线性增加(P<0.01),肌肉组织中则呈二次曲线增加(P<0.01),但脂肪组织中PPARγ的表达量没有受到亚麻籽添加的影响(P=0.095)。随着亚麻籽添加时间的延长,脾脏中的TNFαmRNA丰度呈线性降低(P<0.01),肌肉组织中(P<0.01)和脂肪组织(P<0.01)中TNFα的mRNA丰度也随亚麻籽添加时间呈线性降低。随着亚麻籽添加时间的延长,血清中TNFα浓度线性降低(P<0.01)。脾脏中PPARγ与TNFα(R~2=0.77,P<0.001)的mRNA丰度有极显著的负相关。肌肉组织中PPARγ的表达量与TNFα(R~2=0.70,P=0.002)有极显著的负相关。脾脏中PPARγ的表达量与血清中TNFα浓度有极显著的负相关(R~2=0.59,P<0.01)。肌肉组织中PPARγ的表达量与血清中TNFα浓度之间显著的负相关(R~2=0.52,P<0.05)。回归分析发现背最长肌重分别与背最长肌中PPARγ表达量(R~2=0.80,P<0.01)和TNFα表达量(R~2=0.87,P<0.01)有显著的二次曲线关系。结果表明持续添加亚麻籽日粮可能以依赖PPARγ的机制下调TNFα基因表达,从而提高生长肥育猪肌肉块重量。
     第二部分,细胞培养试验。为了进一步研究持续添加亚麻籽日粮对生长肥育猪骨骼肌重的影响机制,体外培养C2C12小鼠骨骼肌细胞。试验分为4组,其中第1组为在培养的小鼠C2C12骨骼肌细胞中添加牛血清蛋白(Bovine serumalbumin,BSA)(正对照组),第2组为添加棕榈酸(Palmitic acid,PTA)(负对照组),第3组为添加α-亚麻酸(α-linolenic acid,LNA),第4组为添加二十碳五烯酸(eicosapentenoic acid,EPA)。在培养的小鼠C2C12骨骼肌细胞中分别添加600μM BSA、PTA、LNA和EPA,培养24小时后,细胞用100nM胰岛素培养10min,采用实时定量PCR方法测定各处理组PPARγ、TNFα及肌肉环状指基因1(muscle RING finger 1,MuRF1)基因的表达量。同时,培养的小鼠C2C12骨骼肌细胞中分别添加300μM、600μM的BSA、PTA、LNA和EPA,培养24小时后,细胞用100nM胰岛素培养10min,采用Western blot方法测定了各处理组骨骼肌细胞中IκBα蛋白量。试验进一步在培养的小鼠C2C12骨骼肌细胞中分别添加300μM、600μM的BSA、PTA、LNA和EPA,培养24小时后,细胞用100nM胰岛素培养10min,采用EMSA方法测定了各处理组骨骼肌细胞中NF-κB活性的影响。主要研究结果如下:
     n-3PUFA对C2C12骨骼肌细胞NF-κB活性和MuRF1基因的影响。在培养的骨骼肌细胞中持续添加的EPA(600μM,24小时)能够提高PPARγmRNA的丰度2.3倍数(P<0.01)。LNA只提高了PPARγmRNA的丰度1.08倍。而600μM棕榈酸,培养24小时,抑制了PPARγ基因的mRNA丰度(P<0.01)。分别在小鼠C2C12骨骼肌细胞中分别添加600μM LNA、EPA,培养24小时,TNFα基因的mRNA丰度分别被抑制了1.06、2.93倍。而棕榈酸通过抑制了PPARγ基因的mRNA丰度,提高了TNFα基因表达(P<0.01)。小鼠C2C12骨骼肌细胞中分别添加300μM LNA、EPA,培养24小时,并没有影响到骨骼肌中IκBα的蛋白质表达量。在同样条件下,分别添加600μM LNA和EPA,LNA依然没有影响到骨骼肌中IκBα的蛋白质表达量,而IκBα的蛋白质表达量被EPA显著提高了86%(P<0.01)。添加棕榈酸(600μM,24小时)能够降低细胞中39%IκBα蛋白质水平。分别添加600μM LNA和EPA,LNA没有影响到C2C12细胞核中NF-κB的蛋白质含量,而EPA降低了细胞核中NF-κB的蛋白质含量;添加600μM PTA提高了C2C12细胞核中NF-κB的蛋白质含量。在本试验中,分别添加600μM LNA和EPA,LNA并没有影响到骨骼肌细胞中MuRF1基因表达,而MuRF1基因表达量被EPA显著抑制了3.38倍(P<0.01)。添加促进IκBα蛋白质降解的棕榈酸(600μM,24小时)极显著提高了MuRF1基因表达(P<0.01)。结果表明,二十碳五烯酸通过PPARγ/TNFα/IκBα/NF-κB信号通路,抑制了MuRF1基因表达,从而减少了骨骼肌蛋白质降解,促进正常生产条件下动物骨骼肌生长。
     结论:1、在生长肥育猪屠宰前30d-90d添加亚麻籽,通过提高组织中n-3PUFA富集量,促进了背最长肌、半腱肌和股薄肌的生长,提高肌肉重。2、持续添加亚麻籽日粮可能以依赖PPARγ的机制下调TNFα基因表达,从而提高生长肥育猪肌肉块重量。3、二十碳五烯酸通过PPARγ/TNFα/IκBα/NF-κB信号通路,抑制了MuRF1基因表达,从而减少了骨骼肌蛋白质降解,促进正常生产条件下动物骨骼肌生长。
The aim of the study was to investigated that the effect of duration of feeding linseed diet on the skeletal muslce growth of the growing-finishing pigs,and the molecular mechanism of n-3PUFA regulating skeletal muscle growth of growing-finishing pigs.
     The contents of the research were mainly composed of two parts:the first part was the animal feeding experiments,which was to investigated that the effect of duration of feeding linseed diet on the skeletal muslce growth of the growing-finishing pigs and explore the relationship between gene expression and muslce mass;the second part was in vitro experiment,which investigated the molecular mechanism of n-3PUFA regulating skeletal muscle growth of growing-finishing pigs.
     The fisrt part:the animal feeding experiments.Two isoenergetic and isonitrogenous diets were formulated,and one of which was the basal diet and another one was the linseed diet including linseed at the level of 10%.Twenty-four Landrace×Yorkshire barrows weighing 35±3.7 kg were randomly assigned to four treatments with six individuals per treatment.Pigs in treatment 1(T1) fed the control diet throughout the experimental period,while pigs in T2,T3 and T4 fed the control diet except for 30,60,and 90 d prior to slaughter when the linseed diet were fed.The experiment was conducted for 90 days.Carcass quality and meat quality data were collected and analyzed.The longissimus dorsi muscle mass,posas minor muscle mass and each muscle mass in the hind leg were weighted.Additionally,fatty acid composition(%) of the diet,the longissimus dorsi muscle and the backfat were analyzed by gas chromatography method.PPARγand TNFαmRNA expression levels in muscle,spleen and adipose tissue,and plasma concentrations of TNFαdata were measured and analyzed.
     1.Duration of dietary linseed feeding affects the intramuscular fat,muscle mass and fatty acid composition in pig muscle.No significant difference(P>0.05) was observed for average backfat thickness,lean meat percentage,loin muscle area, whereas the intramuscular fat content increased linearly(P<0.01) as prolonged the time of feeding linseed diet.As prolonged the time of feeding linseed diet,the longissimus dorsi muscle mass,quadriceps femoris muscle mass and semitendinosus muscle mass increased linearly(P<0.01).Duration of feeding linseed diet linearly increased(P<0.01) the LNA,EPA and C22:5n-3 concentrations in the longissimus dorsi muscle and backfat.There was significant quadratic relation between the intramuscular fat content and the n-3 polyunsaturated fatty acids(PUFA) enrichment (R~2=0.87,P<0.01),or LNA enrichment(R~2=0.91,P<0.01) in the longissimus dorsi muscle.Likewise,the longissimus dorsi muscle mass was also quadratically related to the n-3PUFA enrichment(R~2=0.89,P<0.01),or LNA enrichment(R~2=0.86,P<0.01) in the longissimus dorsi muscle.These results revealed that duration of feeding linseed diet may stimulate intramuscular fat accumulation,and promote the hypertrophy of the longissimus dorsi muscle,quadriceps femoris muscle and semitendinosus muscle mass by increasing the n-3PUFA enrichment,especially LNA enrichment in the longissimus dorsi muscle.
     2.Duration of feeding linseed diet influences peroxisome proliferator-activated receptorγand tumor necrosis factor gene expression,and muscle mass of growing-finishing barrows.The expression of PPARγin longissimus muscle and spleen increased(P<0.01) linearly as prolonged the time of feeding linseed diet,while the expression of PPARγin adipose tissue were not affected(P=0.095).Duration of linseed addition linearly decreased(P<0.01) TNFαgene expression levels in the longissimus dorsi muscle,adipose and spleen,and serum concentration of TNFαas well.The expression levels of PPARγnegatively correlated with the expression of TNFαin muscle(R~2=0.70,P<0.001) and spleen(R~2=0.77,P<0.001) respectively. Likewise,PPARγexpression level in spleen(R~2=0.59,P<0.01) or muscle(R~2=0.52, P<0.05) negative correlated with serum TNFαconcentration.There were significant quadratic relation between muscular PPARγ(R~2=0.80,P<0.01) or muscular TNFα(R~2=0.87,P<0.01) expression and the longissimus dorsi muscle mass.These results demonstrated that duration of feeding linseed diet lead to a linear decrease of TNFαgene expression,which may increase the muscle mass in growing-finishing barrows, at least in part,through a PPARγ-dependent mechanism.
     The second part:in vitro experiment.In order to investigate the molecular mechanism of n-3PUFA regulating skeletal muscle growth of growing-finishing pigs. C2C12 myotube were incubated with BSA(the postive control),PTA(the negative control),ALA an EPA,respectivley.After treatment with 600μM BSA,LNA,EPA or PTA for 24 hours PPARγ,TNFαand MuRF1 mRNA expression levels were measured by Real-time quantitative PCR method.After incubation of C2C12 myotubes with 300μM,600μM BSA,LNA,EPA or PTA for 24 hours,respectively,the abundance of IκBαwas measured by Western blot method.Additionally,C2C12 myotubes were incubated with 600μM LNA,600μM EPA,600μM PTA or for 24 h.Total nuclear protein was subsequently isolated and analyzed by EMSA for NF-κB DNA binding activity.
     The effect of n-3PUFA on NF-κB activation and MuRF1 gene expression in C2C12 skeletal muscle Cells.C2C12 myotubes incubated in the presence of 600μM EPA for 24 hours resulted in a 2.3-fold induction of the PPARγepression(P<0.01).A 1.08-fold induction(P<0.01) was observed in the presence of 600μM LNA for 24 hours.However,24-h incubation period with 600μM palmitate decreased PPARγexpression(P<0.01).Treatment with 600μM LNA or EPA for 24 hours caused a 1.06-fold and 2.93-fold reduction in the mRNA levels of TNFαin C2C12 myotubes (P<0.001),respectively.Whereas 24-h incubation period with 600μM palmitate increased TNFαexpression(P<0.01).Incubation of C2C12 myotubes with 300μM LNA,EPA or palmitate for 24 hours did not affect the abundance of IκBα.However, 600μM EPA addition to cells caused approximately a 86%(P<0.01) increase in the abundance of IκBα,and 600μM palmitate addition to cells caused approximately a 39%(P<0.01) decrease in the abundance of IκBα.Incubation of C2C12 myotubes with 600μM EPA for 24 hours decreased the NF-κB DNA binding activity.However, Treatment with 600μM LNA or EPA for 24 hours increased the NF-κB DNA binding activity.C2C12 myotubes incubated in the presence of 600μM EPA for 24 hours caused a 3.38-fold induction in the levels of MuRF1 mRNA(P<0.01).Whereas 24-h incubation period with 600μM palmitate increased MuRF1 expression(P<0.01). These results revealed EPA treatment of skeletal muscle cells represses MuRF1 expression through mechanisms involving the activation of the axis PPARγ/TNFα/IκBα/NF-κB,decreases skeletal muscle protein degradation,and promotes the skeletal muscle growth.
引文
1.柴家科,盛志勇.严重烧伤脓毒症骨骼肌蛋白分解代谢的机制及意义.解放军医学杂志,2003,28:947-951
    2.陈丹英,翟中和,舒红兵.NF-κB激活的调节机理.科学通讯,2003,48(18):1893-1911
    3.李朝飞,庞义.泛素—蛋白水解酶复合体通路与病毒侵袭.生物工程学报,2004.20:151-156
    4.Aggarwal B B,Sethi G,Nair A,and Ichikawa H.Nuclear Factor-κB:A Holy Grail in Cancer Prevention and Therapy.Curr Signal Transduct Ther,2006,1:25-52
    5.Arrington J L,Chapkin R S,Switzer K C.Dietary n-3 polyunsaturated fatty acids modulate purified murine T-cell subset activation.Clin Exp Immunol,2001,125(3):499-507
    6.Arrington J L,McMurray D N,Switzer K C.Docosahexaenoic acid suppresses function of the CD-8 costimulatory membrane receptor in primary murine and Jurkat T cells.J Nutr,2001,131(4):1147-1153
    7.Aya K,Alhawagri M,Hagen-Stapleton A,Kitaura H,Kanagawa O,Veis Novack D.NF-κB-inducing kinase controls lymphocyte and osteoclast activities in inflammatory arthritis.J Clin Invest,2005,115(7):1848-1854
    8.Baier L J,Permana P A,Yang X,Pratley R E,Hanson R L,Shen G,Mott D,Knowler W C,Cox N J,Horikawa Y,Oda N,Bell G I,Bogardus C.A calpain-10gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance.J.Clin.Invest,2000,106:69-73
    9.Bailey S T,Ghosh S.'PPAR'ting ways with inflammation.Nat.Immunol,2005,6:966-967
    10.Baldi L,Brown K,Franzoso G.Critical role for lysines 21 and 22 in signal-induced,ubiquitin-mediated proteolysis of IκBα.J Biol Chem,1996,271:376-379
    11.Berger J and David E M.The mechanisms of action of PPARs.Annu.Rev.Med,2002,53:409-435
    12. Billiar T, Bankey P, Svingen B, Curran R D, West M A, Holman R T, Simmons R L, and Cerra F B. Fatty acid uptake and Kupffer cell function: fish oil alters eicosanoid and monokine production to endotoxin stimulation. Surgery, 1988, 104:342-349
    13. Blackwell T S, Christman J W. Sepsis and cytokines: current status. B J Anaesth, 1996,77:110-117
    14. Bligh E G, Dyer W J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Phyisol, 1959, 37:911-917
    15. Bodine S C, Latres E, Baumhueter S, Lai V K, Nunez L, Clarke B A. Identification of ubiquitin ligases required for skeletal muscle atrophy. Science, 2001,294:1704-1708
    16. Borden K. L, and Freemont P S. The RING finger domain: A recent example of a sequence-structure family. Curr. Opin. Struct. Biol, 1996,6:396-401
    17. Bourke R S, Nelson K M, Naumann R A, Young O M. Studies of the production and subsequent reduction of swelling in primate: Cerebral cortex under isomotic conditions in vivo. Exp. Brain. Res. 1970,10:427-446
    18. Boutard V, Fouquery B, Philippe C, Perez J and Baud L. Fish oil supplementation and essential fatty acid deficiency reduce nitric oxide synthesis by rat macrophages. Kidney Int, 1994,46:1200-1286
    19. Braissant O, Foufelle F, Scotto C, Dauca M, and Wahli W. Differential expression of peromisome proliferator-activated receptors (PPARs): tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat. Endocrinology, 1996,137:354-366
    20. Breuille D, Farge M C, Rose F, Arnal M, Attaix D, Obled C. Pentoxifylline decreases body weight loss and muscle protein wasting characteristics of sepsis. Am. J. Physiol, 1993,265:E660-E666
    21. Brown A J, Wood J D, Pig carcass evaluation; measurement of composition using anatomical dissection. Memo. Meat Res. Inst. 1979,42
    22. Buck M, Chojkier M. Muscle wasting and dedifferentiation induced by oxidative stress in a murine model of cachexia is prevented by inhibitors of nitric oxide synthesis and antioxidants. EMBO. J, 1996, 15:1753-1765
    23. Cabrero A, Laguna J C, Va'zquez M. Peroxisome proliferator-activated receptors and the control of inflammation. Curr. Drug Targets Inflamm. Allergy, 2002, 1:243-248
    24. Cai D, Frantz J D, Tawa N E, Melendez P A, Lidov H G W, Hasselgren P O. IKKbeta/NF-kappaB activation causes severe muscle wasting in mice. Cell, 2004, 119:285-298
    25. Calder P C. Fatty Acids and Gene Expression Related to Inflammation. Nestle Nutrition Workshop Series Clinical & Performance Program, 2002,7:19-40
    26. Castrillo A, Diaz-Guerra M J, Hortelano S, Martin-Sanz P, Bosca L. Inhibition of IkappaB kinase and IkappaB phosphorylation by 15-deoxy-Delta(12,14)-prostaglandin J(2) in activated murine macrophages. Mol. Cell Biol, 2000,20:1692-1698
    27. Caterina D R, Cybulsky M I, Clinton S K, Gimbrone M A, Libby P. The omega-3 fatty acid docosahexaenoate reduces cytokine-induced expression of proatherogenic and proinflammatory proteins in human endothelial cells. Arterioscler Throm, 1994,14:1829-1836
    28. Caughey G E, Mantzioris E, R. Gibson A, Cleland L G and James M J. The effect on human tumor necrosis factor a and interleukin 1 B production of diets enriched in n-3 fatty acids from vegetable oil or fish oil, Am. J Clin. Nuts, 1996, 63:116-122
    29. Centner T, Yano J, Kimura E, McElhinny A S, Pelin K, Witt C C. Identification of muscle specific ring finger proteins as potential regulators of the titin kinase domain. J. Mol. Biol, 2001,306:717-726
    30. Chaet M S, Garcia V F, Arya G and Ziegler M M. Dietary fish oil enhances macrophage production of nitric oxide. J Surg Res, 1994, 57:65-68
    31. Chandrasekar B, Fernandes G. Decreased pro-inflammatory cytokines and increased antioxidant enzyme gene expression by ω-3 lipids in murine lupus nephritis. Biochem Biophys Res Commun, 1994,200:893-898
    32. Chen L, and Green W. Shaping the Nuclear Action of NF-κB. Nat Rev Mol Cell Biol, 2004. 5:392-401
    33. Chen Z, Hagler J, Palombella V J. Signal-induced site-specific phosphorylation targets IκB to the ubiquitinproteasome pathway. Genes Dev, 1995,9:1586-1597
    34. Chung J H, Seo A Y, Chung S W, Kim M K, Leeuwenburgh C, Yu B P, Chung H Y. Molecular mechanism of PPAR in the regulation of age-related inflammation. Ageing Res Rev, 2008, 7(2): 126-36
    35. Chung S W, Kang B Y, Kim S H, Pak Y K, Cho D, Trinchieri G, Kim T S. Oxidized low density lipoprotein inhibits interleukin-12 production in lipopolysaccharide-activated mouse macrophages via direct interactions between peroxisome proliferator-activated receptor-g and nuclear factor-kB. J. Biol. Chem, 2000,275:32681-32687
    36. Chung S, Brown J M, Provo J N, Hopkins R, and McIntosh M K. Conjugated Linoleic Acid Promotes Human Adipocyte Insulin Resistance through NFKB-dependent Cytokine Production. J Bio Chem, 2005,280 (46):38445-38456
    37. Combaret L, Ralliere C, Taillandier D, Tanaka K, Attaix D. Manipulation of the ubiquitin-proteasome pathway in cachexia: pentoxifylline suppresses the activation of 20S and 26S proteasomes in muscles from tumor-bearing rats. Mol. Biol. Rep, 1999,26:95-101
    
    38. Cooper A L, Gibbons L, Horan M A, Little R A and Rothwell N J. Effect of dietary fish oil supplementation on fever and cytokine production in human volunteers. Clin. Nuts, 1993,12:321-328
    39. Costelli P, Carbo N, Tessitore L, Bagby G J, Lopez-Soriano F J, Argiles J M, and Baccino F M. Tumor necrosis factor-a mediates changes in tissue protein turnover in a rat cancer cachexia model. J. Clin. Invest, 1993,92:2783-2789
    40. Curtis C L, Hughes C E, Flannery C R, Little C B, Harwood J L, Caterson B. n-3 Fatty acids specifically modulate catabolic factors involved in articular cartilage degradation. J Biol Chem, 2000,275:721 -724
    41. D'Arrigo M, et al.Effect of dietary linseed oil on pig hepatic tissue fatty acid composition and susceptibility to lipid peroxidation. Nutr Res, 2002, 22:1189-1196
    42. Davis T A, Fiorott M L, and Reeds P J. Amino acid compositions of body and milk protein change during the suckling period in rats. J Nutr, 1993,123:947-956
    43. Dehoux M J M, van Beneden R P, Fernandez-Celemin L, Lause P L, and Thissen J P M.. Induction of MafBx and Murf ubiquitin ligasemRNAs in rat skeletal muscle after LPS injection. FEBS Lett, 2003, 544:214-217
    44. Delerive P, Fruchart J C, Staels B, Peroxisome proliferatoractivated receptors in inflammation control. J. Endocrinol, 2001,169:453-459
    45. Delerive P, Gervois P, Fruchart J C, Staels B. Induction of IkappaBalpha expression as a mechanismcontributing to the anti-inflammatory activities of peroxisome proliferator-activated receptor alpha activators. J. Biol. Chem, 2000, 275:36703-36707.
    46. Demirel G, Wachira A M, Sinclair L A, Wilkinson R G, Wood J D. Enser, M., Effects of dietary n-3 polyunsaturated fatty acids, breed and dietary vitamin E on the fatty acids of lamb muscle, liver and adipose tissue. Br. J. Nutr. 2004, 91:551-565
    47. DeRuisseau K C, Kavazis A N, Deering M A, Falk D J, Van Gammeren D, Yimlamai T, Ordway G A, and Powers S K. Mechanical ventilation induces alterations of the ubiquitin-proteasome pathway in the diaphragm. J. Appl. Physiol, 2005,98:1314-1321
    48. Didonato J A, Mercurio F, Rosette C. Mapping of the inducible IκB phosphorylation sites that signal its ubiquitination and degradation. Mol Cell Biol, 1996,16:1295-1304
    49. Dinarello C A. The biological properties of interleukin-1. European Cytokine Network. 1994, 5(6):517-531
    50. Ding S T, McNeel R L, Mersmann H J. Modulation of adipocyte determination and differentiation-dependent factor 1 by selected polyunsaturated FA. In Vitro Cell. Dev. Biol. Ani, 2002,38:352-357
    51. Ding S T, Schinckel A P, Weber T E, Mersmann H J. Expression of porcine transcription factors and genes related to fatty acid metabolism in different tissues and genetic populations, J. Anim. Sci, 2000, 78:2127-2134
    52. Ebisui C, Tsujinaka T, Morimoto T, Kan K, Iijima S, Yano M, Kominami E, Tanaka K, and Monden M. Interleukin-6 induces proteolysis by activating intracellular proteases (cathepsins B and L, proteasome) in C2C12 myotubes. Clin. Sci, 1995, 89:431-439
    53. Endres S, Ghorbani R, Kelley V E, Georgilis K, Lonnemann G, Cannon J G, Rogers T S, Klempner M S, Wever P C, Schaeffer E J, Wolef S M and Dinarello C A. The effect of dietary supplementation with n-3 polyunsaturated fatty acids on the synthesis of interleukin-1 and tumor necrosis factor by mononuclear cells. N. Eng. J. Med, 1989, 320:265-271
    54. Endres S, Meydani S N, Ghorbani R, Schindler R and Dinarello C A. Dietary supplementation with n-3 fatty acids suppresses interleukin-2 production and mononuclear cell proliferation. J. Leuk. Biol, 1993, 54:599-603
    55. Enser M, Hallett K G, Hewett B, Fursey G A J, Wood J D, Harringtong G. The polyunsaturated fatty acid composition of beef and lamb liver. Meat Sci, 1998, 49:321-327
    56. Enser M, Richardson R I, Wood J D, Gill B P, Sheard P R. Feeding linseed to increase the n-3 PUFA of pork: fatty acid composition of muscle, adipose tissue, liver and sausages. Meat Sci, 2000,55:201-212
    57. Erol A. PPARalpha activators may be good candidates as antiaging agents. Med. Hypotheses, 2005,65:35-38
    58. Espat N J, Copeland E M, Moldawer L L. Tumor necrosis factor and cachexia: a current perspective. Surg. Oncol, 1994,3:255-262
    59. Ezaki O. Regulatory elements in the insulin-responsive glucose transporter (GLUT4) gene. Biochem. Biophys. Res. Comm, 1997,241:1-6
    60. Fernandes G, Bysani C, Venkatraman J T, Tomar V and Zhao W. Increased TGF-β and decreased oncogene expression by ω-3 fatty acids in the spleen delays onset of autoimmune disease in B/W mice. J. Immunol, 1994,152:5979-5987
    61. Field C J, Ryan E A, Thompson A B, Clandinin M T. Diet fat composition alters membrane phospholipid composition, insulin binding, and glucose metabolism in adipocytes from control and diabetic animals. J. Biol. Chem, 1990, 265:11143-11150
    62. Folch J, Lees M, Sloane-Stanley G H. A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Chem, 1957, 226:497-509
    63. Fontanillas R, Barroeta A, Baucells M D, Guardiola F. Backfat fatty acid evolution in swine fed diets high in either cis-monounsaturated, trans, or (n-3) fats. J. Anim. Sci, 1998, 76:1045-1055
    64. Frost R A, Nystrom J, and Lang C H. Lipopolysaccharide and proinflammatory cytokines stimulate interleukin-6 expression in C1C12 myoblast: Role of the Jun NH_2-terminal kinase. Am. J. Physiol. Regul. Integr. Comp. Physiol, 2003, 285:R1153-1164
    65. Frost R A, Nystrom J, and Lang C H. Lipopolysaccharide regulates proinflammatory cytokine expression in mouse myoblasts and skeletal muslce. Am. J. Physiol. Regul. Integr. Comp. Physiol, 2002,283:R698-709
    66. Fujita J, Tsujinaka T, Yano M. Anti-interleukin-6 receptor antibody prevents muscle atrophy in colon-26 adenocarcinoma-bearing mice with modulation of lysosomal and ATP-ubiquitin-dependent proteolytic pathways. Int J Cancer, 1996. 68:637-643
    67. Gabler N K and Spurlock M E. Integrating the immune system with the regulation of growth and efficiency. J Anim Sci, 2008,86:E64 - E74
    68. Gaines A M, Carroll J A, Yi G F, Allee G L, Zannelli M E. Effect of menhaden fish oil supplementation and lipopolysaccharide exposure on nursery pigs II. Effects on the immune axis when fed simple or complex diets containing no spray-dried plasma. Domest. Anim. Endocrinol, 2003,24:353-365
    69. Gallai V, Sarchielli P, Trequattrini A, Franceschini M, Floridi A, Firenze C, Alberti A, Di Benedetto D and Stragliotto E. Cytokine secretion and eicosanoid production in the peripheral blood mononuclear cells of MS patients undergoing dietary supplementation with n-3 polyunsaturated fatty acids. J Neuroimmunol. 1993,56:143-153
    70. Garcia-Martinez C, Lopez-Soriano F J, Argiles J M. Acute treatment with tumour necrosis factor-alpha induces changes in protein metabolism in rat skeletal muslcle. Mol. Cell. Biochem, 1993, 125:11-18
    71. Goll D E, Thompson V F, Christiansen J A. Role of the calpain system in muslce growth. Biochimie, 1992, 74:225-237
    72. Gomes M D, Lecker S H, Jagoe R T, Navon A, and Goldberg A L. Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy. Proc. Natl. Acad. Sci. U.S.A., 2001, 98:14440-14445.
    73. Grindflex E, Sundvold H, Klungland H, Lien S. Characterisation of porcine peroxisome proliferator-activated receptors gamma 1 and gamma 2: detection of breed and age differences in gene expression. Biochem. Bioph|ys. Res. Commun, 1998,249:713-718
    74. Hammad H, Heer H J, Soullie T, Angeli V, Trottein F, Hoogsteden H C, Lambrecht B N. Activation of peroxisome proliferators-activated receptor-γ in dendritic cells inhibits the development of eosinophilic airway inflammation in a mouse model of asthma. Am. J. Pathol, 2004,164:263-271
    75. Hardardottir I and Kinsella J E. Increasing the dietary (n-3) to (n-6) polyunsaturated fatty acid ratio increases tumor necrosis factor production by murine resident peritoneal macrophages without an effect on elicited peritoneal macrophages. J. Nutr. 1992,122:1942-1951
    76. Hardardottir I and Kinsella J E. Tumour necrosis factor production by murine resident peritoneal macrophages is enhanced by dietary n-3 polyunsaturated fatty acids, Biochim. Biophys. Acta, 1991,1095:187-195
    77. Hovenier R, Kanis E, Verhoeven J A. Repeatability of taste panel tenderness scores and their relationships to objective pig meat quality traits. J. Anim. Sci, 1993,71:2018-2025
    78. Hsu J M, Ding S T. Effect of polyunsaturated FA on the expression of transcription factor ADD1 and of lipogenic and FA oxidation enzymes in porcine differentiating adipocytes. Br. J. Nutr, 2003,90:507-513.
    79. Hsu J M, Wang P H, Liu B H, Ding S T., The effect of dietary docosahexaenoic acid on the expression of porcine lipid metabolism-related genes. J. Anim. Sci, 2004, 82:683-689
    80. Huang F R, Zhan Z P, Luo J, Liu Z X, Peng J. Intramuscular fat, muscle mass, and n-3 PUFA enrichment of growing-finishing barrows improved by duration of feeding linseed. Livest. Sci, 2008, Accepted.
    81. Hubbard N E, Chapkin R S and Erickson K L. Effect of dietary linseed oil on tumoricidal activity and eicosanoid production in murine macrophages. Lipids, 1994,29:651-655
    82. Hunter R B, and Kandarian S C. Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy. J. Clin. Invest, 2004,114:1504-1511
    83. Irie M, Sakimoto M. Fat Characteristics of pigs fed fish oil containing eicosapentaenoic and docosahexaenoic acids. J. Anim. Sci, 1992, 70:470-477
    84. Isabel B, lopez-Bote C J, Hoz L D, Timon M, Garcia C, Ruiz J. Effects of feeding elevated concentrations of monounsaturated fatty acids and vitamin E to swine on characteristics of dry cured ham. Meat Sci, 2003,64:475-482
    85. Jackson P K, and Eldridge A G.. The SCF ubiquitin ligase: An extended look. Mol. Cell, 2002,9:923-925
    86. Jacobi S K, Gabler N K, Ajuwon K M, Davis J E, Spurlock M E. Adipocytes, myofibers, and cytokine biology: New horizons in the regulation of growth and body composition. J. Anim. Sci, 2006, 84:E140-E149
    87. Jiang C, Ting A T, and Seed B. PPAR-gamma agonists inhibit production of monocyte inflammtory cytokines. Nature, 1998,391:82-86
    88. Johnson, R. W. Inhibition of growth by pro-inflammatory cytokines: an integrated view. J Anim Sci, 1997, 75:1244-1255
    89. Jove M, Planavila A, Laguna JC, Vazquez-Carrera M. Palmitate-induced interleukin 6 production is mediated by protein kinase C and nuclear-factor kappaB activation and leads to glucose transporter 4 down-regulation in skeletal muscle cells. Endocrinology, 2005,146(7):3087-95
    90. Karin M, and Ben-Neriah Y. Phosphorylation meets ubiquitination: the control of NFκB activity. Annu Rev Immunol, 2000,18:621-663
    91. Kauffman R G, Eikelenboom G, van der Wal P G, Engel B, Zaar M. A comparison of methods to estimate water-holding capacity in post-rigor porcine muscle. Meat Sci, 1986, 18:307-322
    92. Kedar V, McDonough H, Arya R, Li H H, Rockman H A, and Patterson C. Muscle-specific RING finger 1 is a bona fide ubiquitin ligase that degrades cardiac troponin I. Proc. Natl. Acad. Sci. U. S. A, 2004, 52:18135-18140
    93. Klasing K C, and Johnstone B J. Monokines in growth and development. Poult. Sci, 1991,90:1781-1789
    94. Korver D R, Klasing K C. Dietary fish oil alters specific and inflammatory immune responses in chicks. J. Nutr, 1997, 127:2039-2046
    95. Kouba M, Enser M, Whittington F M, Nute G R, Wood J D. Effect of a high linolenic acid diet on lipogenic enzyme activities, fatty acid composition and meat quality in the growing pig. J. Anim. Sci, 2003, 81:1967-1979
    96. Ladner K J, Caligiuri M A, and Guttridge D C. Tumor necrosis factor-regulated biphasic activation of NF-κb is required for cytokine-induced loss of skeletal muscle gene products. J Biol Chem, 2002,278:2294-2303
    97. Latres E, Amini A R, Amini A A, Griffiths J, Martin F J, Wei Y.. IGF-1 inversely regulates atrophy-inducedgenes via the PI3K/Akt/mTOR pathway. J. Biol. Chem, 2005,280:2737-2744
    98. Lecker S H, Solomon V, Price S R, Kwon Y T, Mitch W E, and Goldberg A L. Ubiquitin conjugation by the N-end rule pathway and mRNAs for its components increase in muscles of diabetic rats. J. Clin. Invest, 1999,104:1411-1420
    99. Leifert W R, McMurchie E J, Saint D A. Inhibition of cardiac so2 dium currents in adult rat myocytes by n23 polyunsaturated fatty acids. J Physiol, 1999, 520 (1):6712679
    100. Leonardo A, Moraes L P, David B B. Peroxisome proliferator-activated receptors and inflammation. Pharm Therap, 2006,110:371-385
    101. Li H H, Kedar V, Zhang C, McDonough H, Arya R, Wang D Z. Atrogin-1/muscle atrophy F-box inhibits calcineurin-dependent cardiac hypertrophy by participating in an SCF ubiquitin ligase complex. J. Clin. Invest, 2004,114:1058-1071
    
    102. Li M, Pascual G, Glass C. Peroxisome proliferator-activated receptor g-dependent repression of the inducible nitric oxide synthase gene. Mol. Cell. Biol, 2000,20:4699-4707
    103. Li Y P, Chen Y, Li A S, and Reid M B. Hydrogen peroxide stimulates ubiquitin conjugating activity and expression of genes for specific E2 and E3 proteins in skeletal muscle myotubes. Am. J. Physiol. Cell. Physiol, 2003, 285:C806-C812
    104. Li Y P, Schwartz R J, Waddell I D, Holloway B R, Reid M B. Skeletal muslce myocytes undergo protein loss and reactive oxygen-mediated NF-κB activation in response to tumor necrosis a. FASEB J, 1998, 12:871-880
    105. Lin Y, Lee H, Berg A H, Lisanti M P, Shapiro L, and Scherer P E. The lipopolysaccharide-activated Toll-like receptor (Tlr)-4 induces synthesis of the closely related receptor Tlr-2 in adipocytes. J. Biol. Chem, 2000, 275:24255-24263
    106.Llovera M, Garcia-Martinez C, Agell N, Lopez-Soriano F J, Argiles J M. Anti-TNF treatment reverts increased muscle ubiquitin gene expression in tumor-bearing rats. Biocherm Biophys Res Commun, 1996,221:653-655
    107.Llovera M, Garcia-Martinez C, Agell N, Lopez-Soriano F J, Argiles J M. TNF can directly induce the expression of Ubiquitin-dependent proteolytic system in rat soleus muscles. Biochem Biophys Res Commun, 1997,230:238-241
    108.Llovera M, Garcia-Martinez C, Lopez-Soriano J. Role of TNF receptor 1 in protein turnover during cancer cachexia using gene knockout mice. Mol Cell Endocrinol, 1998,142:183-189
    109.Lokesh B R, Sayers T I, Kinseila J E. Interleukin-1 and tumor necrosis factor synthesis by mouse peritoneal macrophages is enhanced by dietary n-3 polyunsaturated fatty acids. Immunol Lett, 1990,23:281
    110.Loskesh B R, Sayers T J, and Kinseila J E. Interleukin-1 and tumor necrosis factor synthesis by mouse peritomneal macrophages is enchanced by dietary n-3 polyunsaturated fatty acids. Immunol. Lett, 1990,23:281-286
    111.Mangelsdorf D J, Thummel C, Beato M, Herrlich P, Schutz G, Umesono K, Blumberg B, Kastner P, Mark M, and Chambon P. The nuclear receptor superfamily: the second decade. Cell, 1995, 83:835-839
    
    112. Matthews K R, Homer D B, Thies F, Calder P C. Effect of whole linseed (Linum usitatissimum) in the diet of finishing pigs on growth performance and on the quality and fatty acid composition of various tissues. Br. J. Nutr, 2000, 83:637-643
    113. May S G, Savell J W, Lunt D K, Wilson J J, Laurenz J C, Smith S B. Evidence for preadipocyte proliferation during culture of subcutaneous and intramuscular adipose tissues from angus and angus and wagyu crossbred steers. J. Anim. Sci, 1994,72:3110-3117
    
    114.McElhinny A S, Kakinuma K, Sorimachi H, Labeit S, and Gregorio C C. Muscle-specific RING finger-1 interacts with titin to regulate sarcomeric M-line and thick filament structure and may have nuclear functions via its interaction with glucocorticoid modulatory element binding protein-1. J. Cell. Biol, 2002, 157:125-136
    115.McMurray D N, Jolly C A, Chapkin R S. Effects of dietary n-3 fatty acids on T cell activation and T cell receptor-mediated signaling in a murine model. J Infect Dis, 2000, 182 (Suppl 1):S103-S107
    116.Meadus W J, Maclnnis R, Dugan M E R. Prolonged dietary treatment with conjugated linoleic acid stimulates porcine muscle peroxisome proliferator activated receptor gamma and glutamine-fructose aminotransferase gene expression in vivo. J. Mol. Endo, 2002,28:79-86
    117.Melchior D, Seve B, Floc'h N L. Chronic lung inflammation affects plasma amino acid concentrations in pigs. J Anim Sci, 2004,82:1091-1099
    118.Mendez M, LaPointe M C. PPARgamma inhibition of cyclooxygenase-2, PGE2 synthase, and inducible nitric oxide synthase in cardiac myocytes. Hypertension, 2003,42:844-850
    119.Meydani S N, Lichtenstein A H, Cornwall S, Meydani M, Goldin B R, Rasmussen H, Dinarello C a and Schaefer E J. Immunologic effects of national cholesterol education panel step-2 diets with and without fish-derived n-3 fatty acid enrichement. J. Clin. Invest, 1993,92:105-113
    120. Miles E A, Wallace F A, Calder P C. Dietary fish oil reduces intercellular adhesion molecule 1 and scavenger receptor expression on murine macrophages. Atherosclerosis. 2000,152:43-50
    121.Molvig J, Pociot F, WorsaaeH, Wogensen L D, Baek L, Christensen P, Mandrup-poulsen T, Andersen K, Madsen P, Dyerberg J and Nerup J. Dietary supplementation with o-3 polyunsaturated fatty acids decreases mononuclear cell proliferation and interleukin-1/3 content but not monokine secretion in healthy and insulin-dependent diabetic individuals. Scand. J. Immunol, 1991, 34:399-410
    122.Murao K, Imachi H, Momoi A, Sayo Y, Hosokawa H, Sato M, Ishida T, Takahara J. Thiazolidinedione inhibits the production of monocyte chemoattractant protein-1 in cytokine-treated human vascular endothelial cells. FEBS Lett, 1999,454:27-30
    123.Nakashima J, Tachibana M, Ueno M, Baba S, Tazaki H. Tumor necrosis factor and coagulopathy in patients with prostate cancer. Cancer Res, 1995, 55:4881-4885
    124.Nano J L, Nobili C, Girard-Pipau F. Effects of fatty acids on the growth of Caco22 cells. Prostaglandins Leukot Essent Fatty Acids, 2003,69 (4) :207-215
    125.Neurath M F, Becker C, Barbulescu K. Role of NF-κB in immune and inflammatory responses in the gut. Gut, 1998,43:856-860
    126. Newman R E, Bryden W L, Kirby A C, Storlien L H, Downing J A. Dietary n-3 and n-6 fatty acids alter avian glucose metabolism. Br. Poult. Sci, 2006, 46:104-113
    127. Nguyen LQ, et al. Mathematical relationships between the intake of n-6 and n-3 polyunsaturated fatty acids and their contents in adipose tissue. Meat Sci, 2003, 65:1399-1406
    128. Nuernberg K, Fischer K, Nuernberg G, Kuechenmeister U, Klosowska D, Eliminowska-Wenda G, Fiedler I, Ender K. Effects of dietary olive and linseed oil on lipid composition, meat quality, sensory characteristics and muscle structure in pigs. Meat Sci, 2005,70:63-74
    129.Olsen H, Haldosen L A. Peroxisome proliferators-activated receptor gamma regulates expression of signal transducer and activator of transcription 5A. Exp. Cell. Res, 2006,312 (8): 1371-1380
    130. Park K S, Giaraldi T P, Lindgren K, Abrams-Carter L, Mudaliar S, Nikoulina S E, Tufari S R, Veerkamp J H, Vidal-Puig A, Henry R R. Troglitazone effects on gene expression in human skeletal muscle of type II diabetes involve up-regulation of peroxisome proliferators-activated receptor-gamma. J. Clin Endocrinol. Metab, 1998, 83:2830-2835
    131.Pasceri V ,Wu H D, Willerson J T, Yeh E T. Modulation of vascular inflammation in vitro and in vivo by peroxisome proliferator-activated receptor-gamma activators. Circulation, 2000, 101:235-238
    132.Pascual G, Fong A L, Ogawa S, Gamliel A, Li A C, Perissi V, Rose D W, Willson T M, Rosenfeld M G, and Glass C K. A SUMOylation-dependent pathway mediates transrepression of inflammatory response genes by PPARγ. Nature, 2005,437:759-763
    133.Pcmpos L J, Fritsche K L. Antigen-driven murine CD4~+ T lymphocyte proliferation and interleukin-2 production are diminished by dietary (n-3) polyunsaturated fatty acids. J Nutr, 2002,132(11):3293-3300
    134.Pegorier J P, May C L, Girard J. Control of gene expression by fatty acids. J. Nutr, 2004,134 (9):2444S-24449S
    135. Pie S, Lalles J P, Blazy F, Laffitte J, Seve B, Oswald I P. Weaning is associated with an upregulation of expression of inflammatory cytokines in the intestine of piglets. J. Nutr. 2004,134:641-647
    136.Pizon V, Iakovenko A,Van DerVen P F, Kelly R, Fatu C, Furst D O. Transient association of titin and myosin with microtubules in nascent myofibrils directed by the MURF2 RING-finger protein. J. Cell. Sci, 2002,115:4469-4482
    137.Poynter M E, Daynes R A. Peroxisome proliferators-activated receptor a activation modulates cellular redox status, represses nuclear factor-κB signaling, and reduces inflammatory cytokine production in aging. J. Biol. Chem, 1998, 273:32833-32841
    138.Pritts E A, Zhao D, Sohn S H, Chao V A, Waite L L, Taylor R N. Peroxisome proliferator-activated receptor-gamma ligand inhibition of RANTES production by human endometnotic stromal cells is mediated through an upstream promoter element. Fertil. Steril, 2003, 80:415-420
    139. Ramsay T G, White M E, Wolverton C K. Glucocorticoids and the differentiation of porcine preadipocytes. J. Anim. Sci, 1989, 67:2222-2229
    140. Reeds P J, Fjeld C R, Jahoor J. Do the differencesbetween the amino acid compositions of acute-phase and muscle proteins have a bearing on nitrogen loss in traumaticstates? J. Nutr, 1994,124:906-910
    141.Reiterer G, Toborek M, and Hennig B. Peroxisome proliferators activated receptors a and 7 require zinc for their anti-inflammatory properties in porcine vascular endothelial cells. J Nutr. 2004, 137(7):1711-1715
    142.Renier G, Skamene E, Sanctis J D and Radzioch. Dietary n-3 polyunsaturated fatty acids prevent the development of atherosclerotic lesions in mice: modulation of macrophage secretory activities. Arterio. Thromb, 1993, 13:1515-1524
    143. Rhind S G, Shek P N, Shephard R J. The impact of exercise on cytokines and receptor expression. Exerc Immunol Rev, 1995,1:97-148
    144.Ricote M, Glass C K. PPARs and molecular mechanisms of transrepression. Biochim. Biophys. Acta, 2007,1771:926-935
    145.Ricote M, Li A C, Willson T M, Kelly C J, and Glass C K. The peroxisome proliferator-activated receptor-gamma is a negative regulator of macrophage activation. Nature, 1998, 391:79-82
    
    146. Riley P A, Enser M, Nute G R, Wood J D. Effects of dietary linseed on nutnonal value and other quality aspects of pig muscle and adipose tissue. Anim. Sci, 2000, 71:483-500
    
    147. Robinson D R, Urakaze M, Huang R, Taki H, Sugiyama E, Knoell C T, Xu L, Yeh E T H, Auron P E. Dietary marine lipids suppress continuous expression on interleukin-1β gene expression. Lipids, 1996,31(suppl):S23-S31
    148. Romans J R, Johnson R C, Wolf D M, Libal G W, Costello W J. Effects of ground flaxseed in swine diets on pig performance and on physical and sensory characteristics and omega-3 fatty acid content of pork: I. Dietary level of flaxseed. J. Anim. Sci, 1995 a, 73:1982-1986
    149. Romans J R, Wolf D M, Johnson R C, Libal G W, Costello W J. Effects of ground flaxseed in swine diets on pig performance and on physical and sensory characteristics and omega-3 fatty acid content of pork: II. Duration of 15% dietary flaxseed. J. Anim. Sci, 1995 b, 73:1987-1994
    150. Rooyackers O E, Nair K S. Hormonal regulation of human muscle protein metabolism. Annu. Rev. Nutr, 1997, 17:457-485
    151.Saitoh H,Hinchey J.Functional heterofeneity ubiquitin related protein modifiers SUMO-1 versus SUMO-2/3.Bio chem.2000,275:6252-6258
    152.Santoli D,Zurier RB,Prostaglandin E precursor fatty acids inhibit human IL-2production by a prostaglandin E-dependent mechanism.Lmmunol,1989,143:1303
    153.Schoonjans K,Staels B,and Auwerx.The peroxisome proliferator activated receptors(PPARs) and their effects on lipid metabolism and adipocyte differentiation.Biochim.Biophys.Acta,1996,1302:93-109
    154.Schreiber S,Nikolaus S,and Hampe J.Activation of nuclear factor κB in inflammatory bowel disease.Gut,1998,42:477-484
    155.Schutze S,Machleidt T,Kronke M.Mechanisms of tumor necrosis factor action.Semin.Oncol,1992,2:16-24
    156.Sen R,Baltimore D.Inducibility of the immunolglobulin enhancer-bingding protein NF-κB bγ a posttranslational mechanism.Cell,1986,47:921-928
    157.Shao J,Sheng H.Prostaglandin E2 induces the expression of IL-1 alpha in colon cancer cells.J Immunol,2007,178(7):4097-4103
    158.Sokolowska M,Kowalski M L,Pawliczak R.Peroxisome proliferator-activated receptors-γ(PPAR-γ) and their role in immunoregulation and inflammation control.Postepy Hig Med Dosw,2005,http://www.phmd.pl/pub/phmd/vol_59/8218.pdf Accessed Oct.29.
    159.Spencer W E,Christensen M J.Multiplex relative RT-PCR method for verification of differential gene expression.Biotechniques,1999,27:1044-1052
    160.Spurlock M E.Regulation of Metabolism and growth during immune challenge:an overview of cytokine function.J Anim Sci,1997,75:1773-1783
    161.Storlien L H,Kraegen E W,Chisholm P J,Bruce P G,Pascor W S.Fish oil prevents insulin resistance induced by high fat feeding in rats.Science,1987,237:885-887
    162.Subbaramaiah K,Lin D T,Hart J C,Dannenberg A J.Peroxisome proliferator-activated receptor gamma ligands suppress the transcriptional activation of cyclooxygenase-2.Evidence for involvement of activator protein-1and CREB-binding protein/p300.J.Biol.Chem,2001,276:12440-12448
    163. Sung B, Park S J, Yu B P, Chung H Y. Amelioration of age-related inflammation and oxidative stress by PPARg activator: suppression of NF-κB by 2,4-thiazolidinedione. Exp. Gerontol, 2006,41:590-599
    164. Takano H, Nagai T, Asakawa M, Toyozaki T, Oka T, Komuro I, Saito T, Masuda Y. Peroxisome proliferator-activated receptor activators inhibit lipopolysaccharide-induced tumor necrosis factor-alpha expression in neonatal rat cardiac myocytes. Circ. Res, 2000,87:596-602
    165.Tappia P S and Grimble R F. Complex modulation of cytokine induction by endotoxin and tumor necrosis factor from peritoneal macrophages of rats by diets containing fats of different saturated, monounsaturated and polyunsaturated fatty acid composition. Clin. Sci, 1994, 87:173-178
    166.Tawa N E, Odessey J R, Goldberg A L. Inhibitors of the proteasome reduce the accelerated proteolysis in atrophying rat skeletal muscles. J. Clin. Invest, 1997, 100:197-203
    167.Tilley S L, Coffman T M, Koller B H. Mixed messages: modulation of inflammation and immune responses by prosglandins and thromboxanes. J Clin Invest, 2001,108:15-23
    
    168. Tintignac L A, Lagirand J, Batonnet S, Sirri V, Leibovitch M P, and Leibovitch S A. Degradation of MyoD mediated by the SCF (MAFbx) ubiquitin ligase. J. Biol. Chem, 2005,280(4):2847-2856
    169.Tracey K L, Wei H, Manogue K, Fong Y, Hesse D G, Nguyen H T, Kuo G C, Beutler B, Cotran R S, Cerami A, and Lowry S F. Cachectin/tumor necrosis factor induces cachexia, anemia, and inflammation. J. Exp. Med, 1988, 167:1211-1227
    170.Traenckner E B, Pahl H L, Henkel T. Phosphorylation of human IκB on serines 32 and 36 controls IκB proteolysis and NF-κB activation in response to diverse stimuli. EMBO J, 1995, 14: 2876-2883
    171.Turek J J, Schoenlein I A and Bottoms G D. The effect of dietary n-3 and n-6 fatty acids on tumor necrosis factor-a produciton and leucine aminopeptidase levels in rat peritoneal macrophages. Prost. Leuk. Ess. Fatty Acids, 1991, 43:141-149
    172. Van den Eijnden M, Lahaye L L, and Strous G J. Disulfide bonds determine growth hormone receptor folding, dimerisation and ligand binding. J Cell Sci, 2006,119:3078-3086
    173. Virella G, Kilpatrick JM, Rugeles MT, Hyman B, Russell R. Depression of humoral responses and phagocytic functions in vivo and in vitro by fish oil and eicosapentaeonoic acid. Clin Immunol Immunopathol 1989; 52:257
    174.Vreugdenhil G, Lowenberg B, Van Eijk H G, Swaak A J. Tumor necrosis factor-α is associated with disease acitivity and the degree of anemia in patients with rheumatoid arthritis. Eur. J. Clin. Invest, 1992, 22:488-493
    175. Wang N, Verna L, Chen N G, Chen J, Li H, Forman B M, Stemerman M B. Constitutive activation of peroxisome proliferatoractivated receptor-g suppresses pro-inflammatory adhesion molecules in human vascular endothelial cells. J. Biol. Chem, 2002,277:34176-34181
    176.Watanabe S, Hayashi H, Onozaki K and Okuyama H. Effect of dietary α-linolenated/linoleate balance on lipopolysaccharide-induced tumor necrosis factor production in mouse macrophages. Life Sci, 1991,48:2013-2020
    177.Waterlow J C. Protein-energy malnutrition: challenges and controversies. Proc. Nutr. Soc. India, 1991,37:59-86
    178. Werman A, Hollenberg A, Solanes G, Bjorbaek C, Vidal-Puig A J, and Flier J S. Ligand-independent activation domain in the N terminus of peroxisome proliferator-activated receptor gamma (PPAR gamma). Differential activity of PPAR gammal and -2 isoforms and influence of insulin. J. Biol. Chem, 1997, 272:20230-20235
    179. Whitehouse A S, Smith H J, Drake J L, Tisdale M J. Mechanism of attenuation of skeletal muscle protein catabolism in cancer cachexia by eicosapentaenoic acid. Cancer Res, 2001, 61(9): 3604-3609
    180. Williamson D L, Kimball S R, and Jefferson L S. Acute treatment with TNF-{alpha} attenuates insulin-stimulated protein synthesis in cultures of C2C12 myotubes through a MEK1-sensitive mechanism. Am. J. Physiol. Endocrinol. Metab,2005,E95-E104
    181.Wingertazhn M A. Proceedings of the society for experimental. Biology and Medicine, 1998,218:244-250
    182. Wood J D, Richardson R I, Nute G R, Fisher A V, Campo M M, Kasapidou E, Effects of fatty acids on meat quality: a review. Meat Sci, 2003,66:21-32
    183. Wray C J, Mammen J M, Hershko D D, and Hasselgren P O. Sepsis upregulates the gene expression of multiple ubiquitin ligases in skeletal muscle. Int. J. Biochem. Cell. Biol, 2003,35:698-705
    184.Wu D, Ren Z, Pae M, Guo W, Cui X, Merrill A H, Meydani S N. Aging up-regulates expression of inflammatory mediators in mouse adipose tissue. J. Immunol, 2007,179:4829-4839
    185.Xi S, Cohen, D, Barve S, Chen L H. Fish oil suppressed cytokines and nuclear factor-kappa B induced by murine AIDS virus infection. Nutr. Res. 2001, 21:865-878.
    186.Yaqoob P anc Calder P C. Effects of dietary lipid manipulation upon inflammatory mediator production by murine macrophages. Cell. Immunol, 1995, 163:120-128
    187. Yaron A, Hatzubai A, Dabis M. Identification of the receptor component of the IκBα-ubiquitin ligase. Nature, 1998, 396:590-594
    188.Yu B P, Chung H Y. The inflammatory process in aging. Rev. Clin. Gerontol, 2007, 16:179-187
    189.Zamir O, Hasselgren P O, Kunkel S L, Frederick J, Higashiguchi T, and Fischer J E. Evidence that tumor necrosis factor participates in the regulation of muscle proteolysis during sepsis. Arch. Surg, 1992, 127:170-174
    190.Zamir O, Hasselgren P O, von Allmen D, and Fischer J E. In vivo administration of interleukin-1a induces muscle proteolysis in normal and adrenalectomized rats. Metabolism, 1993b, 41:204-208
    191. Zhang X, Rodriguez-Galan M C, Subleski J J, Ortaldo J R, Hodge D L, Wang J M, Shimozato O, Reynolds D A, Young H A. Peroxisome proliferators-activated receptor-γand its ligands attenuate biologic functions of human natural killer cells. Blood, 2004, 104:3276-3284
    192. Zhao G, Etherton T D, Martin K R, Vanden Heuvel J P, Gillies P J, West S G, and Kris-Etherton P M. Anti-inflammatory effects of polyunsaturated fatty acids in THP-1 cells. Biochem Biophys Res Commun, 2005, 336:909-917.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700