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首页> 外文期刊>Journal of Agricultural and Food Chemistry >Sodium Butyrate Mitigates iE-DAP Induced Inflammation Caused by High-Concentrate Feeding in Liver of Dairy Goats
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Sodium Butyrate Mitigates iE-DAP Induced Inflammation Caused by High-Concentrate Feeding in Liver of Dairy Goats

机译:丁酸钠减轻IE-DAP诱导由奶牛羊肝中的高浓缩饲料引起的炎症

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摘要

The aim of this study is to explore the impact of sodium butyrate on D-glutamyl-meso-diaminopimelic acid (iE-DAP)-induced liver inflammation in dairy goats during subacute ruminal acidosis (SARA) caused by high-concentrate feed. To achieve this aim, 12 lactating dairy goats were randomly divided into two groups: a high-concentrate feed group (n = 6, concentrate/forage = 6:4) as the control group and a sodium butyrate (SB) with high-concentrate feed group (n = 6, concentrate/forage = 6:4, with 1% SB by wt.) as the treatment group. A rumen pH below 5.6 lasted for at least 4 h/d due to long-term HC feeding. The concentration of iE-DAP was significantly lower (11.67 +/- 3.85 mu g/mL, and 7.74 +/- 1.46 mu g/mL, at the fourth h and sixth h of feeding, respectively) in the SB-treated group than that in the HC group (51.45 +/- 5.71 mu g/mL, and 18.31 +/- 3.83 mu g/mL, at the fourth h and sixth h of feeding, respectively). Meanwhile, SB significantly suppressed the mRNA expression of inflammatory genes (NOD1, RIPK2, TAK1, NF-kB/p65, ERK, JNK2, p38, IL-1 beta, TNF-alpha, CCL5, CCL20, CXCL12, FOS, beta-defensin/LAP). Moreover, the protein expression of NOD1, p-IKB alpha, p-NF-kB/p-p65, p-ERK1/2, p-JNK, p-p38, and HDAC3 was significantly downregulated in the HC+SB group. In conclusion, iE-DAP-induced inflammation and liver disruption generated by the HC diet was mitigated by SB treatment.
机译:本研究的目的是探讨丁酸钠对D-glutamyl-Meso-二氨基甲酸(IE-DAP)的影响,在高浓缩饲料引起的亚尾酸中毒(SARA)期间乳制品山羊中诱导的肝脏炎症。为了实现这一目标,将12个哺乳酸乳制山羊随机分为两组:作为对照组的高浓缩饲料组(n = 6,浓缩/饲料= 6:4)和高浓缩的丁酸钠(Sb)进料组(n = 6,浓缩/饲料= 6:4,用WT为1%SB)作为治疗组。由于长期HC喂养,瘤胃pH低于5.6以下至少4小时。 IE-DAP的浓度显着降低(11.67 +/-3.85μg/ ml,分别在SB处理组中的第四H和第六小时,在第四H和第6次H和第6毫升)比在HC组(51.45 +/-5.71μmg/ ml,和18.31 +/-3.83μg/ ml,分别在喂养的第四H和第六小时)。同时,Sb显着抑制炎症基因的mRNA表达(NOD1,RIPK2,TAK1,NF-KB / P65,ERK,JNK2,P38,IL-1β,TNF-α,CCL5,CCL20,CXCL12,FOS,β-防御素/ leap)。此外,在HC + Sb组中,NOD1,P-IKBα,P-NF-KB / P-P65,P-ERK1 / 2,P-JNK,P-P38和HDAC3的蛋白质表达显着下调。总之,通过Sb治疗减轻了通过HC饮食产生的IE-DAP诱导的炎症和肝脏破坏。

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