首页> 美国卫生研究院文献>Journal of Animal Science >Glutathione content and expression of proteins involved with glutathione metabolism differs in longissimus dorsi subcutaneous adipose and liver tissues of finished vs. growing beef steers
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Glutathione content and expression of proteins involved with glutathione metabolism differs in longissimus dorsi subcutaneous adipose and liver tissues of finished vs. growing beef steers

机译:牛背最长背肌皮下脂肪和牛公牛与生长牛公牛的肝组织中谷胱甘肽含量和涉及谷胱甘肽代谢的蛋白质表达不同

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摘要

Increased tissue redox state may result in sub-optimal growth. Our goal was to determine if glutathione ( ) content and expression of proteins involved with GSH metabolism change in longissimus dorsi ( ), subcutaneous adipose ( ), and liver tissues of growing vs. finishing steer phenotypes. Tissues were taken from 16 Angus steers (BW = 209 ± 29.4 kg) randomly assigned ( = 8) to develop through Growing (final BW = 301 ± 7.06 kg) vs. Finished (final BW = 576 ± 36.9 kg) growth phases, and at slaughter had achieved different rib-eye area (REA) (53.2, 76.8 cm ), marbling scores (296, 668), and 12th rib adipose thickness (0.54, 1.73 cm), respectively (Amino Acids, doi:10.1007/s00726-018-2540-8). GSH content (mg/g wet tissue) was determined by a commercial assay and the relative content of target protein and mRNA in tissue homogenates was determined by Western blot and reverse-transcribed PCR analyses, respectively. The effect of growth phase (Finished vs. Growing) was assessed by ANOVA using the GLM procedure of SAS. The LD of Finished steers had more ( < 0.04) GSH (42%) and GSH synthesizing (GCLC, 61%; GCLM, 21%) and metabolizing (GPX1, 42%; GPX3, 73%; GGT1, 56%) enzymes, and less ( 0.02) GPX2 (46%), EAAC1 (30%) and glutamine synthetase (GS) (28%), whereas GTRAP3-18 and ARL6IP1 did not differ ( 0.57). Principal component analysis found that GSH content of LD was associated with REA and marbling score. The SA of Finished steers had less ( < 0.04) GSH (38%), GSH metabolizing (GPX4, 52%; GGT1, 71%) enzyme mRNA, and GTRAP3-18 (123%) and ARL6IP1 (43%), whereas the mRNA content of GSH-synthesizing enzymes and content of EAAC1 and GS did not differ ( 0.32). The liver of Finished steers had less ( 0.02) mRNA content of GSH synthesizing (GCLC, 39%; GSS 29%) and metabolizing (GPX1, 30%) enzymes, and more ( 0.01) GSTM1 metabolizing enzyme (114%). The change in GSH content as steers fattened indicate an increased antioxidant capacity in the LD of Finished steers, and a decreased antioxidant capacity in SA, consistent with changes in enzyme and transporter expression. Changes in liver enzyme and transporter expression were consistent with no change in GSH content. The relationship of EAAC1 regulatory proteins (GTRAP3-18, ARL6IP1) to GSH, EAAC1, and GS content differs and changes as Growing steers develop into Finished phenotypes. These findings provide mechanistic insight into how antioxidant capacity occurs in tissues of economic and metabolic importance as cattle fatten.
机译:组织氧化还原状态增加可能会导致生长欠佳。我们的目标是确定在长背鳍表型和末代背齿表型的背最长肌,皮下脂肪和肝组织中,谷胱甘肽含量和与GSH代谢有关的蛋白质表达是否发生变化。从随机分配(= 8)的16个安格斯ste牛(BW = 209±29.4 kg)中抽取组织,以通过生长(最终BW = 301±7.06 kg)与完成(最终BW = 576±36.9 kg)的生长阶段进行发育,屠宰时的肋眼面积(REA)(53.2,76.8 cm),大理石花纹得分(296、668)和第12肋脂肪厚度(0.54、1.73 cm)(氨基酸,doi:10.1007 / s00726- 018-2540-8)。 GSH含量(mg / g湿组织)通过商业化测定确定,组织匀浆中靶蛋白和mRNA的相对含量分别通过Western印迹和反转录PCR分析确定。使用SAS的GLM程序通过ANOVA评估生长阶段(完成与生长)的影响。最终ers牛的LD具有更多(<0.04)GSH(42%)和GSH合成酶(GCLC,61%; GCLM,21%)和代谢酶(GPX1,42%; GPX3,73%; GGT1,56%),较少(0.02)GPX2(46%),EAAC1(30%)和谷氨酰胺合成酶(GS)(28%),而GTRAP3-18和ARL6IP1没有差异(0.57)。主成分分析发现LD的GSH含量与REA和大理石花纹分数相关。成年公牛的SA较少(<0.04)GSH(38%),GSH代谢(GPX4,52%; GGT1,71%)酶mRNA和GTRAP3-18(123%)和ARL6IP1(43%),而GSH合成酶的mRNA含量与EAAC1和GS的含量无差异(0.32)。精制ste牛肝脏的GSH合成酶(GCLC,39%; GSS 29%)和代谢酶(GPX1,30%)的mRNA含量较少(0.02),而GSTM1代谢酶的含量更高(0.01)。 ste牛皮增肥过程中GSH含量的变化表明成品ste牛皮的LD中抗氧化能力增强,而SA中的抗氧化能力下降,这与酶和转运蛋白表达的变化一致。肝酶和转运蛋白表达的变化与谷胱甘肽含量没有变化一致。 EAAC1调节蛋白(GTRAP3-18,ARL6IP1)与GSH,EAAC1和GS含量之间的关系不同,并且随着生长的ers牛发展成最终表型而改变。这些发现为牛增肥时在具有经济和新陈代谢重要性的组织中如何发生抗氧化能力提供了机械原理。

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