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首页> 外文期刊>Annals of Clinical and Laboratory Science: Official Journal of the Association of Clinical Scientists >Evaluation of Stable Isotope Labeling Technique in Measuring the Tissues' Protein Fractional Synthesis Rates in Rats
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Evaluation of Stable Isotope Labeling Technique in Measuring the Tissues' Protein Fractional Synthesis Rates in Rats

机译:稳定同位素标记技术在测量大鼠组织蛋白质分数合成速率中的评价

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Aims: The objective of this study was to evaluate the technique for measuring tissues' protein fractional synthesis rates with [L-N-15] Leucine. Materials and methods: Sixty male Sprague-Dawley rats were randomly assigned to different groups. After intravenous injection with [L-N-15] Leucine, the enrichment of N-15 in different time intervals was measured with the same dosage and at the same time by variable dosage. Results: During the period from 0 to 30 minutes, there was nearly a linear increase in enrichment of N-15 in both the free amino acid pool and the bond amino acid pool in rats' tissues, and the peak was achieved at 30 minutes. With the increase of dosage, the fractional synthesis rates rose. However, when the dosage was more than 1.0 mmol/kg, there was no significant discrepancy. Conclusions: For measuring the tissues' protein fractional synthesis rates with [L-N-15] Leucine in rats, 30 minutes post-injection is optimal, and 1.0 mmol/kg is the most suitable dosage.
机译:目的:本研究的目的是评估使用[L-N-15]亮氨酸测量组织蛋白质分数合成率的技术。材料和方法:60只雄性Sprague-Dawley大鼠随机分为不同的组。静脉内注射[L-N-15]亮氨酸后,以相同的剂量和不同的剂量在同一时间测量N-15在不同时间间隔的富集。结果:在0至30分钟内,大鼠组织中游离氨基酸库和键合氨基酸库中N-15的富集几乎呈线性增加,并在30分钟时达到峰值。随着剂量的增加,部分合成速率增加。但是,当剂量大于1.0 mmol / kg时,则没有显着差异。结论:为测定[L-N-15]亮氨酸在大鼠组织中的蛋白质分数合成速率,注射后30分钟为最佳,最合适的剂量为1.0 mmol / kg。

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