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[绵羊体内15N-14C-乙酰脲的代谢]

[Metabolism of 15N-14C-acetylurea in the sheep].

作者信息

Bergner H, Görsch R, Kijora C, Adam K, Müller J

出版信息

Arch Tierernahr. 1975 Dec;25(9-10):609-27. doi: 10.1080/17450397509423229.

Abstract

3 male sheep (phi 48.3 kg) were fed a semisynthetic diet containing acetyl urea as sole protein source and 15N-14C labelled acetyl urea (urea-C labelled) by intraruminal tube. A half life period of 4 hrs was established for the removal of labelled acetyl urea from the TCE-soluble portion of the ruminal fluid. The degree of 14C labelling in ruminal proteins was very low whereas the extent of 15N labelled protein synthesis was quite marked reaching a maximum between the 18th and 24th hour of experiment. The steepest rise of 15N incorporation into ruminal proteins was found to occur between 8 to 12 hrs after start of the experiment, i.e. at the time of peak level of 15N returned from 15N urea via the rumino-hepatic circulation. 23.3% of the amount of 14C activity administered (mean of all 3 experimental animals) was excreted through respiration. The curve patterns of both isotopes in the TCE soluble portion of the ruminal fluid were similar to that of the degasified TCE soluble portion of the blood blasma. At the peak time (8 hrs) a concentration of the nitrogen isotope of about 4 atom% excess of 15N was observed. The level of 14C labeling in blood plasma proteins was insignificant when compared with that of 15N labelling. The ratio at the peak time was 1:10; the same ratio was found for ruminal proteins. From this it can be concluded that the process of labelling of blood plasma proteins proceeds mainly through microbial protein synthesis. Sheep I and III excreted an average of 60.6% of 14C activity and 57.0% of the administered excess of 15N in the urine. 6 hrs after the beginning of the experiment 81% of the amount of urinary 14C activity was found to occur as acetyl urea; after 48 hrs this amount had decreased to 50%. All experimental sheep excreted a urinary sediment consisting mainly of acetyl urea. The level of faecal 14C excretion (1.4%-2.9% of the amount administered) was considerably lower than that of 15N excretion (9.1%--15.6% of the administered dose). The TCE soluble fraction of the faeces contained up to 2% of the 14C dose and 3% of the 15N dose. The true digestibility data of 15N from 15N acetyl urea varied between 96.4% and 98.2%. An average of 40.9% was obtained for the 15N balance over the 7-day trial period.

摘要

选用3只雄性绵羊(体重48.3千克),通过瘤胃管给它们饲喂一种半合成日粮,该日粮以乙酰脲作为唯一蛋白质来源,并添加15N - 14C标记的乙酰脲(尿素 - C标记)。从瘤胃液的三氯乙烷(TCE)可溶部分中去除标记的乙酰脲的半衰期为4小时。瘤胃蛋白质中14C标记程度非常低,而15N标记的蛋白质合成程度相当显著,在实验的第18至24小时达到最大值。发现15N掺入瘤胃蛋白质的最陡上升发生在实验开始后的8至12小时,即从15N尿素通过瘤胃 - 肝循环返回的15N达到峰值水平时。所给予的14C活性量(所有3只实验动物的平均值)的23.3%通过呼吸排出。瘤胃液的TCE可溶部分中两种同位素的曲线模式与血浆的脱气TCE可溶部分相似。在峰值时间(8小时),观察到氮同位素的浓度约为15N过量4原子%。与15N标记相比,血浆蛋白质中的14C标记水平微不足道。峰值时间的比例为1:10;瘤胃蛋白质也发现相同比例。由此可以得出结论,血浆蛋白质的标记过程主要通过微生物蛋白质合成进行。绵羊I和III在尿液中平均排出60.6%的14C活性和57.0%所给予的过量15N。实验开始6小时后,发现尿液中81%的14C活性以乙酰脲形式存在;48小时后,该量降至50%。所有实验绵羊都排出了主要由乙酰脲组成的尿沉渣。粪便中14C排泄水平(所给予量的1.4% - 2.9%)远低于15N排泄水平(所给予剂量的9.1% - 15.6%)。粪便的TCE可溶部分含有高达2%的14C剂量和3%的15N剂量。15N乙酰脲中15N的真实消化率数据在96.4%至98.2%之间变化。在7天的试验期内,15N平衡平均为40.9%。

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