Bergner H, Simon O, Sommer A, Görsch R, Ceresnáková Z, Chrastinova L, Szakacs J, Stoyke M
Arch Tierernahr. 1985 Oct;35(10):733-45. doi: 10.1080/17450398509425229.
The experiments were carried out on 3 bulls (body weight: 172, 229 and 193 kg), equipped with ileo-caecal cannulas and with catheters in the jugular veins on both sides. The offered pelleted ration consisted of straw 73%, molasses 12%, cereals 10%, ammonium hydrogen carbonate 3% and urea 2%. Feed intake amounted to about 3 kg per animal and day. During a preliminary period of 5 days 50% of ileal digesta were collected for 12 hours daily, deep-freezed and stored. In the main experiment 15N-urea was infused intravenously for 24 hours. During this period and during the following 6 hours ileal digesta were collected and replaced by precollected, unlabelled digesta. The urea metabolism was estimated by the 15N-labelling of blood urea, by the 15N-excretion via faeces and urea, by the appearance of 15N in ileal digesta and by the 15N-labelling of faecal NAN, NH3 and bacterial fraction. The time course of the 15N-labelling of plasma urea during infusion can be described by an exponential function. The urea flux rate was estimated from the calculated plateau value. The flux rate for the 3 animals was 28.8, 30.7 and 34.8 mumol per minute per kg0.75, respectively. During the infusion of 15N-urea 1.0-2.4% of the infused amount of 15N' appeared in ileal digesta, half of it in the TCA precipitable fraction. At the same time the 15N-labelling of faecal NH3 increased sharply, however, the 15N-labelling of the faecal bacterial fraction was smaller by one order of magnitude. Deficiency of fermentable substrates and problems of inhomogenity of the NH3 pool are supposed as reasons for this result. 30 to 50% of the urea flux entered the digestive tract, the direct entry of urea into the large intestine seems to be only very low.
实验在3头公牛(体重分别为172、229和193千克)身上进行,这些公牛安装了回肠 - 盲肠插管以及两侧颈静脉导管。提供的颗粒饲料由73%的稻草、12%的糖蜜、10%的谷物、3%的碳酸氢铵和2%的尿素组成。每头动物每天的采食量约为3千克。在为期5天的预实验期内,每天收集12小时的回肠消化物,深度冷冻并储存。在主要实验中,静脉注射15N - 尿素24小时。在此期间以及随后的6小时内,收集回肠消化物,并用预先收集的未标记消化物进行替换。通过血尿素的15N标记、粪便和尿液中15N的排泄、回肠消化物中15N的出现以及粪便NAN、NH3和细菌部分的15N标记来评估尿素代谢。输注期间血浆尿素15N标记的时间进程可用指数函数描述。从计算出的平台值估算尿素通量率。这3头动物的通量率分别为每分钟每千克0.75体重28.8、30.7和34.8微摩尔。在输注15N - 尿素期间,输注的15N量的1.0 - 2.4%出现在回肠消化物中,其中一半在三氯乙酸可沉淀部分。与此同时,粪便NH3的15N标记急剧增加,然而,粪便细菌部分的15N标记小一个数量级。推测可发酵底物缺乏和NH3池不均匀问题是导致该结果的原因。30%至50%的尿素通量进入消化道,尿素直接进入大肠的量似乎非常低。