Factors affecting the urinary excretion of urea nitrogen in cattle. I. Sodium chloride and water loads

1970 ◽  
Vol 21 (1) ◽  
pp. 131 ◽  
Author(s):  
RF Thornton

Urea metabolism in cattle was studied under conditions of different nitrogen, sodium chloride, and water intakes. Urea supplementation increased the concentrations of ammonia and trichloroacetic acid-insoluble nitrogen in ventral rumen fluid, raised the plasma urea concentration, and increased the excretion of faecal nitrogen and urinary urea and non-urea nitrogen. Sodium chloride loading increased the free water intake and urine flow rate, and the added sodium was quantitatively recovered in the urine. Plasma urea concentration was linearly related to urinary urea excretion but the slope of this relationship was influenced by the urine flow rate. Urea clearance and the fraction of filtered urea excreted were both related to the urine flow rate and to the urine-concentrating ability of the kidney, but not to the urinary urea output. During low nitrogen intakes, urinary urea excretion was influenced more by urine flow than by solute load.

1970 ◽  
Vol 21 (1) ◽  
pp. 145 ◽  
Author(s):  
RF Thornton

The relationships between the plasma urea concentration and clearance variables associated with urinary urea excretion were investigated in urea-supplemented cattle. The plasma urea concentration was related to the urinary urea output, and thus to the urea clearance and the fraction of filtered urea excreted. It is suggested that the urine flow rate was influenced by urinary urea excretion, which in turn was influenced by the plasma urea concentration and therefore by the filtered load of urea. The probable influence of the recycling of urea to the rumen on the excretion of urinary urea is discussed.


1967 ◽  
Vol 21 (2) ◽  
pp. 353-371 ◽  
Author(s):  
M. R. Cocimano ◽  
R. A. Leng

1. The entry rates of urea into the urea pool of the body fluids have been measured in sheep given rations varying in crude protein percentage from 3.5 to 27.3.2. Results obtained with a single injection and with continuous infusions of [14C]urea were essentially the same.3. The difference between the entry rate and the rate of excretion of urea in the urine was taken to indicate the quantity of urea degraded in the alimentary tract.4. Plasma concentrations and urea entry rates were significantly and linearly related.5. The relationship between excretion rate and plasma urea concentration was best described by a cubic equation.6. Degradation of urea in sheep was found to be extensive in all the animals studied; as the protein intake increased, the quantity of urea degraded also increased but the percentage of urea entering the body pool that was degraded was decreased. Animals given a ration containing 3.5% crude protein degraded 76–92% of the urea entering the body pool.7. A rectilinear relationship was found between pool size and plasma urea concentration. The urea space in animals given low-protein rations was significantly less than in animals on high-protein rations.8. The effects of starvation for 2, 4 and 6 days on urea metabolism in sheep were investi-gated. In a11 the sheep starved for 2 days there was a significant increase in urea pool size, but the entry rate was markedly depressed indicating a retention of urea in the body pool on starvation.9. A significant amount of nitrogen was found to go through the system: rumen ammonia → portal blood ammonia→blood urea→rumen ammonia.10.Urea excretion rate, urea clearance by the kidney, urine flow rate and the ratio of the concentration of urea in urine to that in plasma (urea U:P ratio) were also examined.11. There were significant correlations between urine flow rate and urea excretion and between plasma urea concentration and urine flow rate.


1970 ◽  
Vol 21 (2) ◽  
pp. 337 ◽  
Author(s):  
RF Thornton

Urea was infused intravenously into sheep whose rumen contents were removed and replaced with physiological saline. Despite large differences in plasma urea concentration the rate of nitrogen accumulation in the rumen, as urea plus ammonia, was similar at 6-7 mmoles/hr. The maximum concentration of nitrogen, as urea plus ammonia, was not influenced by plasma urea concentrations higher than 15-17 mg N/100 ml. Urinary urea excretion was positively related to plasma urea concentration but within any level of plasma urea concentration there was a close association between urine flow and urinary urea excretion.


1957 ◽  
Vol 188 (3) ◽  
pp. 477-484 ◽  
Author(s):  
Bodil Schmidt-Nielsen ◽  
Knut Schmidt-Nielsen ◽  
T. R. Houpt ◽  
S. A. Jarnum

The nitrogen excretion was studied in the one-humped camel, Camelus dromedarius. When a growing camel was maintained on a low N intake (dates and hay) the amount of N excreted in the form of urea, NH3 and creatinine decreased to 2–3 gm/day. This decrease was caused by a drop in urea excretion from 13 gm to 0.2–0.5 gm/day. Urea given intravenously during low N intake was not excreted but was retained. (The camel like other ruminants can utilize urea for microbial synthesis of protein.) The renal mechanism for urea excretion was investigated by measuring urea clearance and glomerular filtration rate during a period of 7 months. During normal N intake about 40% of the urea filtered in the glomeruli were excreted in the urine while during low N intake only 1–2% were excreted. The variations in urea clearance were independent of the plasma urea concentration and of glomerular filtration rate, but were related to N intake and rate of growth. No evidence of active tubular reabsorption of urea was found since the urine urea concentration at all times remained higher than the simultaneous plasma urea concentration. The findings are not in agreement with the current concept for the mechanism of urea excretion in mammals. It is concluded that the renal tubules must either vary their permeability to urea in a highly selective manner or secrete urea actively.


2007 ◽  
Vol 85 (4) ◽  
pp. 1006-1013 ◽  
Author(s):  
N. E. Sunny ◽  
S. L. Owens ◽  
R. L. Baldwin ◽  
S. W. El-Kadi ◽  
R. A. Kohn ◽  
...  

1970 ◽  
Vol 16 (4) ◽  
pp. 347-349
Author(s):  
E Melvin Gindler

Abstract Two nomograms are given for use in calculating standard, C[unknown], or maximum, Cm, urea clearance. The first nomogram calculates the urine flow rate, f, from the urine collection time and volume data. With the second nomogram, values of f and urea nitrogen concentrations in blood serum (or plasma) and urine are used to calculate either C[unknown] or Cm, according to the value of f. There is no intermediate calculation of √f. Examples of the use of the two nomograms in the calculation of C[unknown] or Cm are given.


1972 ◽  
Vol 42 (4) ◽  
pp. 423-432 ◽  
Author(s):  
John R. Gill ◽  
Catherine S. Delea ◽  
F. C. Bartter

1. The response to an infusion of 4% (w/v) fructose in water was determined in fifteen women on a daily sodium intake of 100 mEq/day. The results were compared with those obtained during a similar infusion on another day after treatment with deoxycorticosterone (20 mg/day; seven subjects), or spironolactone (200 mg/day; eight subjects), for 1 day before the day of study. 2. Treatment with deoxycorticosterone significantly (P < 0·01) decreased sodium excretion (from a mean value of 391 to 192 μEq/min) and urine flow rate (from 14·3 to 12·4 ml min−1 100 ml−1 of glomerular filtrate) without a change in urinary osmolality or the clearance of inulin. The steroid also increased the fractional reabsorption of sodium at the diluting segment of the nephron, but this increase in reabsorption was not sufficient to compensate for the decrease in delivery of sodium to the site, so that absolute free-water clearance decreased. 3. Treatment with spironolactone significantly (P < 0·01) increased sodium excretion (from 349 to 437 μEq/min) and urine flow rate (from 12·5 to 14·4 ml min−1 100 ml−1 of glomerular filtrate) with essentially no change in urinary osmolality or in inulin clearance. Spironolactone also decreased the fractional reabsorption of sodium at the diluting segment of the nephron, but the degree of inhibition of reabsorption was not sufficient to prevent an increase in free-water clearance as a result of increased delivery of sodium to the site. 4. The findings support the concept that changes in circulating aldosterone can alter the renal excretion of sodium in man by affecting its reabsorption in the proximal tubule as well as in the distal tubule.


1970 ◽  
Vol 21 (2) ◽  
pp. 323 ◽  
Author(s):  
RF Thornton

Cattle and sheep were offered the same diet in amounts according to the ratio of their metabolic body size, and were intravenously infused with urea in amounts according to the same ratio. An apparent limit to the transfer of urea from the blood to the rumen occurred at lower plasma urea and rumen ammonia concentrations in cattle than in sheep. Associated with ingestion of feed there was a decline in the concentrations of both rumen ammonia and plasma urea, and in urinary urea excretion. It is suggested that (a) the transfer of urea from the blood to the rumen and the urinary excretion of urea are reciprocally related, and (b) the transfer of urea from the blood to the rumen and the consequent reduction in plasma urea concentration associated with feed ingestion may account for the decline in urinary urea excretion after ingestion of feed, rather than changes in the urine flow rate and in renal tubular mechanisms.


1989 ◽  
Vol 257 (1) ◽  
pp. R162-R167 ◽  
Author(s):  
T. D. Williams ◽  
K. P. Walsh ◽  
R. Canepa-Anson ◽  
M. I. Noble ◽  
A. J. Drake-Holland ◽  
...  

The effects of rapid atrial pacing on central hemodynamics, plasma hormones, and renal function were investigated in eight control and nine cardiac-denervated dogs under chloralose anesthesia. Pacing at approximately 250 ppm for 60 min caused similar increases in pulmonary wedge and right atrial pressures, systemic vascular resistance, and plasma atrial natriuretic peptide (ANP) in both groups. In control dogs, pacing produced a fall in both plasma vasopressin (AVP) and plasma renin activity (PRA) and a rise in urine flow rate associated with an increase in free water but not sodium clearance. In contrast, in cardiac-denervated dogs, both plasma AVP and PRA increased during pacing; urine flow rate did not change, and marked sodium retention occurred. This study supports the concept that the increase in urine flow during rapid atrial pacing is mediated by inhibition of renin and AVP secretion through intact cardiac nerves. The secretion of ANP is unaffected by cardiac denervation. The natriuretic and vasodilator actions of high plasma ANP concentrations during rapid atrial pacing can be inhibited either by neurally mediated cardiorenal effects in normal animals or by stimulation of the renin-angiotensin system after cardiac denervation.


1976 ◽  
Vol 36 (3) ◽  
pp. 353-368 ◽  
Author(s):  
Sarah A. Allen ◽  
E. L. Miller

1. Plasma urea entry rate, urinary urea excretion and, by difference, urea recycling in the body, together with the flow of non-ammonia N through the abomasum and digestion of dry matter (dm) before the abomasum were determined in both wethers and lambs receiving cereal-starch diets supplemented with urea to give 60–120 g crude protein (N × 6.25)/kgdm.2. Lambs excreted less urea in urine than wethers given the same diet.3. Relationships between plasma urea entry rate or urine urea excretion rate and plasma urea concentration were different for lambs compared to wethers suggesting greater conser vation of body N by renal control in lambs.4. Recycling of urea was not related to plasma urea concentration in wethers but was related exponentially in lambs, suggesting recycling is controlled rather than the result of simple diffusion from the blood to the gastro-intestinal tract.5. Abomasal non-ammonia-N flow was similar for wethers and lambs and increased linearly with urea supplementation.6.dmdigestion prior to the abomasum was not significantly altered, although there was a tendency for decreased digestion of the basal diet given to lambs.7. Maximum microbial N flow to the abomasum was estimated as 30 g N/kg organic matter (OM) fermented in the rumen.8. This work and the literature reviewed suggested maximum net microbial production can be obtained when the diet supplies an amount of fermentable N equal to the microbial N output. It is calculated the diet should supply approximately 26 g fermentable N/kg digestible OM or 1.8 g fermentable N/MJ metabolizable energy. This corresponds to a fermentable crude protein supply varying from 65 to 130 g/kg DM as digestible OM content increases from 400 to 800 g/kg DM.


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