scholarly journals ECONOMICAL FATTENING OF BUFFALO CALVES USING DIFFERENT SOURCES OF NON-PROTEIN NITROGEN

1996 ◽  
Vol 33 (1) ◽  
pp. 113-122
2021 ◽  
Vol 38 (2) ◽  
pp. 144-150
Author(s):  
D. Kumar ◽  
S.P. Yadav ◽  
D.S. Sahu ◽  
G. Chandra ◽  
P.S. Maurya

1978 ◽  
Vol 91 (2) ◽  
pp. 309-316 ◽  
Author(s):  
N. S. Malik ◽  
P. N. Langar ◽  
A. K. Chopra

SUMMARYThe nutritive value of uromol, a heated product of urea and molasses, was compared with raw urea–molasses and groundnut meal in three metabolic trials on buffalo calves. The non-protein nitrogen (NPN) as urea or uromol contributed about 65, 48 and 30% of the nitrogen in the experimental concentrate mixtures, replacing partially or completely the groundnut meal of the control diets. The results showed that at 65% nitrogen replacement, the crude fibre and cellulose digestibilities and the nitrogen retention of the uromol diet was similar to that of the control but was significantly (P < 0·05) higher than the urea–molasses diet. At 48% nitrogen replacement the nitrogen retention in the uromol-fed animals was still significantly (P < 0·05) higher than the urea–molasses fed group. At 30% nitrogen replacement, the differences between the control, urea–molasses and uromol groups were not significant.In vivo rumen studies with the diets containing 50% NPN replacement showed lower but sustained ammonia-N with uromol than the urea–molasses diet. The total volatile fatty acids (TVFA) in rumen fluid, though initially higher in the control and uromol groups, were not significantly different from the urea–molasses group. Abomasal studies with diets containing 65% N as urea or uromol indicated a higher total nitrogen content in the abomasal fluid of the control and uromol-fed animals than the urea-fed animals. The 24 h abomasal passage of total-N/100 g nitrogen consumed was 95·5, 93·5 and 77·9 g in control, uromol and urea groups, respectively. The TCA-precipitatable-N (TCA-N) was also higher in the first two groups. These studies suggest that uromol is safer and has a better feeding value than urea–molasses at high rates of nitrogen replacement.


1996 ◽  
Vol 1996 ◽  
pp. 43-43
Author(s):  
H.J. Kim ◽  
W.J. Maeng ◽  
H. Park ◽  
M.A. Neville ◽  
R.T. Evans ◽  
...  

Synchronising the availability of energy and nitrogen to the rumen microbes is considered to be important for enhancing output of microbial protein from the rumen. This is particularly relevant to diets based on grass silage (Chamberlain and Choung, 1995). In the rumen ammonia, is rapidly released from the substantial content of non-protein nitrogen compounds in grass silage and this requires a similarly rapid release of energy in the rumen to ensure efficient capture of ammonia. Different sources of carbohydrate may enhance rumen function to varying degrees. The aim of this study was to examine the effects of various carbohydrate sources on intake, rumen fermentation characteristics and digestibility in steers fed on grass silage.


1987 ◽  
Vol 57 (01) ◽  
pp. 029-034 ◽  
Author(s):  
Göran Urdén ◽  
Joanna Chmielewska ◽  
Tomas Carlsson ◽  
Björn Wiman

SummaryPolyclonal antibodies have been raised against the inhibitor moiety in the purified complex between tissue plasminogen activator and its fast inhibitor (PA-inhibitor) in human plasma/ serum. A radioimmunoassay for quantitation of PA-inhibitor antigen was developed. The polyclonal antiserum and a previously described monoclonal antibody against the PA-inhibitor (14) have been used to study the immunological relationship between PA-inhibitors from plasma, serum, platelets, placenta extract and conditioned media from Hep G2 and HT 1080 cells. It was demonstrated that the ratio between PA-inhibitor activity and antigen varied considerably between the different sources. In the plasma samples studied, similar activity and antigen concentrations were found, suggesting that the PA-inhibitor in these samples mainly was in an active form. On the other hand the other sources seemed to contain variable amounts of inactive PA-inhibitor forms. Immunoadsorption experiments revealed that the PA-inhibitor (activity and antigen) from all the sources were specifically bound to the insolubilized antibodies (polyclonal and monoclonal). In no case, however, could active PA-inhibitor be eluted from the immunoadsorption columns. Also the competitive radioimmunoassays suggested that the PA-inhibitors from the different sources studied, were closely immunologically related.


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