scholarly journals Concurrent studies of the flow of digesta in the duodenum and of exocrine pancreatic secretion of calves

1975 ◽  
Vol 33 (2) ◽  
pp. 181-196 ◽  
Author(s):  
J. H. Ternouth ◽  
J. H. B. Roy ◽  
S. Y. Thompson ◽  
Joyce Toothill ◽  
Catherine M. Gillies ◽  
...  

1. The flow of digesta through the duodenum and the concurrent secretion of the pancreas were studied in four Friesian calves given four milk-substitute diets. The diets were: reconstituted, ‘mildly’ pre-heated, spray-dried skim-milk powder with (SKF) or without (SK) margarine fat or with 50% of the skim-milk powder in diet SKF replaced by soya-bean flour (ASKF) or fish-protein concentrate (BSKF), together with dried whey. The diets were given ad lib. twice daily from 13 to 37 d of age, each diet being given for 6 consecutive days. Collections of duodenal digesta and pancreatic secretions, from cannulas, were made for 12 h after feeding the 6th and 12th meals (‘experimental’ meals) for each diet2. The diets fed as ‘experimental’ meals contained polyethylene glycol (PEG) as a fluid (whey) marker and goat's milk containing [3H]lysine as a marker for total protein; β-carotene was added as a lipid marker to the three diets containing margarine fat3. Over the 12 h postprandial period, the patterns of duodenal digesta flow and secretion of pancreatic fluid did not differ markedly between the four diets. The abomasal outflow of both nitrogen and lipid in a 12 h postprandial period was related to their intakes from the ‘penultimate’(5th and 11th) meals for diets SKF and SK but to their intakes at the ‘experimental meals’ for diets ASKF and BSKF. Secretion of pancreatic enzyme activity was highest during the 1st hour after feeding but the main outflow from the abomasum of total N and lipid occurred 5–10 h after feeding4. The time required for all the whey marker (PEG) to pass through the duodenum was similar for diets SKF and SK, but only 53 and 42% respectively of the ingested protein marker passed through the duodenum in the 12 h after feeding. More acid appeared to be secreted by the abomasum when diet SK was given; also less undigested protein passed out of the abomasum after giving this diet. It is concluded that the physical absence of fat globules in the abomasal clot increases the degree of proteolysis5. The secretions of pancreatic fluid and pancreatic enzyme activity were all markedly lower for diet SK than for diet SKF6. With diets containing non-milk proteins (ASKF and BSKF), abomasal proteolysis was less efficient and the ingested protein passed out of the abomasum more rapidly than for diet SKF. There was no difference in the rate of abomasal outflow of the whey fluids between diets SKF, ASKF and BSKF7. In comparison with diet SKF, diets ASKF and BSKF tended to induce less pancreatic enzyme secretion over a 12 h postprandial period, with the exception of lipase8. There appeared to be no direct relationship between the quantities of any of the pancreatic enzymes secreted during a postprandial period and either the concurrent flow of duodenal digesta or the total quantities of dietary constituents passing through the duodenum.

1974 ◽  
Vol 31 (1) ◽  
pp. 13-26 ◽  
Author(s):  
J. H. Ternouth ◽  
J. H. B. Roy ◽  
R. C. Siddons

1. The duodenal flow of digesta and the concurrent pancreatic secretion were compared when six Ayrshire calves, with duodenal re-entrant and pancreatic sac cannulas, were fed on three reconstituted milks. The diets were: reconstituted, ‘mildly’ preheated, spray-dried skim-milk powder (SK); the same skim milk containing 20 g fat/l (SKF); and reconstituted, ‘severely’ preheated skim-milk powder containing 20 g fat/l (HSKF). The calves were fed ad lib. from teats twice daily from 9 to 21 d of age, each diet being offered for 4 d. Collections of duodenal digesta and pancreatic secretions were made for 12 h after the fourth and eighth meals on each diet.2. The calves tended to have the highest liquid intakes when diet SK was given. After adjustment for differences in intake, diet SK resulted in the appearance of more hydrogen, chloride and potassium ions but less undigested protein nitrogen in the duodenal digesta than with either diet SKF or HSKF.3. Compared with diets SK and SKF, the whey fluids from diet HSKF took significantly longer to leave the abomasum, less H+ passed through the duodenum during the first 6 h after feeding and less Cl− during the whole postprandial period. More undigested protein N and fat from diet HSKF passed through the duodenum during the first 6 h after feeding, although this difference was significant only for protein N during the 1st hour after feeding.4. Over the 12 h postprandial period, the duodenal digesta contained almost exactly the same quantities of polyethylene glycol (PEG), N and fat as those in the meal. The total volume of digesta was 2.25 l greater than the quantity of milk ingested. When the hourly duodenal flows of PEG and fluid were expressed as the square root of the hourly quantities recovered, the pattern of abomasal emptying was rectilinear. The flows of N and fat were curvilinear, when expressed on the same basis.5. The concentration of ‘sodium-free’chloride in the duodenal digesta, in excess of that ingested in the milk, was used as an indicator of the quantity of acid secreted by the abomasum. The relative quantity of acid secreted was greatest with diet SK and least with diet HSKF.6. The pancreatic secretion of fluid was highest during the period 5–9 h after feeding but the secretion of enzyme activity was highest during the first 2 h after feeding.7. Considerable variability in the secretion of enzyme activity was observed and the rate of secretion did not appear to be related to any component of the duodenal digesta.8. Diet SKF was associated with a greater volume of pancreatic secretion and more pancreatic protease secretion than either diet SK or HSKF, but most amylase activity was secreted when diet HSKF was given. Evidence is presented which suggests that pancreatic enzyme activity adaptation occurred when diet HSKF was offered in succession to diet SK or SKF. The secretion of trypsin activity did not differ between diets.


2011 ◽  
Vol 94 (4) ◽  
pp. 1043-1059 ◽  
Author(s):  
Petra Lutter ◽  
Véronique Parisod ◽  
Hans Weymuth

Abstract The protection of allergic consumers is crucial to the food industry. Therefore, accurate methods for the detection of food allergens are required. Targeted detection of selected molecules by MS combines high selectivity with accurate quantifcation. A confrmatory method based on LC/selected reaction monitoring (SRM)-MS/MS was established and validated for the quantifcation of milk traces in food. Tryptic peptides of the major milk proteins β-lactoglobulin, β-casein, αS2-casein, and κ-casein were selected as quantitative markers. Precise quantifcation was achieved using internal standard peptides containing isotopically labeled amino acids. For each peptide, qualifer and quantifer fragments were selected according to Commission Decision 2002/657/EC. A simple sample preparation method was established without immunoaffnity or SPE enrichment steps for food matrixes containing different amounts of protein, such as baby food, breakfast cereals, infant formula, and cereals. Intermediate reproducibility, repeatability, accuracy, and measurement uncertainty were determined for each matrix. LOD values of 0.2–0.5 mg/kg, e.g., for β-lactoglobulin, were comparable to those obtained with ELISA kits. An LOQ of approximately 5 mg/kg, expressed as mass fraction skim milk powder, was validated in protein-rich infant cereals. The obtained validation data show that the described LC/SRM-MS/MS approach can serve as a confrmatory method for the determination of milk traces in selected food matrixes.


1984 ◽  
Vol 51 (4) ◽  
pp. 623-628 ◽  
Author(s):  
Donald Stead

SummaryA method which was developed for assaying the extracellular lipases of psychrotrophic bacteria in milk (Stead, 1983, 1984) and which uses the fluorogenic substrate 4-methylumbelliferyl oleate has been adapted for use with skim milk powder (SMP), whey powder (WP) and whey protein concentrate (WPC). A five-fold increase in the concentration of sodium taurocholate (NaTC), in the mixture of NaTC and cetyltrimethylammonium bromide needed to dissociate lipase from milk proteins, removed the excessive sensitivity of the assay to variations in the concentrations of SMP, WP or WPC incorporated. Commercially available pancreatic lipase provided a suitable standard of lipolytic activity and as little as 1–2 μ could be detected in each assay system.


2014 ◽  
Vol 36 (1) ◽  
pp. 21-28 ◽  
Author(s):  
L.P. Martínez-Padilla ◽  
V. García-Mena ◽  
N.B. Casas-Alencáster ◽  
M.G. Sosa-Herrera

2004 ◽  
Vol 16 (2) ◽  
pp. 252 ◽  
Author(s):  
M.A. Coutinho da Silva ◽  
G.E. Seidel ◽  
E.L. Squires ◽  
Y.H. Choi ◽  
E.M. Carnevale

The ability of sperm to bind to zonae pellucidae (ZP) has been correlated with fertilizing capacity of sperm in several species. Limited numbers of equine oocytes are available to perform such assays. Therefore, use of heterologous ZP to perform gamete binding tests with stallion sperm would be useful. We have found that addition of 10% of skim milk-based extender with glucose [EZ-Mixin®, Animal Reproduction Systems, Chino, USA;; (EZ)] to TALP significantly increased the number of stallion sperm bound to bovine ZP. Objectives of the present experiments were to determine: (1) if stallion sperm bind in similar numbers to equine and bovine ZP, and (2) the effects of skim milk, milk proteins and glucose on sperm binding to ZP. Denuded bovine (immature) and equine (mature) oocytes were stored at 5°C in salt solution (1.5M MgCl2, 40mM HEPES, 0.1% PVP). In Experiment I, 4 ejaculates from 2 stallions were centrifuged at 300g for 6min, and sperm pellets were resuspended in 1mL of TALP or EZ. Sperm were stained with Hoechst 33342, centrifuged, and resuspended to 2×106 sperm mL−1. Oocytes were placed into droplets of 45μL of TALP (7 to 10 oocytes/trt/ejac). Extended sperm (5μL) were added to oocytes, resulting in 2times105 sperm mL−1, and the mixutre was incubated for 2h at 38.5°C. Oocytes then were pipetted in TALP to remove loosely attached sperm and observed with fluorescence microscopy;; mean numbers of sperm bound to bovine and equine ZP for TALP were 29±1.9 and 36±2.6 (P>0.1) and for EZ, 149±5 and 152±6.3 (P>0.1), respectively. More sperm bound to ZP with EZ than to ZP with TALP (P<0.001). Experiment II used 4 ejaculates from 4 stallions. After initial centrifugation, sperm were resuspended in 1mL of each of six extenders: TALP, EZ, TALP containing 89.5mM glucose (TG), TALP containing 163.5mM glucose (THG), TALP containing 2.4mgmL−1 of skim-milk powder (TSM), and INRA 96® (IMV Technologies, L’Aigle, France) that contains 27mgmL−1 of native phosphocaseinate. Hoechst 33342-stained sperm and bovine oocytes were processed as described for Experiment I. Treatments containing milk proteins resulted in more sperm binding (P<0.01) than those without milk proteins (Table 1). In conclusion, use of bovine oocytes led to similar results for equine and bovine oocytes;; therefore, bovine oocytes can be used for binding assays with stallion sperm. High concentrations of glucose increased numbers of sperm bound to ZP;; however, presence of milk or milk proteins was more effective in enhancing binding of sperm to ZP. INRA96 contains relatively low glucose (67mM) and one milk protein. Therefore, we hypothesize that native phosphocaseinate may cause increased sperm binding to ZP. Table 1 Mean sperm bound per ZP±SEM (n=38–40/group)


Author(s):  
Shishir Sinha ◽  
Shalini Sinha

Proteases are enzymes that hydrolyze peptide bonds and, therefore, lead to the disassembly of proteins. Commercially these are extremely important as more than 60% of the total enzyme market is made up of proteases, out of which 40% are acid proteases. The objective of this study was to compare the available standard strains, Rhizopus oligosporus MTCC-556, Rhizomucor miehei MTCC-546 and Aspergillus awamori MTCC-548, which were examined for the production of acid protease by submerged fermentation. Aspergillus awamori showed maximum proteolytic activity and was selected for further optimization studies. During the course of study the medium was altered. Effect of different carbon sources (lactose, sucrose, and combination of these two in same ratios and glucose) on the proteolytic activity of acid protease produced by A. awamori MTCC 548 was studied and it was found that glucose showed highest proteolytic activity. The effect of various concentrations of glucose was also studied on the acid protease production and its 1% concentration was found to be optimum; it showed proteolytic activity of 0.11 U/ml. Among the different nitrogen sources, such as casein, peptone, skim-milk powder and peanut meal, the peanut meal was found better for enzyme production. Peanut meal, with a concentration of .2% in the medium, increased proteolytic activity up to 0.218 U/ml. The effect of additives, such as Tween-80 and chemicals like CaCl2 and skim-milk powder, was also studied and it was found that 0.05% Tween-80 was effective in enzyme production and a proteolytic activity of 0.225 U/ml was obtained. The enzyme extract was separated in the form of supernatant by using centrifuge and the enzyme activity was analyzed by Anson’s method using a spectrophotometer. The enzyme produced was recovered by using a saturated solution of 80% ammonium sulphate and protein content was determined by Lowery method using a spectrophotometer. It was found that the specific enzyme activity was increased from 0.155 U/mg proteins to 0.174 U/mg proteins showing a purification fold by a factor of 1.12 by using 80% saturated ammonium sulphate.


2021 ◽  
pp. 106757
Author(s):  
Jianfeng Wu ◽  
Simin Chen ◽  
Teng Wang ◽  
Hao Li ◽  
Ali Sedaghat Doost ◽  
...  

2021 ◽  
pp. 104997
Author(s):  
Sejeong Kim ◽  
Jae Yeon Joung ◽  
Daekyoung Kang ◽  
Nam Su Oh ◽  
Yohan Yoon

1983 ◽  
Vol 36 (1) ◽  
pp. 147-150 ◽  
Author(s):  
W. S. Thickett ◽  
N. H. Cuthbert ◽  
T. D. A. Brigstocke ◽  
M. A. Lindeman ◽  
P. N. Wilson

ABSTRACTResults are presented from six trials dealing with aspects of management on the cold ad libitum system of calf rearing using an acidified milk replacer containing over 600 g skim milk powder per kg.Thirty-six calves were housed in pens of six for each trial and were fed through a teat and pipeline from a storage barrel. Acidified milk replacer, pH 5·6, was mixed cold at 125 g/1 and made available ad libitum to 3 weeks. A rationed allowance was given daily, on a reducing scale, over the following 2 weeks with weaning completed at 35 days. A pelleted dry food containing 180 g crude protein per kg, together with water in buckets and barley straw in racks, was available ad libitum throughout. Each trial lasted 8 weeks. Results for the mean of the six cold ad libitum trials involving 216 calves were compared with the mean results of 10 conventional bucket-fed trials carried out separately at the same unit, involving 912 calves. All calves were purchased British Friesian male (bull) calves.Calves on the ad libitum system showed improved live-weight gains of 9·4 kg at 3 weeks, 8·8 kg at 5 weeks and 7·5 kg at 8 weeks, compared with the conventional system. The consumption of milk replacer powder was higher in ad libitum trials at 29·4 kg cf. 12·5 kg by bucket but intake of pelleted dry feed was lower on the ad libitum system at 50·7 kg cf. 71·3 kg to 8 weeks. Calf appearance scores were significantly improved on the ad libitum system which gave the main improvement in performance in the first 3 weeks.


1955 ◽  
Vol 53 (4) ◽  
pp. 387-397 ◽  
Author(s):  
P. H. R. Anderson ◽  
Doris M. Stone

SummaryEight explosive outbreaks of food poisoning, occurring in school canteens in England during 1953 and affecting 1190 known cases, are described. The clinical features were characteristic of the toxin type of illness. No deaths occurred.The food causing all of these outbreaks was prepared from spray-dried skim milk powder. It was not subsequently heat-treated and was usually consumed 3–4 hr. after preparation.The spray-dried milk powder proved to contain a high content of bacteria, including large numbers of Staph. aureus, of a phage pattern often associated with food poisoning. The assumption was therefore made that these outbreaks were caused by staphylococcal enterotoxin.Because the food was often consumed within 3–4 hr. of reconstitution of the milk powder—before, in fact, the staphylococci had had time to grow—it is concluded that the poisoning must have been due mainly to pre-formed toxin.Consideration is given to the opportunities for the formation of toxin in a spray-drying plant, and reasons are brought forward for believing that it is formed mainly in the balance tank where the warm milk is kept, sometimes for several hours, before passing into the final drying chamber.The processing of the milk and the precautions for preventing contamination of the finished product are discussed.


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