scholarly journals Age, sex, and weight at weaning influence organ weight and gastrointestinal development of weanling pigs

2003 ◽  
Vol 54 (5) ◽  
pp. 515 ◽  
Author(s):  
J. R. Pluske ◽  
D. K. Kerton ◽  
P. D. Cranwell ◽  
R. G. Campbell ◽  
B. P. Mullan ◽  
...  
Keyword(s):  
Specific Activity ◽  
Cellular Growth ◽  
Weanling Pigs ◽  
Large White ◽  
Organ Weights ◽  
Weaning Age ◽  
Villous Height ◽  
Specific Activities ◽  
Ad Libitum

The present study was designed to determine the interrelationships between sex, weaning age, and weaning weight on aspects of physiological and gastrointestinal development in pigs. Forty-eight Large White × Landrace pigs were used in a factorial arrangement with the respective factors being: age at weaning (14 or 28 days), weight at weaning (heavy or light), sex (boar or gilt), and time after weaning (1, 7, and 14 days). At weaning, 48 pigs were removed from the sow: 16 pigs were then fasted for 24 h before euthanasia for determination of organ weights, gut histology, and enzymology, and 32 pigs were offered a high quality pelleted weaner diet ad libitum for subsequent assessment of organ weights, histology, and enzymology at 7 and 14 d after weaning. On Day 6 and 13 after weaning, 2 pigs from each group had their feed removed, and 24 h later were euthanased and similar measurements were taken. In general, the data highlighted the overall gastrointestinal underdevelopment of pigs weaned at 2 weeks of age and of pigs weaned light-for-age at either 2 or 4 weeks. Heavier body organs, gastrointestinal organs, and accessory digestive organs observed after weaning, except for the spleen, presumably reflected the increase in substrates available for cellular growth as feed intake increased after weaning, and the development of organs required to process this feed. Interestingly, the relative weights (% of liveweight) of the stomach and small intestine and, to a lesser extent, the caecum and colon, were greater in the light, 14-day-old weaned pigs, but these differences diminished with increasing time after weaning. Consistent effects due to age, weight, and sex were not observed for villous height and crypt depth, or for the specific activities of the brush-border and pancreatic enzymes measured. However, increases (P < 0.001) in the activities of maltase (P�<�0.001), glucoamylase (P < 0.001), and sucrase (P = 0.020) (all expressed per gram of mucosa), and that of trypsin (per gram of pancreas), occurred by 14 days after weaning. This most likely reflected the inducible nature of these enzymes in response to the increasing intake of substrates provided in the diet. In contrast, the specific activity of lactase declined (P = 0.012) in the first 14 days after weaning. These data suggest that pigs weaned at 2 weeks of age and pigs weaned light-for-age at either 2 or 4 weeks have a less developed gastrointestinal tract, and that its development after weaning might proceed differently to that of pigs weaned older and heavier.

Lifetime and post-weaning determinants of performance indices of pigs

2003 ◽  
Vol 54 (4) ◽  
pp. 363 ◽  
Author(s):  
F. R. Dunshea ◽  
D. K. Kerton ◽  
P. D. Cranwell ◽  
R. G. Campbell ◽  
B. P. Mullan ◽  
...  
Keyword(s):  
Growth Rate ◽  
Treatment Group ◽  
Performance Indices ◽  
Subsequent Growth ◽  
High Quality ◽  
Large White ◽  
Weaning Age ◽  
Available Lysine ◽  
Ad Libitum

The present study was designed to determine the interrelationships between sex, weaning age, and weaning weight on subsequent growth performance. Ninety-six Large White × Landrace pigs were used in a 2 × 2 × 2 factorial experiment with the respective factors being: age at weaning (14 or 28 days), weight at weaning (heavy or light), and sex (boar or gilt). Eighty pigs were offered a high quality pelleted weaner diet ad libitum while the remaining 16 pigs (2 pigs from each treatment group) were removed from the sow and fasted for 24 h before being euthanased for determination of gut histology and enzymology. The remaining pigs were weaned into individual pens and given an ad libitum diet containing 15.5 MJ DE/kg and 0.95 g available lysine/MJ DE. On Day 6 and 13 after weaning, 2 pigs from each group at each time had their feed removed and, 24 h later, were euthanased. From 3 weeks post-weaning, the remaining pigs were group-penned with contemporary pigs and fed commercial rations until slaughter at 23 weeks of age. In the first week after weaning, the heavy pigs and those weaned at 28 days ate more feed and grew faster, and gilts ate more and grew faster than boars over the same time. Pigs that were heavier at weaning were also heavier at every subsequent age. At slaughter, heavy boars weighed more than heavy gilts (110.5 v. 103.7 kg, P = 0.027), whereas this was not the case for light boars and gilts (94.1 v. 94.4 kg, P = 0.96). Whereas there were no effects of sex or weight at weaning on P2 backfat depth, pigs weaned at 14 days had more backfat at 23 weeks than pigs weaned at 28 days (13.1 v. 10.9 mm, P = 0.009). In conclusion, these data clearly indicate that the greatest determinants of immediate post-weaning performance under the present conditions were the age and weight of the pigs at weaning. However, the key determinant of lifetime growth rate appeared to be weight of pigs at weaning or, by inference, birth. Although age at weaning had no effect on lifetime growth rate, early-weaned pigs were fatter at slaughter.

Prediction of the phosphorus content of herbage consumed by grazing cattle

1977 ◽  
Vol 88 (3) ◽  
pp. 533-538 ◽  
Author(s):  
D. A. Little ◽  
R. W. McLean ◽  
W. H. Winter
Keyword(s):  
Intravenous Infusion ◽  
Phosphorus Content ◽  
Specific Activity ◽  
Accurate Prediction ◽  
Degree Of Reduction ◽  
Grazing Cattle ◽  
Specific Activities ◽  
Highly Correlated

SUMMARYThe determination of feed phosphorus content using oesophageally fistulated cattle is reported in this paper, from an experiment in which salivary phosphorus was labelled with 32P.An intravenous infusion of Na232PO4 to cattle produced an immediate increase in the specific activity of salivary phosphorus, which then fell rapidly to an essentially linear asymptote by 3 h after the infusion. The phosphorus content of consumed feed was calculated from the degree of reduction in salivary specific activity by the feed phosphorus, expressed as the ratio of the specific activities of bolus and saliva phosphorus.A dose of 100 /μCi 32P allowed the accurate prediction of phosphorus content ranging from 0·07 to 0·25% in various feeds, at intervals from 3 to 24 h after the infusion; the predicted and actual phosphorus concentrations were highly correlated (r = 0·95). Similar observations for feeds ranging from 0·14 to 0·25% phosphorus suggested that accurate prediction was also possible 144 h after infusion. Comparison of estimated feed phosphorus content of grazed material with that measured in hand-plucked herbage indicated that this approach is applicable to grazing studies.

scholarly journals Dual-digitonin-pulse perfusion. Concurrent sampling of periportal and perivenous cytosol of rat liver for determination of metabolites and enzyme activities

1987 ◽  
Vol 243 (1) ◽  
pp. 87-95 ◽  
Author(s):  
B Quistorff ◽  
N Grunnet
Keyword(s):  
Lactate Dehydrogenase ◽  
Glutamine Synthetase ◽  
Rat Liver ◽  
High Purity ◽  
Alanine Aminotransferase ◽  
Specific Activity ◽  
Perfusion Technique ◽  
Short Intervals ◽  
Specific Activities

A previously described digitonin-perfusion technique [Quistorff, Grunnet & Cornell (1985) Biochem. J. 226, 289-297], by which intracellular material of rat liver could be liberated, has been refined, now allowing release of cytosol of high purity from both periportal and perivenous parts of the same liver. The cytosolic fractions are obtained by perfusing the liver for short intervals (10-20 s) with digitonin (4-5 mg/ml), first in the normal perfusion direction and then, after an interval of 1-2 min, in the retrograde direction, the eluate being collected during and after both intervals. The technique is termed ‘dual-digitonin-pulse perfusion’. The eluate fractions showed a peak specific activity of the cytosolic enzymes alanine aminotransferase (ALAT), lactate dehydrogenase (LDH) and pyruvate kinase (PK) of 3-5-fold higher than obtained in a biopsy from the same liver. For glutamine synthetase (GS) a 10-fold higher specific activity was obtained. Zonation, defined as the ratio of the specific activities in periportal and perivenous eluates, of ALAT, LDH and PK was 10, 1.7 and 0.70 respectively. Zonation of GS was less than 0.01. These factors may be modified by a slight zonation of cytosolic protein of 1.2-1.3. Peak concentrations in the eluate of ATP, ADP, Pi, NAD+ and glycerol 3-phosphate were 32.5 +/- 11.4, 19.9 +/- 4.3, 71.9 +/- 25.4, 2.41 +/- 0.83 and 6.84 +/- 2.74 nmol/mg of protein for periportal eluates. There was no difference between periportal and perivenous eluates except for glycerol 3-phosphate, which was significantly higher in perivenous eluates, 12.8 +/- 4.5 nmol/mg of protein.

Use of 14CO2 in estimating rates of hepatic gluconeogenesis

1992 ◽  
Vol 263 (1) ◽  
pp. E36-E41 ◽  
Author(s):  
E. Esenmo ◽  
V. Chandramouli ◽  
W. C. Schumann ◽  
K. Kumaran ◽  
J. Wahren ◽  
...  
Keyword(s):  
Blood Glucose ◽  
Specific Activity ◽  
Tricarboxylic Acid Cycle ◽  
Tricarboxylic Acid ◽  
Hepatic Gluconeogenesis ◽  
Acid Cycle ◽  
Specific Activities ◽  
Glucose Formation

Estimating the rate of hepatic gluconeogenesis in vivo from the incorporation of 14C from 14CO2 into glucose requires determination of the rates in liver of equilibration of oxaloacetate with fumarate, conversion of oxaloacetate to phosphoenolpyruvate (PEP), and conversion of PEP to pyruvate, all relative to the rate of tricarboxylic acid cycle flux. With the use of a model of mitochondrial metabolism and gluconeogenesis, expressions are derived relating specific activity of carboxyl of PEP from 14CO2 to those rates and specific activity of mitochondrial CO2. If those rates and specific activity of mitochondrial CO2 are known, specific activity of PEP, calculated using the expressions, should, on a mole basis, be one-half the specific activity of the glucose formed. At steady state, in the 60-h fasted individual, where glucose formation is solely by gluconeogenesis, twice estimated specific activity of PEP should then approximate that of blood glucose. Estimates of relative rates in 60-h fasted humans, previously made from distribution of 14C in glutamate from phenylacetylglutamine excreted when [3-14C]lactate and phenylacetate were given, were applied to the expressions. Specific activity of mitochondrial CO2 was equated to that of CO2 expired by 60-h fasted subjects given NaH14CO3 and alpha-[1-14C]ketoisocaproate. Predicted specific activities approximated actual specific activities of blood glucose when NaH14CO3 was administered. alpha-[1-14C]ketoisocaproate administrations gave underestimates. This is attributable to differences between specific activities of hepatic mitochondrial CO2 and expired CO2, which is evidenced by higher incorporations of 14C in glucose than in expired CO2 from alpha-[1-14C]ketoisocaproate than from NaH14CO3.(ABSTRACT TRUNCATED AT 250 WORDS

Collagen metabolism of rats in various hormonal and dietary conditions

1961 ◽  
Vol 200 (6) ◽  
pp. 1330-1334 ◽  
Author(s):  
Q. T. Smith ◽  
W. D. Armstrong
Keyword(s):  
Specific Activity ◽  
Male Rats ◽  
Total Collagen ◽  
Complete Diet ◽  
Parathyroid Extract ◽  
Specific Activities ◽  
Tail Tendon ◽  
Free Plasma ◽  
Tendon Collagen

Injections of glycine-2-C14 into male rats were followed by determination of specific activity of femur and tail tendon collagen glycine and free plasma glycine. Hydroxyproline contents of bones were used to calculate total collagen glycine radioactivities. Although part of the femur collagen was relatively metabolically stable, a slow replacement appeared to take place. Specific activities of tail tendon collagen glycine, in contrast to femur collagen glycine, increased from 3 to 7 days after isotope administration. This difference appeared to be related to specific activities of free plasma glycine. Animals on an inadequate diet presented a different pattern of isotope content than animals on a complete diet. Results with hypophysectomized animals indicated turnover of femur collagen. Hypophysectomy resulted in a differential effect on femur and tail tendon collagen. Parathyroid-extract treatment increased the total collagen content of femurs. During certain experimental periods, specific activities of femur and tail tendon collagen glycine of parathyroid-treated animals approached the specific activity of free plasma glycine more rapidly than normal animals.

An International Collaborative Study to Investigate Standardisation of Hirudin Potency

1993 ◽  
Vol 69 (05) ◽  
pp. 430-435 ◽  
Author(s):  
Colin Longstaff ◽  
Man-Yu Wong ◽  
Patrick J Gaffney
Keyword(s):  
Specific Activity ◽  
Collaborative Study ◽  
Residual Activity ◽  
Quality Standard ◽  
Upper Limit ◽  
Assay Procedure ◽  
Specific Activities ◽  
International Collaborative ◽  
Range Of Values ◽  
International Collaborative Study

SummaryAn international collaborative study has been carried out to investigate the reproducibility of hirudin assays in 13 laboratories using four recombinant hirudins and one natural, sulphated product. A simple assay procedure was proposed involving the titration of α-thrombin with inhibitor and measurement of residual activity using a chromogenic substrate. A standard α-thrombin preparation was supplied to ensure that this reagent was of uniform quality throughout the study. The method appeared to present no difficulties and laboratories reported similar potencies for the 5 hirudin samples, in line with expected values. This gave 200–222 Thrombin Inhibitory Units/ampoule (TIU/ampoule) of lyophilised hirudin, with geometric coefficient of variation (gcv) values ranging from 10.15–15.97%. This corresponds to specific activities of approximately 14,300–15,900 TIU/mg protein. This is close to the upper limit of previously reported values of specific activity. We conclude that the precision of this determination compared with the wider range of values in the literature (8,000–16,000 thrombin inhibitory units [TIU]/mg) results from the use of good quality standard α-thrombin by all laboratories. This study has important implications for hirudin standardisation.

An Enzyme Linked Immunosorbent Assay for Determination of Tissue Plasminogen Activator Applied to Patients with Thromboembolic Disease

1983 ◽  
Vol 50 (03) ◽  
pp. 740-744 ◽  
Author(s):  
Nils Bergsdorf ◽  
Torbjörn Nilsson ◽  
Per Wallén
Keyword(s):  
Plasminogen Activator ◽  
Tissue Plasminogen Activator ◽  
Specific Activity ◽  
Thromboembolic Disease ◽  
Tissue Type ◽  
Enzyme Linked Immunosorbent Assay ◽  
Type Plasminogen Activator ◽  
Tissue Plasminogen ◽  
Normal Human

SummaryUtilizing the immunoglobulin fraction from a goat antiserum against human uterine tissue plasminogen activator, an enzyme- linked immunoassay for tissue-type plasminogen activator in human plasma has been developed. With the new method, the concentration of t-PA in normal human acidified plasma is found to be 4.0 ± 1.8 (SD) ng/ml. It increases to 12 ng/ml after a tomiquet test, and to 14 ng/ml after strenous physical exercise. In a group of patients with idiopathic thromboembolic disease, the resting t-PA concentration was 5 ng/ml and the post-occlusion value 16 ng/ml. Furthermore, the patients also exhibited a normal post-occlusion rise in the concentration of plasmin-α2-antiplasmin complex. However, in 37% of the post-occlusion patient plasmas, virtually no increase in t-PA could be detected by a specific activity assay. The results indicate that the reason for a defective post-occlusion fibrinolytic activity in a majority of cases may be the presence of increased concentrations of a fast-acting specific t-PA inhibitor.

Determination of Specific Activity of Cholera Chemical Vaccine Components using Cell Culture

2020 ◽  
Vol 36 (3) ◽  
pp. 82-89
Author(s):  
O.V. Gromova ◽  
O.S. Durakova ◽  
S.V. Generalov ◽  
L.F. Livanova ◽  
O.A. Volokh
Keyword(s):  
Cell Culture ◽  
Vibrio Cholerae ◽  
Production Control ◽  
Specific Activity ◽  
Methodological Approach ◽  
Toxin Production ◽  
Submerged Cultivation ◽  
Vaccine Production ◽  
Antigenic Activity

Том 36(2020) №3 стр. 82-89; DOI 10.21519/0234-2758-2020-36-3-82-89А.В. Гаева1*, О.В. Громова1, О.С. Дуракова1, С.В. Генералов1, Л.Ф. Ливанова1, О.А. Волох1 Определение специфической активности компонентов холерной химической вакцины с использованием культуры клеток 1ФКУЗ «Российский научно-исследовательский противочумный институт «Микроб»» Федеральной службы по надзору в сфере защиты прав потребителей и благополучия человека, Саратов 410005 *[email protected] Поступила - 2019-11-26; После доработки - 2020-03-16; Принята к публикации - 2020-05-15 Список литературы Описаны методы определения динамики продукции токсинов штаммом Vibrio cholerae 569B при глубинном культивировании в биореакторе и антигенной активности специфической фракции холерогена-анатоксина по анатоксинсвязыванию с использованием клеточных культур. Показана высокая степень соответствия результатов, полученных методами, применяемыми для контроля этапов производства холерной химической вакцины и рассмотренными в данной работе. Отмечено, что применение клеточной линии СНО-К1 наиболее перспективно для замены биомоделей на промежуточных этапах контроля активных компонентов холерной химической вакцины. Разработанный методический подход впервые предлагается использовать на этапах производства холерной бивалентной химической вакцины. культура клеток, Vibrio cholerae, холерная химическая вакцина, контроль производства, холера. Vol 36(2020) N 3 p. 82-89; DOI 10.21519/0234-2758-2020-36-3-82-89A.V. Gaeva1*, O.V. Gromova1, O.S. Durakova1, S.V. Generalov1, L.F. Livanova1, O.A. Volokh1 Determination of Specific Activity of Cholera Chemical Vaccine Components using Cell Culture 1Russian Research Anti-Plague Institute «Microbe» of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing, Saratov, 410005 *[email protected] Received - 26.11.2019; Accepted - 15.05.2020 References The methods has been described to determine the dynamics of toxin production by the Vibrio cholerae 569B strain during submerged cultivation in bioreactor and of the antigenic activity of specific choleragen anatoxin fraction by anatoxin binding levels using cell cultures. High degree of consistency was observed between the results obtained via the method under consideration and those obtained via control methods at different stages of cholera chemical vaccine production. It was shown that the CHO-K1 cell line is the most promising substitute for biomodels at the intermediate stages of control of active cholera chemical vaccine components. The developed methodological approach was first proposed for use at the stages of cholera chemical bivalent vaccine manufacturing. cell culture, Vibrio cholerae, cholera chemical vaccine, production control, cholera.

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