Abstract:I. Thirty-three cross-bred lambs were given reconstituted dried whole cow's milk from I week of age at different levels of intake and at different frequencies of feeding.
2.Feeding frequency had no effect on live-weight gain, N retention or total body composition.3. Lambs given two feeds daily had significantly heavier abomasums than pair-fed lambs given six feeds daily.
4.The weights of fat, protein (N x 6 2 5 ) and water in the body were closely related to empty body weight; body composition (% of empty body… Show more
“…They were then homogenized (Polytron, model PT 10, Brinkman Instruments Ltd., Rexdale, Ontario) for 30 sec in 10 ml of 2:1 chloroformmethanol and extraction of the lipid continued for 60 min at room temperature under nitrogen. After removal of the residue by filtration the extract was washed with water and the lipids isolated as previously described (19). Total lipids were fractionated by thin layer chromatography (TLC) on Adsorbosil 1 (Applied Science Labs.…”
Section: Methodsmentioning
confidence: 99%
“…Cholesteryl esters, visualized by spraying the plate with Rhodamine 6G and viewing under ultra violet light, were extracted from the gel with freshly redistilled diethyl ether. Methyl pentadecanoate was added as an internal standard, the cholesteryl esters were transesterified with boron fluoridemethanol and the resulting methyl esters purified by TLC (19). The fatty acid composition of the adrenal cholesteryl esters was determined by gas liquid chromatography using the equipment and procedures previously described (19).…”
Section: Methodsmentioning
confidence: 99%
“…Methyl pentadecanoate was added as an internal standard, the cholesteryl esters were transesterified with boron fluoridemethanol and the resulting methyl esters purified by TLC (19). The fatty acid composition of the adrenal cholesteryl esters was determined by gas liquid chromatography using the equipment and procedures previously described (19). The esters from animals fed corn or coconut oil were fractionated on a 150 x 0.2 cm column containing 15% EGSS-X on 80-100 mesh Chromosorb W (Applied Science Labs., Inc.) and operated isothermally at 180-185 C. In order to separate 18:3(n-3) from 20:1 (n-9) and bSelectivity Index = decrease in concentration of ester expressed as per cent of decrease in total ester divided by mole per cent of ester in control (17).…”
Male rats were maintained on diets containing corn oil or hydrogenated coconut oil. The compositions of the adrenal cholesteryl esters were determined in control animals and in those subjected to cold stress (4 C for 30 min). Total sterol ester content was lower in the stressed rats. In those receiving corn oil there were selective decreases in 16∶1, 18∶2 and 20∶4(n−6) esters but not in 22∶4(n−6). In the coconut oil fed, essential fatty acid (EFA) deficient animals, the decreases in 20∶4(n−6) and 22∶4(n−6) were quite selective, but the concentrations of the cholesteryl esters of 20∶3(n−9) and 22∶3(n−9) were also selectively reduced in the stressed animals. Olive oil and corn oilethyl erucate were employed as dietary fats in a second experiment. Plasma corticosterone was lower in animal fed ethyl erucate and subjected to cold stress. Cholesteryl erucate was the major adrenal ester in animals receiving dietary erucate but it was not well utilized in animals subjected to stress. The cholesteryl esters of linoleate and arachidonate were preferentially utilized in both of these dietary groups. Cholesteryl arachidonate was selectively utilized in all four dietary groups studied and may constitute the preferred substrate for rat adrenal cholesteryl ester hydrolase.
“…They were then homogenized (Polytron, model PT 10, Brinkman Instruments Ltd., Rexdale, Ontario) for 30 sec in 10 ml of 2:1 chloroformmethanol and extraction of the lipid continued for 60 min at room temperature under nitrogen. After removal of the residue by filtration the extract was washed with water and the lipids isolated as previously described (19). Total lipids were fractionated by thin layer chromatography (TLC) on Adsorbosil 1 (Applied Science Labs.…”
Section: Methodsmentioning
confidence: 99%
“…Cholesteryl esters, visualized by spraying the plate with Rhodamine 6G and viewing under ultra violet light, were extracted from the gel with freshly redistilled diethyl ether. Methyl pentadecanoate was added as an internal standard, the cholesteryl esters were transesterified with boron fluoridemethanol and the resulting methyl esters purified by TLC (19). The fatty acid composition of the adrenal cholesteryl esters was determined by gas liquid chromatography using the equipment and procedures previously described (19).…”
Section: Methodsmentioning
confidence: 99%
“…Methyl pentadecanoate was added as an internal standard, the cholesteryl esters were transesterified with boron fluoridemethanol and the resulting methyl esters purified by TLC (19). The fatty acid composition of the adrenal cholesteryl esters was determined by gas liquid chromatography using the equipment and procedures previously described (19). The esters from animals fed corn or coconut oil were fractionated on a 150 x 0.2 cm column containing 15% EGSS-X on 80-100 mesh Chromosorb W (Applied Science Labs., Inc.) and operated isothermally at 180-185 C. In order to separate 18:3(n-3) from 20:1 (n-9) and bSelectivity Index = decrease in concentration of ester expressed as per cent of decrease in total ester divided by mole per cent of ester in control (17).…”
Male rats were maintained on diets containing corn oil or hydrogenated coconut oil. The compositions of the adrenal cholesteryl esters were determined in control animals and in those subjected to cold stress (4 C for 30 min). Total sterol ester content was lower in the stressed rats. In those receiving corn oil there were selective decreases in 16∶1, 18∶2 and 20∶4(n−6) esters but not in 22∶4(n−6). In the coconut oil fed, essential fatty acid (EFA) deficient animals, the decreases in 20∶4(n−6) and 22∶4(n−6) were quite selective, but the concentrations of the cholesteryl esters of 20∶3(n−9) and 22∶3(n−9) were also selectively reduced in the stressed animals. Olive oil and corn oilethyl erucate were employed as dietary fats in a second experiment. Plasma corticosterone was lower in animal fed ethyl erucate and subjected to cold stress. Cholesteryl erucate was the major adrenal ester in animals receiving dietary erucate but it was not well utilized in animals subjected to stress. The cholesteryl esters of linoleate and arachidonate were preferentially utilized in both of these dietary groups. Cholesteryl arachidonate was selectively utilized in all four dietary groups studied and may constitute the preferred substrate for rat adrenal cholesteryl ester hydrolase.
“…(Faichney & Colebrook, 1979). The wethers were fitted with harnesses and faecal collecting apparatuses of the type described by Walker & Faichney (1964).…”
Two merino ewes were fed 800 and then 1000 g of lucerne chaff per day and renal responses and extracellular fluid volume (E.C.F.) were determined. Urine urea nitrogen, glomerular filtration rate (G.F.R.), urine volume, effective renal plasma flow (E.R.P.F.) and E.C.F. increased in both animals with the greater nitrogen intake. In a second experiment, five merino wethers and four merino ewes were infused intraruminally with increasing quantities of urea, whilst being fed a mainly roughage ration, and the above parameters were determined. No significant changes in G.F.R., E.R.P.F. or E.C.F. were noted. Urinary excretion maintained a linear response to nitrogen input until 20·6 g of urea nitrogen per day were infused. At this level of infusion, an increased fractional reabsorption of urea resulted in a large increase in plasma urea concentration, but when 500 mmol of NaCl or KCl were added to the infusate, urine urea nitrogen excretion increased from 10·4 to 11·4 and 11·9 g/d respectively and plasma urea concentration decreased from 68·0 to 35·2 and 37·3 mg nitrogen/100 ml. Urea clearance virtually trebled with both electrolyte infusions and E.C.F. and G.F.R. increased by aproximately 10 and 25% respectively. It is concluded that urea alone has limited diuretic ability and that the increased electrolyte content of higher protein dry roughage diets aids urine urea excretion by increasing G.F.R., and the urine flow rate by an osmotic diuretic effect.
“…A three-day administration of EFA was chosen to test whether short-term rectal administration of linoleic acidrich MG is feasible and effective, and because changes in the fatty acid composition of liver lipids of EFAdeficient rats were already apparent within 24 hr after linoleic acid administration (23). Full recovery including restoration of 20:4oJ6 to normal values would have taken much longer (24). The amount of linoleic acid administered represents about 0.32% of the calories, and the 7-wk-old EFA-deficient rats consumed about 11 g of fat-free diet per day.…”
The potential of the rectal route for administration of essential fatty acids (EFA) as monoglyceride (MG) was investigated. EFA-deficient rats were supplemented with 14 mg linoleic acid/day for 3 days. Supplementation was either by oral administration as corn oil, orally as corn oil-derived MG or rectally as MG. The patterns of polyunsaturated fatty acids (PUFA) in liver and serum lipids, characteristic of EFA deficiency, were altered in the direction of normalcy in similar magnitude by all modes of supplementation, indicating that the rectal route may be useful for administration of EFA. The amounts of phospholipids (PL) and free fatty acids (FFA) in liver changed by all modes of administration. The magnitude of change of total PL and of FFA in liver depended upon the chemical form in which linoleic acid was administered and the route of administration, indicating that these factors affect lipid metabolism.
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