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Forty crossbred steers of similar birth date and fed the same growing-finishing diet were used to study adipocyte changes in six fat depots during growth from 11 to 19 mo of age. Steers were slaughtered at 2-mo intervals. Adipose tissue samples were obtained from kidney, mesenteric and brisket fat and subcutaneous, intermuscular and intramuscular fat from the 10th to 12th rib section. The osmium tetroxide fixation technique was used for determination of cell size and number. Except for three brisket fat samples, distributions of adipocyte diameters from six different fat depots were monophasic during the age range considered in this study. At 17 mo of age, the mean adipocyte diameter, in decreasing order, was: kidney fat greater than mesenteric greater than subcutaneous greater than intermuscular greater than intramuscular greater than brisket fat. Fat deposition during growth to 19 mo of age occurred mainly by hypertrophy of adipocytes. An apparent cell hyperplasia occurred in the intramuscular fat depot from 11 to 15 mo and in the brisket fat depot after 15 mo of age. Based on cellularity characteristics, evidence exists to classify intramuscular and brisket fat depots as late-developing ones. Cell number/gram of intramuscular adipose tissue was a better predictor of marbling score than was fat cell diameter.

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A study was conducted to compare catecholamine concentrations in nervous tissues of stress-susceptible (SS) and stress-resistant (SR) pigs that were physically stressed. Ten pigs were included in each group on the basis of results of halothane screening tests, blood typing analysis, and examination for serum creatine kinase (CK) activities at 6 weeks of age. The nervous tissues analyzed included the substantia nigra (SN) and the caudate nucleus (CN) which were taken from pigs as soon as possible after death and frozen in liquid nitrogen. Tissues were radioenzymatically assayed for dopamine, norepinephrine, and epinephrine concentrations. The SS pigs exhibited significantly greater (P less than 0.001) CK activity concentrations than did those SR pigs before and after physical stress. Concentrations of dopamine, norepinephrine, and epinephrine in the CN of SS pigs were significantly lower (P less than 0.05) than those in the CN of SR pigs. Similarly, the SN of SS pigs had lower dopamine, norepinephrine, and epinephrine concentrations than did the SN of SR pigs. The catecholamine deficiencies observed in the porcine stress syndrome seem to have similarities with certain human extrapyramidal diseases.

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Four freezing rates for ground beef patties were evaluated for product quality effects and microstructural changes. These rates were further evaluated for different pattie formulations involving post-rigor and pre-rigor meat. Both light microscopy (LM) and scanning electron microscopy (SEM) were utilised for microstructural comparisons. Fast freezing rates had a positive effect on pattie quality, resulting in increased juiciness, tenderness and overall acceptability. Photomicrographs showed increased ice cavity size with decreased freezing rates, which probably contributed to increased cooking shrink and tenderness changes observed. Pre-rigor patties compared very favourably with conventional post-rigor beef patties and showed no obvious structural differences.

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Samples of subcutaneous, intermuscular and mesenteric adipose tissues from beef steers were fixed with osmium tetroxide, and freed adipocytes were counted with an automatic particle counter to determine whether a lognormal distribution function would describe adipocyte size distributions more accurately than a normal distribution function. Modes and medians of size distributions generally were larger than means for adipocyte size distributions modeled with a lognormal distribution function. Normalized third and fourth moments of predicted lognormal distributions often were close to 0 and 3, respectively, which are expected values for a normally distributed population. Considerable variation was observed in the skewness of adipocyte size distributions. Both normal and lognormal models for adipocyte size distribution yielded similar means. The lognormal model yielded a greater standard deviation than the normal model for adipocyte size distributions. Smaller chi-square values were found for size distributions modeled with a lognormal than with a normal distribution function. Results suggest that a lognormal distribution function more accurately models the size distributions of bovine adipocytes.

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In vitro rates of lactate metabolism were determined in stress-susceptible (SS) and stress-resistant (SR) pigs. Three SR and three SS pigs were given 20 muCi of [U-14C] L-lactate by a single injection method and resting blood lactate kinetics were measured. Seventeen blood samples were taken during the 60 min after injection. Lactate was separated from the deproteinized plasma by silicic acid column chromatography, and specific radioactivity was determined. Kinetic characteristics were calculated from plots of specific activity versus time. Pigs met steady-state requirements during the sampling period. There were no differences in kinetic characteristics of resting SS and SR pigs. Later, a second isotope injection was given after 5 min of electrical stress. Lactate pool sizes increased similarly in both types of pigs after stress; however, SS pigs had greater plasma lactate concentrations after stress. It is concluded that SS and SR pigs respond differently to stress but have similar capacities to metabolize lactate while resting.

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Rates of fatty acid synthesis from lactate and acetate and activities of selected lipogenic and NADPH-generating enzymes were determined in subcutaneous, intermuscular and intramuscular adipose tissues of cattle that were 11-19 months of age. Fatty acid synthesis from lactate and acetate increased from 11 to 13 months of age in subcutaneous and intermuscular adipose tissues; synthesis from lactate increased until 17 months of age. In intramuscular adipose tissue, synthesis from lactate also increased until 17 months of age while that from acetate continually increased. Activities of NADPH-generating enzymes increased in all three fat depots from 11 to 13 months of age, and little change occurred thereafter. Acetyl-CoA carboxylase activity was constant over entire growth period in all depots. Activity of ATP-citrate lyase increased from 11 to 13 months of age in subcutaneous and intermuscular adipose tissues, but did not increase until 19 months of age in intramuscular adipose tissue. In all cases, activities of ATP-citrate lyase were sufficient to support synthesis from lactate; therefore, lactate conversion to fatty acids in bovine adipose tissues seems to use the citrate cleavage pathway for generation of cytosolic acetyl-CoA.

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Eight stress-susceptible and eight normal pigs were used in the first portion of the study. Urine samples were collected for 24 hr over 4 consecutive days while the pigs were kept in metabolism cages. Each 24-hr sample was assayed for epinephrine, norepinephrine and dopamine. Urinary levels of dopamine were lower (P < .01) in the stress-susceptible pigs. No significant differences in urinary epinephrine or norepinephrine were observed. The second portion of the study evaluated the catecholamines in the caudate nucleus of the brain. Six stress-susceptible and six control pigs were examined. Immediately after exsanguination, caudate nuclei were excised and frozen in liquid nitrogen. The caudate nuclei were assayed for catecholamines within 2 to 3 days of freezing. Caudate nuclei dopamine levels were lower (P < .01) in stress-susceptible pigs (5,961 ng/g) than in control pigs (10,878 ng/g). No significant differences in norepinephrine levels of the caudate nuclei were observed between the two groups.

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Eight stress-susceptible and eight normal pigs weighing 35 to 50 kg were studied to determine if caffeine administration would trigger the stress syndrome and affect blood CPK levels. The pigs were littermates of Yorkshire descent. One gram of caffeine (dissolved in 10 ml of saline-sodium benzoate solution) was infused into the pigs through a jugular catheter at a rate of 1.0 ml/min. Blood samples were collected through the catheter before caffeine administration and at specific intervals up to 8 hr after the caffeine administration for the determination of blood creatine phosphokinase levels. The pigs were sacrificed approximately 48 hr after caffeine administration, and M. longissimus pH and reflectance values were obtained 45 min and 24 hr postmortem. Caffeine administration stimulated the development of the signs associated with the porcine stress syndrome in seven of the eight pigs genetically classified as stress-susceptible, and only one control pig exhibited an early sign of the stress syndrome, muscle tremors. Blood CPK levels did not differ significantly between the normal and stress-susceptible groups until visual signs of the stress syndrome were no longer observed (approximately 45 min after caffeine administration). Stress-susceptible pigs had significantly higher blood CPK levels than controls 45 min after the initial caffeine administration. Physical stress received by the pigs during transport and the stress from being held in a new environment resulted in a greater elevation of blood CPK than did the stress administered through the caffeine infusion.

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Rates of conversion of lactate, alanine and aspartate to glucose and oxidation of each to CO2 were determined in incubated liver slices from nine stress-susceptible (SS) and seven stress-resistant (SR) Yorkshire pigs ranging in body weight from 24 to 54 kg. Pigs were screened for stress susceptibility by exposure to halothane at 7 weeks of age. Stress was minimized before slaughter, and liver samples were obtained immediately after death. Rates of lactate and aspartate conversion to glucose were not significantly different between pig types. Mean rates of lactate conversion to glucose in livers of SS and SR pigs were 637 and 413 nmoles/(100 mg X 2 hours), respectively. Mean rates of aspartate conversion to glucose were 441 and 540 nmoles/(100 mg X 2 hours) in SS and SR pigs, respectively. Alanine conversion to glucose in livers of SS pigs was slower than that in SR pigs [527 and 813 nmoles/(100 mg X 2 hours), respectively]. Rates of hepatic gluconeogenesis from lactate probably do not predispose SS pigs to the lactic acidosis observed during the porcine stress syndrome. Rates of lactate, alanine and aspartate oxidation to CO2 in livers of SS pigs were 61, 59 and 76%, respectively, of the rates observed in SR pigs. Decreased rates of substrate oxidation to CO2 may contribute to the development of the syndrome in SS pigs.

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In vitro rates of lactate conversion to glucose and oxidation to CO2 were determined in livers of stress-susceptible (SS) and stress-resistant (SR) pigs because we hypothesized that livers of SS pigs had a lower capacity than livers of SR pigs to remove lactate from blood. Stress-susceptibility was determined by reaction to halothane at 7 weeks of age. At approximately 9 weeks of age, pigs were assigned to one of three experimental diets. Pigs weighing 95 kg were slaughtered immediately after stress, and liver samples were obtained. Incorporation of lactate into glucose in liver of SS pigs was 38% of that in SR pigs. Addition of either vitamin C or vitamins C and E plus magnesium oxide and collagen extract to a corn-soy diet did not alter lactate conversion to glucose, but depressed lactate oxidation to CO2. No differences were detected in either activities of lactate dehydrogenase, HAD-malate dehydrogenase, phosphoenolpyruvate carboxykinase, fructose-1,6-diphosphatase, and glucose-6-phosphatase or concentration of glycogen in livers of SS and SR pigs. Our data indicate that livers of SS pigs possess a lower capacity to incorporate lactate into glucose and to oxidize lactate to CO2; maximal activities of enzymes measured in this study are not the cause of these differences. Reduced capacity of lactate metabolism in livers of SS pigs seems a part of the etiology of the porcine stress syndrome.

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The studies reported here were undertaken to better characterize the role of the adrenal cortex in the increased susceptibility to stress observed in porcine stress syndrome. Since adrenal hypofunction was suggested during early studies as a factor in events leading to porcine stress syndrome it was decided to produce such a state by the exogenous administration of the glucocorticoids prednisolone and fluoroprednisolone.A total of 34 pigs (weighing 90 to 100 kg) received a series of graded doses (given intramuscularly) of one or the other of the foregoing compounds and were necropsied 48, 72, and 120 hours after the last treatment. The major adrenocortical changes produced by these treatments were atrophy, an accentuation of degenerative changes which could be observed in milder form in many of the 30 control pigs examined, a marked increase in stainable lipid 120 hours after the last fluoroprednisolone treatment and, ultrastructurally, an increase in lysosome-like bodies and cellular debris ("myelin bodies").Adrenocortical atrophy is not a feature of porcine stress syndrome nor were the localized depositions of stainable lipid within the zona reticularis, described in porcine stress syndrome, found in the glucocorticoid treated pigs. Consequently, the findings reported here bear a somewhat limited resemblance to those observed in pigs affected by porcine stress syndrome and cast some doubt on whether adrenal hypofunction plays a role in the pathogenesis of the latter condition.

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