Effect of exercise and pre-slaughter stress on pork muscle characteristics

The effects of exercise, stress and chill temperature on pork muscle characteristics were studied in a 3 × 2 × 2 factorial experiment in which treatments were assigned to blocks made up of six pigs of the same sex from the same litter. Pigs were fed a corn-soybean meal diet with the two littermate pigs on each treatment fed together. Treatments were (1) a control group receiving no exercise and fed in an 8 m(2) pen; (2) a treatment group fed in an 8 m(2) pen and driven 1·6 km/day for 100 days prior to slaughter; and (3) a treatment group fed in pens with 40 m(2) floor space with feeders placed 5 m from their waterers. When the animals averaged approximately 105 kg in weight, one animal from each pair treated alike was subjected to standardized stress. After slaughter, one side was chilled at 2-3°C and the other at 13-15°C for 24 h. Both sides were then chilled at 2-3°C for an additional 24 h. Exercise did not affect average daily gain (ADG), feed efficiency, yield of total wholesale cuts, muscle pH, protein solubility, fiber diameter and sarcomere length of the Longissimus dorsi (LD) and Quadriceps femoris (QF) muscles or the tenderness of the QF muscle. Exercise decreased backfat thickness and the subjective tenderness of the LD muscle. The effects of stress on the characteristics evaluated were consistent with those that have been previously reported. Chilling temperature and interactions involving chilling temperature did not affect any of the characteristics studied. No exercise × stress interactions were observed. Protein solubility values indicated that pale, soft exudative (PSE) muscle was not a factor in any of the treatments. It was concluded that exercise will produce leaner carcasses but less tender muscle and that exercise will not counteract the effects of pre-slaughter stress.     

Transillumination of the skull in premature infants

Transillumination of the skull in infants is a simple technique which can be used to detect several major abnormalities of the central nervous system. The usefulness of transillumination has been limited, however, by the lack of standard techniques for its performance and by the absence of normal values, especially in premature infants. In healthy premature infants, there is a progressive increase in transillumination with increasing gestational age over three sites--the anterior fontanelle, the frontotemporal fossa, and the parieto-occipital eminence.     

Metabolites of phencyclidine

The results of the animal experiment demonstrate that oxidative hydroxylation is the major mode of metabolism of phencyclidine. It is evident that this process takes place in all three rings of the molecule. Hydroxylation of the piperidyl moiety probably also accounts for the formation of the N-dealkylated metabolites. Metabolism of phencyclidine in humans appears, at least in part, to be similar to that in the rat. Hydroxylation is still the principal mode in the case of humans though of a lesser extent. Metabolites hydroxylated in the phenyl moiety as well as dihydroxy derivatives of phencyclidine have so far not been observed in humans. Furthermore, most of the monohydroxy metabolites exist as conjugates in the human urine. It should also be pointed out that no metabolites have yet been detected in human blood samples.     

Malignant tumors of the pleura in the post-pneumothoracic cavities

The single nephron glomerular filtration rate (SNGFR) was determined in superficial (S) and juxtamedullary (JM) nephrons of 10 anesthetized rabbits by the 14C ferrocyanide infusion technique. The length of the proximal tubules and the volume of the glomeruli were also determined for the same nephrons. SNGFR was higher in JM than in S: 28.6 +/- 3.4 versus 22.6 +/- 3.0 nl/min, P less than 0.001. In JM nephrons, glomeruli were larger than in S: 1.3 +/- 0.1 versus 0.9 +/- 0.1 nl, P less than 0.001, whereas there was no difference between proximal tubule length in either category (s, 8.7 +/- 0.3 and JM, 8.9 +/- 0.5 mm). In 6 out of 8 animals, SNGFR was significantly correlated to glomerular volume. Lack of correlation was observed between SNGFR and length of proximal tubule in all animals but one. These results show that the rabbit, as well as small rodents and the dog, has a higher SNGFR in juxtamedullary than superficial glomeruli. Although this functional difference is not related to the length of the proximal tubule in each individual animal, the ratio between the mean SNGFR value and the mean length of the proximal tubule in superficial rabbit nephrons is similar to the ratio found in other species.     

Influence of dietary inclusion level of manganese on pork quality during retail display

Boneless pork loins (n = 112) were used to test the influence of dietary manganese (Mn) inclusion level on pork quality traits during retail display. Crossbred barrows and gilts were fed diets formulated with 0, 20, 40, 80, 160, or 320 ppm Mn from Availa^®Mn (AvMn; a Mn–amino acid complex) from 23.8 to 106.8 kg live weight. At approximately 48 h postmortem, boneless pork loins were fabricated into longissimus thoracis et lumborum (LM) chops, which were subsequently placed in open-topped, coffin-chest display cases (2.6 °C) under continuous warm-white, fluorescent lighting (1600 lx) for 7 days. Dietary Mn level had no effect on LM pH (P = 0.47), purge volume (P = 0.60) and loss (P = 0.53), or moisture loss (P = 0.95) during retail display. Chops from pigs fed 80 ppm Mn received higher (P < 0.05) American and Japanese color scores than pigs fed 0 and 40 ppm Mn. Even though the LM from pigs fed 80, 160, and 320 ppm Mn tended to be darker (lower L^* values; P = 0.07) than chops from pigs fed 40 ppm Mn, a^* (redness) and b^* (yellowness) values, as well as hue angle and chroma, were not (P  0.19) affected by dietary Mn. On days 0 and 1, the reflectance ratio of 630 nm/580 nm was similar (P > 0.05) among dietary Mn supplementation levels; yet, by day 4 of retail display, chops from pigs fed 80 ppm Mn had higher (P < 0.05) reflectance ratios than chops from pigs fed 0, 20, 40, and 160 ppm, whereas LM chops from pigs fed 40 ppm Mn had lower (P < 0.05) reflectance ratios than all other dietary treatments on day 7 (Mn supplementation level × display day; P = 0.04). Although TBARS were greater (P < 0.001) on day 7 than 0 of retail display, TBARS values did not (P = 0.43) differ among dietary Mn levels. Results indicate that supplementing swine diets with 80 ppm Mn may improve pork color during retail display without increasing the likelihood of lipid oxidation.     

Comparison of different magnesium sources on lamb muscle quality

Wether lambs (n=20) were used to compare the effect of dietary magnesium oxide (MgO), unweathered Magnesium Mica® (UMM) and weathered Magnesium Mica® (WMM) on muscle quality. Lambs were fed a corn-based, control diet (Ctrl), or the Ctrl supplemented with either MgO, UMM, or WMM for 95 days before harvest. Following a 24-h chill, carcasses were fabricated, and L*, a* and b* values were determined on the triceps brachii (TB), longissimus thoracis (LT), semimembranosus (SM), and semitendinosus (ST) muscles. Supplemental magnesium had no (P > 0.10) effect on live and carcass weights, fat thickness, loin eye area, and USDA yield grade. Carcasses from lambs supplemented with MgO had higher (P < 0.10) flank streaking scores and USDA quality grades than those from lambs fed diets containing UMM. Although magnesium-supplementation had no (P > 0.10) effect on marbling scores, the LT from Ctrl-fed lambs had more (P < 0.05) intramuscular lipid than lambs fed diets containing UMM or WMM. Lambs supplemented with UMM had greater (P < 0.05) LT shear force values than lambs fed MgO or WMM. Magnesium-supplementation had no (P > 0.10) effect on muscle color; however, supplementing finishing diets with UMM may result in less palatable lamb.     

Disruption of cellular translational control by a viral truncated eukaryotic translation initiation factor 2alpha kinase homolog

Phosphorylation of eukaryotic translation initiation factor 2alpha (eIF2alpha) is a common cellular mechanism to limit protein synthesis in stress conditions. Baculovirus PK2, which resembles the C-terminal half of a protein kinase domain, was found to inhibit both human and yeast eIF2alpha kinases. Insect cells infected with wild-type, but not pk2-deleted, baculovirus exhibited reduced eIF2alpha phosphorylation and increased translational activity. The negative regulatory effect of human protein kinase RNA-regulated (PKR), an eIF2alpha kinase, on virus production was counteracted by PK2, indicating that baculoviruses have evolved a unique strategy for disrupting a host stress response. PK2 was found in complex with PKR and blocked kinase autophosphorylation in vivo, suggesting a mechanism of kinase inhibition mediated by interaction between truncated and intact kinase domains.     

Selective reduction of GluR2 protein in adult hippocampal CA3 neurons following status epilepticus but prior to cell loss

Kainic acid (KA) induces status epilepticus and delayed neurodegeneration of CA3 hippocampal neurons. Downregulation of glutamate receptor 2 (GluR2) subunit mRNA [the alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) subunit that limits Ca2+ permeability] is thought to a play role in this neurodegeneration, possibly by increased formation of Ca2+ permeable AMPA receptors. The present study examined early hippocampal decreases in GluR2 mRNA and protein following kainate-induced status epilepticus and correlated expression changes with the appearance of dead or dying cells by several histological procedures. At 12 h, in situ hybridization followed by emulsion dipping showed nonuniform decreases in GluR2 mRNA hybridization grains overlying morphologically healthy-appearing CA3 neurons. GluR1 and N-methyl-D-aspartate receptor mRNAs were unchanged. At 12-16 h, when little argyrophilia or cells with some features of apoptosis were detected by silver impregnation or electron microscopy, single immunohistochemistry with GluR2 and GluR2/3 subunit-specific antibodies demonstrated a pattern of decreased GluR2 receptor protein within CA3 neurons that appeared to predict a pattern of damage, similar to the mRNA observations. Double immunolabeling showed that GluR2 immunofluorescence was depleted and that GluR1 immunofluorescence was sustained in clusters of the same CA3 neurons. Quantitation of Western blots showed increased GluR1:GluR2 ratios in CA3 but not in CA1 or dentate gyrus subfields. Findings indicate that the GluR1:GluR2 protein ratio is increased in a population of CA3 neurons prior to significant cell loss. Data are consistent with the "GluR2 hypothesis" that reduced expression of GluR2 subunits will increase formation of AMPA receptors permeable to Ca2+ and predict vulnerability to a particular subset of pyramidal neurons following status epilepticus.