Evaluation of L-selectin expression and assessment of protein tyrosine phosphorylation in bovine polymorphonuclear neutrophil leukocytes around parturition

Impaired polymorphonuclear neutrophil leukocyte (PMN) function around parturition has been associated with increased clinical mastitis in dairy cows. Rolling and attachment of PMN to the endothelium is the first step in the recruitment process and is accomplished by interaction between L-selectin on PMN and its ligand on endothelial cells. Furthermore, tyrosine phosphorylation is involved in the initiation of many PMN functions. The objective of this work was to determine changes in expression of L-selectin and tyrosine phosphorylation in the perinatal period. Eight clinically healthy Holstein cows were used as PMN donors at d-21, -14, -7,0 (calving), +1, +2, +7, +14, +28. Evaluation of L-selectin expression was carried out on activated and resting PMN. Anti-bovine L-selectin monoclonal antibody (MAB) and flow cytometric analysis were used to measure the percentage of PMN fluorescing and receptor expression (log mean fluorescent channel, LMFC). Activated and resting PMN showed similar trends in % PMN fluorescence and LM FC. The percentage of PMN fluorescing tended to decrease at parturition, followed by a significant increase at d +14 and +28 (P < 0.02). For LMFC a decrease was observed on d +1 followed by an increase through d +28 (P < 0.01). Protein tyrosine phosphorylation of lysates prepared from PMN isolated throughout the study was detected by electrophoresis and western blotting using anti-phosphotyrosine MAB. Several protein bands were tyrosine phosphorylated. Two of these bands (42-44 kDa and 90 kDa) varied in intensity over time. The intensity of the 42-44 kDa band gradually increased from d -7, peaked at d +7 (P < 0.03), and steadily decreased to d +28 (P < 0.02). Antibody to activated mitogen protein kinase reacted with the 42-44 kDa band. Reduced PMN function during the periparturient period could be related to reduced L-selectin adhesion molecules on the cell surface, and to modulation in the phosphorylation of functionally important molecules.     

Influence of lidocaine and diazepam on peri-induction intraocular pressures in dogs anesthetized with propofol–atracurium

The purpose of this study was to evaluate the effects on the intraocular pressure (IOP) of lidocaine or diazepam administered intravenously (IV) before induction of anesthesia with propofol-atracurium and orotracheal intubation in normal dogs, as well as the effects on the IOP of lidocaine applied topically to the larynx after induction with propofol-atracurium. We randomly assigned 32 random-source dogs, obtained from municipal pounds, to receive the following: lidocaine, 2 mg/kg IV, with saline, 0.1 mL/kg topically applied to the larynx (LIDOsal); saline, 0.1 mL/kg IV, with lidocaine, 2 mg/kg topically applied to the larynx (SALlido); diazepam (Valium), 0.25 mg/kg IV, with saline, 0.1 mL/kg topically applied to the larynx (VALsal); or saline, 0.1 mL/kg IV, with saline, 0.1 mL/kg topically applied to the larynx (SALsal). We measured arterial pressure directly, by means of an indwelling catheter placed in a peripheral artery. Anesthesia was induced with propofol, 8 mg/kg IV, until loss of jaw tone, followed by atracurium, 0.3 mg/kg IV. We measured the IOP in triplicate in each eye before premedication, before induction, before intubation, and after intubation. After induction, the IOP was significantly increased except in the VALsal group, in which the IOP was significantly lower than in the negative-control group before intubation. After intubation, the IOP was significantly elevated in all the groups compared with the values before induction. Cardiovascular parameters were essentially similar in all the groups, except for a significant increase in blood pressure after intubation in the SALlido group. Thus, propofol-atracurium anesthesia causes an increase in IOP that is blunted by diazepam. However, diazepam does not blunt the increase in IOP observed with intubation.     

Density estimates of rural dog populations and an assessment of marking methods during a rabies vaccination campaign in the Philippines

We estimated the population density of dogs by distance sampling and assessed the potential utility of two marking methods for capture-mark-recapture applications following a mass canine rabies-vaccination campaign in Sorsogon Province, the Republic of the Philippines. Thirty villages selected to assess vaccine coverage and for dog surveys were visited 1 to 11 days after the vaccinating team. Measurements of the distance of dogs or groups of dogs from transect lines were obtained in 1088 instances (N = 1278 dogs; mean group SIZE = 1.2). Various functions modelling the probability of detection were fitted to a truncated distribution of distances of dogs from transect lines. A hazard rate model provided the best fit and an overall estimate of dog-population density of 468/km² (95% confidence interval, 359 to 611). At vaccination, most dogs were marked with either a paint stick or a black plastic collar. Overall, 34.8% of 2167 and 28.5% of 2115 dogs could be accurately identified as wearing a collar or showing a paint mark; 49.1% of the dogs had either mark. Increasing time interval between vaccination-team visit and dog survey and increasing distance from transect line were inversely associated with the probability of observing a paint mark. Probability of observing a collar was positively associated with increasing estimated density of the dog population in a given village and with animals not associated with a house. The data indicate that distance sampling is a relatively simple and adaptable method for estimating dog-population density and is not prone to problems associated with meeting some model assumptions inherent to mark-recapture estimators.     

The longevity of immunoglobulin preservation in canine skin utilizing Michel's fixative

Skin biopsy specimens from 7 dogs with immune-mediated skin diseases diagnosed by routine histology and 5 dogs with other skin diseases were placed in Michel's transport medium for 4 to 9 years. Direct immunofluorescence yielded positive results in tissue samples from 3 dogs with pemphigus foliaceus and 2 dogs with discoid lupus erythematosus. Direct immunofluorescence was not seen in tissue samples from 1 dog with pemphigus foliaceus and 5 dogs with non immune-mediated skin diseases. Direct immunofluorescence was seen in skin biopsy specimens maintained in Michel's medium for 4 to 8 years.     

A stress transformation approach to predicting the failure mode of wood

Summary A simple model, based on the use of transformations of second-order tensors, is presented in this paper to predict the failure mode of wood members stressed in various degrees of parallel-and perpendicular-to-grain tension and parallel-to-grain shear. This type of loading is indicative of structural wood members with cross grain or grain deviations in the vicinity of knots subjected to bending or tension. The model is based on the assumptions that failure is dictated by the presence of any of the aforementioned stresses that exceed the clear wood strength in that mode and that failure does not result from stress interactions. The magnitudes of the applied stresses are normalized relative to the wood strength in that mode. The ratio of applied stress to material strength that is greatest at any particular angle of load to grain is presumed to be the failure mode at that angle. To verify model predictions, optical and microscopic analyses of surfaces of failed specimens loaded in uniaxial tension at angles between 0° and 90° to grain were compared to previously obtained, or otherwise known, surfaces of specimens tested in tension and shear. Specimens tested at various angles to grain demonstrated failed surfaces very much like those associated with specimens loaded in the modes predicted by the model.     

Marking and retention of harlequin bug,Murgantia histrionica (Hahn) (Hemiptera: Pentatomidae), on pheromone-baited and unbaited plants

Harlequin bug (Murgantia histrionica) is an important pest of cole crops in the USA. The adults and nymphs feed on aboveground plant tissues by sucking cell contents and can seriously damage the host. Current insect control measures on cole crops target mainly lepidopteran pests, and the insecticides generally used do not control harlequin bug, so alternative management practices need to be explored. Previous research has established the existence of a male-produced pheromone attractive to both sexes and nymphs of M. histrionica. In this work, two systems of marking bugs were tested to verify if the mark affected fitness traits such as survival and host location. In a second phase, marked individuals were placed on trap host plants baited with synthetic pheromone lures to test whether migration rates were related to M. histrionica density on the trap plants and the presence of the attractants. Neither marking system affected the survival or orientation of the subjects compared to unmarked individuals. The pheromone lures significantly increased the attractiveness of the trap plants, but did not increase the retention time of the plants compared to unbaited plants. Emigration from the trap plants showed a constant rate and seemed unrelated to bug density on the plants. However, a mean peak density of ca. 36 bugs/plant was calculated. Beyond this number, density tended to decrease. These successful marking methods and retention time models support development of M. histrionica management with trap crops, by providing tentative control thresholds and decision rules.