Distribution of a new rosmarinic acid derivative in Eryngium alpinum L. and other Apiaceae

The roots of Eryngium alpinum L. (Apiaceae) demonstrated radical scavenging properties toward the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical in a TLC autographic assay. Isolation of the bioactive compounds allowed the identification of R-(+)-3'-O-beta-D-glucopyranosyl rosmarinic acid, a new rosmarinic acid derivative. The quantitative determination of the antioxidant capacity of the compound by chemoluminescence demonstrated half the activity of R-(+)-rosmarinic acid. To find another source richer in this compound, a chemotaxonomic study was conducted. The higher content was found in the aerial parts of Sanicula europeae L., also belonging to the Saniculoideae subfamily. Although present in most of the Eryngium species, this compound was not detected in Imperatoria ostruthium L., Pimpinella peregrina L., and Levisticum officinalis L. species from the Apioideae subfamily and Hydrocotyle asiatica L. from the Hydrocotyloideae subfamily. The results indicate that the new derivative R-(+)-3'-O-beta-D-glucopyranosyl rosmarinic acid is a potential chemotaxonomic marker of the Saniculoideae subfamily.     

Using Sterols to Detect Pig Slurry Contribution to Soil Organic Matter

Samples of pig slurry, as well as dairy and poultry manures collected in Brittany (western France) were analysed to test the ability of sterol profiles to provide a fingerprint of pig slurry contribution to soil organic matter. The data show that the 5β-stanol, known as coprostanol, is the most abundant sterol present in pig slurry, whereas this compound occurs only in minor amounts in both poultry and dairy manures. Moreover, systematic variations of (campesterol + sitosterol)/cholesterol (i.e., C₂₈₊₂₉/C₂₇) and (coprostanol + epi-coprostanol)/cholesterol (i.e., 5β/C₂₇) ratios allow to discriminate clearly pig slurry from poultry and dairy manures. The robustness of the pig slurry “sterol fingerprint” was tested by analysing the sterol profiles of soil samples from an experimental field that had received a massive pig slurry input between 10 to 14 years ago. The results indicate that the specific sterol profile of pig slurry is conservative once the slurry has been incorporated into the soil. In particular, the diagnostic 5β/C₂₇ ratio proves to be constant with time in soils having received pig slurry application, even 10 years after the end of the application. The “sterol fingerprint” of pig slurry is thus sufficiently distinctive from dairy and poultry manures, and also sufficiently time-resistant, to be of diagnostic value in determining whether a soil sample was once contaminated by pig slurry.     

Pharmacokinetics of chloramphenicol in sheep after intravenous, intramuscular and subcutaneous administration

The pharmacokinetics of chloramphenicol were studied in sheep after 3 single intravenous (IV), intramuscular (IM) and subcutaneous (SC) administrations (30 mg/kg). The two extravascular routes were studied during a crossover trial for a bioequivalence test. After IV and SC administrations, the plasma-concentration time graphs were characteristic of a two-compartment model, and after IM administration it was characteristic of a monocompartment model. The two routes of absorption were not bioequivalent. Using the kinetic values, multidose regimens to maintain the therapeutic chloramphenicol blood level (5 micrograms/ml) were proposed: 60 mg/kg every 12 hours for 72 hours for the IM administration and 45 mg/kg administered subcutaneously according to the same regimen. A study of the chloramphenicol residues in tissues was carried out. Chloramphenicol residues remained at the injection site, and 400 hours would be necessary to obtain the level of 10 micrograms/kg. Determination of the creatinine phosphokinase serum values showed that the subcutaneous route induced less damage to muscle than the intramuscular route.     

Influence of Psoroptes ovis on the energy metabolism of heifer calves

To determine the effect of Psoroptes ovis on the energy metabolism of heifers, 32 calves were randomly assigned to four treatments in a 2 X 2 factorial arrangement. Calves were fed the same diet at two intake levels, high or low, and were either infested or were not infested with P. ovis mites. Calves were housed in antigrooming stanchions. Body composition was determined by urea dilution on Days 0 and 63. Ration digestibility was determined on fecal grab samples using acid-insoluble ash as a marker. Infested calves had developed a severe P. ovis infestation 7 weeks following exposure and had significantly lower daily gain, gain:feed, and energy retention and higher serum glutamic-oxaloacetic transaminase than control calves. P. ovis infestation increased the maintenance energy requirement of calves by greater than 50% (79 vs. 123 kcal of net energy kg-1 body wt.75). For each 10% increase in the body surface affected by P. ovis, maintenance energy requirement increased 0.5 mcal day-1.     

Anatomy of a flaring proto-planetary disk around a young intermediate-mass star

Although planets are being discovered around stars more massive than the Sun, information about the proto-planetary disks where such planets have built up is sparse. We have imaged mid-infrared emission from polycyclic aromatic hydrocarbons at the surface of the disk surrounding the young intermediate-mass star HD 97048 and characterized the disk. The disk is in an early stage of evolution, as indicated by its large content of dust and its hydrostatic flared geometry, indicative of the presence of a large amount of gas that is well mixed with dust and gravitationally stable. The disk is a precursor of debris disks found around more-evolved A stars such as beta-Pictoris and provides the rare opportunity to witness the conditions prevailing before (or during) planet formation.     

Identification of apolipoprotein A‐I in the α‐globulin fraction of avian plasma

Background: Plasma protein electrophoresis is frequently used in birds as a tool for the diagnosis and monitoring of disease. Identification of proteins in individual peaks can help improve our understanding of changes in protein concentration in physiologic and pathologic conditions. Objective: The aim of this study was to verify the presence and identity the protein(s) in the prominent α‐globulin peak of orange‐winged parrots (Amazona amazonica), black kites (Milvus migrans), and rock pigeons (Columba livia). Methods: Heparinized plasma samples were obtained from 12 birds of each species. Agarose gel electrophoresis and total protein concentration were determined using standard techniques. One plasma sample from each species was then electrophoresed using high‐resolution agarose gels to isolate the α‐globulin band. Gel strips were digested in trypsin and peptides were extracted and analyzed using liquid chromatography with tandem mass spectrometry. De novo sequencing was used to identify the protein based on homology scoring against a protein database. Results: Electrophoresis verified the presence of a single prominent α‐globulin peak, usually in the α₁‐region, that had a median concentration of 9.4 g/L (range, 2.1–11.7 g/L, 21.6% of total protein) in parrots, 12.2 g/L (10.4–13.2 g/L, 35.9%) in kites, and 10.7 g/L (9.0–11.5 g/L, 40.0%) in pigeons. Mass spectrometry and sequencing analysis unequivocally identified the protein as a mature circulating form of apolipoprotein A‐I (apo A‐I) in all 3 species. Conclusions: Apo A‐I accounts for the prominent α‐globulin peak and comprises a major proportion of total protein concentration in diverse avian species. As a high‐density lipoprotein and negative acute phase protein with a pivotal role in cholesterol homeostasis, further study is warranted to determine the significance of changes in apo A‐I concentration in avian electrophoretograms.     

Comparison of lidocaine and lidocaine–epinephrine for the paravertebral brachial plexus block in dogs

Objective

To compare the motor and sensory block efficacy and duration of a modified paravertebral brachial plexus block (PBPB) after administration of lidocaine alone (LI) or combined with epinephrine (LE).