Hematochemical parameters in sheep and goats of Sardinian breeds. II) Total blood cholesterol

It has been studied the total plasma cholesterol rate in lactating or dry sheep and goats of Sardinian breed. The values obtained for the four different groups of subjects have been compared with the "t of Student". While the difference between the sheep groups has seemed very accentuated, it has appeared hardly significant between the goat groups. Highly significant difference has also been found between lactating sheep and goats whereas there was no significant difference among the groups of dry subjects.     

The epizootiology of gastrointestinal nematode parasites in Greek dairy breeds of sheep and goats

Gastrointestinal (GI) parasitism represents a severe health problem in small ruminant production systems world-wide. The objective of the present study was three-fold: (i) to assess the prevalence of GI parasitism in dairy breeds of sheep and goats in selected areas of Greece; (ii) to determine the species of existing gastrointestinal parasites; and (iii) to investigate the effect of climatic factors on the seasonal variation of parasite population dynamics in dairy sheep and goats reared in two different geographical areas of Greece. The study was conducted in four flocks of either sheep or goats that were equally allocated in northern and central Greece. In each flock, faecal samples were randomly collected from 30 animals at monthly intervals and were used for nematode egg counts and coprocultures. Two animals from each flock were slaughtered monthly and their GI tract were examined for adult worm population and identification. The study revealed that the parasitic burdens in sheep were significantly (P<0.05) higher than those in goats. Faecal egg counts for both sheep and goats were significantly (P<0.01) affected by the month of the year and there was also a significant interaction between month of the year and area of study (P<0.01). Teladorsagia, Haemonchus, Trichostrongylus and Chabertia were the most prevalent nematode genera in both sheep and goats. Such information could be useful for the development of strategic treatments when sheep and goats are reared under systems similar to those described in this study.     

Electrophoretic and immunological characteristics of non-histone proteins of human skin tumors. I) Methods

The object of the research is to classify the nuclear proteins of the cellular nucleus of some types of human skin tumours (melanotic and amelanotic melanomas, squamous epitheliomas). Nuclear proteins were extracted from the nuclei with a saline buffer. Nuclear proteins were extracted from a melanoma step by step. After prolonged centrifugation to sediment the DNA and the large ribonucleoprotein complexes, the nuclear proteins were chromatographed on columns of Biorex 70+ to remove proteins were chromatographed on columns of Biorex 70+ to remove the histones. Nuclear proteins from a squamous epithelioma were injected into a rabbit to induce specific antibodies.     

Peripheral plasma testosterone levels in two indian breeds of goats and their reciprocal crosses

Plasma testosterone levels were estimated in different male goat age groups. In Black Bengal at 15–30 days, 2–3 months, 3–5 months and in Black Bengal, Beetal, Beetal × Black Bengal and Black Bengal × Beetal at 6 months and > 12 months (n = 6 in each case). The plasma testosterone levels (mean ± s.e.m.) were high (7.1 ± 2.0 ng/ml) at 2–3 months and fell drastically to 2.6 ± 0.5 ng/ml before attaining sexually mature levels of 4.6 ± 0.9 ng/ml at 6 months and 4.1 ± 0.8 ng/ml at > 12 months. The mature bucks of all genetic groups had a plasma testosterone concentration of 4.6 ± 0.8 ng/ml. Genetic group differences were not significant.     

Genetic variations in blood proteins within and between Spanish dairy sheep breeds

Eleven flocks of three Spanish sheep breeds have been studied: four Churra, four Lacha and three Manchega. Genetic variations between flocks of the same and different breeds have been analysed, using eight genetic blood systems and a wide range of statistical methods. The results show that the Churra, Lacha and Manchega breeds present significant differences between each other. Significant intraracial variations have been observed in Churras and Lachas, although they were almost non-existent in Manchegas. In some cases the genetic distances between flocks of the same breed were greater than the distances between flocks of different breeds. The data indicate that the closest breeds genetically are Lacha and Manchega.     

Comparative plasma pharmacokinetics of meloxicam in sheep and goats following intravenous administration

Meloxicam, a novel cyclooxygenase-2 selective nonsteroidal anti-inflammatory drug (NSAID), has been used extensively in humans and recently in some domestic animal species. Although it is an attractive NSAID for use in small ruminants, meloxicam pharmacokinetics have not been investigated in sheep and goats and this information is essential for rational therapeutic use of the drug in these species. In this investigation, comparative pharmacokinetic properties of meloxicam were studied in sheep and goats after a single intravenous dose of 0.5 mg kg(-1) body mass. Blood samples were collected via jugular venepuncture into heparinised tubes at predetermined times after drug administration. Plasma concentrations of meloxicam were determined by reversed-phase high performance liquid chromatography. The plasma concentrations of meloxicam were detectable in sheep and goats up to 72 and 48 h, respectively. The plasma concentration versus time data of meloxicam in both sheep and goats were adequately described by a two-compartment open model. The values obtained for sheep and goats for distribution half-life, volume of distribution at steady state and volume of the central compartment were almost similar in sheep and goats. The elimination half-life (t(1/2beta)), area under the plasma concentration-time curve (AUC), mean residence time (MRT) and total systemic clearance (Cl(B)) in sheep were significantly different from those of goats. The mean+/-S.E. values of t(1/2beta), MRT, AUC and Cl(B) in sheep were 10.85+/-1.21 h, 15.13+/-1.67 h, 31.88+/-2.97 microg h mL(-1) and 0.016+/-0.002 L h(-1) kg(-1), respectively whereas the respective values in goats were 6.73+/-0.58 h, 9.37+/-0.83 h, 19.23+/-2.23 microg h mL(-1) and 0.03+/-0.01 L h(-1) kg(-1). The results indicate that elimination kinetics of meloxicam differ significantly between sheep and goats and the elimination of the drug tends to be faster in goats compared to sheep.     

Detection of genetic variation with radioactive ligands. I. Electrophoretic screening of plasma proteins with a selected panel of compounds.

To detect new genetic variation in human plasma proteins, a panel of 63 radioactive substances were screened as potential radioligands using polyacrylamide gel electrophoresis (PAGE) and autoradiography. Vitamins, hormones, drugs, amino acids, purines, pyrimidines, sugars and lipids labeled with 14C or other radionuclides were among those substances tested. A majority bound to albumin and a smaller fraction to prealbumins and lipoproteins. Several vitamins and hormones bound to specific alpha and beta globulins. (1) Electrophoretic polymorphisms of vitamin D-binding protein (group-specific component), a vitamin B12-binding protein (transcobalamin II), and thyroxine-binding alpha-globulin are described elsewhere. (2) Testosterone-binding beta-globulin (TeBG) showed an electrophoretic polymorphism in Caucasians and a possible deficiency allele. (3) Transcortin showed an electrophoretic doublet in all persons tested but no electrophoretic variation. (4) A protein binding derivative of norepinephrine or epinephrine was identified as transferrin. (5) A nonpolymorphic protein running cathodal to albumin and binding a derivative of riboflavin was tentatively identified as a fraction of albumin with mobility altered as a result of interaction with the ligand.     

Electrophoretic studies of muscle proteins. I. Complex formation between delta protein and F-actin

Complex formation between delta protein and F-actin has been demonstrated by electrophoretic technique. The high turbidity of F-actin solutions has made it necessary to work at low concentrations of this protein (0.8 to 1.6 mg/ml). Delta protein concentrations were four to six times greater. At higher concentrations all F-actin was bound to delta protein, on both limbs. The combination ratio was about 1:1 by weight. We call this complex “delta-actin.” When the complex formed there was a slight fall in viscosity, indicating side-by-side union, but the turbidity greatly increased. The mobility of delta-actin was always less than that of free F-actin and sometimes also less than that of free delta protein. We earlier reported that delta protein is probably a polymer of tropomyosin. Its sedimentation constant (4.4 to 6.0 S) is higher than the of any other form of tropomyosin so far described. It may be the native molecule, its structure preserved by our relatively simple method of extraction and purification. The filaments of the I band may be composed of delta-actin. Since delta protein also forms a complex with myosin the filaments of the A band may be composed of delta-myosin. Delta protein may be a structural component which, in addition to other activities, may direct the building of both filament arrays and strengthen them.     

Electrophoretic polymorphism of proteins in the blood of horses: Studies of eleven pony breeds or populations

The allelic variants (of six genetic systems of blood proteins and enzymes) have been investigated by starch gel electrophoretic phenotyping among French populations of eleven pony breeds. Notable differences were observed between breeds with regard to the number of allelic variants in each system and their estimated frequencies. The distribution of hemotypes shows a much higher proportion of different individuals in pony populations than among thoroughbreds.