Topic:Centrifugation
Centrifugation is a laboratory technique utilized in equine research to separate components of blood or other biological samples based on their density. This process involves spinning samples at high speeds, causing denser elements to move outward and form distinct layers. In equine studies, centrifugation is often employed to isolate plasma or serum from whole blood, facilitating various diagnostic and research applications. It enables the analysis of different blood constituents, such as cells, proteins, and other biomolecules, which are essential for understanding equine physiology and pathology. This page compiles peer-reviewed research studies and scholarly articles that explore the applications, methodologies, and implications of centrifugation in equine science.
[Outbreaks of equine trypanosomiasis caused by Trypanosoma evansi in Formosa Province, Argentina]. Tests on 257 blood samples from 21 herds of horses in Formosa Province of Argentina, using the technique of centrifuging microhaematocrit capillary tubes, revealed Trypanosoma evansi in 90 of 137 animals in eight herds. Application of the direct agglutination test to serum samples from the same animals revealed antibodies to T. evansi in 107 horses. Antibody was also detected in nine horses from two herds where the parasite was not detected. Outbreaks of 'mal de caderas' occurred in the humid (eastern) and sub-humid (central) zones of Formosa. More than 95% of the equine population of the prov...
Chromogenic assay for equine plasminogen. A functional assay for equine plasminogen was established, using urokinase as the activator, a synthetic chromogenic substrate, a computer-assisted centrifugal analyzer, and acidified/neutralized plasma. One documented effect of plasma acidification appears to be inactivation of alpha-2-antiplasmin. Intra- and interassay precision testing yielded coefficients of variation of 4.1% (n = 10) and 5.6% (n = 26), respectively. Plasminogen was stable in equine plasma stored up to 1 week at 4 C and up to 5 months at -70 C. Plasminogen in nonacidified equine plasma was not activated by urokinase, strep...
Isolation of granulocytes and mononuclear cells from the blood of dogs, cats, horses and cattle. A simple discontinuous Percoll density-gradient technique was adapted for isolation of granulocytes and mononuclear cells from cats, dogs, horses and cattle. Separation was accomplished at low speeds using a standard tabletop centrifuge. Cell purity was 100% for both granulocytes and mononuclear cells and cell viability exceeded 95%. Percent recovery of leukocytes ranged from 69 to 83%.
Continuous-flow centrifugation hemapheresis in the horse. In a continuous-flow centrifugation apheresis technique adapted for blood-component separation and collection in horses, hydroxyethyl starch was not required for erythrocyte sedimentation. The efficacy and separation characteristics of whole blood from 10 horses were evaluated at various gravitational forces (700 to 1,500 rpm), using a constant withdrawal rate (100 ml/min). Maximum leukocyte collection occurred at 700 rpm (P less than 0.01), and optimal neutrophil collection occurred at 700 to 750 rpm (P less than 0.01). Although neutrophil counts decreased and lymphocyte counts remained const...
Platelet function, size and yield in whole blood and in platelet-rich plasma prepared using differing centrifugation force and time in domestic and food-producing animals. The effects of centrifugation force and time upon platelets function, mean platelet volume and platelet yield were compared with whole blood platelet counts and size in citrated blood samples from the bovine, canine, caprine, equine, feline, ovine and porcine species. The results were similar, for a given species, irregardless of sample volume. Bovine, caprine, feline and ovine platelet yields and mean platelet volumes were maximal when platelet-rich plasma was prepared using longer centrifugation times and lower gravitational forces. Canine, equine and porcine platelet yields and mean platele...
Isolation and identification of equine lymphocytes and monocytes. Various cell populations of equine mononuclear leukocytes were identified and isolated. Mononuclear leukocytes were concentrated by isopyknic centrifugation, using a solution of Ficoll and Hypaque. Three additional techniques were explored to separate monocytes from lymphocytes, and 3 methods were used to separate lymphocyte types. Cytochemical techniques for the detection of nonspecific esterase readily distinguished equine monocytes from lymphocytes. Peripheral blood lymphocytes were separated into at least 2 populations. One population had surface traits identical to thymocytes [ie, they re...
Separation of mononuclear leukocytes and polymorphonuclear leukocytes from equine blood. The present study describes a two step technique for the separation of mononuclear leukocytes or mononuclear and polymorphonuclear leukocytes from whole equine blood. First, the leukocyte rich plasma was obtained by sedimentation of erythrocytes in the undiluted blood. Subsequently, separation of the different populations of white blood cells was performed by centrifugation with different gradients overlaid with the leukocyte rich plasma. The optimal separation of the mononuclear cells was obtained by the centrifugation of the leukocyte rich plasma overlaying the gradient containing 24 parts o...
Purification and characterization of equine infectious anemia virus. EIA virus was purified from equine fetal kidney cell cultures by PEG-precipitation, two sucrose-gradient sedimentations (5-30 per cent) and (25 to 60 per cent) centrifugation, using the immunodiffusion test to follow the procedure. Purified EIA virus had a density (20 degrees C) of 1.162 and a sedimentation constant of S20w=656. electron microscopy revealed a particle of about 100 nm in diameter with a very flexible but usually spherical shape. The dense core may be at various locations inside the membrane bound particle.
[Anoplocephala sp. prevalence in equines at the Sociedade Hípica Paranaense, Curitiba, PR]. Anoplocephala sp. parasites are among the most frequent tapeworms in equines and are associated with intestinal infections. This survey had the objective to verify Anoplocephala sp. prevalence at Sociedade Hípica Paranaense (SHPr). The animals were treated with ivermectin, which does not have efficacy against Anoplocephala sp.. To determine whether eggs of Anoplocephala sp. were present, a modified centrifugal flotation technique was used and also eggs per gram of faeces (EPG). None of the samples showed Anoplocephala sp. eggs and only 11% of the animals had positive values for EPG. The resul...