Analyze Diet

Topic:Flow Cytometry

Flow cytometry is a technology used to analyze the physical and chemical characteristics of cells or particles in horses. This technique involves suspending cells in a fluid stream and passing them through a laser beam, where they are individually measured for various parameters such as size, complexity, and fluorescence intensity. In equine research, flow cytometry is applied to study immune cell populations, assess cellular responses to pathogens, and evaluate hematological parameters. It is a valuable tool for veterinary diagnostics, allowing for detailed analysis of blood and tissue samples. This page compiles peer-reviewed research studies and scholarly articles that explore the applications, methodologies, and findings related to flow cytometry in equine health and disease.
In vitro calibration and surgical implantation of electromagnetic blood flow transducers for measurement of left coronary blood flow and cardiac output in the pony.
American journal of veterinary research    July 1, 1987   Volume 48, Issue 7 1120-1125 
Ward DS, Fessler JF, Bottoms GD.Electromagnetic flow transducers were implanted via left thoracotomy in 8 ponies (122.7 to 263.6 kg) around the main pulmonary and left main coronary arteries for continuous measurement of mean and pulsatile blood flow. Flow transducers were calibrated in vitro with a gravity flow system. The mean +/- SE pulmonary flow was 73.1 +/- 5.1 ml/kg of body weight/min. Left coronary flow was 0.95 +/- 0.07 ml/kg/min (1.3% of cardiac output) and was not believed to be an accurate measurement. This was caused by the inability to implant a zero-flow occluder, requiring the use of minimum flow during systo...
Continuous-flow centrifugation hemapheresis in the horse.
American journal of veterinary research    February 1, 1986   Volume 47, Issue 2 342-345 
Gordon BJ, Latimer KS, Murray CM, Moore JN.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...
Assessment of spermatozoal function using dual fluorescent staining and flow cytometric analyses.
Biology of reproduction    February 1, 1986   Volume 34, Issue 1 127-138 doi: 10.1095/biolreprod34.1.127
Garner DL, Pinkel D, Johnson LA, Pace MM.Spermatozoa from bulls, boars, dogs, horses, mice, and men were examined using a fluorogenic stain consisting of the membrane-permeant substrate carboxyfluorescin diacetate (CFDA) and the relatively membrane-impermeant nuclear stain propidium iodide (PI). Three distinct populations of spermatozoa were discernible in samples from each species upon microscopic examination. Individual spermatozoa, presumed to be viable because of their motility, retained products of the fluorescein chromophore throughout the cell. A second population of spermatozoa in which the nuclei stained red with PI retained...
A new surface marker on equine peripheral blood lymphocytes. I. Subpopulations of lymphocytes with receptors for Helix pomatia A hemagglutinin (HP).
Veterinary immunology and immunopathology    January 1, 1985   Volume 8, Issue 1-2 35-46 doi: 10.1016/0165-2427(85)90108-4
Broström H, Hellström U, Hammarström S, Obel N, Perlmann P.Untreated and neuraminidase-treated equine peripheral blood lymphocytes were analysed for binding of the A hemagglutinin of the snail Helix pomatia (HP). For optimal staining by direct immunofluorescence, the concentration of neuraminidase had to be increased as compared to that needed for other species. Moreover, higher concentrations of HP were required for optimal staining of equine lymphocytes as compared to lymphocytes from other species. Even so, the maximal number of equine lymphocytes exhibiting positive staining was only about 20%. No, or very few, HP-positive lymphocytes were seen wh...
A new surface marker on equine peripheral blood lymphocytes. II. Characterization and separation of purified blood lymphocytes with receptors for Helix pomatia A hemagglutinin (HP).
Veterinary immunology and immunopathology    January 1, 1985   Volume 8, Issue 1-2 47-61 doi: 10.1016/0165-2427(85)90109-6
Broström H, Hellström U, Ziverts I, Obel N, Perlmann P.In a preceding report we have shown that the lectin Helix pomatia A hemagglutinin (HP) binds to two subpopulations of neuraminidase-treated equine peripheral blood lymphocytes (PBL), constituting about 20% and 75% of PBL, respectively. The aim of the present study was to further characterize these HP+ cells in regard to other surface markers such as receptors for guinea pig erythrocytes (GPR+ cells), membrane-bound immunoglobulins (sIg+ cells), receptors for activated complement (C3R+ cells) and receptors for IgG (Fc alpha R+ cells). This was done by double marker analysis and by lymphocyte fr...
Xenogeneic monoclonal antibodies to cell surface antigens of equine lymphocytes.
American journal of veterinary research    April 1, 1984   Volume 45, Issue 4 626-632 
Newman MJ, Beegle KH, Antczak DF.Monoclonal antibodies to equine lymphocyte antigens were produced, using normal peripheral blood lymphocytes as the immunogen and standard hybridoma techniques. Antibody producing hybridomas were detected by a solid-phase enzyme-linked immunosorbent assay. Antibodies produced by 6 cloned hybrids were characterized further by microlymphocytotoxicity, indirect immunofluorescence, and agglutination assays on peripheral blood lymphocytes, platelets, and erythrocytes. Reaction patterns on leukocytes indicated that these antibodies may recognize at least 3 different cell-surface antigens: (1) an ant...
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.
Thrombosis and haemostasis    December 30, 1983   Volume 50, Issue 4 838-843 
Clemmons RM, Bliss EL, Dorsey-Lee MR, Seachord CL, Meyers KM.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.
American journal of veterinary research    September 1, 1981   Volume 42, Issue 9 1651-1654 
Banks KL, Greenlee A.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 and identification of equine leukocyte populations and subpopulations.
American journal of veterinary research    June 1, 1981   Volume 42, Issue 6 1037-1039 
Dutta SK, Bumgardner MK, Scott JC, Myrup AC.Various methods of separation and identification of major equine leukocyte populations and subpopulations were used. The purity of T and B lymphocytes separated in Sephadex anti-equine F(ab')2 columns was 87% to 99% and 83% of 97%, respectively. The purity of T lymphocytes separated in nylon-wool columns was 89% to 98%. Preparations of B lymphocytes separated in glass-bead columns were 68% to 79% pure. The presence (or absence) of surface immunoglobulin by immunofluorescence was the most consistent and reliable method for the identification of B or T lymphocytes, respectively. However, the ery...
Identification and genetics of horse lymphocyte alloantigens.
Immunogenetics    January 1, 1980   Volume 11, Issue 5 499-506 doi: 10.1007/BF01567818
Bailey E.Six hundred horses were tested with lymphocytotoxic antisera derived from 550 parous mares and 58 antisera produced by alloimmunization with horse blood cells. Seven equine lymphocyte specificities were identified using correlation analysis of the test data, absorption analysis and lysostripping. These specificities are expressed on lymphocytes and platelets, but not on red blood cells (RBC). Therefore, these specificities do not appear to be products of any of the eight known blood group systems of the horse. The distribution of these specificities in 113 Thoroughbred horses and 57 Arabian ho...
[Studies on erythrocyte rosette-forming peripheral T-cells in cattle, swine and horse].
Berliner und Munchener tierarztliche Wochenschrift    November 15, 1978   Volume 91, Issue 22 437-439 
Mayr B, Schleger W.No abstract available
Collateral flow resistance and time constants in dog and horse lungs.
Journal of applied physiology: respiratory, environmental and exercise physiology    January 1, 1978   Volume 44, Issue 1 63-68 doi: 10.1152/jappl.1978.44.1.63
Robinson NE, Sorenson PR.We studied collateral flow resistance in exsanguinated, excised lower lobes and accessory lobes of dog and horse lungs, respectively. A double lumen catheter obstructed a peripheral airway isolating a segment of the lobe. Oxygen flowed into the segment via a rotameter which measured flow (Vcoll) while the inner catheter recorded segment pressure (Ps). Gas delivered into the segment flowed out via collateral channels. Collateral flow resistance was calculated as (Ps - PL)/Vcoll, where PL = static transpulmonary pressure. Rcoll at PL = 20, 10, and 5 cm H2O averaged 0.24, 1.25, and 2.65 cmH2O.ml-...
Erythrocyte rosette formation of equine peripheral blood lymphocytes.
American journal of veterinary research    November 1, 1977   Volume 38, Issue 11 1775-1779 
Tarr MJ, Olsen RG, Krakowka GS, Cockerell GL, Gabel AA.Erythrocyte rosette (ER) formation of equine peripheral blood lymphocytes (PBL) was characterized. Guinea pig and, to a lesser extent, human erythrocytes formed ER; cat, cow, dog, hamster, mouse, rat, and sheep erythrocytes showed negligible rosetting properties. Conditions of the assay were varied to determine which procedure allowed the largest percentage of rosette formation. The PBL from 20 normal horses were then assayed, averaging 38 +/- 2% ER. To characterize the erythrocyte receptor as being on T or B cells, equine thymocytes from 6 foals were assayed; the thymocytes formed an average ...
Hot-film anemometer velocity measurements of arterial blood flow horses.
Circulation research    February 1, 1974   Volume 34, Issue 2 193-203 doi: 10.1161/01.res.34.2.193
Nerem RM, Rumberger JA, Gross DR, Hamlin RL, Geiger GL.No abstract available
Comparative study of platelet aggregation in various species.
Journal of medicine    January 1, 1974   Volume 5, Issue 5 292-296 
Calkins J, Lane KP, LoSasso B, Thurber LE.No abstract available
The separation of peripheral blood cells of the horse.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    January 1, 1974   Volume 38, Issue 1 72-74 
Carter EI, Valli VE, McSherry BJ.The peripheral blood cells from Standard bred horses were subjected to procedures which will separate equine peripheral blood cells with good precision and efficiency into red cell, leukocyte, and platelet fractions. The separated cells have normal morphology and the differential count of the separated granulocytes and lymphocytes is unchanged from that of the original sample.
Comparative study on the composition of platelets from the equine, bovine, ovine and porcine species.
Revista espanola de fisiologia    December 1, 1973   Volume 29, Issue 4 323-327 
Cabezas M, Cabezas JA.No abstract available
1 16 17 18