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Topic:In Vitro Research

In vitro research involving horses refers to the study of equine cells, tissues, or biological molecules outside their normal biological context, typically in controlled laboratory environments. This research approach allows scientists to investigate cellular processes, molecular interactions, and the effects of various treatments without the ethical and logistical complexities of in vivo studies. In vitro studies contribute to understanding equine physiology, pathology, and pharmacology by providing insights into cellular responses to pathogens, drugs, and other stimuli. This page compiles peer-reviewed research studies and scholarly articles that explore various in vitro methodologies and their applications in equine science, including cell culture techniques, molecular assays, and drug efficacy testing.
Isolation of herpesvirus from equine leukocytes: comparison with equine rhinopneumonitis virus.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    January 1, 1970   Volume 34, Issue 1 59-65 
Kemeny L, Pearson JE.An agent which possessed the properties of herpesviruses was isolated from the leukocytes of 71 out of 80 (88.7%) apparently normal Iowa horses. It was ether- and heat-sensitive, DNA type, and produced type-A intranuclear inclusion bodies in cell cultures. Electron micrographs revealed a virion of typical herpesvirus structure. Leukocyte isolate virus could be differentiated from equine rhinopneumonitis virus (ERV) by serum neutralization, by growth differences in rabbit kidney cells, and by fluorescent antibody staining. Specific neutralizing antibody against this agent was found in a pooled ...
Studies on the structure of ferritin and apoferritin from horse spleen. I. Tryptic digestion of ferritin and apoferritin.
Biochimica et biophysica acta    November 11, 1969   Volume 194, Issue 1 34-42 doi: 10.1016/0005-2795(69)90176-7
Crichton RR.No abstract available
Heterogeneity of erythrocyte catalase. Correlations between sulfhydryl group content, chromatographic and electrophoretic properties.
European journal of biochemistry    November 1, 1969   Volume 11, Issue 1 49-57 doi: 10.1111/j.1432-1033.1969.tb00737.x
Mörikofer-Zwez S, Cantz M, Kaufmann H, von Wartburg JP, Aebi H.No abstract available
The transport of oxidized glutathione from the erythrocytes of various species in the presence of chromate.
The Biochemical journal    October 1, 1969   Volume 114, Issue 4 833-837 doi: 10.1042/bj1140833
Srivastava SK, Beutler E.1. Erythrocytes from normal and glucose 6-phosphate dehydrogenase-deficient humans were subjected to hydrogen peroxide diffusion to oxidize the GSH. Studies were carried out in the presence and absence of chromate to inhibit glutathione reductase and with or without the addition of glucose. 2. The GSH content of erythrocytes from other species was oxidized by subjecting them to hydrogen peroxide diffusion in the presence of chromate and glucose. 3. Chromate (1.3mm) inhibited glutathione reductase by about 80%, whereas glucose 6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, hexokin...
The isolation of estrone sulfate and estradiol-17 beta sulfate from stallion testes.
Canadian journal of biochemistry    August 1, 1969   Volume 47, Issue 8 811-815 doi: 10.1139/o69-124
Raeside JI.No abstract available
Stability studies on crude and purified horse serum cholinesterase.
Biochemical pharmacology    July 1, 1969   Volume 18, Issue 7 1701-1705 doi: 10.1016/0006-2952(69)90159-2
Beckett AH, Vaughan CL, Mitchard M.No abstract available
[Cephalexin: microbiological activity in vitro and in vivo].
Antibiotica    June 1, 1969   Volume 7, Issue 2 93-128 
Muggleton PW, Renzini G, Ravagnan G, Orsolini P.No abstract available
Optical rotatory dispersion and circular dichroism of horse myoglobin and its derivatives.
Journal of biochemistry    May 1, 1969   Volume 65, Issue 5 759-766 doi: 10.1093/oxfordjournals.jbchem.a129075
Samejima T, Kita M.No abstract available
[Corecipitation: methods for analysing monovalent antibody fragments. I. Equine antidiphtheria system: hyperimmune sera].
Annales de l'Institut Pasteur    May 1, 1969   Volume 116, Issue 5 657-685 
Iscaki S, Raynaud M.No abstract available
[Chromogenic substrates of choline esterase from the blood serum of horses].
Biokhimiia (Moscow, Russia)    March 1, 1969   Volume 34, Issue 2 277-281 
Brestkin AP, Kats RI, Rozengart LA, Rozengart EV, Soboleva IN, Sokolovskiĭ MA.No abstract available
Studies on tissue culture of equine ovarian cell types: pathways of steroidogenesis.
The Journal of endocrinology    March 1, 1969   Volume 43, Issue 3 403-414 doi: 10.1677/joe.0.0430403
Channing CP.No abstract available
Tissue culture of equine ovarian cell types: culture methods and morphology.
The Journal of endocrinology    March 1, 1969   Volume 43, Issue 3 381-390 doi: 10.1677/joe.0.0430381
Channing CP.No abstract available
Studies on tissue culture of equine ovarian cell types: steroidogenesis.
The Journal of endocrinology    March 1, 1969   Volume 43, Issue 3 391-402 doi: 10.1677/joe.0.0430391
Channing CP, Grieves SA.No abstract available
[Structure of peptides isolated from chymotrypsin hydrolysates of horse myoglobin].
Bulletin de la Societe de chimie biologique    January 30, 1969   Volume 50, Issue 10 1651-1669 
Boulanger Y, Dautrevaux M, Han K, Biserte G.No abstract available
Morphological studies on horse kidney culture cells infected with cytopathic equine orphan (CEO) virus.
National Institute of Animal Health quarterly    January 1, 1969   Volume 9, Issue 3 149-164 
Okaniwa A, Fukunaga Y, Kono Y.No abstract available
Steroid hormone transformations by endocrine organs from pregnant mammals. 3. Biosynthesis and metabolism of progesterone by the Mare placenta in vitro.
Endocrinology    January 1, 1969   Volume 84, Issue 1 91-97 doi: 10.1210/endo-84-1-91
Ainsworth L, Ryan KJ.No abstract available
Changes in the histochemical behaviour of cultured cells due to differences in the serum component of the medium.
Acta histochemica    January 1, 1969   Volume 33, Issue 1 188-190 
Gyévai A, Fazekas I.No abstract available
Cleavage of horse immunoglobulin by cyanogen bromide.
Immunochemistry    November 1, 1968   Volume 5, Issue 6 513-524 doi: 10.1016/0019-2791(68)90088-8
Ernst ML, Arnon R, Sela M.No abstract available
Succinylcholine analogs as substrates and inhibitors of pseudocholinesterase.
Journal of medicinal chemistry    November 1, 1968   Volume 11, Issue 6 1126-1128 doi: 10.1021/jm00312a005
Beckett AH, Vaughan CL, Mitchard M.No abstract available
Electron-microscopic and chemical studies of oligomers in horse ferritin.
The Biochemical journal    November 1, 1968   Volume 110, Issue 2 265-280 doi: 10.1042/bj1100265
Williams MA, Harrison PM.Horse ferritin was fractionated both by starch-gel electrophoresis and by gel filtration on Sephadex G-200. Monomer fractions contained up to 98% of monomer and oligomer fractions up to 76% of oligomers as determined by quantitative electron microscopy. Percentages obtained from electron micrographs correlated well with analytical starch-gel electrophoretograms and ultracentrifuge patterns. Amino acid analyses of monomer- and oligomer-enriched fractions showed no significant differences. Ferritin oligomers did not apparently dissociate on dilution for electron microscopy or on storage. Apoferr...
Preparation and purification of horse antihuman lymphocyte globulin (ALG).
Cleveland Clinic quarterly    October 1, 1968   Volume 35, Issue 4 199-205 doi: 10.3949/ccjm.35.4.199
Konomi K, Deodhar SD.No abstract available
The binding of plutonium to serum proteins in vitro.
Radiation research    October 1, 1968   Volume 36, Issue 1 22-30 
Turner GA, Taylor DM.The interactions between tetravalent plutonium and horse serum proteins were studied in vitro by electrophoresis on cellulose acetate and by gel filtration. The results show that in horse serum, as in other mammalian sera, the plutonium is associated principally with the transferrin component of the beta1-globulins. The formation of the plutonium-transferrin complex requires the presence of HCO3-, and plutonium is displaced from the complex by excess iron, thus indicating that similar binding sites may be involved in the complexing of iron and plutonium. The plutonium complex is considered to ...
Kinetics of cellular and viral DNA synthesis in equine abortion (herpes) virus infection of L-M cells.
Virology    September 1, 1968   Volume 36, Issue 1 104-114 doi: 10.1016/0042-6822(68)90120-7
O'Callaghan DJ, Cheevers WP, Gentry GA, Randall CC.No abstract available
Comparison of protein structure in the crystal and in solution. V. Solubility of horse methemoglobin and azide binding.
Journal of molecular biology    August 14, 1968   Volume 35, Issue 3 477-481 doi: 10.1016/s0022-2836(68)80007-5
Rupley JA, Gates V.No abstract available
Inhibition of the pseudocholinesterase in horse serum by some choline analogues.
Biochemical pharmacology    August 1, 1968   Volume 17, Issue 8 1595-1599 doi: 10.1016/0006-2952(68)90220-7
Beckett AH, Vaughan CL, Mitchard M.No abstract available
Some properties of soluble proteins from chromaffin granules of different species.
Biochemical pharmacology    August 1, 1968   Volume 17, Issue 8 1553-1556 doi: 10.1016/0006-2952(68)90214-1
Strieder N, Ziegler E, Winkler H, Smith AD.No abstract available
The synthesis of some analogues of butyrylcholine and their hydrolysis by a purified horse serum cholinesterase.
Biochemical pharmacology    August 1, 1968   Volume 17, Issue 8 1591-1594 doi: 10.1016/0006-2952(68)90219-0
Beckett AH, Vaughan CL, Mitchard M.No abstract available
Kinetics of viral deoxyribonucleic acid, protein, and infectious particle production and alterations in host macromolecular syntheses in equine abortion (herpes) virus-infected cells.
Journal of virology    August 1, 1968   Volume 2, Issue 8 793-804 doi: 10.1128/JVI.2.8.793-804.1968
O'Callaghan DJ, Hyde JM, Gentry GA, Randall CC.Infection of exponential-phase suspension cultures of mouse fibroblast cells (L-M) with equine abortion virus (EAV) resulted in inhibition of cell growth and marked alterations in host metabolic processes. The synthesis of deoxyribonucleic acid (DNA) and ribonucleic acid was inhibited within 4 hr after infection and was suppressed by more than 90% by the time of maximal virus replication (14 to 18 hr). The overall rate of protein synthesis, however, was similar in uninfected and virus-producing cells as determined by measurements of net protein and isotope incorporation. The time course of vir...
Equine antihapten antibody. VI. Subunits of polyalanylated gamma-G(T)-immunoglobulin.
Biochemistry    July 1, 1968   Volume 7, Issue 7 2462-2468 doi: 10.1021/bi00847a003
Genco RJ, Karush F, Tenenhouse HS.No abstract available
[Determination of the effect in vitro of various antiseptics on the equine rhinopneumonitis virus].
Bulletin de l'Academie veterinaire de France    March 1, 1968   Volume 41, Issue 3 101-106 
Fontaine MP, Fontaine M, Moraillon A, Moraillon R, Brion A.No abstract available