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Topic:Cell Viability

Cell viability refers to the ability of cells to survive and function within their physiological environment. In horses, assessing cell viability is an important aspect of veterinary research, particularly in understanding the effects of various treatments, diseases, and environmental factors on equine cellular health. Techniques such as flow cytometry, trypan blue exclusion, and MTT assays are commonly used to evaluate cell viability in equine studies. These methods help determine the proportion of living cells in a sample, providing insights into cellular responses to different stimuli or conditions. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, applications, and implications of cell viability assessments in equine research.
[The use of Leydig interstitial cells preserved by deep freezing in the testosterone production assay].
Archiv fur experimentelle Veterinarmedizin    May 1, 1988   Volume 42, Issue 3 430-434 
Tiemann U, Falge R, Blödow G, Bergfeld J.No abstract available
Loss of polar trophoblast during differentiation of the blastocyst of the horse.
Journal of reproduction and fertility    May 1, 1988   Volume 83, Issue 1 447-460 doi: 10.1530/jrf.0.0830447
Enders AC, Lantz KC, Liu IK, Schlafke S.Twelve blastocysts, collected 7-12 days after ovulation (Day 0), were examined by light and electron microscopy to investigate the nature of the relationship of the polar trophoblast (Rauber's layer) to the inner cell mass. On Day 7, the polar trophoblast was intact and formed a flattened layer overlying the epiblast cells of the inner cell mass. As blastocysts enlarged to greater than 1 mm in diameter, small discontinuities appeared in the polar trophoblast, where epiblast cells intruded onto the surface. At this time, trophoblast cells adhered closely to adjacent and underlying epiblast cell...
Epidermal cell renewal in the horse.
American journal of veterinary research    April 1, 1988   Volume 49, Issue 4 520-521 
Barker BB, Stannard AA, Maibach HI.Epidermal cell labeling index and cell renewal time were estimated in 8 adult horses, using autoradiography after [3H]thymidine was given intradermally. The mean labeling index was 1.45 +/- 0.47%, and the mean cell renewal time of the viable epidermis was approximately 17 days.
Determination of the minimum time of praziquantel therapy required for the in vitro treatment of protoscoleces of Echinococcus granulosus.
Journal of helminthology    March 1, 1988   Volume 62, Issue 1 10-14 doi: 10.1017/s0022149x00011135
Morris DL, Taylor DH, Daniels D, Riley EM, Richards KS.Ovine and equine protoscoleces of Echinococcus granulosus were cultured for 26 days with our without praziquantel and viability assessed, by eosin exclusion, for cultures in various drug concentrations (50, 250 and 500 micrograms/l) and periods of exposure (1, 3 or 7 days (d] before removing/'rescuing' to drug-free medium. Drug efficacy was proportional to drug concentration and to length of exposure. At higher drug concentrations shorter exposures were required to produce the effect of continuous drug treatment, 1d therapy at 500 micrograms/l killing 96% ovine protoscoleces by day 14 whereas ...
Influence of an epidermal cell extract on skin healing and scar formation.
International journal of tissue reactions    January 1, 1988   Volume 10, Issue 6 381-385 
Silver IA, Eisinger M.We have examined the possible regulatory role of epidermal cell extract(s) (ECE) on skin cells, namely fibroblasts and keratinocytes, both in vivo and in vitro with particular reference to modification of scar formation. In an experimental wound model in pigs, it was found that extracts of cultured human and pig keratinocytes stimulated replication of epidermal cells and their migration from wound edges and remnants of hair follicles and sebaceous glands, together with hair growth, but at the same time suppressed fibroblast proliferation in the dermis. Sections of healing skin wounds that had ...
Induction and characterization of acrosome reaction in equine spermatozoa.
American journal of veterinary research    September 1, 1987   Volume 48, Issue 9 1383-1389 
Varner DD, Ward CR, Storey BT, Kenney RM.Equine spermatozoa were incubated in a chemically defined medium for 8 hours. The medium preserved spermatozoal viability, as assessed by total spermatozoal motility, progressive spermatozoal motility, and spermatozoal exclusion of eosin stain. Effects of time and divalent cation ionophore, A23187, on the occurrence and character of the spermatozoal acrosome reaction were determined. Two light microscopic assays, a triple-stain technique and a chlortetracycline fluorescence assay, were calibrated with transmission electron microscopy for detection of the acrosome reaction. Incubation time and ...
Viability of stored equine embryos.
Journal of animal science    August 1, 1987   Volume 65, Issue 2 534-542 doi: 10.2527/jas1987.652534x
Clark KE, Squires EL, McKinnon AO, Seidel GE.Equine embryos were recovered nonsurgically 6.5 d after ovulation (Exp. 1) and those greater than 200 microns were stored in one of three media: 1) Ham's F10 + 10% fetal calf serum (FCS) under 5% CO2, 5% O2 and 90% N2 at 24 C (Ham's F10); 2) Minimal Essential Medium with Hank's balanced salts + 10% FCS in air (MEM) at 24 C or 3) MEM at 5 C n = 10/treatment). Embryos less than or equal to 200 micron (n = 10) were bisected microsurgically; one-half of each embryo was stored in Ham's F10 and the other half in either Dulbecco's phosphate-buffered saline + 10% FCS in air at 24 C (DPBS), or MEM in a...
Assay for equine peripheral blood lymphocytes blastogenic response using ethidium bromide.
Nihon juigaku zasshi. The Japanese journal of veterinary science    June 1, 1987   Volume 49, Issue 3 567-570 doi: 10.1292/jvms1939.49.567
Tajima M, Fujinaga T, Koike T, Okamoto Y, Otomo K.No abstract available
Effect of povidone-iodine on in vitro locomotion of equine neutrophils.
Equine veterinary journal    May 1, 1987   Volume 19, Issue 3 226-228 doi: 10.1111/j.2042-3306.1987.tb01387.x
Watson ED.Incubation of equine neutrophils with povidone-iodine solutions of greater than or equal to 0.2 per cent resulted in total inhibition of migration under agarose. This was caused by the cytotoxic effects of the solutions as shown by pyknosis and cell lysis. Lower concentrations of povidone-iodine, however, did not adversely affect neutrophil viability or locomotion.
Complement-induced equine neutrophil adhesiveness and aggregation.
Veterinary pathology    May 1, 1987   Volume 24, Issue 3 239-249 doi: 10.1177/030098588702400308
Slauson DO, Skrabalak DS, Neilsen NR, Zwahlen RD.Equine neutrophils (PMN) were isolated from citrated normal blood by density gradient separation on Ficoll-Hypaque to greater than 96% purity and 98% viability and an average of 3.78 x 10(7) PMN/ml. The agonist C5a des Arg was used in serial dilutions of whole zymosan-activated equine plasma (ZAP) or was partially purified from ZAP by column chromatography. Purified equine PMN exhibited rapid aggregation following incubation with C5a des Arg which was further dependent on the availability of divalent cations, especially Mg++. The microfilament disruptive agent cytochalasin B (5 micrograms/50 m...
Inhibition of equine neutrophil chemotaxis and chemokinesis by a Taenia taeniaeformis proteinase inhibitor, taeniaestatin.
Parasite immunology    March 1, 1987   Volume 9, Issue 2 195-204 doi: 10.1111/j.1365-3024.1987.tb00500.x
Leid RW, Grant RF, Suquet CM.Taeniaestatin, a recently isolated Taenia taeniaeformis proteinase inhibitor, was used to inhibit equine neutrophil migration. Taeniaestatin itself was not chemotactic when used as a chemotactic factor but taeniaestatin did inhibit neutrophil chemokinesis when tested in a Zigmond-Hirsch checkerboard assay. A dose-dependent inhibition of both chemokinesis and chemotaxis was observed when zymosan activated bovine sera (ZABS) was used as the chemotactic factor. This inhibition was greater than 95% when 5 mu of taeniaestatin was present on both the cell and chemotactic factor side of the chambers....
Use of different nonglycolysable sugars to maintain stallion sperm viability when frozen or stored at 37 degrees C and 5 degrees C in a bovine serum albumin medium.
Journal of reproduction and fertility. Supplement    January 1, 1987   Volume 35 135-141 
Arns MJ, Webb GW, Kreider JL, Potter GD, Evans JW.Bovine serum albumin (BSA) diluents containing lactose, raffinose or sucrose were not different (P greater than 0.05) in their ability to maintain stallion sperm viability, as determined by percentage motile spermatozoa (PMS) and their rate of forward movement (RFM), when stored at 37 or 5 degrees C for 24 h. These diluents did promote a higher (P greater than 0.05) PMS and RFM, when compared with BSA diluents containing arabinose or galactose. The BSA-arabinose and BSA-galactose diluents did not differ (P less than 0.05) in their ability to support sperm viability and were detrimental to sper...
Concentrations of uterine luminal prostaglandins in mares with acute and persistent endometritis.
Equine veterinary journal    January 1, 1987   Volume 19, Issue 1 31-37 doi: 10.1111/j.2042-3306.1987.tb02574.x
Watson ED, Stokes CR, David JS, Bourne FJ, Ricketts SW.Intrauterine infusion of 1 per cent oyster glycogen solution was used to induce acute endometritis in four genitally normal mares. Numbers of viable neutrophils recovered in uterine washings had increased by 1 h after infusion and remained elevated for at least 72 h. There was a significant correlation between numbers of viable neutrophils and total protein concentrations and between prostaglandin (PG)F and PGE2 concentrations in washings. There was also a significant relationship between concentrations of 15-keto-13, 14-dihydro PGF2 alpha in plasma and PGF in washings. Intrauterine concentrat...
Evaluation of cellulose acetate/nitrate filters for the study of stallion sperm motility.
Journal of reproduction and fertility. Supplement    January 1, 1987   Volume 35 33-38 
Strzemienski PJ, Sertich PL, Varner DD, Kenney RM.Stallion semen was diluted in a Hepes-supplemented buffer (CM) (10(6) spermatozoa/ml) and placed in the upper well of a Sykes-Moore chemotaxis chamber. Chambers were incubated in a humidified atmosphere (5% CO2 in air) at 37 degrees C for 1 and 2 h and spermatozoa were allowed to swim through filters with a mean pore size of 3,5 or 8 micron. Spermatozoa entered filters of all three pore sizes. Distance travelled was greater for each increase in pore size (P less than 0.01) but did not differ (P greater than 0.05) between 1 and 2h of incubation. Extended semen from stallions of different fertil...
Single step purification procedure for the rapid separation of equine leucocytes.
Veterinary research communications    November 1, 1986   Volume 10, Issue 6 445-452 doi: 10.1007/BF02214007
Sedgwick AD, Morris T, Russell BA, Lees P.Percoll gradients have been used to separate relatively pure populations of viable equine polymorphonuclear (PMN) and mononuclear (MN) cells. In preliminary studies, a continuous density gradient of 70% Percoll solution was used to separate two distinct leucocyte-rich bands. After measurement of the density of each band on the continuous gradient, discontinuous Percoll gradients, using 60% and 75% Percoll solutions, were used to provide a rapid means of separating PMN and MN cells. The yield of viable cells per ml of blood was 3.0 X 10(6) and 3.2 X 10(6) for MN and PMN cells, respectively. Cor...
Cell types in the pineal gland of the horse: an ultrastructural and immunocytochemical study.
The Anatomical record    October 1, 1986   Volume 216, Issue 2 165-174 doi: 10.1002/ar.1092160208
Cozzi B.A combined ultrastructural and immunocytochemical study was performed on the pineal gland of the horse in order to identify the cell types present and describe their characteristics. Comparisons have been made with other mammals. Two main cell types are present: pinealocytes and glial cells. Pinealocytes display different degrees of electron density in the nucleus and the cytoplasm, yet no ultrastructural feature supports the idea of separate populations. Putative secretory materials are stored in vesicles related to the Golgi apparatus. A variety of electron-dense bodies are present in the cy...
Equine endothelial cells in vitro.
American journal of veterinary research    April 1, 1986   Volume 47, Issue 4 956-958 
Lamar CH, Turek JJ, Bottoms GD, Fessler JF.Certain in vitro culture conditions were determined for equine endothelial cells obtained from the aorta and pulmonary arteries. Cells were enzymatically isolated from the vessel lumen, using clostridial collagenase (2.5 mg/ml of Hanks's balanced salt solution) incubated at 37 C for 30 minutes. Cells were cultured in alpha minimum essential medium supplemented with plasma-derived and nonplasma-derived bovine fetal sera, endothelial cell-growth supplement, heparin, and antibiotics. Smooth muscle cell growth was not inhibited with nonplasma-derived animal sera, plasma-derived equine serum, or he...
Antibodies to surface antigens of pigmented cells in animals with vitiligo.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)    March 1, 1986   Volume 181, Issue 3 423-426 doi: 10.3181/00379727-181-42275
Naughton GK, Mahaffey M, Bystryn JC.All of 24 animals (dogs, cats, and horses) with vitiligo were found to have antibodies to pigmented cells that could be detected by specific immunoprecipitation of radioiodinated, detergent-soluble surface macromolecules, and by indirect immunofluorescence on viable cells. These antibodies were not detected in 17 normal animals of the same species. The antibodies were directed to an 85-kDa surface antigen selectively expressed by pigmented cells that was not present on nonpigmented control cells. These observations suggest that vitiligo in animals is an autoimmune disease mediated to pigmented...
A new approach to quantification of Sertoli cells that avoids problems associated with the irregular nuclear surface.
The Anatomical record    March 1, 1986   Volume 214, Issue 3 231-237 doi: 10.1002/ar.1092140302
Johnson L.A new approach to quantification of Sertoli cells is described. The number of Sertoli cells per testis was calculated from the number of spermatids per testis, the number of spermatids per Sertoli cell apex, and the correction for the lifespan of spermatids enumerated per testis. To evaluate this method under different physiological conditions, testes from 28 adult (4-20-year) stallions obtained in the nonbreeding season (December-January) and from 28 adult stallions in the breeding season (June-July) were compared. Number of Sertoli cells per gram parenchyma was similar between seasons. Howev...
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...
Cytolytic activity of liposomes containing stearylamine.
Biochimica et biophysica acta    January 16, 1986   Volume 854, Issue 1 93-101 doi: 10.1016/0005-2736(86)90068-4
Yoshihara E, Nakae T.In order to develop the cytotoxic liposome, the cytolytic effect of polycationic liposome was examined. Upon incubation of the stearylamine-containing liposome (stearylamine-liposome) with rabbit erythrocyte, a significant extent of hemolysis was observed. Hemolytic activity of the liposome depends on the amount of stearylamine in the liposome membrane. The plots of the initial rate of hemolysis versus the concentration of stearylamine-liposome showed a sigmoidal curve, suggesting that stearylamine-liposomes act cooperatively on the erythrocyte membrane. Hemolytic activity of stearylamine-lipo...
Survival of rabbit and horse erythrocytes in vivo after changing the fatty acyl composition of their phosphatidylcholine.
Biochimica et biophysica acta    October 10, 1985   Volume 819, Issue 2 170-178 doi: 10.1016/0005-2736(85)90171-3
Kuypers FA, Easton EW, van den Hoven R, Wensing T, Roelofsen B, op den Kamp JA, van Deenen LL.The phospholipid composition and the distribution of phospholipids over the two leaflets of the membrane have been investigated for rabbit and horse erythrocyte membranes. Phosphatidylcholine (PC) comprises 39.4% and 41.3% of the total phospholipid complement of the rabbit and horse erythrocytes, respectively. In both membranes the distribution of this phospholipid is asymmetric: 70% of the PC is present in the outer layer of the rabbit membrane and 60% in that of the horse. The major species of this phospholipid class are the (1-palmitoyl-2-oleoyl)- and the (1-palmitoyl-2-linoleoyl)PC. The di...
In vitro phagocytosis and killing of Corynebacterium equi by alveolar macrophages of foals.
American journal of veterinary research    October 1, 1985   Volume 46, Issue 10 2171-2174 
Zink MC, Yager JA, Prescott JF, Wilkie BN.Bronchoalveolar lavage was performed 5 times, sequentially, on 3 healthy foals while each foal was 6 to 63 days of age. Phagocytosis and bactericidal assays were performed on recovered alveolar macrophages. Corynebacterium equi and alveolar macrophages at a ratio of 10:1 were incubated for 1 hour in medium containing 1% heat-inactivated rabbit anti-C equi serum. After incubation, greater than 90% of the alveolar macrophages contained at least 1 ingested bacterium and each alveolar macrophage contained 9.4 +/- 1.0 bacteria (mean +/- SE). After alveolar macrophages and C equi were incubated for ...
Cell synchronization and dynamic G-banding of equine chromosomes by bromodeoxyuridine.
The Journal of heredity    September 1, 1985   Volume 76, Issue 5 375-376 
Richer CL, Romagnano A.Both dynamic G-banding and cell synchronization produced by bromodeoxyuridine (BrdU), were applied to equine chromosomes. BrdU incorporated during the first half of the S-phase is taken up into the R-bands that are early replicating. These bands, which have incorporated BrdU, cannot contract as usual and remain elongated; only the other regions of the chromosome, i.e., the G-bands, contract normally and are sharply defined. BrdU also can be used for cell synchronization. The addition of BrdU in a high concentration, 15 hours before harvest, and its removal 11 hours later, has two effects: init...
In vitro development of Strongylus edentatus to the fourth larval stage with notes on Strongylus vulgaris and Strongylus equinus.
The Journal of parasitology    August 1, 1985   Volume 71, Issue 4 489-499 
Farrar RG, Klei TR.Strongylus edentatus was successfully cultured in vitro to the fourth larval stage (L4). Some growth continued for periods of 40-50 days at which time reductions in viability were observed in some of the culture systems tested. Various combinations of media, sera, buffers and organ explant cultures were tested. All cultures were incubated at 37 C in an atmosphere of 95% air and 5% CO2. Larvae underwent growth and differentiation to the L4 in all medium-serum combinations with and without organ explant cultures. Development and growth did occur but viability was reduced to insignificant levels ...
Natural cytotoxicity of human lymphocytes against equine target cells in vitro.
Scandinavian journal of immunology    March 1, 1985   Volume 21, Issue 3 245-254 doi: 10.1111/j.1365-3083.1985.tb01427.x
Broström H, Obel N, Perlmann P.Human lymphocytes displayed a frequent natural cytotoxicity (NK) in vitro against normal equine dermal fibroblasts (ED) and against equine tumour cells of a virus-containing cell line (Mc-1). Similarly, human normal sera contained antibodies that induced antibody-dependent cellular cytotoxicity (ADCC) by normal human lymphocytes against the same target cells. Both NK and ADCC varied for different donors. For individual donors, however, cytotoxicity against the two target cells was significantly correlated both in NK and ADCC. For ED there was also a significant correlation between ADCC and NK ...
Spread of equine lungworm (Dictyocaulus arnfieldi) larvae from faeces by Pilobolus fungi.
Nordisk veterinaermedicin    May 1, 1984   Volume 36, Issue 5-6 162-169 
Jørgensen RJ, Andersen S.Between 10 and 25% of the Dictyocaulus arnfieldi larvae excreted in faeces from a naturally infected donkey were harvested as infective stages from faecal cultures by means of Pilobolus fungi. The faeces were collected between 24 and 56 hours after drenching the donor animal with Pilobolus spores and kept at 16 +/- 2 degrees C. Most larvae were collected between the 5th and the 8th day of culturing during which period fructification and sporangium discharge also peaked. The sporangia and the adhering larvae were collected in Petri dishes inserted between the faecal mass and a light source. All...
Spermidine cytotoxicity in vitro: effect of serum and oxygen tension.
In vitro    March 1, 1984   Volume 20, Issue 3 Pt 1 198-204 doi: 10.1007/BF02618188
Hegre OD, Marshall S, Hickey GE.Plasma amine oxidase activities (benzylamine oxidase and spermine oxidase) were determined in the sera of a number of species of various ages. Benzylamine oxidase (BZO) activity, measured spectrophotometrically, was present in bovine, equine, and ovine species examined. Generally its activity in serum increased with the age of the animal. Spermine oxidase activity (SPO) was estimated by a bioassay of in vitro toxicity and did not necessarily correlate with BZO. Cytotoxicity in the presence of spermidine was found only in the sera of the ruminant species examined. Serum activity tended to rise ...
Isolation and partial characterization of equine alveolar macrophages.
American journal of veterinary research    December 1, 1983   Volume 44, Issue 12 2379-2384 
Dyer RM, Liggitt HD, Leid RW.A device was constructed from an equine nasogastric tube, polyethylene tubing, and a 3-way stopcock and used to lavage the lungs of anesthetized ponies. The technique was safe and atraumatic in that 6.4 to 19.7 X 10(7) purified alveolar macrophages were removed from the lungs without harm to the ponies or contamination of the samples with blood. Studies of these highly purified cell suspensions revealed a mean viability of 85% as assessed by eosin dye exclusion with a mean recovery (+/- SD) of 12.5 +/- 4.8 X 10(7) pulmonary alveolar macrophages/pony.
Horse red blood cells frozen with 20% (w/v) glycerol and stored at -150 C for five years.
American journal of veterinary research    November 1, 1983   Volume 44, Issue 11 2200-2202 
Valeri CR, Valeri DA, Gray A, Contreras TJ, Lindberg JR.When equine RBC were frozen with 20% (w/v) glycerol and stored at -150 C for as long as 5 years, there were no adverse effects on freeze-thaw or freeze-thaw-wash recovery or oxygen transport function. The manner in which the glycerol was added to, and removed from, the equine RBC was shown to be an important consideration in ensuring optimal freeze-thaw-wash recovery values.