Evaluation of Pgg-Glucan, a Novel Immunomodulator, in in Vitro and Ex Vivo Models of Equine Endotoxemia
dc.contributor.author | Sykes, Benjamin William | en |
dc.contributor.committeechair | Furr, Martin O. | en |
dc.contributor.committeemember | Donaldson, Lydia L. | en |
dc.contributor.committeemember | McKenzie, Harold C. III | en |
dc.contributor.department | Veterinary Medical Sciences | en |
dc.date.accessioned | 2014-03-14T20:40:09Z | en |
dc.date.adate | 2003-09-01 | en |
dc.date.available | 2014-03-14T20:40:09Z | en |
dc.date.issued | 2003-06-16 | en |
dc.date.rdate | 2009-10-02 | en |
dc.date.sdate | 2003-06-17 | en |
dc.description.abstract | Justification - Endotoxemia is an important contributor to mortality and loss of use in the horse and results in significant losses to the equine industry on an annual basis. Objective - To determine the effect of PGG-Glucan on the cytokine response to endotoxin in the horse. Animals - Part 1; 6 adult horses. Part 2; 12 adult horses. Procedure - Part 1; Whole blood was collected, aliquoted, and incubated in vitro in four groups; saline control, endotoxin (LPS) (100 ng/ml), PGG-Glucan (0.1, 1.0, 10 and 100 μg/ml) and LPS (100 ng/ml) plus PGG-Glucan (0.1, 1.0, 10 and 100 μgg/ml). Supernatants were collected at 0, 6 and 12 hours and assayed for tumor necrosis factor £\ (TNF£\) activity. Part 2; Horses received either PGG-Glucan (1 mg/kg) or an equal volume of isotonic saline (0.9% NaCl) IV over 15 minutes. Twenty four hours later blood was collected and mononuclear cells isolated for cell culture. Cells were treated with LPS (100 ng/ml) and RNA extractions were performed at 0, 6, 12, 24 and 48 hours. Relative mRNA expression of TNFα, interleukin-1β (IL-1β),, interleukin-10 (IL-10) and interferon-γ (IFN-γ) was determined by reverse transcription and real time polymerase chain reaction. Results - Using an in vitro endotoxin challenge method PGG-Glucan altered the production of TNFα in a dose-dependent manner. PGG-Glucan had no effect upon the ex vivo cytokine mRNA expression of TNFα, IL-1β, IL-10 or IFN-γ. Conclusions and Relevance - Although mild changes were observed in TNFα production in vitro, it is not likely that PGG-Glucan will have a significant effect upon clinical endotoxemia. | en |
dc.description.degree | Master of Science | en |
dc.identifier.other | etd-06172003-143114 | en |
dc.identifier.sourceurl | http://scholar.lib.vt.edu/theses/available/etd-06172003-143114/ | en |
dc.identifier.uri | http://hdl.handle.net/10919/33617 | en |
dc.publisher | Virginia Tech | en |
dc.relation.haspart | Thesis2.pdf | en |
dc.rights | In Copyright | en |
dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
dc.subject | Horses | en |
dc.subject | endotoxemia | en |
dc.subject | PGG-Glucan | en |
dc.title | Evaluation of Pgg-Glucan, a Novel Immunomodulator, in in Vitro and Ex Vivo Models of Equine Endotoxemia | en |
dc.type | Thesis | en |
thesis.degree.discipline | Veterinary Medical Sciences | en |
thesis.degree.grantor | Virginia Polytechnic Institute and State University | en |
thesis.degree.level | masters | en |
thesis.degree.name | Master of Science | en |
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