Please use this identifier to cite or link to this item:
http://dspace.sctimst.ac.in/jspui/handle/123456789/9561
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lekshmi, N | - |
dc.contributor.author | Geetha, CS | - |
dc.contributor.author | Mohanan, PV | - |
dc.date.accessioned | 2017-03-10T03:26:11Z | - |
dc.date.available | 2017-03-10T03:26:11Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | 44 ,6;726-731 | en_US |
dc.identifier.uri | 10.4103/0253-7613.103269 | - |
dc.identifier.uri | http://dspace.sctimst.ac.in/jspui/handle/123456789/9561 | - |
dc.description.abstract | Aim: To detect the interleukin -1 levels from single and pooled isolated human lymphocytes in response to lipolysaccharide and lipoteichoic acid. Materials and Methods: Blood collected from healthy individuals (O ve, A ve, B ve, and AB ve) were subjected to gradient centrifugation to isolate lymphocytes. Different lymphocyte concentrations were used for in vitro pyrogen assay. Lymphocytes isolated were challenged with 5 EU of Gram negative (LPS) and 1 g/l of Gram positive (LTA) pyrogens in vitro and the inflammatory cytokine, Interleukin 1 (IL-1) release was measured by Sandwich ELISA method. Results: The results indicated that the release of IL-1 increases immediately after the initiation of incubation and reaches a maximum at 4 to 6 (th) hour and then stabilizes for both the pyrogens. Furthermore, IL-1 release by 5 EU of LPS and 1 g/l of LTA is dependent on lymphocytes concentration. It was also observed that the difference in blood group did not interfere with the IL-1 release. Conclusion: The isolated lymphocyte system can be used as an alternative to the in vivo rabbit pyrogen assay. | - |
dc.publisher | INDIAN JOURNAL OF PHARMACOLOGY | - |
dc.subject | Pharmacology & Pharmacy | - |
dc.title | Detection of interleukin-1 from isolated human lymphocyte in response to lipopolysaccharide and lipoteichoic acid | - |
Appears in Collections: | Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.