Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/4767
Title: Tobacco-specific nitrosamines mediated phospholipid alterations by enhanced phospholipase A2 and acyltransferase activity in yeast and mammalian system
Researcher: Panneerselvam, Vijayaraj
Guide(s): Nachiappan, Vasanthi
Keywords: Tobacco specific nitrosamines
N-nitrosonornicotine
S. cerevisiae
Pulmonary surfactant
Phospholipid
Phospholipase A2
Acyltransferases
Fatty acid
Upload Date: 24-Sep-2012
University: Bharathidasan University
Completed Date: February 2011
Abstract: The present study is the first report of 4-(methyl nitrosamino)-1-(3-pyridyl)-1- butanone (NNK) and N-nitrosonornicotine (NNN) on phospholipid metabolism using two different model systems. Tobacco specific nitrosamines (TSNAs) namely NNK and NNN are potent pulmonary carcinogens present in cigarette smoke and carcinogenicity of these compounds is very well documented. However the impact on lipid metabolism remains enigmatic, since NNK and NNN primarily target the respiratory system and respiratory function is fully dependent on lipid-protein complex called surfactant. Hence the present study was undertaken to investigate the impact of NNK and NNN on phospholipid metabolism. We initiated our objectives with Saccharomyces cerevisiae, a good model system for characterizing phospholipid metabolism. We observed reduced phospholipid content accompanied with enhanced phospholipase B (PLB), particularly plb1p activity with NNK (Vijayaraj et al., 2011b) and NNN (Vijayaraj et al., 2011a) exposure. The results have led us to investigate and confirm these changes in rat pulmonary surfactant metabolism. NNK and NNN primarily target the respiratory system and respiratory function is fully dependent on lipid-protein complex called surfactant. The phospholipids were reduced significantly due to enhanced deacylation by different form of phospholipase A2s (PLA2s) and they prefer to hydrolyse PC and PG in the presence of NNN and NNK respectively. NNK and NNN increased the expression of secretory PLA2s (sPLA2- IIA and sPLA2-V) and lysosomal- PLA2 (LPLA2) in alveolar epithelial type 2 cells (AEC2). Further both NNK and NNN significantly enhanced acyltransferases, LPCAT and LPGAT activity and also induces the expression of LPCAT and LPGAT. Remodelling enzyme reduced dipalmitoyl phosphatidylcholine (DPPC) formation accompanied with increase of other fatty acids, mainly arachidonic acid (AA) in AEC2 exposed to NNK and NNN.
Pagination: 147p.
URI: http://hdl.handle.net/10603/4767
Appears in Departments:Department of Biochemistry

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File88.94 kBAdobe PDFView/Open
02_certificate.pdf34.04 kBAdobe PDFView/Open
03_declaration.pdf33.84 kBAdobe PDFView/Open
04_acknowledgements.pdf65.74 kBAdobe PDFView/Open
05_abbreviations.pdf58.14 kBAdobe PDFView/Open
06_contents.pdf147.65 kBAdobe PDFView/Open
07_abstract.pdf159.46 kBAdobe PDFView/Open
08_chapter 1.pdf696.57 kBAdobe PDFView/Open
09_chapter 2.pdf679.51 kBAdobe PDFView/Open
10_chapter 3.pdf2.59 MBAdobe PDFView/Open
11_summary.pdf230.88 kBAdobe PDFView/Open
12_bibliography.pdf336.91 kBAdobe PDFView/Open
13_publications.pdf1.84 MBAdobe PDFView/Open


Items in Shodhganga are protected by copyright, with all rights reserved, unless otherwise indicated.