Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/4201
Title: Effect of excessive cholesterol and lipopolysaccharide on cerebellar neuronal cells in <i>in vitro</i> and protective role of anti-inflammatory drugs
Authors: Ramanathan, M
Deshmuk, D
Keywords: Cerebellar cells
Cholesterol
Lipopolysaccharide
NSAIDs
Pioglitazone
S-methyl isothiourea
Issue Date: May-2009
Publisher: CSIR
Abstract: The present work was carried out to elucidate the role of NSAIDs, PPARg agonist and HMG CoA inhibitor on cholesterol and lipopolysaccharide (LPS) induced neurodegeneration. The cerebellar neuronal cells were exposed to cholesterol (10 and 50 µg/ml), LPS (1 ng/ml) or both. Neuroprotective effect of ibuprofen, rofecoxib, simvastatin and pioglitazone was assessed by measuring the neuronal loss, MTT dye assay, nitric oxide, LDH and lipid peroxide measurement. The results indicated that incubation of cholesterol and LPS showed less synaptic connections, neurite outgrowth and cell shrinkage as compared to normal cerebellar cells. Significantly decreased survival cells count along with increased LDH, lipid peroxide and nitrite levels were observed in the cells that confirmed neurodegeneration with cholesterol and LPS challenge. In comparison to individual toxins (LPS or cholesterol), combination of LPS and cholesterol produced more deleterious effect indicated synergistic effect of toxins. Interestingly, in comparison to LPS, cholesterol produced significantly low level of nitrites, LDH and lipid peroxides which indicated excessive cholesterol might not influence radical generation directly and might be a secondary effect. Among the drugs studied, NSAIDs showed better effect indicated inflammatory mediator response played vital role in cholesterol and LPS induced neurodegeneration. Simvastatin demonstrated moderate neuroprotective effect. It could be concluded that excessive cholesterol might produce cell death and led to release of nitrites and other cytokines. NSAIDs had better neuroprotective activity than simvastatin that produced moderate effect.
Description: 320-326
URI: http://hdl.handle.net/123456789/4201
ISSN: 0019-5189
Appears in Collections:IJEB Vol.47(05) [May 2009]

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