Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series : World's leading Event Organizer

Back

Natasa Petronijević

Natasa Petronijević

University of Belgrade, Serbia

Title: Molecular targets of aluminum toxicity: Cholinergic system, NADPH oxidase and mitochondrial dysfunction

Biography

Biography: Natasa Petronijević

Abstract

Association of aluminum (Al) and some neurodegenerative disorders, including Alzheimer’s disease (AD), is implicated in 1965 when Al was recognized as neurotoxin. Since then, the role of Al as a pathogenetic factor in AD was suggested by many epidemiological studies. The exact mechanism responsible for changes induced by Al is not known. We have analyzed the effects of ingested Al on the acetylcholinesterase (AChE), NADPH oxidase (NOX2), respiratory chain enzymes and oxidative stress parameters in Mongolian gerbils brain. Also, the protective effects of intrahippocampal application of green tea leaf extract and glucose-6-phosphate dehydrogenase on aluminium-induced brain toxicity were studied. Adult gerbils were acutely (LD25), or subacutely (LD10) exposed to aluminum chloride by gavage and sacrificed 2, 6 or 24 hours after acute and 21 days after sub-acute treatment. Intrahipocampally solutions were injected into the CA1 region using a stereotaxic frame for small animals. The expressions of amyloid and tau protein, as well as, membrane-bound (gp91phox, p22phox) and cytosolic (p40phox, p47phox, p67phox) NOX2 subunits, the activity of AChE and oxidative stress parameters were determined in specific brain structures. Changes of AChE and COX activities, as well as, oxidative stress parameters were seen as the earliest effects of Al treatment. The changes of the expression of NOX subunits were seen six hour after acute poisoning. After subacute Al ingestion the oxidative stress was pronounced. Decreased gp91phox and increased p67phox expressions were seen in cortex while in the hippocampus the decrease of p67phox was noticed. Green tea leaf extract and glucose-6-phosphate dehydrogenase have shown protective effects.