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Volume 8

Journal of Alzheimers Disease & Parkinsonism

Dementia 2018

December 13-15, 2018

Page 22

Notes:

December 13-15, 2018 Abu Dhabi, UAE

13

th

Annual Conference on

Dementia and Alzheimer's Disease

Effects of chronic administration of Memantine on okadaic acid induced spatial short-term memory

impairment

Mariam Chighladze

1

, Manana Dashniani

1

, Maia Burjanadze

1

and Khatuna Rusadze

2

1

Ivane Beritashvili Center of Experimental Biomedicine, Georgia

2

Akaki Tsereteli State University, Georgia

A

lzheimer’s Disease (AD) is a neurodegenerative disease that causes progressive cognitive and behavior impairment in

the elderly. It is widely believed that changes in the cerebral activity of protein phosphatases have been implicated in the

pathogenesis of AD. Okadaic Acid (OA) is a potent and selective inhibitor of protein phosphatases. OA induced memory

deficit and elevation of Ca

2+

was found to be correlated with neurotoxicity and N-Methyl-D-Aspartate (NMDA) receptor

emerged as a plausible link. According to available data, the NMDA receptor antagonists (including memantin) have the

potential to perform neuroprotective role in neurodegenerative processes caused by Ca

2+

ionotoxicity. In the present study, the

possible beneficial effect of memantine on the OA induced spatial short-term memory impairment was examined in spatial

alternation task. OA was dissolved in artificial Cerebro-Spinal Fluid (aCSF) and injected Intra Cerebro Ventriculary (ICV) 200

ng in a volume of 10 μl bilaterally. Vehicle control received aCSF ICV bilaterally. Control and OA injected rats were divided

into two subgroups injected i.p. with saline or memantine (5 mg/kg). Memantine or saline were given daily for 13 days starting

from the day of OA injection. Behavioral study showed that bilateral ICV microinjection of OA induced impairment in spatial

short-term memory and chronic administration of memantine effectively attenuated OA induced spatial short-term memory

impairment. Therefore, ICV injection of OA can be used as an experimental model to study mechanisms of neurodegeneration

and define novel therapeutics targets for AD pathology.

Biography

Mariam Chighladze has completed her PhD from St Andrew the First-Called Georgian University of the Patriarchate of Georgia. She is the Laboratory Assistant at

Ivane Beritashvili Center of Experimental Biomedicine, Laboratory of Behavior and Cognitive Functions. She has published more than four papers.

Mariam Chighladze et al., J Alzheimers Dis Parkinsonism 2018, Volume 8

DOI: 10.4172/2161-0460-C8-057