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Parkinsons 2016

December 05-07, 2016

Volume 6 Issue 6(Suppl)

J Alzheimers Dis Parkinsonism

ISSN: 2161-0460 JADP, an open access journal

conferenceseries

.com

December 05-07, 2016 Phoenix, USA

2

nd

International Conference on

Parkinson’s Disease & Movement Disorders

Jie Wu, J Alzheimers Dis Parkinsonism 2016, 6:6(Suppl)

http://dx.doi.org/10.4172/2161-0460.C1.024

Impact of sirtuin-3 in cognitive deficits of Parkinson’s disease

Jie Wu

Barrow Neurological Institute-St. Joseph’s Medical Center, USA

P

arkinson’s disease (PD) exhibits non-motor symptoms (NMS), including cognitive and neuropsychiatric deficits, and

often appear a decade or more before the first signs of motor symptoms. Sirtuin-3 (SIRT3) is a member of the sirtuin

family of mitochondria NAD(+)-dependent deacetylase that acts as a regulator of mitochondrial protein function. Emerging

evidence demonstrates that activation of SIRT3 exhibits neuroprotection, while reduced SIRT3 exacerbates neuropathogenesis,

suggesting SIRT3 is a critical target for neurodegenerative pathogenesis and therapeutics. Here, we evaluated the impact of

SIRT3 in PD cognitive deficits including hippocampal synaptic and neural network impairments in PD mouse models. First,

we compared hippocampal synaptic function between SIRT3 KO and WT mice, and found that 4-month-old SIRT3 KO mice

showed deficits of hippocampal functions including impaired both hippocampal CA1 LTP maintenance and fEPSP amplitude

after 40 Hz stimulation for 4 seconds. Second, we found that hippocampal theta oscillations (induced by 50 µM CCh) and

gamma oscillations (induced by 100 Hz stimulation for 200 ms) were significantly impaired in SIRT3 KO mice compared to

WET mice. Third, when mice were treated with low dose rotenone (RTN, 0.8 mg/k.g., i.p. for 7 days), WT mice did not show

detectable change of synaptic function and network synchronizations, while SIRT3 KO mice showed impaired hippocampal

CA1 region PPF, LTP and gamma oscillations. Finally, mitochondrial dysfunction in hippocampal slices can be restored by

SIRT3 activator, ketone. Collectively, our data suggest an important role played by SIRT3 in hippocampal synaptic and neural

network function, which may underlie the cognitive deficits in PD.

Biography

Jie Wu has completed his PhD from Sun-Yat Sen University of Medical Sciences, China in 1990 and Post-doctoral studies from Tohoku University, Japan and

New Mexico University School of Medicine, USA between 2013 and 2017. Now, he is a Professor and the Director of Neurophysiological Laboratory at Barrow

Neurological Institute, St. Joseph’s Hospital. He has published more than 140 papers in reputed journals with total citation of 2,883, h-index 31 and i10 index 82.

He has been serving as an Editor in Chief and Editorial Board Member of repute.

Jie.Wu@DignityHealth.org