This proposal is a competitive renewal application in which in the previous cycle we demonstrated that both protein kinase C epsilon (PKCe) and resveratrol emulated ischemic preconditioning (IPC) in brain and that IPC, PKCe and resveratrol upregulate BDNF levels, which played a key role in neuroprotection. We also demonstrated that IPC and resveratrol preconditioning (RPC) induced neuroprotection via SIRT1 activation. SIRT1 activates hypoxia inducible factor-2 alpha (HIF-2?) 1 and Akt 2, transcription factors involved in other preconditioning pathways 3,4,5 and is also known to play a role in epigenetics. Epigenetic changes have been suggested to play a key role in preconditioning 6,7. We now present evidence that RPC neuroprotection lasts at least 14 days and that SIRT1 brain levels are elevated during that time. Resveratrol has previously been shown to be neuroprotective against cerebral ischemia activating many pathways that protect mitochondria 8 and promote angiogenesis 9 to name a few. The main goals of the new funding cycle are to define the specific molecular targets of IPC that promote ischemic tolerance and to further define the molecular mechanisms of a chronic ischemic tolerant state.
The specific aims are 1) to define the maximum window of neuroprotection against cerebral ischemia afforded by resveratrol preconditioning (RPC); 2) to define whether this extended window of neuroprotection by RPC against cerebral ischemia is SIRT1 dependent; 3) to determine mechanisms by which RPC promotes ischemic tolerance in the delayed window; and 4) to define the molecular underpinnings of the long-term neuroprotection conveyed by RPC.

Public Health Relevance

Stroke remains a leading cause of death and disability in the US with only 1 clinically approved treatment for the most common form, ischemic stroke. Given that a host of post-stroke treatments have failed in clinical trials, an alternative approach is prophylactic treatments for patients with cardiovascular disease and high stroke risks. This proposal will study new potential mechanisms and treatments for prophylactic treatments for stroke.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS034773-18
Application #
9502402
Study Section
Brain Injury and Neurovascular Pathologies Study Section (BINP)
Program Officer
Bosetti, Francesca
Project Start
1997-05-01
Project End
2020-05-31
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
18
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Miami School of Medicine
Department
Neurology
Type
Schools of Medicine
DUNS #
052780918
City
Coral Gables
State
FL
Country
United States
Zip Code
33146
Ding, Di; Enriquez-Algeciras, Mabel; Valdivia, Anddre Osmar et al. (2018) The Role of Deimination in Regenerative Reprogramming of Neurons. Mol Neurobiol :
Narayanan, Srinivasan V; Dave, Kunjan R; Perez-Pinzon, Miguel A (2018) Ischemic Preconditioning Protects Astrocytes against Oxygen Glucose Deprivation Via the Nuclear Erythroid 2-Related Factor 2 Pathway. Transl Stroke Res 9:99-109
Xu, Jing; Jackson, Charlie W; Khoury, Nathalie et al. (2018) Brain SIRT1 Mediates Metabolic Homeostasis and Neuroprotection. Front Endocrinol (Lausanne) 9:702
Jackson, Charles W; Escobar, Iris; Xu, Jing et al. (2018) Effects of ischemic preconditioning on mitochondrial and metabolic neruoprotection: 5' adenosine monophosphate-activated protein kinase and sirtuins. Brain Circ 4:54-61
Stradecki-Cohan, Holly M; Youbi, Mehdi; Cohan, Charles H et al. (2017) Physical Exercise Improves Cognitive Outcomes in 2 Models of Transient Cerebral Ischemia. Stroke 48:2306-2309
Cohan, Charles H; Stradecki-Cohan, Holly M; Morris-Blanco, Kahlilia C et al. (2017) Protein kinase C epsilon delays latency until anoxic depolarization through arc expression and GluR2 internalization. J Cereb Blood Flow Metab 37:3774-3788
Koronowski, Kevin B; Khoury, Nathalie; Saul, Isabel et al. (2017) Neuronal SIRT1 (Silent Information Regulator 2 Homologue 1) Regulates Glycolysis and Mediates Resveratrol-Induced Ischemic Tolerance. Stroke 48:3117-3125
Narayanan, Srinivasan V; Perez-Pinzon, Miguel A (2017) Ischemic preconditioning treatment of astrocytes transfers ischemic tolerance to neurons. Cond Med 1:2-8
Khoury, Nathalie; Koronowski, Kevin B; Perez-Pinzon, Miguel A (2016) Long-term window of ischemic tolerance: An evolutionarily conserved form of metabolic plasticity regulated by epigenetic modifications? J Neurol Neuromedicine 1:6-12
Morris-Blanco, Kahlilia C; Dave, Kunjan R; Saul, Isabel et al. (2016) Protein Kinase C Epsilon Promotes Cerebral Ischemic Tolerance Via Modulation of Mitochondrial Sirt5. Sci Rep 6:29790

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