Scientists stop brain cells in mice from dying in potential Alzheimer's treatment breakthrough

How closely is your doctor following up with this research to prevent your 33% chance of developing Dementia/Alzheimers after a stroke.?
The Fox news article here;
http://www.foxnews.com/health/2013/10/10/scientists-stop-brain-cells-in-mice-from-dying-in-potential-alzheimer-treatment/
The abstract here;
Oral Treatment Targeting the Unfolded Protein Response Prevents Neurodegeneration and Clinical Disease in Prion-Infected Mice

1. Julie A. Moreno¹,
2. Mark Halliday¹,
3. Colin Molloy¹,
4. Helois Radford¹,
5. Nicholas Verity¹,
6. Jeffrey M. Axten²,
7. Catharine A. Ortori³,
8. Anne E. Willis¹,
9. Peter M. Fischer⁴,
10. David A. Barrett³ and
11. Giovanna R. Mallucci¹,*

+ Author Affiliations

1. ¹MRC Toxicology Unit, Hodgkin Building, University of Leicester, Lancaster Road, Leicester LE1 9HN, UK.
2. ²GSK Oncology, GlaxoSmithKline, 1250 South Collegeville Road, Collegeville, PA 19426, USA.
3. ³Centre for Analytical Bioscience, School of Pharmacy, University of Nottingham, Nottingham NG7 2RD, UK.
4. ⁴Division of Medicinal Chemistry and Structural Biology, School of Pharmacy, Centre for Biomolecular Sciences, University of Nottingham, Nottingham NG7 2RD, UK.

1. ↵*Corresponding author. E-mail: grm7@le.ac.uk

Abstract

During prion disease, an increase in misfolded prion protein (PrP) generated by prion replication leads to sustained overactivation of the branch of the unfolded protein response (UPR) that controls the initiation of protein synthesis. This results in persistent repression of translation, resulting in the loss of critical proteins that leads to synaptic failure and neuronal death. We have previously reported that localized genetic manipulation of this pathway rescues shutdown of translation and prevents neurodegeneration in a mouse model of prion disease, suggesting that pharmacological inhibition of this pathway might be of therapeutic benefit. We show that oral treatment with a specific inhibitor of the kinase PERK (protein kinase RNA–like endoplasmic reticulum kinase), a key mediator of this UPR pathway, prevented UPR-mediated translational repression and abrogated development of clinical prion disease in mice, with neuroprotection observed throughout the mouse brain. This was the case for animals treated both at the preclinical stage and also later in disease when behavioral signs had emerged. Critically, the compound acts downstream and independently of the primary pathogenic process of prion replication and is effective despite continuing accumulation of misfolded PrP. These data suggest that PERK, and other members of this pathway, may be new therapeutic targets for developing drugs against prion disease or other neurodegenerative diseases where the UPR has been implicated.