A talk on A short intracerebroventricular mTOR Inhibitors causes complete and long-lasting cognitive recovery in an animal model of #Alzheimer #Disease #Neuroscience #Conference June 18-19,2018 #Rome #Italy.
For more details visit – https://bit.ly/2uelcLc
Limited speaker slots available…
Neuroscience 2018 proudly announces #Bence Andras as an invited Speaker for the conference Annual Congress on Advancements in Neurology and Neuroscience scheduled on June 18-19, 2018 at #Rome, #Italy.
What Causes Prion Disease?
Prion diseases are associated with the build up in the brain (and some other organs) of an abnormal or ‘rogue’ form of a naturally occurring cellular protein, known as the prion protein. The rogue protein results from a change in shape of the normal prion protein. Once formed in the body these rogue proteins recruit and convert more of the normal prion protein into the abnormal form, setting off a kind of chain reaction which leads to a progressive accumulation of the rogue protein. In the normal course of events, once they have served their purpose, prion proteins are broken down by enzymes in the body. The abnormal prions however are more resistant to this process; so they accumulate and cause damage in the brain, which interferes with normal brain functioning. All forms of the disease are thought to be associated with an incubation period. This is a clinically ‘silent phase’ during which replication of the rogue protein is thought to be taking place.
At a particular position in the prion gene known as codon 129, there are two possible genetic types, which in turn specify the body to produce different amino acids at this position. These amino acids are called methionine and valine, or M and V for short. In most countries, MM and MV frequencies in the population are roughly equal (40-50%). It has been known for some years that individuals, who are MV, are at much less risk of developing prion disease than are MM or VV individuals .
Prion diseases, also known as transmissible spongiform encephalopathies (TSE’s) are a group of progressive neurodegenerative conditions. These illnesses exist in both animals and humans. Scrapie, a disease affecting sheep and goats, was the first prion disease to be identified in the 1730s.
Most cases of prion disease are sporadic; that is, they arise spontaneously for no known reason. More rarely prion disease is inherited due to a faulty gene, or acquired by medical procedures, transfusions, or contaminated food. Sporadic and inherited prion disease occurs worldwide in all populations. The incidence of sporadic CJD is around 1 per million of the population per annum; males and females are equally affected. The incidence of the various acquired prion diseases, however, is more localised to specific groups and populations.
Stay tuned to know more about Prion Disease ..
1.9 million #brain #cells are destroyed every minute after a #stroke
Here’s how much stroke would be reduced if each were eliminated:
Physical inactivity 35.8%
Lipids (blood fats) 26.8%
Poor diet 23.2%
#Heart causes 9.1%
#Alcohol intake 5.8%
Learn more facts presented in live at : https://bit.ly/2IJPs6s