Prion protein protects against epilepsy
News Jul 09, 2015
Neuroprotective role of PrPC confirmed with unprecedented accuracy
In the most systematic and rigorous study conducted thus far in its field, the Prion Protein (PrPC) has been clearly shown to play a role in preventing the onset of epileptic seizures. PrPC is perhaps best known in its "degenerate" form, the prion, and an infectious agent behind dangerous neurodegenerative diseases such as mad cow disease (bovine spongiform encephalopathy). The study, is published in the journal Scientific Reports.
For some time, scientists have been wondering what the physiological role of PrP is in its normal physiological state. Previous studies suggested that among its functions, one was preventing the onset of seizure discharges in the brain (most likely by modulating the action of specific synaptic channels). However, some scientists had questioned the validity of the research. "The idea in the past was that animal models were not specific enough and that the observations were the product of systematic, experimental error," says Prof. Giuseppe Legname of the International School for Advanced Studies (SISSA) of Trieste. Legname is one of the authors of the new study. "With our work we wanted to dispel any doubt. We used 4 animal models to really test the hypothesis of the neuroprotective function of PrPC against epilepsy. " The Result? "PrPC definitely plays a role in preventing seizures and, when it is lacking, they are much more frequent."
This study has now become an important point of reference in the field: "So far no one else has used this much precision and this large of a case series. The study is also significant in terms of collaboration between international institutes: along with SISSA, the University of Barcelona, the German Centre for Neurodegenerative Diseases of Göttingen, as well as other Spanish institutes," says Legname. "Of course we have no intention to stop here: we are already improving results with a new model we developed using more advanced and precise genetic techniques that can selectively turn off the Prion Protein alone."
Note: Material may have been edited for length and content. For further information, please contact the cited source.
del Río JA et al. Involvement of PrPC in kainate-induced excitotoxicity in several mouse strains. Scientific Reports, Published July 9 2015. doi: 10.1038/srep11971
All in a Droplet: Atomic Resolution of ALS Protein ResolvedNews
Researchers have described atom-by-atom changes in a family of proteins linked to amyotrophic lateral sclerosis (ALS), a group of brain disorders known as frontotemporal dementia and degenerative diseases of muscle and bone.READ MORE
Pupil Size Couples to Cortical States to Protect Deep Sleep StabilityNews
Researchers have found that mice pupil size fluctuates during sleep. They also show that pupil size is a reliable indicator of sleep states.READ MORE
A Place to Think: Persistent neuronal activity in human prefrontal cortex links perception and actionNews
Neuroscientists have tracked the progress of a thought through the brain, showing clearly how the prefrontal cortex at the front of the brain coordinates activity to help us act in response to a perception.READ MORE