Scientists developed drug which could be used to treat brain disorders
Scientists on Thursday said they had a drug that in mice helped prevent prion disease and may also work on Alzheimer\'s, Parkinson\'s and other brain disorders that share a similar mechanism. Still at a very early and experimental stage
, the drug blocks disruption of the brain\'s defence system, something that boosts neurodegenerative disease.
Many of these crippling and tragic diseases start with the buildup of rogue, scrunched-up proteins in the brain.
The organ\'s response to this is to switch on a defence mechanism called the unfolded protein response, or UPR.
The mechanism orders cells to stop producing new proteins so that the problem is not worsened.
But the buildup of misshapen proteins prevents the UPR mechanism from being switched off.
As a result, the misshapen proteins are no longer made -- but nor are normal proteins that are essential for brain-cell survival. Neurons start to die, are not replenished, and the disease progresses.
British researchers, reporting in the US journal Science Translational Medicine, tested a drug that works on a key point in this switching pathway, an enzyme called PERK, to keep protein production open.
Known by its lab name as GSK2606414 -- it is made by British drugmaker GlaxoSmithKline -- the drug was tested on 29 mice with prion disease, a family of disorders that includes Creuzfeldt-Jakob disease.
These were compared against a group of \"control\" mice, whose brain had also been infected with prions but did not receive the drug.
Mice that were treated seven weeks after being infected with the prions suffered no memory loss in a test to recognise a familiar object, but those treated at nine weeks lost their memory.
The mice were killed and autopsied, and examination of samples under a microscope confirmed that brain-cell death among all the treated mice was very low, although less so among the nine-week group.
The University of Leicester team say they are hugely buoyed by the success, although many more years of tests lie ahead.
\"We were extremely excited when we saw the treatment stop the disease in its tracks and protect brain cells, restoring some normal behaviours and preventing memory loss in the mice,\" said Giovanna Mallucci, a professor of toxicology.
\"We\'re still a long way from a usable drug for humans ? this compound had serious side effects,\" Mallucci told Britain\'s Press Association.
\"But the fact we have established that this pathway can be manipulated to protect against brain cell loss, first with genetic tools and now with a compound, means that developing drug treatments targeting this pathway for prion and other neurodegenerative diseases is now a real possibility.\"
If the drug eventually progressed to human patients, people would need treatment \"for years or even decades in many cases,\" the study also cautioned.
In a commentary carried in the same journal, neuroscientists Wiep Scheper and Jeroen Hoozemans of the Free University of Amsterdam said the research may have thrown open \"a new therapeutic strategy.\"
They too urged caution, saying that mouse models designed to replicate human brain disease had limitations, and in humans, loss of the PERK enzyme also had side-effects in promoting diabetes and skeletal defects.
Source: AFP
GMT 07:36 2018 Sunday ,21 January
Black NASA astronaut is replaced in sudden crew shuffleGMT 07:48 2018 Sunday ,14 January
Top takeaways from Consumers Electronics ShowGMT 09:06 2018 Thursday ,11 January
Travis the translator aims to make people understoodGMT 08:48 2018 Tuesday ,09 January
Tech faithful gather to worship at mecca of innovationGMT 10:56 2018 Friday ,05 January
Struggling Westinghouse Electric sold to Brookfield for $4.6 bnGMT 08:32 2018 Thursday ,04 January
High-tech ship en route to resume hunt for MH370GMT 08:20 2017 Sunday ,31 December
Apple apologizes for slowing iPhones, offers discounted batteriesGMT 08:33 2017 Friday ,29 December
Apple, Epson face French legal pressureMaintained and developed by Arabs Today Group SAL.
All rights reserved to Arab Today Media Group 2023 ©
Maintained and developed by Arabs Today Group SAL.
All rights reserved to Arab Today Media Group 2023 ©