Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Tuesday, December 20, 2016

Study finds natural compound extends lifespan of worms

Don't make the leap of judgement that this will help humans. That will require quite a bit of research, unlikely to ever occur with no government funding and our fucking failures of stroke associations not stepping up to fill that funding gap.
https://www.mdlinx.com/family-medicine/top-medical-news/article/2016/12/20/7
Vanderbilt University Medical Center Research News
A compound found in buckwheat seeds extends the lifespan of worms, Vanderbilt investigators have discovered. They reported in the journal Aging that C. elegans worms consuming salicylamine – a compound that inactivates molecules called isoketals – live longer healthy lives compared to worms not receiving the compound.

The findings support the idea that oxidative damage produced by compounds including isoketals contributes to aging–related tissue damage and death.

“There’s a notion that we’re slowly oxidizing ourselves to death,” said L. Jackson Roberts, MD, professor of Pharmacology and Medicine. “If we could overcome that, we predict we would have a longer lifespan.”

Roberts, who is also the William Stokes Professor of Experimental Therapeutics, and his colleagues previously identified isoketals as products of lipid oxidation. The highly reactive isoketals are formed during normal cell metabolism, and they bind to and disrupt the function of proteins and DNA. Isoketal–modified proteins are increased in atherosclerosis, Alzheimer’s disease, hypertension and end–stage renal disease.

“With every breath, we’re generating molecules that can potentially damage us,” said Thuy Nguyen, PhD, who conducted the current studies as a graduate student working with Roberts and Michael Aschner, PhD, at Albert Einstein College of Medicine.

Roberts and his colleagues had discovered that the natural product salicylamine scavenges reactive isoketals and prevents them from damaging proteins.

In the current studies, the researchers found that treating adult worms with salicylamine increased the worms’ median lifespan from 16 to 25 days. They also demonstrated that the longer–lived worms were healthy. Salicylamine reduced the accumulation of fluorescent lipids – worm “age spots” – and slowed the age–related decline in pharyngeal pumping rate, a measure of food consumption.

To explore how salicylamine extended lifespan, Nguyen and colleagues focused on molecular pathways implicated in longevity in C. elegans. They showed that the sirtuin SIR–2.1 was required for salicylamine action and that salicylamine works at the protein level rather than at the genome level.

Future studies will focus on which proteins — in addition to SIR–2.1 — are being protected by salicylamine.

In contrast to many studies, which have used genetic tools or altered developmental pathways to extend lifespan, salicylamine is a pharmacologic intervention that can be started in adulthood, Nguyen said.

In previous studies, the researchers demonstrated that salicylamine prevented age–related deficits in working memory in a mouse model of Alzheimer’s disease. Mice consumed salicylamine for more than a year and did not exhibit any adverse side effects, Roberts said.

Metabolic Technologies Inc., a natural products company co–founded by Vanderbilt faculty member Naji Abumrad, MD, expects to market salicylamine as a natural supplement in the next few months. Roberts is convinced it will prevent oxidative damage and extend healthy life.

“I think everyone should take this compound,” he said.

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