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.

Saturday, May 21, 2016

Black sugarcane decoction reduces rat brain ischemia

Further research would be needed to see if this delivered in the hyperacute stage would reduce ischemia. But that will never occur, we have NO fucking stroke leadership or strategy.
http://www.univmed.org/ejurnal/index.php/medicina/article/view/142 
 
ety sari handayani, zainuri sabta nugraha, Titis Nurmasitoh, Kuswati Kuswati, Dwi N. Ahsani, Ajeng G. Nanda

Abstract


Background
There are people in Yogyakarta, who use black sugarcane decoction (BSD) to prevent stroke. BSD contains policosanol and antioxidants. It has been proven that policosanol can reduce global ischemia in Mongolian gerbils. This study aims to evaluate the effect of BSD on brain ischemia in a rat stroke model.

Methods
A laboratory experiment using eighteen 3-month old male Wistar rats without any defects, of 175-250 g body weight. Brain ischemia was produced by a 20-minute bilateral carotid artery ligation (BCAL). Using a rat stroke model, brain ischemia was produced by a 20-minute bilateral carotid artery ligation (BCAL). The rats were randomized into three groups: BSD treated stroke model rats (group 1), non treated stroke model rats (group 2), and sham operated rats (group 3). BSD was administered by gavage for 1 week before BCAL. Decapitation of rats was performed two hours post BCAL. Brain tissues were stained with 2,3,5-triphenyltetrazolium chloride (TTC). Ischemic areas were analyzed using Image J softwere. Statistical analysis was conducted by one way ANOVA test.

Results
The mean percentages of rat brain ischemic area differed between group 3 (0.0 ± 0.0 %), group 2 (3.13 ± 0.59 %) and group 1 (1.15 ± 0.47 %) p =0.001). Post hoc test showed that there was no difference between group 3 with group 1. Instead, there was a significant difference between group 2 and the other groups.

Conclusion
The administration of BSD reduced rat brain ischemia after bilateral carotid artery ligation.

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