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, October 4, 2022

Integrity of neuronal size in the entorhinal cortex is a biologic substrate of exceptional cognitive aging

What is your doctor doing to test this in you, AND WHAT PROTOCOLS ARE GIVEN to increase this integrity. No protocols, you don't have a functioning stroke doctor.

Integrity of neuronal size in the entorhinal cortex is a biologic substrate of exceptional cognitive aging

Caren Nassif, Allegra Kawles, Ivan Ayala, Grace Minogue, Nathan P. Gill, Robert A. Shepard, Antonia Zouridakis, Rachel Keszycki, Hui Zhang, Qinwen Mao [MD, PhD], Margaret E. Flanagan [MD], Eileen H. Bigio [MD], M.-Marsel Mesulam [MD], Emily Rogalski [PhD], Changiz Geula [PhD] and Tamar Gefen [PhD]

Abstract

Average aging is associated with a gradual decline of memory capacity. SuperAgers are humans over age 80 who show exceptional episodic memory at least as good as individuals 20-30 years their junior. This study investigated whether neuronal integrity in entorhinal cortex (ERC), an area critical for memory and selectively vulnerable to neurofibrillary degeneration, differentiated SuperAgers from cognitively-healthy younger individuals, cognitively-average peers (“Normal Elderly”), and individuals with amnestic Mild Cognitive Impairment (aMCI). Postmortem sections of the ERC were stained with cresyl violet to visualize neurons, and immunostained with PHF-1 to visualize neurofibrillary tangles. The cross-sectional area (i.e., size) of layer II and layer III/V ERC neurons were quantified. Two-thirds of total participants were female. Unbiased stereology was employed to quantitate tangles in a subgroup of SuperAgers and Normal Elderly. Linear mixed-effect models were used to determine differences across groups. Quantitative measurements found the soma size of layer II ERC neurons in post-mortem brain specimens were significantly larger in SuperAgers compared to all groups (p<0.05)—including younger individuals 20-30 their junior (p<0.005). SuperAgers had significantly fewer stereologically quantified AD-related neurofibrillary tangles in layer II ERC than Normal Elderly (p<0.05). This difference in tangle burden in layer II between SuperAgers and Normal Elderly suggest that tangle-bearing neurons may be prone to shrinkage during aging. The finding that SuperAgers show ERC layer II neurons that are substantially larger even compared to individuals 20-30 years younger is remarkable, suggesting that layer II ERC integrity is a biologic substrate of exceptional memory in old age.

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