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.

Sunday, June 15, 2025

Aspartate in the Brain: A Review

 Ask your competent? doctor what will be done with this knowledge to get you recovered. NOTHING, LIKE USUAL? 

All this earlier research which I bet your doctor knows nothing!

  • arginine (2 posts to December 2016)
  • arginine-rich peptides (1 post to February 2015)
  • Cationic arginine-rich peptides (1 post to March 2020)
  • poly-arginine peptides (1 post to February 2015)
  • beta-amyloid peptides (2 posts to February 2019)
  • nitric oxide (120 posts to March 2011)
  • endothelial nitric oxide (2 posts to January 2019)
  • Do you prefer your doctor and hospital incompetence NOT KNOWING? OR NOT DOING?

    Aspartate in the Brain: A Review

    Review
  • Open access
  • Published:
  • Volume 50, article number 199, (2025)Cite this articleDownload PDF

    You have full access to this open access article

    Abstract

    l-Aspartate (aspartic acid; C4H7NO4; 2-aminobutanedoic acid) is a non-essential α-amino acid found ubiquitously throughout the body, including in the brain. Aspartate is one of the protein-forming amino acids and the formation of tRNA-aspartate complex is catalysed by aspartyl tRNA synthetase. Free aspartate, which is the main subject of this review, plays key roles in metabolism, as an amino donor and acceptor. It contributes to the synthesis of protein, arginine and nitric oxide, asparagine, N-acetylaspartate and N-methyl-d-aspartate. Its major metabolic role in the brain is recycling reducing equivalents (protons) between the cytoplasm and mitochondrial matrix as part of the malate-aspartate shuttle. l-Aspartate’s actions on synaptic receptors, as well as its possible presence in nerve terminals and synaptic vesicles, are, in principle, consistent with a role as an excitatory neurotransmitter. The evidence is far from conclusive and at times controversial. The role of d-aspartate in brain function is even less certain but, it appears that, rather than being a minor neurotransmitter, d-aspartate is more likely to be involved in fine regulation of endocrine and homeostatic processes. Much research remains to be done in this area. The diversity of its functions and chemistry make aspartate a complex molecule to investigate and measure in vivo. Perturbations of aspartate metabolism have been described in a range of neurological deficits, particularly those of white matter. Here, we examine what is known about the various roles of aspartate in brain, its metabolism, transport and compartmentation, its role as a neurotransmitter or a more general signalling molecule, and what is currently known about its role(s) in disease processes.

    More at link.

    Malate Aspartate Shuttle—Linkage to Phosphorylation State

    The malate-aspartate shuttle (Fig. 1) plays a major role in the movement of reducing equivalents (NADH) into, or out of, the mitochondrion.

    Fig. 1
    figure 1

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