Brain memory storage

Blood glucose levels appear to directly influence brain memory storage (Koehn and Hilbish, 1987). Adrenaline, because it influences blood glucose concentration, also has an effect on memory retention. 

New codes with huge memory storage controlling flow in brains ... 

Bontempi, B., Luanrant-Demir, C., Destrade, C. and Jaffard, R. Time-dependent reorganization of brain-circuitry underlying long-term memory storage. Nature 400 671-675,1999. 

Dalmaz C, Introini-CoUison IB, McGaugh JL. 1993. Noradrenergic and cholinergic interactions in the amygdala and the modulation of memory storage. Behav Brain Res 58(1-2) 167-174. 

Martinez JL, Jensen RA, Messing RB, Vasquez BJ, Soumireu-Mourat B, Gedden D, Liang KC, McGaugh JL (1980) Central and peripheral actions of amphetamine on memory storage. Brain Res 182 151-116. 

We have found [1] that orthogonalization of the correlated vectors not only takes care of the above problem very effectively but also gives vital insight into the phenomenon of memory storage in the brain. The orthogonalization process in fact acts like a decision making process wherein when a new object is compared with the stored ones, the nature of its correlation with them decides, in an efficient (or economical) manner, in what form it should be stored. The noise is also eliminated using this approach. 

The sheer quantity of medical information, even within a single speciality, is often beyond the power of one person to comprehend. People, that is, the human brain, simply cannot cope with the amoimt of information that they need to function safely and effectively. For instance, more than 600 drugs require adjustment of doses for multiple levels of renal dysfunction an easy task for a computer, but one which will inevitably be performed poorly by a person (Bates and Gawande, 2003). Machines can therefore aa as a kind of extended memory, which we can access at will, to overcome the transience and limitations of human memory storage. However, these are not the only problems of memory there are other limiting factors which are not always appreciated. 

The newborn rat is a natural split-brain preparation for olfactory learning protocols it can be trained to associate an odor with a milk reward via just one nostril. If the other nostril is tested, the animal shows no preference. However, at 12 days of age or later, the two sides of the brain are connected and a learned preference occurs with either nostril open. The information is stored M/nlaterally the animal shows unilateral preference if the commissure is cut after training. The maturation of the commissure pathways occurs between 6 and 12 days of age. In summary, unilaterally represented memories remain unilateral, even after bilateral retrieval processes have developed. The mnemonic storage capacity of the brain is increased by confining memory to one side (Kucharski and Hall, 1987). 

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