English is not my native language, but I am going to put this the best way so it seems understanable that maybe a different way to use novel substances to boost brain power, than trying to supplement and "push" the brain for increased energy or neural growth. I am not sure if something similar has been discussed before, but I would appreciate any input even speculative on the nature of regular short-term mental exsaustion and how this may affect maximum brain development in the long-term.
This is my first post, I cannot add links, so I would copy/paste two articles and a part from wikipedia for the quite interesting for me Myostatin.
1. Does Thinking Really Hard Burn More Calories? An online article from scientific American. It gives current research that glucose depletion does not seem to be a major issue with mental exsaustion. Especially telling (at least for my thinking) is the last paragraph in the end of the article.
"My general hypothesis is that the brain is a lazy bum," he says. "The brain has a hard time staying focused on just one thing for too long. It's possible that sustained concentration creates some changes in the brain that promote avoidance of that state. It could be like a timer that says, 'Okay you're done now.' Maybe the brain just doesn't like to work so hard for so long."
Myostatin, and why everyone could possibly have the body of a bodybuilding champion.
I have read a bit about myostatin and its effects on body composition and is interesting from an evolutionary point of view, I was wondering if something similar applies on "brain composition", that is a natural brake in brain's possibly maximum development.
A paragraph from wikipedia follows
Clinical research
Further research into myostatin and the myostatin gene may lead to therapies for muscular dystrophy.[21][22] The idea is to introduce substances that block myostatin. A monoclonal antibody specific to myostatin increases muscle mass in mice.[23] Similar results in monkeys were obtained.[5]
A two-week treatment of normal mice with soluble activin type IIB receptor, a molecule that is normally attached to cells and binds to myostatin, leads to a significantly increased muscle mass (up to 60%).[24] It is thought that binding of myostatin to the soluble activin receptor prevents it from interacting with the cell-bound receptors.
It remains unclear as to whether long-term treatment of muscular dystrophy with myostatin inhibitors is beneficial, as the depletion of muscle stem cells could worsen the disease later on. As of 2012[update], no myostatin-inhibiting drugs for humans are on the market, but an antibody genetically engineered to neutralize myostatin was developed by New Jersey pharmaceutical company Wyeth.[25] The inhibitor is called MYO-029, but, after an initial clinical trial, Wyeth says they will not be developing the drug.[26] Some athletes, eager to get their hands on such drugs, turn to the internet, where fake "myostatin blockers" are being sold.[5]
Myostatin levels are effectively decreased by creatine supplementation.[27][not in citation given]
A technique for detecting mutations in myostatin variants has been developed.
Myostatin seems to be an "evolutionary brake", in developing too much mass for the organism to sustain through food intake. I was wondering if there is a similar mechanism that put "brakes" on short-term brain endurance and most importantly for the long term maximum possible brain development. Searching online I found the article below that is close to the logic here.
Boston, MA-Scientists at Schepens Eye Research Institute have identified specific molecules in the brain that are responsible for awakening and putting to sleep brain stem cells, which, when activated, can transform into neurons (nerve cells) and repair damaged brain tissue. Their findings are published online this week in the Proceedings of the National Academy of Science (PNAS).
An earlier paper (published in the May issue of Stem Cells) by the same scientists laid the foundation for the PNAS study findings by demonstrating that neural stem cells exist in every part of the brain, but are mostly kept silent by chemical signals from support cells known as astrocytes.
"The findings from both papers should have a far-reaching impact," says principal investigator, Dr. Dong Feng Chen, who is an associate scientist at Schepens Eye Research Institute and an assistant professor of ophthalmology at Harvard Medical School. Chen believes that tapping the brain¹s dormant, but intrinsic, ability to regenerate itself is the best hope for people suffering from brain-ravaging diseases such as Parkinson¹s or Alzheimer¹s disease or traumatic brain or spinal cord injuries.
Until these studies, which were conducted in the adult brains of mice, scientists assumed that only two parts of the brain contained neural stem cells and could turn them on to regenerate brain tissue-- the subgranular zone (SGZ) of the hippocampus and the subventricular zone (SVZ). The hippocampus is responsible for learning and memory, while the SVZ is a brain structure situated throughout the walls of lateral ventricles (part of the ventricular system in the brain) and is responsible for generating neurons reponsible for smell. So scientists believed that when neurons died in other areas of the brain, they were lost forever along with their functions.
In the second (PNAS) study, the team went on to discover the exact nature of those different chemical signals. They learned that in the areas where stem cells were sleeping, astrocytes were producing high levels of two related molecules--ephrin-A2 and ephrin-A3. They also found that removing these molecules (with a genetic tool) activated the sleeping stem cells.
The team also found that astrocytes in the hippocampus produce not only much lower levels of ephrin-A2 and ephrin-A3, but also release a protein named sonic hedghoc that, when added in culture or injected into the brain, stimulates neural stem cells to divide and become new neurons.
The eventual development of techniques to create youthful neural stem cells will provide stem cells that can be safely stimulate to grow without running a cancer risk. But How to replace the old stem cells with young ones? It is not enough to add the newer younger stem cells to the brain (and just getting the new stem cells into all the spots in the brain they need to go is a challenge). We need to get rid of the old stem cells so that a drug that boosts stem cell growth will only stimulate the new stem cells and not the old stem cells too.
I wrote a post back in November 2004 about the ability of sonic hedgehog to triple brain stem cell growth. The use of sonic hedgehog for this purpose is well known among the researchers in this area.
The point I am trying to make is that by inhibiting chemicals in the brain that make us "mentally lazy" and stop neural growth, and by taking the time to work even more intensely in our interests, we could train our brain much more efficiently, having long term advantages in brain boosting effects and better mastery in our fields or hobbies.