kineticz
Member
Understanding ketogenesis, mitochondria and ATP production
I repeat a missing piece of context.
Even if cells can replicate indefinitely, this does not solve the issue of brain ATP and undermethylation.
High oxidative stress, due to low ATP and low glutathione, will promote angiotensin and toxify cells. The phospholipid exchange breaks the deadlock because it gives the signal that the brain, combined with magnesium, is becoming less calcified.
Hence your liver can start making it's own glutathione again.
Also, Humans are not tightly regulated like insects or petri-dishes. We have information overload, and a huge amount of toxic factors due to capitalism.
Mammals might benefit from 'superior brains', because the point of the phospholipid exchange isn't a high PUFA diet, it's to improve brain ATP.
Notice how he said extremely small amount, rather than zero. The brain myelin sheath only needs a very small amount, especially when you are methylating properly.
I repeat a missing piece of context.
Even if cells can replicate indefinitely, this does not solve the issue of brain ATP and undermethylation.
High oxidative stress, due to low ATP and low glutathione, will promote angiotensin and toxify cells. The phospholipid exchange breaks the deadlock because it gives the signal that the brain, combined with magnesium, is becoming less calcified.
Hence your liver can start making it's own glutathione again.
Also, Humans are not tightly regulated like insects or petri-dishes. We have information overload, and a huge amount of toxic factors due to capitalism.
Mammals might benefit from 'superior brains', because the point of the phospholipid exchange isn't a high PUFA diet, it's to improve brain ATP.
Notice how he said extremely small amount, rather than zero. The brain myelin sheath only needs a very small amount, especially when you are methylating properly.