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Individuals with Alzheimer’s have alterations in the BBB where they have
increased permeability which therefore allows greater stress on the brain (12).
This happens through 3 major mechanisms
1) Hypoglycemia: Low blood sugar causes a partial starvation of the brain
tissue and the body responds by opening up the BBB to allow for more
nutrients to cross. This also allows for more toxins and oxidative stress to
effect brain tissue (13).
2) Hyperglycemia: High blood sugar causes more oxidative stress that
damages the endothelial lining of the BBB, weakening this protective shield
and making it more permeable to larger compounds. This causes increased
stress on the brain tissue and leads to insulin resistance in the brain.
Increased insulin levels are associated with the neurofibrillary tangles and
amyloid plaque found in Alzheimer’s disease (14, 15).
3) Magnesium Deficiency: Blood sugar imbalances deplete magnesium and
many B vitamin stores in the body. Magnesium plays a key role in the
capillary tone of the endothelial membrane. Magnesium deficiency weakens
the endothelial lining and makes it more permeable to heavy metals such as
aluminum which is classically found in Alzheimer’s disease (16, 17, 18).
The MicroBiome and Alzheimer’s
There has been a tremendous amount of research linking the gut microbiome
and neurological health. Research has indicated that low levels of healthy
lactobacillus and bifidobacterium are linked with increased brain excitability
and neurological inflammation (19, 20).
These microbes help to break down the excititory neurotransmitter glutamate
into the inhibitory neurotransmitter GABA. Low levels of GABA production
are associated with anxiety, seizures, depression, dementia and Alzheimer’s
(21, 22).
Additionally, it has been shown that some microbes secrete amyloid as a
byproduct of their metabolism. This endotoxin is linked to the pathogenesis
of Alzheimer’s disease. It is thought that high levels of amyloid producing
bacteria are a significant factor in the development of Alzheimer’s (23, 24).
Aluminum and Alzheimer’s:
Aluminum is found in high amounts within the neurofibrillary tangles of
Alzheimer’s disease patients. How does it get in there? Through a
combination of blood sugar dysregulation, gut dysbiosis and chronic
inflammation and environmental aluminum exposure.
Aluminum is used in the processing of many different industrial products.
We are exposed to aluminum in vaccines, deoderants, medications, canned
foods and tap water. Aluminum has an affinity for brain tissue due to 2 major
mechanisms (25, 26, 27)
1) Slow Absorption and Uptake Rates: Because aluminum is absorbed by
the body slowly and the uptake into the brain is progressive, many scientists
believe it is a safe additive in food and drinking water treatment.
2) Aluminum’s Ionic Size: This particle is similar to iron in size and uses
iron-evolved mechanisms to enter the highly active, iron-dependent cells
responsible for memory processing. Aluminum accumulates in these iron-
dependent cells and dysregulates the iron homeostasis which causes brain
hypoxia and neuronal cell death.
AD is a human form of chronic aluminum neurotoxicity. The causality
analysis demonstrates that chronic aluminum intake causes AD.
Mitochondrial Dysfunction:
Every cell of the body has mitochondria within it that produce energy for the
cell. The mitochondria are the battery packs of the cell and they are
extremely important. High levels of oxidative stress wear down the
mitochondria and cause a dysfunctional state. Studies have found that
individuals with Alzheimer’s disease have an advanced state of mitochondrial
dysfunction (28, 29).
Individuals suffering from AD are evidenced to have massive cell death of
the hippocampus and amygdala regions of the brain (30). Research has
shown that this is initiated by a profound glutathione (GSH) decrease and a
mitochondrial dysfunction.
Glutathione Depletion and Nrf2:
In AD, the cells are under so much stress that there main protective shield
(GSH) gets worn down and oxidative stress damages the mitochondria and
the DNA leading to cell death. Poor blood sugar control and high
environmental toxinexposure are known to deplete glutathione levels and
impair mitochondrial function (31).
A key pathway that maintains cellular glutathione levels and the ability of the
cell to adapt to stress is called Keap1-Nrf2. When this pathway breaks down
it causes increased levels of oxidative stress within the cell that leads to the
glutathione depletion and mitochondrial dysfunction (32).
This pathway must be addressed in order to prevent or reverse AD symptoms
(33).
Anti-Inflammatory Nutrition:
An anti-inflammatory nutrition plan that is low in carbohydrate and rich in
healthy fats and anti-oxidants is critical to preventing and treating
Alzheimer’s disease. The brain is primarily water, fat and cholesterol. These
are all key building blocks for promoting healthy brain function and
rebuilding a damaged brain.
The proper nutrition plan to beat AD is rich in phytonutrient dense
vegetables, healthy fat and clean protein sources. Healthy fat sources such as
coconut, avocados, olive oil & sprouted nuts and seeds must take a central
role in the diet to promote healthy brain function.
Healthy Proteins & Anti-Oxidants:
Healthy proteins include wild-caught fish, grass-fed red meat and organic
chicken, turkey and eggs. Grass-fed beef is loaded with long-chain omega 3
fatty acids, saturated fat, cholesterol, vitamin B12, and conjugated linoleic
acid which are all necessary for healthy neurological function.
Additionally, you can use lavendar, chamomile and peppermint essential oils
to relax the nervous system, oxygenate the body and induce deeper sleep.
Healthy melatonin levels help the brain to clean up damaged cells
(autophagy) including the NFT’s that are characteristic of AD.
Good sleep and optimal melatonin secretions also positively influence healthy
genetic expression, circadian rhythms that improve anti-aging characteristics
and human growth hormone levels which boost immunity, reduce
inflammation and build lean body tissue and a healthy physique.
Stimulating NeuroGenesis:
One of the biggest breakthroughs in neuroscience over the last 20 years has
been the discovery of neurogenesis. This refers to the ability of the brain to
generate new healthier and stronger cells and synaptic junctions. The brain
can literally re-wire itself. In the case of AD, the brain is breaking down
faster than it can rebuild which is called neurodegeneration.
In order to grow stronger and healthier neuronal cells the neurons secrete a
compound called Brain derived neurotrophic growth factor (BDNF).
BDNF encourages the growth and differentiation of new neurons and
synapses. In the brain, it is most active in the hippocampus and cortex and is
vital to learning, memory and higher thinking (34).
Key ways to simulate BDNF include regular exercise, novel movement
patterns such as using your non-dominant hand for activities, doing cross-
crawl style movements, aromatherapy, learning new concepts, listening to
classical music, social interaction and laughing.
Mental health struggles are slow, silent killers sapping us of energy and
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2. Alzheimer.net – Alzheimer’s Research Spending vs. Annual Care Costs Link Here
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GJ, Agranoff BW, Albers RW, et al., editors. Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th
4. Sabuncu MR, Desikan RS, Sepulcre J, Yeo BT, Liu H, Schmansky NJ, Reuter M, Weiner MW, Buckner RL,
Sperling RA, Fischl B; Alzheimer’s Disease Neuroimaging Initiative. The dynamics of cortical and hippocampal
5. Brion JP. Neurofibrillary tangles and Alzheimer’s disease. Eur Neurol. 1998 Oct;40(3):130-40. PMID: 9748670