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Welcome to From the Spectrum Podcast. This is a podcast about autism. It is my goal to explain

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what is autism. I plan to use a mixture of scientific literature, personal experience,

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and opinion. With opinion, I will explain why, I fill the way I do, and give examples. I will

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provide links to various references for each episode. For each episode, we will discuss various

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aspects of autism. For today's episode, we will need two things. One, it's critical thinking,

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and two, it's curiosity. I cannot help but to wonder why autism just appears in society. I can't

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help to think about what people think is causing autism. I can't help but to play a game of tug

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of war with Barb Wire. For today's episode, I can't help but to expand on implications to

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embryogenesis, neuroectoderm, the genetic lineage, and tying these to one common environmental factor

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that is proven to be significant to human biology. I will tie other health implications

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things seen across societies and across the lifespan. For today's episode, we will cover the

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cause of autism. The question that needs to be asked, do you know about the energy in light?

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Light is an electromagnetic strip. The second question is, do you know how living organisms on

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earth use this energy? These are facts. The power grid dates back to 1880s. The World's Fair

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event in Chicago was 1893. Those lights were incandescent. More on that later. Dementia,

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studied by Alois Alzheimer's. First patient was 1906. Alzheimer's disease first named in 1910.

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Rates of type 1 diabetes are increasing. And the age of onset has kind of shifted. Previously,

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it was referred to as juvenile diabetes. But now, it's not uncommon that adults get diagnosed with

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type 1 diabetes. At one time, type 1 diabetes was associated with a lot of sugar intake,

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carbohydrates, eating things like candy and being obese. But this is largely false.

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Autism, our subject, you know, was first observed in 1938. The rates of obesity are increasing.

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The rates of type 2 diabetes increasing. Sometimes, those are related. Or scientifically speaking,

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type 2 diabetes and Alzheimer's can be a sequela to obesity. However, obesity is not required.

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Degenerative conditions are alarming too. But all of these conditions tied together and mentioned

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are alarming. Developmental delays and intellectual disabilities are increasing. The so-called

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attentional and hyperactivity are increasing. Mood disorders too, especially at younger ages.

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Society's answer, because it is comfortable to them, is increasing support in schools. Often,

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you will hear, we don't have enough providers or services. Those comments lack critical thinking.

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Those are stimulus response comments. Spoken words to return the speaker to comfort,

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to homeostasis. This is not the answer. This does not explain the problem. This does not fix

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the root cause. In addition, cardiovascular diseases, or CVD, are alarming and still a

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common cause of death. A majority of society, especially above the age of 40, is on a certain

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type of medication. Yet, leading causes of death are still CVDs. Same scenario as earlier. Not the

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answer. Doesn't explain the problem. Does not hit the root cause. Okay, let's go back to development.

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We've discussed genetic implications. Even the known common genetic implications tie to autism.

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If you have these, it does not mean the individual has autism. Why are those conditions connected?

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And why are they connected to the light source? Remember, the brain and skin are connected long

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before birth. This creates our complex nervous system. This is in the embryo. From the moment,

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the first cell divides. The moment embryogenesis begins. All the way to death. Let's paint this

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picture in a linear graph. A cell divides is the beginning, the beginning of the human. The moment

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the individual passes. This is a linear timeline. At some point, autism exists on this timeline.

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Now, one. 100 years ago, autism did not exist. At least, it was not recognized in literature.

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A side note. Remember Leo Kanner mentioned in 1938, the first observation. And these were roughly

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8 to 10 year olds. Same for Hans Asperger's. So roughly 1930 or so, for the birth. It's possible.

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Autism existed at smaller scales. Let's say in the 1920s or so. But that is not so important to

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our conversation. What is important is autism just magically shows up in human evolution.

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And two. Decade over decade, rates are increasing. Now, the moment autism begins on that linear

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timeline is early in development. Be it in the embryo or just after birth. We reviewed altered

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salience brain connectivity at six weeks old. The crucial consideration is, autism is new and

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follows the trends of those earlier mentioned conditions. Crucial in development are. Well,

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there are many crucial biological components for development. Some regions of interest for our

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conversation are vitamin A, various vitamin B's, vitamin D, the aromatic amino acids,

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histidine, water, melanin, melanopsin, pro-opio-melanocortin, or pom-C for short. And light, of course.

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And light. These are all crucial for our conversation. In addition to the genetic lineage and what we

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know about heritability, we also need to consider the environment the mother is in during pregnancy.

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This is crucial and it's shown. It is a worthy consideration about how the light is a primary

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environmental factor when people discuss environmental factors. The environment of the

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pregnant woman is also different from 100 years ago or 150 years ago. DNA is a magnetic strip and

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codes for proteins. Proteins are wide band gap semiconductors. For reference, see Albert St.

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Georgie's. When the magnetic footprint changes, implicated, it changes the light. It changes the

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power, function of our cells, because it changes the charge. Atoms and oxidated stress is this,

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is a cause. Humans use roughly 20 amino acids. Remember, these are proteins. These 20 amino

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acids are responsible for tens and tens of thousands of different proteins based on unique

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sequencing. Various elements from the periodic table and water and melanin and light are the

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components. Look at a periodic table. We use some, but not all. This powers or energizes our cells.

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So we use some of the elements from the periodic table, water, melanin and light. The aromatic

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amino acids receives light and targets various elements such as calcium, magnesium and sodium.

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Light is underestimated. Light is the only change. Light is the only change. One, a shift from the

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light source. Previously, it was more sunlight. Now, we have the ability to light the environment

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with artificial light. And we can extend the day under artificial light. And to the type of light

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from incandescent to the modern day LED and tech light. You know, children, especially at extremely

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young ages, have access to technology. And we can see, we know that children, young age, are right

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on top of the technology on the screen. The younger and developing brain is more implicated to this.

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And this is true. Now, by the time the child has access to this blue light and this tech, this

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technology, autism likely already exists. It's already manifested in the biology of that individual.

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However, what is the purpose here is blue light or modern light more generally implicates our

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biology. It's not so much autism occurs directly for that individual with the exposure to the blue

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light. It's more, this is more the lineage. This is more generational. Now, autism around 1938 was

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first discovered. And the light sources remember 1880. And then the power grid 1893. So this is,

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we've discussed this, this is just a couple of generations. So that makes sense for the lineage

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that hand me down of this biological implication. Blue light dehydrates cells, whereby, something

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called a TCA cycle is implicated. This involves cellular respiration and some oxidation. This

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was discovered by a Nobel laureate, Hans Krebs. You know, mitochondria. This is occurring in the

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mitochondria, more on mitochondria later. But the TCA cycle generates ATP. Now, if mitochondria is

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the energy source for the cell, it's the ATP that's creating this. Mitochondria absorbs light. Light

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is a major source of energy here. Various wavelengths. We'll discuss longer wavelengths in

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the red light later. But shorter wavelengths are here too. And melanin and some elements from the

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periodic table. All cells, except for bacteria, have the TCA cycle. In addition, water is a main

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factor here. Water is commonly known as being a part of the human body. This is occurring at the

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mitochondria metabolism. However, not common is the knowledge of the role water has and the

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differences of water. In mitochondria, there are cytochromes. Cytochromes are proteins. Specifically,

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cytochrome C1 or cytochrome 1 transfers electrons during phosphorylation. Phosphorous, iron and

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sulfur are huge here. But not to be overlooked is light. Cytochromes receive light. Specifically,

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red light and near infrared and infrared light. They are red light chromophores. This is a part

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of the oxidation process. This involves an enzyme called cytochrome C oxidase. It turns oxygen

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into water. And we will talk more about this through the episode. But this generates the ATP

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that is most commonly known when we think about mitochondria. The P is phosphate. Phosphate is

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phosphorous and oxygen. You're going to see oxygens playing a huge role here in cell health. And

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probably lastly, because this is getting in depth, but phosphate is a type of ion, adene ion,

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whereby it has more electrons than protons. Okay, last thing here. And just all of that

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explanation, all of that build up just to say this, mainly just to say this. Modern light

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dehydrates cells whenever it's just isolated to blue light. Now think about the embryo and that

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cell dividing and cell differentiation and migration development and the complex living

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organism coming to life, coming into life form. We know autism develops early, probably within

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the embryo, probably. But even after birth, postnatal, all of these things are huge. When cells

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function, whenever they are functioning properly, this is a very dynamic structure, a very dynamic

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operation, I should say, whereby it's using energy from the environment, like such as the light,

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and it uses the periodic elements and is creating energy. This could be the most important thing

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in the whole episode right here. This is instead of adding something to the biological processes,

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such as pesticides or vaccines or whatever it is that we want to add to the components of the

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biological processes. Let's just take the normal biological processes, these normal ingredients

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or components that we've discussed, such as the light, the periodic elements, the water, and so

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forth. And let's just change that. Let's just change one and see what it does to development and

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our cell functioning and our nervous system. Autism is a form of neuroplasticity. Neuroplasticity,

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we've changed, autistic people have changed based on the environment that they are in. And I think

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this is what's happening. Neuroplasticity is not limited to learning something new, such as

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knowledge or learning a new motor skill. Yes, that's neuroplasticity, but there are more complex

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types of neuroplasticity. Perhaps the most fascinating one is people that are blind will

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repurpose their visual cortex for the Braille reading. That's the type of neuroplasticity

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that we need to discuss and consider. Autism is an example of that type of neuroplasticity,

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whereby the living organism changed because something in the environment. Just know this,

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humans can harm themselves unlike any other species. We have, you've heard me say, never underestimate

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a human's capacity to think. This has a chance to be good and it has a chance to be bad, an

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infinite amount of good and bad. Somewhere along the line, we have to recognize that we can do harm

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to ourselves, maybe even indirectly. Of course. Remember, you know I've said the nervous system

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just wants to respond. It doesn't want to work. Now carry that out a little downstream to our

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behaviors. I don't think this is all that complicated. If this environmental factor,

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this environmental component that gets little attention can implicate cells like this, just

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imagine what it's doing in the embryo and through the lifespan, such as with the Alzheimer's and

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dementia. Now, innocence will happen. Yes, we can normalize for this. We will age, but the type

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of aging we are doing now and all of the health trends, just pick any health trend that you want

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to look up. Are we doing it right? Do we have any understanding of it? Now let's consider autism.

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So this is at the beginning of life, of course, but at the end of life, on the other end of the

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lifespan, the rates of dementia, the rates of autism, the rates of dementia are very similar.

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Obesity is also alarming. Remember leptin, it wasn't discovered until 1994. Dementia and even

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obesity can be picked up in an eye. Using an OCT scan, an ophthalmologist or optometrist can do

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this and this is shown. This is in the scientific literature. They can pick up eye damage with

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this melanin back in the eye, the retina, on an OCT scan years, many years before dementia and those

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symptoms that we know manifest later in life. It starts in the eye. It starts with the photoreceptors

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and these light sources. I don't think none of this is very complicated if we just look at it

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differently. If we just give ourselves a chance or said differently, just to wrap all of these

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things up, the rates of chronic diseases are concerning. The second thing is we can look

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up maps from space. NASA does this to look at Earth and the artificial light from let's say the

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1940s to the 60s to the 80s to the 2000s about every 20 years or so. You can see this artificial

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light at night expanding. It's a rapid increase. We are more exposed to this type of light. So a

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shift from the light source and then the increase of this artificial light. This is my opinion.

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Artificial light looks innocent. It doesn't look like much is going on other than it allows us to

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light up the inside environment. It allows us to light up our houses and we can extend the day

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and we can light up the house so we can enjoy our pleasures, enjoy our activities, our modern

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activities and pleasures. Further, it allows us to light up organization so we can have more job

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opportunities during the night and we can have more goods produced. But then we get shift work

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and all of these health implications associated with that which aren't a surprise in the medical

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literature. It might be a surprise to the lay public but that doesn't make it right. It doesn't

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make lighting up the homes at night and this being suffocated in artificial light right. We

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like that artificial light at night. We like it. We're drawn to that nightlife with those shiny

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lights, spotlighting, things to do, activities. Oh look at this. The artificial light even during

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the day allows us to be more comfortable but that doesn't make it right. And here's my last opinion

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because I want to move on. It's off topic. The light during that industrial revolution was really

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serious. It really allowed profits to be made and those goods to be produced like we mentioned

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earlier. And now after several generations of it, after all of these generations, it's just normal

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part of life now. Couldn't imagine living without it or reducing it or only using it at certain

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times, optimal times that's okay for your biology. Okay, let's talk more light and biology. Photo

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electric effect is photons hitting the surface and giving energy to electrons. In our case,

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different proteins require or activate based on various wavelengths of light. Artificial light

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has certain wavelengths, very specific wavelengths. Most modern light such as LED and tech light is

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blue light about 460 to 480 nanometer light. We've covered this. However, I don't think it hit.

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Incandescent light was mostly green all the way up to red and infrared light. Candles are red light

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to near infrared light and fire is too. The sun includes UVB about 250 nanometer light all the

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way up to 3100 nanometer light. And that includes various infrareds. So it's UVB, UVA, and then the

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visual light spectrum, the rainbow from violet to red light. So from 390 to 760. And then from 760

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to 3100 are various forms of infrared. I bet 99% 99% of society does not understand or know that

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infrared light is a tool against cancer cells. It is known. Go to your search bar right now and type

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in infrared light, Jack Hammers cancer cells, I believe to my knowledge. This is the latest research.

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And it comes out of Texas A&M. They use Jack Hammers whenever they discuss what infrared light is

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doing to a cancer cell. The sun is roughly 43 to 47% red and infrared light. So almost half of the

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sunlight that we get is in this range. Melatonin is going to be the human's powerhouse here. The

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human secret weapon for this. Here are some interesting data. These data are very interesting.

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Vitamin D and autism are anti correlated, whereby the higher the vitamin D, the less likelihood

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for autism. Okay. Autism rates closer to the equator are also lower. Now, artificial light in

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this modernization is becoming more and more. However, the sun and the power of the sun is

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still going to kind of cancel out. I know, I know. A biological cell is a so-called dissipative

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structure. A dissipative structure is built atomically to capture energy from the environment.

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It captures this energy and stores it. Melanin and water are major players here in the cell to

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capture that energy. The energy from the sunlight and that lux is the way this happens. What we

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want to look at is the sun power, the lux provided by the sun versus artificial light. So something

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to consider is the lux between artificial light and indoors versus outdoors in the sunlight.

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Indoors, roughly 3 to 500 lux is about the most that you will receive. And remember,

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it's a very specific wavelength. However, the sun, a sunrise and sunset are roughly 20,000 to 30,000

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lux. And the afternoon sun is upwards to 100,000 lux. And this is the energy source. This is the

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difference in energy source too. Remember the light as an electromagnetic strip and how we use that

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light. Here are just some brief benefits or some highlighted benefits of each wavelength of light

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and sun and the relationship to human biology. This list is not exhaustive. UVB, which is roughly

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250 or so to 315 nanometer light. Vitamin D, vitamin D and cholesterol have a close relationship. It's

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a very coordinated dance whereby they need to sulfate. They need to work together with UVB light

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for lipid metabolism. This is the lipid metabolism that is a problem in society today. And some

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details about that medication I mentioned previously in the episode. Testosterone. Remember

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testosterone's role in human biology. Sipolsky says testosterone makes effort feel good. The

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aromatic amino acids phenylalanine, tryptophan, tyrosine, tryptophan and methionine, another

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amino acid are very unique. They have one codon and methionine is the start signal for all protein

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and DNA sequencing. And histidine. Histidine is one of those amino acids that are vital for protein

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synthesis. It helps synthesize proteins, which is also a region of interest for us. Endogenous

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analgesic. So those pain receptors or that pain perception also associated with a pro opioid

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bolano-cortin. That wonderful subdivision in the hypothalamus. Leptin sensitivity. Now we've

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we've hit on that. So UVA, so roughly 315 to 390 nanometer light. Nitric oxide. This is huge for

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CVD. UVA is powerful for our cardiovascular system. UVA regulates blood pressure. Infrared light. So

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760 all the way up to 3100 light. Melatonin. Infrared creates a sun callus. So prevents harm

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from too much UV. The more you get infrared, which is really high in morning and evening,

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closer to sunset. This protects. This is an endogenous healthy sunscreen. This is Mother Nature

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sunscreen. Water. Infrared is huge for our water. The human body is roughly 80% water at birth. And

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this decreases decade over decade as we age. See Jared Pollock for water. This is primarily why

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younger humans are more resilient. And infrared is a wonderful anti-inflammatory. And of course,

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the wonderful cancer fighting abilities. Infrared can even penetrate bone. It penetrates bones. A

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process called DC electric current. And this is a semiconductor method here. The higher the

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wavelength of light, such as the red light at around 700 all the way up to the 3100 in the

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infrared light. The higher that number is, the more it penetrates the human body. A combination of

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UVA and infrared, a type of infrared light, regenerates photoreceptors. A lot of what we're

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talking about today is those photoreceptors that receives the light energy. Red light,

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which is 620 to 760 nanometer light. Mitochondria function. It's huge for mitochondria. That

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cytochrome C oxidase mentioned earlier, it has four chromophores. And they are all red light.

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You might ask, and you ought to ask, why are red light chromophores deep inside the mitochondria?

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And you ought to consider, where are we getting red light now? Artificial light doesn't have it.

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The sunlight does, but where are humans getting the red light if they're not outside? And think

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about the consequences. And thinning out blood viscosity, we don't want thick blood. So red

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light to infrared is wonderful for the cardiovascular. Red light also lowers blood glucose. Studies

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show by 27, 27% just the light. This is nature's way of giving us energy, giving us improving

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our metabolism. In contrast to the red light, blue light stimulates glucose corticoids. That's

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right. The blue light will cause us to generate cortisol and glucose without eating. And this

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is all through the POMC gene. Modern light is full of the blue light spectra, about 440

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to 480, 490. It's huge for circadian rhythm, those natural rhythms we had to follow before

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the creation of artificial light. We've talked about melanopsin. Melanopsin is a blue light

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chromophore. We've discussed this. Remember, melanopsin wasn't discovered until 1998. That's

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when it was discovered in the human eye. However, how it's sequenced and melanopsin being present

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in tissues, organs, and deep inside the brain didn't exist until six, eight, 10, 12 years

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ago. So all of this has happened recently. Why do we have this blue light chromophore

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all over the place? That's the question. That's the question you have to ask if you're going

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to follow along here and understand and give yourself a chance to consider what is going

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on. And the downstream implications or the power melanopsin have to all of the bodily

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physiology. This is very crucial and an alarming consideration for our health now in the modern

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world. The smaller the wavelength, such as in the UV area and the blue light, have greater

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photonic energy. You know this. You know UV light is strong. Visual light, which is the

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only light humans can see, the 390 to 760. Most modern light now, most artificial light,

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are shorter wavelengths because that light contains more energy. So it requires less

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electricity to power it. So let's expand on melanin, a black pigment now found across

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the brain that serves several purposes. Melanin is a semiconductor whereby each one, U melanin,

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few melanin, and neuro melanin, uses a different element on the periodic table. One uses nitrogen,

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one uses sulfur, and one uses phosphorus. Melanin comes from tyrosine and UVB. You know

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about color. You know about certain types of melanin. You melanin and feel melanin for

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the eyes, skin, and hair. However, neuro melanin, as we discussed previously, likely you've

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just heard melanin without detail, without understanding the purposes. Neuro melanin

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is slightly different. One, it protects against oxidative stress. Oxidative stress is extremely

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harmful for cells. And a major factor, maybe the primary factor for CVD and aging complications.

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Oxidative stress is a common theme throughout this whole episode. Everything we're talking

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about essentially is involving oxidative stress, specifically the mitochondria and the cytochrome.

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And two, neuronal function. Here we go. Cell function, beginning in the embryogenesis.

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Mitosis. Mitosis is trillions of cells dividing, giving life to a complex living organism.

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Cells begin to increase at rapid paces. They migrate. We've discussed cell migration. In

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episode three, one of the first things we discussed in episode three. Now autism and cell migration

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is a problem. This is a very big problem. In things like the cell functioning, the cells

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capability and the hydration, the cell metabolism, all of these things will factor into the migration.

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And blue light does not do any favors for this. In the complex living organism, such

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as the human, this is detrimental in the development, early in development, from embryogenesis

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and all the way up through lifehood to the whole lifespan. Remember that linear timeline

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that we painted earlier in the episode. This can implicate cells and problems and increase

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senescence all through lifespan. And you can see this in society. Melanin and light will

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be our best friend for this, for protection, for proper cell growth, migration, for proper

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cell function. Melanogenesis comes from UV light, UV radiation that up regulates melanocytes

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from pro-opioid melanocortin or POMC. This is a subdivision in the hypothalamus. We've

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discussed the hypothalamus. There are three types of melanocytes. Our region of interest

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is alpha melanocyte stimulating hormone. We've introduced this in episode four. We've introduced

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this to autism during that time. But this is far beyond autism. This is all cells for

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all conditions. Common with genetic implications with autism is cell and synapsis development.

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That is, much of those implications are tied to cell development and function and synaptic

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development and function. Both the pre and the post synapses. Neuromellanin is black.

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And this is why we use the melanin. The black absorbs all frequency of light. It receives

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all of that energy from that electromagnetic strip. Remember the sun spectrum from 250

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to 3100 and remember how certain wavelengths provide certain benefits to our biology. Now

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remember artificial light has very specific wavelengths. Another role with neuromellanin

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is protecting the cell whereby the pigments remove toxins and metals. Here we go. Society

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loves to speak about toxins and metals as a general cause and general reasons for rates

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of autism diagnosis. They think this is what's causing the increase. This reason is missing

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critical information. This is true about toxins and pesticides and metals and so forth. The

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reason would be neuromellanin. Neuromellanin protects the cell against those toxins, the

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pesticides and metals and so forth. It is mostly known. Neuromellanins role in degenerative

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conditions. As you know, it's role in cell health and protection. Interesting. Neuromellanin

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is the topic for Parkinson's. Most people would think dopamine and that's true. But

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neuromellanin and dopamine are closely related. It's in the biosynthesis. A hot spot for

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Parkinson's is a Cisthantia nigra or black substance. Neuromellanin is also plentiful

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and the locus ceruleus. The spot for brain adrenaline. Dopamine, melanin, adrenaline are

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all synthesized by tyrosine, one of the aromatic amino acids. This tyrosine protein needs 200

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nanometer light or UVB light. Within the past month, Neuroscience News highlighted a study,

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a recent study showing people with autism have a three fold increase, times three increase,

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chance of developing Parkinson's. If you go to PubMed and type in Neuromellanin, you

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can see trend of articles released. The articles are increasing mainly because, one, people

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are understanding its role in different than the peripheral melanin discussed earlier with

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the eye, hair and skin color. And two, the rates of Parkinson's. People, science is

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starting to study this more. Melanin is involved in the cell body. All cells and it is not

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limited to Parkinson's or any degenerative condition. Okay, moving on to tryptophan,

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another aromatic amino acid. Tryptophan is a wide band semiconductor for the eyes. The

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eyes are no way only vision. It's a passage into our deep biology and development. The

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eyes is a highway into our biology. This involves photoreceptors. We've discussed

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melanopsin and physiology and development, timing, etc. Also, we've discussed all

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opsin, have a weak covalent bond with vitamin A. You have probably heard how important vitamin

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A is for the eyes. As a kid, probably told carrots are good for your eyes. Anyway, blue

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light destroys this bond, vitamin A to opsin. Remember the implications, the damage of opsin

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and vitamin A, those weak covalent bonds. Vitamin A in the aldehyde form damages cells when

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the bond is broken. Remember, blue light breaks this bond and create free radicals. That broken

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bond of vitamin A in this aldehyde form is toxic to cell membranes, an area called lipid

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rafts and it causes a so-called dielectric collapse of the cell. This means we cannot

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control or understand the electromagnetic information coming in from the light. We cannot

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create order from that electromagnetic strip. And this seems to be at the core of a lot

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of the aging complications of modern day and chronic diseases. Free radicals in our biology

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is no good. It is an unstable molecule that promotes or creates ROS, that oxidative condition

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that is no good. ROS is reactive oxygen species and this damages DNA and cells, lipid and

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proteins and they are also responsible for cancer and aging. It sounds familiar. It sounds

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like this episode. Yes, free radicals is a normal part of the cell metabolism. However,

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it's the amount and it's the amount of antioxidants we have internally built into us that intends

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to keep us safe. However, these internal mechanisms rely on sunlight to create these antioxidants.

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Humans did not evolve with the need of exogenous antioxidants so much in a supplement form

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or medication or relying on nutrients from food. We have these already and they come

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from the sun. Vitamin A is crucial for eyes and skin and influences cell development. No

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surprise, cell growth and cell differentiation. All crucial parts of human development. Okay,

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from tryptophan is serotonin. Remember an aromatic amino acid activating for UVB light.

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Serotonin is the first molecule studied in autism from the 1960s. It was 1961 when it

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hit medical literature. Serotonin has a vital or is a vital molecule for modulating the

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nervous system. Today it is believed to be the closest to a biomarker for autism. That

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is according to Mueller et al. including Jeremy Finstra, Vanderwill. This paper was a collaboration

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between Vanderbilt and Columbia. They study serotonin and autism quite extensively. Serotonin

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is in the brain of course and in the gut and platelets and cutaneous tissues. Serotonin

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is synthesized on the skin. This is one biosynthesis path from the eyes and the skin. Remember

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the brain and skin are connected. There are two isoforms responsible for serotonin production.

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And the central nervous system or the brain serotonin. Remember our conversation about

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this as a neural modulator. And remember the RAFE located on the brain stem. This is tryptophan

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hydroxylase 2 or TPH2 which is an enzyme used for the biosynthesis of tryptophan into serotonin.

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And second for the peripheral nervous system synthesized by tryptophan hydroxylase 1 or

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TPH1 which is in the epidermis. More specifically the keratinocytes. So this is right on the

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skin surface essentially. The keratinocytes make up 90% of the epidermis and have a large

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role with cell proliferation and differentiation. This serotonin does not enter the brain. And

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remember 95% of all serotonin is located in the gut. Now something never mentioned on

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this podcast is the relationship between autism and GI issues. This is well documented, well

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studied. Just this week Nature Microbiology released a paper. I'm looking forward to

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learning more about how archaea and bacteria are involved here. Peripheral serotonin is

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vast for development and during pregnancy. Serotonin in the maternal pancreas is in the

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process of serotonin in the fetal forebrain. I'll say it again. Serotonin from the maternal

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pancreas is included in the process of serotonin for the fetal forebrain. Okay the gut serotonin

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has a large role in peripheral physiology. Additional roles in development includes and

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these processes ought to be familiar to us now. They include serotonin helps modulate

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the nervous system. Also cell proliferation, migration and differentiation. Perhaps the

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most interesting and a region of interest for us is serotonin's role in sensory processing.

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Scientifically referred to as somatosensory system. Somatosensory is more specific to

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object recognition, discriminating between textures and processing sensory to motor feedback

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and exchanging in social cues. Sounds familiar, sounds like autism. We as humans, we have

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a sensory map and this map is implicated. In addition, a path that is implicated is the

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thalamocortical connection. We've discussed this. So the thalamus to the cortex. In other

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words, the thalamus which is where all senses are processed to the cortex. The area that

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extends the head up more than any other species. The area that makes us dominant. However, a

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reason that gives humans an enormous capacity to think. This is a human function. This is

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a human feature. The somatosensory explains a lot with autism explains the autistic phenotype

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including all three social communication and interaction criteria. Remember criteria A,

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A1, A2 and A3 and it explains some criteria B, B1 and B4. Melanin is involved in all five

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senses. Melanin is in between the sitting organ and the brain. Different individuals

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and different species have different amounts of melanin in between certain senses and the

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brain. Think about dogs. Think about dogs and their ability for smell. Their olfaction process.

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Dogs have more melanin located at their olfaction senses. Remember at the beginning of the biosynthesis

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is tryptophan on the surface eyes, skin and gut. Additionally, serotonin is crucial for

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visual and auditory cortex. Undisputed, tryptophan is massive for the human eye. Please don't

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underestimate the biosynthesis of serotonin from the surfaces. Eyes, skin and skin via

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the gut. Returning to an earlier conversation, blue light or modern light implicates vitamin

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A and melatonin which is synthesized via tryptophan and serotonin. This is vast for mitochondria

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DNA and autophagy. Now, I've mentioned this briefly, mitochondria and this is very important

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for cells. It is very important for all human cells and autism. However, we haven't discussed

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it much and that is not because it is not important. It is very important. Mostly when

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we discuss a cell, we discuss the mitochondria. It uses photosynthesis. 95% of the body's

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melatonin is synthesized here in the mitochondria which comes from tryptophan. Remember, more

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need for UVB. Melatonin is the body's number one antioxidant. And remember what I just

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said about photosynthesis. Humans are solar powered. Humans use photosynthesis just the

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same as what you might know in chlorophyll to a plant. Humans are solar powered. Damage

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here is no good for cells. No good for aging. No good for anything downstream from these

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processes which are massive. The eyes are upstream in this process. Destroying this,

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everything is damaged. This is degeneration. This is accelerated aging. Okay, some things

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to note. Blue light, LED, tech light, all or most, modern light causes hypoxia. Hypoxia

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is well researched in autism and oxidative stress. This explains cancer. This explains

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accelerated aging. It also implicates development. Our region of interest. Remember that process

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in the mitochondria. Oxidation to water. This is not news. This is known. This developmental

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problem early on is known with the cell proliferation, differentiation, migration, etc. and how cells

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develop and function. But think about all of those processes running in reverse. This

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is the implications to aging and the cancer and dementia. All of these processes are kind

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of unwinding, if you will. And that's what we're seeing in society. If you have implications

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during development, yes, you'll see things like autism, ADHD, the neurodevelopmental

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problems, even schizophrenia, etc. But not all, obviously not all people have these.

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But on the back end, it's not necessary. You can be normal. You can be healthy or your

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biology can be perfect. But this exposure will begin to unwind this. You do not have

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to look hard to see examples of this. This is all known in medical research. Where we

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fell is it is not known by the masses. But why? Think about the human baby. We are much

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different than other species, other primates, especially chimps. We are 99% exact gene matches

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as chimps. Yet, from the first cell dividing in that embryogenesis to birth, let's say

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to three years old. I want to cut off here. There is massive things changing. Everything

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involved in these processes that we've discussed today. Autism is happening somewhere along

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this linear timeline. Humans, after birth, are very underdeveloped compared to other

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primates. To other species, regardless of a primate or not, our brains are very underdeveloped.

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We take on mass of changes from different life spans, different stages of the lifespan.

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We are also overweight. We are chubby, if you will. Chubby babies with underdeveloped

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brains. Our evolution, however, requires certain things for this undertaking, for this development

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of the brain and the nervous system. The energy system, our metabolism. We lose the baby weight.

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We grow a brain, a functional brain. At birth, we can even sit up. We have no muscle strength.

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With autism, we have the dyspraxia, that underdevelopment. But even with a normal child, they're still

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delayed here compared to other species. Remember how GABA, that inhibitory neuron,

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is excitatory during the critical period. Think about birth to that critical period,

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the end of it, and how it's pretty common that children will learn different languages

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that pick up on different languages quite easily. There's this rapid development occurring.

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However, with the spectrum, let's talk about the spectrum here. How some people with autism

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range from the high functioning, or the Asperger's so-called little professors, to the profound

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autism. We've discussed profound in that level three type. That's a big difference.

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But we can see that how these cells are implicated during the development, starting in the embryo

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likely, how this will manifest for the young child, two, three, four years old. It could

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be speech and language. It could be motor coordination. It could be sensory processing.

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It could be low social motivation, or desires in social motivation. Poor social communication.

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It could be poor eye gaze is common. And remember how much we've spoken about the eyes, and

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the downstream processes from the eyes. This is something. And then at the other end of

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the spectrum, children can, they need so much support, such as using the bathroom or riding.

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Riding is a common problem with autism, or feeding, getting dressed, etc. All of these

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basic life skills are missing. Or maybe the person with autism has GI issues. Some do,

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some don't. But with the cell proliferation, migration, and differentiation. This is it.

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The sun, and all of these mechanisms that we've discussed, is a part of this crucial

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part. It is all very underestimated. I don't know if it's direct or intentional or indirect.

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We just bypass it. And I think it could be, because we don't want that conflict within

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ourselves while we're discovering this. We're studying this. Humans hate when our beliefs

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are offended, when we can't figure out something. We need to figure it out. We need something

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that makes sense to us. Maybe, if you made it this far, you do have some critical thinking

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and curiosity. All of this stuff is known. Everything we've discussed is known. This

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isn't me. This isn't the medical literature. This isn't decentralized medicine. You can

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find people, doctors, PhDs, etc. Neurosurgeons talking about this stuff. But the masses,

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they don't know. Okay. Before we end, there's, vitamin Bs are very important in autism and

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development. I should say, in development. There's a couple of B vitamins here that we

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will discuss. Beginning with a well-studied vitamin B folate. It's vitamin B9. This is

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altered by light pollution and water. Remember, light controls DNA expression. Folate requires

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water. This water is made from the cells mitochondria metabolism. Easy water. You might have heard

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or fourth phase of water. Folate is involved in creating those neuromodulators previously

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discussed epinephrine, nor epinephrine and dopamine. All very crucial in the human nervous

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system. Folate provides one carbon for the regulation of DNA methylation and DNA synthesis.

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You know this process is abnormal in autism. Folate requires UVB light. B12 does too. Low

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folate potentially increases risk of CVD, colon cancer, anemia, pregnancy and birth complications,

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mood disorders and dementia. Melanin assist in the process. Remember those protective

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roles. Blue light also called modern light provides vast consequences for this process.

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Natural folate synthesis is broken today. Now it comes from supplement or exogenous and

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supplement form increases autism risk. It comes from manmade foods also in exogenous

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form. Those are synthetic also known as folic acid and bypasses crucial components of the

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natural biosynthesis. And that's a problem. I know a lot of people are going to discount

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this conversation today. We need critical thinking, curiosity to even consider. Autism

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just arrives in human evolution about 100 years ago. Autism just magically appears. There's

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a lot of effort going into discovering which genes. I want to know what is causing it.

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I want to know what would happen if a high likelihood children during birth, during pregnancy,

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if there's a family history, if the pregnant woman would spend time outdoors instead of

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underneath blue light. Would that help? Would changing the environment during pregnancy help?

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But instead the focus is on medication and maybe a shot. There I even say, it even pains

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me to say maybe there will be an autism vaccination. That does not sound like a fix to me.

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If you are listening and enjoy the episode or enjoy the podcast, please feel free to

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leave a review or rating. In podcasting reviews, ratings and downloads are crucial. And I very

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much appreciate your feedback. You can email me info.fromthespectrum.com. Thank you for

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listening to From the Spectrum podcast.

