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

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explain 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 show the way I do and give examples.

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

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discuss various aspects of autism. For today's episode, we will cover mitochondria. The

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mitochondria, which is plural, mitochondrion, is singular, or vast for living organisms.

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Often, mitochondria are considered the powerhouse of the cell. We've covered light, water, and

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magnetism as the central foundation of life, including human life. Today, we will have

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more understanding of these three critical components in our living organism.

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Today's episode is an introduction because mitochondria is very critical in this discussion

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and we cannot cover everything. We will prepare for a future episode featuring an expert, an

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MD, and a PhD in biophysics to explain the roles of autism and mitochondria. If you

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go to PubMed and type in just a broad search of mitochondria into the PubMed's search

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engine, you will see recently, over the last one to two decades, the number of publishings

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on mitochondria has a vast and sharp increase. The understanding of mitochondria is becoming

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more apparent. The roles in human biology and health versus senescence and death is becoming

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more recognized. What we will talk about are not topics that help our life. They are topics

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in our biology that gives us life. Most cells have mitochondria. All cells accept red blood

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cells and two types of cells from the autism and gastrointestinal episodes. Bacteria and

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archaea. Red blood cells use deuterium water and you will find out mitochondria is a role

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of producing water. Mitochondria needs a different type of water than blood or hemoglobin. Red

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blood cells use hemoglobin which allows optimal oxygen transportation. You will soon find

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out oxygen and the mitochondria is delicate. Bacteria and archaea, their absence of mitochondria

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is because those are prokaryotic cells. Prokaryotic cells are less complex and then eukaryotic

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cells are more complex. All the organelles within a cell nucleus including mitochondria,

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it's believed that everything in the cell nucleus was once independent or separate from

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each other. And the collection of these different organelles coming together in the cell nucleus

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gives rise to more complex living organisms to more complex life. In the prokaryotic bacteria

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and archaea it shares a cytochrome c-oxidase with eukaryotic mitochondria cells. In eukaryotic

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cells that more complex cell nucleus and mitochondria, cytochrome c-oxidase is the fourth of five

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cytochromes. We've talked about humans use photosynthesis. This is here and crucial parts

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of hemoglobin and mitochondria. Hemoglobin and chlorophyll are nearly the same except

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hemoglobin uses iron. Chlorophyll uses magnesium. Iron will be a critical part for today. Iron

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in both blood and the mitochondria have magnetic properties. This is a heme sometimes called

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hemo protein. These are molecules containing iron which binds to oxygen. Remember the magnetic

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part of the story. Hems store and transport globins. Hence hemo-globin conserves energy.

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Another area for today photosynthesis and respiratory cytochromes which will be most

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of our conversation is also a catalyst meaning starting or accelerating and hemes since changes

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in redox states. So more involvement with oxygen. So a brief recap the elements that

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we will discuss. It's energy, oxygen, water, proteins, ions both negative ions which are

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electrons and positive ions which are protons and the electromagnetic fields. Light is a

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driving force. Light or a lack of light depending on the cellular state and function. Meaning

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if the cell is active and functioning and healthy it's receiving optimal light, optimal

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electromagnetic fields. If the cell is lacking energy or cell death even it is neglected

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from these energy properties. The powerhouse of the cell, the mitochondria and cellular

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respiration. There are three components that we will spend most of the time on. These are

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all energy producing paths. One is glycolysis. Two is citric acid cycle or sometimes called

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TCA cycle or even Crab cycle. This is briefly mentioned in cause of autism episode. Hans

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Krebs the Nobel winner this was mentioned around minute 16 of the cause of autism episode.

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Also Albert St. George's another Nobel winner has critical roles here with that the protein

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discovering the semiconductor. Essentially what we're talking about with all of those

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ingredients mentioned earlier those elements we are creating semiconductor properties.

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And the third component of the cellular respiration is oxidative phosphorylation. This will include

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the electron transport chain also briefly mentioned in previous episodes. The ATPase

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and chymiosmosis or the movement of ions across membranes and across the gradient. First is

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glycolysis. This is glucose metabolism that creates two molecules of pyruvate. You probably

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know glucose is released for energy. This is where it takes action. This is the cells

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cytoplasm. The goal is to break down glucose and use a transporter to enter the mitochondria.

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Glucose binds to insulin and there is a straw like feature for a transporter which allows

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the glucose to enter. Pyruvate kinase isoform M2 or PKM2 is labeled metabolic budgeting

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system. This is a factor in autistic biology. Pyruvate has ATP and NADH outputs. ATP is

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adenosine triphosphate which transfers energy. This is what we are trying to achieve in

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cellular respiration. The NADH carries electrons. With oxygen and pyruvate, acetyl coenzyme

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A sometimes shown as aceto coa is created and the citric acid the TCA cycle needs it.

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It needs it. The citric acid cycle. This occurs in the mitochondria matrix and is central

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driver for cellular respiration. The cycle is used to release stored energy from oxidation

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of acetyl coenzyme A which is derived from carbohydrates and fats or protein into carbon

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dioxide and chemical energy of ATP. It also produces NADH and FADH2. These are coenzymes.

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FADH2 is a cofactor. These are required for metabolism. FADH2 and NADH are catabolism

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which breaks down complex molecules which we've discussed into simpler forms. Simpler

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molecules, then mechanisms can use these simple forms for energy. This is life. This is upstream

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metabolism. NADH and FADH2, the electron carriers are crucial. We will cover all five of the

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cytochromes in the electron transport chain and the ATPase momentarily. Both glycolysis

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and the citric acid cycle uses NAD plus breaking it down to NADH. Glycolysis and the citric

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acid cycle just many components moving parts. They are like conveyor belts feeding into

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the cytochromes in the electron transport chain. Now oxidative phosphorylation. This

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is where the magic happens but without glycolysis and without the citric acid oxidative phosphorylation

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suffers. This is the final stage of cellular respiration. This includes the electron transport

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chain and ATP synthase and chymiosmosis. ATP generated in one of these two metabolic pathways

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glycolysis and or oxidative phosphorylation. We've discussed just briefly the electron

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transport chain and the cytochromes involved. Cytochromes are chromophores. In other words

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these are a unique type of protein. This translates into color and carriers of chromophores. I'll

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say again translates into color and carriers of. It means they absorb specific wavelengths

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of light and you know the position on the cause of autism and all of the chronic diseases

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that are just downstream of essentially everything we're talking about today. Today's conversation

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will take us essentially as far upstream in human functioning, human metabolism and biological

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sequencing as we can go. Cytochrome 1 or sometimes called ubiquinone. The products of glycolysis

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are oxidized here transferring two electrons from NADH to FMN or Flavin. You might have

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heard of Flavin products such as green tea or supplemental form. The electrons are then

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used in CoQ10. You might have even heard about this or seen it on your supplement aisle in

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your supplement store or grocery store. CoQ10 is a coenzyme and these are lipophilic and

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it's reduced form ubiquinol also in cytochrome 1 or 8 iron sulfur clusters. So here we are

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with the iron. Remember the magnetic field and hydrogen. Hydrogen and electrons are produced.

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They are broken down from these separate processes and produced here. Then we move to cytochrome

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2. This uses electrons from succunate in the citric acid cycle and we are passing electrons

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down the path using iron sulfur clusters and CoQ10 to cytochrome 3. Succunate is a catalyst

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of the oxidative process being fed to cytochrome 3 which will turn these products into water.

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Essentially we are making water and ATP. You might have heard of ROS, reactive oxidative

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stress. This is cytochrome 3, this process that we are working up to will take oxygen

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and create water. The whole purpose of breaking these molecules down into smaller molecules

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is this. Cytochrome 3 is called cytochrome C reductase. Heme proteins and iron sulfur

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clusters are used. Heme groups alternate between ferrous and ferric. Proton gradients begin

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to add up a two step Q cycle is used to move into cytochrome C oxidase. This is a transfer

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in breaking down of processes or elements because cytochrome C can only accept a single

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electron at one time. So this occurs in two steps. The cytochrome 3 also releases the

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four protons. Just a special note about the hydrogen 2. Hydrogen is building up and is

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necessary. So we are processing different elements, different molecules I should say,

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into the matrix and the inter membrane. And this brings us to maybe the most underrated

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or not appreciated process in the whole mitochondria. And that's the creation of water. Now I ran

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through the first processes to get to this point fairly quickly and I did not highlight

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the elements or the molecules that's being produced, the amount of them and essentially

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I didn't mention the reasons. However, we are here for these reasons right now. One

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is to get to cytochrome C oxidase as fast as possible and two there are obviously lots

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of molecules and atomic processes going on here. I want to be mindful of the podcast.

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I want to be mindful of the information regarding autism because you might think we haven't

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even talked about autism. However, I would hold off on that thought. So cytochrome C

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oxidase. Remember this has four red light chromophores from the cause of autism episode

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from 620 to 860 nanometer light. This process creates water. The electrons we've been transferring

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and creating and the oxygen that's being created into water. Light. Remember the light story

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the whole purpose of this topic. Light charge separates water. Water equals H plus the hydrogen

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and oxygen and two electrons. So how does light create more water? We've established light

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is electromagnetic. Understand it? We've established autism is a light story. Low electrons, low

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melanin is a modern human phenomena. Also we've established isolated light, especially blue

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light, dehydrates cells. Well this is it. This is where the damage is in the lipid rafts

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of the process of exchanging these molecules from smaller molecules and transferring them

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down the process. And here is a big takeaway because we've now explained the creation of

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water and the mitochondria. Not all water is equal. It changes its physics based on

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the environment it's in. Mitochondria is the reverse process of photosynthesis. Instead

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of producing oxygen and sugar like the photosynthesis of a plant, the mitochondria produces carbon

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dioxide and water. This water is an electromagnetic capacitor. It is a battery. An old car battery

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uses this process. A key note here is water is a dipole, meaning the electrons has negative

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charges and protons as positive charges. You know that we are creating electrons and

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protons which are crucial ingredients to this process. Now you can understand that the

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iron and some oxygen and water, the magnetic properties of these elements are crucial.

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In addition, water is a paradoxity, meaning it is very responsible for the clock timing

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mechanisms occurring within this mitochondrial matrix. Our clock timed mechanisms are crucial

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and that begins in the SCN. We've discussed the SCN. How and when are all of these elements

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and these biological ingredients functioning are critical. And another note about the water

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here in the mitochondria and just water in general. Water is very heat tolerant and we

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want our mitochondria to be this heat and dissipative structure. We want massive amounts

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of energy and production here. Mother Nature chose water. It uses water accurately here.

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It's by design. Water with heat tolerant, it can endure so much and be very reliable.

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You can also remember melanin from the cause of autism episode. How melanin is also very

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enduring and can absorb all frequencies of light. The light which is, you know, a vast

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component of this story and also within melanin being that neuroprotective. We've discussed

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that neuroprotective role here. It keeps this process functioning. Different light has different

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effects on water, has different effects on our electron transport chain. Light has different

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effects on the glucose getting to the cytoplasm released from the organs. Light, remember the

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pom-C story. Remember now that we've discussed glycolysis and remember the previous conversations

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about pom-C. Pro, opioid, malano, cortin and how cortisol and alpha malano site stimulating

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hormones, the melanin found throughout the body on the surface and deep inside of us

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and tissues and organs are implicated from the light source. Melanin here is a different

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story. Melanin and light takes the water and is the semi-conductive properties. It uses

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this in a dissipative structure. In other words, it is a method of creating more energy

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and remember the pom-C and how insulin is generated from here, from CLIP, CLIP. If glucose

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is affected and insulin sensitivity is infected, the process getting to the mitochondria for

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glycolysis are implicated. Remember the blue light, our modern light now, about 440 to 480

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nanometer light. That's modern LED and tech light. Most, nearly all of the light exposure

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humans get now falls within this range and this dehydrates cells. Now maybe you can understand

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why. We've talked about cytochrome c-oxidase. These dehydrated cells, the implications to

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water production from cytochrome c-oxidase will cause hetero plasma which is a decrease

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of water and this is where disease manifests in the body. This is lower dissipative ability.

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Meaning as we age, water production drops. Okay, so there's an understanding that humans

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are roughly 70% water or so. I don't know what the paradigm suggests but at birth we

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are about 80% water and that is shown to be we decrease water about 10% every decade.

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Now Doug Wallace is a good source of this and so is Jack Cruz. As we age and reduce our

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water production we need to increase the electrons getting to the mitochondria level to produce

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more water. We have to supplement our aging and the decrease of electrons with proper,

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that's key here, proper electromagnetic fields. The melanin story which is frequently discussed

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or mentioned at least throughout the several episodes of the podcast. This is underrated

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here too. Melanin charge separates water like no other element or molecule in the human

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body and lastly on the cytochrome c-oxidase for now. I mentioned there are four red light

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chromophores and this one protein. Why are there four red light chromophores and cytochrome

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c-oxidase? Why and how are humans using this? Especially with our modern light. Based on

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some information from a decentralized neuro surgeon, he has over 10,000 surgeries in his

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career. He suggests that the red light chromophores and cytochrome c-oxidase where water is produced

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links the entire mitochondrial matrix including the protein metabolism, the TCA cycle glycolysis

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and the red light chromophores. Red light is what spins the FO head and ATP synthase

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which is the fifth and final cytochrome. Now you can understand maybe you can kind of attach

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the rates of autism follows almost identically with the sources of light. One, the timing

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of artificial light that we are under beginning back in the 1930s with an incandescent type

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all the way up through the LED production and the shift to LED and now technology, technology

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follows essentially every single human being especially around the ages of 6 to 8. I guess

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maybe closer to 8 to 10 people are getting cell phones now and autism is a generational

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issue. With this light exposure people's water production is decreasing and our melanin

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inside of us is decreasing. This is why light and melanin are the key candidates for the

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cause of autism. The light exposure follows identically the rates of autism. And second

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thing we need to consider is that power source the sun spectra at 280 to 3100 nanometers our

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biology is missing those components. Okay so we make water and now let's get to the

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cytochrome 5 which is ATP synthase ATPase. The hydrogen charge separated in cytochrome

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c-oxidase to produce water that charge separation or protons. The protons are H plus ions,

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positive charged ions this is hydrogen. On the ATPase is an FO head. FO is a proton

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channel. In ATPase the head spins 9000 to 12000 times per second and every 3 or 4 spins

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creates 1 ATP. Okay so here's some more magnetic properties here the FO head with that spinning

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that rapid spinning creates a magnetic field. This is a quantum nano rotary engine that

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works on red light. Where are modern humans getting red light? Remember the rant just

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a couple of minutes ago the sun is 43 to 47 percent red but it requires humans to spend

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time under it and remember our photosynthesis. Okay so why the red light? You remember from

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the cause of autism episode and probably some other episodes that red light penetrates the

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body deeper than any other specter of light including bones. Red light penetrates bones

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and remember the antioxidant effect here with the with the cancer treatment. Red light

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is very powerful against carcinoma and tumors and that is shown in many many articles in

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PubMed. In addition what people might fail to understand is our mitochondria is where

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95 percent of our melatonin is generated. Melatonin is a light hormone that works at night the

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absence of light and this is our number one antioxidant. So this is all from longer wavelengths

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of light on one side of the sun spectra but also you can kind of come together here and

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understand that this is more and more of the light story light water magnetism with the

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light story it doesn't just include those longer wavelengths of light vitamin D receptors

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are involved. Okay so more sun this is UVB remember the biosynthesis discussed in autism

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and gastrointestinal problems it goes the biosynthesis it goes pre vitamin D2 and D3

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is 216 nanometer light. Tachysterol the next process is 280 nanometer light and then pro

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vitamin D3 is 293 nanometer light and then we get to vitamin D the full synthesis of

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vitamin D is 312 nanometer light. The VDR blocks electron transport chain but that's

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okay here that just means we don't need to eat as much when we are outside if you've

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ever noticed that maybe you don't eat as much whenever you're outside in the sun that's

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because that glucose used during glycolysis is kind of supplemented here with the VDR

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structures. Our photobiomodulation and the mitochondria as dissipative structures in

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the sense of nonlinear optics used in human biology. Healthy human biology is built in

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mechanism to create energy and we do this we've discussed pom-C and that release of

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cortisol and that coincides with glucose this is what it's all about we evolved under

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the sun and this natural electromagnetic fields we've taken the electrons from the

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sun and used it for energy production inside of us inside the so-called powerhouse of the

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cell. Modern humans and all of our chronic diseases are electron deficient. Most ATP

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from the cell happens from sun on cytochrome c-oxidase and ATPase from infrared and UV

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on VDR receptors. Now you can begin to understand the obesity epidemic. Now you can understand

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type 2 diabetes. Remember how we've mentioned the insulin sensitivity and the release of

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glucose and metabolizing all of this energy production. Obesity is a cause of people

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losing energy to the environment. It's not all cases of calories in versus calories

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out food intake and the lack of movement and exercise. Now the lack of movement and exercise

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could be explained here too because people don't have energy because they're not they're

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not producing water. For the autism story now you can even understand the roles of autism

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and metabolism and autism and inflammation. Cells and our biology are not adapted to our

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new environments. You understanding this? We are adapting but these are not healthy adaptations.

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Autism is neuroplasticity to our light and energy change. Research and people's beliefs

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are in the wrong place. There are all of these autism and XYZ. I am tired of autism and XYZ.

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I am tired quite frankly of autism and allergies or autism and eczema or autism and gastrointestinal

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problems. Autism and dyspraxia. Autism has a higher rate of higher chance of Alzheimer's

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and Parkinson's. On that note you ought to be able to understand a little bit better

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now the role of light and these rapid cognitive declines that we are now seeing. And I've

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said Alzheimer's is a reverse process of autism. Hopefully you can kind of make sense

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of this. Now as we discussed the cell metabolism, the way that the cell is functioning, the

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powerhouse with autism you know the problems exist on the cellular level and the synaptic

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level. The cellular level here is explained. This is why cells aren't developing. Also

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to note that remember our genes response to the environment. In other words our environmental

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signals informs the genes how to respond. The environmental signals are the cues for

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DNA sequencing and guess what? In the cell nucleus the organelle of DNA sequencing and

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mitochondria are closely related. Genetic studies receives much attention. There's a

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lot of money thrown at GWAS studies. This genome sequencing and genome-wide understanding

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and with autism there are over 100 so-called risk genes. Now what this is saying is there

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are many complicated factors here. There are many genes involved that might cause autism

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or might not cause autism. This because you have duplications or deletions, copy number

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variants and so forth of this gene. Well it might mean autism. In my opinion autism

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research because of the amount of funding and attention thrown at it. But the genes

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has reached a dead end and at the dead end it takes bulldozers and just kind of barrels

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through trying to find some sort of hidden treasure. And this is all wrong. The genes

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of humans the DNA is vastly different than the mitochondria genes. Mitochondria has

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its own DNA. There are only 37 total for mitochondria. Now this is a huge difference and with everything

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we've just discussed you ought to understand that huh mitochondria is very important to

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the cell health, to our life. Not only is it just 37 genes but the cytochromes, the powerhouses,

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the source of energy processing these electrons and protons and creating water and creating

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ATP. There are only 13 DNA responsible of the mitochondria for this function. This meaning

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13 genes that we can study to really find out some more information about. What is autism?

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If you are listening to the podcast or listening to the episode please feel free to leave a

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review or rating. In podcasting reviews, ratings and downloads are crucial and I very much

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appreciate your feedback. You can contact me on X at RPS 47586. We can have discussions

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about autism and especially the cause of autism. These atomic molecular levels. You can email

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me info.fromthespectrum.com. Thank you for listening to From the Spectrum podcast.

