WEBVTT

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I would like to take a moment and mention a pressing

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issue we are seeing in our modern world. And

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that is tech use and tech light. The data are

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impressive and concerning on isolated wavelengths

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of light, especially shorter wavelengths, which

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is blue light. For those that don't know, We

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have chromophores, which are special proteins

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that absorbs specific wavelengths of light. For

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blue light, the light that is LED light and tech

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light, that protein is called melanopsin. Melanopsin

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is responsible for our circadian biology, physiology,

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and cell functioning. hormone regulation, and

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even a connection to an area huge for mood. A

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consideration we should include is this protein

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was not even discovered until 1998. It seems

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important for us to understand how our biology

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uses the different wavelengths of light. for

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various aspects of our biology. This blue light

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chromophore is our master controller, our master

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clock. Remember circadian rhythm is a two -part

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process, two independent parts, light and dark.

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For a quick reference, see the 2017 Nobel Prize

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in Physiology medicine. But for now, I have something

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exciting. I want to introduce a product unlike

00:02:01.920 --> 00:02:06.799
any other product available. A highlight is the

00:02:06.799 --> 00:02:10.759
product from Daylight Computer Company created

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their product based on these factors. The Daylight

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Computer is completely blue light free. It has

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no flicker. Short wavelength flicker. is extremely

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harmful for our eyes and downstream biology.

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Light flicker is constantly turning our central

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nervous system on and off. Essentially it is

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like going to a light switch and repeatedly turning

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it on and off. The problem is blue light and

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LED light does this and it is so rapid You cannot

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even perceive this in real time. The daylight

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computer is the lowest stimulation and foremost

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for sensory sensitive users. It is no question

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that the alternative product, especially when

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used at night, do not address or consider this

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in their product. It is so toxic to human biology.

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Big tech corporations have patents on how their

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short wavelength implicate the human nervous

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system. And a bonus, despite daylight computer

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not having backlight, it is very functional for

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outdoor use. And of course, increased sunlight

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is always preferred. I am happy to offer a discount

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for the Daylight Computer. You can use the code

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Autism for a $25 off coupon. Again, use the code

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Autism and the discount code for $25 off. See

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the link in the show notes to Daylight Computer

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Company or just give it a quick search in your

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internet browser. Use the code Autism. for $25

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off. For today's episode, we will explore a dense

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part of human biology, a hot topic as well. We

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will cover a popular protein of the podcast,

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tryptophan, an aromatic amino acid, and introduce

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microtubules and expand on mitosis. For tryptophan,

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this is a very special protein whereby it has

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one codon. Tryptophan and methionine have only

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one. Remember methionine provides a donor, SAM,

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S -A -M, for M -T -H -F -R, the methylene tetrahydrofolate

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reductase. And folate, the vitamin B9, is heavily

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used for DNA methylation in this process. Anyway,

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tryptophan, the one codon is UGG. This is really

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upstream in our biology and I don't really want

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to go here. I don't like to go here. Mainly because

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some of the data is mucky and I am afraid I won't

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come back from this area. It's too easy with

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the obsessions and the restricted fixated interest

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that are abnormal in intensity or focus. But

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the DNA is A, T, C, H. Apple tree and car in

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garage. The A in T and the C in G. It's high

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school biology. In RNA, the T is changed to U.

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So for tryptophan, the DNA is TGG. The RNA is

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UGG. For microtubules, these are train tracks

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for cells. They are tiny tubes and provide a

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track for movement and a frame for the cell to

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develop around. Mitosis, how cells copy each

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other. One, cells copy the DNA. The microtubules

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provide a spindle which grabs the DNA and then

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splits it. An easy example of this process happening

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is skin repairing after a cut. For tryptophan,

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this is an essential amino acid and a building

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block of proteins. Remember, we only have 20

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amino acids, and then within those 20, you can

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break those down into subtypes, subcategories,

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and so forth. The aromatic amino acids, are very

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special. The tryptophan provides a tubulin which

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is primary protein component for these microtubules.

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Microtubules are dynamic cytoskeletal structures

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involved in cellular processes like the mitosis

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or intracellular transport and maintaining the

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cell's shape. This is all going to be important

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for autism. Now, admittedly, this isn't really

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involved much with autism research, but I have

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a problem with it. We need to look at these normal

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processes, these underlying processes of building

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the living organism, and find out from these

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upstream processes where autism is developing.

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What is going on? What is wrong? and what is

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causing these problems. And for that reason,

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these upstream processes are heavily important.

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So the tryptophan and tubulin. Tryptophan residues

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are present in the amino acid sequence for the

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tubulin in an alpha and beta subunit. And these

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residues are contributors for the proteins' folding,

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stability, and these interactions with other

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molecules. Hence, the building block. An example

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of this is tryptophan's hydrophobic and the aromatic

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properties will influence tubulin and its binding

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to the microtubule -associated proteins, or called

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MAPs. The aromatics have an indole group. So

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this is a carbon, hydrogen, and nitrogen. The

00:09:16.350 --> 00:09:22.190
endo group is a benzene ring fused with additional

00:09:22.190 --> 00:09:28.710
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and performance. Shapiro launched Chroma to restore

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Chroma makes serves a purpose to create devices

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that are precise, durable, and effective for

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improving human life. Remember, humans use different

00:11:42.730 --> 00:11:45.649
wavelengths of light for different functions

00:11:45.649 --> 00:11:51.789
of life. Remember when I ask, what do you think

00:11:51.789 --> 00:11:58.409
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00:11:58.409 --> 00:12:03.450
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00:12:27.490 --> 00:12:34.840
at checkout for a 10 % off discount. What's special

00:12:34.840 --> 00:12:39.299
about these aromatic amino acids as they fluoresce?

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We've talked about this mainly in the Cause of

00:12:41.659 --> 00:12:44.480
Autism episode and a few other episodes from

00:12:44.480 --> 00:12:50.399
time to time. These proteins fluoresce. So this

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means that tryptophan's natural fluorescence

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means they absorb light and then emit light.

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What's fascinating about this is Once these proteins

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absorb or are excited by UV light, remember 200

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to 400 nanometer light, and the tryptophan peaks

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at 280 on the absorption, and it fluoresces,

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it emits light around mid 300s, I think. But

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in studies, scientists can use this property

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and monitor how the tubulin assembles into the

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microtubules. because of the ability to observe

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the light. There will be a link that shows a

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fascinating video of this, maybe two videos.

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There's a part one and part two. But tryptophan

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and the microtubules, this is a recent video

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too, early to mid -March. So mitosis. This is

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the process by which a eukaryotic cell, mitosis

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is only eukaryotic cells, and this involves dividing

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its nucleus, the cell nucleus, to produce two

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separate cells. Each of the cells need the identical

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set of chromosomes. That is key here. It's a

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key part of the cell cycle in ensuring that genetic

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material is accurately distributed to each of

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the daughter cells, each of the two split cells.

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Mitosis is crucial for the growth of the living

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organism and tissue repair. Remember the cut

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skin. This is a big reason on how the living

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organism kind of maintains and lives efficiently.

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So an overview of the mitosis. Mitosis is a five

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-step process. And then there's the cytokinesis,

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a division of the actual cytoplasm. So the microtubules,

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as part of that mitotic spindle mentioned earlier,

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have a key role in moving the chromosomes apart

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and into these additional cells. So the first

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phase of mitosis is prophase. What happens here

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is chromatin. which are loose DNAs, condenses

00:15:25.360 --> 00:15:29.779
into very distinct chromosomes. And they do their

00:15:29.779 --> 00:15:34.299
magical work with chromatids and centromeres.

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I'm not going to get into that. But the nuclear

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envelope will start to break down. And then this

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mitotic spindle, mentioned earlier, that structure

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from the microtubules will begin to form. And

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this is a very crucial process. in the transfer

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of information. Second stage is pro -metaphase.

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So what happens here is the nuclear envelope

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will fully disassemble and this allows a spindle

00:16:05.230 --> 00:16:08.570
of the microtubules to access these chromosomes.

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Remember that they are transferring. They provide

00:16:12.309 --> 00:16:20.190
tracks. The microtubules grow here. Some of them

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latch onto the various biology or molecules.

00:16:25.389 --> 00:16:29.929
And some of them, they just stabilize the spindle.

00:16:30.570 --> 00:16:34.009
And chromosomes here will start moving as the

00:16:34.009 --> 00:16:37.830
microtubules tug on them. Observe this in the

00:16:37.830 --> 00:16:42.250
video provided. The third phase is metaphase.

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The chromosomes will begin to align at the cell's

00:16:46.250 --> 00:16:50.669
equator plane. This is huge here. This will start

00:16:50.669 --> 00:16:53.649
to pull into position by the spindle and each

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chromosome is attached to a microtubule from

00:16:57.490 --> 00:17:01.509
opposite poles. The microtubule here provides

00:17:01.509 --> 00:17:04.910
tensions and ensures chromosomes are perfectly

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centered. This is a very dynamic process, very

00:17:09.529 --> 00:17:13.470
fascinating thing. And the cells can check that

00:17:13.470 --> 00:17:17.730
all of these molecules deeply attached here are

00:17:17.730 --> 00:17:21.690
attached before processing before moving forward.

00:17:23.170 --> 00:17:26.910
The fourth phase is anaphase. What happens here

00:17:26.910 --> 00:17:32.190
is sister chromatids are pulled apart and the

00:17:32.190 --> 00:17:35.210
microtubules will begin to shorten and this separates

00:17:35.210 --> 00:17:39.430
into individual chromosomes. These cells, they

00:17:39.430 --> 00:17:43.450
begin to elongate as the microtubules begin to

00:17:43.450 --> 00:17:48.089
expand and lengthen. A huge role here for the

00:17:48.089 --> 00:17:55.440
microtubules They shrink and they drag the chromosomes

00:17:55.440 --> 00:17:59.180
to the opposite poles. They kind of make room

00:17:59.180 --> 00:18:05.079
for these other molecules being attached. And

00:18:05.079 --> 00:18:07.940
lastly, the fifth and final phase is telophase.

00:18:08.420 --> 00:18:10.680
So the chromosomes will begin to reach these

00:18:10.680 --> 00:18:15.500
poles, their destination, and begin to decondense

00:18:15.500 --> 00:18:19.380
back into a chromatin. The nuclear envelopes

00:18:19.380 --> 00:18:23.119
reform around each set of the chromosomes and

00:18:23.119 --> 00:18:26.460
this provides two separate, two different nuclei.

00:18:27.400 --> 00:18:30.559
Then the spindle disassembles. It's gone. It's

00:18:30.559 --> 00:18:35.359
done. The microtubule here will break down and

00:18:35.359 --> 00:18:41.359
make room for the two distinct nuclei. Cytokinesis

00:18:41.359 --> 00:18:44.259
will then happen and this is when the cytoplasm

00:18:44.259 --> 00:18:48.720
divides. This splits the cell into two daughter

00:18:48.720 --> 00:18:53.680
cells, which has its own nucleus, as we just

00:18:53.680 --> 00:18:58.119
discovered, and the organelles. So in mammalian

00:18:58.119 --> 00:19:03.019
cells, these complex cells, the eukaryotic cells,

00:19:03.759 --> 00:19:07.619
a cleavage will happen, and it forms into actin

00:19:07.619 --> 00:19:10.880
filaments, which have very dynamic roles as an

00:19:10.880 --> 00:19:13.720
organelle as well. Remember, the eukaryotic cells

00:19:13.720 --> 00:19:16.990
are more complex. than the prokaryotic cells.

00:19:17.410 --> 00:19:20.509
Some roles of the actin filaments are cell movement

00:19:20.509 --> 00:19:25.569
and the cell shape, cell adhesion. Remember the

00:19:25.569 --> 00:19:29.769
conversation about T3 that the process of the

00:19:29.769 --> 00:19:33.890
the thyroid and providing T3 and T4 and T3's

00:19:33.890 --> 00:19:37.549
roles those surprising roles with cells. And

00:19:37.549 --> 00:19:40.990
also actin filaments are involved in signal transduction.

00:19:41.730 --> 00:19:45.579
These are all in the The cytoplasm with things

00:19:45.579 --> 00:19:48.619
like the mitochondria and so forth, the DNA and

00:19:48.619 --> 00:19:52.440
the nucleus. So a little review here. The chromosomes

00:19:52.440 --> 00:19:56.240
carry the genetic information that's being divided.

00:19:56.660 --> 00:20:00.579
These are little messengers. They're like the

00:20:00.579 --> 00:20:04.259
post office workers, Pony Express even. The microtubules

00:20:04.259 --> 00:20:07.619
will form the spindle which will then help move

00:20:07.619 --> 00:20:11.460
the chromosomes and tryptophan is a part of this

00:20:11.460 --> 00:20:15.319
for the tubulin. and the tryptophan contributes

00:20:15.319 --> 00:20:20.519
to the structure. So this is important. The mitosis

00:20:20.519 --> 00:20:25.019
is important because it ensures each of the split

00:20:25.019 --> 00:20:28.359
divided cells will inherit an identical copy

00:20:28.359 --> 00:20:33.140
of the genome. And with autism, you know this

00:20:33.140 --> 00:20:37.380
is implicated here. This is a region of interest

00:20:37.380 --> 00:20:43.279
here. So the mitosis and these microtubules are

00:20:43.279 --> 00:20:46.759
huge in prenatal development. Because mitosis

00:20:46.759 --> 00:20:51.140
is a very critical part during the embryonic

00:20:51.140 --> 00:20:53.680
development, especially in this formation of

00:20:53.680 --> 00:20:56.759
the brain. Remember, neuralation. Remember those

00:20:56.759 --> 00:21:00.779
subtypes of cells with the proencephalon, the

00:21:00.779 --> 00:21:04.460
mesencephalon, the romencephalon, and how the

00:21:04.460 --> 00:21:09.559
brain is developed here. The neural tube. We've

00:21:09.559 --> 00:21:12.289
discussed the neural tube. Right? This is developing

00:21:12.289 --> 00:21:15.390
the central nervous system. And this comes early

00:21:15.390 --> 00:21:19.750
in pregnancies around that week 3 to 4, days

00:21:19.750 --> 00:21:23.069
22 to 28 is what we're talking about here. Remember

00:21:23.069 --> 00:21:27.809
the episodes on neuralation. Cells undergo rapid

00:21:27.809 --> 00:21:30.930
mitotic division here. This is how the complex

00:21:30.930 --> 00:21:36.410
living organism becomes so complex. Microtubules

00:21:36.410 --> 00:21:40.980
made of these tubulin proteins. from the tryptophan.

00:21:41.819 --> 00:21:44.059
When these things that we're talking about today

00:21:44.059 --> 00:21:48.859
are disrupted, these microtubule functions or

00:21:48.859 --> 00:21:52.680
these any part of the mitosis cycle, this affects

00:21:52.680 --> 00:21:57.200
how neurons proliferate, migrate, and connect.

00:21:58.200 --> 00:22:00.480
Sounds like autism. Sounds like everything we

00:22:00.480 --> 00:22:04.660
cover in autism with the migration problem and

00:22:04.660 --> 00:22:10.579
the hyper and hypo connectivity. For brain size,

00:22:11.420 --> 00:22:14.500
we've also covered this. The research shows that

00:22:14.500 --> 00:22:18.220
some children have larger brain sizes. It's not

00:22:18.220 --> 00:22:22.640
uncommon that they have microcephaly. I think

00:22:22.640 --> 00:22:27.039
UC San Diego probably does the most work on this

00:22:27.039 --> 00:22:31.660
topic. So if these neuro progenitor cells, if

00:22:31.660 --> 00:22:35.279
they divide too much or too quickly due to that

00:22:35.279 --> 00:22:40.160
microtubule dysregulation, it becomes a problem

00:22:40.160 --> 00:22:44.099
for the cortical tissues. And remember the roles

00:22:44.099 --> 00:22:49.400
of P10, phosphatase, Tencin, in regulating this

00:22:49.400 --> 00:22:54.160
process here. In addition, post birth, this is

00:22:54.160 --> 00:22:57.200
huge up into the, let's say, the critical period.

00:22:58.559 --> 00:23:01.480
The living organism, the human baby, the infant,

00:23:02.740 --> 00:23:07.210
undergoes vast and massive development. at rapid

00:23:07.210 --> 00:23:11.029
paces here. This is a problem here. All of these

00:23:11.029 --> 00:23:15.549
things need to be in sync with exquisite timing.

00:23:17.430 --> 00:23:20.529
So the hypo and hyper connections in autism is

00:23:20.529 --> 00:23:23.730
very common. It's very well established. It's

00:23:23.730 --> 00:23:29.269
undisputed. With the neuron proliferation and

00:23:29.269 --> 00:23:31.910
the migration, there's a problem here during

00:23:31.910 --> 00:23:36.029
prenatal development. Because these neurons the

00:23:36.029 --> 00:23:39.549
ventricular zone, tying this back to that ventricular

00:23:39.549 --> 00:23:42.230
zone when the neural tube starts to fold and

00:23:42.230 --> 00:23:46.430
the crest becomes alive. They migrate to their

00:23:46.430 --> 00:23:50.589
destinations. They migrate based off of the tracks

00:23:50.589 --> 00:23:54.410
and the guides from the microtubules and these

00:23:54.410 --> 00:23:58.509
base structures like the radial glia. We've covered

00:23:58.509 --> 00:24:01.529
that in the neuralation and the conversations

00:24:01.529 --> 00:24:05.730
with migration. And if the mitosis produces too

00:24:05.730 --> 00:24:11.069
many neurons, or if migration goes abnormal,

00:24:12.029 --> 00:24:14.750
where are the neurons going to go? How are they

00:24:14.750 --> 00:24:17.450
going to get there, or where they're supposed

00:24:17.450 --> 00:24:20.789
to go? Remember, they're supposed to migrate

00:24:20.789 --> 00:24:24.490
to similar cells, just like we flock to friends,

00:24:24.650 --> 00:24:27.890
we flock to similarities. That's the process

00:24:27.890 --> 00:24:33.789
of these neurons ought to be doing. With hyperconnectivity,

00:24:34.710 --> 00:24:38.849
this also explains the excessive synaptic connections.

00:24:38.950 --> 00:24:43.710
Remember the neurorexin, the Shenk 3, and the

00:24:43.710 --> 00:24:47.589
neuroligand. There's a big problem with the synaptic

00:24:47.589 --> 00:24:52.809
connections with the autistic phenotype. With

00:24:52.809 --> 00:24:56.990
that is a process called synaptic pruning. And

00:24:56.990 --> 00:25:00.369
after the birth, the brain trims excessive connections

00:25:00.369 --> 00:25:04.039
in a process called synaptic pruning, which also

00:25:04.039 --> 00:25:06.480
involves the microtubules for transporting the

00:25:06.480 --> 00:25:12.180
materials to these areas. With autism, there's

00:25:12.180 --> 00:25:16.000
a problem with the pruning. And this leaves these

00:25:16.000 --> 00:25:18.359
crowded areas, these hyper -connected areas,

00:25:18.700 --> 00:25:23.539
locally. Remember the sensation processing episodes

00:25:23.539 --> 00:25:27.220
where there's studies showing that early on in

00:25:27.220 --> 00:25:31.119
the process of sensory, when we're processing

00:25:31.420 --> 00:25:37.000
like a visual cue or auditory cue. Early in this

00:25:37.000 --> 00:25:40.799
process, we're sending these sensations down

00:25:40.799 --> 00:25:44.240
through the brain for perception to make sense

00:25:44.240 --> 00:25:49.180
of the environment. Early in this process, the

00:25:49.180 --> 00:25:53.539
first stages, there's a problem with the sensory

00:25:53.539 --> 00:25:57.980
processing. And the downstream connections here,

00:25:58.200 --> 00:26:01.720
these distal connections, will phase out. With

00:26:01.720 --> 00:26:04.440
autism, at these initial parts of the sensory

00:26:04.440 --> 00:26:08.599
processing, it's overloaded, it's hyper -connected,

00:26:08.640 --> 00:26:11.680
so it's too much too fast. And then it phases

00:26:11.680 --> 00:26:15.099
out before it reaches more like cortical capacities

00:26:15.099 --> 00:26:18.059
or areas of the brain that can help make sense

00:26:18.059 --> 00:26:21.039
of this. The sensory processing problem is a

00:26:21.039 --> 00:26:26.420
huge phenomena here. It is no surprise that autistics,

00:26:26.839 --> 00:26:29.839
one of the most common comorbid problems is sensory

00:26:29.839 --> 00:26:33.630
sensitivities. Remember part two of the sensory

00:26:33.630 --> 00:26:39.089
processing episode when we reviewed four papers

00:26:39.089 --> 00:26:43.609
on sensory processing and paper three showed

00:26:43.609 --> 00:26:47.930
90 % of their subjects had sensory processing

00:26:47.930 --> 00:26:53.829
complications and paper four showed 95 % of the

00:26:53.829 --> 00:26:59.440
subjects had sensory processing problems. A problem

00:26:59.440 --> 00:27:03.039
with this is that cortical development, especially

00:27:03.039 --> 00:27:06.599
in the somatosensory cortex. And this process

00:27:06.599 --> 00:27:11.240
is touched in the auditory cortex. And remember

00:27:11.240 --> 00:27:15.220
the mesencephalon with the superior and inferior

00:27:15.220 --> 00:27:20.299
colliculi. This mesencephalon is a very important

00:27:20.299 --> 00:27:25.029
area, I think. And its goal here is to... bias

00:27:25.029 --> 00:27:27.990
our attention to the environment, make us aware

00:27:27.990 --> 00:27:33.329
of the environment. With autism, we don't care

00:27:33.329 --> 00:27:38.069
about the environment. So with the cortical development,

00:27:38.130 --> 00:27:42.329
if these microtubules that are responsible for

00:27:42.329 --> 00:27:47.069
the migration or division are abnormal, these

00:27:47.069 --> 00:27:50.309
areas won't be able to go downstream, go to their

00:27:50.309 --> 00:27:56.579
destination. In addition, A common topic is the

00:27:56.579 --> 00:28:00.880
excitation inhibition imbalance. This is big

00:28:00.880 --> 00:28:04.279
with the sensory processing as well because it

00:28:04.279 --> 00:28:08.099
requires a balance, a more balanced seesaw instead

00:28:08.099 --> 00:28:11.980
of one side always high, one side always low.

00:28:12.480 --> 00:28:16.380
For autism, it's mostly high excitation and low

00:28:16.380 --> 00:28:19.539
inhibition. And the roles of this tryptophan

00:28:19.539 --> 00:28:22.470
being that aromatic amino acid and providing

00:28:22.470 --> 00:28:26.250
the tubulence for these microtubules. This is

00:28:26.250 --> 00:28:30.089
a region of interest and likely an untouched

00:28:30.089 --> 00:28:33.589
region of interest for some reason. We need to

00:28:33.589 --> 00:28:37.930
go here. Some implications with the prenatal

00:28:37.930 --> 00:28:44.230
with the autism. We've mentioned Shenk 3 and

00:28:44.230 --> 00:28:48.690
how this helps regulate the mitosis and the microtubule

00:28:48.690 --> 00:28:52.319
function for that synaptic formation. and the

00:28:52.319 --> 00:28:57.599
P10. The environment is a problem. There are

00:28:57.599 --> 00:29:00.680
a lot of environmental toxins being identified

00:29:00.680 --> 00:29:06.000
now for autism. My question is, is it do we not

00:29:06.000 --> 00:29:10.579
have enough DHA and melanin and so forth, melatonin

00:29:10.579 --> 00:29:15.059
and so forth, glutathione, or are the toxins

00:29:15.059 --> 00:29:18.339
just that much increased? Are we that much more

00:29:18.339 --> 00:29:23.019
exposed? probably a little bit of both. But the

00:29:23.019 --> 00:29:25.640
main environmental toxin here that's going to

00:29:25.640 --> 00:29:30.420
do these insults is the light environment. Because

00:29:30.420 --> 00:29:32.980
we are not getting that proper sunlight from

00:29:32.980 --> 00:29:36.700
that full light spectrum, I should say, to develop.

00:29:37.119 --> 00:29:40.059
We are no different from the tree or your favorite

00:29:40.059 --> 00:29:43.400
plant outside. If we're not getting that light,

00:29:43.720 --> 00:29:47.880
we're not going to develop. But if you block

00:29:47.880 --> 00:29:50.460
the Sun from the tree, you're going to think,

00:29:50.720 --> 00:29:52.900
oh, well, that's why it's dying or that's why

00:29:52.900 --> 00:29:57.059
it didn't develop through germination. Why are

00:29:57.059 --> 00:30:02.859
we so complicated on this? Some other functions

00:30:02.859 --> 00:30:05.960
of the microtubules in early embryonic stages

00:30:05.960 --> 00:30:09.500
are during the fertilization. Why I want to mention

00:30:09.500 --> 00:30:12.720
this is because the environment of the mother

00:30:12.720 --> 00:30:16.589
here has vastly changed and this is occurring

00:30:16.589 --> 00:30:20.750
immediately. These processes once sperm meets

00:30:20.750 --> 00:30:25.230
egg and we undergo this mitosis on all these

00:30:25.230 --> 00:30:29.930
cell proliferations this comes fast. It turns

00:30:29.930 --> 00:30:34.650
the zygotic cell two cells and then four cells

00:30:34.650 --> 00:30:39.650
and then it just keeps on multiplying. A key

00:30:39.650 --> 00:30:42.670
detail here is tryptophan residues. Remember

00:30:42.670 --> 00:30:45.369
those residues in that tubulin. This will help

00:30:45.369 --> 00:30:49.849
stabilize this. If it's off immediately, everything

00:30:49.849 --> 00:30:53.509
downstream here will be off. That's why I want

00:30:53.509 --> 00:30:57.630
to go more upstream. In the womb, this happens

00:30:57.630 --> 00:31:01.430
fast, within days of conception, before you even

00:31:01.430 --> 00:31:05.170
know, weeks, maybe months before you even know

00:31:05.170 --> 00:31:08.990
that this is happening in your body. it is happening

00:31:08.990 --> 00:31:15.670
in your body. This can begin as far as or as

00:31:15.670 --> 00:31:19.170
soon as around day six or seven that the embryo

00:31:19.170 --> 00:31:23.730
travels down the tube towards the implantation

00:31:23.730 --> 00:31:27.210
and there are things that you can look up like

00:31:27.210 --> 00:31:31.349
blastocyst which is the microtubules here will

00:31:31.349 --> 00:31:35.750
help establish the cell polarity and then the

00:31:35.750 --> 00:31:39.400
so -called blastocyst gives rise to the inner

00:31:39.400 --> 00:31:42.400
cell mass, which is that future embryo. And then

00:31:42.400 --> 00:31:46.900
the outer, the outer blast, which is the placenta.

00:31:47.140 --> 00:31:49.940
Remember Dr. Hannah Stevens taking us through

00:31:49.940 --> 00:31:52.440
the role of the placenta from the mother and

00:31:52.440 --> 00:31:56.339
the womb, how this is developed. And already

00:31:56.339 --> 00:32:01.299
these microtubules, they will function to make

00:32:01.299 --> 00:32:04.859
sure that these inner cell masses and that embryo

00:32:04.859 --> 00:32:08.819
is properly being exported and transferred and

00:32:08.819 --> 00:32:13.119
developed, then giving rise to gastrolation.

00:32:13.900 --> 00:32:16.480
We didn't talk about gastrolation during the

00:32:16.480 --> 00:32:20.460
neuralation episodes, but this is occurring between

00:32:20.460 --> 00:32:24.000
weeks two and three, and just briefly here. Some

00:32:24.000 --> 00:32:27.799
of these roles will include transforming the

00:32:27.799 --> 00:32:30.259
cells into three layered structures. This is

00:32:30.259 --> 00:32:33.539
the part with the ectoderm, the mesoderm, and

00:32:33.539 --> 00:32:36.619
the endoderm. that we discussed. And the microtubules

00:32:36.619 --> 00:32:40.400
here will ensure that the cells reach their designated

00:32:40.400 --> 00:32:44.559
germ layers. And then we start to form our tissues

00:32:44.559 --> 00:32:47.900
in these organs in the different nervous systems.

00:32:49.980 --> 00:32:53.759
So microtubules role in that neuralation are

00:32:53.759 --> 00:32:57.519
critical for the neural tube formation. The neural

00:32:57.519 --> 00:33:02.339
plate folding. And these microtubules will bundle

00:33:02.339 --> 00:33:04.700
these neuroepithelial cells that we've talked

00:33:04.700 --> 00:33:09.099
about. And the mitosis of these neuroprogenitors,

00:33:09.839 --> 00:33:13.799
and a huge part here for autism, working alongside

00:33:13.799 --> 00:33:16.660
the microtubules, working alongside the radial

00:33:16.660 --> 00:33:22.519
glia, these are important, vastly important for

00:33:22.519 --> 00:33:26.220
the scaffolds responsible for the cell migration.

00:33:27.559 --> 00:33:33.039
Do you understand how complex and small this

00:33:33.039 --> 00:33:36.200
process is and how easily it could be disrupted?

00:33:36.920 --> 00:33:40.539
If you think about not having the proper exposure

00:33:40.539 --> 00:33:45.799
for the living organism to properly grow. Something

00:33:45.799 --> 00:33:48.180
we discussed quite heavily in the autism and

00:33:48.180 --> 00:33:52.779
the womb episode. Several, several episodes ago,

00:33:52.799 --> 00:33:55.900
last summer, we talked about neurogenesis. This

00:33:55.900 --> 00:34:00.839
happens around weeks four to over 20 weeks into

00:34:00.839 --> 00:34:04.099
embryonic development or prenatal development.

00:34:04.940 --> 00:34:07.599
Microtubules here are heavily involved with these

00:34:07.599 --> 00:34:12.679
neurogenesis including the axonal growth and

00:34:12.679 --> 00:34:15.599
also the synaptogenesis. Remember that episode

00:34:15.599 --> 00:34:18.880
long ago? We talked about synaptogenesis as well.

00:34:19.400 --> 00:34:24.260
This is late prenatal to postnatal even. The

00:34:24.260 --> 00:34:27.039
microtubules here will transport materials like

00:34:27.039 --> 00:34:29.860
the vesicles and the mitochondria. We've talked

00:34:29.860 --> 00:34:33.579
about the mitochondria in quite detail. The eukaryotic

00:34:33.579 --> 00:34:37.440
cells need these. There are many, many mitochondria

00:34:37.440 --> 00:34:40.699
in one cell nucleus. Thousands, I believe maybe

00:34:40.699 --> 00:34:45.679
even 5 ,000. And the microtubules are also responsible

00:34:45.679 --> 00:34:48.420
for the axons and the dendrites to form these

00:34:48.420 --> 00:34:53.480
synapses. This begins late in pregnancy and ramps

00:34:53.480 --> 00:34:57.619
up after the birth. Remember that accelerated

00:34:57.619 --> 00:35:01.039
growth after birth. Humans are different than

00:35:01.039 --> 00:35:05.480
other primates whereby we are vastly underdeveloped.

00:35:05.500 --> 00:35:08.340
Remember the Lepton -Milano -Corton pathway episode

00:35:08.340 --> 00:35:12.340
and how the biophotons helps accelerate this

00:35:12.340 --> 00:35:16.300
process and Lepton being like an on -off switch

00:35:16.300 --> 00:35:20.460
here. And remember the episode with Dr. Eric

00:35:20.460 --> 00:35:27.000
Weiss, how his embryonic stem cell is rescuing

00:35:27.000 --> 00:35:30.599
this. This is what I think. These nutrients and

00:35:30.599 --> 00:35:32.920
this development here that we're talking about

00:35:32.920 --> 00:35:36.500
is abnormal in the autistic phenotype, but he

00:35:36.500 --> 00:35:41.320
can use the umbilical cord stem cells to rescue

00:35:41.320 --> 00:35:43.420
this. I think this is what's actually happening.

00:35:46.280 --> 00:35:51.280
So the mother that receives or that gives this

00:35:51.280 --> 00:35:56.340
umbilical cord for this process, that mother

00:35:56.340 --> 00:36:00.679
during pregnancy did not have as many or any

00:36:00.679 --> 00:36:03.619
of these insults that will implicate these processes

00:36:03.619 --> 00:36:06.699
that we're talking about. And remember, Dr. Eric

00:36:06.699 --> 00:36:09.539
Weiss also saying that sometimes that doesn't

00:36:09.539 --> 00:36:13.639
work. Maybe, just maybe, the mother that donated

00:36:13.639 --> 00:36:17.059
that umbilical cord She did have some insults

00:36:17.059 --> 00:36:20.079
that will just not align with the autistic phenotype

00:36:20.079 --> 00:36:23.980
receiving this transfusion. I say that to say

00:36:23.980 --> 00:36:26.840
this because Dr. Eric Weiss talked about this.

00:36:27.019 --> 00:36:29.320
Because of the inflammation, and remember the

00:36:29.320 --> 00:36:31.840
episode with Dr. Richard Fry with the immune

00:36:31.840 --> 00:36:35.519
dysfunction, the mitochondrial dysfunction, and

00:36:35.519 --> 00:36:39.019
the inflammation, the terrible trios, he called

00:36:39.019 --> 00:36:42.860
it. Inflammation here for the maternal immune

00:36:42.860 --> 00:36:47.260
activation. And these cytokines. Cytokines are

00:36:47.260 --> 00:36:49.679
very fascinating and there are very many of them.

00:36:49.679 --> 00:36:52.219
We just keep adding a number to them. Dr. Eric

00:36:52.219 --> 00:36:55.400
Weiss highlights this in quite detail. But something

00:36:55.400 --> 00:36:58.579
like IL -6, which is heavily involved in autism

00:36:58.579 --> 00:37:02.340
research, this can stimulate the neural stem

00:37:02.340 --> 00:37:06.280
cell division in the fetus. This is a very interesting

00:37:06.280 --> 00:37:09.159
topic and a very common topic when we're talking

00:37:09.159 --> 00:37:11.980
about autism, pathophysiology, and so forth.

00:37:12.400 --> 00:37:18.269
IL -6. If you are listening to the podcast, listening

00:37:18.269 --> 00:37:21.150
to the episode, please feel free to leave a review

00:37:21.150 --> 00:37:25.590
or rating. In podcasting, reviews, ratings, and

00:37:25.590 --> 00:37:28.329
downloads are huge, and I very much appreciate

00:37:28.329 --> 00:37:32.389
your feedback. You can contact me on X at RPS

00:37:32.389 --> 00:37:37.329
47586 where we can have conversations about autism.

00:37:38.449 --> 00:37:40.969
You can check out the hop link for links to all

00:37:40.969 --> 00:37:44.239
of the podcasts across different platforms. you

00:37:44.239 --> 00:37:46.539
can check out the YouTube channel for full length

00:37:46.539 --> 00:37:52.599
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00:37:52.599 --> 00:38:00.099
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00:38:00.099 --> 00:38:03.280
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