Latest / Do You F*cking Mind? / Top 3 Brain Facts
Transcript
- 0:11Speaker 1: Hello, beautiful beans, Welcome to this episode. Often now it's
- 0:15Speaker 1: not necessarily an encore, it's more of a best off episode.
- 0:19Speaker 1: And in this episode we are going through the top
- 0:21Speaker 1: three brain facts, your favorite brain facts of last year.
- 0:26Speaker 1: So settle in, enjoy. If you're into if you're having
- 0:30Speaker 1: like a science moment, if you want to feel super
- 0:33Speaker 1: smart at the next engagement that you're at social engagement
- 0:37Speaker 1: not necessarily romantic engagement party, then you can drop some
- 0:40Speaker 1: of these fun fucking brain facts. Enjoy. Keep enjoying your
- 0:45Speaker 1: time off if you have it. If you don't have
- 0:46Speaker 1: time off, slay the day regardless, Love you so much,
- 0:50Speaker 1: Love you so much, and enjoy the episode. Brain Fact
- 0:56Speaker 1: is on CT which is chronic traumatic and cephalopathy. Now,
- 1:02Speaker 1: in a nutshell, that is what is kind of in
- 1:05Speaker 1: the media more recently, where at least in Australia. It
- 1:08Speaker 1: is about this degenerative disease that occurs when people have
- 1:12Speaker 1: repeated head trauma. So you're thinking boxing, rugby, anything where
- 1:17Speaker 1: you are being dealt repeated blows to the head is
- 1:21Speaker 1: something that might arise later on. Now, if you've watched
- 1:25Speaker 1: the Aaron Hernandez documentary on Netflix, that is he was
- 1:31Speaker 1: an American football player who after he died, they found
- 1:36Speaker 1: in his autopsy that he actually had this CTE and
- 1:39Speaker 1: it might have been the cause for his psychological downfall, Okay,
- 1:44Speaker 1: and he then took his life unfortunately. So it's very,
- 1:47Speaker 1: very very good series on Netflix. Highly recommend if you
- 1:51Speaker 1: don't mind watching something that's quite fucking deep and intense.
- 1:54Speaker 1: But let's talk about it.
- 1:55Speaker 2: So what is it?
- 1:56Speaker 1: What is CTA chronic traumatic and obviously chronic trauma because
- 2:00Speaker 1: then it happens more than once encephalopathy, So it's a
- 2:03Speaker 1: progressive and fatal brain disease. And it is associated with
- 2:08Speaker 1: repeated traumatic brain injuries, so such as concussions and repeated
- 2:14Speaker 1: blows to the head. Now, when you think concussion, I
- 2:18Speaker 1: want you to realize that concussion does not mean you
- 2:20Speaker 1: have to be knocked unconscious. You can have concussion and
- 2:24Speaker 1: be conscious conscious. I think there was this belief, at
- 2:27Speaker 1: least a long time ago, that that was yet to
- 2:29Speaker 1: be knocked out. But now we're realizing that concussion can
- 2:32Speaker 1: happen and you don't even realize that you've been concussed.
- 2:35Speaker 1: So that's why it can be quite dangerous. It is
- 2:38Speaker 1: also associated with the development of dementia. Now, what occurs
- 2:43Speaker 1: in CTA is the death of nerve cells or neurons
- 2:46Speaker 1: nerve cells neurons in the brain, and this is what
- 2:49Speaker 1: is known as degeneration. So I talk about degeneration all
- 2:52Speaker 1: the fucking time. This is one of the forms of
- 2:55Speaker 1: degeneration and progressive, meaning that it gets worse over time. Okay,
- 2:59Speaker 1: but the only way to definitively diagnose CTE is post
- 3:04Speaker 1: mortem in an autopsy. Okay, you cannot diagnose it when
- 3:09Speaker 1: the person is alive, and that is due to the
- 3:11Speaker 1: fact that the only way that you can actually probably
- 3:14Speaker 1: diagnose it is by dissecting the brain. Okay, you can't
- 3:18Speaker 1: see it through scans. You can only guess based on
- 3:20Speaker 1: the symptoms and based on the person's history that they
- 3:24Speaker 1: have CTE or some form of dementia because you're obviously
- 3:27Speaker 1: seeing all these symptoms. No one has CTE and it's
- 3:30Speaker 1: perfectly fine and then dies and you're like, oh, wow,
- 3:31Speaker 1: they had it. It's obvious that something's up, but it
- 3:34Speaker 1: could be confused with other degenerative diseases as well, so
- 3:37Speaker 1: you can only confirm it after death. Now, it does
- 3:42Speaker 1: not seem to be related to a one off head injury,
- 3:45Speaker 1: but instead repeated head injury, so you're not seeing this
- 3:48Speaker 1: happen with someone who's had one big blow to the head.
- 3:51Speaker 1: So we often see it in contact sports or people
- 3:54Speaker 1: involved in combat, and it has been seen in people
- 3:58Speaker 1: who are in abusive relationships. They were being hit quite
- 4:01Speaker 1: hard over the head. Okay, So basically it doesn't really
- 4:06Speaker 1: matter where the blow is coming from, but we are
- 4:07Speaker 1: talking repeated blows to the head and it becomes noticeable
- 4:12Speaker 1: years but for some people decades after the head trauma
- 4:16Speaker 1: has occurred. And this is because it's got this progressive nature.
- 4:19Speaker 1: So you could be somebody like Aaron Hernandez whil was
- 4:22Speaker 1: relatively young. You know, you could have all these head
- 4:24Speaker 1: traumas that occur when you're a teenage, teenager or an
- 4:27Speaker 1: early adult, and then it manifests this disease and the
- 4:30Speaker 1: symptoms of the disease manifest just a couple of years,
- 4:33Speaker 1: and for a lot of players or like Boxes, you
- 4:36Speaker 1: might see it manifest twenty years after they retire, Okay,
- 4:41Speaker 1: And that is because, like I said, it's progressive, so
- 4:43Speaker 1: it is progressively getting worse, and you're not saying, like, oh,
- 4:48Speaker 1: it's a flare up. Then it goes away, then it's
- 4:49Speaker 1: a flare up. No, it's like a sliding scale that's
- 4:51Speaker 1: just going to get worse with time. The symptoms include
- 4:56Speaker 1: Wait before I go into the symptoms, I want to
- 4:58Speaker 1: say that we see in a association of CTE developing
- 5:02Speaker 1: alongside something called second impact syndrome. This is very important
- 5:07Speaker 1: to pay attention to. Second impact syndrome is a syndrome
- 5:11Speaker 1: where you get a second head injury that occurs before
- 5:16Speaker 1: the first injury has resolved or the individual has recovered
- 5:20Speaker 1: from it. This is where it can be really dangerous
- 5:22Speaker 1: because you still have this head trauma, potential swelling, potential
- 5:27Speaker 1: neurinal shearing. There's all this shit that goes down in
- 5:31Speaker 1: the brain when you get concussion or whiplash or something
- 5:33Speaker 1: like that. Then when the brain's trying to recover, and
- 5:35Speaker 1: then if you get a second blow, we're talking more swelling,
- 5:38Speaker 1: more trauma on top of existing swelling and trauma that
- 5:42Speaker 1: could then cause major problems in the brain more so
- 5:45Speaker 1: than just the initial head trauma. Okay, so that is
- 5:49Speaker 1: called second impact syndrome. If you are somebody that plays
- 5:52Speaker 1: a contact sport, you have to be so fucking careful
- 5:55Speaker 1: that you are not getting this second impact syndrome. If
- 5:59Speaker 1: you get a blow to the head, you've got to
- 6:00Speaker 1: do everything in your power to make sure. Firstly, you've
- 6:03Speaker 1: got to avoid blows to the head at the best
- 6:05Speaker 1: of times. If you have had the blow to the head,
- 6:08Speaker 1: you want to make sure you're fully recovered. Nothing is
- 6:11Speaker 1: more important than your brain health, No contract, no sport, nothing. Okay,
- 6:14Speaker 1: So just I mean, I love watching rugby, but that
- 6:17Speaker 1: it gives me anxiety when I see that the blows
- 6:19Speaker 1: to the head that these people get. It's full on.
- 6:21Speaker 1: So the symptoms include emotional instability, trouble with thinking just
- 6:27Speaker 1: in general, memory loss, a lot of difficulty planning or organizing,
- 6:33Speaker 1: difficulty carrying out tasks. Then it gets more serious and
- 6:36Speaker 1: we've got aggression. A lot of people become really aggressive.
- 6:39Speaker 1: We've seen cases people with CT that have turned into murderers.
- 6:43Speaker 1: But obviously this is not in every case. It's just
- 6:45Speaker 1: one of the symptoms that some people may get. Impulsivity,
- 6:49Speaker 1: suicidal thoughts, A really common one is depression and apathy,
- 6:53Speaker 1: substance abuse, and then parkinsonism, which is shaking or slowed
- 6:59Speaker 1: movement that comes along with trouble with speech, trouble with balance,
- 7:05Speaker 1: and walking, and also modeor neuron disease, which affects cells
- 7:09Speaker 1: that control breathing, speaking, swallowing, walking.
- 7:12Speaker 2: So it's pretty serious this shit.
- 7:14Speaker 1: Okay. Now, not all symptoms have to be present for
- 7:18Speaker 1: the individual to have CTA. It might just be a
- 7:20Speaker 1: combination of some of the ones that I just mentioned.
- 7:22Speaker 1: And experts think that it comes in two waves. So
- 7:25Speaker 1: the first one early on is close to the time
- 7:28Speaker 1: of the injury. So often here you see the first
- 7:32Speaker 1: wave of symptoms is the mental health issues, the behavioral issues,
- 7:36Speaker 1: the aggression that happens a lot closer to the time
- 7:39Speaker 1: of the injury. Okay, and you might put all of
- 7:42Speaker 1: that down, the irritability, all of that down to something else.
- 7:46Speaker 1: But then you might realize, you know, in combination with
- 7:48Speaker 1: what you see later on in the future, that oh
- 7:50Speaker 1: that was actually CTE. It wasn't that they were just
- 7:52Speaker 1: under stress. You know. The second wave occurs later in
- 7:57Speaker 1: their life, in their sixties, and this is where you
- 8:00Speaker 1: get the impact on memory, thinking, this degenerative progression which
- 8:05Speaker 1: kind of progresses to dementia, like you know, symptoms. That's
- 8:09Speaker 1: kind of what the what it comes across as. Now,
- 8:13Speaker 1: what is happening in the brain. Why why is this happening?
- 8:18Speaker 1: We're basically seeing a build up of a protein called
- 8:21Speaker 1: TAO around the blood vessels. We also see this TOW
- 8:26Speaker 1: that's accumulation found in Alzheimer's disease and other kinds of dementia. However,
- 8:30Speaker 1: this TAW build up and how it occurs in CT
- 8:34Speaker 1: is different to how it occurs in dementia. That is
- 8:37Speaker 1: how you can differentiate the two in post mortem or
- 8:40Speaker 1: in an autopsy. Because of this and also other factors,
- 8:44Speaker 1: the brain atrophies. Now, when you hear atrophy, it means
- 8:47Speaker 1: it breaks down, and because it's breaking down, it gets smaller. Basically,
- 8:51Speaker 1: it's wasting away because the cells when you get this atrophy,
- 8:55Speaker 1: cells can't carry the signal properly. And if cells can't
- 8:59Speaker 1: carry a signal properly, that cell is no longer being used.
- 9:03Speaker 1: And when something's not being used, that an you lose it. Okay,
- 9:08Speaker 1: So when you if you don't use it, you lose it.
- 9:11Speaker 1: It's not getting the nutrients, it's not being able to
- 9:14Speaker 1: send off signals properly, communicate with other cells. It gets
- 9:18Speaker 1: eaten up, broken down by the brain, among many other
- 9:21Speaker 1: things that are also happening in the brain. There is
- 9:25Speaker 1: no way to treat it. You cannot treat CTE. Okay.
- 9:30Speaker 1: The only thing you can do is prevention, minimize head trauma,
- 9:34Speaker 1: and if you can also you know that second impact syndrome.
- 9:38Speaker 1: Be very careful around second impact syndrome. Okay. So I
- 9:43Speaker 1: just want to dive in a little bit deeper with
- 9:45Speaker 1: TAO and what that is so you get a bit
- 9:46Speaker 1: more of an understanding. But basically, TAO this protein is
- 9:50Speaker 1: an abbreviated or alternative term for something called microtubule associated
- 9:56Speaker 1: protein TAU or MAPPED or MAPT. But we're just go
- 10:00Speaker 1: into it as tow TAU is how it's spelled. Now,
- 10:03Speaker 1: we've got something called microtubules, which are needed for cellular
- 10:07Speaker 1: nutrients and other things to travel down the axon of
- 10:11Speaker 1: the cell. So in your cell, you've got a neuron.
- 10:13Speaker 1: The axon is the main highway that sends a signal
- 10:16Speaker 1: to another cell. Now, to strengthen the axon, you've got
- 10:20Speaker 1: all these building blocks that make that axon strong, and
- 10:22Speaker 1: one of those things is microtubules. Okay, So we need
- 10:27Speaker 1: these tubules for the cell to be able to propagate
- 10:30Speaker 1: a signal. Basically, Tao's role in all of this is
- 10:34Speaker 1: to stabilize these tubules. Without it, it's not stable. So
- 10:38Speaker 1: you want to think about it like a highway where
- 10:40Speaker 1: goods are being traveled along and tow is what keeps
- 10:42Speaker 1: that highway running smoothly. Stable. It's not breaking apart now
- 10:47Speaker 1: in these conditions, and it's unclear why it is. But
- 10:50Speaker 1: in these conditions, this tow after trauma, swelling, inflammation, all
- 10:55Speaker 1: of that taw becomes unstable. It becomes hyperphosphorol. That means
- 11:00Speaker 1: that they're getting too much phosphate added to these protein groups,
- 11:05Speaker 1: which you don't need to know about the details of that.
- 11:08Speaker 1: And when this happens, they dissociate from the microtubule, as in,
- 11:12Speaker 1: they detach from the microtribule. So this TAEL protein is
- 11:14Speaker 1: no longer attached to the microtribule. Means that the microatribules
- 11:18Speaker 1: gets weaker, it's shittier, its structure, its integrity has been
- 11:24Speaker 1: fucking compromised, and they float off. The towel floats off
- 11:29Speaker 1: the microattribules into the cell bodies of the neurons and
- 11:32Speaker 1: also into the dendruts, which is other parts of the neurons,
- 11:35Speaker 1: and they clump together and form something called an NFT,
- 11:38Speaker 1: which is a neurofibrillary tangle, and this process is what
- 11:42Speaker 1: causes impaired function in the axon because you're having difficulty
- 11:46Speaker 1: sending the message and then you're also having these clumps
- 11:49Speaker 1: of shit that's not supposed to be in certain parts
- 11:51Speaker 1: of the brain. There these tangles of TAU. But the
- 11:54Speaker 1: mechanism behind all of this, when you get deeper and
- 11:57Speaker 1: deeper into the y is still not completely understood. Okay, Now,
- 12:01Speaker 1: when you're looking at the brain in an autopsy, the
- 12:03Speaker 1: damage from tower across brain regions differs from that of
- 12:06Speaker 1: patients with Alzheimer's, So we see it spread through the
- 12:08Speaker 1: neocortex first, then the medial temporal lobe, the basal ganglia brainstem.
- 12:13Speaker 1: In Alzheimer's disease, we see these tangles develop in the
- 12:16Speaker 1: brain stem first, but not in the neocortex, and it
- 12:21Speaker 1: kind of spreads from brain stem out whereas it looks
- 12:24Speaker 1: like there's a different process of spreading and different locations
- 12:26Speaker 1: when you're talking about CTE. So basically, in a nutshell,
- 12:30Speaker 1: look after your fucking heads. Do whatever you can to
- 12:32Speaker 1: not get a concussion. If you have a concussion, your
- 12:35Speaker 1: number one and your only priority is to recover fully
- 12:39Speaker 1: from that concussion, and I feel like I want to
- 12:40Speaker 1: do a whole another episode and my own research on
- 12:45Speaker 1: the concussion tests that they do in NRL. So when
- 12:49Speaker 1: someone gets hit sometimes I see the biggest blows to
- 12:51Speaker 1: heads and then they get pulled off and they get
- 12:53Speaker 1: this concussion test, and then ten minutes later they're back
- 12:56Speaker 1: on the field. I would love to know how extensive
- 13:00Speaker 1: concussion tests are, because if you've just been dealt a
- 13:02Speaker 1: massive blow to the head and you've passed this concussion
- 13:05Speaker 1: test and then you're back on the field and you
- 13:06Speaker 1: get another blow to the head, I'm not confident that
- 13:09Speaker 1: that's a good idea. Basically, in a nutshell, without getting
- 13:12Speaker 1: too passionate about it, I don't know anyway, take care
- 13:15Speaker 1: of your heads. You've got one.
- 13:17Speaker 2: You've got one fucking brain.
- 13:37Speaker 1: I have a brain factor. Now full disclosure, this is
- 13:41Speaker 1: a brain factor that I have done in the past,
- 13:43Speaker 1: but I wanted to add a little bit more into
- 13:45Speaker 1: it because we're talking about l F Andine and Lthanin
- 13:50Speaker 1: is something that well, I'm going to talk about it
- 13:51Speaker 1: in a second. But one thing that I didn't really
- 13:54Speaker 1: mention in the last time that I spoke about l
- 13:56Speaker 1: f andin was how much lf andine is in mucha.
- 14:00Speaker 1: I did mention about green tea and different types of
- 14:03Speaker 1: green tea, but I want to specifically talk about macha
- 14:06Speaker 1: and why macha is such a great source of lth
- 14:09Speaker 1: aanine versus other also really good sources. Okay, So the
- 14:14Speaker 1: brain factor of today is basically elthaanine. So what is it?
- 14:17Speaker 1: How does it affect the brain, How does it alleviate stress,
- 14:22Speaker 1: Its implications on mood disorders, how it affects anxiety, It
- 14:27Speaker 1: can also assist with sleep. So what is it? Basically,
- 14:30Speaker 1: it's a naturally occurring non protein amino acid, and it
- 14:36Speaker 1: is found in very high quantities in green tea, in
- 14:39Speaker 1: all different kinds of green tea. Okay, Now, the reason
- 14:43Speaker 1: why it's such an interesting amino acid, why a lot
- 14:45Speaker 1: of people you might hear a lot of people banging
- 14:47Speaker 1: on about why you should be taking althaenine is because
- 14:50Speaker 1: of this these amazing effects that it has on the brain,
- 14:53Speaker 1: not just on human brains, but you see it in
- 14:55Speaker 1: a lot of studies on rat models and in mice
- 14:59Speaker 1: models as well. I was about to say, in rice models,
- 15:02Speaker 1: rat and mice models. So it's pretty cool all the
- 15:05Speaker 1: benefits that your brain will get from consuming lthanine, and
- 15:09Speaker 1: I'm going to talk about a study that was done
- 15:12Speaker 1: as well, and hopefully it will inspire you to get
- 15:16Speaker 1: amongst it. And if you're someone that's like I've tried mucha,
- 15:19Speaker 1: I'm not about it. It is not fucking it for me,
- 15:24Speaker 1: then green tea is still sensational for you and for
- 15:28Speaker 1: your brain. Okay, you'll be wanting to fucking drink a
- 15:30Speaker 1: cup of much of green tea daily, if not twice
- 15:33Speaker 1: a day after listening to this, So basically, let's talk
- 15:36Speaker 1: about it. The molecular structure. I fucking love molecules so much.
- 15:40Speaker 1: I love talking about molecules and molecular structure and drugs
- 15:42Speaker 1: and pharmacology and all that shit. So this is right
- 15:44Speaker 1: at my alley. The molecular structure of lthanine is very
- 15:48Speaker 1: close to that of L glutamic acid. So it's believed
- 15:52Speaker 1: that this lthanine performs its actions and is basically mediated
- 15:57Speaker 1: via glutamate receptors. Okay, so I'm gonna speak about gabon
- 16:01Speaker 1: and glutamate in a little bit more depth, but basically
- 16:04Speaker 1: it acts on the same receptors that this L glutamic
- 16:08Speaker 1: acid acts on because of its molecular structure. That's all
- 16:11Speaker 1: you need to really think about. And what's happening is
- 16:14Speaker 1: that it's also competing at this at the binding site
- 16:18Speaker 1: where glutamate binds too. Okay, now I've spoken about glutamat
- 16:22Speaker 1: a thousand times. Glutamate is the major excitatory neurotransmitter within
- 16:27Speaker 1: the brain versus gabba, which is the major inhibitory neurotransmitter.
- 16:31Speaker 1: So excitation, we're seeing more activity in the brain. Whether
- 16:35Speaker 1: it's good or bad, it's just more activity. More synaps
- 16:39Speaker 1: is more firing, just more. And then inhibition is using
- 16:44Speaker 1: a reduction in excitability or excitation within the brain. Okay.
- 16:50Speaker 1: So another good thing about the molecular structure of l
- 16:54Speaker 1: anine is that it is based on its shape and structure,
- 16:57Speaker 1: it is able to cross the blood brain barrier. So
- 17:01Speaker 1: it has really really strong effects within the central nervous system.
- 17:04Speaker 1: And remember the central nervous system is your brain, brain stem,
- 17:07Speaker 1: and spinal cord. Okay, So anything that can cross the
- 17:09Speaker 1: blood brain barrier, you're getting those effects in the central
- 17:13Speaker 1: nervous system, which is in this scenario great. Another thing
- 17:16Speaker 1: that it can do is it can block glutamate receptors
- 17:19Speaker 1: within the central nervous system. And when it's blocking or
- 17:22Speaker 1: when it's kind of modulating or modifying what's going on
- 17:25Speaker 1: at the glutamate receptor, you're getting this limitation of excitability.
- 17:29Speaker 1: You're not stopping excitability altogether, that's just an insurmountable task.
- 17:35Speaker 1: You pretty much have to knock someone out for that
- 17:37Speaker 1: to happen, but you are limiting this excitability all right.
- 17:40Speaker 1: So a lot of different mood disorders, depression, anxiety, it's
- 17:48Speaker 1: got to do with excitability and inhibition. Okay, you're seeing
- 17:52Speaker 1: there's either too much excitability or a dysregulation in excitability.
- 17:56Speaker 1: So when you look at different drugs that target depression
- 18:00Speaker 1: for example, or anxiety for example, you're looking at different theories,
- 18:05Speaker 1: and you've got like the monoamine theory, which is the
- 18:07Speaker 1: drugs that target things like serotonin and dopamine and chemicals
- 18:13Speaker 1: like that. But then you've got the kind of glutamate hypothesis,
- 18:21Speaker 1: which is where you're using drugs such as ketamine to
- 18:24Speaker 1: target kind of the glutamate pathway or the idea that
- 18:28Speaker 1: glutamate might be behind all these different mood disorders. So
- 18:31Speaker 1: here we're seeing something that is a modulator or modifying
- 18:34Speaker 1: what's going on at the glutamate receptor in the form
- 18:37Speaker 1: of lpanine, which you can have in a t that
- 18:40Speaker 1: can also have similar effects in modulating this amount of
- 18:44Speaker 1: excitability within the brain. Okay, so we're seeing that lthanine
- 18:49Speaker 1: can do that with glutamate. It can also exert its
- 18:51Speaker 1: effects on GABBA receptors, which enhance sas GABBA activity. And
- 18:56Speaker 1: because of this enhancement of GABA activity, it's also helping
- 18:58Speaker 1: increase dopamine and serotonin because dopamine and serotonin are linked
- 19:03Speaker 1: to activity with GABBA as well. Okay, so lthanine it's
- 19:07Speaker 1: not a sedative, it's not going to cause sleepiness. It's
- 19:12Speaker 1: not going to cause drowsiness. It just allows the body
- 19:15Speaker 1: to be in a more relaxed state in general because
- 19:18Speaker 1: of its effects on GABBA and glutamate. Fucking epic. Okay,
- 19:23Speaker 1: So we want to look at elthanine, this amino acid
- 19:26Speaker 1: as being a neuromodulator. It's basically modulating the levels of neurotransmitters,
- 19:32Speaker 1: so helps bring you into this nice, calm, relaxed state
- 19:35Speaker 1: and therefore it is conducive to overall better sleep. So
- 19:38Speaker 1: if you're increasing your levels of l phanine. It is
- 19:41Speaker 1: helping you later on in the day with sleep, okay um,
- 19:47Speaker 1: And it's it's obviously not making you drowsy, it's just
- 19:49Speaker 1: making you more relaxed. Now, it's not endogenously produced, which
- 19:53Speaker 1: means that it is not made by your own body.
- 19:56Speaker 1: It can't be produced by your own body, so endogenous
- 19:59Speaker 1: versus XO genus. But it's not an essential amino acid,
- 20:03Speaker 1: so we don't need it to survive. So an essential
- 20:05Speaker 1: amino acid, I've spoken about this before, is something that
- 20:08Speaker 1: you need to survive, but you can't make it with
- 20:10Speaker 1: your own body, so you need it from your diet.
- 20:13Speaker 1: This is not essential, although I think it should be essential,
- 20:15Speaker 1: but it's not essential for your survival all right. Now,
- 20:19Speaker 1: where do you get it? It's found in many sources,
- 20:22Speaker 1: but it's believed that the highest quantity is naturally other
- 20:25Speaker 1: than because you can get it in supplements as well,
- 20:26Speaker 1: which you'll speak about in a second, but is the
- 20:29Speaker 1: highest is in green tea. So macha is when it
- 20:33Speaker 1: comes to elthanine, going to be the most superior source
- 20:37Speaker 1: of elthanine versus other kinds of green tea. Mucha can
- 20:41Speaker 1: contain up to five times more than other kinds of
- 20:45Speaker 1: green tea, five times more elthanine than other kinds of
- 20:48Speaker 1: green tea. And the reason for this is because mucha
- 20:53Speaker 1: the mucha tea grows in the shade, okay, and the shade,
- 20:59Speaker 1: the role that shade plays in the growth process mitigates
- 21:02Speaker 1: this photosynthesis in the leaves, therefore preserving the ltheneine within
- 21:07Speaker 1: the leaves among other amino acids as well. Okay, So
- 21:11Speaker 1: teas that grow in hectic sunlight are going to have
- 21:14Speaker 1: lower levels of elthene and this is due to oxidization.
- 21:17Speaker 1: So that is why macha is just going to be
- 21:20Speaker 1: a superior source for lthanein. But if you don't like maucha,
- 21:23Speaker 1: there's still great sources of lthen in in regular green tea.
- 21:26Speaker 1: It's still very very very good source of elthene in,
- 21:29Speaker 1: so do not fret okay. Now, Also, macha does contain caffeine,
- 21:36Speaker 1: but in general it's going to be less than the
- 21:38Speaker 1: average cup of coffee. So we're talking about averages here.
- 21:41Speaker 1: So on average, in a cup of macha, you're getting
- 21:45Speaker 1: roughly seventy milligrams of caffeine versus a cup of coffee.
- 21:48Speaker 1: You get between one hundred and one hundred and forty
- 21:52Speaker 1: milligrams of caffeine in coffee. Okay. You've also got other
- 21:57Speaker 1: kinds of green tea, white tea, oo, long tea, and
- 22:00Speaker 1: then lower down is black tea. So all the other
- 22:03Speaker 1: t's are going to have higher levels of elthan in
- 22:05Speaker 1: before black ta okay. And then there are some mushrooms
- 22:10Speaker 1: as well. I don't know which ones, but there are
- 22:12Speaker 1: some mushrooms. Elthanin also has an antioxidant effect on the brain,
- 22:17Speaker 1: and we love antioxidants, especially when it's something that can
- 22:20Speaker 1: cross the blood brain barrier, like this molecule in elthenin can, okay,
- 22:27Speaker 1: So it's very neuroprotective in that matter. It's going to
- 22:30Speaker 1: help reduce inflammation. It helps with oxidization within the brain
- 22:33Speaker 1: because it's its targets can be within the central nervous system,
- 22:38Speaker 1: and its bioavailability is very high. So bioavailability means how
- 22:43Speaker 1: much of this is actually available within your body to
- 22:48Speaker 1: exert its effects. That's not being eaten up through digestion
- 22:52Speaker 1: and through other things that your body can interfere with.
- 22:54Speaker 1: When you consume a substance. There are many different vitamins
- 22:58Speaker 1: and supplements and minerals on the market that claim all
- 23:02Speaker 1: these things, but once you ingest it orally, the bioavailability
- 23:05Speaker 1: is just not that great based on how we digest
- 23:07Speaker 1: or how our body process. Is that thing lthnin brilliant bioavailability,
- 23:11Speaker 1: So it's between seventy two and seventy four percent. It
- 23:15Speaker 1: crosses the blood brain barrier within an hour of consumption,
- 23:19Speaker 1: and some studies also claim that it might aid in
- 23:22Speaker 1: ADHD symptoms. Sorry, and also some studies are claiming that
- 23:30Speaker 1: it might aid in ADHD symptoms for certain individuals. This
- 23:34Speaker 1: is not across the board. It's obviously individual dependent because
- 23:38Speaker 1: it is a neuromodulator, so it's helping kind of calm
- 23:40Speaker 1: down activity in certain parts of the brain without being
- 23:42Speaker 1: a sedative. Based on its effects on the glutamate pathways,
- 23:47Speaker 1: you're enhancing dopamine release, You're getting all this regulation of
- 23:50Speaker 1: GABBA as well and of glutamate. So it goes a
- 23:52Speaker 1: really long way in lowering the rate of mood disorders
- 23:55Speaker 1: such as depression and anxiety, because, like I mentioned, people
- 24:00Speaker 1: with mood disorders are going to have, you know, specific
- 24:03Speaker 1: abnormalities in these like two major excitatory and inhibitory neurotransmitters.
- 24:08Speaker 1: Um So. Also, studies have found that if you pair
- 24:12Speaker 1: lthan in with caffeine, it's going to be a really
- 24:16Speaker 1: effective way to increase focus during demanding like focus tasks. Okay,
- 24:20Speaker 1: So macha, green tea, these are really great sources because
- 24:24Speaker 1: it's already combined. For you've got your caffeine and you've
- 24:27Speaker 1: got your fucking lthen in. Okay, so you're getting this
- 24:30Speaker 1: stimulating effect of the caffeine, but you're also getting this
- 24:33Speaker 1: a lot but calming effect of the l the inin.
- 24:37Speaker 1: So basically, go fucking have a mucha tea right now,
- 24:40Speaker 1: is what I'm trying to get at, or a green
- 24:42Speaker 1: tea if you prefer. And the beauty of it is
- 24:46Speaker 1: is like you don't need crazy obscene amounts of caffeine
- 24:49Speaker 1: because you've got that combination of the l fene in
- 24:51Speaker 1: and of like the the smaller amount of caffeine that's
- 24:54Speaker 1: in the in the green tea and also in macha. Now,
- 24:57Speaker 1: I am going to mention a study that I did
- 24:59Speaker 1: mentionlast time that I spoke about this about elfenin in
- 25:02Speaker 1: brain fact, and the study was done by Shinsuku in
- 25:06Speaker 1: twenty nineteen and it was a randomized placebo controlled crossover
- 25:11Speaker 1: double blind trial. That is the best, most elite kind
- 25:15Speaker 1: of study that you can do. Okay, for many many
- 25:18Speaker 1: different reasons. Where you do a double blind means that
- 25:22Speaker 1: the researcher and the individual is blinded to if they're
- 25:26Speaker 1: getting the place ebo if they're not. Place Ebo controlled
- 25:29Speaker 1: means that they're testing the actual substance and they're doing
- 25:32Speaker 1: a place ebo, and crossover means that every single individual
- 25:35Speaker 1: has a certain amount of time with the drug that's
- 25:39Speaker 1: being tested or the substance, and then they also have
- 25:41Speaker 1: a wash out period and then they're doing a certain
- 25:43Speaker 1: period of time with the place ebo, but no one
- 25:45Speaker 1: knows which one is what. So this is a very
- 25:48Speaker 1: and every participant is trying both. So it's the most
- 25:51Speaker 1: superior fucking kind of study that you can do. Obviously,
- 25:55Speaker 1: not every kind of study can be done this way,
- 25:57Speaker 1: but if you can do it this way, that's ideal.
- 26:02Speaker 1: It's also really good at knocking out potential co founding
- 26:05Speaker 1: variables and things like that. That's why it's such a
- 26:07Speaker 1: good study. So basically it was done to examine what
- 26:09Speaker 1: kind of effect four weeks of elthan in administration on
- 26:12Speaker 1: stress symptoms and on cognitive function could have on healthy adults.
- 26:16Speaker 1: So this study was carried out for over four weeks,
- 26:18Speaker 1: but we're looking at the four week effect and it
- 26:21Speaker 1: was done on a quote unquote healthy population. So what
- 26:24Speaker 1: they deemed healthy population to be were people with no
- 26:28Speaker 1: psychiatric disorders, but who did suffer from sleep issues and
- 26:32Speaker 1: mood and cognitive problems. Because we're trying to look at
- 26:35Speaker 1: is it benefiting them or not? Okay, So they were
- 26:37Speaker 1: given two hundred milligrams per day of health and INN
- 26:40Speaker 1: in tablet form and that's how they did the place
- 26:43Speaker 1: ebo control because they didn't know what they were taking
- 26:45Speaker 1: the tablet. Is it just a sugar pill or is
- 26:46Speaker 1: it going to be or like a plain pill whatever,
- 26:49Speaker 1: or is it going to be the elth And then
- 26:51Speaker 1: they had a wash out period. So a wash out
- 26:52Speaker 1: period is a period of time where you're not taking anything.
- 26:54Speaker 1: It often is around the two week mark, but it
- 26:56Speaker 1: depends on the study. So they do the four weeks
- 26:59Speaker 1: or just over four weeks. Then you've got to wash
- 27:01Speaker 1: out period of nothing. Then you return back and you
- 27:03Speaker 1: do another four weeks doing the other one that you
- 27:05Speaker 1: didn't do. So they found that after four weeks, stress
- 27:13Speaker 1: symptoms went down, anxiety traits depressive treats also went down,
- 27:16Speaker 1: sleep quality improved. They also found that cognitive function when
- 27:20Speaker 1: tested on verbal fluency and executive function improved, which is amazing.
- 27:24Speaker 1: And this is just in four weeks. So this is
- 27:27Speaker 1: what two hundred milligrams of l fen in over four
- 27:30Speaker 1: weeks can do, which is extremely impressive. So you could
- 27:33Speaker 1: start by having one cup two cups of green tea
- 27:36Speaker 1: a day, one or two cups of much a day,
- 27:39Speaker 1: and hopefully you're going to start really noticing a difference. Now,
- 27:44Speaker 1: if you don't like green tea or much, you can
- 27:47Speaker 1: have a supplement form. Now, the supplements do tend to
- 27:50Speaker 1: be a little bit exy because it's apparently quite difficult
- 27:55Speaker 1: to extract the lpnn and put it into supplement form,
- 27:58Speaker 1: so it's not the cheap process. But look, if you
- 28:02Speaker 1: like green tea, if you're willing to force yourself to
- 28:04Speaker 1: like it, then that's going to be a much cheaper,
- 28:06Speaker 1: very very good alternative to the supplements. But supplements are
- 28:09Speaker 1: there as an option and it's going to give you
- 28:10Speaker 1: the same benefits. Okay, So fucking yes, that's the brain
- 28:15Speaker 1: fact of today, and I really hope that all of
- 28:18Speaker 1: you that when I release this brain fact last time,
- 28:21Speaker 1: the obsession that I had from everyone being like, Oh
- 28:24Speaker 1: my fucking god, I'm drinking green tea. Now I'm having
- 28:27Speaker 1: much a tea I'm having I'm doing the lth and
- 28:29Speaker 1: Out of all the things you've told me to take,
- 28:31Speaker 1: this is the most exciting one. So I really have
- 28:34Speaker 1: these high hopes that I've got this big surge of
- 28:36Speaker 1: excitement from you guys to do this for your brain.
- 28:40Speaker 1: You're not only doing your brain a favor from the
- 28:42Speaker 1: neuroprotective benefits, You're doing your mood a favor. You're doing
- 28:46Speaker 1: your happiness a favor. It's just so fucking good. I
- 28:49Speaker 1: am the spokesperson for lth Anden, and I love it.
- 28:54Speaker 1: You're gonna talk about a brain fact. And the brain
- 28:56Speaker 1: fact is motion sickness. It's also known as keinatosis. Okay,
- 29:02Speaker 1: why do we get motion sickness? And I'm also going
- 29:06Speaker 1: to explain kind of exactly what's going on in the brain.
- 29:09Speaker 1: Obviously that's the point of the fucking brain factor. That's
- 29:11Speaker 1: a very redundant sentence that I just said. All right,
- 29:13Speaker 1: so let's get straight into it. What fucking is motion
- 29:15Speaker 1: fucking sickness. It is feeling dizzy, fatigue, feeling nausea due
- 29:21Speaker 1: to movement off you know, like when you're in a
- 29:24Speaker 1: vehicle or a boat. Okay, so thirty percent of the
- 29:28Speaker 1: population experiences motion sickness. Okay, for some people it's while
- 29:34Speaker 1: they're doing a specific task. So for example, you'll only
- 29:37Speaker 1: experience it when you're reading while driving, but if we
- 29:41Speaker 1: hopefully you're not reading while you're driving, but when someone
- 29:43Speaker 1: else is driving, but if you're looking out the window,
- 29:45Speaker 1: you don't experience it. For some people, it's more just
- 29:48Speaker 1: on a boat in the ocean, but they're fine in
- 29:50Speaker 1: a car. So it varies from person to person. But
- 29:54Speaker 1: some people even experience it in a cinema as well.
- 29:58Speaker 1: If there's like a lot of movement, or if it's
- 30:00Speaker 1: three D vision where it's really realistic, they may even
- 30:03Speaker 1: experience motion sickness at the movies, which is fucking wild.
- 30:07Speaker 1: But basically, what is going on, and I'll break it
- 30:10Speaker 1: down a little bit deeper, is that we're getting this
- 30:14Speaker 1: mismatch between the sensory information the sensory input that your
- 30:18Speaker 1: brain is receiving, and the result of that mismatch is nausea,
- 30:23Speaker 1: and I'll explain exactly why that is or the main
- 30:25Speaker 1: theory as to what neuroscientists believe is behind this. So
- 30:30Speaker 1: this mismatch involves primarily two regions. You've got your vestibular system,
- 30:36Speaker 1: which is the inner ear. I've done a whole brain
- 30:39Speaker 1: fact on the vestibular system and your visual system and
- 30:43Speaker 1: a little bit of appropriate reception as well. But your
- 30:46Speaker 1: visual system obviously your eyes. And when you get a
- 30:48Speaker 1: mismatch of the input that's coming in, that's where the
- 30:52Speaker 1: problem is and that's what we become motion sickness. That's why
- 30:55Speaker 1: they say, if you're reading, don't read, look out the
- 30:56Speaker 1: window and the motion sickness will go away. You'll understand
- 30:59Speaker 1: that in a sect. So first let's talk about the
- 31:01Speaker 1: vestibular system. So the vestibular system, this is in your
- 31:03Speaker 1: inner ear. It's basically its role is to detect motion, balance,
- 31:10Speaker 1: spatial orientation, and it's got these three semicircular canals. And
- 31:16Speaker 1: if you look, if you were to google an image
- 31:18Speaker 1: of the vestibular system the inner ear, you'll see these
- 31:20Speaker 1: kind of three canals that go on different planes, like
- 31:23Speaker 1: the vertical, the horizontal, so they're all on different planes,
- 31:27Speaker 1: and they detect rotational and linear movement. This is also
- 31:33Speaker 1: where I think I did a brain fact on this,
- 31:35Speaker 1: where I talk about how you've actually got rocks in
- 31:37Speaker 1: your head, but we've got these tiny, tiny, tiny little
- 31:39Speaker 1: crystals in our inner ear. And when the crystals kind
- 31:42Speaker 1: of roll from one side to the other, like literally
- 31:45Speaker 1: rocks in your head. So when someone said you got
- 31:46Speaker 1: rocks in your head, being like, as do you, as
- 31:48Speaker 1: do we all, but these little crystals they kind of
- 31:52Speaker 1: like will roll, and the inner ear detects that movement
- 31:56Speaker 1: and helps determine your orientation and where you are as
- 32:00Speaker 1: far as like what direction you're heading, what plane you're on,
- 32:03Speaker 1: what like movement, how fast you're going all of that, okay,
- 32:07Speaker 1: um and rotation and all of that. So, when you
- 32:11Speaker 1: are in a moving vehicle such as a car, a boat,
- 32:13Speaker 1: this vestibular system senses the movement of that vehicle even
- 32:18Speaker 1: if you're seated, because its senses acceleration, it sensors movement, okay,
- 32:24Speaker 1: forward movement in general. The visual system obviously is providing
- 32:29Speaker 1: information to your brain about your surrounding environment what you
- 32:34Speaker 1: can see, Okay, So when you are in a moving
- 32:37Speaker 1: car or boat, you can either see the changing scene
- 32:40Speaker 1: from outside of you and it's coming into the brain
- 32:42Speaker 1: being like, yep, the scener is changing, the vestibular system
- 32:45Speaker 1: is saying, yep, we're moving, so all is well. Versus
- 32:48Speaker 1: if you're looking at something still while your vestibular system
- 32:52Speaker 1: is telling your brain we are moving, but I'm looking
- 32:53Speaker 1: at something still, so my visual system is saying we're
- 32:55Speaker 1: not moving, the vestibulait is saying we are moving. Okay.
- 33:00Speaker 1: So that's where you're getting a different input with the
- 33:03Speaker 1: visual system. Then proprioception and sensor integration also plays a role.
- 33:07Speaker 1: So that's your body's awareness of like due to your
- 33:11Speaker 1: muscles and your joints and stuff where your physical body
- 33:14Speaker 1: is in space. That also plays a bit of a role. Now,
- 33:19Speaker 1: the theory is called the sensory mismatch theory. So the
- 33:21Speaker 1: most widely accepted theory from euroscientists for motion sickness is
- 33:27Speaker 1: this sensory mismatch theory or sensory conflict theory, okay, And
- 33:32Speaker 1: it basically suggests that motion sickness is occurring when you're
- 33:36Speaker 1: receiving contradictory signals from the vestibular, visual, and proprioception systems
- 33:42Speaker 1: within the brain. Okay, so you're getting one part saying
- 33:44Speaker 1: we're moving, the other part saying we're not moving. But
- 33:47Speaker 1: why that's all well and good, But why do we
- 33:50Speaker 1: get sick? Why do we need to vomit? So your
- 33:52Speaker 1: brain stem, which is the part of the brain that's
- 33:56Speaker 1: in between your spinal cords. Your spinal cord goes up,
- 33:58Speaker 1: then you've got the brain stem and and you've got
- 34:00Speaker 1: your hemispheres and cerebellum like the main part of the
- 34:02Speaker 1: brain that you've seen in drawings or pictures of a brain.
- 34:06Speaker 1: This brainstem plays a very significant role in coordinating sensory information.
- 34:11Speaker 1: That's one of the major roles that the brain stem has. Okay,
- 34:14Speaker 1: And when conflicting information reaches the brainstem, it really struggles
- 34:18Speaker 1: to resolve this conflict of information. It doesn't really understand
- 34:23Speaker 1: what's going on, but it knows that something's wrong because
- 34:25Speaker 1: that shouldn't be happening, okay. And then because of that,
- 34:29Speaker 1: the brain stem activates the autonomic nervous system. It's like,
- 34:33Speaker 1: something's not right. It's going to trigger a response in
- 34:35Speaker 1: the automatic nervous system, and the ANS is responsible for
- 34:38Speaker 1: involuntary bodily functions. One of those things is digestion, but
- 34:41Speaker 1: of course also vomiting, nausea or sweating, being dizzy, increased
- 34:46Speaker 1: heart rate, things like that. So what these neuroscientists believe,
- 34:51Speaker 1: or what this theory is saying, is that the brain
- 34:54Speaker 1: interprets this sensory mismatch as a sign of potential neurotoxicity.
- 34:59Speaker 1: So it thinks that maybe we've ingested some kind of
- 35:03Speaker 1: toxin or some kind of poison, because sometimes the side
- 35:06Speaker 1: effect of a toxin or a poison is a sensory mismatch.
- 35:10Speaker 1: So your brain already identifies, it knows that when there
- 35:13Speaker 1: is a mismatch in the signals, when there's a discrepancy
- 35:16Speaker 1: in what's being interpreted in the brain stem, you've probably
- 35:19Speaker 1: ingested a toxin, you've probably ingested a poison. And of
- 35:22Speaker 1: course the body responds to a potential threat of toxicity
- 35:26Speaker 1: or poisoning by making you vomit. It tries to expel
- 35:31Speaker 1: anything that you may have ingested to rid itself of
- 35:34Speaker 1: these perceived toxins. Okay, so that's the theory, which in
- 35:38Speaker 1: my opinion, I mean, obviously theories come with a lot
- 35:41Speaker 1: of research, a lot of you know, supporting evidence. It's
- 35:44Speaker 1: not to say it's definitely one hundred percent it, But
- 35:46Speaker 1: that's kind of where the belief is, and I think
- 35:48Speaker 1: it really makes a lot of sense, especially if you
- 35:50Speaker 1: if you understand the anatomy of the brain and where
- 35:52Speaker 1: these regions are located, it makes a lot of sense
- 35:54Speaker 1: that this is the reason. Now there is room for
- 35:59Speaker 1: adaptation and something called habituation as well. So if you
- 36:03Speaker 1: are repeatedly exposed to this thing, For example, if you
- 36:06Speaker 1: were to start reading regularly while in a car or
- 36:10Speaker 1: on a train, if you were to start going out
- 36:12Speaker 1: on ocean trips where the water is quite chopping in,
- 36:14Speaker 1: the boat's moving a bit really regularly, then for a
- 36:17Speaker 1: lot of people you will kind of become habituated to
- 36:21Speaker 1: that thing. Your brain adapts, and that's why you know,
- 36:26Speaker 1: you can have people that will first go on a
- 36:28Speaker 1: boat and they can't handle it, but if they worked
- 36:30Speaker 1: on a boat, they're like, oh my god, I can't
- 36:31Speaker 1: believe I used to be motionsick. Now it's fine because
- 36:33Speaker 1: the brain understands. It's like, oh, well, this obviously isn't
- 36:35Speaker 1: a threat. This is obviously an environment that we're put
- 36:37Speaker 1: in for whatever reason. It's happening repeatedly. It's not hurting me.
- 36:41Speaker 1: So then I'm going to stop sending these signals to
- 36:43Speaker 1: make you vomit, because, for whatever reason, I now need
- 36:45Speaker 1: to interpret this mismatch as just part of your every
- 36:48Speaker 1: day okay. So it basically loans to like integrate these
- 36:53Speaker 1: conflicting signals as just another part of what you were
- 36:56Speaker 1: doing in your everyday behavior. So that is the fu
- 37:00Speaker 1: Can brain fact for today. And I think that's really
- 37:02Speaker 1: really interesting