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00:03 last week we finished talking about Gaba signaling and we started talking about Gaba

00:11 And in particular we looked at the a receptor activation of Gaba A.

00:18 Gaba neurotransmitter will cause hyper polarization. , I don't know, tropic.

00:24 A. Is a channel and chloride come in through this channel inside the

00:31 will hyper polarized with plasma membrane. also has binding sides which means that

00:38 protein, this receptor protein has binding for substances like ethanol, alcohol,

00:46 , barbiturates, the neuro steroids that all be opening up this channel and

00:53 lot of the pharmaceutical medications that target channels. They increase the inhibitory tone

01:03 the brain and by increasing the inhibitory , increasing the inhibition of the

01:10 There's a control or attempt to balance excitation and in position. So this

01:16 how you can see glutamate will cause lot of excitation and if there's too

01:22 glutamate, we talked about really made toxicity. Then pharmacologically you would want

01:29 either reduce glutamate or you would want stimulate the inhibitory neural translation through the

01:36 neurotransmitter systems. We then talked about Gaba a receptor is a channel item

01:44 tropic channel that allows chloride to flux and Gaba B. Is a member

01:50 the tropic receptor that is linked to . Pro dams and these do custodians

01:57 linked to potassium channels systematically. They open potassium channels opening the potassium real

02:06 for the potassium to leave the cell potassium leaving the south. What will

02:15 the cell will become more hyper So both Gaba a influx of chloride

02:23 hyper polarization through Gaba B. Protein opening of potassium channel also causes

02:30 polarization. The gap of the receptors also linked to calcium channels as you'll

02:36 and blocking the calcium channels especially pre in control neurotransmitter release in this

02:44 In a very similar fashion that you've when we were talking about the retrograde

02:49 the phenomenon signaling. So this is very good diagram and the picture that

02:58 everything that we've been studying together and kind of extensive diagram but this diagram

03:07 the figure legend here but also has reference where it has been taken

03:17 And it also has a really neat and this key and all of the

03:24 descriptions you should recognize PSD stands for synaptic density of the screen. You

03:30 see that in these excitatory when you glutamate release, post synaptic densities will

03:36 excitatory glutamate synopsis and the cielo is MGM. This chapter will cause the

03:44 of housing. You also have blue which are Gabba A channels and these

03:52 kind of a yellow receptors which is B receptors, potassium channels and

04:00 You should be able to understand everything this diagram from what you've learned and

04:05 two models. So if we look example into this Gaba ergic synapse here

04:12 the left. You have the production Gaba. So these cells will be

04:17 G. A. D. God that we talked about where chloride is

04:22 sorry when Gaba is released into the cleft it will bind to Gaba A

04:30 personality quickly causing hyper polarization, fluoride in and also posting graphically you can

04:38 that there are Gabba B receptors, are the winged like G protein coupled

04:45 and these G protein coupled receptors. they will do as in previous slide

04:51 that they will open up potassium So when they open up the potassium

04:57 , potassium will be the flux ng the post synaptic cell the positive charge

05:05 will cause further hyper polarization. This the inhibitors and interestingly in latin inhibitory

05:12 also contained Gaba B auto receptors. called auto receptors because these synopsis with

05:21 terminals their release Gaba. And if Gaba films over here to the pre

05:29 side in the case of the ambient will bind to Gaba and Gaba

05:34 Boston optically. But if there is Gabba being released precision optical, it

05:39 bind to its own gabardine metadata tropic protein coupled receptor which will close both

05:48 calcium channels and well basically decrease or off the influx of calcium is you

05:56 , calcium influx through these channels is . We send applicability for the secular

06:03 and neurotransmitter release. So if basically Gabbert 16 oz so active that the

06:13 spills over it will shut down its release and this mechanism is similar than

06:20 cannabinoids which will control precinct topically calcium . So well controlled free south africa

06:27 gather now what is happening in the synapse And why are these called auto

06:36 here? These are called auto receptors Gabba that produces these neurons that produce

06:43 Gaba also gather minds to its own synaptic receptors is auto receptors gathered the

06:50 that auto receptors and this excited there's on the ride. You have a

06:55 production of glutamate in different color black . Black following kills here good and

07:01 gets released. It binds the Tampa and NBA receptors in this case and

07:08 receptor is highlighted in M. A receptor as we know is a

07:12 source of calcium influx all of them receptors. Also this calcium now can

07:18 with calcium Fine A. Says. the calcium will bind and activate these

07:25 and if you remember those kindnesses cause relations they donate the P.

07:30 For growth and so through this intracellular of calcium chinese you can actually activate

07:39 B receptors. Do you produce and for me receptors here cost synoptic aly

07:47 the activity and if you open potassium possum topically if this will be hyper

07:55 . So this glutamate synapse through the influx and campinas mechanisms and Gaba

08:01 That is passed synaptic will be regulating post synaptic effect at the level of

08:08 membrane because now if there is hyper that's an M. D. A

08:12 is not going to be active. . So and there isn't gonna be

08:17 of calcium. This is how boston Gabby baby can regulate santa tourism do

08:25 couple this afternoon. Also notice that channels these these these calcium channels that

08:34 talked about. These voltage gated calcium are located symmetrically on excitatory synapses

08:41 And then our gaba B. They're hetero receptors that are located preseason

08:48 They're called Gabby hetero receptors which is receptors because they located an excitatory synapses

08:55 as you know, excited. Their do not synthesize Gaba. So the

08:59 way these hetero receptors can be affected if there is significant amount of Gaba

09:05 spills over from the inhibitors synapses on left and then it spills over.

09:11 can do two things. It can synaptic quickly activate these Gaba be heavier

09:18 that will reduce the influx of calcium will reduce the release of glutamate their

09:24 receptors because they're located and excited for . Or this Gabba spillover from the

09:31 . Synopsis can affect Gaba B receptor cost synaptic code and by affecting them

09:39 optically they will open precaution channels so you protein coupled mechanisms and opening of

09:46 potassium channels will cause hyper polarization, optical. So now you can see

09:53 if you have inhibitor and excitatory synapses nearby. You can see how Gaba

10:02 metabolic tropic and i on a tropic in the in this inhibitory synapse will

10:08 hyper polarization here in the south. it can also control prison epic mechanisms

10:14 Gaba glutamate release and also the cost hyper polarization in the excited tourist synapses

10:22 this medical tropic gap to be So I hope that you're all putting

10:28 all together and everything that we've learned far. And typically this is the

10:34 that you would see if you stimulated fiber and that fiber produced an excitatory

10:41 . And E. P. P. This is very sharp PPE

10:44 that you're seeing here that the PSP going to be followed and sculpted by

10:49 PS PS. The Gaba A. PSP which is going to be hyper

10:55 . And when Gaba a receptor channel activated there's a flux of chloride and

11:02 is trying to drive the number and to its equilibrium potential for chloride and

11:08 the G protein coupled mechanisms and opening the potassium channel causes further hyper polarization

11:17 potassium leaving the cell will try to its equilibrium in the number of potential

11:22 its own equilibrium potential value of about 19 results in this case gather.

11:28 and that would be about hyper gather is faster because it's ion on

11:34 channel rather be is slower because of meadow with tropic their specific blockers for

11:43 and Gaba bees or mike you Callum a specific antagonist or blocker for gaba

11:49 receptor. And this shows that in here at the bottom number one when

11:54 is a stimulation there's a nice P. S. P. And

11:58 a smaller PSP that is being sculpted and controlled by immediately activation of

12:07 I. Ps PS inhibition here and trace number two. You applied by

12:12 and when you apply by cooking this little small excited to response in

12:18 absence of inhibition becomes this massive deep , what we call the depot arising

12:26 potential. And if you use to drugs to sack with them which is

12:32 gather B the receptor antagonist that doesn't got but he doesn't really produce this

12:44 response. But instead it kind of the response because it's in the latter

12:50 of the I. P. B. So for metabolic tropic signaling

12:57 general we're going to very briefly look the structure of the G protein coupled

13:02 that are 1234567 uh membrane spanning alpha that the link to G proteins.

13:14 if you look at the stable below a variety of metabolic trophic receptors And

13:19 we talk about the civil Colin masculinity , there is a variety of subtypes

13:24 masculinity receptors and they will slightly have , they will have slightly different

13:31 And one and two and three and and five stands for different subtypes of

13:35 in the casino code. And glutamate glue ours, there's probably 12 to

13:43 Mw ours now that have been Gaba gaba B receptor one, Gaba

13:51 receptor to serotonin five HT one A c d alpha D beta E F

13:58 HT 25. HT four. These different subtypes but they're all g protein

14:05 neurotransmitter receptors, dopamine norepinephrine. We comparing north enough from alpha versus north

14:14 alpha beta or alpha and beta, is linked to g stimulatory protein

14:20 alpha linked to g inhibitory profile form protein Catelyn we didn't talk about in

14:27 kingdom. Cannabinoids CB one and CB receptors are both medical tropics. G

14:32 coupled receptors and a TB. That molecule will bind to a dentist and

14:40 the denison receptor A one, A , A two, B A three

14:45 also P two Y type of So remember the A T. P

14:50 an energy molecule but it is also neurotransmitter and denison which is the core

14:56 http contributes and is also a neurotransmitter contributes to the control of the present

15:04 neural transmission and maybe we'll get a to review it quickly next lecture.

15:11 these are our transmitter gated channels that talked about which are different placido colon

15:18 . These are the two still Killeen binding sites. Each one of these

15:24 will have four trans membrane segments and shows that there is a similarity in

15:32 structure between receptors that are ion a South versus acetylcholine, You can see

15:41 will all have a similar structure and through M4 in this case it's segments

15:50 each sub unit and that they will a collection of five of these

15:57 Now you can have different combinations of subunits. So for example, if

16:03 look at Gaba receptor subunits, there's and there's one through six different subtypes

16:10 the alpha subunit. So when these come together you may have to alpha

16:16 this case it's acetylcholine molecule, the receptor channel. But it would be

16:22 in other receptor channels like two alpha gamma one beta one delta. You

16:28 have two alpha to beta one two alpha to beta one delta.

16:35 now have, if you look at A, you have at least six

16:39 , at least four betas, at four gammas roll and so on.

16:44 how many combinations of different subtypes of A receptors? You could potentially

16:53 It's very, very diverse. And by having this slightly different composition of

17:00 sub units or the alpha, beta and gamma will influence the kinetics in

17:06 function of these receptor channels. So of the things that are on the

17:12 here are the things that will be for the examining the quiz. So

17:16 example, acetylcholine nicotine, it must agonist nicotine musk urine antagonist security.

17:23 has to know that norepinephrine and what need to know for norepinephrine. We

17:28 talk about the agonist and antagonist but did talk about the alpha and beta

17:33 functions. You know the difference is you have one pushing cyclic GMP production

17:41 is up to another one. Pulling receptor from producing more cycling can be

17:48 . We talked about ample and an . D. A. Agonists and

17:52 and an M. D. That's easy antagonists that CN Q.

17:56 . And a P. Five or PV. So you should know this

18:00 we talked about a little lethargic signaling depth. We talked about the AMP

18:06 . And an M. B. . I. V. Curves where

18:09 had a linear curve and NBA nonlinear . And we discussed what happens to

18:14 via curved in the presence of A . D. Gamma gamma A gamma

18:21 . We know that natural endogenous agonists but you also have these chemicals agonists

18:28 we really kind of just highlighted by organism antagonists for Gaba a risk

18:35 So just know that YaBA A. eye on a tropic. It conducts

18:40 Gaba B. Is measurable tropic and linked to the opening of the percussion

18:46 And that if you blog Abba With bike UK Poland then excitation is

18:51 . Then it can be very prolonged sustained in the same synapses that otherwise

18:57 have gone to A. In the ATP receptor subtypes as p. two

19:03 and a type agonist for the P X type receptors http which is a

19:10 agonist or for the A type for and receptors is in a denizen.

19:16 a denizen uh will activate the dynamism . Now the antagonist for a denizen

19:25 caffeine. That's something that most of probably 90 plus percent consumed every day

19:32 we do that in the morning because of denison, a tie perceptive by

19:40 molecules reduces glutamate release priests in africa the metabolic tropic signaling. So dennison

19:48 glutamate release and dennison levels go up the evening and at night and there

19:55 less of glutamate release in the I'm not saying there's none the less

20:01 then the denison levels typically go down the morning and glutamate release increases.

20:06 dennison controls the medical tropic mechanism prison algorithm it released, it reduces it

20:14 caffeine does caffeine is an antagonist of of Dennis and receptor. And because

20:20 denison reduces glutamate caffeine actually increases recently and that's part of the waking up

20:30 having a cup of coffee or tea anything that contains caffeine in it.

20:41 maybe it's partly a placebo effect but I think that it helps us wake

20:46 our brains get engaged and I think definitely the neurochemistry behind it that you

20:52 are aware of. Okay, so concludes our neural transmission section and we're

21:00 going to move into the exciting this exciting world, the macro view

21:09 the brain, which is great time overview some of the things that we

21:17 in the first section, Some of structures that we mentioned in the first

21:21 of this course and as we look some of the gross anatomy, structure

21:29 function of the brain parts and talked little bit about the development them.

21:38 think having a background ah in the section and having all of this

21:45 you are going to be very well into understanding the major sensory and somatic

21:52 systems in the brain and the circuits the functions in these circuits that we

21:58 talk about in the next uh I we have about 11 lectures, we're

22:04 lucky. We are over the hump the sports more than halfway through in

22:10 the material. Congratulations, you are one centimeter. This is the scale

22:16 on the left and this is the brain. Yeah, it's about one

22:20 . This is to scale on the video, the rabbit brain. A

22:24 bigger cat brain, not so A few cents a centimeter. Shoot

22:27 from kinds of brain. Human dolphin brains. If we were to

22:33 to virologists, we were too believe size is all that matters and the

22:41 the size of the organ, the its performance and computational power uh,

22:50 then obviously developments have larger brains relative to humans and they should be smarter

22:58 us and should be on top of food chain. But this is not

23:04 scale on the ride. And it's as you can see how some of

23:09 brains are relatively smooth. They don't a lot of these imaginations and the

23:14 order species, the higher you go the more and more complex these imaginations

23:19 actually in the higher order species, in non human primates and other forces

23:27 . Whenever you talk about anatomy the location of anatomical structures, we

23:32 to talk about some of the basic . You don't have to talk about

23:39 . Some of the terms that we in describing where the structures are located

23:45 planes, you already know dorsal which the back Of the spinal cord.

23:51 know, the sensor information comes in . And the trouble is the front

23:55 the spinal cord. Notice that in here and the rat there is not

24:00 bent between the brain and the spinal . Between humans is bent would be

24:05 90° because we're standing up on two . This is the interior or

24:11 All this is the posterior card or in the middle is medial, anything

24:16 the side is lateral. There are major planes or cuts that we perform

24:24 the brain ross told to coddle. you're performing it like this slicing the

24:29 in this direction, it's called mid . This is the horizontal plane of

24:34 slices and this is corona lil sections the brain of corona slices through the

24:39 . And that's important because for we can look at the brain

24:45 for example, the entire brain structures have been stained with missiles stained.

24:51 we can read the instructions sisters it's in the occipital lobe, or

24:55 in the parietal lobe. It's this coordinates, and we're going to understand

25:00 structure we're looking at. It's very to us. If somebody said,

25:06 know when you talk to directing well, you know, it's the

25:10 over there and then you have to a right and if you locate

25:14 and that's where you're gonna look to left and you should be able to

25:18 the classroom we're looking at. So is the instructions that we get is

25:22 anonymous, you're looking at mythological cut through So, and so we're

25:28 okay, well, I know which directly major parts of the brains.

25:34 re brooms are a ballot and brainstem cord. And this is an exaggerated

25:39 , which allows you to have an view from the mid line, all

25:42 way to the lateral and medial collateral of the brain. Now, all

25:49 the information and the in the the and cerebral hemispheres is contra lateral sensory

26:00 motor information. That means that all the sensor information actually from the body

26:05 face. It comes in to the that information travels from collateral with all

26:10 the output. Motor commands on my hemisphere will command my left side of

26:16 body, and left hemisphere will control lot of right right side of the

26:22 . The cerebellum is different. Cerebellum involved in a lot of the control

26:26 movement, but sarah balham right here green in the back of the

26:31 The projections are absolute lateral, meaning they control the movement on the same

26:38 of the bridge and it's a little different. Learn more democracy about

26:42 View. Brain stem is where you a lot of the cerebro cerebellum to

26:50 cerebrum to sarah balham and from sarah Arabella cerebral interconnections of these two structures

26:57 very tightly interconnected. And especially the of this arm balance is very important

27:03 the motion control and learning the motion or what we call procedural memory such

27:12 riding a bicycle, which is very to forget what you learned and it's

27:17 in the structure like cerebellum brainstem right , brainstem is responsible for vital body

27:25 , breathing, consciousness, heartbeat, of body temperature. So this is

27:32 controlled release. Very interesting nuclear that located here in brain stomach. We'll

27:37 about some of the next couple of , we have peripheral nervous system and

27:44 don't talk much about the peripheral nervous . Uh it's motor and sensory,

27:51 everything skin joints and muscles that we talked about a little bit about the

27:55 muscular junction. We don't get to about the autonomic nervous system, the

28:02 system that is present and the sierra internal organs, blood vessels and glands

28:10 the autonomic nervous system and the complexity the autonomic nervous system and the

28:16 That's a terek for example, nervous is just as complex potential.

28:25 Uh And it is a very interesting field of study as well. The

28:32 is protected, it is surrounded by protected the ninjas. He's protected

28:39 There are three of them. The mater which is the hard mother,

28:45 arachnoid, this spider like membrane of underneath the dura mater and the PM

28:52 and the general mother number. And lays right on the surface of the

28:59 great and different societies that the dura is really really tough. It's very

29:06 to penetrate. So the brain already protected by the skull. It's a

29:11 , it's hard to crack and break bone. It's very hard and I

29:16 that bone cracks or breaks underneath. is this really thick mater. Okay

29:26 the thingies and this meninges is quite to penetrate. You cannot just poke

29:32 it with a finger. I actually a scalpel to cut through duro

29:38 So it's very very thick, thick rather resilient thingies on the surface right

29:48 the skull. Now, do you ? We talked about the trepidations.

29:55 prepper nations and he said, well are some of the reasons? Of

29:58 , pressure build up in the brain build up in the brain. Pain

30:02 up in the brain. One of fluids that can build up in the

30:07 . As you can see here, have the vasculature that's going through this

30:11 space and penetrating into the brain tissue the microbe assholes. But if there

30:16 a rupture of the broad, thus here, you may experience what is

30:22 a subdural hematoma where there's going to a coagulation of blood and hardening these

30:31 blood pools essentially underneath the dura, E. And the only way that

30:38 can clean up the wound is to a trip to a nation and the

30:45 and make a small opening in the and clear up and clean up the

30:52 and and potentially maybe even patch it or put something in this as far

30:58 the ancient forms of medicine available at time. So these are the three

31:04 energies and the environment within them. fluid, This is cerebrospinal fluid and

31:11 when the brain shakes, the brain protected by the ninjas and by the

31:16 this environment the fluid, the cerebral fluid or CSF super spinal fluid is

31:26 in these areas? The forward in ventricles lateral ventricles here that are

31:33 ventricles in the brain. There are and they contain a lot of fluid

31:37 that fluid gets constantly refraction produced and generate new, completely turned over your

31:44 spinal fluid over the day and the spinal fluid is circulating and to the

31:53 , ventricular system and the brain going the sort of paranoid space and is

31:58 drained. Now this is another reason you would potentially have brain entrepreneur nations

32:07 a condition that happens during development is hydrocephalus. Water in the brain.

32:13 there is too much of the fluid is being produced, let's say the

32:17 Alexis's overproducing the fluid or the drainage the fluid is not proper from the

32:25 ins and subdural spaces. And what then is there can be a build

32:32 of fluid in the ventricles and as fluid collects in the ventricles. And

32:37 it happens during early development such as case with hydrocephalus, the ventricles are

32:44 going to start pushing on the brain and the surrounding brain tissue and that

32:49 tissue is going to start pushing on skull, the skull during the first

32:54 years of life, especially his soft the skull plates have not used

33:01 And so you have the ability to move and reshape the skull. And

33:07 if there is abnormal balloon like formation the ventral course is going to we

33:13 the soft tissue of the brain and the hard skull tissue and that's not

33:21 . And so the only way to rid of these fluids is to drain

33:25 . And in modern days you can the tube into the ventricles and you

33:32 drain the fluids into the intra peritoneal here and you can have these fluids

33:40 during the development of the monitor. in the ancient prehistoric times that is

33:46 likely that they saw a child developing abnormal head. And maybe they even

33:53 there are fluids or something like But they would probably perform a

33:57 entrepreneur nation and entrepreneur nation would be in order to drain the fluids and

34:04 they're accumulating and drain them again. , so this is the formation of

34:11 central nervous system and how the central system comes about the process of no

34:20 . So this primordial state, you you have the three types of

34:26 The end of the term the meso and the actor. The M dot

34:34 becomes a lining of internal form. an investor mas a term in the

34:42 becomes skeleton, bones and muscles. the act a damn becomes nervous system

34:51 skin to skin cells actually have the pra morelia ah uh stem like similarities

35:05 would say skin cells with neurons with cells. And then first you have

35:12 neural plate formation here. If you these three structures, you have this

35:17 play and then you have the formation the neural form. You have the

35:23 of the girl falls. These false closing out and the form the neural

35:32 here surrounded by so am I. over here and on top of that

35:39 ceo neural crushed. So what happens essentially this plate falls and produces the

35:49 and this dude from ross tral all way to the Qatar land and then

35:54 have the closing of the studio. my rights that are shown here become

36:01 column, scalpel, uh muscles, vertebral column and the projections of this

36:10 Muslims. In this process of formation the neural tube is called no relation

36:19 general. If you think about the brains are very complex. We

36:24 about billions of cells and trillions of and one of the brain is

36:31 it is self assembling into this very structure and in general we don't have

36:38 many abnormalities and developmental abnormalities. They're one in 1000 maybe during the

36:46 But they do have and if they related to the tube formation obviously developmental

36:56 and if there is an effect on roster all side of this no relation

37:02 and do formations somehow improper holding on rostrum side that can result of insufferably

37:12 basically is not having the cerebrum ah it's not sustainable and if there's problems

37:23 the cardinal and of the neural tune this no relation process given I haven't

37:31 a bifida. So it's fine or spinal cord will be sticking out abnormally

37:38 of being properly surrounded by the vertebral which is the sodomites. And this

37:44 a irreparable problem with the surgery but is still significant treatable. So once

37:53 have this neural tube, your harvest rel and right here we're gonna zoom

38:00 to the rasta rel end of this too, which is further subdivided into

38:06 pros and suffering or the forebrain. suffering on the membrane or rum and

38:11 for the hind brain. From here the spinal forwards. The forebrain further

38:21 the first you have no relation Then you have the formation of the

38:28 vesicles. Those primary bicycles differentiated secondary and and with subsequent development you have

38:37 and more specific differentiation, structural differentiation these different three regions, forebrain,

38:45 and hind brain. Here you see four brains subdivided into talents of our

38:53 coast because tell himself along, becomes cortex this is diana cephalon we'll see

39:02 diet cephalon becomes stalinists and hypothalamus. are the optic classic als of the

39:09 of the stock here coming off Uh stop Coming off a year of

39:18 four brand. And this is where retina there's going to forms off the

39:25 . That's why everybody that studies optometry ophthalmology is also a neuroscientist because recognized

39:32 part of the central nervous system, you have the further differentiation of selling

39:40 . So talents a folic hemisphere has the two cerebral hemispheres. And as

39:45 can see that with this differentiation you more and more of the refinement,

39:52 more complex structure and architecture emerging in brain in the mid brain. You

39:58 the formation of these four nuclei that called corporate quadra gemini. Again,

40:05 lot of neuron anatomical anatomical terms are on latin. But you can decipher

40:15 everything corpora, corpora, body For gemini gemini nuclei sides, the

40:28 of the four sides. So where can translate it all now you can

40:33 these are the arctic cups that's going be the formation of the retina and

40:38 optic nerve that preserve of the The cerebral hemispheres tell himself along the

40:45 cephalon, subdivided into the thalamus on the hypothalamus at the bottom. You

40:53 see the formation of these lateral ventricles , the third country floor in the

40:58 , the fourth ventricle going down and spinal canal for the spinal cord corpus

41:05 . That is shown here is the of the major attract and the fibers

41:11 will be interconnecting the two hemispheres. you know that there's a lateralization of

41:17 brain function. There is not only localization of specific brain function but there's

41:22 lateralization of the brain function because when talk about Broca's area and when we

41:28 about Bernie Kosar was on the left of the brain. To the speech

41:33 and speech areas will be dominated by left side of the brain. Does

41:37 mean that the right side of the is not informed of what's left the

41:43 are doing. And there is a of information between the two hemispheres through

41:48 major interconnecting fiber bridge called the corpus from the thalamus. There's other types

41:57 fibers that are referred to as internal and those internal capsules are the white

42:02 , the myelin ated neuron fibers that go from the columns into the cortex

42:08 actually from the cortex back into the . So there is inter connectivity between

42:13 sub cortical structures that we call bad like almost in contra thomas between cortex

42:20 those structures back and forth and also the cerebral hemispheres through the the corpus

42:27 bridge. So this is don doesn't long romp and suffering behind brain and

42:34 spinal cord. Again, the talents the line becomes the cortex uh Palomas

42:40 can see on top there is a of dying cephalon thalamus. Underneath this

42:45 of thalamus the membrane differentiates and attacked and to give momentum to detect um

42:53 where we just saw the structures here the dorsal side of mine spectrum is

43:00 the roof. So protect yourself from rain on the dorsal side? How

43:05 can remember and take amount them. have a serb alan here emerging from

43:09 roman suffer long hind brain and pause the dual oblon gata all are emerging

43:16 roman and finally in the yellow. have a spinal form so the ventricular

43:22 would drown through these lateral ventricles and left and right hemisphere and the third

43:28 . Then you have the fourth cerebral aqueduct and the spinal canal supplying

43:35 the spinal fluid all the way and the bottom of the spinal cord by

43:43 by the very um sequel vertebra. you can see that the brain has

43:52 side and it has gyre I and side are the grooves and gyro are

43:58 region's religious cortex is the seat of and cognition. So a lot of

44:10 perceptions, reasoning um sensory modalities, sensory modalities together. This is all

44:27 in the cortex which has major frontal lobe, parietal lobes separated by

44:33 sulcus a big cool. You have occipital lobe of the temporal lobe.

44:41 is the three dimensional structure of the of the brain. The lateral

44:46 the third, the fourth ventricle was canal. A lot of similarities on

44:51 gross level between right in the human of course of course of course human

45:00 a lot more conflicts that contain a more south side and joy ride.

45:06 But in general you'll see the ventricular 1st and 2nd and the 3rd and

45:12 ventricles. You'll see the cerebellum. the pawns armadillo of long gotta all

45:18 recognizable in many different species. Higher lower order species. Neocortex is only

45:28 in mammals. The neocortex is this cephalon that becomes a telling stuff along

45:36 here becomes telling symbolic hemispheres becomes cerebral , becomes vortex. Neocortex is the

45:48 surface of the cortex. It's a cortex. It's new in the sense

45:55 evolution. That's what Neo stands It's the most sophisticated and the latest

46:02 structure and this human and adam a models. And what's interesting is if

46:11 took a piece of neocortex from an by the way, look at these

46:16 the frontier. Alligator has these huge bulbs because that's what gators do around

46:23 . They swim around the bayous and swarms. By the way you can

46:28 can see so many alligators if you're here, you probably know if you're

46:35 from here, Brazos Bend State Park 35 minutes. 40 minutes from the

46:42 the big city. He has incredible of alligators and you can observe them

46:49 in the sun. Have to be when you walk your pets around there

46:53 they they may snap them on a . Natural wildlife preserve heading east Beaumont

47:04 to in large populations of alligators. have these massive olfactory balls because that's

47:12 they do they swap around and they around this smell the food. They

47:20 incredible sense of smell. You can on the rats they have these very

47:26 olfactory bulbs but there's a factory balls the rat and the road of which

47:31 very important. The rats are We'll have to go to Brazos Bend

47:36 Park, perhaps are everywhere plenty of Houston. They also have a factor

47:44 . You saw a factory balls are as big, you can see as

47:48 are an alligator. So you have different variations in animal structures but interesting

47:54 some canonical structures that are preserved canonical , meaning that if you want to

47:59 a piece of neocortex, an alligator or a matter of fact from

48:03 you would have these primal cells with optical dendrites and basil gun rights.

48:07 will have a certain six layer structure your vortex is a six layer structure

48:12 will be replicable and would be founded and rats and as you can see

48:18 , there is this canonical for repeatable and structures and even the shapes of

48:26 styles and anatomical arrangements in the new cortex. Of course there's different levels

48:32 processing and complexity in these animals. there are some very recognizable structures that

48:38 will find across different species. So last slide that I will very briefly

48:45 to is actually shows the neocortex is six layer structure. The most superficial

48:51 or the skull is number one, deepest layers. # six. There

48:56 a column of connectivity and that means the selves that are arranged themselves with

49:04 in the neocortex and Weigert stain is stain that will stay in axons and

49:08 can see how their bundles of axons what is called the column in the

49:15 . This is a missile statement you know will stain all of the cells

49:19 this is a gold. The statement stay in precisely the anatomy of a

49:23 of the cells only. This is stain that shows all of the six

49:29 cortical layers. The thickness of neocortex vary from frontal cortex to occipital cortex

49:37 bridal cortex or motor cortex. With overall this canonical structure and this column

49:46 well as laminar. So the column you have columns and two connected columns

49:51 south and the neocortex and laminar as have these layers and the columns communicate

49:58 adjacent columns through the slab on earth connections. So when we come back

50:04 will look at greater detail at neocortex continue talking about the development and going

50:11 more precise detail from different brain different brain areas and also studying the

50:19 nerves and the great detail as So thank you very much for joining

50:25 online today, this will conclude our today. I will see everyone at

50:31 next lecture in person and please stand to get the information about the quiz

50:37 soon as I have it, I inform everyone in class and I will

50:44 everyone on thursday. Thank you and care

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