Exam 7: February 27 - March 3 Flashcards

1
Q

what information does your vestibular system give?

A

it’s the part of your sensory NS that tells you about your head position and motion

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2
Q

what receptors does your vestibular system use?

A

mechanoreceptors

stereocilia specifically

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3
Q

what are the components of your vestibular system?

A

1) semicircular canals

2) otolith organs

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4
Q

how many semicircular canals do you have?

A

3

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5
Q

what do your semicircular canals help with? which vectors?

A

help you tell how your head is moving in a 3D space because each plane gives you a vector of movement and you do vector addition

rotation, acceleration, and deceleration

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6
Q

what is the reference that your simicircular canals use?

A

when you solve this 3 plane problem, you get the line that you’re moving but you don’t know if it’s positive or negative direction….you need a reference!

Gravity is always working on us and will tell us which way is “down”

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7
Q

what does otolith mean?

A

“lith” means stone

“oto” means ear

if you have rocks in your ears and you tilt you head, the rocks would follow gravity and roll so rocks in your head would be helpful because they would tell us which way gravity is pulling on us

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8
Q

how many otolith organs do you have? why do you have that specific number? what are they called?

A

2! because your head can tilt side to side or back and forth so you need one for each

utricle and saccule

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9
Q

what are the otolith organs made of?

A

your utricle and saccule are calcium stones

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10
Q

when do your otolith organs have difficulty determining orientation? how do you fix this?

A

gravity has a low impact on us when we’re in water

when someone is under water and gets disoriented they have a hard time figuring out which way is up because we’re buoyant in water so gravity doesn’t pull down and the rocks don’t roll right

so how do you solve the problem of which way is up? Bubbles! Follow the bubbles because they will always go towards the surface

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11
Q

what do your otolith organs give you information about?

A

your otolith organs give you the information of acceleration relative to gravity

the rocks can only roll so far so you only get the initial component

the rocks are about changes in motion, not constant motion – kind of like cans in your car trunk

with the use of your semicircular canals you know if you’re staying in that position

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12
Q

what information does your chemosensory system give?

A

it’s a part of your sensory nervous system that tells us about dissolved chemicals

our eyes are filled with fluid

we breath in air and bring things into our mouth but we have to dissolve them to be able to register

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13
Q

what receptors does the chemosensory system use?

A

chemoreceptors

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14
Q

what are the components of the chemosensory system?

A

taste and smell

internal and external!!

this is just the way we gather information from the outside – how the chemicals are changing around us or how they’re changing inside us – so these are just the external measurements

internal: pH, O2, CO2 levels – make sure we’re staying in SS and are in homeostasis

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15
Q

what is another name for taste?

A

gustation?

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16
Q

where do we find the chemoreceptors associated with taste?

A

Your mouth overall because you have your tongue and the back of your throat too

you also have receptors in your GI track and your lungs as well so that’s why when you breath sometimes you feel like you taste it

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17
Q

what causes an aftertaste with food?

A

there are different chemoreceptors in the back of your throat

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18
Q

what helps to increase the number of taste receptors?

A

where we have these receptors, there’s lots of surface area

our tongue isn’t nice and smooth, it’s bumpy so that you can have lots of receptors (10,000 taste receptors in association)

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19
Q

why do we put stuff in our mouth?

A

it’s most likely going to end up going in to your digestive track

you need to decide if you want to swallow something or spit it back up

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20
Q

what are primary taste receptors?

A

things that are critical to maintaining homeostasis are important so for knowing if it’s something you want to digest

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21
Q

what are the 6 primary taste receptors?

A

1) salty
2) sour
3) sweet
4) bitter
5) umami
6) fat

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22
Q

what is your salty primary taste receptor do?

A

need Na for membrane potential, action potential, your nervous system – historically sodium was lacking in our environment – Na acts on the receptors and causes an influx of Na which activates membrane potential

it gives us information about a compound that is of critical importance so we know it’s something we want to swallow and we need more of

we’ve become successful at accumulating salt from our environment but back in time we weren’t and used salt as a monetary unit

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23
Q

why do you need sodium?

A

need Na for membrane potential, action potential, your nervous system

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24
Q

what is your sour primary taste receptor?

A

H+ blocks normal K+ movement

H+ impacts the ability of the regular movement of K into these receptors and therefore impacts membrane potential of these receptors

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25
Q

when would we want sour foods?

A

sour is important for pH regulation of blood: we don’t want to be acidic or basic

if we’re lacking in H+ we’ll want sour things but if we’re already acidic we won’t want to take in sour things

it all depends on your current situation

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26
Q

what does a sour taste indicate?

A

another thing this sour taste tells us is when proteins break down they release H+ so a sour taste typically indicates that that food is spoiled

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27
Q

what does your sweet primary receptor tell you? what activates these receptors?

A

binding of glucose activates these receptors

we need the glucose to do glycolysis and feed into Krebs cycle/ETC

we can run these processes off proteins and fats but it’s not as efficient – this has changed in our history but we’ve also become efficient at extracting sugar out of our environment

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28
Q

why do we need glucose?

A

to do glycolysis and feed into Krebs cycle/ETC

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29
Q

what does your bitter primary taste receptor tell you?

A

it’s unlike the other 5 categories in that it’s a group category

it’s a grouping of at least 30 compounds that bind to a similar Rs so they historically all get us the same response

they’re typically alkaloids (caffeine) and toxins that bind to these bitter receptors

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30
Q

why do bitter things taste bitter?

A

the compounds that bind to bitter receptors are typically alkaloids (caffeine) and toxins

this makes sense because alkaloids play with pH and toxins are bad

when you taste something bitter you don’t ingest it typically – this is why a lot of pharmaceuticals don’t have a good taste because they’re toxins which makes it hard to give medicine to kids

historically bitter things you avoid ingesting so you avoid toxins and don’t have a pH change – how we deal with them now we can consciously say that it’s okay because it might be healthy actually like kale

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31
Q

what does umami mean?

A

a pleasant or savory taste in Japanese

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32
Q

what is the umami primary taste receptor?

A

it’s when you can’t put a name to it when you’re eating it but wow it tastes good - it’s most likely your umami receptors responding

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33
Q

what activates umami receptors?

A

binding of glutamate is what activates umami receptors

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34
Q

what makes food taste better?

A

monosulfate glutamate = MSG

binding of glutamate compounds makes food taste good!

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35
Q

why do we like bacon?

A

glutamate is needed for Krebs

having enough glutamate helps keep aerobic cell metabolism working properly

we also know that lots of our AA can act as neurotransmitter so therefore Glu also acts as a NT so without it there’s nervous system communication problems and ATP production problems

umami are also a protein indicator

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36
Q

what can umami receptors also be an indicator for?

A

umami are also a portion indicator

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37
Q

what activates fat primary taste receptors?

A

binding of a fat that activates these receptors

how that’s happening is still being worked out

it’s about a critical need and that it’s something historically was quite low in the environment – we can turn fats into energy!

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38
Q

what’s another name for smell?

A

olfaction

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39
Q

where does olfaction happen?

A

3 cmˆ2 patch on the roof of your nasal cavity

not wide spread like taste receptors

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40
Q

which receptors does smell use?

A

chemoreceptors

5 million receptors with 1000 types in this small little patch of area so we don’t really categorize or group them

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41
Q

what is your sense of smell?

A

it’s about detecting changes in the environment but you don’t have intimate contact with it or bring it into your body

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42
Q

what happens when you can’t smell?

A

when your nose is a wet area so when your nose dries out your lose your sense of smell because you need the moisture to dissolve

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43
Q

how long do your smell receptors last?

A

2 months = high turnover area

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44
Q

how do receptors in the smell and taste turn over?

A

when individual receptors in our mouth turnover but the categories stay the same

with our sense of smell we add and take away categories all the time

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45
Q

what is being nose blind?

A

your nose receptors have a high turnover rate and you add and take away categories of receptors all the time

being nose blind to things is if you’re around something all the time, you’ll put away the receptors it and literally stop smelling it like in the febrile commercials

if it’s always in your environment, it’s not interesting like how you don’t need to know that you’re wearing clothes – this is why you need to change your perfume and cologne regularly because you stop realizing how much you’re putting on

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46
Q

how do you register smells?

A

your olfactory bulb is the patch in the roof of our nasal cavity

at this spot we’re just picking up the information, we do some initial processing with it so it’s your initial sorting

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47
Q

how do you process smell?

A

you initially sort smells at the olfactory bulb

this initial sort then goes to a section of your brain in your cerebral cortex called your primary olfactory cortex which is your secondary processing center that starts getting you to act on what you’ve smelled before you even consciously register it such as getting closer or farther away from the source

when you become conscious of those smells its because of processing done in your orbitofrontal cortex in your cerebral cortex

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48
Q

what is the primary olfactory cortex?

A

subconscious coordination with behavior

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49
Q

what happens when you become conscious of a smell?

A

when you become conscious of those smells it’s because of processing done in your orbitofrontal cortex in your cerebral cortex

this one gives you conscious knowledge of that particular smell and now you register it

you might already be reacting to it before this conscious registering happens which gives you more detail of what you’re detecting

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50
Q

what is your vomeronasal organ?

A

it’s related to olfactory

it’s not about general chemicals being registered like in olfaction, it’s about chemicals being registered from another organism = receiving signals that are released from another human and come to you to act on your cells

they’re between person signals instead of between your own cells which are called pheromones

you respond to them and recognize and give off certain pheromones that tell information about you and get other individuals to respond to that information you’re giving them – it’s not within smell, it’s similar though

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51
Q

what is perception?

A

it’s not identical to detection

ex. obvious case and point is smell because we’re reacting to smell before we consciously know that they’re even there
ex. pheromones we don’t even know they’re there but we’re responding to them

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52
Q

how does perception work?

A

o Within the interpretation of these signals, the brain sees no reason to keep them as separate entities and often merges them together

you have 6 categories of taste receptors but when your nose gets stuffed up things don’t taste the same because what we perceive as the sense of taste is actually a combination of smelling it, tasting it, hearing it, and seeing it

it’s not just about how it hits and individual’s tongue, it’s also about presentation because if it looks great it’ll influence how you feel about it when you taste it – if you get a bag of chips but can’t hear a crunch, you perceive that it’s stale

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53
Q

what kind of process is the interpretation of signals?

A

the interpretation of signals is a cerebral process

so when you drink your taste and perception change…

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54
Q

what are consequences of perception?

A

we often combine signals so you have to be careful about saying something is just from one area because you’re likely responding to multiple things that are happening at that time

we are often very unconsciously acting on the signals that we gather where as we think we’re only consciously acting on them – guys can pick up on signals girls are sending based on what time in her cycle she’s in

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55
Q

what does your somatic nervous system do?

A

the somatic NS controls skeletal muscles only, not cardiac or smooth muscle

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56
Q

which muscles are striated? which are not?

A

skeletal and cardiac are striated

smooth muscles are not striated

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57
Q

does your mouth or nose have more receptors?

A

your mouth has less receptors and less types of receptors than your nose

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58
Q

which muscles are voluntary vs involuntary?

A

skeletal muscle is under voluntary control, we are making them move in a conscious matter, it’s not under the autonomic nervous system

our cardiac and smooth muscle (size of blood vessels, GI tract) are involuntary

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59
Q

what do our different types of muscles do?

A

skeletal muscles move bonds

cardiac muscles are changes in heart volume

smooth muscles are changes in our organ volume

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60
Q

what is the organization of a muscle?

A

cells, tissues, organs, and organ systems are the levels of organization

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61
Q

what is your muscle?

A

your muscle is an organ!

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62
Q

what are the units in a muscle?

A

myfibers → myofibril → myofilaments

myofiber is the container

the myofiber is the straws inside of it

the myofilaments are the stripes on the straw

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63
Q

what are myofibers

A

they’re your individual units that are your muscle fibers

64
Q

what does my mean?

A

muscle

you don’t say muscle cell because fiber helps you with how the cell looks = they’re long and thing

65
Q

how long are myofibers?

A

they run from one end of your muscle to the other end

66
Q

how does a myofiber form? how do you know that’s how it forms?

A

in development, there’s a whole series of cells that crosses that distance but then they all fuse together to create one bigger cell

we know this is what happened because all the nuclei of all the individual cells are all still there

one continuous plasma membrane but they used to be separate plasma membranes so now the cells all have the same PM and you can’t rip them apart

67
Q

what are myofibrils?

A

bundles of myofilaments make up myofibers

myofibrils are part of your myofiber

68
Q

what are myofilaments?

A

they make up myofibrils

69
Q

what are the types of myofilaments?

A

myosin and actin

70
Q

what is the difference between actin and myosin?

A

they are the two types of myofilaments (they’re proteins)

actin is smaller and thinner than myosin

71
Q

what are actin and myosin referred to as?

A

myosin is called the thick myofilament

actin is the thin myofilament

72
Q

what is the sarcoplasmic reticulum?

A

it’s what causes the myofibrils to be grouped up because it wraps around them

without the SR the myofibrils wouldn’t exits because there wouldn’t be any bundling

the SR creates structure

73
Q

what is the primary job of the SR?

A

it’s a holding place within our myofibrils for Ca which you need to do contractions for your muscles (that way you aren’t dependent on the external Ca concentration)

74
Q

what are transverse tubules?

A

they are just extensions of the plasma membrane that come down into the cell to create tubules

they cut all the way across the myofibers aka all the way down to the myofilaments

75
Q

what’s inside the transverse tubules?

A

interstitial fluid

TT are ECF channels because there’s interstitial fluid within the tubules

it’s not intracellular fluid because it hasn’t crossed the PM

76
Q

what are the 6 components of myofilaments?

A

1) z-line/disc
2) sarcomere
3) I band
4) A band
5) M line
6) H zone

77
Q

what is the z-line?

A

it connects up actin = thin filaments

78
Q

what is a sarcomere?

A

it goes from z line to the next z line

79
Q

what is the I band?

A

aka the light band

it’s where we only have thin filaments = actin

80
Q

why is our I band called the light band?

A

the I band is where there’s just actin

it’s called light because our skeletal muscles are striated and where we have only thin filaments, it appears lighter and that’s where you get the white striations

81
Q

what is the A band?

A

aka the dark band

it’s the length of the thick filament = myosin

82
Q

what is the M line?

A

it’s the midpoint between two z lines

aka the midpoint of the sarcomere and the midpoint of the A band

83
Q

what is the H zone?

A

it’s where there’s only thick filament = myosin

matching form of our I band because we only see thick filaments

the H zone must be within the sarcomere and it must be within the A band

84
Q

what’s the functional unit of the muscle?

A

the sarcomere

if you want your muscle to contract, your sarcomere must be able to shorten its length

myosin and actin don’t change size so how do you get the two z lines closer together? they slide relative to each other to make sarcomere smaller and get the z lines closer to each other

85
Q

can the A band change in size?

A

no

it’s the length of myosin so it won’t change during contraction

86
Q

what changes length during a contraction?

A

I band and H band

the I band is just actin and H band is just myosin so as the sarcomere gets smaller these areas also get smaller

87
Q

what happens to the striations during a contraction?

A

as the sarcomeres get smaller, the striation pattern will change and the light part will get smaller and smaller and eventually it’ll all be just dark with tiny strips of light

88
Q

what is actin?

A

it’s a protein

the individual units are called actin and the whole structure is called actin

89
Q

what does actin look like? what’s located on it?

A

it’s round ball type structures but there’s a green spot on them that is the binding site where it can interact with myosin and bind to myosin – it’s the receptor spot for its ligand, myosin

90
Q

what’s the overall structure of actin?

A

actin subunits form up into a double helix chain to form the overall structure of actin

91
Q

what are the associates of actin?

A

troponin and tropomyosin

92
Q

what is troponin?

A

it’s the smaller of the two associates of actin (it’s smaller than tropomyosin)

it looks like a clump of three balls

93
Q

what binding site does troponin have?

A

it’s bound to actin and tropomyosin

it has a binding site for Ca

it’s the only thing on actin that has a binding site aka Ca exclusivity

94
Q

what is tropomyosin?

A

it’s the larger of the two associates of actin

it is a long strand protein that is more fibrous in look

95
Q

how many binding sites does myosin have? what does it bind?

A

2

one binds actin and the other binds ATP

it’s the only one of our components that can bind to/interact with ATP

96
Q

what does myosin look like?

A

long shaft component with a head like a golf club

but they’re lined up in a way that looks like a double sided golf bag

97
Q

what’s a cross bridge?

A

myosin come off sticking in different directions

we know that our myosin can bind to our actin and when it does it looks like a bridge

the cross bridge is flexible and can move however the goldf club head is not! The movement of the cross bridge is what causes the movement of your muscles and allows your forearm to be pulled up to your shoulders

98
Q

what happens at rest during a contraction?

A

tropomysoin blocks myosin binding site on actin

99
Q

what is innervation?

A

our NS tells our myofibrils to get their myosin and actin interacting

it’s our connection of our nervous system that’s coming to impact the effector and get it to work

100
Q

what are motor neurons?

A

the neurons that tell our skeletal muscles what to do but just like receptor potentials, it’s just an added name to what we already know is going on underneath

receptor potentials are just graded potentials and motor neurons are just somatic efferents because they’re going out to an effector

101
Q

what has ATP exclusivity?

A

myosin

102
Q

what has Ca exclusivity?

A

troponin

103
Q

what kind of neurons are motor neurons?

A

somatic efferents because going out to effectors

they help make muscle movements happen

104
Q

what’s the relationship between motor neuron and myofiber?

A

motor neurons can be connected up to multiple myofibers

each myofiber is only being told by one motor neuron what to do

a motor neurons can be connected up to multiple myofibers

105
Q

what’s the relationship between motor neuron an muscle?

A

a particular muscles gets innervated by multiple motor neurons but each of those motor neurons is impacting multiple myofibers

106
Q

what’s a motor unit?

A

one neuron and all of its myofibers that it runs

different muscles have different numbers of motor units so we can have a varying number of motor units getting activated so you create different amount of movement

107
Q

how is the signal getting to the effector?

A

the signal is coming electrically

it’s coming as AP series along myelinated axon that gets turned into an chemical NT message but then you want to put it back into an electrical message

108
Q

what’s the first step of a neuromuscular junction?

A

AP changes membrane potential of axon terminal where we have V.G. Ca channels

if we hit threshold potential, Ca channels open and Ca goes into axon which causes the exocytosis of NT which is Ach

109
Q

what is THE neurotransmitter of our somatic nervous system?

A

acetylcholine is THE neurotransmitter of our somatic nervous system

110
Q

what are motor neurons categorized as?

A

somatic efferents because they’re going out to an effector

111
Q

what is the second step of a neuromuscular junction?

A

after V.G. Ca channels are activated, Ca comes in an exocytoses Ach

Ach will move through interstitial fluid of the synapse and will bind to a receptor that is acting as a channel which will then cause ligand gated/chemically gated Na channels to open and Na will influx into the cell

this will depolarize your myofibril and you’ve now created a graded potential aka you’ve changed the membrane potential of the cell

112
Q

what happens after a graded potential is created in the myofiber?

A

after Ach bind to ligand gated Na channel and Na depolarized myofiber, if graded potential is big enough, a different set of Na channels open so there’s an influx of Na and you’ve now started your AP

then more channels open and AP are triggered section by section in our myofibers and our electrical message is moving along

113
Q

what are all the steps of a neuromuscular junction?

A

1) AP change membrane potential of axon terminal where we have voltage gated Ca channels
2) so if we hit threshold potential, Ca voltage gated channels open and Ca goes in axon
3) the Ca causes exocytosis of NT which is acetylcholine → we have now switched from electrical to chemical message
4) Ach is a NT that will move through interstitial fluid of synapse and it will bind to a receptor that is acting as a channel which then causes ligand gated/chemically gated Na channels open
5) Na will influx which will depolarize your myofibril and you’ve created a graded potential
6) you want this to spread across your myofiber but a graded potential can’t go distance so you need an action potential to travel distance but AP only happen in excitable cells which have to have voltage gated Na and K channels – oh look at that, we have that in our myofibers!
7) So if graded potential turns into a threshold potential, Na channels open so there’s an influx of Na and the start of our AP
8) more channels open and AP are triggered section by section in our myofibers – we now have our electrical message moving along

114
Q

what if you want to stop activity in the neuromuscular junction?

A

our brain stops sending AP so there’s no longer a threshold potential or influx of Ca so exocytosis of Ach will stop

BUT the Na channels are kept open by the Ach that was already there so you need Achase to break down at to allow channels to close

when channels close, there’s no more depolarization, no more AP and the message gets stopped

115
Q

how do TT help muscles contract?

A

AP travel along the PM

we know the plasma membrane of a myofiber doesn’t just stay on the surface, it gives us a new structure called our transverse tubules

our AP will move along plasma membrane just like AP on our axon, and it goes down into transverse tubules also

we need transverse tubules to take AP deep into myofibers to the myofilaments

if the AP was just on the surface the myofibers wouldn’t be as big as they could be

116
Q

what do the AP of our motor neuron do?

A

they get voltage gated Ca channels to open

117
Q

what do the AP that travel along the PM of a myofiber do to the SR?

A

SR sits next to the PM and TT

SR has voltage gated Ca channels that our AP on our PM triggers the opening of

118
Q

Ca levels in the SR and cytosol

A

the cytosol has little Ca

the reason for the SR is to have Ca inside our cell

SR will get triggered by AP traveling across PM and V.G. Ca channels will open and flood out into the cytosol

Ca is coming from sequestered pool of Ca aka it’s intracellular Ca

119
Q

what happens to Ca after it’s released into the cytosol?

A

Ca binds to the troponin in the cytosol

troponin is a protein so when Ca binds there’s a shape change

troponin is bound to actin and tropomyosin so they also shape change → once there’s a shape change tropomyosin will move and uncover the myosin binding site on actin

120
Q

what happens after tropomyosin uncovers the binding site on actin?

A

Ca bind troponin which shape changes and also causes tropomyosin to shape change and uncover myosin binding spot on actin

myosin head binds to actin which causes a shape change

myosin has ADP and Pi attached to it which get released due to the shape change that happened when the myosin bound to actin

energy is released and myosin head pulls and muscle contracts

121
Q

what is cross bridge cycling?

A

it’s about myosin moving (cross bridge) and it’s going to be a cyclic process

myosin and actin are proteins so when we do binding and unbinding we get shape changes

so all crossbridge cycling is, is a series of shape changes caused by binding and unbinding of things in association with these two proteins

122
Q

what is blocking the binding site on actin?

A

tropomyosin

123
Q

what happens when myosin binds to actin?

A

actin binding releases ADP and Pi

because myosin has shape changed but ADP and Pi don’t

when you break a Pi bond energy is released which is used to make shape change to take the moveable head and get it to flex (bigger angle to smaller angle = flex of crossbridge = myosin grabbed the muscle and yanked like in tug a war)

124
Q

what do you have to do to get myosin to release actin?

A

ATP binds to myosin

ATP then hydrolyzes to ADP and Pi which is the reflex/cock of cross bridge

125
Q

what are the steps of the cross bridge cycle?

A

1) Ca binds to troponin
2) troponin shape change moves tropomyosin from the myosin binding site on actin
3) myosin (ADP and Pi) binds actin
4) release of ADP and Pi
5) flex of cross bridge
6) ATP binds to myosin
7) myosin unbinds actin
8) ATP hydrolyzes to ADP and Pi
9) deflex/cock of cross bridge
10) repeat

126
Q

when can’t we get the cross bridge cycle to continue?

A

we can’t run out of Ca because we’re putting it back to the SR

what if we run out of ATP? we can’t have it bind to myosin so we can’t let go = rigor mortis

when you die your cellular processes stop so ATP production stops so your muscles get stuck in the holding position and can’t release

127
Q

how far does a cross bridge cycle get us to move?

A

it gets us a pull/movement but only 10 micrometers of movement per cycle so you need a ton of little pulls happening at the same time

128
Q

how does skeletal muscle relaxation happen?

A

relaxation comes from getting our crossbridge cycling to stop which means we have to stop sending the message on our motor neuron to cause the process to happen

have to tell the effector to stop contracting

129
Q

what’s the catch to skeletal muscle relaxation?

A

skeletal muscles are somatic efferents which can’t inhibit, they can only excite or stop sending signals

130
Q

how do you stop CBC to induce relaxation?

A

no more motor neuron AP → no more Ach released → no opening of V.G. Ca channels → no myofiber AP aka no Ca released from SR

however, you have to get rid of the Ca that was in the cytosol and get it back to the SR

131
Q

how do you get the Ca in the cytosol back to the SR?

A

active transport

you need an ATPase driven pump that will pump the Ca into the SR

pumps don’t work as fast as channels so putting them back is a slower process than releasing them

every time you move Ca back to the SR, it costs us an ATP to relax the muscle

132
Q

what is twitch?

A

the contraction pattern happening in our muscle

it’s the pattern of tension due to a single AP getting created on that myofiber that triggers a cascade of AP and gets Ca channels to open

133
Q

what is tension?

A

is the force that gets generated from the pull from cross bridge cycling

134
Q

what is a latent period?

A

when there’s a delay between when an AP is triggered and when tension actually happens

135
Q

what are our semicircular canals vs. otolith organs?

A

semicircular canals are acceleration due to gravity

otolith are acceleration with our head moving side to side or up and down

Ca stones also have to due with gravity

vestibular is stereocilia in a fluid environment and are mechanoreceptors

136
Q

how does the chemosensory system work?

A

DISSOLVED receptors that are chemoreceptors that can be impacted by tasting something as well as internal concentrations of CO2 or O2

137
Q

why don’t a lot of people like sour and bitter food?

A

sour causes a Ph issue if you eat too much

bitter causes toxin issue if you eat too much

138
Q

what happens if sour receptors stay activated?

A

it H continues to block K channels, whatever you put in your mouth will also taste sour or spoiled

139
Q

what taste receptors are critical to metabolism?

A

umami and fat

140
Q

olfaction receptors between people?

A

Avalon has different smell receptors than me

there’s more olfaction receptors than taste receptors

141
Q

what does the olfactory bulb do?

A

first sorting

will detect that I smelled something and perceive something but don’t know what you smelled

142
Q

what does the primary olfactory cortex do?

A

coordinate body in relation to the smell

move away or towards without registering

143
Q

what does the orbitofrontal cortex do?

A

you consciously understand what you smell

144
Q

what are vomeronasal organ?

A

unconscious with pheromones

145
Q

which muscles are the only unstriated ones?

A

smooth

146
Q

which muscles are autonomic?

A

cardiac and smooth

autonomic is parasympathetic and sympathetic which has different NT released like norepinephrine and Ach

Ach is released in somatic and parasympathetic so if you mess with Ach it’ll effect both but will impact parasympathetic more since it’s the only one used

147
Q

what are types of smooth muscle?

A

stomach and bladder

148
Q

what is your muscle?

A

an organ because it has muscle tissues and cells

149
Q

what are the two functions of the SR?

A

holds Ca and structural component for myofibrils

an SR is a component that runs parallel to myofiber because it wraps around myofibrils

150
Q

what are the transverse tubules made of?

A

interstitial fluid = only one made of IF

run perpendicular to myofibrils

151
Q

what is the SR made of?

A

intracellular fluid

152
Q

what parts of the sarcomere change in size?

A

H band and I zone

H band is space that’s just myosin

I zone is just actin space

153
Q

what does the A band contain?

A

the H zone

154
Q

what does the I band contain?

A

z lines

155
Q

what is the overall thing that’s happening during relaxation of a muscle?

A

Ca put back to SR through ATPase pumps and everything goes back to shape and tropomyosin will cover myosin binding spot

156
Q

can the latent period change?

A

no but the length of the twitch can be changed