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midterm content

QuestionAnswer
anatomy vs physiology anatomy is studying body structures, physiology is studying how those structures work together to carry out functions
levels of organization in the body chemical, cellular, tissue, organ, body system, organism
chemical organization atoms combine to form molecules
cellular organization smallest unit that can carry out life processes
ribosomes protein synthesis
nucleus dna
smooth er fat synthesis
golgi apparatus sorts and packages proteins
lysosome digestive enzyme that breaks down waste
mitochondria atp/energy
tissues groups of cells that perform the same function, they're organized into tissues in multicellular organisms
types of tissue epithelial, connective and excitable
epithelial tissue types exchange, transport, ciliated, protective, and secretory
connective tissue types loose, dense, hardened, adipose, and blood
loose tissue under skin and around organs
dense tissue ligaments and tendons
hardened tissue bone
adipose tissue fat/lipids
excitable tissue types muscle and nervous
muscle tissue types skeletal, cardiac, and smooth
nervous tissue types neurons and glial cells
glial cells cells in the brain that aren't neurons, they support neurons
organs two or more types of primary tissue that work together to perform a specific function
body system group of organisms that perform related functions
organism independent living thing, group of body systems that work together
types of fluid compartments intracellular (ICF) and extracellular fluid (ECF)
intracellular fluid inside of the cells, 2/3 total body water
extracellular fluid outside of the cells, 1/3 total body water. this is further divided into two types
ECF- plasma fluid found in the blood, makes up 1/4 of the ECF
ECF- interstitial fluid around cells, 3/4 of ECF
negative feedback response restores equilibrium by opposing the change
positive feedback response enhances the og chance
feedback look: receptor first step, detects the change
feedback loop: integrator/integration centre second step, carries the message (key words are recognizes/releases)
feedback look: effector third and final step, actually makes the adjustments to restore
nervous system body's primary communication centre
nervous system: 2 parts central (CNS) and peripheral (PNS)
central nervous system (CNS) brain and spinal cord
peripheral nervous system (PNS) nervous that extend beyond the CNS (i.e. everything that isn't the brain or spinal cord). maintains homeostasis by monitoring and rapidly responding to internal and external changes in the environment
PNS: 2 parts efferent and afferent
PNS: motor/efferent nervous system brings information away from CNS. carries motor commands to muscles and glands
PNS/efferent nervous system: 2 parts somatic and autonomic
autonomic nervous system involuntary branch of the efferent/peripheral nervous system
autonomic nervous system: 2 parts sympathetic and parasympathetic
sympathetic nervous system flight or flight. preps the body for strenuous activity and dominates in stressful situations
parasympathetic nervous system rest and digest. promotes body maintenance activities and dominates in quiet and relaxed situations
PNS: sensory/afferent nervous system brings information to the CNS. carries sensory information like pain, touch, temperature etc
neuron excitable cell that can product electric signals (ion/charged particle movement)
membrane potential separation of opposite (positive and negative) charges across the plasma membrane
resting membrane potential -70 mV, different between ICF and ECF charges at rest
equilibrium potential membrane potential when the electric gradient = chemical gradient, so there's no net movement across the membrane
ECF charge positive
ICF charge ICF charge
K+ electric gradient K+ wants to move inside of the cell i.e. from ECF to ICF
K+ chemical/conc. gradient higher conc. of K+ in ICF, so it wants to leave the cell (go to ECF)
K+ net movement chemical > electric gradient so K+ wants to move outside of the cell till -90 mV
Na+ chemical/conc. gradient higher conc. of Na+ in ECF, so Na+ wants to move inside of the cell
Na+ electric gradient Na+ wants to move inside the cell i.e. from ECF to ICF
Na+ net movement chemical = electric gradient so Na+ wants to move inside the cell till +60 mV
changes in membrane potential polarization: uneven distribution of electron density, creating regions of partial +ve and partial -ve charge
depolarization decreases the difference between the +ve and -ve charge (e.g. -70 mV to -50 mV)
repolarization making the cell more -ve again i.e. undoing the depolarization, closer to membrane potential (e.g. from -50 mV to -60 mV)
hyperpolarization increasing the difference between charges more than the initial membrane potential (e.g. -70 mV to -90 mV)
neuron signalling electrochemical process where nerve cells (neurons) receive, process, and transmit information
graded potenial initiates electric signal, opens chemical(ligand)/mechanical gated ion channels. depolarizes that specific location of the membrane then dissipates away
threshold potential the membrane potential where an action potential occurs
action potential large change in membrane potential. happens at threshold potential. opens voltage gated ion channels and sends the signal
graded potential nature can vary in size depending on intensity of stimulus, can add together with other graded potentials to increase size, doesn't self propagate i.e. doesn't send a signal
action potential nature goes to the same maximal height every time, self propagates down the axon which sends the signal
refractory period recovery period right after a stimulus occurs, the excitable cell is unable to respond to another stimulus, has two types
absolute refractory period post action potential, membrane cannot be restimulated because the Na+ channels become inactivated and close
relative refractory period post action potential, membrane can only be restimulated with a greater stimulus/stronger graded potential. K+ channels are still open, allowing K+ to move out of the cell as Na+ tries to move in and depolarize the membrane again
conduction nature/how the action potential moves down the axon
myelin fat/lipid that wraps around the axon and acts as an insulator
contiguous conduction happens in unmyelinated fibres. every portion of the axon membrane has to get an action potential
saltatory conduction happens in myelinated fibres. action potential skips through the parts of the axon membrane that have myelin (because the fats don't like ions, so bno charged particles can get in or out so it just skips over) and travels down the axon really fast
rate of conduction speed/how fast the action potential moves down the axon. determined by myelin (with myelin = faster) and diameter of axon (larger = faster)
dendrites receives inputs
cell body has all the organelles
axon sends the outputs/info
terminal bulb communicates with other cells
afferent/sensory neurons brings info from the PNS to the CNS. starts with receptors in the PNS (instead of dendrites, because they detect the signal not only pass it on), cell body is halfway down the axon
interneurons only in the CNS, make up 99% of neurons. in between afferent and efferent, receives signals from afferent, and interprets the data and sends instructions to the efferent neurons
efferent/motor neurons leave the CNS, cell bodies are in the CNS, and they send the message to something e.g. muscle or gland
synapses verb and noun. it's the connection between neurons (neurons don't actually touch each other), but is also the electric signal that gets passed
presynaptic neuron axon terminal
synaptic vesicle in the presynaptic neuron, holds neurotransmitters
synaptic cleft space in between 2 neurons where neurotransmitters diffuse into
ion channel receptor neurotransmitters bond to this on the postsynaptic neuron
postsynaptic neuron dendrites
neurotransmitter removal once they get released into the synaptic cleft, the effect needs to be turned off so they can get removed in three ways
NT reuptake NT go back up into the presynaptic neuron (where they og. came from) or into surrounding cells
NT inactivation when the effect is done, enzymes come and degrade them
NT diffusion once released they move away from the synaptic clef and go into the blood (so it has little to no effect)
NT and synapse relationship different NT for every synapse, and the same NT is always released at the same synapse
acetylcholine prevalent in the brain, used on efferent neurons (the ones that go out to the body) so it controls movement basically
glutamate amino acid that depolarizes the next neuron, so it's a main excitatory NT
GABA amino acid that acts as an off switch, so it's an inhibitory NT. opens Cl- channels to hyperpolarizes the membrane
norepinephrine monoamine thats mainly used in the fight or flight response in the sympathetic nervous system
dopamine monoamine that triggers pleasure and reward
seretonin monoamine used in mood regulation
synaptic convergence each postsynaptic neuron can receive inputs from thousands of presynaptic neurons. basically a bunch of inputs converge onto one cell, and the sum of those inputs determine the output
synaptic divergence single presynaptic neuron branches out and 'synapses' onto many postsynaptic neurons
postsynaptic potentials whats happening on the postsynaptic cell when it receives the signal (signal being graded potentials)
excitatory post synaptic potential (EPSP) depolarizes and increases the likelihood of reaching threshold
inhibitory post synaptic potential (IPSP) hyperpolarizes and decreases the likelihood of reaching threshold
grand post synaptic potential because of synaptic convergence, a single neuron is receiving thousands of different inputs at a time. there are different ways to determine whether an action potential will happen or not
temporal summation two EPSPs occur close to each other in time, and add up to achieve a larger membrane depolarization i.e. closer to threshold
spatial summation based on location. EPSPs coming from different neurons converging onto one close to each other generates a larger depolarization
EPSP-IPSP if a neuron gets stimulated with an EPSP and IPSP of the same magnitude, they will cancel out and nothing will happen
reflex automatic, involuntary response to a stimulus that happens without conscious thought
botulinum toxin (botox) and NT prevents the release of acetylcholine (which stimulates muscle movement), preventing muscle contraction
tetnus and NT prevents release of GABA (inhibitory neuron that induces muscle relaxation), meaning the muscle stays contracted
SSRI and NT inhibits reuptake of serotonin, so it binds for longer making you happier/improving mood regulation
physiological basis of memory thoughts, perceptions, and memories are based on neural connections
learning process forms new neural connections
memory making process strengthening connections (breaking habits weakens neural connections). neural pathway is created from input, info is stored in short term (connections are briefly strengthened, then repeated stimulus (retrieval and rehearsal) long term is formed
neuroplasticity ability to change neural connections i.e. strengthen, weaken, or form new ones
neurogenesis formation of new neurons
short term memory temporarily strengthens already existing neural connections. limited capacity and limited duration, hippocampus processes and prefrontal cortex stores them
long term memory involves structural/functional changes to neural connections (e.g. new axon terminal being created). infinite capacity and longer duration. hippocampus processes, stored in cerebral cortex, amygdala, and cerebellum
habituation decreased response to a repetitive presentation of an indifferent stimulus
habituation process action potentials fired often, leading to cumulative and prolonged entry of Ca+ into the presynaptic neuron,. sustained membrane depolarization locks voltage gated Ca+ channels into a non-conducting state, so less Ca+ comes in and less NT gets released
sensitization increases response following a strong or painful stimulus
sensitization process interneuron releases serotonin which blocks K+ channels, preventing K+ or Na+ movement, prolonging the action potential. longer AP means more Ca+ gets let in, so more NT leaves, more NT means bigger response
long term potentiation long lasting strengthening of neural connections that happen after repeated or high frequency stimulation
long term potentiation process glutamate release from presynaptic neuron, binding to AMPA receptors (Na+ channels), Na+ enters, depolarization. more glutamate activates NMDA receptor (Ca+ channel). Ca+ makes more AMPA, so the synapse has more Na+ channels allowing more Na+ in next stim
declarative memories (explicit) facts, events, and spaces. hippocampus helps form, stored in cerebral cortex. hippocampus brings neuron projection together, cerebral cortex does the connecting
procedural memories (implicit/autopilot) procedures and habits. formed and stored in the basal nuclei and cerebellum
cerebellum part of brain involved in motor function
retrieve memory recall long term memories for future use
re encoding memories how your memories change with new information
diffuse/decay of memories neural connections are lost, it gets rid of stuff you don't use
interference of memories new memories interfere with our ability to recall old ones
encoding failure of memories the neural connection wasn't very strong
bone: protection of CNS tissue tissues are enclosed in hard bony structures
brain bone protection cranium
spine bone protection vertebral collum
meninges: protection of CNS tissue protective and nourishing membranes. they have 3 types
meninges: dura 'durable'. toughest, thick and strong outermost layer found under the scalp and skull bone/cranium
meninges: arachnoid mater covers blood vessels (that look like spiders like 'arach')
arachnoid mater: subarachnoid space of the brain actually has the blood vessels
meninges: pia mater innermost layer. follows the grooves of the brain, making it hard to separate because they're very closely attached.
cerebrospinal fluid: protection of CNS tissue surrounds and cushions the brain and spinal cord. they're basically floating in this fluid
cerebrospinal fluid process fluid filled spaces of the brain have specialized cells that make the fluid. it travels from these spaces into the subarachnoid space around the brain and spinal cord
blood brain barrier: protection of CNS tissue brain blood vessels are not porous/leaky (like normal blood capillaries are) because they're tightly linked together and wrapped in another layer of cells. nutrients and gases are allowed in, but not things like viruses, which can normally spread
glial cells of CNS cells in the brain that are not neurons (they support neurons)
glial cells: astrocytes have a bunch of projections that make it look like a star (astro). most abundant, holds neurons in place (spatial arrangement), makes up the blood brain barrier (wraps around blood vessels) and maintains ECF
glial cells: ependymal cells lines the brain cavities (spaces) and forms cerebrospinal fluid
glial cells: microglia immune cells of the brain, attacks things that are foreign or damaged
glial cells: oligodendrocytes make myelin that wrap around axons to insulate them and speed up electric signals
spinal cord location goes from base of brain to lumbar/lower back
spinal cord job link between the brain and body, manages reflex activity (involuntary automatic movement)
spinal cord protection same as brain (same meninges and cerebrospinal fluid, but has blood spine barrier and vertebral column instead of cranium)
grey matter in spinal cord found in the middle, is the neuron cell bodies
white matter in spinal cord surrounds the grey matter, made up of tracts that are bundles of axons that are wrapped in myelin (the white is the fat because fat is white)
spinal nerves allow info to come in and out of the spinal cord. has two types of 'roots'. all of the nerves start inside the spinal cord then extend beyond. the nerves are made up of a bunch of neruons
spinal nerve: dorsal root afferent neurons bring info into the spinal cord from PNS to CNS (come from behind, dorsal = back/behind)
spinal nerve: ventral root efferent neurons send messages out into the body from CNS to PNS (the cell starts in the spinal cord)
cervical nerves neck area
thoracic nerves trunk/chest
lumbar nerves lower back
sacral nerves tailbone
coccogeal nerves basically legs
brain's functions homeostasis, perception, voluntary movement, emotions, higher cognitive processes (thoughts and memories)
brain stem vital link. controls digestive, cardiovascular, and respiratory function. starts at base of brain and is continuous with the spinal cord. cranial nerves start here.
reticular activating system (RAS) controls degree of awareness, collection of neurons in the brain stem that activate when we're awake (tells the cerebellum to be awake and alert)
hypothalamus homeostasis, controls body temp, sleep, thirst, controls autonomic nervous system (para and sympathetic nervous system)
pituitary gland found in hypothalamus, produces pituitary hormones which manage metabolism, stress response, growth etc)
thalamus middle of the brain above the hypothalamus. sensory input goes through the thalamus, then the message gets sent to the cerebrum
cerebellum controls balance, muscle movement and tone (degree of contraction/tension of the muscle at rest). stores procedural memories
basal nuclei groups of neurons deeply embedded into the brain, controls posture and smooth voluntary movements (impairment would cause parkinsons's)
cerebrum outerlayer of the brain, has a lot of folds, has a left and right side (which uses the corpus collosum to communicate with each other)
cerebral cortex composition outerlayer = grey matter (cell bodies and dendrites). core = white matter (axons that connect the dif areas of the brain). this is opposite to the spinal cord/ divided into different cortical lobes.
occipital lobe: cerebral cortex at the back, vision
temporal lobes: cerebral cortex at the sides, hearing
parietal lobe: cerebral cortex top back of head, somatosensation. different sections correspond to different areas of the body
frontal lobe: cerebral cortex front of head, voluntary movement
prefrontal cortex: frontal lobe at the very very front, does higher level thinking
primary somatosensory cortex behind central sulus. perceives sensations in the body
wernicke's area: primary somatosensory cortex understands written and spoken language
broca's area: primary somatosensory cortex produces sound, coordinates the motor commands needed to shape words using the mouth
limbic system network of structures in the brain that control emotions and behaviours, survival and perception of species, motivation and sexual behaviours
amygdala: limbic system controls emotions
hypothalamus: limbic system activates autonomic nervous system (para or sympathetic system)
hippocampus: limbic system learning and memory
afferent/sensory nervous system: visceral stimuli internal changes that are not usually consciously perceived
afferent/sensory nervous system: sensory stimuli external stimuli that are consciously perceived. have two types
sensory stimuli: somatic sensation touch, pain, hot/cold, proprioception i.e. physical awareness
sensory stimuli: special senses visual, auditory, olfactory, taste, equilibrium
afferent/sensory nervous system: perception conscious awareness/interpretation of the external world. derived from sensory input (doesn't give true reality)
receptor physiology receptors at the nervous system are structures at the end of afferent neurons (found in CNS). they don't have dendrites because they start with a receptor, they start the signal. turn various stimuli into electrical energy i.e. graded or action potentials
transduction process stimulus, mechanically gated ion channels open, Na+ enters, depolarization, graded potential, more Na+ leads to threshold, voltage gated channels open, threshold reached, action potential
coding of sensory info: type of stimulus processed by a specific receptor, then sent to a particular area in the cerebral cortex
coding of sensory info: location of stimulus where the receptors are (receptive field), and which area of the somatosensory cortex gets activated (which corresponds to an area in the body)
coding of sensory info: intensity of stimulus frequency of action potentials initiated after the neuron is activated/amount of receptors/afferent neurons activated
somatosensation sensations that arise from the body/skin
proprioceptions sensations from muscles, tendons, and joints showing you the position of your limbs
primary somatosensory area located in parietal lobe of the cerebral cortex
somatosensation detection process stimulus, ion channels open, Na+ enters, enough Na+ threshold leads to action potential, info goes to the CNS
ascending pathways transports somatosensation info/signals to the cerebral cortex in the brain (where we have conscious awareness), and uses 3 different neurons
ascending pathways: first order neuron receptor to the CNS. detects and sends info via the dorsal root ganglion (type of afferent neuron)
ascending pathways: second order neuron CNS to thalamus, type of interneuron because it's inside the CNS
ascending pathways: third order neuron thalamus to cerebral cortex, the sensation then gets interpreted, type of interneuron
pain protective mechanism meant to bring conscious awareness that tissue damage is going to happen. helps to prevent/avoid potentially harmful events in the future
nociceptors receptors that detect pain. has 3 different types
mechanical nociceptors detect mechanical damage e.g. cutting, crushing, pinching etc
thermal nociceptors detect temperature extremes
chemical nociceptors detect irritating chemicals
pain transmission process same as other somatosensations (i.e. ascending pathways): nociceptors to brain stem to thalamus to somatosensory cortex (localization of pain). also goes from brain stem to reticular formation (makes u alert), then limbic system (relating emotion to pain)
opiates peptide neurotransmitters in the body that bind to opioid receptors which regulate pain and mood
endorphins endogenous opiates that block pain transmission to the brain
endorphin process pain detected, brain sends message to release endorphins, bc it's an opiate it blocks the first neuron from sending the message to release of substance P, pain subsides
exogenous opiates substances you can take to mimic the effect of opiates. stimulates the release of dopamine. if you take them consistently you can build a tolerance (i.e. need more to get same effect)
exogenous opiate tolerance process GABA released to stop dopamine release, opioids stop GABA, dopamine keeps getting released, GABA gets used to the opioids stopping it, more opioids are need to stop GABA (continue dopamine release)
when on exogenous opiates pain is dulled and dopamine is released
when off exogenous opiates GABA goes full force, completely stopped dopamine release, causing intense pain and a crash
chemical senses taste and smell
taste detection process tastants (chemicals) dissolved in water/saliva to go into taste pores and bind to taste receptors, chemically gated ion channels open, Na+ enters, taste receptors synapse with afferent neurons, action potential, signal travels to brain
salty chemical salts like NaCl
sour acids that have free H+
sweet configurations of glucose
bitter chemically diverse group of alkaloids, toxic plant derivates, poisonous substances
umami meaty/savoury taste evoked by amino acids, especially glutamate
taste perception same process as somatosensation (3 neuron path). taste receptor detect tastants, signal is sent via cranial nerves to the brain stem, brain stem to thalamus, thalamus to glustartory cortex in the cerebral cortex
smell detection process detected by olfactory receptors (at top of nasal cavity), the receptor is afferent neuron, Na+ opens, action potential travels from olfactory bulb to olfactory nerve, scent gets organized in olfactory bulb, interneurons pass the signal to cerebral cortex
olfactory receptors are the only neuron that can be replaced (the other ones cant) because they're renewable and replaceable
how we sense smell have to volatile (vaporized) to reach the olfactory mucosa. when u eat, these scent fumes travel there via pharynx
flavour taste + smell + what you're expecting + vision
pupil round opening in the centre of the iris where light enters
iris thin, pigmented (your eye colour) smooth muscle that forms a ring like structure
iris: sphincter pupillae circular muscles, constrict the pupil, controlled by parasympathetic, protect the retina from bright light by reducing the amount of light that enters the eyes
iris: dilator pupillae radial muscles, dilate the pupil, controlled by sympathetic, helps you see better in the dark by increasing the amount of light that enters the pupil
cornea outermost layer that protects the pupil and iris
sclera outermost layer that covers and protects the rest of the eye (is continuous with the cornea)
retina covers the very back of the eye. has photoreceptors that detect light (this info gets sent to the brain via optic nerve)
fovea at the centre back of the eye, vision is the most clear because it has the most photoreceptors
vision perception process light enters pupil (front of eye), hits retina (back of eye), detected by photoreceptors (rods/cones), message gets passed to bipolar cells, leaves via optic nerve to ganglia cells
photoreceptors layers of membrane embedded with light absorbing pigments. these proteins absorb light, get activated, and undergo chemical alterations to change shape. chemical pathways alter ion channels, then light becomes electric signal
photoreceptor: rods' job for low light bc they're sensitive and get overstimulated in bright light. less activity bc they can't see detail, or colour
photoreceptor: rods' ratio multiple rod cells converge onto one bipolar cell, so less stimulation is needed to generate the signal, but the image is less clear
photoreceptor: cones' job for bright light, they aren't sensitive enough to see in the dark. respond to different wavelengths of light so can see colour. when they get burnt out they see complimentary colours
photoreceptor: cone' ratio 1:1 cone:bipolar cell, so images are very clear
seeing dark process rod don't change shape, ion channels stay open, cell depolarizes, Ca+ opens, NT gets released and blocks the next bipolar cell from sending signals to another
seeing light process photoreceptors absorb, retinal becomes trans retinal (hyper polarizes and changes shape), starts signal that closes Na+ (so Ca+ stay closed), no NT gets released, bipolar cells depolarize, signal to ganglia, optic nerve to visual cortex to get perceived
when photoreceptor cells are stimulated... ...no NT gets released
dark adaptation vision gradually improving when entering a dark environment after being in a light one. photopigment in rods take 20-30min to regenerate and become active (because in bright: rods=off and cones=on)
light adaptation feeling 'blinded' after going from dark to bright. in bright light, rods=bleached/oversaturated and shut down. cones only take a minute to reactivate tho
outer ear pinna, ear canal, and ear drum
pinna floppy part, funnel shaped to funnel sound waves into the ear canal
ear canal external auditory meatus. sound waves travel via this to enter ear drum
ear drum aka tympanic membrane, separates outer ear from middle ear
middle ear auditory ossicles which are 3 different bones
auditory ossicles malleus, incus, and stapes. they amplify and transmit sound waves (so the waves can move through the fluid in the inner ear after easily moving through air within the ear canal/drum)
inner ear oval window, cochlea, organ of corti, basilar membrane, hair cells, tectorial membrane, auditory nerve
oval window start of cochlea/inner ear. sound waves hit the window and get transferred into the cochlea
cochlea fluid-filled and spiral-shaped. basically the entire inner ear
organ of corti where sound waves get transducted into electric signals. sits on the fluid on top of the basilar membrane
hair cells attached to the basilar membrane, they move/bend as the fluid moves and detect movement caused by sound
tectorial membrane stable membrane above the hair cells
auditory nerve where action potentials travel, carry info from the cochlea to the brain
sound transduction sound wave enters cochlea via oval window, cochlear fluid moves, basilar membrane moves, hair cells bend, mechanically gated ion channels open, graded/action potential
sound wave discrimination by different properties of the sound waves, timbre, intensity and pitch
timbre/quality overtones (i.e. different types of sounds like voices and instruments)
intensity/loudness amplitude. greater tympanic membrane movement means great basilar membrane movement, hair cells produce more frequent action potentials, CNS interprets louder sound
pitch frequency of the wave. determined by location (on basilar membrane) of the hair cells that have been activated
high pitch/frequency gets detected at narrow/stuff end of basilar membrane close to the oval window
low pitch/frequency gets detected near the helicotrema
vestibular apparatus sensory system in the inner ear that controls balance, spatial orientation, and movement coordination
semicircular canals 3 tiny, fluid filled tubes (with different orientations) that detect rotational acceleration/deceleration of the head. at the bottom, there's cupola with hair cells
otolith organs in the vestibular apparatus, detects linear acceleration and position of head relative to gravity. their hair cells have gelatinous layer on top, which has a layer of tiny crystals call otoliths
otolith organs: utricle detects horizontal movement
otolith organs: saccule detects vertical movement
otolith organs process movement, hair cells and attached gel moves, otolith crystals don't move bc they're heavier, hairs get pulled back, this bending creates electric signal that gets sent to the CNS
autonomic nerve pathway has two efferent neurons: preganglionic and postganglionic fibre
autonomic nerve pathway process signal travels down preganglionic axon (goes into PNS) of the first neuron (cell body in CNS). synapses with autonomic ganglion/2nd neuron, releasing preganglionic neurotransmitters. signal travels down 2nd neurons axon to the effector organ
parasympathetic preganglionic neuron starts at cranial (brainstem) or sacral (spinal cord/lowerback) and releases acetylcholine which binds to nicotinic receptors
parasympathetic postganglionic neuron releases acetylcholine that binds to muscarinic receptors on the effector organ
sympathetic preganglionic neuron starts at thoracic (spinal cord/middle-upper back) or lumbar (spinal cord/lowerback above sacral), releases acetylcholine that binds to nicotinic receptors on postganglionic fibres
sympathetic postganglionic neuron releases norepinephrine and binds to adrenergic receptors on the effector organ
acetylcholine released by both presynaptic neurons binds onto this nicotinic receptors
acetylcholine released by parasympathetic postganglionic binds onto this muscarinic receptors
norepinephrine binds and released... binds to adregenic receptors on effector organ and is released by the sympathetic postganglionic
autonomic agonist binds to the same receptor as a NT and mimics NT's effect (has the same effect)
autonomic antagonist binds to the same receptor of the NT and blocks the response
control of autonomic activities whether you set off sympathetic or parasympathetic nerves. involves hypothalamus (homeostasis), brainstem/medulla (life processes control centre), and prefrontal cortex (personality
somatic nerve pathway one neuron path. starts in CNS, motor/efferent neurons that control skeletal movement come out of ventral root and go to skeletal muscle
cell bodies of somatic motor neurons are found in... spinal cord grey matter (called spinal nerves)
cell bodies of somatic motor neurons that control face and neck movement are found in... brainstem (called cranial nerves)
voluntary body movement process (somatic nervous system) stimulus, efferent neuron gets action potential, propagates to skeletal muscle along efferent fibres, axon branches out, forming multiple neuromuscular junctions with muscle fibres at the muscle
neuromuscular junctions neuron to muscle. 1 neuron : 1 muscle cell fibre. always excitatory, always action potential.
control of motor neurons motor cortex, basal nuclei, and cerebellum
control of motor neurons: motor cortex sends info to spinal cord (where the nerve is) then the motor neuron takes it to the muscle
control of motor neurons: basal nuclei refines movements and controls posture
control of motor neurons: cerebellum manages balance, muscle done and procedural memories. e.g. if you want to walk, the cerebellum sends program to the motor cortex, motor cortex to neuron, then neuron to muscle
Created by: kaiashea
 

 



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