Module 2: Neurons, Synapses and Nervous Systems Flashcards

1
Q

what are the three stages of information processing?

A

1) sensory input - eye
2) Integration- central nervous system
3) Motor output - peripheral nervous system - effector

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2
Q

describe the structure of a neuron

A
>nucleus
> dendrites
> cell body
> axon hillock 
> axon
> synaptic terminals
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3
Q

what are the different types of neurons and their structure?

A

> sensory neuron - small, few dendrites, long axon, cell body is half way down the axon
Interneuron - lots and lots of dendrites and synaptic terminals, used for collecting information, can form huge tree like structures
motor neuron - long and multiple dendrites, cell body located next to the dendrites, regular axon

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4
Q

describe the structure of a nerve

A

> a collection of neurons
axons
connective tissue
blood vessels

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5
Q

what are glia cells?

A

> supporting cells
vital for structural integrity and normal function
10-50 times more glia then neurons in the mammalian brain
supply nutrients
three types:
1) astrocytes
2) oligodendrocytes and Schwann cells

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6
Q

what are astrocytes

A

> located in the CNS
structural support
regulate extracellular concentrations of ions and neurotransmitters
formation of the blood-brain barrier
prevents things from getting into the brain.

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7
Q

what are oligodendrocytes and Schwann cells?

A

> oli in the CNS
Schwann in the PNS
form myelin shealths around axons - fatty insulators
lipid membranes: insulator
when defective cause multiple sclerosis
have nodes of ranvier between each schwann cells on the axon of a neuron.

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8
Q

what is sodium/potassium ATPase?

A

> maintains the resting potential of the neuron
pumps out 3 x Sodium out of the cell
pumps 2 x potassium into the cell
for each ATP molecule

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9
Q

what are the relative concentrations of ions inside and outside the cell?

A
Extra cellular concentration:
> overall slightly postive
> 5mM K+
> 150mM Na+
>120mM Cl-
Intracellular concentration:
> overall slightly negative 
> 140mM K+
> 15mM Na+
>10mM Cl-
>100mM A- (large anions)
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10
Q

why is the resting membrane potential negative?

A

> Na+/K+-ATPase pumps 3Na+ out and 2 K+ in
the membrane at rest has many open K+ channels and few open Na+ or Cl- channels
K+ outflow leads to a net negative charge inside the cell.
the excess negative charges inside the cell exert attractive force that stops too many K+ ions from leaving the cell
the chemical gradient of K+ is thus opposed by the electrical gradient
this gradient forms -70mV equilibrium potential in human cells.

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11
Q

Which cells are excitable?

A

neurons
myocytes - muscle cells
pancreatic beta cells - release insulin

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12
Q

describe hyperpolarisation

A

inside of membrane becomes more negative
> opening of voltage-gated K+ channels
> K+ travels out

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13
Q

describe depolarisation

A

inside of membrane becomes more positive
> opening of voltage-gated Na+ channels
> Na+ in

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14
Q

what is a graded potential?

A

> can be depolarisation and/or hyperpolarisation
vary in magnitude with the strength of the stimulus
local and die out

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15
Q

what is an action potential?

A

> always depolarisation
reach a certain threshold (-50mV in humans) then all or nothing response
travel along axons
magnitude is independent of the strength of the original stimulus
1-2 millisecond and high frequency

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16
Q

what are voltage-gated ion channels?

A
open when a certain voltage reaches them
Na+:
> closed --depolarisation--> open --> inactivated by peptide tail ---> closed again
> fast
> into cell
K+:
> closed --depolarisation--> open ---> closed
> slower
> out of cell.
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17
Q

describe the process of producing an action potential

A

1) resting state - voltage-gated ion channels are closed
2) a stimulus cause a few Na+ channels to open. Na+ rushes in
3) depolarisation occurs if threshold is reached by incoming Na+ ions. lots of Na+ channels open. lots of Na+ rushes in
4) repolarisation. K+ channels open and K+ rushes out. Na+ channels inactivated and then start to close
5) undershoot. Small hyperpolarisation. also need Na+/K+-ATPase to restore Na+ and K+ concentrations.

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18
Q

what are refractory periods?

A

> Absolute refractory period:

  • voltage-gated Na+ channels inactivated during repolarisation
  • no action potential can be generated because Na+ channels open then inactivate

> relative refractory period
- an action potential can only be generated if a large enough stimulus is applied
- because some Na+ channels have closed again and are ready to be opened to let in Na+ to create a depolarisation event.
limits firing frequency
the action potential can only travel in one direction

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19
Q

what is the mechanism for local anaesthetics?

A

> local anaesthetics prevent action potentials by blocking voltage-gated Na+ channels from returning to the closed state, leaving them as inactive.

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20
Q

how does the conduction of action potentials work?

A

1) an action potential is generated as Na+ flows inward across the membrane at one location
2) the depolarisation of the action potential spreads to the neighbouring region of the membrane, reinitiating the action potential there. to the left of this region, the membrane is repolarising as K+ flows outward.
3) the depolarisation-repolarisation process is repeated in the next region of the membrane. in this way, local currents of ions across the plasma membrane cause the action potential to be propagated along the length of the axon.

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21
Q

how does axon diameter effect action potentials?

A

> the larger the diameter, the less resistance = faster conduction
invertebrates: speeds vary from a few cm/s to 100m/s in giant squid axon

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22
Q

what are the factors that effect the speed of action potentials?

A

1) axon diameter
2) temperature
3) degree of myelination

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23
Q

how does temperature effect action potential speed?

A

> any chemical reaction, i.e., an action potential, occurs faster at warmer temperatures

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24
Q

how does the degree of myelination of the axon effect action potentials?

A

> myelin insulates the axon membrane in vertebrates = faster conduction speed
conduction speed is affected more by myelination than axon diameter
unmyelinated nerve fibre - smooth, slower conduction
myelinated nerve fibre - saltatory conduction
- action potential only has to be propagated at the nodes of ranvier

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25
Q

what is saltatory conduction?

A

> Schwann cells produce a myelin sheath around the axon
the depolarising current during an action potential at one node of Ranvier spreads along the interior of the axon to the next node, where voltage-gated sodium channels enable reinitiation. Thus, the action potential jumps from node to node to node as it travels along the axon.
can reach conduction speeds of 120m/s

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26
Q

list and explain the two types of communication that can occur at the synapses

A
Electrical synapses
> at gap junctions
> direct electric current between cells
> relatively few synapses of this type
Chemical synapses
> involves release of a chemical neurotransmitter
> neurotransmitter released by presynaptic neuron
> vast majority of synapses
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27
Q

what are the steps that occur at a chemical synapse in direct synaptic transmission?

A

1) an action potential arrives, depolarising the presynaptic membrane
2) the depolarisation opens voltage-gated channels triggering an influx of Ca2+.
3) the elevated Ca2+ concentration causes synaptic vesicles to fuse with the presynaptic membrane, releasing neurotransmitter into the synaptic cleft.
4) the neurotransmitter binds to the ligand-gated ion channels in the postsynaptic membrane. In the example, binding triggers opening, allowing Na+ and K+ to diffuse through.

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28
Q

what happens after the neurotransmitter is released from the presynaptic neuron?

A

> either an excitatory postsynaptic potential (EPSP) if depolarisation at postsynaptic membrane - another action potential
or an inhibitory postsynaptic potential (IPSP) is hyperpolarisation at postsynaptic membrane

29
Q

what are the different types of summation?

A

Temporal summation:
> several ESPSs from the same synapse just after each other - summation over time
> if they can reach threshold at the axon hillock, than an action potential is created.
Spatial summation:
> two or more EPSPs from different synapses
> same time at different parts of the cell body.

30
Q

know the graphs for subthreshold: no summation, temporal and spatial summation

A

on notes

31
Q

what is the difference between a postsynaptic potential ans an action potential?

A
Postsynaptic potential:
> excitatory (EPSP) or inhibitory (IPSP)
> graded
>local
> at the cell body or dendrites
Action potential:
>depolarisation - always
> "all or nothing"
> EPSPs can add up and cause an action potential
> generated at the axon hillock
> travels along the axon
32
Q

what are the types of chemical synaptic transmission?

A

Direct synaptic transmission:
> neurotransmitter opens ion channels on the postsynaptic membrane
> action via ligand-gated ion channels

Indirect synaptic transmission:
> neurotransmitter binds to a receptor on the postsynaptic membrane
> activates a signal transduction pathway
> involves a second messenger

33
Q

which receptor types are direct and which are indirect synaptic transmission?

A

DIRECT:
> ion channel receptors
INDIRECT:
> G-protein coupled receptors

34
Q

What are the components of direct synaptic transmission?

A

> neurotransmitter opens ion channels on the postsynaptic membrane
- leads to a postsynaptic potential - graded
excitatory postsynpatic potential
- depolarisation
IPSPs
- hyperpolarisation

35
Q

what are the amino acid transmitters and what is their function?

A
> GABA (gamma-aminobutyric acid)
- brain
-inhibitory
> Glutamate
- CNS
- excitatory
> Glycine
- CNS outside the brain - i.e., spinal cord
- inhibitory
> Aspartate 
- excitatory
36
Q

what are the amine neurotransmitters?

A

> acetylcholine

  • ligand-gated ion channel
  • excitatory
  • PNS and CNS
  • In heart muscles g-protein - inhibitory effect
37
Q

What are the biogenic amine neurotransmitters?

A

> Norepinephrine/noradrenaline
- excitatory in the autonomic nervous system
Dopamine and serotonin
- brain
- affect sleep, mood, attention and learning.

38
Q

how are neurotransmitters removed from the synaptic cleft?

A

1) recycled by selective uptake by transporters e.g., NET, SERT into presynaptic neuron
2) diffusion (very slow)
3) taken up by astrocytes
4) broken down by enzymes e.g., acetylcholinesterase
- only neurotransmitter with this mechanism

39
Q

what are the different types of nervous systems in primitive organisms?

A

> nerve net - hydra
radial nerve and nerve ring - seastar
brain, nerve chord and transverse nerve - planarian

40
Q

what are the different types of nervous systems in more complex invertebrates?

A

> segmentally arranged clusters of neurons = ganglia
ganglia = PNS
connected to CNS
brain, ventral nerve chord, segmental ganglion
e.g., leech and insect

41
Q

what are the different types of nervous systems in molluscs?

A

> mollusc organisation depends on lifestyle
anterior nerve ring, longitudinal nerve chords, ganglia - chiton
brain, ganglia - squid
giant axon of the squid as experimental model in physiology
aplysia (sea hare) - used for studies on the cellular basis of memory

42
Q

what are the different types of nervous systems in vertebrates?

A

> central nervous system and peripheral nervous system

> regional specialisation

43
Q

what is involved in the central nervous system?

A

Brain and spinal cord

44
Q

what is involved in the PNS?

A
cranial nerves
> 12 pairs in mammals
ganglia outside CNS
spinal nerves
> contain both sensory and motor neurons
> 31 pairs in mammals
45
Q

describe the reflex arc

A

DIAGRAM
> skin senses stimulus
> send information via the posterior sensory neuron to the dorsal root ganglion where the cell body is located
> then this travels to the spinal cord where it synapses with a interneuron
> interneuron synapses with a motor neuron on the anterior side.
> travels through the motor neuron in the ventral root to the muscle.

46
Q

what are the components of the peripheral nervous system?

A

> somatic nervous system - motor neurons - voluntary
autonomic nervous system - mostly involuntary
includes:
- sympathetic division
- parasympathetic division
- enteric dividion

47
Q

describe the components of the autonomic nervous system

A
Sympathetic:
> 'fight or flight'
> bronchi dilate
> heart beats faster
> glycogen to glucose
> adrenaline secretion
> digestion is inhibited - precapillary sphincters
Parasympathetic:
> 'rest and digest'
> calming
> often opposite response to the sympathetic division
48
Q

what are the anatomical components of the sympathetic nervous system?

A

> nerves arise from the thoracic or lumbar regions of the spinal cord
short preganglionic neurons
long postganglionic neurons

49
Q

what are the anatomical components of the parasympathetic nervous system?

A

> nerves arise from the cervical and sacral regions of the spinal cord
long preganglionic neurons
short postganglionic neurons

50
Q

what parts of the brain developed from embryonic?

A

> forebrain - cerebrum and diencephalon
midbrain - part of the brainstem
hindbrain - part of brainstem, cerebellem

51
Q

what is cerebrospinal fluid?

A

> protects the CNS
clear fluid
subarachnoid space (between the skull and cortex)
ventricles (4) and central canal
supply nutrients and hormones; removes waste
blocked flow in hydrocephalus

52
Q

what is the brain made of?

A

> gray matter (dendrites, unmyelinated axons, cell bodies)
white matter (myelinated axons in tracts
ventricles

53
Q

wha is the spina cord made of>

A

gray and white matter

54
Q

what is the brainstem?

A

> evolutionary older part
‘basic’ functions
homeostasis, movement
transfers information to the rest of the brain
reticular formation - selectivity filter that determines arousal and sleep
consists of: pons, midbrain and medulla oblongata (respiration)

55
Q

what is the cerebellum?

A

> coordination
motor function
cognitive and perceptual functions

56
Q

what is the diencephalon?

A

> Epithalamus
thalamus
hypothalamus

57
Q

what is the cerebrum?

A
contains:
> left cerebral hemisphere
> right cerebral hemisphere
> neocortex = 80% of total brain mass
> cerebral cortex
> corpus callosum 
- communication between left and right
> basal nuclei
- important for movement
- deep in brain
- release dopamine
58
Q

what are the four lobes of the human cortex?

A

frontal, parietal, occipital, temporal

59
Q

what is in the frontal lobe?

A
> prefrontal cortex
- decision making, planning
> Broca's area
- forming speech
> motor cortex
- control of skeletal muscles
60
Q

what is in the parietal lobe?

A

> somatosensory cortex
- sense of touch
sensory association cortex
- integration of sensory information

61
Q

what is in the occipital lobe?

A

> visual cortex
- processing visual stimuli and pattern recognition
visual association cortex
- combining images and object recognition

62
Q

what is in the temporal lobe?

A

> auditory cortex
- hearing
Wernicke’s area
- comprehending language

63
Q

what areas of the brain can a stroke effect?

A

> Broca’s area - decribed patients who could understand language but not speak - active during speech generation
Wernicke’s area - described patients with the opposite effect, could speak but not comprehend speech - active when speech is heard

64
Q

describe the limbic system

A
> emotional system
> Thalamus
> hypothalamus
> Olfactory bulb
> Hippocampus: memory
> Amygdala: fear
65
Q

what areas are active in memory?

A

> short term memory: constantly active - hippocampus
long term memory: is something worth remembering? cerebral cortex - stored memories
short-term memory is activated when long term memory needs to be accessed.

66
Q

how does long term memory potential work in vertebrates?

A

> high frequency transmission of glutamate
results in increase in size of the postsynaptic potentials at synapse
lasts for days or weeks
a fundamental process for storing memories and hence for learning

67
Q

What is the epithalamus?

A
  • connects limbic system (emotional centre) to the rest of the brain
  • pineal gland: melatonin (sleep)
68
Q

What is the thalamus?

A
  • relay station
  • input from sensory neurons
  • output via motor neurons
69
Q

What is the hypothalamus?

A
  • homeostatic regulation - hormones
  • biological clock
  • temperature regulation
  • survival - hunger , thirst etc.