Unit 15: Control & Coordination (JW) Flashcards

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1
Q

Describe endocrine system

A

endocrine glands -> ductless glands
- in good blood supply -> secrete hormones into bloodstream as soon as possible

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2
Q

Define and describe hormones

A

Hormones = cell-signalling molecules secreted to bloodstream
- only affect cells with receptors that the hormone can bind to
- water-soluble -> cannot cross phospholipid bilayer of CSM
- binds to receptor -> which activates 2nd messenger to transfer signal throughout cytoplasm

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3
Q

Extra: steroid hormones and their properties?

A

other hormones such as testosterone, oestrogen & progesterone are steroid hormones
- lipid soluble
- can cross phospholipid bilayer
- bind to receptors in cytoplasm/nucleus of target cells

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4
Q

compare the features of the nervous system and the endocrine system

A
  • Impulse vs hormone
  • Electrical vs. chemical
  • Neurone vs blood
  • Muscle/gland vs target organ (organs, tissue, cells)
  • Faster vs slower
  • Specific vs widespread
  • Short-term vs long-lasting
  • CSM vs CSM/within cell

Both: (similarities)
- Involve cell signalling
- Involve signal molecule binding to receptor
- involve chemicals

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5
Q

Describe the function of 3 diff types of neurone

A

Sensory neurone - transmit impulse from receptor to intermediate neurone
Motor neurone - transmit impulse from intermediate neurone to effector/muscle/gland
intermediate neurone - connect sensory & motor neurone

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6
Q

outline the role of sensory receptor cells

A

detect stimuli, e.g. light, heat
act as transducers by converting stimuli energy to electrical energy
produces receptor potential
Passes impulse to sensory neurone

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7
Q

Describe structure of motor neurones

A
  • Dendrites -> dendron -> to cell body in centre
  • Nucleus in cell body
  • Many mito & rER
  • 1 long axon
  • Synaptic knobs furthest from cell body
  • Schwann cells
  • Nodes of Ranvier
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8
Q

Describe structure of sensory neurones

A

nucleus in, cell body / soma ;
(long) dendron ;
3 (short) axon ;
4 many mitochondria (in cell body) ;
5 many, RER / ribosomes or presence of Nissl’s granules (in cell body) ;
6 synaptic, knobs / terminals / boutons ;
7 Schwann cells / myelin sheath ;
8 nodes of Ranvier

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9
Q

describe the sequence of events that results in an action potential in a sensory neurone

A

Na+ ions enter chemoreceptor cell through microvilli
CSM depolarised
receptor potential > threshold
Ca2+ channels open, Ca2+ enter cytoplasm
vesicles move towards and fuse with presynaptic membrane
released to synaptic cleft by exocytosis
diffuses across synaptic cleft
binds to receptors on sensory neurone
Na+ enters sensory neurone
depolarisation
such that receptor potential > threshold potential

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10
Q

Describe how a resting potential is set up and maintained in a myelinated neurone

A

Na+ moves out of, cell and K+ moves into cell ;
3 Na+ for every 2 K+ ;
by, active transport / use of ATP ;
sodium-potassium pump / Na+ K+ pump ;
against concentration gradient ;

K+ diffuses out of cell and Na+ diffuses into cell ;
by facilitated diffusion / diffusion through (ion) channels ;
membrane more permeable to K+ / more K+ goes out than Na+ in ;
inside of, cell / membrane, more negative than outside ; ora
membrane / cell, polarised / repolarised ;
(resting potential is), –60 mV / –65 mV / –70 mV ;
AVP ; e.g. ion movement only at nodes of Ranvier

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11
Q

Describe refractory period

A

Neurone is unresponsive as it is recovering
until repolarisation occurs and resting potential is established, axon membrane undergoes refractory period
when resting potential close to being reestablished, K+ close, Na+ open -> responsive to depolarisation again

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12
Q

describe and explain the rapid transmission of an impulse in a myelinated neurone

A
  • Schwann cells wrap around axon
  • myelin sheath insulates axon
  • Ions cannot pass through
    Na+ channels only occur at nodes of Ranvier
    depolarisation only occurs at nodes
  • APs occur at nodes of Ranvier only
  • Longer circuits/currents
  • APs must jump from node to node (saltatory conduction)
  • Faster transmission of impulses (approx 50x faster)
    1 way transmission
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13
Q

Explain the importance of the refractory period in determining the frequency of impulses

A

Ensures AP are discrete events - prevent merging into one another

So, 1 way transmission = establish minimum time between APs occuring only at 1 place along neurone

Ensures new APs are generated ahead, rather than behind original AP - as region behind is recovering from AP that has just occurred

Length of refractory period determines maximum frequency of impulse transmission

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14
Q

Describe the structure of a cholinergic synapse and explain how it functions, including the role of calcium ions

A

AP reaches presynaptic neurone =
Ca2+ channels open = Ca2+ enters presynaptic neurone
causes vesicles containing ACh to move towards & fuse with presynaptic membrane

ACh released to synaptic cleft by exocytosis

ACh diffuses across synaptic cleft
binds to receptors on postsynaptic membrane

Na+ channels open = Na+ enter = Postsynaptic neurone
Depolarised

Acetylcholinesterase breaks down ACh

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15
Q

Explain the role of acetylcholinesterase in a synapse.

A

Enzyme that breaks down ACh = ACh leaves the binding site = recycles ACh too

Depolarisation stops in postsynaptic neurone = so stops continuous APs

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16
Q

Explain the effects of inhibition of acetylcholinesterase at a synapse.

A

ACh not broken down =
Na+ channels remain open = Na+ diffuse into postsynaptic neurone
continued to be depolarised

Continuous transmission of APs

17
Q

Outline the roles of synapses in the nervous system.

A
  • Ensure one-way transmission
  • Filter out infrequent impulses
  • Allow interconnection of nerve pathways
  • Involved in memory / learning
18
Q

describe the roles of neuromuscular junctions, the T-tubule system and SR in stimulating contraction in striated muscle

A

AP at presynaptic membrane
Ca2+ channels open = Ca2+ enter

Vesicles fuse with presynaptic membrane =
ACh released to neuromusclar junction by exocytosis =
ACh diffuses across neuromuscular junction & binds with receptor on sarcolemma

Na+ channels open = Na+ enter =
Depolarisation of sarcolemma =
Depolarisation spreads through T-tubules =
Depolarisation of SR

Ca2+ channels in SR open =
Ca2+ move out of SR =
Ca2+ diffuse into sarcoplasm =
Ca2+ bind to troponin

19
Q

Describe the ultrastructure of a striated muscle fibre.

A

Muscle fibres are multinucleate

CSM = sarcolemma = deep tube-like projections known as T-tubules running to close to SR

Cytoplasm = sarcoplasm = has many mitochondria

Myofibrils has 2 types of protein filaments
i) Thick filament = myosin = fibrous protein with globular head
ii) Thin filament = actin = chain of globular protein molecules

20
Q

Explain the sliding filament model of muscular contraction

A

Ca2+ ions released from SR into sarcoplasm =
Ca2+ ions bind to troponin and tropomyosin

Troponin and tropomyosin change position = expose myosin binding site on actin

Myosin head binds forms cross bridge =
Myosin head tilts =
Power stroke

Myosin head hydrolyses ATP =
Myosin head lets go of actin

Myosin head goes back to previous orientation= binds closer to the Z disc =
Process repeated

Sarcomere shortens

21
Q

Describe how tropomyosin and myosin are each involved in the sliding filament model of muscle contraction.

A

Tropomyosin:
covers / uncovers myosin binding sites on actin
when Ca2+ bind to troponin, tropomyosin changes shape
allows myosin to bind to actin

Myosin (ATPase):
ATP hydrolysis
causes myosin head to pivot back to original position

Myosin head binds to actin to form cross bridges with actin = ADP and Pi detaches

When myosin head swings back, ATP binds and is hydrolysed = myosin detaches

(So remember, when it detaches, ADP and Pi is still there, and will detach once cross bridge is formed)

22
Q

Explain the precise function of ATP in sliding filament model

A

ATP binds to myosin head

Hydrolysed by ATPase
head detaches from actin

Head tilts back to original position

23
Q

Describe the main structural features of thick filaments and thin filaments in the sarcomere

A

Thick filaments:
Myosin
fibrous protein
globular heads

Thin filaments:
Actin
globular protein

Troponin and tropomyosin covers binding site for myosin

24
Q

Describe the role of Ca2+ ions in the contraction of striated muscle

A

SR depolarised
Ca2+ channels open
Ca2+ released from SR
Binds to troponin
troponin changes shape
moves tropomyosin
exposes myosin-binding site on actin
allows myosin to bind to actin - form cross-bridge
myosin binds to actin
myosin head tilts
actin pulled

25
Q

Describe how Venus fly trap closes.

A

Concept is:
i) mechanical energy converted to electrical
ii) sensory hair cell is receptor

Cell membrane of SH depolarises if at least 2 hairs touch within 35 seconds = AP occurs = AP spreads over lobe to midrib cells

H+ pumped into cell walls = cross-links broken = calcium pectate dissolves in middle lamella = Ca2+ ions enter cells = water follows by osmosis = cells turgid

Trap shuts quickly in less than 1 second = convex to concave

Further stimulation of SH = calcium ions to enter gland cells = stimulate exocytosis of vesicles with digestive enzymes

26
Q

Explain the role of auxin in elongation growth by stimulating proton pumping to acidify cell walls

A

Binds to receptor on CSM = stimulates proton pumps to pump protons into cell wall = lowers pH

Causes 2 things
i) Expansins activated = loosens bond between cellulose microfibrils
ii) Potassium ion channels stimulated to open = potassium ions enter = decreases WP = more water enter by osmosis = increase turgor pressure

So, cell wall streteches = cell elongates

27
Q

describe the role of gibberellin in the germination of barley

A

Seed absorbs water
Embryo produces gibberellin
Gibberellin binds to receptors on CSM of aleurone layer where production of amylase occurs

Gene coding for amylase expressed
translation of mRNA to produce amylase
Amylase hydrolyses starch in endosperm to maltose
Embryo uses sugars for respiration & growth
Gibberellin affect synthesis of mRNA coding for amylase