6.1 and 6.2 Flashcards

1
Q

What is a stimulus?

A

a change in an organisms internal or external environment

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2
Q

Why is important that organisms respond to stimuli?

A

Organisms increase their chance of survival, responding to internal environment allows them to maintain optimum conditions for metabolism

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3
Q

What is a tropism?

A

Growth of a plant in response to a directional stimulus. Positive= towards stimulus, negative= away from stimulus

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4
Q

Summarise the role of growth factors in flowering plants:

A

Specific growth factors e.g auxins (IAA) move via phloem or diffusion from growing regions (shoot/root tips) where they’re produced to other tissues where they regulate growth in response to directional stimuli (tropisms)

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5
Q

How does indoleacetic acid affect cells in roots/shoots?

A

In shoots, high concenration of IAA stimulates cell elongation
In roots, high concentrations of IAA inhibits cell elongation

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6
Q

Explain gravitropism in the shoots of flowering plants:

A

Cells in tip of shoot produces IAA
IAA diffuses down shoot, and moves to lower side of shoot so concentration increases. This stimulates cell elongation so shoots bend away from gravity

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7
Q

Explain gravitropism in the roots of flowering plants:

A

Cells in tip of root produce IAA.
IAA diffuses down root, and moves to lower side so concentration increases. This inhibits cell elongation so shoots bend towards gravity

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8
Q

Explain phototropism in shoots of flowering plants:

A

Cells in tip of shoot produce IAA
IAA diffuses down shoot and moves to shaded side, so concentration increases. This stimulates cell elongation so shoots bend towards light

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9
Q

Explain phototropism in the roots of flowering plants:

A

Cells in tip of root produce IAA
IAA diffuses down root and moves to shaded side of root, so concentration increases. This inhibits cell elongation so root bends away from light

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10
Q

What is taxes/tactic response?

A

Directional response, movement towards or away from a directional stimulus

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11
Q

What is kinesis/kinetic response?

A

Non-directional response. Speed of movement/ rate of direction change changes in response to a non directional stimulus, depending on intensity of stimuli

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12
Q

Explain the protective effect of a simple reflex:

A

Rapid, as only 3 neurones and few synapses
Autonomic as doesn’t involve conscious regions of brain so doesn’t have to be learnt
Protects from harmful stimuli, e.g escape predators or prevents damage to body tissues

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13
Q

Describe how a generator potential is established in a Pacinian corpuscle:

A

Mechanical stimuli deforms lamellae and stretch mediated sodium ion channels
Na+ channels in membrane open and Na+ diffuse into sensory neurone.
Greater pressure causes more Na+ channels to open and more Na+ to enter
This causes depolarisation, leading to a generator potential.
If generator potential reaches threshold it triggers an action potential

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14
Q

Why are rods more sensitive to light?

A

Several rods connect to a single neurone (retinal convergence) so there is spatial summation to reach/overcome threshold to generate an action potential

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15
Q

Why are cones less sensitive to light?

A

Each cone connected to a single neurone and so no spatial summation

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16
Q

Why do rods give lower visual accuity?

A

Several rods connected to a single neurone and so several rods send a single set of impulses to brain so can’t distinguish between separate sources of light

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17
Q

Why do cones give higher visual acuity?

A

Each cone connected to a single neurone and so cones send separate sets of impulses to brain and can distinguish between separate sources of light

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18
Q

Why do rods allow monochromatic vision?

A

Only one type of pigment (rhodopsin) so only one type of rod cell

19
Q

Why do cones allow colour vision?

A

3 types of cones- red, blue and green sensitive. Each have different pigments of iodopsin so absorb different wavelengths. Stimulating different combos of cones give a range of colours

20
Q

Define myogenic:

A

Able to contract and relax without receiving electrical impulses from nerves

21
Q

Describe the myogenic stimulation of the heart:

A

SAN acts as a pacemaker, releasing regular waves of electrical activity across atria- causes atria to contract simultaneously
Non-conducting tissue between atria and ventricles prevents impulses passing directly to ventricles, preventing immediate contraction of ventricles
Waves of electrical activity reach AVN which delays impulse, allowing atria to fully contract and empty before ventricles contract
AVN sends wave of electrical activity down bundle of His, conducting wave between ventricles to apex where it branches into Purkyne tissue, causing ventricles to contract simultaneously from the base up

22
Q

Where are chemo- and pressure-/baro- receptors located?

A

In the aorta and carotid arteries

23
Q

Describe how the nervous system controls heart rate in response to a fall in blood pressure/pH:

A

Baroreceptors detect fall in blood pressure/ chemoreceptors detect fall in blood pH
Send impulses to medulla
Which send more frequent impulses to SAN along sympathetic neurones
So more frequent impulses sent from SAN to AVN
Cardiac muscle contracts more frequently and heart rate increases

24
Q

Describe how the nervous system controls heart rate in response to a rise in blood pressure/pH:

A

Baroreceptors detect rise in blood pressure/ chemoreceptors detect rise in blood pH
Send impulses to medulla
Which send more frequent impulses to SAN along parasympathetic neurones
So less frequent impulses sent from SAN to AVN
Cardiac muscle contracts less frequently and heart rate decreases

25
Describe resting potential:
Inside of axon has negative charge relative to outside as more positive ions outside compared to inside
26
Explain how a resting potential is established across the axon membrane in a neurone:
Na+/K+ pump actively transports 3 Na+ out of axon and 2 K+ into axon This creates an electrochemical gradient as higher conc. of K+ inside and higher conc. of Na+ outside Different membrane permeability as membrane more permeable to K+ (move out by facilitated diffusion) than Na+ (closed channels)
27
Explain how changes in membrane permeability lead to depolarisation and the generation of an action potential:
-70mV: Na+ channels open, so membrane permeability to Na+ increases Na+ diffuse into axon down electrochemical gradient, causing depolarisation -55mV: If threshold potential reached an action potential is generated as more voltage gated Na+ channels open so more Na+ diffuse in rapidly 40mV: Voltage gated Na+ channels close, and voltage gated K+ channels open so K+ diffuse out of axon K+ channels are slow to close so slight overshoot where too many K+ diffuse out Resting potential restored by Na+/K+ pump
28
What is the all or nothing principle?
For an action potential to be produced, depolarisation must exceed threshold potential. Action potentials produced are always the same magnitude- bigger stimuli increase frequency of action potentials
29
How do action potential pass along mon-myelinated neurones?
Action potential passes as wave of depolarisation. Influx of Na+ ion one region increases permeability of adjoining region to Na+ by causing voltage gated Na+ channels to open so adjoining region depolarises
30
How do action potentials pass along myelinated neurones?
Myelination provides electrical insulation. Depolarisation of axon at nodes of Ranvier only, resulting in saltatory conduction so there is no need for depolarisation along whole length of axon
31
Suggest how damage to myelin sheathe can lead to slow responses and/or jerky movement?
Less/no saltatory conduction so depolarisation occurs along whole length of axon, and nerve impulses take longer to reach neuromuscular junction so delay in muscle contraction. Ions/depolarisation may pass/leak to other neurones, causing wrong muscle fibres to contract
32
What is the refractory period?
Time taken to restore axon to resting potential when no further action potential can be generated as Na+ channels are closed/inactive/will not open
33
Why is the refractory period important?
Ensures discrete impulses produced (action potentials don't overlap) Limits frequency of impulse transmission at a certain intensity so prevents over reaction to stimulus Also ensures action potentials travel only in one direction
34
What are the three factors that affect the speed of conductance?
Myelination- depolarisation at nodes of Ranvier only (saltatory conduction) so impulse doesn't travel whole length of axon Axon diameter: bigger diameter means less resistance to flow of ions in cytoplasm Temperature: Increases rate of diffusion of Na+ and K+ as more kinetic energy, however proteins/enzymes could denature at too high a temp
35
What is a synapse?
A junction between two neurones/neurone and an effector
36
What are cholinergic synapses?
Synapses that use the neurotransmitter acetyl choline
37
Describe transmission across a cholinergic synapse:
Pre-synaptic neurone: Depolarisation of presynaptic membrane causes opening of voltage gated Ca2+ channels so Ca2+ diffuse into presynaptic neurone/knob This causes vesicles carrying ACh to move and fuse with presynaptic membrane releasing ACh into synaptic cleft by exocytosis Post synaptic membrane: ACh diffuses across synaptic cleft to bind to specific receptors on post-synaptic membrane, causing Na+ channels to open Na+ diffuses into post synaptic knob causing depolarisation. If threshold met, then action potential initiated
38
What happens to ACh after synaptic transmission?
Hydrolysed by acetylcholinesterase into ethanoic acid and choline. Products are reabsorbed by presynaptic neurone to stop overstimulation
39
Explain how synapses result in unidirectional impulses?
Neurotransmitter only made in/released from presynaptic neurone Receptors only on postsynaptic neurone
40
Explain summation by synapses:
Addition of a number of impluses converging on a single post synaptic neurone causing rapid buildup of neurotransmitter so threshold more likely to be reached
41
Describe spatial summation:
Many presynaptic neurones share one postsynaptic neurone and so collectively releases sufficient neurotransmitter
42
Describe temporal summation:
One pre-synaptic neurone release neurotransmitter many times over a short time so sufficient neurotransmitter to reach threshold
43
Describe inhibition by inhibitory synapses:
Inhibitory neurotransmitters hyperpolarise the membrane as Cl- channels open (Cl- move in) and K+ channels open (K+ out) Inside of axon has a negative charge below resting potential So more Na+ required to enter for depolarisation which reduces likelihood of threshold being met
44
What effect do drugs have on a synapse?
Some stimulate the nervous system leading to more action potential - similar shape to neurotransmitter - stimulate release of more neurotransmitter - inhibit enzyme that breaks down neurotransmitter so Na+ continues to enter Some inhibit the nervous system, leading to fewer action potenitals - inhibit release of neurotransmitter (e.g prevent opening of Ca2+ channels) - Block receptors by mimicking shape of neurotransmitter