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Stimulus
Detectable change in the internal/external environment of an organism that leads to a response/ change in the organism
Tropism
When plants respond to a stimuli via growth
Can be positive (towards)
Can be negative (away)
Process of positive phototropism in shoots
1) cells in the tip of the shoot make IAA, which is transported evenly down the shoot
2) light causes IAA to build up on the shaded side of the shoot
3) high concentration of IAA causes elongation of shoot cells on the shaded side
4) shaded side grows faster causing shoot to bend towards the light
Process of positive gravitropism in roots
1) cells in the tip of the root make IAA which in transported evenly across the root
2) gravity causes IAA to move from upper side to lower side of root so IAA builds up on lower side
3) high concentration of IAA inhibits elongation of root cells so cells on the lower side elongate less
4) upper side grows faster which causes shoot to bend downwards towards gravity (anchors the plant in)
IAA
Indoleacetic acid (growth factor)
type of auxin which can control cell elongation in shoots and inhibit growth of cells in the roots
Made in the tip of roots/shoots and can diffuse
Reflex
Rapid, automatic response to an external or internal stimuli
Taxis
organism will move its entire body towards a favourable stimulus or away from an unfavourable stimulus
Kinesis
Organism changes the speed of movement and frequency of direction changes in order to randomly move towards a favourable condition/ away from an unfavourable one
2 main nervous systems
1) the central nervous system (brain and spinal chord)
2) the peripheral nervous system (sensory and motor neurones)
Voluntary nervous system
Carries nerve impulses to body muscles and is under voluntary control
Autonomic nervous system
Carries nerve impulses to glands, smooth muscle an cardiac muscle and is ‘subconscious’
Structure of a motor neurone
soma (main cell and nucleus)
axon
myelin sheath (myelination over Swann cells)
nodes of ranvier (saltatory conduction between them )
Dendrites
The spinal chord
Column of nervous tissue that runs along the back inside the vertebral column for protection (emerging at intervals are pairs of nerves)
Example of a reflex arc (hot stimulus)
Stimulus- hot pan
Receptor- temperature receptors in skin
SEnsory neurone- passes impulse to spinal chord
Intermediate neurone- in spinal cord links the neurones together
Motor neurone passes impulse from spinal cord to muscle in upper arm
Effector- the muscle in upper arm is stimulated to contract
Response- drop saucepan
Importance of reflex arcs
protect the body from harmful stimuli
they are fast, because the neurone pathway is short with very few synapses
Brain is not overloaded with situations in which the response is the same
are involuntary and therefore do not require the decision making powers of the brain the leaving it free to carry out more complex responses
Receptors
Cells which detect specific stimuli to establish a generator potential to cause a response
1) Pacinian corpuscle
2) Rods
3) cones
Pacinian corpuscle
Receptor located deep in skin that responds to mechanical pressure (transducers the mechanical energy of the stimulus into a generator potential
has a capsule/lamellae
Axon membrane which travels into the lamellae
Shwann cells/ myelination
Has stretch-mediated Na+ channels
Method of action in pacinian corpuscle
1) in its resting state, the stretch-mediated Na+ channels are too narrow to allow Na+ through
2) when mechanical pressure is applied the corpuscle changes shape which stretches/deforms the membrane/ lamellae the neurone
3) this widens the channel and the Na+ can now diffuse into the neurone
4) this influx of Na+ changes the potential of the membrane causing depolarisation
5) this creates a generator potential which creates an action potential
Features of rod cells
high in number
Most highly concentrated in periphery of retina (not present at fovea)
See in black and white
Contain rhodopsin which is very sensitive to light (only requires low intensities to be stimulated)
High retinal convergence (multiple rods connected to one bipolar neurone
Low visual acuity
Features of cone cells
fewer in number
Highest concentration at the fovea (fewer in the periphery of retina)
3 different types of cones (RGB) each of which responds to a different wave length of light- allows us to see in colour
Contain iodopsin which is less sensitive to light (therefore need higher light intensities to be stimulated)
No retinal convergence (each cone cell connected to one bipolar neurone)
High visual acuity
Establishing resting potential
1) 3 Na+ ions actively transported out of axon by Na+/K+ATP-ase
2) 2 K+ ions actively transported in to axon by Na+/K+ATP-ase
3) creates an electrochemical gradient (Na+ wants to move in and K+ wants to move out)
4) membrane is more permeable to K+ ions so some K+ ion allowed to diffuse out of axon
Resting = -65mV
Nervous impulse
Self-propagating wave of electrical activity that travels along the atonal membrane (reversal of potential difference)
Process of action potential
1) stimulus causes voltage-gated Na+ channels in the axon membrane (at -55mv/ threshold)
2) causes an influx of Na+ down the electrochemical gradient causing depolarisation
3) neighbouring voltage-gated Na+ channels open ( more Na+ influx up to + 4o mv of depolarisation)
4) at +40mv, voltage-gated channels close and voltage gated K+ channels open
5) K+ ions diffuse out of axon, down their electrochemical gradient, depolarising the axon membrane
6) hyperpolarisation which causes axon to becom more negative than resting potential
How is size of a stimulus perceived?
by the frequency of the action potentials generated
Absolute refractory period
NO more action potential can be generated regardless of how strong the stimulus (during depolarisation)
Relative refractory period
Possible for further action potentials but requires a stronger stimulus (durging hyperpolarisation)
Importance of refractory periods
make sure action potentials are only propagated in one direction
Produces discrete impulses (seperate action potentials)
Limits the frequency of action potentials
How to increase the speed of nervous impulses?
myelination insulates the axon, saltatory conduction between nodes of ranvier allows impulse to hop between nodes
Larger axon diameter= faster speed of conductance
Higher temperature increases diffusion of ions
Explain why. Ions can only be exchanged between nodes of ranvier
Because the remainder of the axon is covered by a myelin sheath that prevents ions being exchanged/ prevents a potential difference being set up
Neurotransmitters
Chemicals used to transmit information between neurones/ neurone and effector
E.g. acetylcholine
Transmission across an excitatory synapse
action potential depolarises pre-synaptic bulb,opening voltage-gated Ca2+ channels
Influx of Ca2+ ions triggers exocytosis of vesicles containing acetylcholine, which is released into the synaptic cleft
Acetylcholine diffuses across the synaptic cleft and binds to receptors on post synaptic membrane
ligand-gated Na+ ion channel open, allowing an influx of Na+ ions,
Once threshold (-55mv) reached, neighbouring voltage-dated Na+ ion channels open. Which generates an action potential in the post synaptic membrane
Acetylcholinesterase hydrolyses acetylcholine
Products are sent back to the pre-synaptic bulb where they undergo endocytosis
ATP resynthesises the products back into acetylcholine to be released again
Inhibitory synapse
Prevents depolarisation
E.g. Causes an influx of Cl- ions so threshold cannot be reached
How are synapses unidirectional?
presynaptic neurone releases the neurotransmitter
Receptors for the neurotransmitter are on the post-synaptic neurone
Spatial summation
multiple pre-synaptic neurones release neurotransmitters into the synaptic cleft to one post-synaptic membrane, to reach threshold and generate an action potential
Temporal summation
One pre-synaptic neurone releases neurotransmitter at a higher frequency (enough to exceed threshold to generate action potential in post-synaptic neurone)
Why are their multiple neuromuscular junctions along the muscle?
To ensure the wave of contraction is stimulated across the full muscle (otherwise the fibres would not contract simultaneously and response would be slow)
Features of a neurone-neurone synapse
inhibitory or exhibitors
Links neurones to neurones to other effectors
Can occur between sensory, intermediate and motor neurones
New action potentials
Multiple different neurotransmitters
Features of a neuromuscular junction
only excitatory
Links neurones to muscles
Only occurs between motor neurones and the muscle
End of action potential pathway
Acetylcholine binds to receptors on membrane of muscle fibre
structure of skeletal muscle
Made up of many fibres share a sarcoplasm and a nucleus
Sarcoplasm contains mitochondria and sarcoplasm if reticulum
Bibles are made up of myofibrils
Myofibrils are made up of two myofilaments (actin and myosin
Structure of actin
thin protein filamanets made up of two twisted strands
Has a troponin complex attached to the protein filament (moved to expose binding sites on tropomyosin)
Structure of myosin
thick protein filament that has two proteins heads which stick out of each molecule
Multiple myosin molecules makes up the thick filament
Fast-twitch muscle fibres
Contract rapidly and powerfully for a short period
have thick myosin filaments
Lots of glycogen
Enzymes involved in glycolysis and phosphocreatine ( ADP to ATP in anaerobic conditions)
Slow twitch muscle fibres
Contracts more slowly and less powerfully but for a longer period of time
lots of myoglobin, which stores o2 for aerobic respiration
Lots of vasculature (delivers glucose and o2)
Lots of mitochondria (aerobic respiration)
Sliding filament theory
1) Action potential from neuromuscular junction travels deep into muscle fibre through T-tubule system
2) Sarcoplasmic reticulum has actively transported Ca+ ions from the sarcoplasm, so con. Of Ca2+ in the sarcoplasm was low
3) Arrival of the action potential opens voltage-gated Ca2+ channels in the sarcoplasmic reticulum, so Ca2+ diffuses into sarcoplasm down their chemical gradient
4) Ca2+ ions bind to troponin and causes tropomyosin to move, exposing actin binding sites
5) ADP molecules attach to the myosin heads, allowing the heads to bind to the actin filaments and form cross-bridges
6) Myosin head change angle, pulling the actin filament along the myosin filament, ADP is released
7) ATP attaches to each myosin head, which detaches from the actin filament
8) ATPase hydrolyses ATP-> ADP. Provides energy to return myosin head to its original position
9) Myosin heads attach further along the actin filament via ADP and the process repeats
Relaxation of muscles
Ca2+ ions actively transported back into the sarcoplasmic reticulum
Allows tropomyosin to block the binding sites so myosin cannot bind
Atrial systole
Contraction of atria
Ventricular systole
Contraction of ventricles
Diastole
Relaxation of the heart
Sinoatrial node
located in the wall of the right atrium
Known as the pacemaker of the heart as sets the rhythm of the heart
Ensure left and right atria contract simultaneously
Atrioventricular node
located at the bottom of the right atrium
Receives electrical impulses (signals) from the SA nods
Delays the impulses to allow all the blood to be squeezed into the ventricles from the atria
Bundle of His
Carries impulses from the AV node down to the ventricles through the septum
Purkinje fibres
smaller fibres that branch off from the bundles of his
Carry the impulses to the lower walls of the ventricle
Stimulate the contraction of the right and left ventricles to contract at the same time
Control of heart rate by chemoreceptors
blood CO2 levels means blood pH is low
Chemoreceptors in carotid body detect this and increase the frequency of impulses sent to the centre of the medulla oblong at a that increases heart rate
Medulla increases frequency of impulses sent to the SA nods via the sympathetic nervous system, increasing heart rate
Increased blood flow allows CO2 to diffuse out more at the lungs, so pH returns to normal
(Vice versa for low CO2 levels)
Control of heart rate by baroreceptors
high blood pressure detected by baroreceptors, which increases the frequency of impulses sent to centre of medulla oblong at a that decreases heart rate
Medulla increases frequency of impulses sent to the SA node via the parasympathetic nervous system, decreasing heart rate
Lead to reduction in blood pressure to normal
(Vice versa for low blood pressure)
Where are alpha and beta cells located?
In islets of Langerhans in the endocrine pancreas
What do Alpha cell secrete, and what does it do?
Release glucagon
increases blood glucose concentration
What doBeta cells secrete, and what does it do?
Secrete Insulin
decreases Blood glucose concentration
How does insulin decrease blood glucose?
insulin binds to its receptor Tyrosine Kinase on cell surface membrane
Receptor phosphorylase’s proteins and causes downstream effects that result in:
GLUT-4 carrier protein that are normally kept in vesicles in the cytoplasm are inserted into membrane so more glucose can be taken up by facilitated diffusion
Activation of enzymes in glycogenesis
Inhibition of glycogensolysis and gluconeogenesis
How does glucagon increase blood glucose?
Glycogen secreted, attaching to receptors on the surface of target cells
When glucagon binds it causes a protein to be activated into adenylate cyclise and to convert ATP into Cyclic AMP (cAMP)
CAMP activates an enzyme, protein kinase that can hydrolyse glycogen into glucose
Activates enzymes involved in gluconeogenesis And glycogenolysis
Inhibits enzymes involved in Glycogenesis
Type I Diabetes
5-10% of cases
Autoimmune disease
Complete lack of insulin
Usually childhood onset
Genetic factor (30-40% concordance in MZ twins)
Treatment:
Insulin replacement (injection/insulin pump)
Correct dose is very important- must match glucose intake
Type II diabetes
85-95% of cases
Caused by insulin resistance- beta cells still releasing it but it is havingg no effect
leads to overcompensation by pancreas leading to beta cell failure
Strongly associated to obesity (80% of cases)
Interestingly, higher genetic factor (60-90% in MZ twins)
Treatment:
Regulate carb in take and match to ammount of exercise
Drugs that stimulate insulin secretion or slow rate of glucose absorption in gut
Functional unit of the kidney
Nephron
Structure of the nephron
cortex (upper level)
Afferent arterioles
Efferent arteriole
Glomerelus
Bowmans’s capsule
Proximal convoluted tube
Distal convoluted tube
Collecting duct
Medulla (lower, salty level)
Ascending loop of Henle
Descending loop of Henle
Efferent arteriole
Collecting duct
Ultrafiltration in glomerulus
afferent arteriole is wider then efferent arteriole
Creates hydrostatic pressure in glomerulus to force small molecules out into Bowman’s capsule against gradient
Endothelium of glomerular capillaries has small spaces between cells, podocytes have foot processes with small slits between them
Allow substances to be filtered out into Bowman’s Capsule
Function of Proximal convoluted Tubule
epithelial cells that line the tubule have
Microvilli- large surface area
Lots of mitochondria- ATP for active transport
Selective reabsorption of: water, glucose, amino acids, Na+, K+, Cl-, HCO3
Na+ ions actively transported out of epithelial cells of tubule into the blood
Na+ ions diffuse down concentration gradient from tubule lumen into epithelial cells through special carrier proteins
Bring other molecules/ions with them
Water moves through aquaporins by itself
Function loop of Henle
Responsible for counter-current multiplication
Descending loop of Henle
Thin
Very permeable to water- lots of water moves out of tubule back into blood via osmosis
Ascending loop of Henle (thick)
Impermeable to water
Na+ ions are actively transported out of Ascending limb
This lowers water potential in interstitial space of the medulla- hence water moves out of descending limb by osmosis
Means water will move out of collecting duct into interstitial space
Function of Distal convoluted tubule
starts to make final adjustments to filtrate
Na+ ions and Cl- ions reabsorbed
Function of Collecting duct
final adjustments made
Water reabsorbed from collecting duct (moves out via osmosis due to Na+ ions in the interstitial space
Reabsorption depends on action of ADH
Hormones and Osmoregulation
osmoreceptors in Hypothalamus detect changes in blood water potential levels
When level is low, water leaves the receptor cell by osmosis, causing them to shrink, which is detected b the hypothalamus- secretes hormones
What does the hypothalamus secrete in response to low water levels?
anti-diuretic hormone (ADH)
ADH is made in the hypothalamus and taken to the pituitary gland, where it is released into blood
ADH travels in the blood to the Kidney
Action of ADH in the Kidney
binds to a receptor on epithelial cells in the collecting ducts (and distal convoluted tubule)
Leads to increased transcription/translation of aquaporins (water channel proteins) and insertion into ell membrane
Increases permeability to water
More water reabsorbed into blood
Also causes upregulation of urea transporters
Increases permeability to urea
Further lowers water potential around the duct in interstitial space
More water leaves the collecting duct and is reabsorbed Ito the blood
Homeostasis
Maintenance of constant internal conditions in spite of internal or external changes
Temperature, water, glucose and pH important
Negative feedback
Reversing a change in order to return the condition to the optimum
stimulus detected by receptor delivered to co-ordination which sends as signal to an effector to produce a response (e.g. lowering or raising blood pressure)
Positive feedback
Deviation from the optimum which causes changes resulting in an even greater deviation from th norm.
This is usually harmful due to the large, unstable change in the body