RESPONDING TO THE
ENVIRONMENT (behaviour and
muscle contraction)
Muscle contraction
NEUROMUSCULAR
JUNCTIONS
this is where motor neurones
terminate and info is transmitted
from motor neurone to effector. this
happens similarly to a synapse
what happens:
1) action potential arrives at neuromuscular
junction which causes vesicles with
neurotransmitter inside, to fuse with
presynaptic membrane and release
acetylcholine into gap
2) acetyle choline binds to (nicotinic
cholinergic) receptors on muscle
membrane causing inflow of na+ ions
which depolarises the sarcolemma
(muscle fibre membrane)
3) if threshold is reached, action potential is
transmitted along the sarcolemme and down
thet-tubules (t-system). these membranes
have the same channel proteins and pumps
as neurons.
4) t system depolarisation leads to
Ca2+ ions release from
sarcoplasmic reticulum into
sarcoplasm. Ca2+ ions act as
second messengers to stimulate
movement of muscle myofibrils.
5) Ca2+ ions bind to protein actin in
muscle, which leads to muscle
contraction
6) acetylcholinesterase in the gap
rapidly breaks down acetylcholine so
contraction only occurs when action
potential arrives continuously
synapses vs neuromusclular junction
BOTH
neurotransmitter
acetylcholine located in
vesicle is pre synaptic
cytoplasm
vesicles release
acetylcholine into cleft
on stimulation (arrival
of ap)
acetylcholine diffuses
across gap and binds to
post synaptic
membrane receptor
binding of
neurotransmitter results
in opening of channels
and depolarisation of post
synaptic membrane
enzyme
acetylcholinesterase
present to break down
acetylcholine into ethanoic
acid and choline to avoid
continual stimulation of
post synaptic membrane
SYNAPSE is neurone to
neurone, NMJ is
neurone to sarcomemre
(muscle cell)
SYNAPSE post synaptic
stimulation leads to ap in
postsynatic neurone, NMJ
postsynpatic stimulation leads
to depolarisation of
sarcolemma and muscle
contraction
SYNAPSE have
synaptic knob which is
smooth and round,
NMJ end plate has
appearance of
microvillia/ brush
border and is flattened
up to muscle cell
SYNAPSE ca2+ ions
diffuse into synaptic
knob, NMJ ca2+ ions
released from
sarcoplasmic
reticulum
elbow joint
when arm goes down bicep
relaxes an tricept contracts. when
arm goes up bicep contracts and
tricep relaxes.
shoulder blade at the top, tendon joins
muscles to bone. bicep on top/right of
humerus and tricep on bottom/left.
radius on palm side lower arm, ulna on
top
ELBOW
in middle is synovial fluid
which lubricates the joint
next layer is synovial
membrane which
produces synovial fluid
ligament surrounds the
rest which holds bones
together and prevents
dislocation
at end of bones is cartilage
which pads wheres bones
meet, reduces friction
during movement and
eases movement
types of muscle
GENERAL
Length of sarcomere when
muscle is relaxed=2.5um and
contracted=2um
THIN FILAMENTS
made up of G/F actin
which is a globular
protein
long chains of actin
molecules: 2 chains
of actin lie side by
side and twist around
one another
actin chains are firmly
anchored in Z lines
TROPOMYOSIN
rod shaped proteins
hich forms long, thin
molecules that lie in
groove between 2 F/G
actin chains
TROPONIN
globular protein
that binds to actin
chains at regular
intervals
composed of 3
polypeptides: 1 binds to
actin, 1 to tropomyosin
and 1 to ca2+ ions
THICK FILAMENTS
made up of bundles of
myosin which is a fibrous
protein
many myosin molecules
lie side by side
each myosin molecules has a
head and bundles are arranged
so that half molecules heads
are one end and half the other
end
where the tails meet forms the M line
Z LINES: border of sarcomeres
M LINES: middle of sarcomeres
H ZONE: distance between ends of
thin filaments, shortens during
contraction as actin and myosin
overlap increases
I BAND: distance between thick
filaments of one sarcomere and
thick filaments of the
subsequent sarcomere, shotens
during contraction as actin
slides over myosin
A BAND: total length of thick
filaments, stays the same on
contraction as myosin length
is unchanged
overall sarcomere reduces in length on
contraction as overlap increases and
actin slides towards myosin, when
relaxed sarcomere is longer
striated muscles look
stripey because I band
has only actin
microfilaments so
appears light and A
band has actin and
myosin microfilaments
so appears dark.
filaments are arranged
regularly giving stripey
look.
SLIDING FILAMENT THEORY
in presence of ATP, thin actin
filaments slide towards the M line
along the thick myosin filaments.
This is the sliding filament model
and explains why H ZONE and I
BANDS shorten by A band does
not during contraction
the filaments dont change size, they just overlap
energy is provided by splitting of ATP
caused by ATPase in the myosin cross
bridge head. The cross bridges can also
attach to actin
Binding sites in resting muscles:
for myosin and actin to slide past
eachother, the myosin head must
bind to the actin-myosin binding site
on the actin filament
in a resting muscle, the
actin-myosin binding site is
bloacked by tropomyosin which
means myofilaments cant slide
past eachother because myosin
head cant bind to actin filaments
1) Arrival of action potential
when ap from motor neurone
stimulates muscle cell, sarcolemma is
depolarised. depolarisation spreads
down t tubules to sarcoplamsic
reticulum where ca2+ ions are released
from into sarcoplasm. influx of ca2+
ions stimulate muscle contraction
ca2+ ions bind to troponin causing it
to change shpe. this pulls attached
tropomyosin out of the actin-myosin
binding site on the actin filament
this exposes binding site so allows
myosin head to bind. the bond
formed when myosin head binds to
actin filament is called an
actin-myosin cross bridge
2) Movement of actin filament
ca2+ ions also activate enzyme
ATPase which breaks down ATP into
ADP + Pi to provide energy for
contraction
energy released from ATP
moves myosin head to the side
which pulls the actin filament
along in a rowing action
3) Breaking of the cross bridge
ATP provides energy to also break cross bridge so myosin
head detached from actin filament after it moved
myosin head then returns to starting position and
reattaches to different binding sie further along the actin
filament
new cross bridge is formed and cycle is repeated. many cross
bridges rapidly form and break pulling actin filament along which
shortens the sarcomere causing muscle to contract
as long as ca2+ is present and bound to troponin, cycle will continue
4) Returning to resting state
when muscle stops being stimulated, ca2+ ions leave binding
sites on troponin molecules are are moved by active transport
back into sarcoplasmic reticulum (needs ATP)
the troponin molecules return to their original
shape, pulling attached tropomyosin molecule
with them so tropomyosin now blocks the
actin-myosin binding sites again
mucle now cant contract as no myosin heads are
attached to actin filaments so there are noa-m cross
bridges
actin filaments slide back to relaxed position
lengthening sarcomere
Behaviour
= an organisms
response to changes in
its external
environment, these
responses help
organisms survive and
reproduce. Behaviour is
influenced by genes and
environment.
INNATE BEHAVIOUR
behaviour organisms do instinctively
genetically determined
requires no thought or learning, respond straight away
eg new born babies
instinctively suckle from their
mothers
not influenced by environment
inherited from parents
it is stereotyped= always carried out in
the same way and by all indiciduals in a
species
Escape Reflexes
the organism moves away
from potential danger
eg cockroaches run away
when threat of being
squashed
Tactic Responses (TAXIS)
directional movement in
response to a stimulus
direction of stimulus
affects response
eg woodlice move away from light
source, keep safe from predators
Kinetic Responses (KINESIS)
non-directional (random)
movement in response to a stimulus
intensity of stimulus
affects the response
eg woodlice under low humidity move from dry air to
more humid air and stay put as this reduces water loss
so improves chances of survival
complex example: bee waggle dance
a display used by worker honey bees to
communicate the direction and distance of a food
source to other worker bees this helps bees find
food source
LEARNED BEHAVIOUR
Habituation
= a reduced response to an
unimportant stimulus after repeated
exposure over time
an unimportant stimulus is a
change that isnt threatening or
rewarding
an animal quickly
learns to reduce or
stop response to
unimportant stimulus
so it doesnt waste time
and energy responding
to unimportant things
however animals remain
alert to unfamiliar stimuli
eg living near busy road,
noise of traffic wont keep
u awake at night as you
stop responding to noise
so sleep through it but an
unfamiliar noise lik ea car
crash will wake you up
Classical Conditioning
= learning to respond naturally to a
stimulus that doesnt normally cause
that response (association)
before conditioning a natural
stimulus (unconditioned stimulus)
can cause natural response
(uncondtioned response)
if neutral stimulus coincides with
unconditioned stimulus enough times,
eventually neutral stimulus (now
conditioned stimulus) will on its own
cause the same response as the
uncondtioned stimulus (condtioned
response)
eg in dogs: uncondtioned
stimulus= food,
unconditioned response=
salivation; if a bell is rung
immediately before dogs
given food, dog will salivate to
sound of bell. neutral
stimulus= bell, is associated
with unconditoned stimulus =
food, triggers salivation
(unconditoned), bell by itself=
conditioned stimulus trigger
conditioned response=
salivation
Operant Conditioning
=learning to associate
particular response with a
reward or punishment
(reinforcement)
when in same sitaution several
times, animal will work out which
response gets reward or
punishment
the response must be rewarded
or punished stright away, this
reinforces behaviour so animal is
more likely to repeat behaviour if
it is rewarded
eg rat put in a cage with
choice of leves, pressing one
lever rewarded rat with food
and the rat was repeatedly put
in same cge so learned which
level to press to get the reward
Latent Learning
=hidden learning
an animal doesnt
immediately show
its learned
something
it involves repetedly doing the same task
animal only shows it's learned
something when its rewarded or
punished
eg three groups of rats put in
same maze repeatedly
group 1 were
reinforced with reward
each time they reached
the end, they quickly
learned their way
around the maze
group 2 were not reinforced (no
reward) and continued to plod
around maze and took ages to
reach the end
group 3 were only rewarded from 11th
time they did the maze, after this they
vert qickly reached the end with hardly
any errors. the rats had been learning
the maze all along without any
reinforcement but they didnt show their
learning until there was a reward
Insight Learning
=solving a problem by working out a
solution using previous experience
solving problems by insight is quicker
than by trial and error as actions are
planned and worked out
eg chimpanzees put in play area with sticks,
clubs and boxes. bunches of bananas were
hung out of reach. chimps used previous
experience of playing with objects to work out
a soltuion: they piled up boxes to reach
banaanas and used the sticks and clubs to
knock them down
=behaviour influenced by environment and
is modified as a result of experience
it is not sterotyped, it varies in
different individuals in the same
species
allows animals to respond to changin conditions
IMPRINTING
=combination of learned behaviour
and innate behaviour
eg animal learns to recognise its parents
and instinctively follows them
a newly born animal has an innate instinct to
follow the first moving object it sees (usually
mother or father) who provide warmth, shelter
and food (helping suvivl)
but the animal has no innate instinct of
what its parents look like- need to learn
this.
once learned imprinting
is fixed and irreversible,
use later in life to
identify mates from
same species
only happens during critical
period (soon after birth)
Lorenz-
ducklings
followed
mother and
him (2
gorups, first
moving
object)
UNDERSTANDING HUMAN BEHAVIOUR
animals behaviour depends of
structure of brain (neurotransmitters,
synapses, receptors etc)
dopamine receptor D4
dopamine= neurotransmitter
can affect mood
and behaviour
5 different receptors
for dopamine (d1-d5)
effects of dopamine vary
depending on which receptor it
binds to
each receptor is coded
for by a different gene
D4 receptor protein is coded
for by the DRD4 gene
too many d4 receptors linked to
abnormal behaviour eg
schizophrenia -disorder effects
thinking, perception, memory and
emotions
evidence for this link: -drugs
that stimualte dopamine
receptors are given to healthy
people, causes abnormal
behaviour -drugs that block D4
receptors reduce symptoms in
schizophrenics -people with
schizophrenia have higher
density of D4 receptors in
brain -one drug used to treat
schiz binds to D4 receptors
better than it binds to other
dopamine receptors
link between D4 receptor and
abnormal behvaiour helps us
understand roel of D4 in normal
behaviour as it is involed in
thinking , perception, memory
and emotions
SOCIAL BEHAVIOUR IN PRIMATES
SB= behaviour involving members of large
groups nteracting with eachother
primates=baboons, apes, humans
social behaviours have advantages
Baboons live in groups of around 50, + large
group is more efficeient at hunting for food,
communicate good food sources
Hireachy of adult males, +
prevents fighting as males
know rank in order
Groom eachother, +hygeinic
and reinforce bonds between
members of group