Coordinatoin & Regulation Nervous Systems Flashcards
organs systems must be
coordinates within an animal and with the enviroment
two majot systems
nervous system (faster) and endocrine system (slower)
nervous system
in all animals except sponges
very rapid coordination
three major roles
three major roles of nervous systems
collects info - from internal and external enviroment, using modified neurons (detection aspect)
process and integrate information - adding info together - evaluates based on past experience or genetics
transmit information - coordinates/regulates effect organ/cells - send info somewhere - to output
sensory process
sensory receptor (eye) - sensory input (afferent) - information INTO nervous system - integration of sum of inputs (cns) - motor input (efferent + pns) - effector cells
neurons
cells of the nervous system
generate bioelectric signals
there used to transmit information
glial cells
support cells
assist neuronal signaling
produce cerebrospinal fluid
maintain enviroment around neurons
provide nutrients to those nurons
more than neurons
motor neuron structure
dendrites - cell body - axon + myelin - axon terminals
sensory neuron structure
dendrites - axon - cell body - axon (myelin) - axon terminals
interneuron structure
dendrites - cell body - axon no myelin - axon terminal - no branching
neuron
individual cell
nerve
a bundle of axons - no cell bodies
acon
a nerve fiber
synapse
connection between axon terminal and effector cell
effector
can be a neuron, muscle, any other cell`
bioelectricity
electrical activity in a biological species
potential
difference in electrical charge between regions - measures in volts or millivolts - if it’s the same charge on both then potential is 0
current
flow of electrical charge between regions
membrane potential
unequal charge distribution across a cell membrane - relative to the inside
biological cell membrane potential
negative on inside relative to outside
size of MP -10 to -90 mV
neurons + muscle cells for MP
- large membrane potentials
- special mechanisms to regulate membrane potentials and currents
3 type of membrane potentials
resting membrane potential
electrotonic potentials
action potentials
- depends on inorganic ions
resting membrane potential
measured when neuron is inactive
-70mV in neurons and muscle cells
due to inequal distribution of ions across membrane
sodium and pottasium
extracellular fluids always have
high sodium concentration and higher than pottasium in intracellular fliud
low pottasium
intracellular fluid
high potassium concentration
low potassium concentration
sodium potassium ATPase
ion gradient pump
found in all cells
moves 3 sodium and 2 potassium in
electrogenic pump - different ion concentration
generates a 10mV potential r
uses ATP since it is going againgradient
resting membrane potentials
measured when cell is inactive
above -70mV
electrogenic -10
aminion proteins -10
passive diffusion -55
amnionic proteins
proteins with negative charge + cannot leave membrane
-5mV
open K channel
leak channel
always open
multiple in one cell
passive diffucion across chemical gradient
end location will be positive
membrane ion channels
- very specific for ion
- some leak channels some regulated
neurons - voltage gated - ion movement depends on the concentration gradient
membrane physiology during RMP
sodium pottasium ATPase + potassium leak channel
RMP sodium concentration
15 inside
150 outside
RMP potassium concentration
150 inside
5 outside
RMP chloride concentration
7 inside
110 outside
RMP A-
110 inside
0 outside
cell is polarized
negative inside less positive
excitable
membrane potential can change - neurons and muscle fibers
depolarized
less negative inside more positive
at rmp
neuron is metabolically active but not chemical
electrotonic potentials
small change in memebrane potentials - around 10 mV
action potentials
large and rapid changes in membrane potentials - nerve impulse
electrotonic potentials
current (ions) travel along the surface - a few microns along the membrane
small
can depolarize or hyperpolarize
only travel a short distance along membrane
what does electrotonic potentials can be used for
used to initiate an AP in axon hilloack
also to conduct AP along axon
action potentials
initiated at axon hillock region
found only in axons
spike initiation (short + quick)
carries the signal from axon hillock to terminals
gets a signal from the cell body to the tip of the axon
special features of AP
- depolarizes membrane (from -70 to +35) cell is polarized
- are all or nothing but transient
- once started conducted along entire axon
- rely on ion current through membrane via voltage ion channels
which channels does action potential rely on
voltage-gates potassium and sodium channels
voltage sodium gate role in action potential
some of them are open before threshold
all of them open after threshold
depolarizes cell - makes inside less negatives
at around 50mV sodium gates get closed and inactivates
potassium voltage gate in action potential
starts at +50
makes inside of cell negative (repolarization) all the way to -80
hyperpolzarization to to -70 which is RMP
threshold
voltage at which AP is initiated
potassium channel
does not inactivate - only closes
refractory period
membrane potential starts arriving at RMP - cannot generate AP
hodgkin huxley cycle
initial depolarization -> opening of Nav channels increases permeability -> increased Na+ flow -> further membrane depolarization (opens more sodium channels( and repeat
AP rise phase is an example of
positive feedback
AP only occurs if
you depolarize and open the sodium channels
why is AP important
conduction
AP initiated in the
axon hilloack/ spike initiating sone
why does the AP start in the axon hillock
large number of sodium channels which then creates a high depolarization
does voltage change in an AP
AP creates an unchanged axon membrane to terminals in which the voltage doesn’t change and only move forward
inter-vertebrate axon
unmyelinated
how does an AP move through an unmyelinated axon
- moves in waves
- started at the axon hillock where the threshold is lower and the sodium channels are high
- once it reaches the peak, the AP moves to the next inactive area and depolarization spreads and makes the MP reach the potential and so on and so forth
- previous section of axon becomes inactive so charge cannot move back
can you have multiple APs
yes
spiking frequency
number of AP sent through per second (neural code for carrying info)
measure of AP speed
larger diameter = AP goes faster