Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
187 Cards in this Set
- Front
- Back
The pathway of muscle contraction is |
corticospinal pathway transmits to spinal cord, synapse in grey matter of spinal cord activates a motor neuron that causes muscle contraction
|
|
All cells are ____ charged compared to outside of the cell.
|
negatively
|
|
The resting potential ranges from _____ to _____ depending on the type of cell.
|
-5 to -100 mV
|
|
The resting potential in neurons and muscle is approximately
|
-60 to -90 mV
|
|
Membranes have a high _______ due to lipids in the membrane.
|
resistance.
|
|
The magnitude of the resting potential is due to
|
1. The concentration differences of ions across the cell, 2. The selective permeabilities of the ions.
|
|
The forces that affect the diffusion of ions across the membrane are
|
1. Electrical (ions move toward the opposite charge), 2. Chemical (concentration gradient).
|
|
Electrochemical potential is
|
the algebraic sum of the electrical and chemical forces for an ion.
|
|
Ohm’s law is
|
V=IR
|
|
In Ohm’s law, V is
|
potential difference (millivolts)
|
|
In Ohm’s law, I is
|
current or movement of ions (picoamps or nanoamps)
|
|
In Ohm’s law, R is
|
resistance to current (megaohms)
|
|
Conductance (g) is
|
the reciprocal of resistance (1/R), and the ability of an ion to move across the membrane (opening channels)
|
|
The equilibrium potential is
|
the membrane potential of zero when the chemical and electrical gradient oppose each other.
|
|
The membrane potential with no net movement of an ion across the membrane is
|
the equilibrium potential.
|
|
The equilibrium potential is negative for ________, but positive for _______.
|
K+ and Cl-; Na+.
|
|
The equilibrium potential for potassium is
|
-89 mV
|
|
The equilibrium potential for sodium is
|
+60 mV
|
|
The equilibrium potential for chlorine is
|
-72 mV
|
|
At rest, the conductance of _____ is approximately 50 times greater than ______.
|
K+, Na+
|
|
Due to ___________, the resting potential is close to the ________ equilibrium potential.
|
the selective conductance of the plasma membrane to potassium over sodium; potassium.
|
|
The leak channels that potassium and sodium pass across the membrane down their chemical gradient are
|
always open and are not gated or activated.
|
|
For the leak channels that potassium and sodium pass across the membrane down their chemical gradient, the number of K+ leaks channels is _____ than the Na+ leak channels.
|
much larger
|
|
The larger number of potassium leak channels gives K+
|
50 times greater conductance than Na+.
|
|
The function of the Na+/K+-ATPase is to
|
maintain Na+ and K+ chemical gradients by pumping out Na+ and in K+.
|
|
The membrane potential can be changed by changing
|
the ion concentration gradients, ion conductance, or both
|
|
Under normal physiological conditions, the ion concentration gradients
|
do not change.
|
|
Under normal physiological conditions, changes in __________ causes changes in the membrane potential.
|
the relative conductance of the ions
|
|
Changes in ion conductance are due to
|
opening or closing of ion channels.
|
|
Depolarizing the plasma membrane is
|
moving closer to 0 mV membrane potential
|
|
Hyperpolarizing the plasma membrane is
|
making the membrane more polarized (more negative mV) compared to resting potential.
|
|
Repolarizing the plasma membrane is
|
return of membrane potential to its resting level.
|
|
The driving force for an ion is
|
the difference between membrane (Vm) and equilibrium (Ex) potentials. It equals Vm – Ex
|
|
The larger the difference between the membrane potential and the ion equilibrium potential,
|
the larger the driving force and current carried by the ion.
|
|
The movement of an ion across the membrane will be dependent on
|
the driving force on the ion and the ion’s valence.
|
|
The ion will move in a direction that will
|
bring the membrane to the ion’s equilibrium potential.
|
|
Because the equilibrium potential for sodium is positive, opening Na+ channels will cause
|
it to flow in the cell and make the membrane potential more positive.
|
|
Because the equilibrium potential for potassium is negative, opening K+ channels cause
|
it to flow out of the cell and make the membrane potential more negative.
|
|
Because the equilibrium potential for chlorine is negative, opening the K+ channels with a -70 mV membrane potential will cause
|
it to flow in the cell and make the membrane potential more negative (-70 mv to -72 mV)
|
|
Because the equilibrium potential for chlorine is negative, opening the K+ channels with a -75 mV membrane potential will cause
|
it to flow out of the cell and make the membrane potential more positive (-75 mv to -72 mV)
|
|
If potassium channels close, the resting membrane potential will
|
become more positive, because potassium will stay in the cell.
|
|
The 3 types of ion channels are
|
ligand-gated, voltage-gated, mechanically-gated
|
|
The opening of a channel is called
|
gating
|
|
The number of ions passing through a channel determines
|
current
|
|
The number of ions passing through a channel depends on
|
the length of time it is open.
|
|
In the nervous system, the ligand-gated channels are activated by
|
neurotransmitters.
|
|
Voltage-gated channels are activated by
|
changes in membrane potential
|
|
Mechano-sensitive channels are also known as
|
stretch receptors
|
|
Mechano-sensitive channels are activated by
|
a change in the shape of a cell.
|
|
Gap junctions are
|
channels between two cells that allow the passage of large molecules.
|
|
Gap junctions are found in abundance in
|
cardiac muscle and certain smooth muscle.
|
|
Gap junctions can be regulated by
|
Ca2+, H+, and voltage
|
|
The pores in Gap junctions close when
|
Ca2+ is elevated and when pH decreases to protect adjacent cells.
|
|
In neuron anatomy, the cell body
|
contains nucleus and protein synthesis
|
|
In neuron anatomy, dendrites
|
receive input from other neurons.
|
|
In neuron anatomy, axons
|
transmit action potentials.
|
|
In neuron anatomy, the axon hillock
|
is the part of the axon next to the cell body
|
|
In neuron anatomy, the axon collaterals
|
are branches of the axon
|
|
In neuron anatomy, the axon terminals
|
are nerve terminals that release neurotransmitters
|
|
In neuron anatomy, the synapse
|
is the junction between nerve and nerve, muscle, or gland.
|
|
90% of cells in the central nervous system are
|
Glia (neuroglia)
|
|
Oligodendrocytes are found in
|
brain and spinal cord
|
|
The role of oligodendrocytes is
|
to wrap around axons to form myelin sheath and nodes of Ranvier.
|
|
Schwan cells are found in
|
the peripheral nervous system.
|
|
The role of Schwan cells is
|
to wrap around axons to form myelin sheaths and nodes of Ranvier.
|
|
Schwann cells are critical for
|
transmission of axon potential.
|
|
The role of astroglia is
|
regulate cerebrospinal fluid and form the blood brain barrier.
|
|
The role of microglia is
|
perform immune functions of the central nervous system.
|
|
Action potentials are
|
a rapid change in membrane potential.
|
|
Action potential are a property of
|
excitable cells (nerve, muscle, glands)
|
|
The excitability in action potentials is provided by
|
opening and closing of voltage-gated channels.
|
|
For a stimulus to cause an action potential, it must
|
reach a threshold of 55 mV
|
|
When the action potential threshold is reached
|
Na+ channels open allowing Na+ influx.
|
|
Influx of Na+ leads to
|
further depolarization of neuron (positive feedback).
|
|
At the peak of the action potential, channels
|
go from open to inactivated.
|
|
Na+ channels inactivate after
|
1 msec.
|
|
Depolarization produced by influx of Na+ causes
|
delayed opening of K+ channels
|
|
Efflux of K+ after an action potential causes
|
repolarization of neuron
|
|
Hyperpolarization after an action potential is due to
|
high K+ conductance.
|
|
The summary of an action potential is
|
1. Neuron at resting potential, 2. Depolarization reaches threshold potential and activates voltage-gated Na+ channels, 3. Influx of Na+ leads to further depolarization, 4. Delayed opening of K+ channels, 5. Na+ channels inactivate, 6. Neuron repolarized by efflux of K+, 7. Hyperpolarization due to K+ conductance, 8. K+ channels close and membrane returns to resting potential.
|
|
The properties of action potentials are
|
1. All-or-none response, 2. Constant amplitude, 3. Threshold, 4. Refractory period
|
|
The all-or-none response of action potentials means
|
once it is initiated, it goes to completion.
|
|
The absolute refractory period is
|
the inactivation of sodium channels immediately after firing.
|
|
The relative refractory period is
|
when some Na+ channels have returned to resting state, but K+ channels remain open.
|
|
The purpose of the refractory period is
|
to limit frequency of action potentials to approximately 100/sec and prevent action potential moving backwards.
|
|
The relative refractory period means subsequence stimuli
|
must be stronger to reach action potential.
|
|
The spreading currents depolarization in an action potential is propagated through
|
voltage-gated Na+ channels activating.
|
|
In nerve cells, action potentials propagate
|
from axon hillock to nerve terminal
|
|
In skeletal muscle fibers, action potentials propagate
|
from middle to ends.
|
|
Myelin insulates the axon to
|
prevent charge from leaking out of the axon.
|
|
Voltage-gated sodium channels and Na+/K+ ATPase in the axon are located only
|
at the Nodes of Ranvier.
|
|
Saltatory conduction is
|
the spread of current from node to node in an axon.
|
|
Condunction of action potential is much faster in ________ neurons.
|
myelinated.
|
|
The conduction velocity of an action potential is increased by
|
myelination and increasing the axon diameter.
|
|
In voltage-gated channels, voltage sensors
|
detect the voltage across the membrane
|
|
In voltage-gated channels, inactivating gates
|
inactivate the channel on the cytoplasmic side by blocking the opening
|
|
In voltage-gated channels, are/are not selective for a given ion.
|
are very selective
|
|
In voltage-gated channels, auxiliary subunits
|
modulate the activity of the channels.
|
|
An alpha motor neuron signals at
|
the neuromuscular junction.
|
|
The neuromuscular junction is located at
|
the End plate.
|
|
One alpha-motor neuron can innervate
|
several muscle fibers.
|
|
The neurotransmitter at the neuromuscular junction is
|
acetylcholine (Ach)
|
|
The postsynaptic receptor at the neuromuscular junction is
|
nicotinic cholinergic receptor.
|
|
The type of receptor of the nicotinic cholinergic receptor is
|
ligand-gated ion channel selective for cations (Na+ and K+)
|
|
The bouton is located
|
on top of the muscle fiber.
|
|
The synaptic cleft is located between
|
the bouton and muscle fiber itself.
|
|
Neurotransmitter release is initiated by
|
arrival of an action potential at nerve terminal.
|
|
The arrival of an action potential at the nerve terminal causes
|
depolarization of nerve terminal to activate voltage-gated calcium channels, increasing intracellular calcium.
|
|
Increased cytosolic calcium causes
|
release of Ach stored in vesicle into synaptic cleft.
|
|
Vesicles containing Ach bind to the plasma membrane to release their contents using
|
SNARE proteins.
|
|
Once released from the vesicles into the synaptic cleft, Ach
|
binds to and activates nicotinic cholinergic receptors (NAChR) on the endplate.
|
|
After binding to the NAChR, the Ach
|
dissociates from the receptor and is removed from the synapse
|
|
Ach in the synaptic cleft is metabolized by
|
acetylcholine esterase (AChE)
|
|
Acetylcholine esterase (AChE) is localized in
|
folds of the endplate.
|
|
AChE hydrolyzes Ach to
|
chline and acetate
|
|
Choline from the hydrolyzed Ach
|
is taken back into the nerve terminal to synthesize new Ach
|
|
Acetate from the hydrolyzed Ach
|
diffuses away from the synaptic cleft.
|
|
Acetyl Chloline (Ach) is regenerated by
|
1. Choline taken back into cell, 2. Choline acetyltransferase transfers acetyl group from acetyl CoA onto Choline.
|
|
Ach is taken back into the vesicle by
|
1. ATP dephosphorylation to ADP pumps H+ into vesicle, 2. H+ countertransported out with Ach in.
|
|
The types of synapses in the CNS are
|
1. Axodendritic, 2. Axosomatic, 3. Axoaxonic (presynaptic inhibition)
|
|
An axodendritic synapse fires on
|
a dendrite
|
|
An axosomatic synapse fires on
|
a cell body (soma)
|
|
An axoaxonic synapse fires on
|
an axon
|
|
The function of graded potentials is
|
generate action potentials
|
|
For graded potentials, local current spread
|
passively, do not propagate.
|
|
For graded potentials, amplitude
|
depends on the strength of stimulus (graded)
|
|
For graded potentials, decremental means
|
amplitude decreases as the distance form site of stimulus increase.
|
|
Graded potentials produce
|
electrical signals over a short distance.
|
|
Stimulus causing graded potentials leads to _______ depending on ________.
|
depolarizing or hyperpolarizing; the channel and ion that goes through it.
|
|
For graded potentials, temporal summation is
|
increasing the frequency of the action potentials of a single neuron will increase the amplitude of graded potentials.
|
|
For graded potentials, spatial summation is
|
multiple action potentials arrive at the same location at the same time.
|
|
The types of graded potentials are
|
1. Synaptic, 2. Pacemaker, 3. Generator, 4. Receptor
|
|
The types of synaptic graded potentials are
|
1. End-plate potentials (EPPs) in skeletal muscle, 2. Excitatory postsynaptic potentials (EPSPs) in neurons), 3. Inhibitory postsynaptic potentials (IPSPs) in neurons.
|
|
Pacemaker graded potentials are found in
|
heart and smooth muscle.
|
|
Generator graded potentials are found in
|
sensory nerve terminals
|
|
Generator graded potentials respond to
|
physical and chemical stimuli (heat, touch, pressure, stretching)
|
|
Receptor graded potentials are found in
|
special sensory tissues
|
|
Receptor graded potentials respond to
|
physical and chemical stimuli (sound, light, chemicals)
|
|
Excitatory postsynaptic graded potentials are produced by
|
excitatory neurotransmitters (excitatory amino acids glutamate and aspartate).
|
|
Excitatory postsynaptic graded potentials affect membrane potential by
|
moving it closer to threshold
|
|
Excitatory postsynaptic graded potentials use
|
ionotropic receptors
|
|
Ionotropic receptors are
|
ligand-gated channels (Na+-K+ channels.
|
|
Ionotropic receptors are activated by
|
glutamate and aspartate
|
|
Inhibitor postsynaptic graded potentials affect membrane potential by
|
moving it further from threshold.
|
|
Inhibitor postsynaptic graded potentials are produced by
|
glycine
|
|
Inhibitor postsynaptic graded potentials use
|
ionotropic receptors (cl-)
|
|
Action potentials are initiated at the axon hillock because
|
it has the lowest threshold
|
|
The greatest concentration of Na+ and K+ voltage gated channels in a neuron is at
|
the axon hillock.
|
|
Action potential is generated by a single/summation of excitatory postsynaptic potentials .
|
summation
|
|
Action potential is inhibited by a single/summation of inhibitory postsynaptic potentials
|
summation.
|
|
The types of muscle are
|
smooth and striated
|
|
The types of striated muscle are
|
skeletal and cardiac
|
|
Skeletal muscle is regulated by
|
voluntary controls
|
|
For skeletal muscle, striations are
|
linear
|
|
The most important skeletal muscle for survival is
|
diaphragm.
|
|
Cardiac muscle is regulated by
|
the autonomic nervous system
|
|
For skeletal muscle, striations are
|
branched
|
|
Smooth muscle is regulated by
|
autonomic, hormonal, and paracrine control
|
|
For smooth muscle, striations are
|
not present.
|
|
For skeletal muscle, though ________ stops at birth, fibers can still _______.
|
cell division; increase in size.
|
|
For skeletal muscle, fascicles are
|
bundles of muscle fibers.
|
|
Individual muscle cells are multi_______.
|
nucleated
|
|
Myofibrils are
|
cylindrical bundles of thick and thin filaments that form muscle fibers.
|
|
A sarcomere is
|
a function unit of the muscle fiber.
|
|
In a sarcomere, thick filaments are composed of
|
myosin
|
|
IN a sarcomere, thin filaments are composed of
|
actin.
|
|
Thick sarcomeric filaments contain
|
cross bridges
|
|
Cross bridges are composed of
|
heavy and light chain, ATP binding sites, actin binding sites.
|
|
Thin sarcomeric filaments contain
|
cross-bridge binding sites.
|
|
A bands are composed of
|
overlapping myosin and actin
|
|
I bands are composed of
|
actin alone
|
|
The molecular mechanism of contraction is
|
a sliding filament mechanism
|
|
The sliding filament mechanism of muscle contraction is
|
1. Shortening of sarcomeres due to thin filaments sliding over thick filaments, 2. I band shortens, but A band length does not change.
|
|
In shortening of sarcomeres, the thick and thin filaments do not change
|
length.
|
|
Swinging of cross bridges creates
|
muscle contraction
|
|
The 4 steps of the cross bridge cycle are
|
1. Energeized cross bridge binds to actin, 2. Phosphate is released and cross bridge rotates (power stroke) and pulls thin filaments towards the center of sarcomere while ADP is released form myosin head, 3. ATP binds to myosin head, cross bridge detaches, 4. Hydrolysis of ATP by ATPase on myosin energizes cross bridge.
|
|
The role of ATP in cross bridge cycle is
|
1. Hydrolysis of ATP energizes the cycle, 2. Binding of ATP breaks the linkage
|
|
Lack of ATP in cross bridge cycle produces
|
rigor mortis.
|
|
Muscle contraction initiates in response to
|
an increase in Ca++
|
|
The two regulator proteins of the cross bridge cycle are
|
tropomysin and troponin
|
|
The roles of troponin in cross bridge cycle are
|
1. Bind to tropomysin and holds it over myosin binding site, 2. Contains Ca++ binding sites, 3. Binding of Ca++ to troponin causes conformation change which makes tropomysin move aside and expose myosin binding sites on actin.
|
|
Action potentials in muscles trigger
|
release of Ca2+ from lateral sacs of the sarcoplasmic reticulum causing contraction.
|
|
______ help propagate action potential within muscle fibers
|
transverse tubules.
|
|
Relaxation in muscles occurs when
|
lateral sacs pump Ca2+ out of cytosol using Ca2+-ATPase pump.
|
|
During relaxation in muscles, the sarcomere
|
extends to its resting length.
|
|
Ca2+ is concentrated in the sarcoplasmic reticulum via
|
Ca2+ binding proteins.
|
|
The steps of Ca2+ release in muscle contraction are
|
1. Action potential travels along muscle fiber and activates L-type Ca2+ channels, 2. Conformation change in L-type Ca2+ channels causes activation of ryanodine receptors, 3. Activation of ryanodine receptors causes the release of Ca2+ from the sarcoplasmic reticulum. |