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136 Cards in this Set

  • Front
  • Back
resting membrane potential of a cell
-70 mV
There is net excess of positive or negative charge inside cell? why?
excess negative charge due to abundace of protein and nucleic acids
which ion is the most permeable at rest?
potassium
which ion is least permeable at rest?
sodium
which two forces cause ions to want to move?
concentration gradient
electical force
T/F Sodium is more concentrated outside the cell at rest.
T
T/F Potassium is more concentrated inside the cell at rest.
T
T/F Sodium has a tendency to want to move out of the cell at rest.
F---it wants to move into cell at rest, down its conc. gradient
T/F Potassium wants to move outside the cell at rest.
T
What is the Nernst Potential?
tells us what the membrane potential would have to be for the electrical force to cancel out the concentration force
What is driving force and how is it calculated?
the net force on an ion to diffuse; is the difference between the membrane potential and the nernst potential for that ion
what is the nernst potential for sodium? Calculate driving force with this information.
+70mV; D.F. = 140 mV (difference between -70mV [membrane potential] and nernst potential)
flux?
permeability * driving force
at rest the most permeable ion is...
potassium
T/F The membrane potential will most closely represent the nernst potential for the most permeable ion.
T
The Na/K pump pumps out how many Na ions and pumps in how many K ions?
pumps out 3 Na ions for every 2 K ions it pumps in. (constantly moving net negative charge into cell)
threshold for generating an action potential
-50 mV
what is depolarization
Na becomes more permeable, leaks into cell "removing" membrane potential from -70mV to 0mV
what is overshoot?
membrane potential becomes positive, up to 30mV
what is repolarization?
membrane potential returns back to -70mV as potassium leaks out of cell
what is afterhyperpolarization?
membrane potential briefly drops below -70mV making it harder to reach threshold and generate another action potential (relative refractory period)
how do we change an ions permeability?
by opening/closing voltage gated ion channels
T/F
sodium channels have two gates and potassium channels have one gate
T
what happens to both K and Na gates as threshold is reached?
they open
Why don't the gates cancel each other out at threshold?
Na has much larger driving force and flows more rapidly into cell; K's gates open slower
what causes afterhyperpolarization?
Na gates closed; K gates still open
T/F At rest, the inactivation gate is open and the activation gate is closed for Na channel.
T
Physiologically, what is the absolute refractory period.
The period of time when the inactivation gate is closed.
When does the inactivation gate reopen?
When membrane potential gets below threshold (-50mV)
When does the potassium gate open?
when threshold is reached
When does repolarization occur?
When Na channels close (inactivation gate closes) and K gates fully open.
When does activation gate close?
during repolarization
define antidromic
an action potential that travels toward the cell body
define orthodromic
an action potential that travels toward axon terminal
glial cells in the peripheral n.s.
Schwann cells
insulating cells in central n.s.
oligodendrocytes
type of pain via "c-fibers"
achy dull pain
T/F action potentials regenerate at the nodes of ranvier b/c this is where the voltage gates channels are located.
T
what is saltatory conduction
the skipping of the action potential from node to node
what prevents reverberation along an axon?
the absolute refractory period---(the node previous to the location of the A.P. cannot depolarize again)
T/F vesicles are loaded with Neurotransmitter via ATP at axon terminal
T
purpose of the presynaptic density
holds vesicles in place
prevents premature fusing of vesicles and exocytosis of NT
two proteins that compose presynaptic density
actin (tether ball post) and synapsin (rope from post into tether ball) [vesicle is tether ball]
type of Ca channels located in region of synapse
n-type Ca channels
what happens to Ca channels when an AP arrives?
they open, allowing Ca to enter the neuron flowing down its Ec gradient
what happens when ca enters the neuron and binds to calcineurin?
inactivates Ca channels
what occurs when Ca enters neuron and binds to calmodulin?
activates calmodulin-dependent protein kinase (CAM kinase)
what does CAM-kinase do?
phosphorylates synapsin which releases vesicle to fuse with membrane and dump NT
purpose of "docking stations"?
activated by Ca, membrane bound proteins that aid exocytosis of NT
fates of NT after it is released?
binds to receptors
diffuse out of cleft and into blood (washout)
metabolized to diff. structure
pumped back in
primary excitatory NT in CNS
glutamate
primary inhibitory NT of brain
GABA
primary inhibitory NT in spinal chord
glycine
type of channels in post-synaptic cells
ligand-gated channels
what is the ligand in the post-synaptic cell?
the NT
What is EPSP?
excitatory post-synaptic potential; a gate opening for both K and Na---mV goes to -20mV, closer to threshold
What is IPSP?
inhibitory post-synaptic potential; gate permeable to Cl that results in hyperpolarization and far from threshold
Two types of summation for IPSP and EPSP
temporal and spatial summation
what is temporal summation?
a second psp occurs before complete decrement of the first psp (same location)
what is spatial summation?
multiple psp's are generated at same time in different locations.
type of summation if an IPSP and an EPSP are summed
spatial (different locations)
where are most EPSPs generated?
dendrites
where are most IPSPs generated?
soma or cell body
Why are ISPSs more poweful than EPSPs?
b/c of sites of origin, ipsps move a shorter distance, lose less charge and can inhibit multiple epsps
n.s. utilized when aware of a decision
somatic nervous system
involuntary n.s.
autonomic nervous system
two parts of autonomic nervous system
sympathetic (F or F)
parasympathetic (rest/dig)
sympathetic n.s. encompasses which portions of vertebral column
thoracolumbar
parasympathetic n.s. encompasses which portions of vertebral column
craniosacral
which nerve plays an important part in parasympathetic activity
vagus nerve
what is a ganglion?
nucleus outside of cns
symp. preganglionic fibers: long or short?
short
all preganglionic fibers: myelinated or unmyelinated?
myelinated
symp postganglionic fibers: long or short?
long
all postganglionic fibers: myelinated or unmyelinated?
unmyelinated
parasympathetic preganglionic fibers: long or short?
long
parasympathetic postganglionic fibers: long or short?
short
T/F: every axon exiting cns is myelinated
T
2 types of receptors for acetylcholine?
nicotinic
muscarinic
T/F: the first synapse involving acetylcholine is a nicotinic receptor?
T
parasympathetic n.s.: type of receptor found on target cells following pre/post ganglionic travel
muscarinic
beta-1 receptors located in...
heart
beta-2 receptors located in....
lungs
beta-3 receptors located in...
adipocytes
two types of receptors for acetylcholine
nicotinic
muscarinic
enzyme that makes acetylcholine
choline acetyltransferase
Ach receptor for somatic activity to muscle cells
nicotinic
Ach receptor type in TARGETcells of para/symp n.s.
muscarinic
Ach receptor type in 1st synapse in para/symp n.s.
usually nicotinic
Ach receptor type fo splanchnic nerve
nicotinic
enzyme that metabolizes Ach after exocytosis into choline and acetate
choline esterases
effect of beta-bungaro toxin (black widow spider venom)
hyper-release of vesicles depleting #
effect of botulism toxim
prevent exocytosis
hemicholinium
deplete Ach--choline is scarce
neostigmine, physostigmine, malathion and nerve gas: mechanism of action
overstimulation; prolongs Ach exocytosis
3 nicotinic agonists
Ach
nicotine
carbachol
3 nicotinic antagonists
curare
succinyl choline
rabies virus
3 muscarinic agonists
Ach
muscarine
pilocarpine
oxotremorine
3 muscarinic antagonists
atropine
scopolamine
how do nicotinic receptors work?
ionophore---nonspecific conductance pore through the membrane (Na and K can pass--EPP)
how do muscarinic receptors work?
use of G-proteins as coupling agents
inhibiting adenylate cyclase does what?
dec. cAMP in cells
guanylate cyclase stimulation..
inc. cGMP in cells
stimulate phospholiase c
inc DAG, IP3, and Ca
what is tyrosine used to make?
catecholamines
three catecholamines..
NE
epi
dopamine
what do the catecholamines share as a precursor?
L-tyrosine
enzyme that adrenal medulla cells express to make epinephrine.
PMNT enzyme
1) L-tyrosine to L-dopa via...
tyrosine hydroxylase
2) L-dopa to dopamine via...
dopa decarboxylase
3) dopamine to norepi via...
dopamine beta hydroxylase
4) norepi to epi via...
PMNT enzyme
action of alpha-methyl tyrosine, alpha methyl dopa, diethyldithiocarbamate:
depletes transmitter
action of amphetamines
initial release but long term depletion (crash later)
what is cortisol? what does it do?
stress hormone; inc. epi synthesis in medulla
action of cocaine, desipramine,
increased NE in cleft but inhibits reuptake; long term depletion
action of reserpine
inhibits recycling of NE
waste product of norepi in urine
vanillylmandelic (VMA)
two enzymes producing endproduct of norepi in urine
monoamine oxidase (MAO)
catechol-o-methyl transferase (COMT)
effect of MAO inhibitors
inc. DA, epi and Norepi in nerve terminals (more into vesicles)
practical uses for MAOI's
antidepressants and blood pressure regulators
T/F Norepi/dopamine are NT in cns as well as pns
T
name of the source of noradrenergic neurons
locus coeruleus
source of dopamine in the brain
substantia nigra
5 subtypes of dopamine receptors
D1 to D5
what do dopamine receptors do?
alter cAMP in target cells (inc. adenylate cyclase activity)
more potent stimulus: epi or norepi?
epi
what are adrenergic receptors
receptors for epi and norepi
T/F adrenergic receptors are located in both the cns and pns
T
primary antagonist for alpha-adrenergic receptors
phenoxybenzamine
primary agonist for all beta-adrenergic receptors
isoproterenol
primary antagonist for all beta-adrenergic receptors
propranolol
agonist for beta-1 adrenergic receptors
dobutamine
antagonist for beta-1 adrenergic receptors
atenolol
where are beta-3 adrenergic receptors located?
adipocytes
beta-2 adrenergic receptor agonist
albuterol