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37 Cards in this Set

  • Front
  • Back
Describe electrical synapses
-ionic currents
- cytoplasmic continuity (gap jxns)
-rapid bidirectional transmission
-electrotonic transmission

(membrane modifications btwn adjacent cells,
common btwn astrocytes & in neurons)
How do astrocytes use gap junctions?
-to form syncytium, compartment around & w/i groups of neurons
-involved in removal of excess K+ from ECF, pH regulation, & Ca2+ waves= modulate synaptic environment
How do intracellular channels promote localized tissue homeostasis?
-maintain electrical potential diff
-buffer differences in secondar messengers & small molecules (Ca2+ & ATP)
-nutrient transport
How do intercellular channels regulate signal transmission?
-propagate electrical signals btwn cells
-cellular differentiation in embryonic tissues
How do intercellular channels maintain cellular organization?
-compartmentalization of cell groups
-amplification or gain control of cell group responses
-coordinate rhythmic drive (neurons) w/ oscillatory activity
Describe chemical synapses
-use neurotransmitters
-cells separated by synaptic cleft (not cytoplasm)
-slow unidirectional transmission
-complex process of excitatory/inhibitory signal amplification
3 components of chemical synapse:
1. presynaptic element
(axon terminal/bouton)
2. synaptic cleft
3. postsynaptic element
(postsynaptic density)
Within the cell membrane of the axon terminal, the _________ contains high concentration of voltage gated calcium channels
active zones
What are the 3 main types of synaptic vesicles?
1. Small clear
(glutamate, GABA, ACh)

2. small/medium spherical dense-core
(catecholamines, serotonin)

3. large spherical dense-core
(neuropeptides- SP, Enk)
Differentiate btwn the vesicles containing glutamate & GABA
glutamate- small spherical, clear vesicles

GABA- small flattened, clear vesicles
The _____________________, within the postsynaptic element. contains Ca2+/calmodulin -dpendent protein kinase II channels and MAGUK & PSD95 proteins
postsynaptic density
What are the 3 common types of synaptic linkages in the CNS?
1. axodendritic
axon terminals contact dendrite/dendritic spine

2. axosomatic
axon terminal contacts soma

3. axoaxonic
axon terminal contacts another axon
(neuropeptides/classical neurotransmitters) are transported in secretory vesicles from the golgi apparatus w/i the soma to axon terminal
(fast axonal transport)
neuropeptides
(neuropeptides/classical neurotransmitters) are synthesized in the axon terminal & loaded into vesicles arriving from the soma
classical neurotransmitters
Describe the role of calcium in vesicle release
1. AP depolarizes membrane , opening voltage gated Ca2+ channels
2. Ca2+ enters terminal, & binds to synaptogamin
3. Synaptogamin promotes membrane fusion & neurotransmitter exocytosis
(SNARE hypothesis)
Vesicles containing _____________ bind to specific target membrane proteins, ______________. The formation of the ______ leads to membrane fusion.
SNARE proteins/v-SNAREs (snaptobrevin/VAMP)

t-SNAREs (SNAP-25 & syntaxin)

SNARE complex
(SNARE hypothesis)
During docking, ____________ is recruited to the SNARE complex, & acts as a calcium sensor.
synaptotagmin
During calcium influx, how does synaptogamin regulate neurotransmitter release?
Synaptotagmin has 2 low-affinity calcium binding domains (C2A & C2B). When bound, acts as a positive regulator of neurotransmitter release, promoting vesicle fusion & exocytosis.
Once neurotransmitters have been released, the SNARE complex is disassembled via _____ & _______.

Which of these is an ATPase that liberates energy to unravel complex?
NSF & SNAP (soluble cytoplasmic proteins)


NSF
What are 2 ways for vesicles to be recycled?
1. endocytosis & formation of clathrin-coated vesicles
2. kiss and run- detached after fusion
How are neurotransmitters removed after use?
1. inactivation
destroyed or modified
2. reuptake
via transporter proteins (endocytosis)
What defines the response that a cell will have to a released neurotransmitter?
the receptor on the neuron

*receptor diversity allows the same neurotransmitter to serve multiple functions
How do receptors on neuroglial cells control synaptic environment?
-inactivation & recycling
-balance of ions
Classify receptors based on function
-Ligated channels, open/close transmembrane pores/channels
-G-protein coupled/2nd messenger
-transmembrane receptors w/ modified enzyme activity
-ligand-dependent regulators of nuclear transcription
-sequestration of intracellular ions (Ca2+)
_______ are involved in sensory transduction, postsynaptic responses (EPSPs, IPSPs)
local potentials

(graded, subthreshold, proportional to intensity)
Describe Battery in relation to the neuronal membrane
built into membrane
concentration gradient creates voltage (Vm)
Describe Resisitance in relation to the neuronal membrane
resists charge movement
membrane channels (Rm)
cytoplasm (Ri)
ECF (Ro)
Describe Capacitance in relation to the neuronal membrane
ability to store charge
2 conductors separated by non-conductor/insulator (Cm)
Speed in which voltage changes across the membrane is determined by its ____________ & ______________
capacitance & resistance
What does the time constant (t) represent?
t= Rm x Cm

-the time it takes for passive voltage to reach 63% Vmax

*fewer channels open = longer time
Current flow in the neurite & change in potential (increases/diminishes) w/ distance from origin
diminished

*increase Rm
*decrease Ri
What does the ration Rm/Ri determine?
the distance that change in membrane potential is passively transmitted
Neurons with greater t (time constant) have (greater/lesser) capacity for temporal summation
greater

*consecutive synaptic potential at same site add together (temporal summation)
Neurons with (greater/lesser) sigma allows for signal to reach trigger zone with less decrement
greater

*synaptic potentials from diff inputs in same area summate (spatial summation)
__________ synapses have greater influence on AP generation due to their proximity to the initial segment
axosomatic
When is inhibitory shunting most effective?
When in close proximity to initial segment

*significant inhibitory inputs in CNS often occurs on neuronal cell body
Where do the bulk of excitatory neuronal inputs in the CNS terminate?
on dendritic spines