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37 Cards in this Set
- Front
- Back
Describe electrical synapses
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-ionic currents
- cytoplasmic continuity (gap jxns) -rapid bidirectional transmission -electrotonic transmission (membrane modifications btwn adjacent cells, common btwn astrocytes & in neurons) |
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How do astrocytes use gap junctions?
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-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 |
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How do intracellular channels promote localized tissue homeostasis?
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-maintain electrical potential diff
-buffer differences in secondar messengers & small molecules (Ca2+ & ATP) -nutrient transport |
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How do intercellular channels regulate signal transmission?
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-propagate electrical signals btwn cells
-cellular differentiation in embryonic tissues |
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How do intercellular channels maintain cellular organization?
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-compartmentalization of cell groups
-amplification or gain control of cell group responses -coordinate rhythmic drive (neurons) w/ oscillatory activity |
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Describe chemical synapses
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-use neurotransmitters
-cells separated by synaptic cleft (not cytoplasm) -slow unidirectional transmission -complex process of excitatory/inhibitory signal amplification |
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3 components of chemical synapse:
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1. presynaptic element
(axon terminal/bouton) 2. synaptic cleft 3. postsynaptic element (postsynaptic density) |
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Within the cell membrane of the axon terminal, the _________ contains high concentration of voltage gated calcium channels
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active zones
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What are the 3 main types of synaptic vesicles?
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1. Small clear
(glutamate, GABA, ACh) 2. small/medium spherical dense-core (catecholamines, serotonin) 3. large spherical dense-core (neuropeptides- SP, Enk) |
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Differentiate btwn the vesicles containing glutamate & GABA
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glutamate- small spherical, clear vesicles
GABA- small flattened, clear vesicles |
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The _____________________, within the postsynaptic element. contains Ca2+/calmodulin -dpendent protein kinase II channels and MAGUK & PSD95 proteins
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postsynaptic density
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What are the 3 common types of synaptic linkages in the CNS?
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1. axodendritic
axon terminals contact dendrite/dendritic spine 2. axosomatic axon terminal contacts soma 3. axoaxonic axon terminal contacts another axon |
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(neuropeptides/classical neurotransmitters) are transported in secretory vesicles from the golgi apparatus w/i the soma to axon terminal
(fast axonal transport) |
neuropeptides
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(neuropeptides/classical neurotransmitters) are synthesized in the axon terminal & loaded into vesicles arriving from the soma
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classical neurotransmitters
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Describe the role of calcium in vesicle release
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1. AP depolarizes membrane , opening voltage gated Ca2+ channels
2. Ca2+ enters terminal, & binds to synaptogamin 3. Synaptogamin promotes membrane fusion & neurotransmitter exocytosis |
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(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 |
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(SNARE hypothesis)
During docking, ____________ is recruited to the SNARE complex, & acts as a calcium sensor. |
synaptotagmin
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During calcium influx, how does synaptogamin regulate neurotransmitter release?
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Synaptotagmin has 2 low-affinity calcium binding domains (C2A & C2B). When bound, acts as a positive regulator of neurotransmitter release, promoting vesicle fusion & exocytosis.
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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 |
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What are 2 ways for vesicles to be recycled?
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1. endocytosis & formation of clathrin-coated vesicles
2. kiss and run- detached after fusion |
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How are neurotransmitters removed after use?
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1. inactivation
destroyed or modified 2. reuptake via transporter proteins (endocytosis) |
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What defines the response that a cell will have to a released neurotransmitter?
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the receptor on the neuron
*receptor diversity allows the same neurotransmitter to serve multiple functions |
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How do receptors on neuroglial cells control synaptic environment?
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-inactivation & recycling
-balance of ions |
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Classify receptors based on function
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-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+) |
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_______ are involved in sensory transduction, postsynaptic responses (EPSPs, IPSPs)
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local potentials
(graded, subthreshold, proportional to intensity) |
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Describe Battery in relation to the neuronal membrane
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built into membrane
concentration gradient creates voltage (Vm) |
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Describe Resisitance in relation to the neuronal membrane
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resists charge movement
membrane channels (Rm) cytoplasm (Ri) ECF (Ro) |
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Describe Capacitance in relation to the neuronal membrane
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ability to store charge
2 conductors separated by non-conductor/insulator (Cm) |
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Speed in which voltage changes across the membrane is determined by its ____________ & ______________
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capacitance & resistance
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What does the time constant (t) represent?
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t= Rm x Cm
-the time it takes for passive voltage to reach 63% Vmax *fewer channels open = longer time |
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Current flow in the neurite & change in potential (increases/diminishes) w/ distance from origin
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diminished
*increase Rm *decrease Ri |
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What does the ration Rm/Ri determine?
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the distance that change in membrane potential is passively transmitted
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Neurons with greater t (time constant) have (greater/lesser) capacity for temporal summation
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greater
*consecutive synaptic potential at same site add together (temporal summation) |
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Neurons with (greater/lesser) sigma allows for signal to reach trigger zone with less decrement
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greater
*synaptic potentials from diff inputs in same area summate (spatial summation) |
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__________ synapses have greater influence on AP generation due to their proximity to the initial segment
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axosomatic
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When is inhibitory shunting most effective?
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When in close proximity to initial segment
*significant inhibitory inputs in CNS often occurs on neuronal cell body |
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Where do the bulk of excitatory neuronal inputs in the CNS terminate?
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on dendritic spines
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