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Neurobiology Test 2

Quiz yourself by thinking what should be in each of the black spaces below before clicking on it to display the answer.
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Question
Answer
Presynaptic   cell before the synapse  
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Postsynaptic   after synapse  
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synaptic cleft   space between cells in chemical synapses  
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gap junctions   connections between two cells in electrical symnapses  
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connexons   Gap junctions are formed by these proteins  
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Chemical synapses   most neuron-neuron; all neuron-muscle  
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Otto Lowei (1926)   tested the idea that cells communicate by releasing chemicals; experimented on the vagus nerve through the frog heart.  
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Chemical Response (1-5)   1. Neurotransmitter synthesized and packed into vesicles in the terminal. 2. Action potential through synaptic bouton. 3. Presynaptic terminal depolarized; opens Voltage gated channels. 4. Ca2+ influx. 5. Ca2+ helps vesicles fuse w/membrane.  
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Chemical Response (6-10)   6. Neurotransmitter released. 7. Diffuses across cleft and bind to receptor proteins in PostSyn. 8. Binding leads to channels opening. 9. Resting membrane poten. changes as ions move. 10. NT removed or inactivated from cleft. 11. Vesicle membrane recycled  
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Neurotransmitter   1. Must be present w/in the presynaptic neuron. 2. Must be released in response to presynaptic depolarization and the release must be calcium dependent. 3. Must bind to specific receptors on the postsynaptic cell.  
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Examples of Neurotransmitters   Acetylcholine, Serotonin, Dopamine, Substance P.  
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ACh binds to AChR   AChR is activated and becomes an open channel. K+ out and Na+ influx. Depolarization in post synaptic cell (causes muscle contraction).  
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Acetylcholinesterase (AChE)   The enzyme that recycles ACh and allows the receptors to close  
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Miniature Endplate Potentials (MEPPs)   Falt & Katz. Caused by random calcium causing a few vesicles to fuse and stimulate the channels to open. Proves vesicle size is uniform at 1 mV--quantal release (packet release)  
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Endplate potential   another term for an action potential that is exclusive to neuron and muscle interaction  
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Quantal release   the release of neurotransmitters in packets  
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Neurotoxins   chemicals that negatively impact the ability of neurotransmitters or the neural system, i.e. EDTA, Botulinum, black widow spider venom, bungarotoxin  
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Calcium Influx blockers (vesicle fusion and ACh release)   EDTA (binds calcium), Ca Ionophores (create artificial calcium channels)  
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Vesicle Fusion (Dockin and exocytosis)   botulinum prevents docking, black widow spider venom causes all vesicles to dock and release  
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Block AChR   bungarotoxin (binds to the site), Curare  
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Block AChE   atropine gives a longer last muscle response, belladona  
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Compound action potential   summation of many cells (recording from many nerves)  
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End plate current (EPC)   the measure of ion flow across the membrane, inward flow of sodium down, outward flow of potassium up  
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EPSP (excitatory post synaptic potential)   takes cells closer to threshold (all EPP in muscle cells)  
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IPSP (inhibitory post synaptic potential)   keeps cells from reaching threshold by opening channels to bring - ions (chloride) in  
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Muscle cells   always excitatory, always have one input  
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Temporal summation   time (closer) and it builds  
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Spatial summation   potentials originating in differing parts of the cell build on one another  
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plasticity   changeability, amenability  
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Facilitation   an increase in the second post-synaptic response (PSP) after closely spaced stimuli due to prolonged calcium levels in the pre-synaptic cell  
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Postsynpatic depression   due to an absence of neurotransmitter vesicles in the presynaptic cell  
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Potentiation   tetanic stimulus/tetany and post-tetanic response  
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Tetanic stimulus/tetany   rapid stimuli that cause tatanic responses/hyper-responses that are together  
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Post-tetanic potentiation   the increased EPSP following a distance of time after tetany  
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Habituation   when a response to a repeated stimulus decreases (ex. gill contraction and siphon in Aplysia)  
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sensitization   generalization of one stimulus to another stimulus  
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Why sensitization (short term) happens   1. Interneuron releases serotonin. 2. Serotonin binds to receptors on sensory terminal. 3. Internal signal transduction pathway. 4. Presynaptic K+ channels get phosphorylated and it closes them  
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Long term sensitization   Action of CREB  
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sensory information processing   1. Environmental stimulus (light, sound, touch, pressure, heat, pain, etc). 2. Sensory transduction changes signal from one energy to electrical. 3. Intensity coding. 4. Sensory analysis. 5. Sensorimotor integration. (6) Motor output  
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Afferent   towards the CNS (sensory)  
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Efferent   away from the CNS (motor)  
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Sensory system   1. Peripheral receptors. 2. Sensory neurons. 3. Dorsal root ganglia. 4. Spinal cord. 5. [Brainstem]. 6. Thalamus. 7. Cerebral cortex.  
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Grey matter   where cell bodies are located  
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white matter   where neurons/axons are located  
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How to determine stimulus intensity   Stimulus intensity is either positively or negatively correlated to the frequency  
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Stimulation function   stimulation generates a receptor potential--channels are opened--excitation occurs and depolarization of sensory cell--can become an action potential--mechanical to electrical/chemical  
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sensation   the ability to transduce, encode, and perceive information generated by internal and external stimuli  
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mechanoreceptors   afferent fibers encapsulated by special receptor cells- generally with lower threshold and a higher sensitivity to stimulation  
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free nerve endings   afferent fibers that lack specialized receptor cells  
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Afferents differ in:   axon diameter, temporal dynamics, and receptive fields  
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two-point discrimination   the minimum inter-stimulus distance required to perceive two distinct stimuli  
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Rapidly adapting   response lessons or stops after repeated stimulation - useful for perceiving changes in stimulus  
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slowly adapting   useful for providing spatial attributes of the stimulus such as size and shape  
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Nociceptors   pain receptors--unmyelinated or slow  
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Parallel pathways   differing somatic responses to the same stimuli  
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Haptics   active touching--involves complex spatiotemporal pattern interpretation  
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Stereognosis   being able to identify an object based on manipulation  
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Merkel cell afferents   slow adapting fibers, 25% of afferents in hand, create ridges that form fingerprints, adept at points edges and curvature, differentiate ~0.5mm  
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Meissnerr afferents   rapid, even more dense ~40%. Adept at grip and vibrations.  
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Pacinian corpuscles   rapid, 10-15%, 10 nm perception displacement, huge range, detect movements using tools  
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Ruffini   slowly adapting fibers, 20%, recognize finger stretches  
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Proprioception   sense of self in space.  
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muscle spindles   4-8 special intra-fusal muscle fibers found in connective tissue--recognize changes in muscle length  
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Golgi tendon organs   composed of extrafusal muscle fibers, detect tension in muscles  
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joint receptors   similar to skin receptors, not used for proprioception, but used for positioning of fingers  
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Dorsal column   the area of white matter in the spinal cord that takes in a majority of the sensory information  
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Lateral inhibition   the capacity of an excited neuron to reduce the activity of its neighbor  
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thermoreceptors   detect changes in temperature (specifically, heat and lack of heat)  
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