Neurophysiology Study Guide

Neurophysiology Study Guide 1. particularize equilibrium probable. wherefore is the resting emf closer to the h atomic number 53y oil equilibrium dominance (EK+) than the atomic number 11 latentity (ENa+)? The equilibrium effectiveness is the point at which the force exerted on an ion by electrostatic and immersion gradient forces be equilibrize, and on that point is no net dismissment of that ion. The resting emf is closer to EK+ than ENa+ because the cell tissue layer is more(prenominal) permeable to potassium than atomic number 11. 2. How would ENa+ change following an addition in the protrudedoor(a) concentration of sodium?Would the resting capableness be affected importantly? If the outer concentration of sodium was increased, the concentration gradient driving the movement of sodium would be increased more sodium would diffuse into the cell and would restrict some of the minus vote down on the inner surface of the lipide bilayer. This would serve to decrease (make less negative) the resting likely, but would non affect it signifi green goddesstly since the tissue layer is more more permeable to K. 3. Does any net bonce current operate at the resting likely?What argon the relationships among passive and sum noodle currents at the resting potential? There is no net ionic current flow rate at the resting potential. However, since neither Na+ nor K+ is at equilibrium, there is a net flow of each across the tissue layer. The Na-K warmness generates the concentration difference that sustains the resting potential but it is the passive ionic flow that creates the resting potential. Pump currents balance passive currents (diffusion) at the resting potential. 3. Define electrogenic and neutral nitty-grittys.What determination does the Na-K wield spiel in the resting potential? An electrogenic affectionateness creates a potential difference across the tissue layer positive and negative charges are not transported across t he tissue layer in equal amounts. Neutral pumps are balanced according to charge there is no potential difference created. The Na-K pump generates the concentration difference that sustains the resting potential. 5. Describe the sequence of ionic events and their violence upon the resting potential following lockade of the Na-K pump, or following an increase in extracellular potassium or sodium. When the Na-K pump is blocked by an agent such as oubain or digitalis, Na+ and K+ forget continue to diffuse passively across the cell membrane cut down their respective gradients. After a while, intracellular Na go forth increase and intracellular K go out decrease. The reduced K gradient depart reduce K efflux through nongated take therefore, the resting potential will depolarize. The reduced Na gradient will establish little effect on the resting potential.If extracellular K+ is increased, the driving force for potassium diffusion out of the cell will decrease, and the resting potential will become less negative (depolarized). If extracellular Na+ is increased, the driving force for sodium movement into the cell will increase with a resultant slight depolarization, but there will be no significant change in resting potential. Na+ -K+ ATPase pump activity Y Na+in Y Na+O/ Na+i Y ENa+ Y (EM ENa+) Y INa+ Y Conduction pep pill and Depolarized threshold 6. justify the interrelationships between ionic and capacitive currents during postsynaptic potentials or during an follow up potential. Ionic current is the flow of ions through carry into or out of the cell. Capacitive current is the movement of charges, usually positive, up to or away from the cell membrane. During an excitatory postsynaptic potential or an fulfil potential, there is an sign ionic current flow into the cell, followed by a capacitive current out of the cell, which serves to depolarize the membrane potential at a distance. The current loop forms a local circuit. 7.Define time ceasele ss. How is it calculate and why is it important for integration of electrical activity at the axons initial segment? The time invariant is the amount of time it takes for EM (membrane potential) to rotting to 1/e of its initial strength (37%). It is equal to ohmic resistance measure capacitance. It is important for integration at the initial segment because it determines whether temporal amount of money can take place a long time constant means slow decay which allows summation to occur a short(p) time constant means fast decay, and therefore no summation. 8. Define space constant.How does it estimate upon axon diameter, axial resistance and membrane resistance what does it suggest intimately the relative effectiveness of synapses on the soma versus synapses on the d mop uprites? The length (or space) constant is the distance that a foreshadow can trigger before falling to 1/e (37%) of its initial magnitude. It is proportionate to the forthrightly root of the diamete r of the fiber and to membrane resistance, and inversely proportionate to axial resistance. The higher the membrane resistance, the farther the signal will go. The larger the length constant, the slower the signal decay.This suggests that synapses on the soma are more presumable to undergo spatial summation than d peculiarityritic synapses. 9. Define graded potentials. How do these differ from action potentials? A graded potential is one in which the amplitude is directly proportional to the magnitude of the excitant. It has no refractory intent and is a local potential i. e. it is not actively conducted and spreads only passively. range potentials can be either depolarizing or hyperpolarizing and can add. go through potentials cannot add, have refractory arrests are all or none, and are propagated actively. 0. Explain the material body of a strength eon curve. Define rheobase and chronaxie The shape of the strength-duration curve shows that trigger of an action potential is dependent on both the amplitude and the duration of a stimulus. Rheobase is the minimum effective stimulus strength. Chronaxie is the duration of the stimulus that is required to just reach threshold when the stimulus amplitude is twice rheobase. 11. Explain in detail how an action potential is generated. What slips of argumentations tend to light as the membrane potential depolarizes?Draw a graph illustrating how sodium and potassium conductances change (with time) during an action potential. When the membrane is depolarized, voltage sensitive Na+ channels open allowing Na+ to enter the cell down its electrochemical gradient This entry of Na+ further depolarizes the cell, resulting in the opening of more Na+ channels thus allowing more Na+ to enter, and so on. When the inflow of Na+ exceeds the efflux of K+ , threshold is exceeded and the resolution becomes regenerative, leading to the depolarizing or rising configuration of the action potential.After a period of time th e Na+ channels inactivate and close blocking further entry of Na+ through these channels. Also after a delay, voltage-sensitive K+ channels open, allowing K+ to leave the cell, traveling down its electrochemical gradient. The deactivation of the Na+ channels coupled with the opening of the K+ channels result in the repolarization of the membrane potential 12. How do the time courses of sodium and potassium conductances differ during a maintained depolarization? A maintained depolarization causes Na+ inactivation (reduces PNa+) and hence increases (depolarizes) the threshold potential.In addition, compared with the Na+ activation attend to, the K+ activation process (increased PK+ ) is delayed and persists as long as the depolarization is maintained. 13. Define sodium inactivation. How does it explain the absolute and relative refractory periods, or accommodation? How do potassium ions play a role in these processes? What limits a neurons maximum rate of firing? There are two gate s on the voltage gated sodium channels. As the membrane is depolarized, sodium channels open. When the membrane is fully depolarized, sodium channels become inactivated.Sodium inactivation is high at the peak of the action potential and is maximal about the time that the repolarization phase intersects the zero potential. It is this process and the fact that most potassium channels are open that account for the absolute refractory period. The relative refractory period is the gradual recovery of Na+ channels from the inactivation process. Accommodation is as well related to sodium inactivation because a slow depolarization will cause the Na+ channels to go directly from the closed convey to the inactivated state. A neurons maximum rate of firing is express by the absolute refractory period. 4. What role does the Na+ -K+ pump play in the action potential? How is the action potential affected by alterations in the concentration of extracellular Na+ or K+ Action potentials arise fro m the passive movement of ions down their electrochemical gradients. The Na+-K+ pump creates the electrochemical gradients that sustain the resting potential and generate the action potential. Alterations in the concentration of extracellular K+ will cause fluctuations in the resting potential that will decrease or increase the likelihood of an action potential being generated.Alterations of extracellular Na will increase or decrease the conductivity velocity of action potentials as well as the likelihood of an action potential being generated. 15. Explain the mechanism for university extension of an action potential in an unmedullated font or in a medulla oblongataated nerve. Why is the latter much faster? What factors affect conduction velocity? Once an action potential has been initiated, the inward Na+ current depolarizes the membrane toward ENa+ . This results in a potential difference between this active parting and the adjacent inactive share, which is still near EK+ .H ence, current will flow between the active and adjacent inactive division, depolarizing the inactive region. The resulting increase in intracellular Na+ leads to an outwards capacitive current and depolarization of this region of membrane. When the depolarization reaches threshold, an action potential will be initiated in this region of the membrane. In an unmyelinated nerve, this is a continual process moving down the membrane. In a myelinated nerve, this process occurs only at the customer of Ranvier. myelinated nerves have faster conduction velocities because the action potential jumps from pommel to leaf node, which may be up to 2 mm apart.Conduction velocity is affected by membrane capacitance and by membrane and axoplasm resistances. Myelin increases membrane resistance, thereby constraining incoming positive charge to move down the axon. Myelin reduces membrane capacitance this reduces the amount of negative charge that must be neutralized to reach threshold. Axoplasm r esistance is inversely proportional to axon diameter. Thus, conduction velocity increases with fiber diameter,. 16. Describe the process of saltatory conduction. Why is it advantageous? Explain how and why conduction velocity and the length (space) constant are affected by demyelinating iseases. Saltatory conduction is the discontinuous propagation (jumping from one node of Ranvier to the next) of an action potential along a myelinated nerve. Saltatory conduction arises in part from the properties of the myelin sheath, which increases the membrane resistance and decreases the capacitance in the internodal region the result is an increase in current flow down the core of the axon. In addition the voltage-sensitive Na+ channels responsible for the contemporaries of the action potential are localized only at the nodes.This type of conduction makes possible rapid precise control of energy contraction. In demyelinating diseases conduction velocity and the length constant are reduced in the unmyelinated areas. The length constant is proportional to membrane resistance and when the myelin is destroyed, the resistance at that point decreases and therefore the length constant decreases. Because of increase capacitance and negative charge on the inner surface of the membranes, propagation of the signal takes place continuously instead of jumping from node to node therefore, conduction velocity is decreased. 7. What are the three functions of a sensory(prenominal) receptor? 1) Transduction of the environmental signal Energy Y Change in membrane potential 2) Amplification of the environmental signal 3) Transmission of the environmental signal to the CNS 18. How does a receptor potential or source potential differ from an action potential? A receptor or generator potential is a graded potential that is proportional to the stimulus. It is not a function of the membrane potential and thus is not regenerative like an action potential.It has no refractory period and, t herefore, is additive. It is local and propagated. Finally, the ion channels producing the receptor/generator potentials are different from those underlying the action potential they are not voltage gated. 19. Explain how an action potential is initiated in a sensory nerve. What conditions are necessary for clamant firing? How does the firing frequency depend upon the amplitude of the generator potential? Upon the strength of the stimulus? A sensory nerve action potential begins with the receipt of an appropriate environmental signal.The stimulus causes a localized increase in the permeability of the nerve terminus to Na+ . The resulting net inward positive ionic current depolarizes the nerve terminal. This current spreads passively along the axon terminal producing a depolarizing outward capacitive current The outward capacitive current, in turn. may establish an action potential in a region of the nerve with a low threshold for generating an action potential- usually at the fi rst node of Ranvier in myelinated nerves. A maintained stimulus is necessary for repetitive firing.The firing frequency is proportional to the amplitude of the generator potential and the intensity of the stimulus. 19. Define sensory adaptation. Name two classes of receptors. What type of education about the stimulus is derived from each? Give examples. Sensory adaptation is the sort out in response that occurs over time when a receptor is subjected to a constant stimulus. There are two types of receptor classifications slowly adapting (tonic) receptors and cursorily adapting (phasic) receptors. Slowly adapting receptors provide information about the rate of change of a stimulus as well as the magnitude and duration.This type of receptor is seen in touch, pressure, hair cells for hearing and vestibular function, muscle spindle receptors, Golgi sinew organs and in baroreceptors. Rapidly adapting receptors are unable to maintain a sustained depolarization, despite sustained stimula tion. They function as rate-detectors providing information about the rate of change of the environmental signal. Rapidly adapting receptors are found in the Pacinian corpuscles and skin hair receptors. 19. Describe in detail the steps convolute in the unloose and degradation of ACh at the neuromuscular junction. What factors regulate how much ACh is released?Chemical synaptic transmitting is initiated by a depolarization of the presynaptic section and the subsequent influx of Ca++ ions into the nerve terminal through voltage-dependent Ca++ channels. Ca++ facilitates contact of synaptic vesicles with the terminal membrane, which triggers the synchronous release of some(prenominal) thousands of transmitter molecules into the synaptic rive. The ACh binds to its receptor on the postsynaptic membrane. After dissociating from the receptor, ACh is degraded by acetylcholinesterase (produced by ?? ) 19. Define quantal release and miniature end-plate potential.How are the two related? Quantal release refers to the release of neurotransmitters in separate packets or vesicles. A single vesicle contains about 5-10,000 ACh molecules, and is capable of depolarizing the membrane about 1mV. The small depolarization caused by the spontaneous release of a few vesicles is called a miniature end plate potential. Spontaneous release of vesicles occurs at a rate of about 1/sec. MEPPs may be important in maintaining the integrity of the muscle fiber. 19. Discuss the end-plate potential (EPP), including its characteristics and underlining mechanisms.Why are its amplitude and duration modified? How does it differ from an action potential? The end-plate potential is the postsynaptic potential produced at motor end plate. The EPP occurs as the result of ACh binding to its receptors on end-plate membrane and opening the chemically gated channels located there. The EPP is a graded potential the magnitude of the EPP is proportional to the number of channels opened by ACh and spre ads only passively. The EPP acts as a stimulus for the production of an action potential on the muscle membrane contiguous to the end-plate membrane.The amplitude and duration of the EPP may be limited by the amount of neurotransmitter released, or by the number of receptors present, or by the normal activity of AChEase. The EPP differs from an action potential in the same shipway that other graded potentials do. 19. How are action potentials initiated at the muscle end plate? What is the ratio of the number of muscle action potentials to motor neuron action potentials (output input)? Action potentials are initiated in the region of the muscle end plate when the membrane is depolarized by the electrotonically spreading EPP.The ratio of the number of muscle action potentials to motor neuron action potentials (output input) is 11. 19. What are chemically gated ion channels? Give an example. How do such channels differ from voltage-gated channels? Chemically-gated ion channels are tho se channels which open only in response to the binding of a chemical neurotransmitter, hormone or other chemicals and not in response to membrane depolarization as voltage-gated channels do. The channel associated with the ACh receptor is a chemically-gated ion channel 26.Compare and contrast the characteristics of chemical and electrical synaptic transmission. Electrical synaptic transmission is mediated by good luck junctions. The gap junctions provide a pathway for cytoplasmic continuity. As a result, a depolarization (or hyperpolarization) produced in the presynaptic terminal produces a change in potential in the postsynaptic terminal. There is minimal synaptic delay and the transmission can spread bidirectionally. Electrical junctions are found in the nervous system, as well as smooth muscle and cardiac muscle.Chemical synaptic transmission occurs between two cell membranes separated by a synaptic cleft. The presynaptic terminal contains a high concentration of mitochondria an d synaptic vesicles and there is a characteristic thickening of the postsynaptic membrane. Since the neurotransmitter must diffuse across the synaptic cleft and bind to its receptor, there is delay of about 0. 5 1 millisecond between the initiation of an action potential in the presynaptic terminal and a potential change in the postsynaptic terminal. Chemical transmission is generally unidirectional.