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Resting membrane potential
The steady voltage difference across the membrane of an unstimulated cell, with the inside negative relative to the outside
What it means for a neuron to have a resting membrane potential
Electrical charges are separated across the plasma membrane so the intracellular side is negative relative to the extracellular side, creating stored electrical potential energy
Typical neuronal resting membrane potential
A typical neuron rests near negative 70 mV, although resting potentials vary among cells depending on their ion gradients and relative membrane permeabilities
Electrochemical gradient
The combined effect of an ion concentration gradient and the electrical gradient across the membrane that determines the direction an ion tends to move
Equilibrium potential
The membrane potential at which the electrical force on a particular ion exactly opposes its concentration gradient so there is no net movement of that ion
Nernst equation
Calculates the equilibrium potential for a single ion from its concentration gradient and charge
Ionic basis of the resting membrane potential
Resting membrane potential depends mainly on Na positive, K positive, and sometimes Cl negative concentration gradients together with the membrane permeability to each ion
Why potassium dominates resting membrane potential
Resting neurons have many more open K positive leak channels than Na positive leak channels, so the membrane is much more permeable to K positive and resting potential lies near the K positive equilibrium potential
Potassium movement at rest
K positive tends to leave the cell through leak channels down its concentration gradient, leaving the inside relatively negative
Sodium movement at rest
A small amount of Na positive enters through leak channels and pulls the membrane potential away from the K positive equilibrium potential toward the Na positive equilibrium potential
Role of the sodium potassium pump in resting potential
The Na positive K positive ATPase maintains Na positive and K positive concentration gradients by pumping 3 Na positive out and 2 K positive in. Its direct electrical effect is small but its indirect role is essential
Resting potential as a steady state
Na positive continuously leaks inward and K positive leaks outward, but the sodium potassium pump balances these movements so ion concentrations and membrane potential remain stable
How permeability affects membrane potential
Increasing permeability to an ion makes that ion exert a greater influence on membrane potential and moves the membrane potential toward that ion's equilibrium potential
Effect of increasing sodium permeability
More Na positive enters the cell and membrane potential moves toward the positive Na positive equilibrium potential, causing depolarization
Effect of increasing potassium permeability
More K positive leaves the cell and membrane potential moves toward the negative K positive equilibrium potential, generally causing hyperpolarization
Depolarization
A change in membrane potential that makes the inside of the cell less negative than at rest
Repolarization
Return of membrane potential toward its resting value after depolarization
Hyperpolarization
A change that makes membrane potential more negative than the resting level
Goldman Hodgkin Katz equation
Calculates membrane potential from the concentration gradients and relative membrane permeabilities of multiple ions rather than considering only one ion
GHK equation main principle
Each permeable ion pulls membrane potential toward its own equilibrium potential, and ions with greater permeability have a greater effect on the final membrane potential
Why GHK predicts different resting potentials in different cells
Different cell types have different relative permeabilities to Na positive, K positive, and Cl negative, so their weighted contributions to membrane potential differ
Major parts of a neuron
A neuron contains a cell body, dendrites, an axon hillock, an axon, axon branches, and axon terminals
Cell body of a neuron
Contains the nucleus and protein synthesis machinery and serves as the major metabolic and control center of the neuron
Dendrites
Highly branched processes that receive incoming signals from other neurons. Dendritic spines increase surface area for receiving synaptic input
Axon hillock and initial segment
Region where the axon begins and where graded potentials are integrated. Its high density of voltage gated Na positive channels makes it the usual trigger zone for action potentials
Axon
Long neuronal process that conducts outgoing electrical signals away from the cell body toward target cells
Axon terminals
End regions of axons that communicate with target cells and release neurotransmitters at chemical synapses
Synapse
Region where the axon terminal of a presynaptic neuron communicates with a postsynaptic target cell
Major parts of a chemical synapse
The presynaptic axon terminal contains neurotransmitter vesicles and voltage gated Ca2 positive channels, the synaptic cleft separates the cells, and the postsynaptic membrane contains neurotransmitter receptors
Presynaptic versus postsynaptic cell
The presynaptic cell releases the signal while the postsynaptic cell receives the signal through receptors
Major glial cells
Schwann cells, oligodendrocytes, satellite cells, astrocytes, microglia, and ependymal cells provide different forms of neuronal support
Schwann cells and oligodendrocytes
Schwann cells form myelin around axons in the PNS while oligodendrocytes form myelin in the CNS. One Schwann cell myelinates part of one axon while one oligodendrocyte can myelinate portions of several axons
Astrocytes
CNS glial cells that regulate extracellular ions and neurotransmitters, support neurons metabolically, contribute to the blood brain barrier, and help guide neuronal development
Microglia
Specialized immune and scavenger cells of the CNS
Ependymal cells
CNS glial cells that line fluid filled spaces and help regulate cerebrospinal fluid. The slides also identify them as a source of neural stem cells
Satellite cells
PNS glial cells associated with neuron cell bodies that provide support and are described in the slides as nonmyelinating Schwann type cells
Current flow
Movement of electrical charge. In neurons, ion movement through channels creates electrical current
Resistance
Opposition to electrical current. Higher resistance means less current can flow for a given voltage difference
Conductance
The ability of ions to flow through a membrane and is opposite to resistance. Opening more ion channels increases conductance and decreases resistance
Ohm's law
Voltage equals current times resistance. Therefore at a constant voltage, lowering resistance increases current and raising resistance decreases current
Membrane resistance and internal resistance
Membrane resistance opposes current leaking across the plasma membrane while internal resistance opposes current flow through the cytoplasm
Graded potentials
Local membrane potential changes whose amplitude varies with stimulus strength. They may depolarize or hyperpolarize, can summate, have no threshold or refractory period, and decrease in strength with distance
Action potentials
Rapid all or none depolarizations used for long distance signaling. They require threshold, use voltage gated channels, have refractory periods, and regenerate without decreasing in amplitude
Graded potentials versus action potentials
Graded potentials vary in size, can summate, decrease with distance, and have no threshold while action potentials are all or none, cannot summate, require threshold, have refractory periods, and propagate without decrement
Stimulus intensity in graded versus action potentials
A stronger stimulus creates a larger graded potential, but once threshold is reached action potential amplitude stays the same. Stronger stimuli are represented by greater action potential frequency rather than larger action potentials
Threshold potential
Critical membrane potential at which enough voltage gated Na positive channels open to initiate the positive feedback phase of an action potential
Action potential depolarization
Threshold opens many voltage gated Na positive channels. Na positive rapidly enters the cell and further depolarization opens additional Na positive channels through positive feedback
Action potential peak
As membrane potential becomes positive, voltage gated Na positive channels begin to inactivate and slower voltage gated K positive channels open
Action potential repolarization
Na positive permeability falls as Na positive channels inactivate while K positive permeability rises. K positive leaves the cell and drives membrane potential back toward negative values
Action potential afterhyperpolarization
Voltage gated K positive channels close slowly, so K positive continues leaving after resting potential is reached and temporarily makes the membrane more negative than resting
Return to resting membrane potential after an action potential
Voltage gated K positive channels close, voltage gated Na positive channels reset, and normal leak channel permeabilities again dominate membrane potential
Why Na positive and K positive channels have different roles in an action potential
Voltage gated Na positive channels open rapidly and then inactivate while voltage gated K positive channels open more slowly and close slowly, creating depolarization followed by repolarization and hyperpolarization
Absolute refractory period
Period when another action potential cannot occur regardless of stimulus strength because voltage gated Na positive channels are already open or inactivated and have not yet reset
Relative refractory period
Period after the absolute refractory period when another action potential is possible but requires a stronger stimulus because some Na positive channels remain unavailable and K positive channels are still open
Functions of refractory periods
They limit maximum action potential frequency, keep individual action potentials separated, and help prevent backward propagation along the axon
Action potential propagation
Local current from an active region depolarizes the adjacent membrane to threshold, opening voltage gated Na positive channels and regenerating the action potential farther along the axon
Myelin
Multiple layers of glial cell membrane that electrically insulate axons and increase membrane resistance, reducing current leakage across the membrane
How myelin speeds action potential conduction
Less charge leaks through myelinated membrane so local current spreads farther and brings the next node of Ranvier to threshold more rapidly
Nodes of Ranvier
Gaps between myelin segments with a high density of voltage gated Na positive channels where action potentials are regenerated
Saltatory conduction
Propagation in a myelinated axon in which action potentials are regenerated only at nodes of Ranvier, making the signal appear to jump from node to node
Why myelin improves efficiency
Because ions cross primarily at nodes, fewer ions must later be restored by membrane pumps, making myelinated conduction faster and less metabolically expensive
Electrical versus chemical synapses
Electrical synapses directly connect neighboring cells through gap junction channels while chemical synapses release neurotransmitter across a synaptic cleft to receptors on a postsynaptic cell
Chemical synaptic transmission sequence
An action potential reaches the terminal, depolarization opens voltage gated Ca2 positive channels, Ca2 positive enters, vesicles fuse with the presynaptic membrane, neurotransmitter is released, neurotransmitter crosses the cleft and binds postsynaptic receptors
Direct trigger for neurotransmitter release
Ca2 positive entry through voltage gated Ca2 positive channels activates regulatory proteins and triggers synaptic vesicle exocytosis
Neurotransmitter
Chemical messenger released from a presynaptic neuron that binds receptors on a target cell and alters its activity
Termination of neurotransmitter signaling
Neurotransmitter can be removed by reuptake into the presynaptic terminal, uptake into glial cells, diffusion away, or enzymatic degradation
Ionotropic receptor
Postsynaptic receptor that contains an ion channel in its structure so neurotransmitter binding directly changes ion flow and produces a relatively rapid response
Metabotropic receptor
Postsynaptic receptor that acts through G proteins or second messenger pathways to indirectly alter ion channels and cellular activity, generally producing slower and more complex effects
Fast versus slow synaptic responses
Fast responses commonly involve direct ionotropic receptor effects on ion channels while slower responses involve metabotropic pathways and intracellular signaling that can last longer
Excitatory postsynaptic potential or EPSP
A depolarizing graded potential that moves the postsynaptic membrane closer to threshold, commonly because opening cation channels produces greater Na positive influx than K positive efflux
Inhibitory postsynaptic potential or IPSP
A graded response that hyperpolarizes or stabilizes the postsynaptic membrane and reduces the chance of reaching threshold, commonly through opening Cl negative or K positive channels
Why opening potassium channels is inhibitory
Increased K positive permeability allows more K positive to leave the cell, moving membrane potential toward the negative K positive equilibrium potential and away from threshold
Why opening chloride channels can be inhibitory
Cl negative entry can hyperpolarize the cell or stabilize membrane potential near rest so incoming positive charge from excitatory synapses has less effect
Postsynaptic inhibition
An inhibitory neurotransmitter acts directly on the postsynaptic neuron and produces an IPSP or stabilizes its membrane potential, making an action potential less likely
Presynaptic inhibition
A modulatory neuron acts on the presynaptic terminal and decreases neurotransmitter release before the signal reaches the postsynaptic cell
Presynaptic versus postsynaptic inhibition
Presynaptic inhibition reduces how much neurotransmitter is released from the sending neuron while postsynaptic inhibition directly changes the receiving neuron's membrane potential or excitability