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Membrane Potentials
● Basic Principles of Electricity
○ I. Separated electrical charges create the potential to do work, as occurs
when charged particles produce an electrical current as they flow down a
potential gradient. The lipid barrier of the plasma membrane is a
high-resistance insulator that keeps charged ions separated, whereas ionic
current flows readily in the aqueous intracellular and extracellular fluids.
● The Resting Membrane Potential
○ I. Membrane potentials are generated mainly by the diffusion of ions and
are determined by both the ionic concentration differences across the
membrane and the membrane’s relative permeability to different ions. + +
■ a. Plasma membrane Na /K -ATPase pumps maintain low
intracellular Na+ concentration and high intracellular K+
concentration.
■ b. In almost all resting cells, the plasma membrane is much more
permeable to K+ than to Na+, so the membrane potential is close to
the K+ equilibrium potential—that is, the inside is negative relative
to the outside.
■ c. The Na+/K+-ATPase pumps directly contribute a small
component of the potential because they are electrogenic.
● Graded Potentials and Action Potentials
○ I. Neurons signal information by graded potentials and action potentials
(APs).
○ II. Graded potentials are local potentials whose magnitude can vary and
that die out within 1 or 2 mm of their site of origin.
○ III. An AP is a rapid change in the membrane potential during which the
membrane rapidly depolarizes and repolarizes. At the peak, the potential
reverses and the membrane becomes positive inside. APs provide
long-distance transmission of information through the nervous system.
■ a. APs occur in excitable membranes because these membranes
contain many voltage-gated Na+ channels. These channels open as
the membrane depolarizes, causing a positive feedback opening of
more voltage-gated Na+ channels and moving the membrane
potential toward the Na+ equilibrium potential.
■ b. The AP ends as the Na+ channels inactivate and K+ channels
open, restoring resting conditions.
■ c. Depolarization of excitable membranes triggers an AP only when
the membrane potential exceeds a threshold potential.
■ d. Regardless of the size of the stimulus, if the membrane reaches
threshold, the AP generated is the same size.
■ e. A membrane is refractory for a brief time following an AP.
■ f. APs are propagated without any change in size from one site to
■ another along a membrane.
■ g. In myelinated nerve fibers, APs are regenerated at the nodes of
■ Ranvier in saltatory conduction.
■ h. APs can be triggered by depolarizing graded potentials in
sensory neurons, at synapses, or in some cells by pacemaker
potentials.
Synapses
● Activation of the Postsynaptic Cell
○ An excitatory synapse brings the membrane of the postsynaptic cell
closer to threshold
○ An inhibitory synapse prevents the postsynaptic cell from approaching
threshold by hyperpolarizing or stabilizing the membrane potential.
○ Whether a postsynaptic cell fires action potentials depends on the number
of synapses that are active and whether they are excitatory or inhibitory.
○ Neurotransmitters are chemical messengers that pass from one neuron to
another and modify the electrical or metabolic function of the recipient cell.
● Functional Anatomy of Synapses
○ Electrical synapses consist of gap junctions that allow current to flow
between adjacent cells.
○ In chemical synapses, neurotransmitter molecules are stored in synaptic
vesicles in the presynaptic axon terminal, and when released transmit the
signal from a presynaptic to a postsynaptic neuron.
● Mechanisms of Neurotransmitter Release
○ Depolarization of the axon terminal increases the Ca2+ concentration within
the terminal, which causes the release of neurotransmitter into the synaptic
cleft.
○ The neurotransmitter diffuses across the synaptic cleft and binds to
receptors on the postsynaptic cell; the activated receptors usually open ion
channels.
● Activation of the Postsynaptic Cell
○ At an excitatory synapse, the electrical response in the postsynaptic cell is
called an excitatory postsynaptic potential (EPSP).
○ At inhibitory synapses, it is either an inhibitory postsynaptic potential
(IPSP) or a stabilization of the membrane potential near resting levels.
○ Usually at an excitatory synapse, nonspecific cation channels in the
postsynaptic cell open, but Na+ flux dominates, because it has the largest
electrochemical gradient. At inhibitory synapses, channels to Cl− or K+
open.
● Synaptic Integration
○ The postsynaptic cell’s membrane potential is the result of temporal and
spatial summation of the EPSPs and IPSPs at the many active excitatory
and inhibitory synapses on the cell.
○ IAction potentials are generally initiated by the temporal and spatial
summation of many EPSPs.
● Synaptic Strength
○ Synaptic strength is modified by presynaptic and postsynaptic events,
drugs, and diseases (see Table 6.5).
○
● Neurotransmitters and Neuromodulators
○ In general, neurotransmitters cause EPSPs and IPSPs
○ Neuromodulators cause, via second messengers, more complex metabolic
effects in the postsynaptic cell.
○ The actions of neurotransmitters are usually faster than those of
neuromodulators.
○ A substance can act as a neurotransmitter at one type of receptor and as a
neuromodulator at another.
○ The major classes of known or suspected neurotransmitters and
neuromodulators are listed in Table 6.6.
■
● Neuroeffector Communication
○ Neuroeffector junction: the synapse between a neuron and an effector
cell is called a
○ The events at a neuroeffector junction (release of neurotransmitter into an
extracellular space, diffusion of neurotransmitter to the effector cell, and
binding with a receptor on the effector cell) are similar to those at synapses
between neurons.