chapter 4.5 Flashcards

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1
Q

Axodendritic synapses

A

synapses of axon terminal buttons on dendrites.

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2
Q

Dendritic spines

A

nodules of various shapes that are located on the surfaces of many dendrites. Many axodendritic synapses terminate on these.

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3
Q

Axosomatic synapses

A

synapses of axon terminal buttons on somas (cell bodies).

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4
Q

Dendrodendritic synapses

A

often capable of transmission in either direction.

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5
Q

Axoaxonic synapses

A

can mediate presynaptic facilitation and inhibition. An axoaxonic synapse on, or near, a terminal button can selectively facilitate or inhibit the effects of that button on the postsynaptic neuron.

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6
Q

Advantage of presynaptic facilitation and inhibition

A

is that they can selectively influence one particular synapse rather than the entire presynaptic neuron.

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7
Q

Directed synapses

A

synapses at which the site of neurotransmitter release and the site of neurotransmitter reception are in close proximity.

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8
Q

Nondirected synapses

A

synapses at which the site of release is at some distance from the site of reception.

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9
Q

String-of-bead synapses

A

neurotransmitter molecules are released from a series of varicosities (bulges or swellings) along the axon and its branches and thus are widely dispersed to surrounding targets.

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10
Q

Neuropeptides

A

large neurotransmitters; short amino acid chains comprising between 3 and 36 amino acids; in effect, they are short proteins. Assembled in the cytoplasm, like other proteins, of the cell body on ribosomes; they are then packed in vesicles by the cell body’s Golgi complex and transported by microtubules to the terminal buttons at a rate of about 40 cm a day.

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11
Q

Small-molecule neurotransmitters

A

typically synthesized in the cytoplasm of the terminal button packed in synaptic vesicles by the button’s Golgi complex. Once filled with neurotransmitters, the vesicles are stored in clusters next to the presynaptic membrane.

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12
Q

The vesicles that contain neuropeptides

A

are usually larger than those that contain small-molecule neurotransmitters, and they do not usually congregate as closely to the presynaptic membrane as the other vesicles do.

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13
Q

Coexistence

A

many neurons contain two neurotransmitters.

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14
Q

Exocytosis

A

the process of neurotransmitter release.

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15
Q

When a neuron is at rest

A

synaptic vesicles that contain small-molecule neurotransmitters tend to congregate near sections of the presynaptic membrane that are particularly rich in voltage-activated calcium channels.

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16
Q

Voltage-activated calcium channels

A

when stimulated by action potentials, these channels open, and Ca2+ ions enter the button. The entry of the Ca2+ ions cases synaptic vesicles to fuse with the presynaptic membrane and empty their contents into the synaptic cleft.

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17
Q

Small neurotransmitters are typically released in a pulse

A

each time an action potential triggers a momentary influx of Ca2+ ions through the presynaptic membrane.

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18
Q

Neuropeptides are typically released gradually

A

in response to general increases in the level of intracellular Ca2+ ions, such as might occur during a general increase in the rate of neuron firing.

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19
Q

Once released, neurotransmitter molecules

A

produce signals in postsynaptic neurons by binding to receptors in the postsynaptic membrane.

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20
Q

Receptors

A

a protein that contains binding sites for only particular neurotransmitters; thus, a neurotransmitter can influence only those cells that have receptors for it.

21
Q

Ligand

A

any molecule that binds to another is referred to as its ligand. Ex. A neurotransmitter is thus said to be a ligand of its receptor.

22
Q

Receptor subtypes

A

the different types of receptors to which a particular neurotransmitter can bind. The various receptor subtypes for a neurotransmitter are typically located in different brain areas, and they typically respond to the neurotransmitter in different ways.

23
Q

Ionotropic receptors

A

associated with ligand-activated ion channels. When the neurotransmitter molecule binds to this receptor, the associated ion channel usually opens or closes immediately, thereby inducing an immediate postsynaptic potential.

24
Q

Metabotropic receptors

A

associated with signal proteins and G proteins (guanosine-triphosphate-sensitive proteins). More prevalent than ionotropic receptors, and their effects are slower to develop, longer-lasting, more diffuse, and more varied. Many different kinds, but each is attached to a serpentine signal protein that winds its way back and forth through the cell membrane seven times. Attached to a protein of the signal poteen outside the neuron; G protein is attached to a portion of the signal protein inside the neuron.

25
Q

EPSPs (depolarizations)

A

usually occur because the neurotransmitter opens sodium channels, thereby increasing the flow of Na+ ions into the neuron.

26
Q

IPSPs (hyperpolarizations)

A

usually occur because the neurotransmitter opens potassium channels or chloride channels, thereby increasing the flow of K+ ions out of the neuron or the flow of CI- ions into it.

27
Q

When a neurotransmitter binds to a metabotropic receptor

A

a subunit of the associated G protein breaks away. Then, depending on the particular G protein, the subunit may move along the inside surface of the membrane and bind to a nearby ion channel, thereby inducing an EPSP or IPSP or it may trigger the synthesis of a chemical called a second messenger. Once created, a second messenger diffuses through the cytoplasm and may influence the activities of the neuron in a variety of ways.

28
Q

first messenger

A

neurotransmitters

29
Q

autoreceptors

A

one type of metabotropic receptor; have two unconventional characteristics: they bind to their neuron’s own neurotransmitter molecules; and they are located on the presynaptic, rather than the postsynaptic, membrane. Usual function is to monitor the number of neurotransmitter molecules in the synapse, to reduce subsequent release when the levels are high, and to increase subsequent release when they are low.

30
Q

Small-molecule neurotransmitters tend to be released

A

into directed synapses and to activate either ionotropic receptors or metabotropic receptors that act directly on the ion channels.

31
Q

Neuropeptides tend to be released

A

diffusely, and virtually all bind to metabotropic receptors that act through second messengers.

32
Q

The function of small-molecule neurotransmitters appears to be

A

the transmission of rapid, brief excitatory or inhibitory signals to adjacent cells.

33
Q

The function of neuropeptides appears to be

A

the transmission of slow, diffuse, and long-lasting signals.

34
Q

Two message-terminating mechanisms

A

reuptake by transporters and enzymatic degradation.

35
Q

reuptake

A

more common; the majority of neurotransmitters, once released, are almost immediately drawn back into the presynaptic buttons by transporter molecules.

36
Q

Enzymatic degradation

A

neurotransmitters are degraded in the synapse by the action of enzymes, which are proteins that stimulate or inhibit biochemical reactions without being affected by them.

37
Q

Acetylcholine

A

one of the few neurotransmitters for which enzymatic degradation is the main mechanism of synaptic deactivation and is broken down by the enzyme acetylcholinesterase.

38
Q

Once released, neurotransmitter molecules or their breakdown products are

A

drawn back into the button and recycled, regardless of the mechanism of their deactivation.

39
Q

The vesicles, once they have done their job, are drawn

A

back into the neuron from the presynaptic membrane and are used to create new vesicles.

40
Q

Astrocytes have been shown

A

to release chemical transmitters, to contain receptors for neurotransmitters, to conduct signals, and to influence synaptic transmission between neurons.

41
Q

Gap junctions

A

are narrow spaces between adjacent cells that are bridged by fine, tubular, cytoplasm-filled protein channels, called connexins. Connect the cytoplasm of two adjacent cells, allowing electrical signals and small molecules (ex. second messengers) to pass from one cell to the next. Sometimes called electrical synapses. Transmit signals more rapidly than chemical synapses.

42
Q

Recent research has established that glial cells (particularly astrocytes) and gap junctions

A

play major roles in brain function.

43
Q

Cerebral gap junctions

A

occur between all classes of cerebral cells; however, the majority of them seem to occur between cells of like kind.

44
Q

One function of gap junctions

A

appears to be to synchronize the activities of like cells in a particular area.

45
Q

Astrocytic organization

A

suggests that they too play a role of synchronizing activities of like cells in a particular area.

46
Q

Unlike neurons, astrocytes are

A

distributed evenly throughout a particular area, with only one astrocyte per location and little overlap between the projections of adjacent astrocytes. Suggests that each astrocyte coordinates the activities of neurons in its domain, and with as many as 40,000 processes, each astrocyte has a great potential to coordinate activity.

47
Q

Gap junctions on astrocytes

A

tend to occur at the end of each process, where it comes in contact with processes from adjacent astrocytes.

48
Q

The fact that many astrocytic processes wrap around synapses and are connected to both presynaptic and postsynaptic neurons by gap junctions suggests

A

that each astrocyte may coordinate the activity of synapses in its domain.

49
Q

Tripartite synapse

A

the hypothesis that synaptic transmission depends on communication among three cells (presynaptic neuron, postsynaptic neuron, and astrocyte) via gap junctions.