Synapse Flashcards

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1
Q

Charles Scott Sherrington

A

physiologically demonstrated that communication between one neuron and the next differs from communication along a single axon

tested reflex of dog and found flexion and extension reflexes

based on timing of reflex he figured out that the reflexes are slower than an action potential on the length of the axon

he inferred that there were gaps between axons that were slowing things down

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2
Q

synapse

A

a specialized gap between neurons

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3
Q

flexion reflex

A

sensory neuron excites a second neuron, which in turn excites a motor neuron, which excites a muscle

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4
Q

reflex arc

A

The circuit from sensory neuron to muscle response

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5
Q

temporal summation

A

repeated stimuli within a brief time have a cumulative effect

although the subthreshold excitation in the postsynaptic neuron decays over time, it can combine with a second excitation that follows it quickly

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6
Q

presynaptic neuron

A

neuron that delivers transmission

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7
Q

postsynaptic neuron

A

the one that receives the transmission

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8
Q

excitatory postsynaptic potential (EPSP)

A

graded depolarization

partial depolarization is a graded potential

results from a flow of sodium ions into the neuron

if an EPSP does not cause the cell to reach its threshold, the depolarization decays quickly.

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9
Q

spatial summation

A

summation over space

Synaptic inputs from separate locations combine their effects on a neuron.

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10
Q

Inhibitory Synapses

A

A pinch on the foot sends a message along a sensory neuron to an interneuron (an intermediate neuron) that excites the motor neurons connected to the flexor muscles of that leg and the extensor muscles of the other legs

the interneuron sends messages to inhibit the extensor muscles in that leg and the flexor muscles of the three other legs

input from an axon hyperpolarizes the postsynaptic cell.

it increases the negative charge within the cell, moving it farther from the threshold and decreasing the probability of an action potential

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11
Q

inhibitory postsynaptic potential (IPSP)

A

occurs when synaptic input selectively opens the gates for potassium ions to leave the cell (carrying a positive charge with them) or for chloride ions to enter the cell (carrying a negative charge)

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12
Q

spontaneous firing rate

A

a periodic production of action potentials even without synaptic input

EPSPs increase the frequency of action potentials above the spontaneous rate, whereas IPSPs decrease it

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13
Q

discovery of chemical transmission at synapse

A

Otto Loewi

repeatedly stimulated the vagus nerve, thereby decreasing a frog’s heart rate

collected fluid from around that heart, transferred it to a second frog’s heart, and found that the second heart also decreased its rate of beating

did the same to increase the heart rate and did the same

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14
Q

Sequence of Chemical Events

at a Synapse

A
  1. The neuron synthesizes chemicals that serve as neu- rotransmitters. It synthesizes the smaller neurotransmit- ters in the axon terminals and synthesizes neuropeptides in the cell body.
  2. Action potentials travel down the axon. At the presynap- tic terminal, an action potential enables calcium to enter the cell. Calcium releases neurotransmitters from the terminals and into the synaptic cleft, the space between the presynaptic and postsynaptic neurons.
  3. The released molecules diffuse across the narrow cleft, attach to receptors, and alter the activity of the postsynap- tic neuron. Mechanisms vary for altering that activity.
  4. The neurotransmitter molecules separate from their receptors.
  5. The neurotransmitter molecules may be taken back into the presynaptic neuron for recycling or they may diffuse away.
  6. Some postsynaptic cells send reverse messages to control the further release of neurotransmitter by presynaptic cells.
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15
Q

neurotransmitters

A

chemicals that affect another neuron

hundred or so kinds known or suspected

includes amino acids, modified amino acids, monoamines, neuropeptides, purines, gases

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16
Q

nitric oxide

A

gas released by many small local neurons

neurons release nitric oxide when they are stimulated

influencing other neurons, nitric oxide dilates the nearby blood vessels, thereby increasing blood flow to that brain area

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17
Q

tryptophan

A

precursor to serotonin

serotonin levels rise after you eat foods richer in tryptophan, such as soy, and fall after something low in tryptophan, such as maize

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18
Q

Serotonin

A

Involved in many functions, including mood, appetite, sleep, and aggression.

Low levels of serotonin are associated with depression, and some drugs designed to treat depression (known as selective serotonin reuptake inhibitors, or SSRIs) serve to prevent their reuptake.

likely matabotropic

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19
Q

Glutamate

A

The most common neurotransmitter, it’s released in more than 90% of the brain’s synapses. Glutamate is found in the food additive MSG

Excess glutamate can cause overstimulation, migraines and seizures.

Usually ionotropic

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20
Q

GABA (gamma-aminobutyric acid)

A

The major inhibitory neurotransmitter in the brain.

Alcohol stimulates the release of GABA, which inhibits the nervous system and makes us feel drunk. Low levels of GABA can produce anxiety, and GABA agonists (tranquilizers) are used to reduce anxiety

mostly ionotropic

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21
Q

Endorphins

A

Released in response to behaviors such as vigorous exercise, orgasm, and eating spicy foods.

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22
Q

Dopamine

A

Involved in movement, motivation, and emotion, Dopamine produces feelings of pleasure when released by the brain’s reward system, and it’s also involved in learning

likely metabotropic

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23
Q

Acetylcholine

A

A common excitatory neurotransmitter used in the spinal cord and motor neurons to stimulate muscle contractions. It’s also used in the brain to regulate memory, sleeping, and dreaming.

acetylcholine attaches as in Figure 2.15b, the receptor folds outward, widen- ing the sodium channel

24
Q

synthesis of neurotrnsmitters

A

Most neurotransmitters are synthesized in the presynaptic terminal, near the point of release

25
Q

vesicles

A

presynaptic terminal stores high concentrations of neurotransmitter molecules in vesicles, tiny nearly spherical packets

26
Q

MAO (monoamine oxidase)

A

Neurons that release serotonin, dopamine, or norepinephrine contain an enzyme, MAO (monoamine oxidase), that breaks down these transmitters into inactive chemicals, thereby preventing the transmitters to accumulate to harmful levels.

27
Q

exocytosis

A

bursts of release of neurotransmitter from the presynaptic neuron

depolarization opens voltage- dependent calcium gates in the presynaptic terminal, 1 or 2 milliseconds (ms) after calcium enters the terminal, it causes exocytosis

spreads across the cleft to the postsynaptic receptor

neurons release a combination of two or more transmitters at a time

28
Q

ionotropic effects

A

on-off effect of neurotransmitters on a receptor site; brief on off effect;

like a paper bag twisted opening and closing to allow a particular type of ion through

29
Q

transmitter-gated or ligand-gated

A

(A ligand is a chemical that binds to something.)

compared to voltage gated

when the neurotransmitter attaches, it opens a channel. Ionotropic effects begin quickly, sometimes within less than a millisecond after the transmitter attaches

effect decays very quickly

30
Q

Glycine

A

another common inhibitory transmitter

31
Q

inhibitory ionotropic neurotransmitters

A

opens chloride gates, enabling chloride ions, with their negative charge, to cross the membrane into the cell more rapidly than usual

32
Q

Metabotropic Effects and Second

Messenger Systems

A

initiating a sequence of metabolic reactions that start slowly but last longer than ionotropic effects

effects emerge 30 ms or more after the release of the transmitter

it bends the receptor protein that goes through the membrane of the cell. The other side of that receptor is attached to a G protein—that is, a protein coupled to guanosine triphosphate (GTP), an energy- storing molecule

Bending the receptor protein detaches that G protein, which is then free to take its energy elsewhere in the cell

the result of that G protein is increased concentration of a second messenger, such as cyclic adenosine monophosphate (cyclic AMP), inside the cell. Just as the “first messenger” (the neurotransmitter) carries information to the postsynaptic cell, the second messenger communicates to areas within the cell

by way of its second messenger, influences activity in much or all of the cell and over a longer time.

33
Q

Ionotropic vs metabotropic synapses

A

vision and hearing, the brain needs rapid, up-to-date information, the kind that ionotropic synapses bring

metabotropic synapses are better suited for more enduring effects such as taste; also important for many aspects of arousal, attention, pleasure, and emotion

34
Q

neuropeptides

A

neuromodulators, because they have properties that set them apart from other transmitters

synthesized in the cell body and then slowly transports them to other parts of the cell

neuropeptides are released mainly by dendrites, and also by the cell body and by the sides of the axon

neuropeptide release requires repeated stimulation

they resemble hormones diffuse widely, slowly affecting many neurons in their region of the brain

important for hunger, thirst, and other long-term changes in behavior and experience

35
Q

acetylcholine inactivation

A

broken down by a specific enzyme into acetate and choline

choline diffuses back to the presynaptic neuron and reconnects it with acetate already in the cell

36
Q

catecholamines

A

serotonin, dopamine, norepinephrine, and epinephrine

37
Q

reuptake

A

presynaptic neuron takes up much or most of the released neurotransmitter molecules intact and reuses them

occurs through special membrane proteins called transporters

one not taken up are broken down by another enzyme and excreted through blood and urine

38
Q

amphetamine and cocaine

A

inhibit the transporters for dopamine, serotonin, and norepinephrine, thus decreasing reuptake and prolonging the effects of the neurotransmitters

39
Q

autoreceptors

A

many presynaptic terminals have receptors sensitive to the same transmitter they release

receptors that respond to the released transmitter by inhibiting further synthesis and release

40
Q

Other Forms of Negative Synaptic Feedback

A

some postsynaptic neurons respond to stimu- lation by releasing chemicals that travel back to the pre- synaptic terminal to inhibit further release of transmitter

nitric oxide
hydrogen ions

41
Q

Cannabinoids

A

the chemicals in marijuana decrease both excitatory and inhibitory messages from neurons that release glutamate, GABA, and other transmitters. In various cases the result can be either brief or more long-lasting suppression of release

resulting in decreased anxiety

42
Q

Electrical Synapses

A

faster than even the fastest chemical trans- mission, electrical synapses have evolved in cases where ex- act synchrony between two cells is important

eg, rhythmic breathing

43
Q

gap junction

A

the membrane of one neuron comes into direct contact with the membrane of another, in electrical synapses

large pores of the membrane of one neuron line up precisely with similar pores in the membrane of the other cell where sodium and other ions pass readily

act is if a single neuron

44
Q

Hormones

A

a chemical secreted by cells in one part of the body and conveyed by the blood to influence other cells

function like a radio instead of a telephone

useful for coordinating long-lasting changes in multiple parts of the body

45
Q

Two types of hormones

A

protein hormones and peptide hormones

proteins are longer and peptides are shorter

attach to membrane receptors, where they activate a second messenger within the cell—exactly like a metabotropic synapse

46
Q

pituitary gland

A

responsible for producing hormones

consists of anterior pituitary and the posterior pituitary

47
Q

posterior pituitary

A

composed of neural tissue, can be considered an extension of the hypothalamus. Neurons in the hypothalamus synthesize the hormones oxytocin and vasopressin

migrate down axons to the posterior pituitary, where they are released into the blood

48
Q

anterior pituitary

A

composed of glandular tissue, synthesizes six hormones, although the hypothalamus controls their release

hypothalamus secretes releasing hormones, which flow through the blood to the anterior pituitary. There they stimulate or inhibit the release of other hormones.

49
Q

hypothalamus

A

maintains fairly constant circulating levels of certain hormones through a negative feedback system

eg,
when the level of thyroid hormone is low, the hypothalamus releases TSH-releasing hormone, which stimulates the anterior pituitary to release TSH, which in turn causes the thyroid gland to secrete more thyroid hormones

50
Q

COMT

A

(catechol-o-methyltransferase) any transmitter molecules that the transporters do not take will instead break down by an enzyme called COMT

51
Q

amphetamine and cocaine,

A

Stimulant drugs, including amphetamine and cocaine, inhibit the transporters for dopamine, serotonin, and norepinephrine, thus decreasing reuptake and prolonging the effects of the neurotransmitters

52
Q

LSD/Hallucinogenic drugs

A

attach to serotonin type 2A (5-HT2A) receptors and provide stimulation at inappropriate times or for longer-than-usual durations. LSD increases the connections among brain areas that ordinarily do not communicate much with one another.

53
Q

Nicotine

A

stimulates a family of acetylcholine receptors, conveniently known as nicotinic receptors. Because nicotinic receptors are abundant on neurons that release dopamine, nicotine increases dopa- mine release

54
Q

Opiate drugs

A

opiates relieve pain by act- ing on receptors in the brain as well as in the skin.

opiates attach to specific receptors in the brain

bind to same receptors as endorphons?

55
Q

Cannabinoids

A

bind to anandamide or 2-AG receptors on presynaptic neurons, indi- cating, “The cell got your message. Stop sending it.

56
Q

anandamide and 2-AG

A

like nitric oxide, other reverse transmitters

respond to stimu- lation by releasing chemicals that travel back to the pre- synaptic terminal to inhibit further release of transmitter