Jose's Deck Flashcards

1
Q

Neurotransmitters are identified using four experimental criteria: _______, _______, ________, and _______.

A

synthesis, release, receptor action, inactivation

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2
Q

The three broad classes of chemically related neurotransmitters are ______, _______, and ______. All three classes, encompassing the approximately 100 likely neurotransmitters active in the nervous system, are associated with both _______, and _______ receptors.

A

small-molecule transmitters, peptide transmitters, transmitter gases; ionotropic, metabotropic

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3
Q

Contrast the major characteristics of ionotropic and metabotropic receptors.

A
  • An ionotropic receptor contains a pore or channel that can be opened or closed to regulate the flow-through of ions, directly bringing about rapid and usually excitatory voltage changes on the cell membrane.
  • Metabotropic receptors are generally inhibitory, are slow acting, and activate second messengers to indirectly produce changes in the function and structure of the cell.
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4
Q

Although neurons can synthesize more than one _______, they are usually identified by the principal ______ in their axon terminals.

A

neurotransmitter; neurotransmitter

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5
Q

In the peripheral nervous system, the neurotransmitter at somatic muscles is ______; in the autonomic nervous system, ______ neurons from the spinal cord connect to _____ neurons for parasympathetic activity and with ______ neurons for sympathetic activity,

A

acetylcholine; acetylcholine; acetylcholine; norepinephrine

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6
Q

The four main activating systems of the brain are _____, _______, ________, and _______.

A

cholinergic, dopaminergic, noradrenergic, serotonergic

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7
Q

How would you respond to the comment that a behavior is caused solely by a “chemical imbalance in the brain”?

A

This idea has been attractive for a long time because there is a clear relationship between DA los and Parkinson’s disease, and acetylcholine and norepinephrine are clearly related to somatic and autonomic behaviors. But for other neurotransmitters in the brain, establishing a clear one-to-one relationships has proved difficult.

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8
Q

Most drugs that have psychoactive effects influence chemical reactions at neuronal _______. Drugs that influence communication between neurons do so either as ______ (increasing the effectiveness of neurotransmission) or as _______ (decreasing the effectiveness of neurotransmission)

A

synapses; agonists; antagonists

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9
Q

The body eliminates drugs through:

A

urine, feces, sweat, breath, breast milk

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10
Q

Antianxiety and sedative-hypnotic drugs affect the _______ receptor, which through ______ influx hyperpolarizes neurons.

A

GABAa; Cl-

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11
Q

Among the antidepressant drug types, ______ increase the amount of serotonin available in the presynaptic terminal while ______ block serotonin reuptake at the synapse.

A

MAO inhibitors; SSRIs

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12
Q

Opiods mimic the action of _____ by binding to the same receptors

A

endorphins

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13
Q

Amphetamine stimulates ______ and cocaine blocks ______ at the _______ synapse

A

release, reuptake, D2

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14
Q

On which neurotransmitters do drugs that produce psychotropic effects act?

A

Psychotropic drugs act on many neurotransmitters, including acetylcholine, anandamide, dopamine, epinephrine, glutamate, norepinephrine, and serotonin.

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15
Q

_________ are energy filters that transduce incoming physical energy into neural activity.

A

sensory receptors

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16
Q

______ fields locate sensory events. Receptor _____ determines sensitivity to sensory stimulation.

A

receptive; density

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17
Q

We distinguish one sensory modality from another by its _______

A

target in the brain

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18
Q

Neurons that project into the brain from the retina and form the optic nerve are called ______.

A

retinal ganglion cells

19
Q

The two major pathways from the retina into the brain are ______ and ______.

A

geniculostriate; tectopulvinar

20
Q

Damage to the fusiform face area in the temporal lobe can produce ______.

A

facial agnosia or prosopagnosia

21
Q

Contrast the paths and functions of the dorsal and ventral streams.

A

The dorsal stream to the parietal lobe processes the visual guidance of movements (the how). The ventral stream to the temporal lobe processes the visual perception of objects (the what)

22
Q

blob

A

`Region in the visual cortex that contains color-sensitive neurons, as revealed by staining for cytochrome oxidase.

23
Q

interblobs

A

Neurons in the interblobs participate in form and motion perception.

24
Q

thin stripes

A

receive input from V1’s color-sensitive neurons

25
Q

thick stripes

A

receive input from the movement-sensitive neurons in region V1

26
Q

pale zones

A

receive input from V1’s form-sensitive neurons.

27
Q

_______ retinal ganglion cells receive input mostly from cones and carry information about color and fine detail, whereas ______ retinal ganglion cells receive input mostly from rods and carry information about light but not color

A

P or parvocellular; M or magnocellular

28
Q

What is the excitatory transmitter in the amphibian heart and mammalian heart

A

amphibian - EP

mammalian - NE

29
Q

What neural pathway is involved in Parkinson’s disease?

A

the pathway connecting the substantia nigra to the basal ganglia

30
Q

Type I synapses

A
  • Excitatory
  • Located on the shafts or the spines of dendrites
  • round synaptic vesicle
  • Denser material on pre/post-synaptic membrane than Type II synapses
  • wider synaptic cleft
  • larger active zone
31
Q

Type II synapses

A
  • Inhibitory
  • located at cell body
  • flattened vesicles
  • less dense membrane
  • narrower synaptic cleft
  • smaller active zone
32
Q

How does the body get Acetylcholine?

A

Typically synthesized from dietary nutrients and packaged ready for use in axon terminals. Small-molecule transmitters can have their level and activity influenced by diet.

33
Q

How do neuroactive drugs typically reach the brain?

A

the digestive track

34
Q

Steps of acetylcholine synthesis

A
  1. Acetyl CoA carries acetate to the transmitter-synthesis site.
  2. ChAT transfers acetate to choline to form ACh
  3. In the synaptic cleft, AChE detaches acetate from choline.
  4. The products of the breakdown can be taken up and reused
35
Q

What are the main excitatory and inhibitory neurotransmitters in the forebrain and cerebellum?

A

excitatory - glutamate

inhibitory - GABA

36
Q

What is a second messenger?

A
  • It is activated by the enzyme which was activated by an alpha subunit.
  • the second messenger can:
    1) bind to an ionotropic channel and alter ion flow
    2) initiate a reaction that causes protein molecules to become incorporated into the cell membrane
    3) instruct the cell’s DNA to initiate or cease the production of a protein
37
Q

Are any neurotransmitters associated with a single receptor type?

A

NO. A neurotransmitter may bind either to an ionotropic receptor and have an excitatory effect on the target cell or to a metabotropic receptor and have an inhibitory effect.
- ACh has an excitatory effect on skeletal muscles by activating ionotropic receptors. ACh has an inhibitory effect on heart rate by activating metabotropic receptors.

38
Q

What single main receptor serves the SNS?

A

nicotinic ACh receptor (nAChr)

  • when Ach binds to this receptor, its pore opens to permit ion flow, thus depolarizing the muscle fiber.
  • the pore of a nicotinic receptor is large and permits the simultaneous efflux of K+ and influx of Na+
39
Q

What prepares the body for “fight or flight”

A

ACh neurons in the CNS synapse with sympathetic NE neurons prepare the body’s organs

40
Q

What prepares the body for “rest and digest”

A

ACh neurons in the CNS synapse with autonomic ACh neurons in the parasympathetic division

41
Q

What type of channel do GABAa receptors have?

A

A Cl- channel

42
Q

Group I: Antianxiety agents and sedatives

A

Benzos, Barbituates, Anesthetics: GHB, ketamine, PCP

43
Q

MAOI

A

Antidepressant drug that blocks the enzyme monoamine oxidase from degrading neurotransmitters such as dopamine, noradrenaline, and serotonin.

44
Q

tricyclic antidepressant

A

First-generation antidepressant drug with a chemical structure characterized by three rings that blocks serotonin reuptake transporter proteins.