Unit 1 Flashcards

(41 cards)

1
Q

Who was Cajal and what did he contribute? What specific technique helped him make this contribution?

A

A scientist who found that there was a gap between the synapses by using Golgi stains

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2
Q

What are two basic types of cells in the brain and spinal cord?

A

Neurons & Glia Cells (astrocytes, oligodendrocytes, microglia, radial glia)

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3
Q

Structure components of a neuron

A

Soma, axon, dendrites, myelin, synaptic cleft, axon hillock

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4
Q

Internal components of a neuron

A

Nucleus, ribosomes, mitochondria, endoplasmic reticulum (ER), membrane

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5
Q

Describe the cell membrane.

A

A lipid bilayer that halts most chemicals aside from those with a protein channel (i.e., water, sodium, potassium, calcium,, chloride, etc.)

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6
Q

What are dendrites and spines? What is their functional role?

A

They are lined with synaptic receptors, and they help to receive messages from other neurons. The more spines and dendrites there are, the greater the surface area for synapses

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7
Q

Astrocytes

A

Creates blood-brain barrier, limit where neurotransmitters go

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8
Q

Oligodendrocytes

A

Creates the myelin sheaths along the axon in central nervous system

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9
Q

Radial Glia

A

Help in development for neurons to migrate, can change over time and become different neurons

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10
Q

Microglia

A

Very powerful in removing waste material and signal for immune resins

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11
Q

Discuss the blood brain barrier. What is active transport?

A

Blocks most chemicals, viruses, and bacteria from entering the brain, but also blocks out useful chemicals. Active transport is a protein-mediated process that expends energy to pump chemicals from the blood to the brain.

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12
Q

What is the action potential and what does it have to do with neurons?

A

Also known as a nerve impulse, it is the electrical signal that is transmitted down the axon of a neuron. Within the neuron, it is a rapid depolarization

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13
Q

Labels on a nerve impulse graph

A
  1. resting
  2. threshold
  3. depolarization
  4. AP
  5. repolarization
  6. hyper polarization
  7. refractory period
  8. resting
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14
Q

Describe the electrical gradient. How is it maintained?

A

The difference of electrical charges between inside and outside the membrane, who maintains the gradient.

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15
Q

What is the resting potential? Describe it and state the charge associated with it.

A

Difference in voltage in a resting neuron that is about -70 mv.

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16
Q

What are voltage-activated channels, and how do they work?

A

Permeability depends on the voltage difference across the membrane. As the membrane depolarizes, sodium rushes in to create an AP while potassium rushes out.

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17
Q

What is something that helps to maintain the resting state?

A

Sodium potassium pump restores ion distribution

18
Q

What is myelin and what makes myelin in the CNS and the PNS?

A

It is composed of fats and proteins that helps the AP to regenerate at each Node of Ranvier. Oligodendrocytes make myelin

19
Q

Describe salutatory conduction. How do demyelinating disorders disturb this process?

A

Jumping of an AP from node to node and it provides rapid conduction of impulses & conserves energy. Without the myelin, the axon lacks sodium channels causing most APs to die out between one node and the next.

20
Q

What are local neurons and graded potentials?

A

Local neurons have short axons and do not produce APs. Instead, they produce graded potentials, a membrane potential that varies in magnitude in proportion to the intensity of the stimulus

21
Q

What are three main contributions that Sherrington made? What term did he coin?

A
  1. Validation of the synapse (term he coined) - reflexes are slower than conduction along one axon
  2. Summation - several weak stimuli can produce a stronger reflex
  3. Interneuron inhibition - as one set of muscles contracts, the other relaxes
22
Q

How is the vagus nerve related to the brain, the gut, and other organs like the heart?

A

The gut, also known as the second brain, communicates with the actual brain via the vagus nerve. (Loewi decreases the heart rate of a second frog by stimulating the vagus nerve on the first and transferring that NT to it)

23
Q

Explain temporal and spatial summation. What are EPSPs & IPSPs? What does the axon hillock have to do with EPSPs & IPSPs?

A

Temporal: repeated stimuli over a time has a cumulative and stronger effect
Spatial: several small stimuli on a similar location produced a reflection when a single stimulus did not
EPSPs: positive grade potential that decays over time and space
IPSPs: synaptic input selectively opens the gates for potassium (+) to leave or for chloride (-) to enter
Summation occurs on the axon hillock

24
Q

State the major categories of NTs.

A

Amino acids, monoamines, acetylcholine, neuropeptides, purines, gases, nitric oxide

25
What are the steps in the chemical events at the synapse?
1. Synthesis 2. Transported 3. Release with calcium 4. Binds 5. Separates 6. Removed (Diffusion, reuptake, enzymatic degradation) 7. Feedback
26
Describe the process of NT release; use the terms (e.g., vesicles and exocytosis). What is a negative feedback loop?
The AP causes the vesicles to fuse/merge with the membrane which causes the NT to be excreted out through exocytosis. IT is a feedback mechanism that alters activity of the presynaptic neuron
27
Discuss the role of hormones and how they work. Explain the general role of the pituitary gland and the hypothalamus.
They coordinate long-lasting changes in multiple parts of the body by being transported through the blood stream to any receiver tuned in to the right station. The hypothalamus contains the pituitary and causes it to release hormones and maintains fairly constant circulating levels of certain hormones through a neg. feedback system
28
Define the relevant terms (e.g., agonist, antagonist, efficacy, and affinity).
Agonist: mimics or increase the effects of NTs Antagonist: blocks the effects of NTs Efficacy: tendency to activate receptor (key turns lock) Affinity: ability to bind to receptor (key in)
29
Characterize (explain) some of the ways that drugs can alter synaptic activity. What are the terms you learned?
It can: alter the synthesis of NTs, cause vesicles to leak, increase release of NTs, decrease reuptake of NTs, block enzymatic breakdown, stimulate or block receptors
30
Describe Olds and Milner’s experiment.
They placed rats in boxes where they could press a lever to produce electrical self-stimulation of the brain. The rats pressed the lever up to 2000 times per hour, the stimulation causing the release of Da.
31
State the major drug categories that we covered in lecture.
Stimulants, analgesics, cannabinoids, hallucinogens, depressants
32
How are the nucleus accumbens and dopamine related to substance abuse and addictions?
Axons would directly or indirectly increase the release of dopamine or norepinephrine in the nucleus accumbens (accumbens activated when imagine something pleasant).
33
How do amphetamines and cocaine alter synaptic activity?
Amphetamines increase the release of Da, reversing the transporter, while cocaine blocks the reuptake of Da, causing it to linger in the synapse longer and bind to receptors.
34
What is the drug classification for opioids and how do they alter synaptic activity?
Analgesics, they bind to the medulla.
35
How do endorphins work and what is their purpose?
Endorphins inhibit an inhibitor (neurons that release GABA), thereby increasing dopamine release. They are endogenous morphines and relieve pain by acting on receptors in the brain
36
Describe how cannabinoids alter synaptic activity and state what is unusual about their mechanism of action.
The receptors are located on the presynaptic neuron, making it different, and use retrograde transport by sending messages backwards that can bind to the receipt and tell it to slow down or stop (modulates activity going backwards).
37
What did you learn about alcohol, toxicity, acetaldehyde, and enzymes? What are some of the physiological effects of alcohol- include the BBB and GABA.
Alcohol disrupts the lipid bilayer causing it to increase in membrane fluidity which damages the DNA as it leaks. As alcohol is metabolized, it is transformed into acetaldehyde by alcohol dehydrogenase, and then turned into acetic acid by acetaldehyde hydrogenase. It easily passes through the BBB, enhances response of GABA receptors, and inhibits potassium and sodium ions.
38
What does conditioning and environmental stimuli have to do with drug addiction?
- Positive reinforcement (perceived effects, makes them an addicts) & negative (withdrawal avoidance, reinforcement maintains) - classical conditioning in which the body often engages in a compensatory process - incentive-sensitization where drug related stimuli are linked to the reinforcement effects of Da release
39
Define tolerance and withdrawal.
Tolerance: can handle larger and larger amounts of the drug Withdrawal: physiological and psychological changes when the drug is not in the system
40
Conditioning
Cravings in response to cues
41
Brain reorganization
Other kinds of reinforcing experiences become less powerful, less able to compete with the drug