Lecture 3 Flashcards

1
Q

What processes take place in the cell nucleus?

A

Genetic and metabolic

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2
Q

What kinds of neurites are there?

A

Entrance (carry information to the soma) = dendrites
Exit neurites (carry information away from the soma) = axon

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3
Q

What is in the soma?

A

membrane (encasing of the whole cell), nucleus (with DNA in it that codes for proteins), mitochondria, ribosomes (genetic material is translated into proteins), endoplasmatic reticulum, golgi complex (molecules like proteins are packaged, “stamped with an address” and sent off to another place in the cell)

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4
Q

Dendritic spines

A

Structures on the dendrites, onto which other neurons can synapse

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5
Q

Along what are packaged proteins transported from the soma to the axon terminal?

A

Microtubulin of the axon by the kinesin

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6
Q

What can happen with the proteins in the axon terminal?

A
  1. Taken up into the membrane
  2. Catalyze chemical reactions if it’s an enzyme
  3. If it’s a neurotransmitter protein it’s kept in a vesicle and then after stimulus, it might be released
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7
Q

Axon per cell

A

1, but it might branch enabling contact with many neurons

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8
Q

Membrane proteins involved in neurotransmission

A

Channel, gated channel, pump

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9
Q

Classification of neurons by location

A

Projection neuron, interneuron, other (motor, sensory neurons)

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10
Q

Classification of neurons by structure

A

multipolar, bipolar, pseudo-unipolar

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11
Q

Neurons use it as fuel

A

Glucose (it can pass through the blood-brain barrier, can be synthesized by the liver)

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12
Q

Types of glial cells

A

Astrocytes, Oligodendrocytes, Schwann-cells, microglia

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13
Q

Astrocytes functions

A

-Give the brain structure
-Important role in blood-brain barrier (assist in making the vessels that go into your brain really impermeable) - Play an important role in maintaining the tight junctions between the cells that make up the blood vessels
-‘Covers’ the synapse, clears excess neurotransmitters

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14
Q

Oligodendrocyte function

A

Makes myelin - extensions that roll around axons, can service multiple cells,

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15
Q

Schwann cell function

A

Make myelin - multiple Schwann cells are needed to cover one projection axon

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16
Q

Microglia function

A

Inflammation makes them change shape, and become big. They eat dead material. They are part of the immune system

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17
Q

Regeneration of neurons

A

If soma is damaged –> no regeneration
If the axon gets damaged –> regeneration

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18
Q

Axon regeneration

A

The part still attached to the soma may sprout. Myelin sheets that were around it originally, retract, stay where they are and mark where the new axon should go. After the axon sprouts and grows out, the myelin sheath starts forming around it again.

19
Q

Blood-brain barrier

A

The border between blood and brain fluid is more selective in letting things through. Blood vessels are even more selectively permeable in the brain. Passive transport can occur for lipids and for small molecules (e.g. oxygen, CO2). Active transport occurs for bigger molecules like glucose, amino-acids (nutrients).

20
Q

Function of blood-brain barrier

A

Maintain the composition of the brain fluid (keep it constant).

21
Q

General function of glial cells

A

-Formation of myelin
-Insulation of the nerve fiber
-Removing dead neurons and waste
-Uptake and release of neurotransmitters/ions from the synaptic cleft
-Forming tight-junctions
-Guiding migration of neurons (radial glia)

22
Q

Resting potential

A

-70 mV

23
Q

Neurons get charged

A

Because of the protein pumps that pump ions: 3 Na+ is pumped out, 2 K+ gets pumped in - Sodium-potassium pump

24
Q

Ions encounter 2 forces

A
  1. Electrical gradient
  2. Chemical gradient

–> The sum of the 2 forces determines whether an ion will diffuse in or out

25
Q

Cl- concentration

A

Lower inside than outside. When Cl- channel opens, Cl- flows in –> Bigger concentration gradient

26
Q

Graded potentials

A

EPSPs: chemical stimulus in the synapse (neurotransmitter) –> Na+ channels open in the postsynaptic terminal –> Positive charge (Na+ ions) flow in, diffuse along membrane –> local depolarization of the cell-membrane
IPSPs: neurotransmitter is released in the synaptic cleft –> CL- channels–> negative charge flows in –> membrane hyperpolarizes locally

27
Q

Graded potentials move along the cell …

A

Passively, current fades away over distance. (because of outward leakage of K+ ions and diffusion of charge over increasingly large surface)

28
Q

What neurons have only graded potentials?

A

Some local neurons (interneurons)

29
Q

Action potential

A

When depolarization reaches a certain threshold (firing threshold)–> action potential

30
Q

Molecular basis of action potential

A

Voltage-dependent Na+ channels in axon hillock (closed at resting potential) –> Open when the membrane locally depolarizes to a certain threshold level–> Massive influx of Na+ –> action potential is triggered

31
Q

Why can action potentials only happen in the axon?

A

Because voltage-gated channels can only be found there

32
Q

Termination of action potential

A

2 slower processes:
1. Opening of voltage-dependent K+ channels (also open because of depolarization, but with a delay) –> K+ flows out –> cell becomes hyperpolarized
2. Inactivation of voltage-dependent Na+ channels

33
Q

Refractory period

A

Right after the action potential, the cell can’t fire for about 1 ms. Cells have to be stimulated stronger during 2-4 ms after action potential to fire again

34
Q

All or none law

A

All action potentials of cell are equal (in amplitude, duration, propagation speed, shape)

35
Q

Larger stimulation leads to…

A

More action potentials

36
Q

Saltatory conduction

A

Under the myelin: passive conduction
At the nodes of Ranvier active conduction (because there are voltage-dependent Na+ channels.) Action potential is refreshed/renewed at each node of Ranvier.

37
Q

Types of synapses

A

Electrical
Chemical

38
Q

Electrical synapses

A

Gap junctions between the presynaptic and the postsynaptic terminal, through which ions float from one cell to the other (current, electrical propagation from one to the other cell)

39
Q

Chemical synapses

A

Most synapses are chemical

40
Q

How electrochemical synapses work

A

There are neurotransmitters in the vesicles at the presynaptic terminal. Action potential comes down –> Depolarization of presynaptic terminal –> Opening of voltage-gated Ca2+ channels –> Influx of Ca2+ into the terminal –> Ca2+ through a chemical reaction that requires it leads to the fusion of the vesicles with the cell membrane –> neurotransmitter is released and passively diffused into the synaptic cleft–> Neurotransmitter finds the neurotransmitter receptor at the postsynaptic terminal –> receptors open when the neurotransmitter binds to it –> leads to graded potentials in the postsynaptic cell

41
Q

Glial cells in the synaptic cleft

A

Each synapse is surrounded by them (astrocytes mostly), they take up neurotransmitters hovering around in the cleft to remove them from the area –> cleaner situation in the cleft

42
Q

Removal of neurotransmitters from the cleft

A

Glial cells
Enzymatic degradation

43
Q

Types of synapses by function

A

Excitatory- Type 1; asymmetrical (pre and postsynaptic membrane are not equally thickened); influx Na+, Ca+
Inhibitory- Type 2 ; symmetrical, Influx Cl-

44
Q

Types of synapses by connection

A

Axodendritic
Axosomatic
Axoaxonic
Dendrodentritic