OP - 6+7+8 Flashcards

1
Q

What are the types of cells of the nervous system? Both CNS and PNS

A

Neurons
Nuroglia:
–>CNS:
- oligodendrocytes (form myelin sheath around axons)
- microglia (removes cell debris, waste, pathogens)
- astrocytes (form blood brain barrier)
- ependymal cells (assist in producing and circulating cerebrospinal fluid

–>PNS:
- schwann cells (form myelin sheath)
- satellite cells (surround neuron cell bodies in ganglia)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are interneurons?

A

Multipolar neurons located entirely within the CNS G

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Ganglion

A

Grouping of neuron cell bodies outside the CNS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Nucleus

A

Grouping of neuron cell bodies within the CNS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Tract

A

Grouping of axons that interconnect regions of the CNS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Why cant ppl with parkinsons be treated with dopamine - what do they have to be treated with instead?

A

Because the blood-brain barrier has capillaires with very tight junctions that prevent the flow of many substances

Have to be treated with a dopamine precursor called L-dopa

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What maintains resting memb potential and how?

A

The Na/K pump
Pumps 3 Na out for every 2 K pumped in
thus Na conc. in ECF > than K
and K in ICF > than Na

**all cells have resting memb potential - only some excitable

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

does the amplitude and frequency of APs change?

A

Not amplitutde
only frequency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why does K+ leave the cell slowly (from ICF–>ECF) and why does Na move in rapidly?

A

Higher K+ in the ICF than the ECF thus due to conc gradient it moves out
However the inside of the cell is -ve and since K+ is positive there is attraction between the two
But effect of conc gradient is larger acc. to Nernst equation

Higher Na+ in the ECF than the ICF thus Na+ moves into cell
Inside is -ve thus attracts Na+ into the cell
Thus strong pull on Na+ to move into the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What does the Nernst equation let us calculate?

A

It allows us to calculate the equilibrium potential for an ion – which is the membrane potential at which there is no net flux/change in the conc. of ions in the ECF and the ICF

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is potential difference and current +units

A

Potential diff is the diff in charge between two point (V, mV)
Current is the movement of charge (ions) (A, pA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

axon hillock?

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Generation and propagation of an AP

A
  • In resiting condition - sodium voltage gated channels on the membrane are closed
  • A release of some neurotransmitters or other substances due to a stimulus can cause binding to receptors on the membrane of the dendrites and cause the receptors to open
  • Since sodium is high in the ECF, sodium moves in thru these receptor channels
  • The entry of Na raises the membrane potential – these are known as graded potentials
  • HYPOPOLARIZATION: When there are a sufficient amount of graded potentials IN THE AXON HILLOCK for the membrane to reach its threshold potential, the voltage gated Na channels on the cell memb. open and an AP can be generated in the AXON as follows:
  • DEPOLARISATION: Once threshold is reached the neuron depolarises
    – causes opening of Na+ voltage gated channels
    – leads to a rapid influx of sodium into the cell membrane
    – Resulting in the membrane potential becoming more positive until it reaches overshoot phase of extreme positivity.
    —- Na channels close 1msec later during refractory period

-REPOLARISATION: K+ channels open after overshoot phase
– Results in K+ from the ICF moving into ECF (K+ conc. is higher in ICF)
– results in the membrane potential becoming more negative
– K+ channels open at +30mV and close soon after RMP is re-established

HYPERPOLARISATION: Repolarisation leads to this - memb. potential more -ve than resting memb. potential
– K+ leak channels allow for resting memb. potential value to go back up to -70mV.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

When do the diff channels involved open and close

A

Na channels:
- Open when threshold pot. reached
- clsoe 1 msec later during refractory period once depolarisation is over

K channels:
- Open during repolaristaion after depolarisation is complete at +30mV
- After hyperpolarisation
- K+ leak channels help establish RMP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Absolute and relative refractory periods

A

Absolute:
- No new action potential can be generated during this period
- Extends from the entire depolarisation phase (as all Na+ channels are open thus max. inflow is already occurring - no Na+ channels free to generate a new AP) and during part (2/3rds) of the repolarization phase (Na+ channels are completely closed)

Relative refractory period:
- A new action potential can be generated only if the new stimulus is stronger than the previous one (during period after hyperpolarisation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the role of myelin?

A

Myelin sheaths cause aggregation of Na and K+ channels in unmyelinated areas along the axon
These gaps where these channels are present are called nodes of ranvier
These nodes allow for efficient propagation of Action Potentials

SALUTATORY CONDUCTION

17
Q

What is MS

A

Multiple Sclerosis
- Neurodegenerative diseases
- Myelin is absent or degenerating
- Results in inefficient conduction of APs - APs lose amplitude - AP may arrive at next node of ranvier with not enough strength to fire another AP
- Thus axon may fail to propagate APs
- Eventually leads to complete motor control loss

18
Q

How are nerve fibre diameter and conduction speed related

A

Increase diameter - increases conduction speed

19
Q

How is an AP propagated in an unmyelinated axon?

A
20
Q

Local Anaesthetics - how they work?

A
  • reversibly bind to Na channels
  • reduce the ability of memb. potential depolarisation to produce APs
  • Block APs not the synapse
  • Cocaine - Procaine
    Now - Lidocaine and tetracaine
21
Q

Primary Hyperkalaemic paralysis

A
  • high levels of K+ in plasma and ECF
  • due to mutations in Na+ channels
  • Longer lasting APs
22
Q

Depression and antidepressants

A
  • Depression thought to be caused due to failure to transmit info properly
  • Drugs that target enzymes that degrade neurotransmitters and help prevent reuptake
  • Drugs that block the enzyme that degrades neurotransmitter:
    —–> Nardil, Marplan, Monoamine oxidase inhibitors
  • Drugs that prevent reuptake:
    —–> Selective serotonin reuptake inhibitors, prozac, lexapro
23
Q

Calciseptine - what is it

A

Neurotoxin in black mamba
- Blocks Ca channels
- no neurotransmitter release
- paralysis and death

24
Q

Curare

A

Neurotxin from plants - used in hunting
- Blocks ACh from binding to its receptors
- Muscle cant contract
- Paralysis and death from resp. failure

25
Q

EPSPs and IPSPs

A

Excitatory postsynaptic potentials:
– depolarisations that bring memb towards threshold
– occur in dendrites and cell bodies unlike APs which occur in axons
– no threshold - they’re graded
Inhibitory postsynaptic potentials:
– hyperpolarizations that being memb. potential further away from threshold

26
Q

Iberiotoxin

A
  • From red scorpion
  • Blocks K+ channels
27
Q

Saxitoxin

A
  • From shellfish containing microorganisms from red tide
  • Blocks voltage gated Na channels
28
Q

Tetrodotoxin

A
  • from puffer fish
  • Blocks Na channels
  • Blocks APs
  • cant be used as anaesthetic as even 1mg can be fatal