S2: the environment of the brain Flashcards

1
Q

List different types of glial cells

A

Astrocytes – most abundant type of giant cell, supporters
Oligodendrocytes – insulators
Microglia – immune response

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2
Q

List different roles of astrocytes

A
Structural support 
Help to provide nutrition for neurones 
Remove neurotransmitters 
Maintain ionic environment 
Help to form the BBB
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3
Q

How do astrocytes help provide energy for neurones?

A

Neurones do not store or produce glycogen
Astrocytes produce lactate which can be transferred to neurones
-supplements their supply of glucose
-via the glucose lactate shuttle

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4
Q

How do astrocytes help to remove neurotransmitters?

A

Astrocytes have transporters for transmitters such as glutamate
Re-uptake of transmitters, which helps to keep the extracellular concentration low

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5
Q

Describe how astrocytes maintain the ionic environment

A

High levels of neuronal activity could lead to a rise in K+ in brain ECF
Astrocytes take up K+ to prevent this

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6
Q

What is the role of oligodendrocytes?

A

Responsible for myelinating axons in CNS

(NB: in PNS, Schwann cells are responsible for myelination

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7
Q

Describe the function of microglia

A

Immunocompetent cells
Recognise foreign material
Phagocytosis to remove debris and foreign material – brain’s main defence system

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8
Q

Describe the blood brain barrier

A

Limits diffusion of substances from the blood to the brain ECF
Maintains the correct environment
Brain capillaries have: tight junctions between endothelial cells, basement membrane surrounding capillary & end feet of astrocyte processes

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9
Q

Describe the ‘immune privilege’ of the CNS

A

Constant surveillance of the CNS by immune cells, however their activity is tightly regulated
Tight regulation is essential = strong inflammatory response in the brain would lead to swelling and hence raised ICP

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10
Q

List the four main sections of a neurone

A

Cell soma
Dendrites
Axon
Terminals

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11
Q

Describe neurotransmitter release from the synapse

A

Depolarisation in the terminal opens voltage-gated Ca2+ channels
Ca2+ ions enter the terminal
Vesicles fuse and release transmitter
Neurotransmitter diffuses across the synaptic cleft and binds to receptors on the postsynaptic membrane

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12
Q

What does the postsynaptic response depend on?

A

Response depends on:

1) Nature of transmitter
2) Nature of receptor (ligand-gated or GPCR)

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13
Q

Describe the three chemical classes of neurotransmitters

A

Amino acids – glutamate, GABA, glycine
Biogenic amines – acetylcholine, noradrenaline, dopamine, serotonin, histamine
Peptides – dynorphin, enkephalins, substance P, somatostatin, CCK, neuropeptide Y

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14
Q

Describe amino acid neurotransmitters

A

Excitatory amino acids – mainly glutamate
-major excitatory neurotransmitter (over 70% of all CNS synapses are glutamatergic)
-present throughout the CNS
Inhibitory amino acids – GABA and glycine

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15
Q

Describe ionotropic glutamate receptors

A

AMPA receptors – Na+/K+
Kainite receptors – Na+/K+
NMDA receptors – Na+/K+ and Ca2+
Ion channel – permeable to Na+ and K+ (and in some cases Ca2+ too)
Activation causes depolarisation – increased excitability

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16
Q

Describe metabotropic glutamate receptors

A

mGluR1-7 (GPCR)
Linked to either:
- Changes in IP3 and Ca2+ mobilisation
- Or inhibition of adenylate cyclase and decreased cAMP levels

17
Q

Describe fast excitatory responses

A

Excitatory neurotransmitters cause depolarisation of the postsynaptic cell by acting on ligand-gated ion channels

  • Excitatory postsynaptic potential
  • Depolarisation causes more action potentials
18
Q

Describe glutamatergic synapses

A

Have both AMPA and NDMA receptors
AMPA receptors mediate the initial fast depolarisation
NDMA receptors are permeable to Ca2+
NDMA receptors need glutamate to bind and the cell to be depolarised to allow ion flow through the channel (glycine acts as a co-agonist)

19
Q

Describe the role of glutamate receptors in learning and memory

A

Activation of NMDA receptors can up-regulate AMPA receptors
Strong, high frequency stimulation causes long term potentiation (LTP)
Ca2+ entry through NMDA receptors important for induction of LTP
Too main Ca2+ entry through NMDA receptors causes excitotoxicity

20
Q

What is long term potentiation?

A

If the synapse is activated strongly and a lot of glutamate is released, then additional AMPA receptors are inserted into the postsynaptic membrane
Mediated by the entry of Ca2+ through NMDA receptors
Extra AMPA receptors means that the synapse will transmit more readily
This is the process of LTP – molecular basis for learning and memory

21
Q

Describe inhibitory amino acids

A

GABA – main inhibitory transmitter in the brain

Glycine – inhibitory neurotransmitter mostly in the brainstem and spinal cord

22
Q

Describe GABA and glycine receptors

A

GABA and glycine receptors have integral Cl- channels
Opening the Cl- channel causes hyperpolarisation
-inhibitory post-synaptic potential = decreased action potential

23
Q

Describe the action of barbiturates and benzodiazepines when they bind to GABA receptors

A

Barbiturates – anxiolytic and sedative actions, but not used for this now
-risk of fatal overdose, also dependence and tolerance
-sometimes used as anti-epileptic drugs
Benzodiazepines – sedative and anxiolytic effects
-used to treat anxiety, insomnia and epilepsy

24
Q

Describe acetylcholine as a neurotransmitter

A

ACh – neuromuscular junction, postganglionic parasympathetic in ANS
Also a central neurotransmitter – acts at both nicotinic and muscarinic receptors in the brain (mainly excitatory)
-receptors often present on presynaptic terminals to enhance the release of other transmitters

25
Q

Describe the cholinergic pathways in the CNS

A

Neurones originate in basal forebrain and brainstem
Give diffuse projections to many parts of cortex and hippocampus
Also local cholinergic interneurons (corpus striatum)
Involved in arousal, learning, memory and motor control
Cholinesterase inhibitors are used to alleviate symptoms of Alzheimer’s disease (degeneration of cholinergic neurones in the nucleus basalis are seen in this disease)

26
Q

Describe the key dopaminergic pathways

A

Nigrostriatal – motor control
Neocortical – mood, arousal and reward
Mesolimbic – mood, arousal and reward

27
Q

Describe conditions associated with dopamine dysfunction

A

Parkinson’s disease – associated with loss of dopaminergic neurones (substantia nigra input to corpus striatum)
Schizophrenia – may be due to release of too much dopamine (overactivity of mesolimbic pathway)
-amphetamine releases dopamine & noradrenaline -> produces schizophrenic like behaviour
-antipsychotic drugs are antagonists at D2 receptors

28
Q

Describe treatment for Parkinson’s

A

Commonly given drug is L-DOPA, converted to dopamine in the brain by the enzyme AADC
L-DOPA crosses the BBB readily via the LNAA
Problem: L-DOPA can also be converted to dopamine in periphery (causes side effects affecting the heart, GI and urinary systems)
Coadministration of carbidopa – inhibits the conversion in the periphery & doesn’t cross the BBB, hence action of L-DOPA in brain is unaffected

29
Q

Describe noradrenaline as a neurotransmitter

A

Transmitter at postganglionic – effector synapse in ANS
Also acts as a neurotransmitter in the CNS
Operates through GPCR alpha and beta-adrenoreceptors (receptors to NA in the brain are the same as in the periphery)

30
Q

Describe noradrenergic pathways in the CNS

A

Cell bodies of NA containing neurones are located in the brainstem (pons and medulla)
Diffuse release of NA throughout cortex, hypothalamus, amygdala and cerebellum

31
Q

Describe the relationship between noradrenaline and behaviour arousal

A

Most NA in the brain comes from a group of neurones in the locus coeruleus
-inactive during sleep
-activity increases during behaviour arousal
-amphetamines increases release of NA and dopamine and increase wakefulness
Depression may be associated with a deficiency of NA

32
Q

Describe serotonergic pathways in the CNS

A

Similar distribution to noradrenergic neurones
Functions: sleep/wakefulness, mood
SSRIs = treatment of depression and anxiety disorders