How drugs control the brain Flashcards

1
Q

What is the main inhibitory system

A

The GABAergic system

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

Outline the features of the GABAergic system

A

Widespread distribution throughout the brain, inhibitory neurons keep the excitation in check.

too much GABA- loss of consciousness and coma
too little GABA- Leads to convulsions and seizures

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

What types of neurones use Gaba and what type uses glutamine

A

GABA uses local interneurons and GLU uses projection neurons

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

What are the two types of GABA receptors

A

GABA ionotropic receptors and GABA metabotropic receptors

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

What are some features of GABA Ionotropic receptors

A

Ligand-gated CL- channel, Fast IPSPs (mainly GABAergic interneurons.

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

What are some features of GABA Metabotropic receptors

A

G-protein coupled receptors, both pre and post synaptic.

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

Name a direct agonist and antagonist for ionotropic receptors

A

Muscimol- agonist, bicuculline- antagonist

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

Name some indirect agonists for ionotropic receptors

A

Benzodiazepine, Barbiturates (increases duration of channel opening, anaesthesia and epilepsy treatment) and alcohol

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

What are the effects of barbiturates and alcohol

A

Both have same effect to enhance GABA activity and the effects are additive, combining may be fatal.

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

Name the agonist for metabotropic receptors and outline some features

A

Baclofen, used as a muscle relaxant to reduce spasticity

results in a slow hyperpolarizing current.

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

Name 3 systems in the dopaminergic system

A

Nigrostriatal system (75% of brain DA), mesolimbic system and mesocortical system

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

What receptors use dopamine

A

Only via metabotropic receptors.

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

Outline the diff dopamine receptors

A

5 diff broad categories, can produce excitatory and inhibitory receptors, D1 Like receptors (1&5) associated with Gs subproteins,
D2-like (2,3&4) is associated with Gi receptors

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

Outline the nigrostriatal system

A

cell bodies in the substantia nigra project to the striatum and dysfunction of this system can lead to: parkinsons disease and huntingtons disease.
types of drugs that can affect the system is: L-DOPA, MAO inhibitors, dopamine receptor agonists- treatment for parkinsons disease.

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

Outline the mesolimbic system

A

cell bodies in the ventral tegmental area project to the limbic system, role in reinforcement of several categoires of stimuli inc drug abuse.

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

Outline the mesocortical system

A

VTA projections to the prefrontal cortex, dysfunction: schizophrenia, drugs: typical antipychotics ( DA receptor antagonists, increases DA turnover and blockade of postsynaptic receptors.

17
Q

Outline the seretonergic system

A

seretonin is synthesised in nine raphe nuclei in reticular formation to a diff part of the brain.

18
Q

What are some functions that seretonin is involved in

A

mood, sleep, pain, emotion and appetite.

19
Q

What type of receptor does seretonin have

A

metabotropic and ionotropic receptors

20
Q

What are some drugs that affect seretonin

A

SSRI’s E.G. Fluoxetine (prozac), increase seretonin function by preventing its uptake, treatment for depression and anxiety disorders.

MDMA, causes seretonin transporters to run in reverse to increase seretonin release and block reuptake.

21
Q

Outline the noradrenergic system

A

projections from the locus coeruleus throughout the brain, role in arousal and attention,

22
Q

Outline the adrenergic system

A

primarily in lateral tegmental area and projects to the thalamus and hypothalamus.

23
Q

Outline the cholinergic system

A

in the periphery, ach at NMJ and synapses in the autonomic ganglia. in the brain we find it in the basal forebrain complex ( cholinergic innervation of the hippocampus and the neocortex) and the brainstem complex which innervates the dorsal thalamus and telencephalon.

24
Q

disorders of the cholinergic system

A

in the periphery: myasthenia gravis- autoimmune disease leads to muscle weakness and loss of muscle acitivity.

brain: alzheimers disease, loss of cholinergic neurons in the basal ganglia.
epilepsy: autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) associated with mutation in the nicotinic receptor genes.

25
Q

outline AChi

A

treatment for alzheimers and myasthenia gravis, by prolonging effect of alzheimers.