11 - Noradrenaline Flashcards

1
Q

Noradrenaline biochemistry

Describe the process of NA synthesis…

A
  1. Tyrosine transported into the presynaptic cell
  2. Tyrosine converted to DOPA by tyrosine hydroxylase
  3. DOPA converted to dopamine by DOPA carboxylase
  4. Dopamine converted to noradrenaline by dopamine β-hydroxylase
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2
Q

Name the two types of noradrenergic receptor and their subclasses…

A

α(1,2) and β(1,2,3)

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3
Q

Noradrenaline is metabolised in the ( pre-synaptic cell / synapse / post-synaptic cell ) by the enzyme…

A

Noradrenaline is metabolised in the pre-synaptic cell by the enzyme monoamine oxidase

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4
Q

Noradrenergic receptors are present at the effector tissues of the ( sympathetic / parasympathetic ) system.

A

Noradrenergic receptors are present at the effector tissues of the sympathetic system.

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5
Q

Noradrenergic receptors are:

a) G-Protein coupled
b) Ionotropic
c) Enzyme-linked
d) All of the above

A

Noradrenergic receptors are:

a) G-Protein coupled

b) Ionotropic
c) Enzyme-linked
d) All of the above

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6
Q

List the alpha 1 noradrenoreceptor mediated effects via the sympathetic system…

A
  • Pupil dilation
  • Blood vessel constriction (to visceral organs and skin)
  • General alertness
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7
Q

State the effect of alpha 2 noradrenoreceptor activation…

A

Inhibition of neurotransmitter release from presynaptic cell

(Alpha 2 NA receptors are presynaptic)

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8
Q

List beta 1 noradrenoreceptor mediated effects…

A
  • Increased heart rate
  • Increased heart force of contraction
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9
Q

List beta 2 noradrenoreceptor mediated effects…

A
  • Ciliary relaxation (increased focal distance)
  • Bronchodilation
  • Dilation of blood vessels to limbs
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10
Q

State the effect of beta 3 noradrenoreceptors…

A

An increase in lipolysis and metabolic rate

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11
Q

List 5 drugs which are noradrenergic agonists

A
  1. Adrenaline (all)
  2. Clonidine (α2)
  3. Dobutamine (β1)
  4. Salbutamol (β2)
  5. Clenbuterol (β2, β3)
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12
Q

List 3 drugs which can act as noradrenergic antagonists

A
  1. Prazosin (α1)
  2. Propanolol (β1, β2)
  3. Atenelol (β1)
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13
Q

Which drug targets NA synthesis?

A

Methyldopa

A false substrate mimicking DOPA. This reduces the amount of NA, as methylnoradrenaline is produced instead (which is also an α2 agonist– decreasing NA release)

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14
Q

Which drug targets NA storage?

A

Reserpine

Disrupts NA storage in the vesicles. This reduces the amount of NA available. Used to treat hypertension.

Remember: Reserp -> reserve -> storage

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15
Q

Which drug targets NA release?

A

Clonidine

Inihibts NA release via α2 agonism (decreased release of NA). Used to treat hypertension.

Remember: Clon. -> Clog = blocked -> release blocked

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16
Q

Drugs targeting NA reuptake

A

Desipramine (TCA) and Reboxetine (SNRI) are noradrenaline reuptake inhibitiors

Remember: Re-box -> Re-uptake

17
Q

Which drug targets NA metabolism?

A

Tranylcypramine (MAOI)

Blocks MAO which along with COMT metabolises NA. This increases recycling of NA, increasing NA availability.

Remember: MAOI -> Metabolism

18
Q

Describe the MAOI ‘cheese reaction’ 🧀

A

MAOIs also block the metabolism of dietary amines (such as those found in cheese, marmite and cold remedies). This leads to accumulation. Accumulated amines have a sympathomimetic* effect, leading to hypertension.

(* sympathomimetic, e.g. mimics the effects of noradrenaline)

19
Q

Noradrenergic antagonists are used to treat…

A

Hypertension

20
Q

Adrenaline is administered by injection, as it is destroyed by the gut.

Give two uses of adrenaline…

A
  • Subcutaneous dose to prolong and isolate anaesthesia
  • Intramuscular delivery to treat anaphylactic shock
21
Q

A common side effect of clonidine is xerostomia (a dry mouth).

Why?

A
  1. Clonidine is an α2 agonist
  2. This inhibits NA release
  3. Post-ganglionic synapse for salivary glands use NA (despite being part of parasymp.)
  4. Salivary gland secretions are reduced
22
Q
A