11 - Noradrenaline Flashcards
Noradrenaline biochemistry
Describe the process of NA synthesis…
- Tyrosine transported into the presynaptic cell
- Tyrosine converted to DOPA by tyrosine hydroxylase
- DOPA converted to dopamine by DOPA carboxylase
- Dopamine converted to noradrenaline by dopamine β-hydroxylase
Name the two types of noradrenergic receptor and their subclasses…
α(1,2) and β(1,2,3)
Noradrenaline is metabolised in the ( pre-synaptic cell / synapse / post-synaptic cell ) by the enzyme…
Noradrenaline is metabolised in the pre-synaptic cell by the enzyme monoamine oxidase
Noradrenergic receptors are present at the effector tissues of the ( sympathetic / parasympathetic ) system.
Noradrenergic receptors are present at the effector tissues of the sympathetic system.
Noradrenergic receptors are:
a) G-Protein coupled
b) Ionotropic
c) Enzyme-linked
d) All of the above
Noradrenergic receptors are:
a) G-Protein coupled
b) Ionotropic
c) Enzyme-linked
d) All of the above
List the alpha 1 noradrenoreceptor mediated effects via the sympathetic system…
- Pupil dilation
- Blood vessel constriction (to visceral organs and skin)
- General alertness
State the effect of alpha 2 noradrenoreceptor activation…
Inhibition of neurotransmitter release from presynaptic cell
(Alpha 2 NA receptors are presynaptic)
List beta 1 noradrenoreceptor mediated effects…
- Increased heart rate
- Increased heart force of contraction
List beta 2 noradrenoreceptor mediated effects…
- Ciliary relaxation (increased focal distance)
- Bronchodilation
- Dilation of blood vessels to limbs
State the effect of beta 3 noradrenoreceptors…
An increase in lipolysis and metabolic rate
List 5 drugs which are noradrenergic agonists…
- Adrenaline (all)
- Clonidine (α2)
- Dobutamine (β1)
- Salbutamol (β2)
- Clenbuterol (β2, β3)
List 3 drugs which can act as noradrenergic antagonists…
- Prazosin (α1)
- Propanolol (β1, β2)
- Atenelol (β1)
Which drug targets NA synthesis?
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)
Which drug targets NA storage?
Reserpine
Disrupts NA storage in the vesicles. This reduces the amount of NA available. Used to treat hypertension.
Remember: Reserp -> reserve -> storage
Which drug targets NA release?
Clonidine
Inihibts NA release via α2 agonism (decreased release of NA). Used to treat hypertension.
Remember: Clon. -> Clog = blocked -> release blocked
Drugs targeting NA reuptake…
Desipramine (TCA) and Reboxetine (SNRI) are noradrenaline reuptake inhibitiors
Remember: Re-box -> Re-uptake
Which drug targets NA metabolism?
Tranylcypramine (MAOI)
Blocks MAO which along with COMT metabolises NA. This increases recycling of NA, increasing NA availability.
Remember: MAOI -> Metabolism
Describe the MAOI ‘cheese reaction’ 🧀
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)
Noradrenergic antagonists are used to treat…
Hypertension
Adrenaline is administered by injection, as it is destroyed by the gut.
Give two uses of adrenaline…
- Subcutaneous dose to prolong and isolate anaesthesia
- Intramuscular delivery to treat anaphylactic shock
A common side effect of clonidine is xerostomia (a dry mouth).
Why?
- Clonidine is an α2 agonist
- This inhibits NA release
- Post-ganglionic synapse for salivary glands use NA (despite being part of parasymp.)
- Salivary gland secretions are reduced