Session 8 ILOs - The Autonomic Nervous System (ANS) Flashcards
List the mechanisms by which drugs influence neurotransmission
In cholinergic synapses:
- Degradation of the transmitter
- Interaction with the post-synaptic receptors
- Inactivation of the transmitter
- Reuptake of the transmitter
- Interaction with pre-synaptic receptors
In adrenergic synapses:
- Metabolism enzymes (monamine oxidases and catechol-O-methyltransferase)
- Post-junctional adrenoceptors
Describe the major drug classes that exert all, or a part of their actions through altering ANS function
Cholinergic drugs:
- Acetylcholinesterase targeting drugs e.g. pyridostigmine for myasthenia graves or Donepezil to treat Alzheimer’s disease
- Muscarinic Ach receptor agonists e.g. Pilocarpine for glaucoma
- Muscarinic Ach receptor antagonists e.g. Ipratropium and tiotropium for some forms of asthma and COPD
Adrenergic drugs:
- Alpha1-adrenoceptor selective antagonists e.g. doxazosin in hypertension
- Beta1-adrenoceptor selective antagonists e.g. atenolol in hypertension
- Beta2-adrenoceptor selective agonists e.g. salbutamol in asthma
Compare and contrast the following in cholingeric and adrenergic synapses:
- Neurotransmitter synthesis
- Neurotransmitter storage
- Neurotransmitter release
- Signal termination
Neurotransmitter synthesis:
- Cholingeric neurotransmitters are synthesised in the pre-synaptic portion, whereas adrenergic neurotransmitters are made in the nerve varicosities (adrenergic neurotransmitters can also be synthesised from other pre-cursors ‘on site’ from e.g. tyrosine)
Neurotransmitter storage:
- Both cholingeric and adrenergic neurotransmitters are stored in vesicles
Neurotransmitter release:
- Both cholingeric and adrenergic neurotransmitters are released upon the depolarisation of the neurone, however in cholingeric neurotransmitters, release is triggered by Ca2+, not the depolarisation itself
Signal termination:
- Cholingeric neurotransmission is terminated by the breakdown first (by acetylcholinesterase), then can be re-taken up by the nerve, whereas adrenergic neurotransmitter is terminated by the high affinity reuptake mechanism for NA direct reuptake