[PHW2:p197]
Parasympathetic nervous system
Preganglionic fibres arise from
CN III, VII, IX, X (3, 7, 9, 10)
* Eye, salivary gland, heart, bronchi, upper GI (up to splenic flexure), ureters
Sacral fibres (S2-4)
* Distal blowel, bladder and genitals
Preganglionic fibres synapse with ganglia which are close to the effector organ
* Release ACh
* Act via nAChRs
Postganglionic fibres also release AChRs and receptors are also nAChRs
Sympathetic nervous system
[PHW2:p188]
Preganglionic fibres arise from lateral horns of the spinal cord from T1-L2
Pathway:
* Lateral horn
--> Anterior primary rami
--> White rami communicans
--> Sympathetic chain or ganglia
Once in sympathetic chain, the preganglionic fibre could
* Synapse at the same level
* Go to an adjacent level and synpase there
* Pass anteriorly through a splanchnic nerve to synapse in a prevertebral ganglion
Preganglionic fibres release ACh, which acts on nAChRs
Post-ganglionic fibres (unmyelinated) go into the adjacent spinal nerve via the grey rami
Post-ganglionic fibres
* Release noradrenaline
--> Acts on adrenergic receptors
Two special cases of the sympathetic nervous system:
Adrenal medulla
* Pre-ganglionic fibres synapse directly with chromaffin cells
--> Release adrenaline into circulation
Sweat gland
* Post-ganglionic sympathetic fibres which innervate sweat glands release ACh (instead of NE) as the neurotransmitter
NB:
ALL pre-ganglionic ANS (sympathetic and parasympathetic) fibres are
* Myelinated
* Release ACh
* Act on nAChRs
[PHW2:p190-193]
Catecholamine
Naturally occurring catecholamine, synthetic agents, others
Naturally occurring catecholamine
adrenaline, noradrenaline, dopamine
[PHW2:p196]
Of the synthetic agents, only isoproterenol, dobutamine, dopexamine are classified as catecholamines because only they contant hydroxyl groups on 3- and 4- positions of the benzene ring
[PHW2:p197]
A direct-acting amine with specific alpha 1 agonist actions.
Similar effects to phenylephrine
?More pronounced reflex bradycardia
No longer in production
[PHW2:p200]
Long-acting beta2 agonist
15 times more potent than salbutamol at beta2, but 4 times LESS potent at beta1
Prevents release of histamine, leukotrienes, and prostaglandin D2 from mast cells
Some antiinflammatory actions
Other effects are similar to salbutamol
======
[James] [???]
If OH group present on C3 and C4 (i.e. a catecholamine) --> metabolise by COMT
Increasing size of amine group substitution --> Increased beta and decreased alpha activity
OH present on both C3 and C4 --> Increased alpha and beta activity (e.g. adrenaline)
OH on C3 and C5 with long amino chain substitution --> Beta2 activity
No OH on C4 --> alpha selective (e.g. phenylephrine)
Alpha methyl group --> Increase alpha selectivity
Levorotatory forms more active