disorder of PNS Flashcards

1
Q

what does the PNS represent ?

A

The PNS represents the output of the CNS and (usually) acts independently to regulate the body’s internal environment.

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2
Q

what does the PNS consists of?

A
  1. Autonomic nervous system (ANS)
    largely outside of voluntary control
  2. Somatic (motor) nervous system (SNS)
    under conscious control
    Efferent nerves control movement by innervating skeletal muscle.
    Afferent nerves respond
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3
Q

what does the autonomic consist of?

A
  1. Parasympathetic nervous system
    Cranial-sacral output, synapse at ganglia close to innervated tissue.
  2. Sympathetic nervous system
    Thoracic-lumbar output, synapse at ganglia either side of vertebral column (sympathetic chain).
    Ganglia distal to innervated tissue.
  3. Enteric nervous system
    Neurones with cell bodies in the wall of the intestine which innervates GI tract, pancreas and gall bladder.
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4
Q

ANS is characterised by 2 neurones outside cns what are they?
and what are released from them

A

The ANS is characterised by having 2 neurones outside the CNS
preganglionic fibres arising from the CNS synapse onto
postganglionic nerve in a ganglia.
Postganglionic neurones terminate at the effector.

Acetylcholine (ACh) is released from
all preganglionic neurones of both parasympathetic and sympathetic nerves
all postganglionic parasympathetic neurones
= cholinergic transmission

Noradrenaline (NA) is released from
most postganglionic sympathetic neurones
= adrenergic (noradrenergic) transmission

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5
Q

what are the neurotransmitters in the ANS?

A
  1. Cholinergic transmission
    all postganglionic parasympathetic nerves release ACh to act on muscarinic acetylcholine receptors (mAChRs)

all motor nerves release ACh which act on nicotinic acetylcholine receptors (nAChRs)

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6
Q

m1 -m5
location
function
g-protein
response
agonist
antagonist

A

check one note

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7
Q

Q. Why is knowledge of receptor subtypes important?

A
  • selectivity
    Allows drug discovery to create better drugs
    (more efficacious, safer)
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8
Q

what are the Actions of mAChR agonists = parasympathetic effects

A

Bradycardia/reduced cardiac output

Vasodilation

Increases secretion (salivation, lacrimation, sweating)

Bronchoconstriction and bronchial secretion

Increased gut motility

Reduction of intraocular pressure (due to pupillary constriction)

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9
Q

Therapeutic uses of mAChR agonists

A
  1. Glaucoma
    Glaucoma is due increased intraocular pressure which can damage the eye’s optic nerve and lead to blindness.
    Pilocarpine (miotic) used as eye drops to reduce intraocular pressure. Pilocarpine is a tertiary amine which is well absorbed into the conjunctival sac and thus action lasts ~ 1 day
  2. Urinary retention and constipation
    Bethanechol has been used to
    relieve urinary retention (usually due to failure of normal reflex pathway)
    increase gut motility
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10
Q

what is SLUDGE?

A

Salivation: stimulation of the salivary glands
Lacrimation: stimulation of the lacrimal glands
Urination: relaxation of the internal sphincter muscle of urethra, and contraction of the detrusor muscles
Defecation: relaxation of the internal anal sphincter
Gastrointestinal upset: smooth muscle tone changes causing gastrointestinal problems, including diarrhea
Emesis: vomiting

SLUDGE is caused by mAChR agonists- this is why therapeutics using these agents is limited

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11
Q

Actions of mAChR antagonists

A

Block secretion -salivation, lacrimation, sweating, bronchial secretion are reduced (can cause dry mouth)

Tachycardia (increased heart rate) - modest effect

Pupillary dilation (mydriasis) and ciliary muscle paralysis (cycloplegia); can lead to increase in intraocular pressure and blurred vision

Inhibits gut motility (can cause constipation)

Paralysis of bladder (can cause urinary retention)

Smooth muscle (except gut) relaxation

CNS effects: excitatory (can cause disorientation, mood swings

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12
Q

Therapeutic uses of mAChR antagonists

A

These anticholinergic drugs all act as competitive antagonists, but are largely unselective and can cause dry mouth/blurred vision/constipation

Ophthalmic
Tropicamide used clinically to dilate pupils (mydriasis) to aid eye examinations; atropine or cyclopentolate paralyse eye (cycloplegia) to treat inflammation

  1. Bronchodilation
    Orally inhaled (aerosol), short-acting drugs such as ipratropium (t1/2 ~ 2-4 hours) used in acute asthma episodes and longer-lasting, M3/M2-selective tiotropium (t1/2 ~ 10 hours) used in chronic obstructive pulmonary disease (COPD)
  2. Reduce intestinal motility
    Atropine or dicycloverine act as smooth muscle relaxants (anti-spasmodic agents) to manage irritable bowel syndrome (IBS) and diverticular disease
  3. Urinary incontinence
    Parasympathetic system controls bladder contraction, so antimuscarinics are used to prevent incontinence (‘overactive bladder’ OAB).

Tolterodine and oxybutynin (10 x selectivity for M1 and M3 > M2 receptors) in extended release formulation can be taken once/day. Desirable drugs are selective M3 antagonist eg. darifenacin, solifenacin

  1. Cardiovascular
    Atropine used to treat bradycardia after myocardial infarction
    1. Nausea and vomiting (CNS)
      Hyoscine (BAN British Approved Name or RINN Recommended International Nonproprietary Name) (scopolamine, USAN) (e.g. Kwells®) given as transdermal patch or orally to treat motion sickness (acts on the ‘vomiting centre’ in the hind brain medulla)
    2. Parkinson’s Disease (CNS)
      In drug-induced PD, dopamine deficiency can cause excessive cholinergic activity eg. trihexyphenidyl hydrochloride
    3. Anaesthesia
      Pre-medication to inhibit salivation and bronchial secretion and to cause drowsiness eg. atropine or hyoscine. During surgery to prevent vagal inhibition of the heart eg. atropine or glycopyrronium
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13
Q

Nicotinic ACh receptor subtypes
muscle
ganglion
cns

molecular form
location
function
agonist
antagonist

A

check one note

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13
Q

subtypes pf nACH receptors

A

Peripheral nAChRs are present at (i) autonomic ganglia and (ii) neuromuscular junctions (NMJs) are molecularly distinct.
However, drugs affecting ANS ganglia do not discriminate between sympathetic and parasympathetic nerves

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14
Q

(i) nAChRs at autonomic ganglia

A

Due to lack of discrimination between sympathetic and parasympathetic ganglia most nACh ligands are therapeutically undesirable; however, nicotine (NiQuitin, Nicorette, Nicotinelle) is used to assist smoking cessation.

Ganglion-blocking drugs (trimetaphan, hexamethonium)
1. Cardiovascular
Effects largely due to block of sympathetic system: vasodilation causes fall
in blood pressure. Trimetaphan was used to produce hypotension in surgery

  1. GastrointestinaI tract
    Effects largely due to block of parasympathetic system: inhibition of motility
  2. Genito-urinary system
    Effects largely due to block of parasympathetic system: impairment of micturition
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15
Q

(ii) nAChRs at the neuromuscular junction

A

Neuromuscular blocking agents work by:
1. Competitive antagonists of nAChRs = competitive blockers
2. Agonists which cause a depolarizing block of the muscle endplate = depolarizing blockers

  1. Uses of competitive blockers
    Widely used as muscle relaxants as an adjunct to anaesthesia, e.g. pancuronium, vecuronium, atracurium
  2. Uses of depolarizing blockers
    Used to cause paralysis during anaesthesia, e.g. suxamethonium (succinylcholine)
16
Q

Cholinergic transmission:
Non-receptor therapeutic targets

A
  1. Acetylcholine synthesis and release (experimental use only)

Vesamicol blocks ACh packaging into vesicles
Hemicholinium blocks choline uptake

  1. Acetylcholine release

Botulinum toxin type A blocks vesicle docking/release
Botulism caused by food poisoning causes dry mouth/blurred vision, but leads easily to respiratory paralysis (LD50 = 10 ng/kg), must be carefully isolated and purified

  1. Cholinesterase inhibitors (anticholinesterases)
    There are 3 main classes of anticholinesterase

short-acting (eg. edrophonium)
medium-duration (eg. neostigmine and pyridostigmine)
irreversible (eg. ecothiopate)

17
Q

Therapeutic applications of botulinum toxin

A
  1. Muscle spasm
    Excessive muscle spasm can result from stroke, brain or spinal cord injury, cerebral palsy or genetic diseases of nerves.
    Botox® treatment also used for:
    focal dystonic spasms (eg, writer’s cramp)
    spasmodic (spastic) dystonia (eg. contraction of laryngeal muscles, eyelid spasm) and neck (torticollis)
    pain associated with continual muscle contraction.
  2. Migraine/headache treatment
    Suggested that facial muscle contraction stimulates headache.
  3. Excessive secretion
    Botox® is used for the treatment of severe underarm sweating (hyperhidrosis) and salivation (drooling) that is not adequately managed with topical agents. Treatment can be effective for 6-10 months.
18
Q

Therapeutic uses of anticholinesterases

A
  1. Myasthenia gravis
    Autoimmune disease leading to depletion of nAChRs at NMJ.
    Neostigmine or pyridostigmine used as they do cross blood/brain barrier
  2. Dementia
    eg. Alzheimer’s disease (AD) associated with a loss of cholinergic neurones in basal forebrain. Small improvement (~10%) seen with newer reversible, anticholinesterase drugs: donepezil, rivastigmine and galantamine,
    used to treat mild to moderate forms of AD (NICE Guidelines, Sept 2007)
  3. Reversal of competitive neuromuscular block after anaesthesia
    Edrophonium (transient action) and neostigmine
19
Q

SUMMARY
The ANS is a major division of the PNS controlling involuntary movement

Major neurotransmitters are acetylcholine (cholinergic transmission in the parasympathetic nervous system) and noradrenaline (adrenergic transmission in the sympathetic nervous system)

Major therapeutic interest is in muscarinic ACh receptor antagonists in the ANS. However, there is a lack of selectively and a number of side effects associated with these drugs

Major therapeutic interest is in nicotinic ACh receptor blockers (muscle relaxants) and non-receptor targets to affect cholinergic transmission in the SNS

A