(PM3B) Local Anaesthetics Flashcards
What is the resting membrane potential of a cell?
-70mV
What is the depolarised membrane potential following the overshoot?
+50mV
How long does an action potential take to generate and be reset?
5msec
What are the stages of action potential generation?
(1) Stimulating current (at -70mV)
(2) Depolarisation
(3) Overshoot (to +50mV)
(4) Repolarisation
(5) Hyperpolarising afterpotential
Which major currents determine an action potential?
(1) Sodium current
- moves inwards
- depolarising current
(2) Potassium current
- moves outward
- hyperpolarising current
Which sodium channel opens following activation?
m-gate (depolarisation)
Which sodium channel opens following inactivation?
h-gate
Which potassium channel opens following activation?
n-gate
What is TTX?
Tetrodotoxin
Which voltage-gated sodium channels are considered tetrodotoxin (TTX) sensitive?
(1) rNav1.1
(2) rNav1.2
(3) rNav1.3
Which voltage-gated sodium channels are considered tetrodotoxin (TTX) non-selective?
(1) rNav1.7
(2) rNav1.4
(3) rNav1.6
Which voltage-gated sodium channels are considered tetrodotoxin (TTX) resistant?
(1) rNav1.5
(2) rNav1.8
(3) rNav1.9
What are the main structures in cocaine, lidocaine, bupivacaine etc?
(1) Aromatic region
(2) Ester/ amide bond
(3) Basic amine
Why are cocaine, procaine, and tetracaine considered to be short-acting?
Have an ester bond
Esters metabolised by plasma esterases
Why are lidocaine and bupivacaine considered to be long-acting?
Have an amide bond
Metabolised by liver
What are the pathways utilised by local anaesthetics?
(1) Hydrophobic
(2) Hydrophilic
Depends on ionisation state of local anaesthetic
What is the hydrophilic pathway, in terms of local anaesthetics?
Major mode of local anaesthetic action
~90%
What is the hydrophobic pathway, in terms of local anaesthetics?
Secondary mode of local anaesthetic action
~10%
Describe the physicochemical properties of local anaesthetics.
Weak bases (pKa ~8-9)
Largely ionised at neutral pH
What ionisation of local anaesthetics is required to act?
Must cross membrane in unionised form
What is use-dependence?
More a channel is open the greater the drug block
Increased access to drug binding site
How is local anaesthetic action characterised?
(1) Duration of action/ degree of tissue penetration
(2) Use-dependent block of sodium channels
(3) Preferential block of small diameter nerve fibres
- nociceptive C and A-delta fibres are blocked more readily than AĆ fibres
(4) Preferential block of inactivated state of sodium channels
- Local anaesthetics have a higher affinity for inactivated state
Describe the onset of action of cocaine.
Medium
Describe the onset of action of procaine.
Medium
Describe the onset of action of lidocaine
Rapid
Describe the onset of action of tetracaine.
Very slow
Describe the onset of action of bupivacaine.
Slow
Describe the onset of action of prilocaine.
Medium
Describe the onset of action of articaine.
Rapid
Describe the duration of action of cocaine.
Medium
Describe the duration of action of procaine.
Short
Describe the duration of action of lidocaine.
Medium