General anaesthesia Flashcards

1
Q

What are the clinical roles of anaesthesia?

A
  • Loss of consciousness (at low conc) - Suppression of reflex responses (at high conc) - Analgesia (relief of pain) - Muscle relaxation - Amnesia
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2
Q

What is the problem with the Meyer-Overton theory

A
  • At pharmacologically relevant concentrations, changes to the lipid bilayer are minute - No-one could understand why is a change in the lipid bilayer would result in a dysfunctional membrane protein
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3
Q

Categrorise different GAs

A
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4
Q

How is anaesthesia usually maintained?

A

Inhalational agent - enflurane

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5
Q

How are the effects of GAs produced?

A
  • Reduced neuronal activity - Altered synaptic function
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6
Q

What is the ideal blood:gas partition coefficient for inhaled anaesthetics?

A

LOW: - The majority of the drug that crosses into the blood remains in gaseous form - Can easily enter brain - Also much easier to clear from brain if poorly dissolved in blood. If it’s high, majority of drug becomes liquid in blood and struggles to enter brain

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7
Q

Which one of inhaled or intravenous GAs will cause achieve other clincal aims of GAS , and why

A

Inhaled due to the fact that is is less selective, and acts on other receptors

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8
Q

How do GAs suppress reflex responses?

A
  • Depression of reflex pathways in the dorsal horn of the spinal cord - Anaesthetic agents that enhance GABA and glycine function in dorsal horn will decrease activity of dorsal pathways - Disconnects brain from sensory info from periphery
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9
Q

In a clinical setting describe what you would use for relif of pain, muscle relaxation and amnesia

A
  • Relief of pain (analgesia)–Opioid (e.g. i.v. fentanyl)
  • Muscle relaxation – Neuromuscular blocking

drugs (e.g. suxamethonium

• Amnesia – Benzodiazepines (e.g. i.v. midazolam)

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10
Q

How do intravenous anaesthetics work?

A

E.g. etomidate, propofol

  • Potentiate GABA A receptor function (altered synaptic function) – most abundant, fast inhibitory, ligand-gated ion channel in CNS
  • B3 subunits present : suppress reflex responses - a5 subunits: amnesia
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11
Q

How do inhaled anaesthetics work?

A
  1. Potentiate GABA A receptor function[50% less powerfully than intravenous] (and glycine receptors) - NOTE: glycine = inhibitory NT - Show less selectivity (altered synaptic function)

a1 subunits present - suppression of reflex responses

  1. Inhibits nAChRs (altered synaptic function) - analgesia
  2. Facilitate TREK (background leak) potassium channel opening (reduced neuronal excitability) - loss of consciousness 4. Reduced NMDA receptor function (altered synaptic function) - nitrous oxide
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12
Q

How is anaesthesia usually induced?

A

Intravenous agent - propofol

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13
Q

What other drugs are used to facilitate general anaesthesia?

A
  1. Opioid (e.g. IV fentanyl) - analgesia 2. NM blocking drug (e.g. suxamethonium) for muscle relaxation 3. Benzodiazepines - amnesia
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14
Q

Are intravenous or inhaled anaesthetics more potent?

A

Intravenous

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15
Q

How do GAs cause loss of consciousness?

A
  • thalamus acts as relay station for info btwn cortex + rest of CNS

Depression of thalamocortical neurones caused by: - Background leak K+ channels –> hyperpolarisation - Enhanced GABA function

RAS - decreased firing of RAS, decreased level of arousal

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16
Q

How does route of administration influence the induction/maintenance of anaesthesia?

A

IV: - Fast induction - Difficult to control rate of excretion as injected straight into blood Inhalation: - Large amount of inhaled gas is excreted back into lungs - Gives rapid control of depth of anaesthesia

17
Q

How do GAs cause amnesia?

A
  • At low dose - Lots of GABA receptors in hippocampus w/a5 subunit - Leads to decrease in synaptic transmission in hippocampus (memory formation)
18
Q

What is the Meyer-Overton theory? What was assumed because of it?

A
  • The potency of a G.A. increases in proportion to its oil:water partition coefficient - Therefore – site of action of G.A.s was the lipid bilayer portion of nerve membranes
19
Q

What is unconsciousness?

A

Massive decrease in cortical activity