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Suxamethonium is the only example of a depolarizing neuromuscular blocker in current clinical use. This drug interacts with the acetylcholine receptor at the neuromuscular junction, initially stimulating it and then preventing further stimulation by endogenous acetylcholine, resulting in paralysis.
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Etomidate has similar effects on the brain to thiopental, producing anaesthesia but no analgesia. The site of action of etomidate is assumed to be activation of GABA receptors. Recovery from etomidate is rapid with no hangover. Compared to thiopental, etomidate has a greater margin of safety between anaesthetic dose and the dose that produces cardiorespiratory depression. The main adverse effects with etomidate are pain on injection and muscle twitching during induction, both of which can be reduced by using an opioid analgesic. It also causes suppression of the adrenal cortex.
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Once absorbed into the blood stream, a drug is distributed around the body.
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