Group |
Example |
Effect |
IV anaesthetic |
Propofol Quickest access |
· ↓L-Ca2+ activity ↑Nitric oxide (NO) release ↓SNS output from medulla ↓CO, ↓↓TPR, ↑depth of anaes |
IV opioid analgesic |
Alfentanil |
· ↓SNS output from medulla · ↔↓CO, ↓↓TPR |
Volatile anaesthetic |
Sevoflurane |
· ↓L-Ca2+ activity, ↓SNS output from medulla · -/↓CO, ↓↓TPR, ↑depth anaes · But slower |
Adrenergic drugs |
Clonidine |
· α2 agonist · ↓NAd release -> ↓TPR |
“” |
Phentolamine |
· α1 and α2 antagonist · ↓TPR, +/-↑HR (initial α2 effect) |
“” |
Phenoxybenzamine |
· α1 and α2 irreversible antagonist · Covalent bond |
“” |
Metoprolol |
· β1 antagonist · ↓CO -> ↓mAP · May precipitate acute LV failure if in setting of ↑↑SVR |
“” |
Labetalol |
· α1, β1 and β2 antagonist · IV 7:1 β:α · ↓CO, ↓TPR |
Nitrate |
Glyceryl trinitrate (GTN) |
· React with ICF sulfhydryl group -> ↑NO -> activate GC -> ↑cGMP -> ↑MLCP activity, ↑Ca2+ reuptake, ↑K+ efflux · Venodilation -> ↓CO · Vasodilation -> ↓TPR |
“” |
NTP |
· Release NO -> same |
Calcium antagonist |
Nifedipine |
· Antagonist at L-Ca2+ · ↓TPR |
“” |
Magnesium |
· Physiological antagonist at L-Ca2+ · ↓TPR |
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