Epistemis

Analytical summary: systemic toxicities and their specific antidotes

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The molecular relationship between xenobiotic aggression and the rescue mechanism of the corresponding antidote is summarized in an integrated manner below.

Xenobiotic / Toxon Affected Cellular Target Antidote of Choice Molecular Mechanism of the Antidote
Paracetamol (Overdose)Hepatic glutathione and NAPQI adductsN-Acetylcysteine (NAC)Restores glutathione and acts as an alternative nucleophilic substrate.
Opioids (Fentanyl, Morphine)Mu (µ) opioid receptors in the CNSNaloxonePure, high-affinity competitive antagonist of mu receptors.
Benzodiazepines (Overdose)Allosteric site of the GABAA receptorFlumazenilCompetitive antagonist of the benzodiazepine binding site in GABAA.
Organophosphates / InsecticidesAcetylcholinesterase (AChE)Atropine + PralidoximeMuscarinic antagonist (atropine) and AChE reactivator by dephosphorylation (oxime).
Methanol / Ethylene GlycolHepatic Alcohol Dehydrogenase (ADH)FomepizoleUltra-potent competitive inhibitor of ADH, prevents toxic acid metabolites.
Ferric Iron (Fe3+)Mitochondrial oxidative cellular metabolismDeferoxamineSelective chelating agent, hydrophilic form of ferrioxamine that can be eliminated through urine.
Dabigatran (Pradaxa)Soluble and clot-bound thrombinIdarucizumab (Praxbind)Humanized Fab fragment that sequesters dabigatran with ultra-high affinity.
Rocuronium / VecuroniumACh receptors in muscle motor plateSugammadex (Bridion)Modified synthetic cyclodextrin that irreversibly encapsulates the drug.

Epistemis is educational review material. It is not a medical device, does not diagnose or prescribe treatment, and does not replace formal medical training, current clinical guidelines, or professional clinical judgment.

System
Immunology, Oncology and Toxicology
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