A therapeutic oxygen carrier isolated from Arenicola marina decreases amanitin-induced hepatotoxicity
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Updated: Oct 28, 2025

Unveiling Xenobiotic Transport and Effects in Isolated Mitochondria: Insights from Respirometric and Enzymatic Assays
Published on: March 7, 2025
Brendan Le Daré1, Pierre-Jean Ferron2, Nessrine Bellamri2
1Pharmacy, Pontchaillou University Hospital, F-35000, Rennes, France; Univ Rennes, INSERM, INRAE, Institut NuMeCan (Nutrition, Metabolisms and Cancer), F-35000, Rennes, France.
Abstract:
The amanitins (namely α- and β-amanitin) contained in certain mushrooms are bicyclic octapeptides that, when ingested, are responsible for potentially lethal hepatotoxicity. M101 is an extracellular hemoglobin extracted from the marine worm Arenicola marina. It has intrinsic Cu/Zn-SOD-like activity and is currently used as an oxygen carrier in organ preservation solutions. Our present results suggest that M101 might be effective in reducing amanitin-induced hepatotoxicity and may have potential for therapeutic development.
Insights
Marine worm hemoglobin (M101) may reduce liver damage caused by toxic mushroom compounds (amanitins). This finding suggests M101’s potential as a therapeutic agent for amanitin poisoning.
Area of Science:
- Toxicology
- Biochemistry
- Pharmacology
Background:
- Amanitins, bicyclic octapeptides from certain mushrooms, cause severe, potentially lethal hepatotoxicity.
- M101, an extracellular hemoglobin from Arenicola marina, functions as an oxygen carrier and possesses Cu/Zn-SOD-like activity.
Purpose of the Study:
- To investigate the potential of M101 in mitigating amanitin-induced hepatotoxicity.
- To explore M101's therapeutic potential for treating mushroom poisoning.
Main Methods:
- The study evaluated the effects of M101 on liver toxicity induced by amanitins.
- Assays were performed to assess M101's protective mechanisms against cellular damage.
Main Results:
- Preliminary results indicate that M101 demonstrates efficacy in reducing amanitin-induced liver damage.
- M101's intrinsic Cu/Zn-SOD-like activity may contribute to its protective effects.
Conclusions:
- M101 shows promise as a potential therapeutic agent for amanitin poisoning.
- Further research is warranted to fully elucidate M101's mechanism of action and therapeutic utility.
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