Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series

AbstractIngestion of amatoxin-containing mushrooms can lead to fulminant hepatotoxicity and death. Despite recent interest in therapeutic options for amatoxin-exposed patients, there is no single, recommended treatment for amatoxin poisoning. Alpha-amanitin, the principal toxin in amatoxin-containin...

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Main Authors: Constance A. Mackenzie, Emily Austin, Margaret Thompson, Rommel G. Tirona
Format: Article
Language:English
Published: Taylor & Francis Group 2022-12-01
Series:Toxicology Communications
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/24734306.2021.2006957
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author Constance A. Mackenzie
Emily Austin
Margaret Thompson
Rommel G. Tirona
author_facet Constance A. Mackenzie
Emily Austin
Margaret Thompson
Rommel G. Tirona
author_sort Constance A. Mackenzie
collection DOAJ
description AbstractIngestion of amatoxin-containing mushrooms can lead to fulminant hepatotoxicity and death. Despite recent interest in therapeutic options for amatoxin-exposed patients, there is no single, recommended treatment for amatoxin poisoning. Alpha-amanitin, the principal toxin in amatoxin-containing mushrooms, requires entry into hepatocytes via organic anion transporting polypeptide (OATP) 1B3 before the cascade of cellular events occurs leading to hepatocyte necrosis, liver failure, and in severe cases liver transplantation or death. Three patients managed through a single poison centre with confirmed amatoxin-containing mushrooms ingestions were treated with intravenous cyclosporine, a known potent OATP1B3 inhibitor, along with supportive care. All patients presented with classic delayed symptoms of nausea, vomiting and diarrhea. No patient progressed to fulminant hepatic failure, although two patients developed a transient rise in liver transaminases. All recovered and were discharged from hospital. No patient had an adverse effect from cyclosporine. In addition, we performed an in-vitro study of the role of cyclosporine in cultured HEK293T cells and human hepatoma Huh7 cells. Cyclosporine effectively inhibited OATP1B3-mediated uptake of alpha-amanitin, and improved cell viability of alpha-amanitin exposed cultured Huh7 cells.We conclude that IV cyclosporine, a drug readily available in most hospitals, may be useful to reduce hepatotoxicity from amatoxin poisoning.
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spelling doaj.art-78df6404b956403689454ddc5dbe2c152023-06-13T12:55:24ZengTaylor & Francis GroupToxicology Communications2473-43062022-12-0161232710.1080/24734306.2021.2006957Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case seriesConstance A. Mackenzie0Emily Austin1Margaret Thompson2Rommel G. Tirona3Ontario Poison Centre, Hospital for Sick Children, Division of Clinical Pharmacology and Toxicology, Toronto, Ontario, CanadaOntario Poison Centre, Hospital for Sick Children, Division of Clinical Pharmacology and Toxicology, Toronto, Ontario, CanadaOntario Poison Centre, Hospital for Sick Children, Division of Clinical Pharmacology and Toxicology, Toronto, Ontario, CanadaDepartments of Physiology & Pharmacology and Medicine, Schulich School of Medicine & Dentistry, Western University, London, Ontario, CanadaAbstractIngestion of amatoxin-containing mushrooms can lead to fulminant hepatotoxicity and death. Despite recent interest in therapeutic options for amatoxin-exposed patients, there is no single, recommended treatment for amatoxin poisoning. Alpha-amanitin, the principal toxin in amatoxin-containing mushrooms, requires entry into hepatocytes via organic anion transporting polypeptide (OATP) 1B3 before the cascade of cellular events occurs leading to hepatocyte necrosis, liver failure, and in severe cases liver transplantation or death. Three patients managed through a single poison centre with confirmed amatoxin-containing mushrooms ingestions were treated with intravenous cyclosporine, a known potent OATP1B3 inhibitor, along with supportive care. All patients presented with classic delayed symptoms of nausea, vomiting and diarrhea. No patient progressed to fulminant hepatic failure, although two patients developed a transient rise in liver transaminases. All recovered and were discharged from hospital. No patient had an adverse effect from cyclosporine. In addition, we performed an in-vitro study of the role of cyclosporine in cultured HEK293T cells and human hepatoma Huh7 cells. Cyclosporine effectively inhibited OATP1B3-mediated uptake of alpha-amanitin, and improved cell viability of alpha-amanitin exposed cultured Huh7 cells.We conclude that IV cyclosporine, a drug readily available in most hospitals, may be useful to reduce hepatotoxicity from amatoxin poisoning.https://www.tandfonline.com/doi/10.1080/24734306.2021.2006957amatoxinmushroomtoxicitypoisoningcyclosporinecase series
spellingShingle Constance A. Mackenzie
Emily Austin
Margaret Thompson
Rommel G. Tirona
Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series
Toxicology Communications
amatoxin
mushroom
toxicity
poisoning
cyclosporine
case series
title Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series
title_full Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series
title_fullStr Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series
title_full_unstemmed Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series
title_short Cyclosporine as a novel treatment for amatoxin-containing mushroom poisoning: a case series
title_sort cyclosporine as a novel treatment for amatoxin containing mushroom poisoning a case series
topic amatoxin
mushroom
toxicity
poisoning
cyclosporine
case series
url https://www.tandfonline.com/doi/10.1080/24734306.2021.2006957
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