Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance

Penitrem A is a mycotoxin mainly produced by Penicillium crustosum, a fungal species occurring in all climate zones, ranging from tropical to arctic areas. P. crustosum produces a wide range of toxic metabolites, including penitrems, thomitrems and roquefortine C. The major metabolite, penitrem A, h...

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Published in:World Mycotoxin Journal
Main Authors: Eriksen, G.S., Moldes-Anaya, A., Fæste, C.K.
Format: Article in Journal/Newspaper
Language:English
Published: Wageningen Academic Publishers 2013
Subjects:
Online Access:http://dx.doi.org/10.3920/wmj2013.1574
https://www.wageningenacademic.com/doi/pdf/10.3920/WMJ2013.1574
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spelling crwagacadpubl:10.3920/wmj2013.1574 2023-05-15T15:16:58+02:00 Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance Eriksen, G.S. Moldes-Anaya, A. Fæste, C.K. 2013 http://dx.doi.org/10.3920/wmj2013.1574 https://www.wageningenacademic.com/doi/pdf/10.3920/WMJ2013.1574 en eng Wageningen Academic Publishers World Mycotoxin Journal volume 6, issue 3, page 263-272 ISSN 1875-0710 1875-0796 Public Health, Environmental and Occupational Health Toxicology Food Science journal-article 2013 crwagacadpubl https://doi.org/10.3920/wmj2013.1574 2022-04-01T19:34:23Z Penitrem A is a mycotoxin mainly produced by Penicillium crustosum, a fungal species occurring in all climate zones, ranging from tropical to arctic areas. P. crustosum produces a wide range of toxic metabolites, including penitrems, thomitrems and roquefortine C. The major metabolite, penitrem A, has been associated with several episodes of mycotoxicosis in dogs. The clinical symptoms of acute penitrem A intoxication include classical signs of neurotoxicity, such as tremors, convulsions, ataxia and nystagmus. The outcomes of penitrem A intoxication in animals range from total recovery to death, depending mainly on the level of exposure. Cases of suspected human mycotoxicosis following exposure to P. crustosum infected food, beer or inhalation of dust have also been reported. The toxicokinetics of penitrem A is scarcely studied. The toxin is rapidly absorbed, as demonstrated by the rapid onset of symptoms after exposure, but the absorption has not been quantified. Penitrem A is transported systemically after absorption and has been found in liver, kidney and brain as well as in serum and the gastrointestinal tract in exposed animals. Five phase I metabolites have been found in liver extracts of mice 60 min after oral exposure to penitrem A, while three metabolites were found after in vitro incubations with primary rat hepatocytes and rat liver microsomes. Only penitrem A was found in the brains of exposed mice or intoxicated dogs. The elimination has not been studied. Penitrem A is probably the main tremorgenic compound in Penicillium-infected food and feed commodities, since analogues had lower toxic potentials in comparative studies. Penitrem A affects the central as well as the peripheral nervous system. The toxin blocks the high-conductance Ca 2+ -activated potassium channels (BK) and impairs the GABAergic neurotransmission in the cerebellum. Animal poisoning by penitrem A is probably underdiagnosed due to a lack of knowledge among veterinarians. Article in Journal/Newspaper Arctic Wageningen Academic Publishers (via Crossref) Arctic World Mycotoxin Journal 6 3 263 272
institution Open Polar
collection Wageningen Academic Publishers (via Crossref)
op_collection_id crwagacadpubl
language English
topic Public Health, Environmental and Occupational Health
Toxicology
Food Science
spellingShingle Public Health, Environmental and Occupational Health
Toxicology
Food Science
Eriksen, G.S.
Moldes-Anaya, A.
Fæste, C.K.
Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
topic_facet Public Health, Environmental and Occupational Health
Toxicology
Food Science
description Penitrem A is a mycotoxin mainly produced by Penicillium crustosum, a fungal species occurring in all climate zones, ranging from tropical to arctic areas. P. crustosum produces a wide range of toxic metabolites, including penitrems, thomitrems and roquefortine C. The major metabolite, penitrem A, has been associated with several episodes of mycotoxicosis in dogs. The clinical symptoms of acute penitrem A intoxication include classical signs of neurotoxicity, such as tremors, convulsions, ataxia and nystagmus. The outcomes of penitrem A intoxication in animals range from total recovery to death, depending mainly on the level of exposure. Cases of suspected human mycotoxicosis following exposure to P. crustosum infected food, beer or inhalation of dust have also been reported. The toxicokinetics of penitrem A is scarcely studied. The toxin is rapidly absorbed, as demonstrated by the rapid onset of symptoms after exposure, but the absorption has not been quantified. Penitrem A is transported systemically after absorption and has been found in liver, kidney and brain as well as in serum and the gastrointestinal tract in exposed animals. Five phase I metabolites have been found in liver extracts of mice 60 min after oral exposure to penitrem A, while three metabolites were found after in vitro incubations with primary rat hepatocytes and rat liver microsomes. Only penitrem A was found in the brains of exposed mice or intoxicated dogs. The elimination has not been studied. Penitrem A is probably the main tremorgenic compound in Penicillium-infected food and feed commodities, since analogues had lower toxic potentials in comparative studies. Penitrem A affects the central as well as the peripheral nervous system. The toxin blocks the high-conductance Ca 2+ -activated potassium channels (BK) and impairs the GABAergic neurotransmission in the cerebellum. Animal poisoning by penitrem A is probably underdiagnosed due to a lack of knowledge among veterinarians.
format Article in Journal/Newspaper
author Eriksen, G.S.
Moldes-Anaya, A.
Fæste, C.K.
author_facet Eriksen, G.S.
Moldes-Anaya, A.
Fæste, C.K.
author_sort Eriksen, G.S.
title Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
title_short Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
title_full Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
title_fullStr Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
title_full_unstemmed Penitrem A and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
title_sort penitrem a and analogues: toxicokinetics, toxicodynamics including mechanism of action and clinical significance
publisher Wageningen Academic Publishers
publishDate 2013
url http://dx.doi.org/10.3920/wmj2013.1574
https://www.wageningenacademic.com/doi/pdf/10.3920/WMJ2013.1574
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_source World Mycotoxin Journal
volume 6, issue 3, page 263-272
ISSN 1875-0710 1875-0796
op_doi https://doi.org/10.3920/wmj2013.1574
container_title World Mycotoxin Journal
container_volume 6
container_issue 3
container_start_page 263
op_container_end_page 272
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