Fate of ptaquiloside-A bracken fern toxin-In cattle.

Ptaquiloside is a natural toxin present in bracken ferns (Pteridium sp.). Cattle ingesting bracken may develop bladder tumours and excrete genotoxins in meat and milk. However, the fate of ptaquiloside in cattle and the link between ptaquiloside and cattle carcinogenesis is unresolved. Here, we pres...

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Main Authors: Paulo César Dos Reis Aranha, Lars Holm Rasmussen, Godelind Alma Wolf-Jäckel, Henrik Michael Elvang Jensen, Hans Christian Bruun Hansen, Christian Friis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0218628
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spelling doaj-205453a44dc448d49309e8a47ee7269a2021-03-03T20:36:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01146e021862810.1371/journal.pone.0218628Fate of ptaquiloside-A bracken fern toxin-In cattle.Paulo César Dos Reis AranhaLars Holm RasmussenGodelind Alma Wolf-JäckelHenrik Michael Elvang JensenHans Christian Bruun HansenChristian FriisPtaquiloside is a natural toxin present in bracken ferns (Pteridium sp.). Cattle ingesting bracken may develop bladder tumours and excrete genotoxins in meat and milk. However, the fate of ptaquiloside in cattle and the link between ptaquiloside and cattle carcinogenesis is unresolved. Here, we present the toxicokinetic profile of ptaquiloside in plasma and urine after intravenous administration of ptaquiloside and after oral administration of bracken. Administered intravenously ptaquiloside, revealed a volume of distribution of 1.3 L kg-1 with a mean residence-time of 4 hours. A large fraction of ptaquiloside was converted to non-toxic pterosin B in the blood stream. Both ptaquiloside and pterosin B were excreted in urine (up to 41% of the dose). Oral administration of ptaquiloside via bracken extract or dried ferns did not result in observations of ptaquiloside in body fluids, indicating deglycosolidation in the rumen. Pterosin B was detected in both plasma and urine after oral administration. Hence, transport of carcinogenic ptaquiloside metabolites over the rumen membrane is indicated. Pterosin B recovered from urine counted for 7% of the dose given intravenously. Heifers exposed to bracken for 7 days (2 mg ptaquiloside kg-1) developed preneoplastic lesions in the urinary bladder most likely caused by genotoxic ptaquiloside metabolites.https://doi.org/10.1371/journal.pone.0218628
collection DOAJ
language English
format Article
sources DOAJ
author Paulo César Dos Reis Aranha
Lars Holm Rasmussen
Godelind Alma Wolf-Jäckel
Henrik Michael Elvang Jensen
Hans Christian Bruun Hansen
Christian Friis
spellingShingle Paulo César Dos Reis Aranha
Lars Holm Rasmussen
Godelind Alma Wolf-Jäckel
Henrik Michael Elvang Jensen
Hans Christian Bruun Hansen
Christian Friis
Fate of ptaquiloside-A bracken fern toxin-In cattle.
PLoS ONE
author_facet Paulo César Dos Reis Aranha
Lars Holm Rasmussen
Godelind Alma Wolf-Jäckel
Henrik Michael Elvang Jensen
Hans Christian Bruun Hansen
Christian Friis
author_sort Paulo César Dos Reis Aranha
title Fate of ptaquiloside-A bracken fern toxin-In cattle.
title_short Fate of ptaquiloside-A bracken fern toxin-In cattle.
title_full Fate of ptaquiloside-A bracken fern toxin-In cattle.
title_fullStr Fate of ptaquiloside-A bracken fern toxin-In cattle.
title_full_unstemmed Fate of ptaquiloside-A bracken fern toxin-In cattle.
title_sort fate of ptaquiloside-a bracken fern toxin-in cattle.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Ptaquiloside is a natural toxin present in bracken ferns (Pteridium sp.). Cattle ingesting bracken may develop bladder tumours and excrete genotoxins in meat and milk. However, the fate of ptaquiloside in cattle and the link between ptaquiloside and cattle carcinogenesis is unresolved. Here, we present the toxicokinetic profile of ptaquiloside in plasma and urine after intravenous administration of ptaquiloside and after oral administration of bracken. Administered intravenously ptaquiloside, revealed a volume of distribution of 1.3 L kg-1 with a mean residence-time of 4 hours. A large fraction of ptaquiloside was converted to non-toxic pterosin B in the blood stream. Both ptaquiloside and pterosin B were excreted in urine (up to 41% of the dose). Oral administration of ptaquiloside via bracken extract or dried ferns did not result in observations of ptaquiloside in body fluids, indicating deglycosolidation in the rumen. Pterosin B was detected in both plasma and urine after oral administration. Hence, transport of carcinogenic ptaquiloside metabolites over the rumen membrane is indicated. Pterosin B recovered from urine counted for 7% of the dose given intravenously. Heifers exposed to bracken for 7 days (2 mg ptaquiloside kg-1) developed preneoplastic lesions in the urinary bladder most likely caused by genotoxic ptaquiloside metabolites.
url https://doi.org/10.1371/journal.pone.0218628
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