Cargando…

Toxic metabolite profiling of Inocybe virosa

Wild mushroom foraging involves a high risk of unintentional consumption of poisonous mushrooms which is a serious health concern. This problem arises due to the close morphological resemblances of toxic mushrooms with edible ones. The genus Inocybe comprises both edible and poisonous species and it...

Descripción completa

Detalles Bibliográficos
Autores principales: Sai Latha, S., Shivanna, Naveen, Naika, Mahadeva, Anilakumar, K. R., Kaul, Ankur, Mittal, Gaurav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426861/
https://www.ncbi.nlm.nih.gov/pubmed/32792538
http://dx.doi.org/10.1038/s41598-020-70196-7
_version_ 1783570773323022336
author Sai Latha, S.
Shivanna, Naveen
Naika, Mahadeva
Anilakumar, K. R.
Kaul, Ankur
Mittal, Gaurav
author_facet Sai Latha, S.
Shivanna, Naveen
Naika, Mahadeva
Anilakumar, K. R.
Kaul, Ankur
Mittal, Gaurav
author_sort Sai Latha, S.
collection PubMed
description Wild mushroom foraging involves a high risk of unintentional consumption of poisonous mushrooms which is a serious health concern. This problem arises due to the close morphological resemblances of toxic mushrooms with edible ones. The genus Inocybe comprises both edible and poisonous species and it is therefore important to differentiate them. Knowledge about their chemical nature will unambiguously determine their edibility and aid in an effective treatment in case of poisonings. In the present study, the presence of volatile toxic metabolites was verified in Inocybe virosa by gas chromatography. Methyl palmitate, phenol, 3,5-bis (1,1-dimethyl ethyl) and phytol were the identified compounds with suspected toxicity. The presence of the toxin muscarine was confirmed by liquid chromatography. The in vitro study showed that there was negligible effect of the digestion process on muscarine content or its toxicity. Therefore, the role of muscarine in the toxicity of Inocybe virosa was studied using a bioassay wherein metameters such as hypersalivation, immobility, excessive defecation, heart rate and micturition were measured. Administration of muscarine resulted in an earlier onset of symptoms and the extract showed a slightly stronger muscarinic effect in comparison to an equivalent dose of muscarine estimated in it. Further, the biological fate of muscarine was studied by pharmacokinetics and gamma scintigraphy in New Zealand white rabbits. Significant amount of the toxin was rapidly and effectively concentrated in the thorax and head region. This study closely explains the early muscarinic response such as miosis and salivation in mice. By the end of 24 h, a relatively major proportion of muscarine administered was accumulated in the liver which stands as an explanation to the hepatotoxicity of Inocybe virosa. This is one of the rare studies that has attempted to understand the toxic potential of muscarine which has previously been explored extensively for its pharmaceutical applications.
format Online
Article
Text
id pubmed-7426861
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-74268612020-08-14 Toxic metabolite profiling of Inocybe virosa Sai Latha, S. Shivanna, Naveen Naika, Mahadeva Anilakumar, K. R. Kaul, Ankur Mittal, Gaurav Sci Rep Article Wild mushroom foraging involves a high risk of unintentional consumption of poisonous mushrooms which is a serious health concern. This problem arises due to the close morphological resemblances of toxic mushrooms with edible ones. The genus Inocybe comprises both edible and poisonous species and it is therefore important to differentiate them. Knowledge about their chemical nature will unambiguously determine their edibility and aid in an effective treatment in case of poisonings. In the present study, the presence of volatile toxic metabolites was verified in Inocybe virosa by gas chromatography. Methyl palmitate, phenol, 3,5-bis (1,1-dimethyl ethyl) and phytol were the identified compounds with suspected toxicity. The presence of the toxin muscarine was confirmed by liquid chromatography. The in vitro study showed that there was negligible effect of the digestion process on muscarine content or its toxicity. Therefore, the role of muscarine in the toxicity of Inocybe virosa was studied using a bioassay wherein metameters such as hypersalivation, immobility, excessive defecation, heart rate and micturition were measured. Administration of muscarine resulted in an earlier onset of symptoms and the extract showed a slightly stronger muscarinic effect in comparison to an equivalent dose of muscarine estimated in it. Further, the biological fate of muscarine was studied by pharmacokinetics and gamma scintigraphy in New Zealand white rabbits. Significant amount of the toxin was rapidly and effectively concentrated in the thorax and head region. This study closely explains the early muscarinic response such as miosis and salivation in mice. By the end of 24 h, a relatively major proportion of muscarine administered was accumulated in the liver which stands as an explanation to the hepatotoxicity of Inocybe virosa. This is one of the rare studies that has attempted to understand the toxic potential of muscarine which has previously been explored extensively for its pharmaceutical applications. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426861/ /pubmed/32792538 http://dx.doi.org/10.1038/s41598-020-70196-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sai Latha, S.
Shivanna, Naveen
Naika, Mahadeva
Anilakumar, K. R.
Kaul, Ankur
Mittal, Gaurav
Toxic metabolite profiling of Inocybe virosa
title Toxic metabolite profiling of Inocybe virosa
title_full Toxic metabolite profiling of Inocybe virosa
title_fullStr Toxic metabolite profiling of Inocybe virosa
title_full_unstemmed Toxic metabolite profiling of Inocybe virosa
title_short Toxic metabolite profiling of Inocybe virosa
title_sort toxic metabolite profiling of inocybe virosa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426861/
https://www.ncbi.nlm.nih.gov/pubmed/32792538
http://dx.doi.org/10.1038/s41598-020-70196-7
work_keys_str_mv AT sailathas toxicmetaboliteprofilingofinocybevirosa
AT shivannanaveen toxicmetaboliteprofilingofinocybevirosa
AT naikamahadeva toxicmetaboliteprofilingofinocybevirosa
AT anilakumarkr toxicmetaboliteprofilingofinocybevirosa
AT kaulankur toxicmetaboliteprofilingofinocybevirosa
AT mittalgaurav toxicmetaboliteprofilingofinocybevirosa