In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract

Biocolourants could be a sustainable option for dyes that require fossil-based chemicals in their synthesis. We studied the in vitro toxicity of anthraquinone aglycone extract obtained from <i>Cortinarius sanguineus</i> fungus and compared it to the toxicity of its two main components, e...

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出版年:Journal of Fungi
主要な著者: Johanna Yli-Öyrä, Mikko Herrala, Harri Kovakoski, Eevi Huuskonen, Peppi Toukola, Riikka Räisänen, Jaana Rysä
フォーマット: 論文
言語:英語
出版事項: MDPI AG 2024-05-01
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オンライン・アクセス:https://www.mdpi.com/2309-608X/10/6/369
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author Johanna Yli-Öyrä
Mikko Herrala
Harri Kovakoski
Eevi Huuskonen
Peppi Toukola
Riikka Räisänen
Jaana Rysä
author_facet Johanna Yli-Öyrä
Mikko Herrala
Harri Kovakoski
Eevi Huuskonen
Peppi Toukola
Riikka Räisänen
Jaana Rysä
author_sort Johanna Yli-Öyrä
collection DOAJ
container_title Journal of Fungi
description Biocolourants could be a sustainable option for dyes that require fossil-based chemicals in their synthesis. We studied the in vitro toxicity of anthraquinone aglycone extract obtained from <i>Cortinarius sanguineus</i> fungus and compared it to the toxicity of its two main components, emodin and previously studied dermocybin. Cell viability, cytotoxicity, and oxidative stress responses in HepG2 liver and THP-1 immune cell lines were studied along with skin sensitisation. In addition, genotoxicity was studied with comet assay in HepG2 cells. Cellular viability was determined by MTT, propidium iodide, and lactate dehydrogenase assays, which showed that the highest doses of both the aglycone extract and emodin affected the viability. However, the effect did not occur in all of the used assays. Notably, after both exposures, a dose-dependent increase in oxidative stress factors was observed in both cell lines as measured by MitoSOX and dihydroethidium assays. <i>C. sanguineus</i> extract was not genotoxic in the comet assay. Importantly, both emodin and the extract activated the skin sensitisation pathway in the KeratinoSens assay, suggesting that they can induce allergy in humans. As emodin has shown cytotoxic and skin-sensitising effects, it is possible that the adverse effects caused by the extract are also mediated by it since it is the main component present in the fungus.
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spelling doaj-art-e89e880f175a4d4a9685f62906c3bcdf2025-08-19T23:12:46ZengMDPI AGJournal of Fungi2309-608X2024-05-0110636910.3390/jof10060369In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone ExtractJohanna Yli-Öyrä0Mikko Herrala1Harri Kovakoski2Eevi Huuskonen3Peppi Toukola4Riikka Räisänen5Jaana Rysä6School of Pharmacy, University of Eastern Finland, 70210 Kuopio, FinlandSchool of Pharmacy, University of Eastern Finland, 70210 Kuopio, FinlandSchool of Pharmacy, University of Eastern Finland, 70210 Kuopio, FinlandSchool of Pharmacy, University of Eastern Finland, 70210 Kuopio, FinlandCraft Studies, University of Helsinki, 00014 Helsinki, FinlandCraft Studies, University of Helsinki, 00014 Helsinki, FinlandSchool of Pharmacy, University of Eastern Finland, 70210 Kuopio, FinlandBiocolourants could be a sustainable option for dyes that require fossil-based chemicals in their synthesis. We studied the in vitro toxicity of anthraquinone aglycone extract obtained from <i>Cortinarius sanguineus</i> fungus and compared it to the toxicity of its two main components, emodin and previously studied dermocybin. Cell viability, cytotoxicity, and oxidative stress responses in HepG2 liver and THP-1 immune cell lines were studied along with skin sensitisation. In addition, genotoxicity was studied with comet assay in HepG2 cells. Cellular viability was determined by MTT, propidium iodide, and lactate dehydrogenase assays, which showed that the highest doses of both the aglycone extract and emodin affected the viability. However, the effect did not occur in all of the used assays. Notably, after both exposures, a dose-dependent increase in oxidative stress factors was observed in both cell lines as measured by MitoSOX and dihydroethidium assays. <i>C. sanguineus</i> extract was not genotoxic in the comet assay. Importantly, both emodin and the extract activated the skin sensitisation pathway in the KeratinoSens assay, suggesting that they can induce allergy in humans. As emodin has shown cytotoxic and skin-sensitising effects, it is possible that the adverse effects caused by the extract are also mediated by it since it is the main component present in the fungus.https://www.mdpi.com/2309-608X/10/6/369allergyanthraquinone<i>Cortinarius sanguineus</i>cytotoxicityemodingenotoxicity
spellingShingle Johanna Yli-Öyrä
Mikko Herrala
Harri Kovakoski
Eevi Huuskonen
Peppi Toukola
Riikka Räisänen
Jaana Rysä
In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract
allergy
anthraquinone
<i>Cortinarius sanguineus</i>
cytotoxicity
emodin
genotoxicity
title In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract
title_full In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract
title_fullStr In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract
title_full_unstemmed In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract
title_short In Vitro Toxicity Assessment of <i>Cortinarius sanguineus</i> Anthraquinone Aglycone Extract
title_sort in vitro toxicity assessment of i cortinarius sanguineus i anthraquinone aglycone extract
topic allergy
anthraquinone
<i>Cortinarius sanguineus</i>
cytotoxicity
emodin
genotoxicity
url https://www.mdpi.com/2309-608X/10/6/369
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