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Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing

Drug-based treatment of alveolar echinococcosis (AE) with benzimidazoles is in most cases non-curative, thus has to be taken lifelong. Here, we report on a 56-year-old male AE patient who received standard benzimidazole treatment and biliary plastic stents, and additionally self-medicated himself wi...

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Autores principales: Karpstein, Tanja, Chaudhry, Sheena, Bresson-Hadni, Solange, Hayoz, Michael, Boubaker, Ghalia, Hemphill, Andrew, Rufener, Reto, Kaethner, Marc, Schindler, Isabelle, Aebi, Yolanda, Cunha, Antonio Sa, Largiadèr, Carlo R., Lundström-Stadelmann, Britta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537204/
https://www.ncbi.nlm.nih.gov/pubmed/34684284
http://dx.doi.org/10.3390/pathogens10101335
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author Karpstein, Tanja
Chaudhry, Sheena
Bresson-Hadni, Solange
Hayoz, Michael
Boubaker, Ghalia
Hemphill, Andrew
Rufener, Reto
Kaethner, Marc
Schindler, Isabelle
Aebi, Yolanda
Cunha, Antonio Sa
Largiadèr, Carlo R.
Lundström-Stadelmann, Britta
author_facet Karpstein, Tanja
Chaudhry, Sheena
Bresson-Hadni, Solange
Hayoz, Michael
Boubaker, Ghalia
Hemphill, Andrew
Rufener, Reto
Kaethner, Marc
Schindler, Isabelle
Aebi, Yolanda
Cunha, Antonio Sa
Largiadèr, Carlo R.
Lundström-Stadelmann, Britta
author_sort Karpstein, Tanja
collection PubMed
description Drug-based treatment of alveolar echinococcosis (AE) with benzimidazoles is in most cases non-curative, thus has to be taken lifelong. Here, we report on a 56-year-old male AE patient who received standard benzimidazole treatment and biliary plastic stents, and additionally self-medicated himself with the Peruvian plant extract Maca (Lepidium meyenii). After 42 months, viable parasite tissue had disappeared. Based on this striking observation, the anti-echinococcal activity of Maca was investigated in vitro and in mice experimentally infected with Echinococcus multilocularis metacestodes. Albendazole (ABZ)-treated mice and mice treated with an ABZ+Maca combination exhibited a significantly reduced parasite burden compared to untreated or Maca-treated mice. As shown by a newly established UHPLC-MS/MS-based measurement of ABZ-metabolites, the presence of Maca during the treatment did not alter ABZ plasma levels. In vitro assays corroborated these findings, as exposure to Maca had no notable effect on E. multilocularis metacestodes, and in cultures of germinal layer cells, possibly unspecific, cytotoxic effects of Maca were observed. However, in the combined treatments, Maca inhibited the activity of ABZ in vitro. While Maca had no direct anti-parasitic activity, it induced in vitro proliferation of murine spleen cells, suggesting that immunomodulatory properties could have contributed to the curative effect seen in the patient.
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spelling pubmed-85372042021-10-24 Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing Karpstein, Tanja Chaudhry, Sheena Bresson-Hadni, Solange Hayoz, Michael Boubaker, Ghalia Hemphill, Andrew Rufener, Reto Kaethner, Marc Schindler, Isabelle Aebi, Yolanda Cunha, Antonio Sa Largiadèr, Carlo R. Lundström-Stadelmann, Britta Pathogens Article Drug-based treatment of alveolar echinococcosis (AE) with benzimidazoles is in most cases non-curative, thus has to be taken lifelong. Here, we report on a 56-year-old male AE patient who received standard benzimidazole treatment and biliary plastic stents, and additionally self-medicated himself with the Peruvian plant extract Maca (Lepidium meyenii). After 42 months, viable parasite tissue had disappeared. Based on this striking observation, the anti-echinococcal activity of Maca was investigated in vitro and in mice experimentally infected with Echinococcus multilocularis metacestodes. Albendazole (ABZ)-treated mice and mice treated with an ABZ+Maca combination exhibited a significantly reduced parasite burden compared to untreated or Maca-treated mice. As shown by a newly established UHPLC-MS/MS-based measurement of ABZ-metabolites, the presence of Maca during the treatment did not alter ABZ plasma levels. In vitro assays corroborated these findings, as exposure to Maca had no notable effect on E. multilocularis metacestodes, and in cultures of germinal layer cells, possibly unspecific, cytotoxic effects of Maca were observed. However, in the combined treatments, Maca inhibited the activity of ABZ in vitro. While Maca had no direct anti-parasitic activity, it induced in vitro proliferation of murine spleen cells, suggesting that immunomodulatory properties could have contributed to the curative effect seen in the patient. MDPI 2021-10-15 /pmc/articles/PMC8537204/ /pubmed/34684284 http://dx.doi.org/10.3390/pathogens10101335 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Karpstein, Tanja
Chaudhry, Sheena
Bresson-Hadni, Solange
Hayoz, Michael
Boubaker, Ghalia
Hemphill, Andrew
Rufener, Reto
Kaethner, Marc
Schindler, Isabelle
Aebi, Yolanda
Cunha, Antonio Sa
Largiadèr, Carlo R.
Lundström-Stadelmann, Britta
Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing
title Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing
title_full Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing
title_fullStr Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing
title_full_unstemmed Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing
title_short Maca against Echinococcosis?—A Reverse Approach from Patient to In Vitro Testing
title_sort maca against echinococcosis?—a reverse approach from patient to in vitro testing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537204/
https://www.ncbi.nlm.nih.gov/pubmed/34684284
http://dx.doi.org/10.3390/pathogens10101335
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