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Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast

Overweight and obesity prevalence has increased worldwide. Apart from conventional approaches, people also resort to botanical supplements for reducing body weight, although several adverse events have been associated with these products. In this context, the present study aimed at evaluating the to...

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Autores principales: Di Giacomo, Silvia, Di Sotto, Antonella, Percaccio, Ester, Scuotto, Erica, Battistelli, Cecilia, Mazzanti, Gabriela, Menniti-Ippolito, Francesca, Ippoliti, Ilaria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525400/
https://www.ncbi.nlm.nih.gov/pubmed/37760074
http://dx.doi.org/10.3390/antiox12091771
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author Di Giacomo, Silvia
Di Sotto, Antonella
Percaccio, Ester
Scuotto, Erica
Battistelli, Cecilia
Mazzanti, Gabriela
Menniti-Ippolito, Francesca
Ippoliti, Ilaria
author_facet Di Giacomo, Silvia
Di Sotto, Antonella
Percaccio, Ester
Scuotto, Erica
Battistelli, Cecilia
Mazzanti, Gabriela
Menniti-Ippolito, Francesca
Ippoliti, Ilaria
author_sort Di Giacomo, Silvia
collection PubMed
description Overweight and obesity prevalence has increased worldwide. Apart from conventional approaches, people also resort to botanical supplements for reducing body weight, although several adverse events have been associated with these products. In this context, the present study aimed at evaluating the toxicity of Garcinia cambogia-based products and shedding light on the mechanisms involved. The suspected hepatotoxic reactions related to G. cambogia-containing products collected within the Italian Phytovigilance System (IPS) were examined. Then, an in vitro study was performed to evaluate the possible mechanisms responsible for the liver toxicity, focusing on the modulation of oxidative stress and Nrf2 expression. From March 2002 to March 2022, the IPS collected eight reports of hepatic adverse reactions related to G. cambogia, which exclusively involved women and were mostly severe. The causality assessment was probable in three cases, while it was possible in five. In the in vitro experiments, a low cytotoxicity of G. cambogia was observed. However, its combination with montelukast greatly reduced cell viability, increased the intracellular ROS levels, and affected the cytoplasmic Nrf2 expression, thus suggesting an impairment of the antioxidant and cytoprotective defenses. Overall, our results support the safety concerns about G. cambogia-containing supplements and shed light on the possible mechanisms underpinning its hepatotoxicity.
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spelling pubmed-105254002023-09-28 Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast Di Giacomo, Silvia Di Sotto, Antonella Percaccio, Ester Scuotto, Erica Battistelli, Cecilia Mazzanti, Gabriela Menniti-Ippolito, Francesca Ippoliti, Ilaria Antioxidants (Basel) Article Overweight and obesity prevalence has increased worldwide. Apart from conventional approaches, people also resort to botanical supplements for reducing body weight, although several adverse events have been associated with these products. In this context, the present study aimed at evaluating the toxicity of Garcinia cambogia-based products and shedding light on the mechanisms involved. The suspected hepatotoxic reactions related to G. cambogia-containing products collected within the Italian Phytovigilance System (IPS) were examined. Then, an in vitro study was performed to evaluate the possible mechanisms responsible for the liver toxicity, focusing on the modulation of oxidative stress and Nrf2 expression. From March 2002 to March 2022, the IPS collected eight reports of hepatic adverse reactions related to G. cambogia, which exclusively involved women and were mostly severe. The causality assessment was probable in three cases, while it was possible in five. In the in vitro experiments, a low cytotoxicity of G. cambogia was observed. However, its combination with montelukast greatly reduced cell viability, increased the intracellular ROS levels, and affected the cytoplasmic Nrf2 expression, thus suggesting an impairment of the antioxidant and cytoprotective defenses. Overall, our results support the safety concerns about G. cambogia-containing supplements and shed light on the possible mechanisms underpinning its hepatotoxicity. MDPI 2023-09-16 /pmc/articles/PMC10525400/ /pubmed/37760074 http://dx.doi.org/10.3390/antiox12091771 Text en © 2023 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
Di Giacomo, Silvia
Di Sotto, Antonella
Percaccio, Ester
Scuotto, Erica
Battistelli, Cecilia
Mazzanti, Gabriela
Menniti-Ippolito, Francesca
Ippoliti, Ilaria
Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast
title Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast
title_full Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast
title_fullStr Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast
title_full_unstemmed Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast
title_short Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast
title_sort interaction of garcinia cambogia (gaertn.) desr. and drugs as a possible mechanism of liver injury: the case of montelukast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10525400/
https://www.ncbi.nlm.nih.gov/pubmed/37760074
http://dx.doi.org/10.3390/antiox12091771
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