Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip

Abstract Due to the increasing availability of hemp-derived products for recreational and medicinal use, it is imperative to understand the hepatotoxicity of the naturally occurring phytocannabinoids. Though, traditionally animal models or in vitro techniques are used to evaluate hepatotoxicity, the...

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Main Authors: Jacob D. Larson, Sushma Jadalannagari, Jake Chaff, James Velez, Josiah Sliz, Lorna Ewart, Donna Webster, Jiang Hu
Format: Article
Language:English
Published: Nature Portfolio 2025-08-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-12846-2
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author Jacob D. Larson
Sushma Jadalannagari
Jake Chaff
James Velez
Josiah Sliz
Lorna Ewart
Donna Webster
Jiang Hu
author_facet Jacob D. Larson
Sushma Jadalannagari
Jake Chaff
James Velez
Josiah Sliz
Lorna Ewart
Donna Webster
Jiang Hu
author_sort Jacob D. Larson
collection DOAJ
description Abstract Due to the increasing availability of hemp-derived products for recreational and medicinal use, it is imperative to understand the hepatotoxicity of the naturally occurring phytocannabinoids. Though, traditionally animal models or in vitro techniques are used to evaluate hepatotoxicity, these methods often fail due to the species differences and lack of the needed complexity. Thus, this study investigated the hepatotoxicity potential of Cannabidiol (CBD), Cannabinol (CBN), Cannabichromene (CBC), and Cannabigerol (CBG) using the Emulate Quad-Culture Liver-Chip model. Liver-Chips were dosed with three concentrations (0.24, 3, or 4.7 µM) of each cannabinoid for 7 days continuously, and acetaminophen (APAP) at 1, 3 or 10 mM dose was also tested as positive control. CBD, CBN, and CBG demonstrated the lowest hepatotoxic potential, as evidenced by unchanged liver injury markers and albumin secretion. CBN at the mid and high dose and CBD at the high dose began to show signs of toxicity on day 7 as observed through morphological changes (CBN) and proinflammatory cytokine and LDH release (CBD), suggesting that increased exposure may result in more severe toxicity. CBC treatment caused increased lactate dehydrogenase (LDH), cytokine release, and decreased albumin production, suggesting moderate hepatotoxicity. Liver-Chip also revealed varying adverse effects of cannabinoids on reactive oxygen species (ROS) and mitochondrial function in both hepatocytes and non-parenchymal cells (NPCs), giving further insights into the mechanism of liver injury. These results indicated differences in cannabinoid toxicity profiles while demonstrating the Liver-Chip model as an alternative tool for live toxicity screening.
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spelling doaj-art-aadfcff6460a43ebb66d0749415e2ba22025-08-20T04:01:52ZengNature PortfolioScientific Reports2045-23222025-08-0115112010.1038/s41598-025-12846-2Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chipJacob D. Larson0Sushma Jadalannagari1Jake Chaff2James Velez3Josiah Sliz4Lorna Ewart5Donna Webster6Jiang Hu7Herbalife International of America Inc.Emulate Inc.Emulate Inc.Emulate Inc.Emulate Inc.Emulate Inc.Herbalife International of America Inc.Herbalife International of America Inc.Abstract Due to the increasing availability of hemp-derived products for recreational and medicinal use, it is imperative to understand the hepatotoxicity of the naturally occurring phytocannabinoids. Though, traditionally animal models or in vitro techniques are used to evaluate hepatotoxicity, these methods often fail due to the species differences and lack of the needed complexity. Thus, this study investigated the hepatotoxicity potential of Cannabidiol (CBD), Cannabinol (CBN), Cannabichromene (CBC), and Cannabigerol (CBG) using the Emulate Quad-Culture Liver-Chip model. Liver-Chips were dosed with three concentrations (0.24, 3, or 4.7 µM) of each cannabinoid for 7 days continuously, and acetaminophen (APAP) at 1, 3 or 10 mM dose was also tested as positive control. CBD, CBN, and CBG demonstrated the lowest hepatotoxic potential, as evidenced by unchanged liver injury markers and albumin secretion. CBN at the mid and high dose and CBD at the high dose began to show signs of toxicity on day 7 as observed through morphological changes (CBN) and proinflammatory cytokine and LDH release (CBD), suggesting that increased exposure may result in more severe toxicity. CBC treatment caused increased lactate dehydrogenase (LDH), cytokine release, and decreased albumin production, suggesting moderate hepatotoxicity. Liver-Chip also revealed varying adverse effects of cannabinoids on reactive oxygen species (ROS) and mitochondrial function in both hepatocytes and non-parenchymal cells (NPCs), giving further insights into the mechanism of liver injury. These results indicated differences in cannabinoid toxicity profiles while demonstrating the Liver-Chip model as an alternative tool for live toxicity screening.https://doi.org/10.1038/s41598-025-12846-2CannabinoidsHepatotoxicityLiver-ChipDrug Induced Liver Injury (DILI)
spellingShingle Jacob D. Larson
Sushma Jadalannagari
Jake Chaff
James Velez
Josiah Sliz
Lorna Ewart
Donna Webster
Jiang Hu
Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip
Scientific Reports
Cannabinoids
Hepatotoxicity
Liver-Chip
Drug Induced Liver Injury (DILI)
title Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip
title_full Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip
title_fullStr Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip
title_full_unstemmed Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip
title_short Hepatotoxicity evaluation of cannabidiol, cannabinol, cannabichromene and cannabigerol using a human quad culture liver chip
title_sort hepatotoxicity evaluation of cannabidiol cannabinol cannabichromene and cannabigerol using a human quad culture liver chip
topic Cannabinoids
Hepatotoxicity
Liver-Chip
Drug Induced Liver Injury (DILI)
url https://doi.org/10.1038/s41598-025-12846-2
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