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Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress
Antipsychotics used to treat schizophrenia can cause drug-induced liver injury (DILI), according to the Roussel Uclaf Causality Assessment Method. The role of oxidative stress in triggering injury in these DILI cases is unknown. We repeatedly administrated two second-generation antipsychotics, aripi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368927/ https://www.ncbi.nlm.nih.gov/pubmed/35955425 http://dx.doi.org/10.3390/ijms23158292 |
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author | Kramar, Barbara Pirc Marolt, Tinkara Monsalve, Maria Šuput, Dušan Milisav, Irina |
author_facet | Kramar, Barbara Pirc Marolt, Tinkara Monsalve, Maria Šuput, Dušan Milisav, Irina |
author_sort | Kramar, Barbara |
collection | PubMed |
description | Antipsychotics used to treat schizophrenia can cause drug-induced liver injury (DILI), according to the Roussel Uclaf Causality Assessment Method. The role of oxidative stress in triggering injury in these DILI cases is unknown. We repeatedly administrated two second-generation antipsychotics, aripiprazole and olanzapine, at laboratory alert levels to study underlying mechanisms in stress prevention upon acute oxidative stress. The drugs were administered continuously for up to 8 weeks. For this, hepatoma Fao cells, which are suitable for metabolic studies, were used, as the primary hepatocytes survive in the culture only for about 1 week. Four stress responses—the oxidative stress response, the DNA damage response and the unfolded protein responses in the endoplasmic reticulum and mitochondria—were examined in H(2)O(2)-treated cells by antioxidant enzyme activity measurements, gene expression and protein quantification. Oxidant conditions increased the activity of antioxidant enzymes and upregulated genes and proteins associated with oxidative stress response in aripiprazole-treated cells. While the genes associated with DNA damage response, Gadd45 and p21, were upregulated in both aripiprazole- and olanzapine-treated cells, only aripiprazole treatment was associated with upregulation in response to even more H(2)O(2), which also coincided with better survival. Endoplasmic reticulum stress-induced Chop was also upregulated; however, neither endoplasmic reticulum nor mitochondrial unfolded protein response was activated. We conclude that only aripiprazole, but not olanzapine, protects liver cells against oxidative stress. This finding could be relevant for schizophrenia patients with high-oxidative-stress-risk lifestyles and needs to be validated in vivo. |
format | Online Article Text |
id | pubmed-9368927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93689272022-08-12 Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress Kramar, Barbara Pirc Marolt, Tinkara Monsalve, Maria Šuput, Dušan Milisav, Irina Int J Mol Sci Article Antipsychotics used to treat schizophrenia can cause drug-induced liver injury (DILI), according to the Roussel Uclaf Causality Assessment Method. The role of oxidative stress in triggering injury in these DILI cases is unknown. We repeatedly administrated two second-generation antipsychotics, aripiprazole and olanzapine, at laboratory alert levels to study underlying mechanisms in stress prevention upon acute oxidative stress. The drugs were administered continuously for up to 8 weeks. For this, hepatoma Fao cells, which are suitable for metabolic studies, were used, as the primary hepatocytes survive in the culture only for about 1 week. Four stress responses—the oxidative stress response, the DNA damage response and the unfolded protein responses in the endoplasmic reticulum and mitochondria—were examined in H(2)O(2)-treated cells by antioxidant enzyme activity measurements, gene expression and protein quantification. Oxidant conditions increased the activity of antioxidant enzymes and upregulated genes and proteins associated with oxidative stress response in aripiprazole-treated cells. While the genes associated with DNA damage response, Gadd45 and p21, were upregulated in both aripiprazole- and olanzapine-treated cells, only aripiprazole treatment was associated with upregulation in response to even more H(2)O(2), which also coincided with better survival. Endoplasmic reticulum stress-induced Chop was also upregulated; however, neither endoplasmic reticulum nor mitochondrial unfolded protein response was activated. We conclude that only aripiprazole, but not olanzapine, protects liver cells against oxidative stress. This finding could be relevant for schizophrenia patients with high-oxidative-stress-risk lifestyles and needs to be validated in vivo. MDPI 2022-07-27 /pmc/articles/PMC9368927/ /pubmed/35955425 http://dx.doi.org/10.3390/ijms23158292 Text en © 2022 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 Kramar, Barbara Pirc Marolt, Tinkara Monsalve, Maria Šuput, Dušan Milisav, Irina Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress |
title | Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress |
title_full | Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress |
title_fullStr | Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress |
title_full_unstemmed | Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress |
title_short | Antipsychotic Drug Aripiprazole Protects Liver Cells from Oxidative Stress |
title_sort | antipsychotic drug aripiprazole protects liver cells from oxidative stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368927/ https://www.ncbi.nlm.nih.gov/pubmed/35955425 http://dx.doi.org/10.3390/ijms23158292 |
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