Olanzapine-induced liver injury in mice: aggravation by high-fat diet and protection with sulforaphane
| Autor: | Robin H. Isaacson, Juliane I. Beier, Nicholas K.H. Khoo, Bruce A. Freeman, Zachary Freyberg, Gavin E. Arteel |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
0301 basic medicine
Olanzapine Endocrinology Diabetes and Metabolism Clinical Biochemistry Biochemistry Antioxidants chemistry.chemical_compound Mice 0302 clinical medicine Isothiocyanates Prevalence Diet Fat-Restricted Liver injury education.field_of_study Nutrition and Dietetics Liver Sulfoxides 030211 gastroenterology & hepatology Female medicine.symptom Chemical and Drug Induced Liver Injury medicine.drug Antipsychotic Agents medicine.medical_specialty NF-E2-Related Factor 2 Population Diet High-Fat Article 03 medical and health sciences Internal medicine medicine Animals Humans Obesity education Molecular Biology business.industry Body Weight Lipid metabolism medicine.disease Lipid Metabolism Fatty Liver Mice Inbred C57BL Oxidative Stress 030104 developmental biology Endocrinology chemistry Steatosis business Weight gain Dyslipidemia Sulforaphane |
| Zdroj: | J Nutr Biochem |
| Popis: | Olanzapine is effective to treat for schizophrenia and other mood disorders, but limited by side effects such as weight gain, dyslipidemia, and liver injury. Obesity in the US is at epidemic levels, and is a significant risk factor for drug-induced liver injury. Obesity incidence in the psychiatric population is even higher than in the US population as a whole. The purpose of this study was to test the hypothesis that obesity worsens olanzapine-induced hepatic injury, and to investigate the potential protective effects of sulforaphane. 8-week old female C57BL/6 mice were fed either a high-fat or low-fat control diet (HFD and LFD). Mice also received either olanzapine (8 mg/kg/d) or vehicle by osmotic minipump for 4 weeks. A subset of mice in the HFD + olanzapine group was administered sulforaphane, a prototypical Nrf2 inducer (90 mg/kg/d). Olanzapine alone increased body weight, without a commensurate increase in food consumption. Olanzapine also caused hepatic steatosis and injury. Combining olanzapine and HFD caused further dysregulation of glucose and lipid metabolism. Liver damage from concurrent HFD and olanzapine was worse than liver damage from high-fat diet or olanzapine alone. Sulforaphane alleviated many metabolic side effects of olanzapine and HFD. Taken together, these data show that olanzapine dysregulates glucose and lipid metabolism and exacerbates hepatic changes caused by eating a HFD. Activation of the intrinsic antioxidant defense pathway with sulforaphane can partially prevent these effects of olanzapine and may represent a useful strategy to protect against liver injury. |
| Databáze: | OpenAIRE |
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