Nootkatone improves anxiety‐ and depression‐like behavior by targeting hyperammonemia‐induced oxidative stress in D‐galactosamine model of liver injury. Issue 4 (3rd December 2020)

• Record Type: Journal Article
• Authors: Yan, Tingxu; Li, Fuyuan; Xiong, Weilin; Wu, Bo; Xiao, Feng; He, Bosai; Jia, Ying
• Is Part Of: Environmental toxicology. Volume 36:Issue 4(2021)
• Page Start: 694
• Page End: 706
• Publication Date: 2020-12-03
• Subjects: anxiety -- depression -- D‐GalN -- Nootkatone -- oxidative stress; Water quality bioassay -- Periodicals; Water -- Pollution -- Toxicology -- Periodicals; Microbiological assay -- Periodicals; Toxicity testing -- Periodicals; Environmental toxicology -- Periodicals; Environmental Pollution -- Periodicals; Environmental Pollutants -- Periodicals; Environmental Monitoring -- Periodicals; Écotoxicologie -- Périodiques; Pollution -- Périodiques; 615.902
• DOI: 10.1002/tox.23073
• Languages: English
• ISSNs: 1520-4081

Abstract

Abstract: Acute or chronic liver injury is closely related to hyperammonemia, which will result in oxidative stress and damage to nerve cells, and these factors are vital to the development of anxiety and depression. In this study, the effect of Nootkatone (NKT) on the anxiety‐ and depression‐like behavioral changes in mice induced by liver injury was investigated. Liver injury was induced by D‐galactosamine (D‐GalN; 350 mg/kg) three times a week for 4 weeks. NKT (5 mg/kg or 10 mg/kg) was given as co‐treatment daily for 4 weeks. NKT (5 mg/kg) co‐treatment remarkably ameliorates D‐GalN‐induced anxiety‐ and depression‐like behaviors as evident from the results of sucrose preference test, forced swimming test, tail suspension test, and novelty suppressed feeding test. Results showed that NKT could induce an elevation in serum alanine transaminase and aspartate transaminase level, alleviate the oxidative stress induced by hyperammonemia through activating Keap1/Nrf2/HO‐1 antioxidant pathways, decrease the expression of inducible nitric oxide synthase and NOX2 in hippocampus and prefrontal cortex, enhance the vitality of superoxide dismutase, catalase, and glutathione levels in serum, liver, and brain, and significantly reduce the generation of malondialdehyde. At the same time, NKT also reduces the level of ammonia in serum and brain and upgrades the activity of glutamine synthetase in the hippocampus and prefrontal cortex. Taken together, the present results suggested that NKT has a significant antidepressant effect through modulation of oxidative stress induced by D‐GalN administration.