GSR is not essential for the maintenance of antioxidant defenses in mouse cochlea: Possible role of the thioredoxin system as a functional backup for GSR

• Published in: PloS one Vol. 12; no. 7; p. e0180817
• Main Authors: Han, Chul, Kim, Mi-Jung, Ding, Dalian, Park, Hyo-Jin, White, Karessa, Walker, Logan, Gu, Tongjun, Tanokura, Masaru, Yamasoba, Tatsuya, Linser, Paul, Salvi, Richard, Someya, Shinichi
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 07.07.2017; Public Library of Science (PLoS)
• Subjects: Abnormalities; Aging; Amplitudes; Animals; Antioxidants; Antioxidants - metabolism; Auditory system; Bacteria; Biology and Life Sciences; Brain stem; Cochlea; Cochlea - metabolism; Cysteine; Cytosol; Damage; Defects; Degeneration; Diquat; Enzymes; Evoked Potentials, Auditory, Brain Stem - physiology; Female; Flies; Gene Expression; Geriatrics; Glutamate-cysteine ligase; Glutamate-Cysteine Ligase - genetics; Glutamate-Cysteine Ligase - metabolism; Glutamic acid; Glutathione; Glutathione - metabolism; Glutathione Disulfide - metabolism; Glutathione peroxidase; Glutathione Peroxidase - genetics; Glutathione Peroxidase - metabolism; Glutathione reductase; Glutathione Reductase - deficiency; Glutathione Reductase - genetics; Hair; Hearing loss; Hyperoxia; Infections; Kidneys; Laboratories; Life span; Male; Markers; Medicine and Health Sciences; Mice; Mice, Inbred CBA; Mice, Knockout; Mitochondrial DNA; Mutation; Noise; Oxidative Stress; Peroxidase; Physiology; Redox properties; Research and Analysis Methods; Rodents; Studies; Thioredoxin; Thioredoxin-Disulfide Reductase - genetics; Thioredoxin-Disulfide Reductase - metabolism; Thioredoxins; Thioredoxins - genetics; Thioredoxins - metabolism; Thresholds; New York; United States > US
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0180817

Glutathione reductase (GSR), a key member of the glutathione antioxidant defense system, converts oxidized glutathione (GSSG) to reduced glutathione (GSH) and maintains the intracellular glutathione redox state to protect the cells from oxidative damage. Previous reports have shown that Gsr deficiency results in defects in host defense against bacterial infection, while diquat induces renal injury in Gsr hypomorphic mice. In flies, overexpression of GSR extended lifespan under hyperoxia. In the current study, we investigated the roles of GSR in cochlear antioxidant defense using Gsr homozygous knockout mice that were backcrossed onto the CBA/CaJ mouse strain, a normal-hearing strain that does not carry a specific Cdh23 mutation that causes progressive hair cell degeneration and early onset of hearing loss. Gsr-/- mice displayed a significant decrease in GSR activity and GSH/GSSG ratios in the cytosol of the inner ears. However, Gsr deficiency did not affect ABR (auditory brainstem response) hearing thresholds, wave I amplitudes or wave I latencies in young mice. No histological abnormalities were observed in the cochlea of Gsr-/- mice. Furthermore, there were no differences in the activities of cytosolic glutathione-related enzymes, including glutathione peroxidase and glutamate-cysteine ligase, or the levels of oxidative damage markers in the inner ears between WT and Gsr-/- mice. In contrast, Gsr deficiency resulted in increased activities of cytosolic thioredoxin and thioredoxin reductase in the inner ears. Therefore, under normal physiological conditions, GSR is not essential for the maintenance of antioxidant defenses in mouse cochlea. Given that the thioredoxin system is known to reduce GSSG to GSH in multiple species, our findings suggest that the thioredoxin system can support GSSG reduction in the mouse peripheral auditory system.