Intermittent hypoxia, brain glyoxalase-1 and glutathione reductase-1, and anxiety-like behavior in mice

• Autor(a) principal: Carissimi, Alicia
• Data de Publicação: 2018
• Outros Autores: Martinez, Denis, Kim, Lenise Jihe, Martinez, Cintia Zappe Fiori, Vieira, Luciana Rodrigues, Rosa, Darlan Pase da, Pires, Gabriel Natan
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UFRGS
• Texto Completo: http://hdl.handle.net/10183/200480
• topic: Biomarcadores; Síndromes da apneia do sono; Hipóxia encefálica; Ansiedade; Ratos; Lactoilglutationa liase; Glutationa redutase; Estresse oxidativo; Sleep; Biological markers; Molecular biology; Stress; Anxiety

Objective: Sleep apnea has been associated with anxiety, but the mechanisms of the sleep apneaanxiety relationship are unresolved. Sleep apnea causes oxidative stress, which might enhance anxietylike behavior in rodents. To clarify the apnea-anxiety connection, we tested the effect of intermittent hypoxia, a model of sleep apnea, on the anxiety behavior of mice. Methods: The rodents were exposed daily to 480 one-minute cycles of intermittent hypoxia to a nadir of 761% inspiratory oxygen fraction or to a sham procedure with room air. After 7 days, the mice from both groups were placed in an elevated plus maze and were video recorded for 10 min to allow analysis of latency, frequency, and duration in open and closed arms. Glyoxalase-1 (Glo1) and glutathione reductase-1 (GR1) were measured in the cerebral cortex, hippocampus, and striatum by Western blotting. Results: Compared to controls, the intermittent hypoxia group displayed less anxiety-like behavior, perceived by a statistically significant increase in the number of entries and total time spent in open arms. A higher expression of GR1 in the cortex was also observed. Conclusion: The lack of a clear anxiety response as an outcome of intermittent hypoxia exposure suggests the existence of additional layers in the anxiety mechanism in sleep apnea, possibly represented by sleepiness and irreversible neuronal damage.