4.7 Article

Soy isoflavones protects against cognitive deficits induced by chronic sleep deprivation via alleviating oxidative stress and suppressing neuroinflammation

Journal

PHYTOTHERAPY RESEARCH
Volume 36, Issue 5, Pages 2072-2080

Publisher

WILEY
DOI: 10.1002/ptr.7354

Keywords

cognitive function; inflammatory system; oxidative stress; sleep deprivation; Soy isoflavones

Funding

  1. China Agriculture Research System [CARS-04]
  2. Knowledge Innovation Program Funding of Institute of Food Science and Technology, Chinese Academy of Agricultural Sciences [125161015000150013]
  3. Science and Technology Innovation Project of Chinese Academy of Agricultural Sciences [CAAS-ASTIP-2020-IFST-04]
  4. Central Public-Interest Institution Basal Research Fund [S2020JBKY-20]
  5. Central Public-Interest Scientific Institution Basal Research Fund [Y2020LM05]

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Mounting evidence suggests a close association between chronic sleep deprivation (CSD) and cognitive deficits. This study investigated the effects of soy isoflavones (SI) on CSD-induced memory impairment. The results showed that SI administration improved cognitive performance, reduced oxidative stress, and suppressed inflammation in CSD-treated mice.
Mounting evidence suggests that there is a close association between chronic sleep deprivation (CSD) and cognitive deficits. The animal model of CSD-induced cognitive deficits is commonly used to seek potential treatments. Soy isoflavones (SI) have been reported to possess antioxidant, anti-inflammation, and neuroprotective effects. In the present study, the effects of SI on CSD-induced memory impairment were investigated. The mice were subjected to the sleep interruption apparatus and continuously sleep deprived for 2 weeks, while orally administrated with SI (10, 20, and 40 mg/kg) or Modafinil (MOD,100 mg/kg) during the CSD process. Immediately after the SD protocol, cognitive performance of mice was evaluated by the object location recognition (OLR) test, the novel object recognition (NOR) test, and the Morris water maze (MWM) task, as well as the hippocampus, was extracted for evaluation of oxidative stress parameters and inflammation levels through biochemical parameter assay and western blotting analysis. The results showed that SI administration remarkably improved the cognitive performance of CSD-treated mice in OLR, NOR, and MWM tests. In addition, SI significantly elevated total antioxidant capacity and superoxide dismutase enzyme activities, decreased malondialdehyde level, promoting antioxidant element nuclear erythroid-2-related factor 2, and its downstream targets, including heme oxygenase 1, and quinone oxidoreductase 1 protein expressions. Moreover, SI treatment significantly suppressed nuclear factor kappa B p65, nitric oxide synthase, and cyclooxygenase 2 activation, as well as the pro-inflammatory cytokines (Tumor necrosis factor-alpha [TNF-alpha], interleukin-6 [IL-6], and interleukin-1 beta [IL-1 beta]) release in the hippocampus of CSD-treated mice. In summary, the current study provides an insight into the potential of SI in treatment of cognitive deficits by CSD.

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