AI Article Synopsis

  • Yokukansankachimpihange (YKSCH) is a traditional Japanese medicine aimed at treating neurosis, insomnia, and children's night crying, showing potential effects in Alzheimer's patients and healthy individuals.
  • In a study with male ddy mice, YKSCH had no impact on sleep latency or duration in group-housed mice but significantly improved sleep duration in socially isolated mice.
  • The sleep-enhancing effect was linked to the GABAergic pathway and was associated with increased levels of allopregnanolone in the olfactory bulb, suggesting a specific mechanism for its action against social isolation-induced insomnia.

Article Abstract

Yokukansankachimpihange (YKSCH), a traditional Japanese medicine composed of 9 crude drugs, is designed to improve neurosis, insomnia in adults, and night crying in children. YKSCH has been reported to improve diurnal rhythm in patients with Alzheimer's disease and prolong the total sleeping time in healthy subjects. However, little is known about how YKSCH alleviates sleep disorders. Here, we investigated whether and how YKSCH treatment affected sleep latency and duration in group-housed and socially isolated mice. Male ddy mice were treated with YKSCH [1,500 mg/kg, per os (p.o.)] in group-housed or socially isolated conditions for 3-4 weeks. After the last injection, mice were intraperitoneally (i.p.) administered with pentobarbital (60 mg/kg) and the sleep latency and duration was evaluated. The results show that pretreatment with YKSCH had no effect on sleep latency or duration in group-housed mice. However, YKSCH treatment significantly improved the reduced sleep duration in socially isolated mice. This effect of YKSCH was inhibited by the administration of bicuculline (3 mg/kg, i.p.), a GABA receptor antagonist. Furthermore, we showed that YKSCH treatment improved the decrease in allopregnanolone content and its synthase expression levels in the olfactory bulb. These results suggest that YKSCH treatment improved social isolation stress-induced insomnia via the GABAergic pathway and that the mechanism of action of YKSCH is partly due to improvement of allopregnanolone levels of expression.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026005PMC
http://dx.doi.org/10.3389/fnut.2020.00008DOI Listing

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