A Standardized Phlorotannin Supplement Attenuates Caffeine-Induced Sleep Disruption in Mice.

Sangoh Kwon, Minseok Yoon, Jaekwang Lee, Kwang-Deog Moon, Dohyeon Kim, Seon-Bong Kim, Suengmok Cho
Author Information
  1. Sangoh Kwon: S&D Research and Development Institute, Cheongju 28156, Korea. so-kwon0004@hanmail.net.
  2. Minseok Yoon: Research Division of Food Functionality, Korea Food Research Institute, Wanju-gun 55365, Korea. msyoon@kfri.re.kr.
  3. Jaekwang Lee: Research Division of Food Functionality, Korea Food Research Institute, Wanju-gun 55365, Korea. jklee@kfri.re.kr.
  4. Kwang-Deog Moon: Major in Food Biotechnology School of Food Science & Biotechnology, Kyungpook National University, Daegu 41566, Korea. kdmoon@knu.ac.kr.
  5. Dohyeon Kim: S&D Research and Development Institute, Cheongju 28156, Korea. concisenews@naver.com.
  6. Seon-Bong Kim: Department of Food Science and Technology, Pukyong National University, Busan 48513, Korea. owlkim@pknu.ac.kr.
  7. Suengmok Cho: Department of Food Science and Technology, Pukyong National University, Busan 48513, Korea. scho@pknu.ac.kr. ORCID

Abstract

In our previous studies, a standardized phlorotannin (brown seaweed polyphenol) supplement (PS) exhibited sleep-promoting effects via type A γ-aminobutyric acid-benzodiazepine receptors in mice. In addition, in human clinical trials, it decreased wake after sleep onset in adults with sleep disturbance. In this follow-up study, we investigated whether PS attenuates caffeine-induced sleep disruption in mice. The effects of PS were evaluated in a caffeine model by analyzing sleep architecture based on electroencephalogram and electromyogram findings, and were compared with the effects of a well-known sedative-hypnotic drug zolpidem (ZPD). As expected, oral administration of caffeine (25 mg/kg) significantly increased sleep latency and decreased the amount of non-rapid eye movement sleep (NREMS). In the caffeine + PS and caffeine + ZPD groups, PS (500 mg/kg) attenuated caffeine-induced sleep disruption, and its effects were comparable with those of ZPD (10 mg/kg). In particular, PS inhibited the arousal effects of caffeine without change in delta activity during NREMS, whereas ZPD produced a decrease in the delta activity. Considering global trends in coffee and energy drink consumption, our finding suggest that PS may be useful to relieve transitory insomnia symptoms caused by caffeine consumption, unlike the prescription drug ZPD.

Keywords

References

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Grants

  1. S0180300-01/S&D Research and Development Institute, Republic of Korea

MeSH Term

Animals
Caffeine
Electroencephalography
Electromyography
Follow-Up Studies
Hypnotics and Sedatives
Mice
Phytotherapy
Plant Preparations
Polyphenols
Receptors, GABA-A
Seaweed
Sleep
Sleep Aids, Pharmaceutical
Sleep Initiation and Maintenance Disorders
Zolpidem

Chemicals

Hypnotics and Sedatives
Plant Preparations
Polyphenols
Receptors, GABA-A
Sleep Aids, Pharmaceutical
Caffeine
Zolpidem

Word Cloud

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