KMID : 1161420110140111456
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Journal of Medicinal Food 2011 Volume.14 No. 11 p.1456 ~ p.1462
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(?)-Epigallocatechin-3-O-Gallate Augments Pentobarbital-Induced Sleeping Behaviors Through Cl? Channel Activation
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Park Kwang-Soon
Han Jin-Yi Moon Dong-Cheul Hong Jin-Tae Oh Ki-Wan
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Abstract
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This experiment investigated whether (?)-epigallocatechin-3-O-gallate (EGCG) (5?20?mg/kg, p.o.) has hypnotic effects and/or enhances pentobarbital-induced sleeping behaviors and whether these effects are mediated by ¥ã-aminobutyric acid (GABA) receptors. EGCG prolonged sleeping time induced by pentobarbital (42?mg/kg, i.p.) and reduced sleeping latency induced by pentobarbital similarly to muscimol (0.2?mg/kg, i.p.), a GABAA receptor agonist in mice. EGCG also increased sleeping rate and sleeping time when co-administered with pentobarbital (28?mg/kg, i.p.) at a subhypnotic dosage. In addition, EGCG and pentobarbital increased chloride (Cl?) influx in primary cultured cerebellar cells. EGCG and pentobarbital decreased GABAA receptors ¥á-subunit expression and had no effect on the expression of ¥â- and ¥ã-subunits and of glutamic acid decarboxylase in the hippocampus of rats. In conclusion, the EGCG enhancement of Cl? influx may play an important role in pentobarbital-induced sleeping behaviors.
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KEYWORD
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¥ã-aminobutyric acidA receptors, chloride ion influx, (?)-epigallocatethin-3-O-gallate, glutamic acid decarboxylase, pentobarbital
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