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Jujuboside A

Clinical trial

Mechanism of Action

Sedative and hypnotic via GABAergic enhancement; anxiolytic; inhibits hippocampal glutamate excitotoxicity
Jujuboside A acts as a positive allosteric modulator of GABA-A receptors, enhancing inhibitory GABAergic neurotransmission in the hypothalamus and hippocampus. It increases chloride ion influx through GABA-A receptor channels, promoting neuronal hyperpolarization and reducing neuronal excitability. Additionally, jujuboside A has been shown to inhibit glutamatergic excitatory transmission and modulate the hypothalamic-pituitary-adrenal (HPA) axis, reducing corticosterone levels and attenuating stress-induced wakefulness.

Research Notes

Jujuboside A is the primary sedative compound. Animal studies confirm sedative-hypnotic effects. Clinical use for insomnia has traditional and modern support.

Animal studies have demonstrated that jujuboside A significantly increases total sleep time and reduces sleep latency in pentobarbital-induced sleep models in mice, with effects comparable to diazepam at doses of 10–40 mg/kg. A 2019 study published in Biomedicine & Pharmacotherapy showed that jujuboside A promoted sleep by upregulating GABA-A receptor alpha-1 subunit expression in the hippocampus. In vitro electrophysiology studies confirmed its direct potentiation of GABA-evoked currents in cultured hippocampal neurons.

Found In 2 Herbs

3D Molecular Structure

Triterpenoid saponin (dammarane-type)
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Jujuboside A

Triterpenoid saponin (dammarane-type)Modified terpenes with diverse biological activities

Representative pattern: C₁₁H₁₄O₆

Atoms
Carbon
Oxygen

Related Compounds (Triterpenoid saponin (dammarane-type))

Live Research

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