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Jujuboside B inhibits febrile seizure by modulating AMPA receptor activity. | LitMetric

Jujuboside B inhibits febrile seizure by modulating AMPA receptor activity.

J Ethnopharmacol

Department of Pharmacology, Institution of Chinese Integrative Medicine, Hebei Medical University, Research Unit of Digestive Tract Microecosystem Pharmacology and Toxicology, Chinese Academy of Medical Sciences, Shijiazhuang, Hebei, 050017, China. Electronic address:

Published: March 2023

AI Article Synopsis

  • - The study investigates Jujuboside B (JuB), a compound from the Ziziphi Spinosae Semen herb, for its neuroprotective effects against febrile seizures in children under five.
  • - It was found that JuB significantly increased the time before seizures occurred and decreased their intensity in a mouse model, while also reducing the excitability of hippocampal neurons.
  • - The mechanism of action involves inhibiting AMPA receptors, which leads to lower levels of calcium inside the neurons, ultimately helping to alleviate the seizures.

Article Abstract

Ethnopharmacological Relevance: Febrile seizure is a common neurologic disorder with limited treatment occurring in infants and children under the age of five. Jujuboside B (JuB) is a main bioactive saponin component isolated from the Chinese anti-insomnia herbal medicine Ziziphi Spinosae Semen (ZSS), seed of Ziziphus jujuba Mill, which has been proved to exhibit neuroprotective effects recently.

Aim Of The Study: In this study, we aimed at elucidating the effect of JuB on suppressing febrile seizure and the potential mechanisms.

Methods: Electroencephalogram (EEG) recording was used to monitor the severity of febrile seizures. The JuB in the brain was identified by mass spectrometry. Neuronal excitability was investigated using patch clamp.

Results: JuB (30 mg/kg) significantly prolonged seizure latency and reduced the severity in hyperthermia-induced seizures model mice. Hippocampal neuronal excitability was significantly decreased by JuB. And JuB significantly reduced the excitatory synaptic transmission mediated by α-amino-3-hydroxy-5-methyl-4-iso-xazolepropionic acid receptor (AMPAR), including evoked excitatory postsynaptic currents (eEPSCs), and miniature EPSCs (mEPSCs) in hippocampal neurons. Furthermore, JuB also significantly inhibited recombinant GluA1 and GluA2 mediated AMPA current in HEK293 cell and decreased the upregulation of [Ca] induced by AMPA in primary cultured cortex neurons.

Conclusions: JuB suppressed the excitability of hippocampal neurons by inhibiting the activity of AMPAR and reducing the intracellular free calcium, thereby relieving febrile seizures.

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Source
http://dx.doi.org/10.1016/j.jep.2022.116048DOI Listing

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