4.7 Article

Ergosterol isolated from cloud ear mushroom (Auricularia polytricha) attenuates bisphenol A-induced BV2 microglial cell inflammation

期刊

FOOD RESEARCH INTERNATIONAL
卷 157, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.foodres.2022.111433

关键词

Bisphenol A; Auricularia polytricha; Ergosterol; Neuroinflammation

资金

  1. National Research Council of Thailand (NRCT) [NRCT5-RGJ63001-003]
  2. 90th anniversary Chulalongkorn University Fund (Ratchadaphiseksomphot Endowment Fund) [GCUGR1125643032D]
  3. National Research Foundation of Korea (NRF) - Korean government [NRF-2018R1A2B2002923]

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The study revealed that Auricularia polytricha extracts have anti-inflammatory and antioxidative effects against BPA-induced neuroinflammation, regulating the occurrence of neuroinflammation through the NF-kappa B signaling pathway.
Bisphenol A (BPA) has been reported to have neurotoxic properties that may increase the risk of neurodegenerative diseases by inducing neuroinflammation. Auricularia polytricha (AP) is an edible mushroom with several medicinal properties. Herein, the anti-neuroinflammatory effects of AP extracts against BPA-induced inflammation of BV2 microglial cells were investigated. Hexane (APH) and ethanol (APE) extracts of AP inhibited BPA-induced neuroinflammation in BV2 microglia by reducing microglial activation and the expression of pro-inflammatory cytokines. These anti-inflammatory effects were regulated by the NF-kappa B signaling pathway. In addition, APH and APE exhibited antioxidative effects by increasing the activity of the SOD-1 enzyme and restoring the accumulation of reactive oxygen species (ROS) in BPA-induced BV2 cells. Moreover, the conditioned medium prepared using BPA-induced BV2 cells demonstrated that the presence of APH or APE could attenuate ROS production in HT-22 cells. Further, ergosterol was isolated from APE and also showed anti-inflammatory and antioxidative activities. In conclusion, AP extracts and ergosterol attenuated neuroinflammation against BPA induction in BV2 microglial cells through the NF-kappa B signaling pathway.

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