AI Article Synopsis

  • The study explored the antiallergic effects of AF-343, a blend of natural plant extracts, on RBL-2H3 cells.
  • AF-343 demonstrated significant inhibition of cell degranulation and proinflammatory cytokine production, specifically reducing b-hexosaminidase release and levels of IL-4 and TNF-a.
  • Additionally, AF-343 showcased strong antioxidant properties and was more effective than individual plant extracts, suggesting its potential as a treatment for various allergic diseases.

Article Abstract

The purpose of this study was to determine the antiallergic effects of AF-343, a mixture of natural plant extracts from L L and on rat basophilic leukemia (RBL-2H3) cells. The inhibitory effects on cell degranulation, proinflammatory cytokine secretion, and reactive oxygen species (ROS) production were studied in compound 48/80-treated RBL-2H3 cells. The bioactive compounds in AF-343 were also identified by HPLC-UV. AF-343 was found to effectively suppress compound 48/80-induced b-hexosaminidase release, and interleukin (IL)-4 and tumor necrosis factor-a (TNF-a) production in RBL-2H3 cells. In addition, AF-343 exhibited DPPH free radical scavenging effects in vitro (half-maximal inhibitory concentration (IC) = 105 μg/mL) and potently inhibited compound 48/80-induced cellular ROS generation in a 2',7'-dichlorofluorescein diacetate (DCFH-DA) assay. Specifically, treatment with AF-343 exerted stronger antioxidant effects in vitro and antiallergic effects in cells than treatment with three single natural plant extracts. Furthermore, AF-343 was observed to contain bioactive compounds, including catechin, aurantio-obtusin, and chicoric acid, which have been reported to elicit antiallergic responses. This study reveals that AF-343 attenuates allergic responses via suppression of b-hexosaminidase release, IL-4 and TNF-a secretion, and ROS generation, perhaps through mechanisms related to catechin, aurantio-obtusin, and chicoric acid. The results indicate that AF-343 can be considered a treatment for various allergic diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288106PMC
http://dx.doi.org/10.3390/molecules25102434DOI Listing

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