4.6 Article

Onion (Allium cepa L.)-Derived Nanoparticles Inhibited LPS-Induced Nitrate Production, However, Their Intracellular Incorporation by Endocytosis Was Not Involved in This Effect on RAW264 Cells

Journal

MOLECULES
Volume 26, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/molecules26092763

Keywords

Allium cepa L; nanovesicles; lipopolysaccharide; endocytosis

Funding

  1. KAKENHI [15K14736]
  2. Japan Health Foundation
  3. Grants-in-Aid for Scientific Research [15K14736] Funding Source: KAKEN

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This study evaluated the anti-inflammatory properties of nanoparticles derived from Allium cepa L. The nanoparticles were found to inhibit nitric oxide production in a cell model without cytotoxic effects, and their cellular uptake was confirmed through microscopy. Overall, the nanoparticles were able to inhibit the LPS response via extracellular mechanisms, suggesting a potential efficient anti-inflammatory effect with consumption of Allium cepa L. without disrupting the nanoparticles.
The aim of this study was to evaluate the involvement of nanoparticles prepared from Allium cepa L. as anti-inflammatory agents. In the present study, we identified nanoparticles from Allium cepa L. using the ultracentrifugation exosome purification method. The nanoparticles were referred to as 17,000x g and 200,000x g precipitates, and they contained quercetins, proteins, lipids, and small-sized RNA. The nanoparticles inhibited nitric oxide production from lipopolysaccharide (LPS)-stimulated RAW264 cells without cytotoxic properties. Cellular incorporation was confirmed by laser microscopic observation after PKH26 staining. The inhibition of caveolae-dependent endocytosis and macropinocytosis significantly prevented the incorporation of the nanoparticles but had no effect on the inhibition of nitric oxide in RAW264 cells. Collectively, the identified nanoparticles were capable of inhibiting the LPS response via extracellular mechanisms. Taken together, the way of consuming Allium cepa L. without collapsing the nanoparticles is expected to provide an efficient anti-inflammatory effect.

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