Protective Role of Polyphenols from Aronia Berry (Aronia melanocarpa) Against LPS-Induced Inflammation in Colon Cells and Macrophages

被引:0
作者
Sreedharan, Shareena [1 ]
Nair, Vimal [1 ]
Bhargava, Prerna [1 ]
Cisneros-Zevallos, Luis [1 ,2 ]
机构
[1] Texas A&M Univ, Dept Hort Sci, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Food Sci & Technol, College Stn, TX 77843 USA
关键词
aronia berry; Aronia melanocarpa; polyphenols; inflammation; oxidative stress; mode of action; pro-inflammatory genes and nuclear receptor; colon cells; macrophage cells; OXIDATIVE STRESS; RICH EXTRACT; ANTHOCYANINS; CANCER; ANTIOXIDANT; ACID; WILD;
D O I
10.3390/nu17101652
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Aronia berry (Aronia melanocarpa) are native to North America, rich in polyphenols and antioxidants with the potential to promote human health through its anti-inflammatory properties. Methods: Through the chemical characterization of phenolic compounds from aronia berries, 11 distinct polyphenols were identified. We investigated the anti-inflammatory activity of a methanolic/acetone/water extract from freeze-dried aronia berries in LPS-stimulated colonic and macrophage cell models. Results: In colon cells, aronia polyphenols suppressed pro-inflammatory gene expression (NFk beta, TNF alpha, IL-6, COX2) by reducing ROS generation while enhancing LXR alpha expression. In macrophages, these compounds decreased NO production through ROS attenuation. Notably, aronia extracts exhibited no cytotoxicity in either cell type across concentrations from 100 to 1000 mu g/mL. The whole-berry methanolic extract contained substantial levels of phenolic compounds (including 3-O- and 5-O-caffeoylquinic acids, quercetin derivatives, and cyanidin derivatives) with high ORAC values, likely contributing to their observed multifaceted anti-inflammatory effects. Conclusions: These findings suggest that freeze-dried aronia berry (AroBerry (R)) may offer protection against low-grade inflammation, providing a foundation for future in vivo studies using murine models of inflammation-associated chronic diseases to establish appropriate dosage regimens.
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页数:15
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