Lipophilic coffee compounds are present in coffee beverages and may also be found in coffee by-products, whose underutilized fractions contain molecules such as β N -alkanoyl-5-hydroxytryptamines (C n -5HTs) and diterpenes. Although members of these groups show anti-inflammatory potential, their combined effects remain unexplored. In this study, C n -5HTs, cafestol, kahweol, and caffeine were tested individually and in mixtures in THP-1 Lucia™ monocytes using an NF-κB reporter gene assay to evaluate additive or synergistic interactions. The most active combinations were further assessed in HCEC-1CT intestinal epithelial cells for effects on TNF-α, IL-6, IL-8, and IL-10 expression and secretion. C 18 -5HT, C 20 -5HT, cafestol, and kahweol reduced NF-κB activation at non-cytotoxic concentrations, while caffeine and longer-chain amides were inactive. C 18 -5HT and kahweol were the most potent, and their co-treatment (3 μM + 40 μM) produced the strongest inhibition, suggesting synergy. In HCEC-1CT cells, treatments lowered pro-inflammatory cytokine mRNA and protein levels, supporting the bioactivity of coffee lipophilic compounds.
Beccari et al. (Sat,) studied this question.
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