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This provides a molecular basis for the observed physiological effects, linking the in vitro findings to in vivo and clinical observations

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[DOI] [PubMed] [Google Scholar] 23.Premaratne K., Karunaratne G., Dias R., Lamahewage A., Samarasinghe M., Corea E., Gunawardena R

Furthermore, it inhibits inflammatory cascades by suppressing the COX enzyme and prostaglandin E-2 (PGE2), also influencing various molecular signaling pathways related to inflammation, apoptosis, and oxidative stress, like PPAR, PI3K, TLR-4, Akt, mTOR, ERK5, AP-1, TGF-, PAK1, Wnt, -catenin, Shh, Rac1, p38MAPK, EBP, NLRP3 inflammasome, Nrf2, Notch-1, AMPK, STAT3, and MyD-88, crucial in IBD development [504]

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