Phytochemicals as Anti-Inflammatory Agents in Animal Models of Prevalent Inflammatory Diseases.
Seong Ah ShinByeong Jun JooJun Seob LeeGyoungah RyuMinjoo HanWoe Yeon KimHyun Ho ParkJun-Hyuck LeeChang Sup LeePublished in: Molecules (Basel, Switzerland) (2020)
Phytochemicals are known to have anti-inflammatory effects in vitro and in vivo, such as in inflammatory disease model systems. Inflammation is an essential immune response to exogenous stimuli such as infection and injury. Although inflammation is a necessary host-defense mechanism, chronic inflammation is associated with the continuous local or systemic release of inflammatory mediators, non-cytokine mediators, such as ROS and NO, and inflammatory cytokines are strongly implicated in the pathogenesis of various inflammatory disorders. Phytochemicals that exhibit anti-inflammatory mechanisms that reduce sustained inflammation could be therapeutic candidates for various inflammatory diseases. These phytochemicals act by modulating several main inflammatory signaling pathways, including NF-κB, MAPKs, STAT, and Nrf-2 signaling. Here, we discuss the characteristics of phytochemicals that possess anti-inflammatory activities in various chronic inflammatory diseases and review the molecular signaling pathways altered by these anti-inflammatory phytochemicals, with a focus on transcription factor pathways. Furthermore, to evaluate the phytochemicals as drug candidates, we translate the effective doses of phytochemicals in mice or rat disease models into the human-relevant equivalent and compare the human-relevant equivalent doses of several phytochemicals with current anti-inflammatory drugs doses used in different types of chronic inflammatory diseases.
Keyphrases
- oxidative stress
- anti inflammatory
- signaling pathway
- dna damage
- transcription factor
- induced apoptosis
- endothelial cells
- emergency department
- type diabetes
- metabolic syndrome
- adipose tissue
- inflammatory response
- insulin resistance
- cell death
- lps induced
- pluripotent stem cells
- drug induced
- toll like receptor
- reactive oxygen species
- induced pluripotent stem cells