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. 2021 Mar 15;29(1):15–38. doi: 10.38212/2224-6614.1151

Table 3.

Anti-inflammatory activity of resveratrol and its derivatives.

Compound Experimental model Cell or animal type Outcomes offered by the compound Reference
Resveratrol In vitro hyperproliferation Human keratinocytes Resveratrol restrained keratinocyte proliferation via aquaporin 3 inhibition [115]
Resveratrol In vivo psoriasiform plaque Balb/c mouse Oral resveratrol alleviated the severity of scaling and skin redness [116]
Resveratrol In vivo psoriasiform plaque Balb/c mouse Topical resveratrol reduced skin thickness and edema [118]
Resveratrol-enriched rice In vivo AD-like lesion NC/Nga mouse The rice reduced scratching frequency and dermatitis severity [120]
Resveratrol In vivo AD-like lesion Balb/c mouse Oral resveratrol reduced skin thickness and immune response [121]
Resveratrol In vivo AD-like lesion Balb/c mouse Oral resveratrol downregulated Th2-type cytokines [122]
Pterostilbene In vivo contact dermatitis-like skin C57BL/6 mouse Oral pterostilbene attenuated erythema and immune cell infiltration [123]
Polydatin In vitro inflammation Human keratinocytes Polydatin inhibited ERK phosphorylation and NF-κB activation [124]
Polydatin In vitro inflammation HaCaT cells Polydatin inhibited MCP-1, TNF-α, and IL-6 [125]
Polydatin In vitro inflammation HaCaT cells Polydatin inhibited TNF-α, IL-6, and IL-8 [126]
Resveratrol and quercetin in liposomes In vitro uptake and in vivo inflammation Dermal fibroblasts and CD-1 mouse The liposomes increased cellular uptake and reduced edema and neutrophil infiltration [127]
Resveratrol in niosomes In vitro skin absorption and in vivo inflammation Wistar rat The enhanced resveratrol skin absorption with reduced edema [129]
Resveratrol and DHA in SLNs In vitro inflammation HaCaT cells DHA could synergize with resveratrol in SLNs to inhibit cytokine expression [131]
Resveratrol in SLNs In vivo contact dermatitis-like skin Mouse SLNs inhibited skin edema [132]

AD, atopic dermatitis; DHA, docosahexaenoic acid; ERK, extracellular signal-regulated kinase; IL, interleukin; MCP-1, monocyte chemotactic protein-1; NF-κB, nuclear factor-κB; SLNs, solid lipid nanoparticles; TNF-α, tumor necrosis factor-α.