Virgin coconut oil (VCO) has been traditionally used as moisturizer since centuries by people in the tropical region. Clinical studies have revealed that VCO improves the symptoms of skin disorders by moisturizing and soothing the skin. However, the mechanistic action of VCO and its benefits on skin has not been elucidated in vitro. The cytotoxicity (CTC50) of VCO was 706.53 ± 2.1 and 787.15 ± 1.1 μg/mL in THP-1 (Human monocytes) and HaCaT (Human keratinocytes) cells respectively. VCO inhibited TNF-α (62.34 ± 3.2 %), IFN-γ (42.66 ± 2.9 %), IL-6 (52.07 ± 2.0 %), IL-8 (53.98 ± 1.8 %) and IL-5 (51.57 ± 2.6 %) respectively in THP-1 cells. Involucrin (INV) and filaggrin (FLG) content increased by 47.53 ± 2.1 % and 40.45 ± 1.2 % respectively in HaCaT cells. VCO increased the expression of Aquaporin-3 (AQP3), involucrin (INV) and filaggrin (FLG) and showed moderate UV protection in HaCaT cells. In vitro skin irritation studies in Reconstructed human epidermis (RHE) and NIH3T3 cells showed that VCO is a non skin irritant (IC50 > 1000 μg/mL) and non phototoxic (PIF < 2). Our study demonstrated the anti inflammatory activity of VCO by suppressing inflammatory markers and protecting the skin by enhancing skin barrier function. This is the first report on anti-inflammatory and skin protective benefits of VCO in vitro. Overall, the results warrant the use of VCO in skin care formulations.

No abstract

Human skin is body’s vital organ constantly exposed to abiotic oxidative stress. This can have deleterious effects on skin such as darkening, skin damage, and aging. Plant-derived products having skin-protective effects are well-known traditionally. Triphala, a formulation of three fruit products, is one of the most important rasayana drugs used in Ayurveda. Several skin care products based on Triphala are available that claim its protective effects on facial skin. However, the skin protective effects of Triphala extract (TE) and its mechanistic action on skin cells have not been elucidated in vitro. Gallic acid, ellagic acid, and chebulinic acid were deduced by LC-MS as the major constituents of TE. The identified key compounds were docked with skin-related proteins to predict their binding affinity. The IC50 values for TE on human dermal fibroblasts (HDF) and human keratinocytes (HaCaT) were 204.90 ± 7.6 and 239.13 ± 4.3 μg/mL respectively. The antioxidant capacity of TE was 481.33 ± 1.5 mM Trolox equivalents in HaCaT cells. Triphala extract inhibited hydrogen peroxide (H2O2) induced RBC haemolysis (IC50 64.95 μg/mL), nitric oxide production by 48.62 ± 2.2%, and showed high reducing power activity. TE also rescued HDF from H2O2-induced damage; inhibited H2O2 induced cellular senescence and protected HDF from DNA damage. TE increased collagen-I, involucrin and filaggrin synthesis by 70.72 ± 2.3%, 67.61 ± 2.1% and 51.91 ± 3.5% in HDF or HaCaT cells respectively. TE also exhibited anti-tyrosinase and melanin inhibition properties in a dose-dependent manner. TE increased the mRNA expression of collagen-I, elastin, superoxide dismutase (SOD-2), aquaporin-3 (AQP-3), filaggrin, involucrin, transglutaminase in HDF or HaCaT cells, and decreased the mRNA levels of tyrosinase in B16F10 cells. Thus, Triphala exhibits protective benefits on skin cells in vitro and can be used as a potential ingredient in skin care formulations.

De‐oiled rice bran is a byproduct of rice processing industries and rich in lipids, carbohydrates, proteins, and fibers. Although rich in nutrients, it is unfit for human consumption and used as animal feed. This study was conducted to explore the therapeutic value of rice bran ceramides. Methanolic extract of de‐oiled rice bran (RBE) was obtained by hot soxhlet extraction method and evaluated for presence of ceramide. Further, the rice bran ceramide extract (RBE) was subjected to column chromatography and the presence of ceramide ascertained by spectroscopic studies. Cytotoxic effect of RBE was tested on THP‐1 and HaCaT cells. The tested concentrations of RBE (100 and 200 µg/mL) dose‐dependently inhibited lipopolysaccharide induced pro‐inflammatory cytokines (TNF‐α, IFN‐γ, IL‐8, IL‐6, and IL‐5) in THP‐1 cells. RBE enhanced skin‐barrier function (involucrin and filaggrin) in HaCaT cells, up‐regulated aquaporin‐3 (AQP‐3) expression, and inhibited hyaluronidase activity in HaCaT cells. Thus, RBE exhibited significant anti‐inflammatory and skin protective benefits in vitro. Practical applications De‐oiled rice bran is cheap, easily procurable, rich in phytonutrients, and possess therapeutic value. In the current study, extract comprising ceramides from de‐oiled rice bran (RBE) showed significant anti‐inflammatory and skin protective effects on THP‐1 and HaCaT cells, respectively. The results of the present investigation highlights the promising use of rice bran ceramides as potential anti‐inflammatory and skin protective ingredient in nutritional and skin‐care formulations or products.