Protection against UVB deleterious skin effects in a mouse model: effect of a topical emulsion containing Cordia verbenacea extract

• Published in: Photochemical & photobiological sciences Vol. 20; no. 8; pp. 1033 - 1051
• Main Authors: Melo, Cristina P. B., Saito, Priscila, Vale, David L., Rodrigues, Camilla C. A., Pinto, Ingrid C., Martinez, Renata M., Bezerra, Julia R., Baracat, Marcela M., Verri, Waldiceu A., Fonseca-Bazzo, Yris Maria, Georgetti, Sandra R., Casagrande, Rubia
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.08.2021
• Subjects: Administration, Topical; Animals; Antioxidants - chemistry; Antioxidants - isolation & purification; Antioxidants - pharmacology; Biochemistry; Biomaterials; Chemistry; Chemistry and Materials Science; Cordia - chemistry; Disease Models, Animal; Emulsions - chemistry; Mice; Mice, Hairless; Original Papers; Oxidative Stress - drug effects; Physical Chemistry; Plant Extracts - administration & dosage; Plant Extracts - chemistry; Plant Extracts - pharmacology; Plant Leaves - chemistry; Plant Sciences; Skin - drug effects; Skin - metabolism; Skin - pathology; Ultraviolet Rays - adverse effects; Oxidative stress; Sunburn cells; Inflammation; COX-2; GSH; Radical scavenger
• ISSN: 1474-905X; 1474-9092; 1474-9092
• DOI: 10.1007/s43630-021-00079-x

Cordia verbenacea DC (Boraginaceae) is a flowering shrub found along the Brazilian Atlantic Forest, Brazilian coast, and low areas of the Amazon. The crude extract of its leaves is widely used in Brazilian folk medicine as an anti-inflammatory, both topically and orally. The aim of this study is to evaluate the activity of C. verbenacea ethanolic leaves extract (CVE) against UVB-triggered cutaneous inflammation and oxidative damage in hairless mice. CVE treatment recovered cutaneous antioxidant capacity demonstrated by scavenging ABTS + free radical and iron-reducing antioxidant potential evaluated by FRAP. CVE also controlled the following UV-triggered events in the skin: reduced glutathione (GSH) depletion, catalase activity decrease, and superoxide anion (O ⋅– ) build-up. Furthermore, mice treated with CVE exhibited less inflammation, shown by the reduction in COX-2 expression, TNF-α, IL-1β, IL-6, edema, and neutrophil infiltration. CVE also regulated epidermal thickening and sunburn cells, reduced dermal mast cells, and preserved collagen integrity. The best results were obtained using 5% CVE-added emulsion. The present data demonstrate that topical administration of CVE presents photochemoprotective activity in a mouse model of UVB inflammation and oxidative stress. Because of the intricate network linking inflammation, oxidative stress, and skin cancer, these results also indicate the importance of further studies elucidating a possible role of C. verbenacea in the prevention of UVB-induced skin cancer and evaluating a potential synergy between CVE and sunscreens in topical products against UVB damaging effects to the skin. Graphic abstract