Antagonist Effects of Veratric Acid against UVB-Induced Cell Damages

Ultraviolet (UV) radiation induces DNA damage, oxidative stress, and inflammatory processes in human epidermis, resulting in inflammation, photoaging, and photocarcinogenesis. Adequate protection of skin against the harmful effect of UV irradiation is essential. In recent years naturally occurring herbal compounds such as phenolic acids, flavonoids, and high molecular weight polyphenols have gained considerable attention as beneficial protective agents. The simple phenolic veratric acid (VA, 3,4-dimethoxybenzoic acid) is one of the major benzoic acid derivatives from vegetables and fruits and it also occurs naturally in medicinal mushrooms which have been reported to have anti-inflammatory and anti-oxidant activities. However, it has rarely been applied in skin care. This study, therefore, aimed to explore the possible roles of veratric acid in protection against UVB-induced damage in HaCaT cells. Results showed that veratric acid can attenuate cyclobutane pyrimidine dimers (CPDs) formation, glutathione (GSH) depletion and apoptosis induced by UVB. Furthermore, veratric acid had inhibitory effects on the UVB-induced release of the inflammatory mediators such as IL-6 and prostaglandin-E2. We also confirmed the safety and clinical efficacy of veratric acid on human skin. Overall, results demonstrated significant benefits of veratric acid on the protection of keratinocyte against UVB-induced injuries and suggested its potential use in skin photoprotection.

[1]  R. Mccauley,et al.  Glutathione , 2003, Reactions Weekly.

[2]  N. Yang,et al.  Ferulic acid, a phenolic phytochemical, inhibits UVB-induced matrix metalloproteinases in mouse skin via posttranslational mechanisms. , 2012, The Journal of nutritional biochemistry.

[3]  M. Saravanakumar,et al.  Veratric acid, a phenolic acid attenuates blood pressure and oxidative stress in L-NAME induced hypertensive rats. , 2011, European journal of pharmacology.

[4]  J. Simon,et al.  Anti-inflammatory activity of edible oyster mushroom is mediated through the inhibition of NF-κB and AP-1 signaling , 2011, Nutrition journal.

[5]  A. García-Lafuente,et al.  Edible mushrooms: role in the prevention of cardiovascular diseases. , 2010, Fitoterapia.

[6]  J. Hong,et al.  Induction of dendritic cell maturation by β-glucan isolated from Sparassis crispa. , 2010, International immunopharmacology.

[7]  B. Narasimhan,et al.  Hansch analysis of veratric acid derivatives as antimicrobial agents. , 2009, European journal of medicinal chemistry.

[8]  Mun Kyung Hwang,et al.  Caffeic acid, a phenolic phytochemical in coffee, directly inhibits Fyn kinase activity and UVB-induced COX-2 expression. , 2008, Carcinogenesis.

[9]  Eunhye Kim,et al.  Phenolic compound concentration and antioxidant activities of edible and medicinal mushrooms from Korea. , 2008, Journal of agricultural and food chemistry.

[10]  J. Rundhaug,et al.  Cyclo‐oxygenase‐2 Plays a Critical Role in UV‐induced Skin Carcinogenesis † , 2008, Photochemistry and photobiology.

[11]  M. Yaar,et al.  Photoageing: mechanism, prevention and therapy , 2007, The British journal of dermatology.

[12]  L. Estevinho,et al.  Effect of fruiting body maturity stage on chemical composition and antimicrobial activity of Lactarius sp. mushrooms. , 2007, Journal of agricultural and food chemistry.

[13]  G. Hedjaroude,et al.  Immunomodulating and anticancer agents in the realm of macromycetes fungi (macrofungi). , 2007, International immunopharmacology.

[14]  S. Katiyar,et al.  Berberine, a natural product, induces G1-phase cell cycle arrest and caspase-3-dependent apoptosis in human prostate carcinoma cells , 2006, Molecular Cancer Therapeutics.

[15]  C. Elmets,et al.  Selective cyclooxygenase-2 inhibition produces heterogeneous erythema response to ultraviolet irradiation. , 2005, The Journal of investigative dermatology.

[16]  B. Jang,et al.  Curcumin inhibits the expression of COX-2 in UVB-irradiated human keratinocytes (HaCaT) by inhibiting activation of AP-1: p38 MAP kinase and JNK as potential upstream targets , 2005, Experimental & Molecular Medicine.

[17]  V. Adhami,et al.  Photochemoprevention of ultraviolet B signaling and photocarcinogenesis. , 2005, Mutation research.

[18]  P. Lacelle,et al.  Epidermal COX-2 induction following ultraviolet irradiation: suggested mechanism for the role of COX-2 inhibition in photoprotection. , 2003, The Journal of investigative dermatology.

[19]  C. Elmets,et al.  Dietary feeding of proanthocyanidins from grape seeds prevents photocarcinogenesis in SKH-1 hairless mice: relationship to decreased fat and lipid peroxidation. , 2003, Carcinogenesis.

[20]  E. Kavanaugh THE COSMETIC, TOILETRY, AND FRAGRANCE ASSOCIATION , 2003 .

[21]  S. Martin,et al.  Caspases: cellular demolition experts. , 2001, Biochemical Society transactions.

[22]  H. Mukhtar,et al.  Green tea polyphenol (−)‐epigallocatechin‐3‐gallate treatment to mouse skin prevents UVB‐induced infiltration of leukocytes, depletion of antigen‐presenting cells, and oxidative stress , 2001, Journal of leukocyte biology.

[23]  Y. P. Lu,et al.  Time course for early adaptive responses to ultraviolet B light in the epidermis of SKH-1 mice. , 1999, Cancer research.

[24]  J. Masferrer,et al.  COX-2 expression is induced by UVB exposure in human skin: implications for the development of skin cancer. , 1998, Carcinogenesis.

[25]  J. Hornung,et al.  Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line , 1988, The Journal of cell biology.

[26]  Stephan D. Flint,et al.  Internal filters: Prospects for UV‐acclimation in higher plants , 1983 .

[27]  A M Kligman,et al.  The soap chamber test. A new method for assessing the irritancy of soaps. , 1979, Journal of the American Academy of Dermatology.