dr samdhattwrites
phospholipidic membranes from UV- induced peroxidation. FerulicAcid, in particular, has exhibited strength in protecting human skin from UVB-induced erythyma and proven its worth as a potent UV absorber in many lotions and sunscreens7
.
Quercetin One of the most common flavonoids, Quercetin serves the skin as a powerful antioxidant when integrated into a pre- and post-sun skin care regimen. Found in Apples, Grapes, Lemons, Onions, Broccoli, Kale, Cottonseed and the herb Gingko Biloba, Quercetin diminishes the harmful effects of UV light.
In a study published in Clinical and Experimental Dermatology, researchers demonstrated that the Flavonoid has the ability to protect the skin’s antioxidant systems glutathione peroxidase, glutathione reductase, catalase and superoxide dismutase against UVA irradiation8
.
Apigenin Another common plant-based Flavonoid, Apigenin may help prevent UVA- and UVB-induced skin cancers, according to two studies published in Anticancer Research and Carcinogenesis. In those studies, tumor incidence decreased with a topical application ofApigenin, which is derived from herbs, such as Endive and Clove, fruits such asApples and Cherries, vegetables and beverages like tea and wine9, 10
.
Genistein Turns out Soybeans not only offer a great phytoestrogenic and protein source for vegans and menopausal women but its valuable phytonutrient Genestein has also been shown to inhibit UVB-induced tumors in mice, according to a study published in Carcinogenesis11
.
Furthermore, a 2001 study published in Photochemistry and Photobiology demonstrated how a topical application substantially inhibited UVB-induced hydrogen peroxide production and contact hypersensitivity and lowered the inflammatory edema reaction in mice12
.
CarnosicAcid Rosemary and Sage’s main constituent, CarnosicAcid is not only a potent antioxidant but also touts wide-ranging chemoprotective effects against carcinogens as demonstrated in a study published in the Journal of the National Cancer Institute ofMedicine13
.
A separate study published in Free Radical Biology &Medicine found human
Dr Sam Dhatt, an award-winning cosmeceutical chemist, founded DermaQuest® in 1999. During his
20-year career he has formulated and manufactured skin care products for over 700 companies. He holds an MS in Chemistry and an MBA in Marketing and Finance.
t: 0845 24 64 666
w:
www.dermaquestinc.co.uk @DermaQuestUK
Silymarin Widely used as medicine in Europe for 2,000 years, Silymarin has been used most commonly for treating liver diseases. However, Silymarin, a standardised extract derived from the seeds of theMilk Thistle, may also have chemoprotective activity against skin cancer, according to several published papers15, 16, 17, 18
.
Topical application is thought to significantly inhibit UVB-induced skin edema and formation of sunburn and apoptotic cells, the destructive cells that cause cell death. It is also known to
References
1. Gao Z, Huang K, Xu H., (2001) Protective effects of flavonoids in the roots of Scutellaria baicalensis Georgii against hydrogen peroxide-induced oxidative stress in HS-SY5Y cells. Pharmacol Res 43,173-8.
2. Afaq F,AdhamiVM,Ahmad N,Mukhtar H. (2002) Botanical antioxidants for chemoprevention of photocarcinogenesis. Front Biosci 7, 784-92.
3. European Journal of Pharmacology,Vol. 650, Issue 1, 10 Jan. 2011 p. 130-137
4. Katiyar SH,Mukhtar H (1997)Tea antioxidants in cancer chemoprevention. J Cell BiochemSuppl 27, 59-67
5.Wei H, Zhang X, Zhao JF,Wang ZY, Bickers DR, LebwohlM. (1999) Scavenging of hydrogen peroxide and inhibition of ultraviolet light-induced oxidative DNA damage by aqueous extracts fromgreen and black teas. Free Radic BiolMed 26, 1427-1435.
6. Katiyar SH,Ahmad N,Mukhtar H (2000) Green tea and
skin.Arch Dermatol. 136, 989-94
7. SaijaA,TomatinoA,Trombetta D, De PasqualeA, Uccella N, BarbuzziT, Paolino D, Bonina F. (2000) In vitro and in vivo evaluation of caffeic and ferulic acids as topical photoprotective agents. Int J Pharm199, 39-47.
8. InalME, KahramantA, KokentT (2001) Beneficial effects of quercetin on oxidative stress induced by ultravioletA. Clin Exp Dermatol 26, 536-9.
9. Birt DF,Mitchell D, Gold B, Pour P, Pinch HC (1997) Inhibition of ultraviolet light induced skin carcinogenesis in SKH-1mice by apigenin, a plant
flavonoid.Anticancer Res 17, 85-92.
10.McVeanM, Xiao H, Isobe K, Pelling JC. (2001) Increase in wild-type p53 stability and transactivational activity by the chemoprotective agent apigenin in keratinocytes. Carcinogenesis 21, 633-9
11.WangY,Yaping E, Zhang X, LebwohlM, DeLeoV,Wei H. (1998) Inhibition of ultraviolet (UVB-induced) c-fos and c-jun expression in vivo by protein kinase inhibitor genistein. Carcinogenesis 19, 649-54.
12.Widyarini S, Spinks N, HusbandAJ, ReeveVE. (2001) Isoflavonoid compounds fromred clover (Trifolium pretense) protect frominflammation and immune suppression induced by UV radiation. Photochem Photobiol 74,465-70.
13. DanilenkoM,Wang X, Studzinski GP. (2001) Carnosic acid and promotion ofmonocytic differentiation of HL60- G cells initiated by other agents. J Natl Cancer Inst. 15, 1224-33.
14. Offord EA, Gautier JC,Avanti O, Scaleta C, Runge F, Kramer K,Applegate LA (2002) Photoprotective potential of lycopene, ß-carotene, vitamin E, vitamin C and carnosic acid in UVA-irradiated human skin fibroblasts. Free Radic BiolMed 23, 1293-303.
15. Afaq F,AdhamiVM,Ahmad N,Mukhtar H. (2002) Botanical antioxidants for chemoprevention of photocarcinogenesis. Front Biosci 7, 784-92.
16. Singh RP,Agarwal R. (2002) Flavonoid antioxidant silymarin and skin
cancer.Antioxid Redox Signal 4, 655–63.
17.Morazzoni P, Bombardelli E. (1994) Silybummarianum (Cardusmarianus). Fitoterapia 66, 3–22.
18. ŠimánekV,Walterová D,Vičar J, Urbaníková J, KřenV, Modrian- skýM, ŠkotováT, Ulrichová J. (2001) “Silymarin” – extrakt z ostropestremariánského (Silybum marianum) – lék nebo potravní doplnek. Ces Slov Farm 50, 66–9.
19. J Dermatol Sci (2007)Apr: 46(1): 21-30. Epub 2007 Feb. 7.
Nextmonth: Dr Sam Dhatt will look at newer, innovative ingredients that have also hit the skin care market for pre- and post-UV exposure.
In a 2007 Czech study, Silymarin was shown to extensively reduced depletion of GSH, the body’s natural antioxidant, glutathione, ROS production and lipid peroxidation in irradiated cells. In this report, Silymarin also significantly decreased formation of UVA-induced DNA damage19
.
Fibroblasts that were pre-treated with CarnosicAcid resulted in suppression of Metalloproteinase-1 (MMP) mRNA, a damaging enzyme caused by UVA irradiation and a biomarker of photoageing14
.
protect against the formation of UVB- induced Cyclobutane-Pyrimidine dimers (CPDs), pre-mutagenic lesions found in DNA and the primary cause of melanoma, according to the animal study published in Frontiers in Bioscience.
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