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Nordihydroguaiaretic Acid from Creosote Bush (Larrea tridentata) Mitigates 12‐O‐Tetradecanoylphorbol‐13‐Acetate‐Induced Inflammatory and Oxidative Stress Responses of Tumor Promotion Cascade in Mouse Skin
Author(s) -
Shakilur Rahman,
Rizwan Ahmed Ansari,
Hasibur Rehman,
Suhel Parvez,
Sheikh Raisuddin
Publication year - 2009
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1093/ecam/nep076
Subject(s) - nordihydroguaiaretic acid , oxidative stress , tumor promotion , chemistry , antioxidant , larrea , pharmacology , lipid peroxidation , glutathione , perilla frutescens , biochemistry , medicine , biology , enzyme , carcinogenesis , botany , lipoxygenase , shrub , gene
Nordihydroguaiaretic acid (NDGA) is a phenolic antioxidant found in the leaves and twigs of the evergreen desert shrub, Larrea tridentata (Sesse and Moc. ex DC) Coville (creosote bush). It has a long history of traditional medicinal use by the Native Americans and Mexicans. The modulatory effects of topically applied NDGA was studied on acute inflammatory and oxidative stress responses in mouse skin induced by stage I tumor promoting agent, 12- O -tetradecanoylphorbol-13-acetate (TPA). Double TPA treatment adversely altered many of the marker responses of stage I skin tumor promotion cascade. Pretreatment of NDGA in TPA-treated mice mitigated cutaneous lipid peroxidation and inhibited production of hydrogen peroxide. NDGA treatment also restored reduced glutathione level and activities of antioxidant enzymes. Elevated activities of myeloperoxidase, xanthine oxidase and skin edema formation in TPA-treated mice were also lowered by NDGA indicating a restrained inflammatory response. Furthermore, results of histological study demonstrated inhibitory effect of NDGA on cellular inflammatory responses. This study provides a direct evidence of antioxidative and anti-inflammatory properties of NDGA against TPA-induced cutaneous inflammation and oxidative stress corroborating its chemopreventive potential against skin cancer.

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