Journal Article

Rosmarinic acid inhibits epidermal inflammatory responses: anticarcinogenic effect of <i>Perilla frutescens</i> extract in the murine two-stage skin model

Naomi Osakabe, Akiko Yasuda, Midori Natsume and Toshikazu Yoshikawa

in Carcinogenesis

Volume 25, issue 4, pages 549-557
Published in print April 2004 | ISSN: 0143-3334
Published online April 2004 | e-ISSN: 1460-2180 | DOI: http://dx.doi.org/10.1093/carcin/bgh034
Rosmarinic acid inhibits epidermal inflammatory responses: anticarcinogenic effect of Perilla frutescens extract in the murine two-stage skin model

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Perilla frutescens extract showed marked reduction on tumorigenesis in a murine, two-stage skin carcinogenesis model. In this model, cancer is initiated by application of 7,12-dimethylbenz[a]anthracene (DMBA) and promoted by application of 12-tetradecanoylphorbol 13-acetate (TPA). Following tumor initiation with DMBA, topical application of a perilla-derived fraction (PF) at doses of 2 mg/mouse/application resulted in significant inhibition of tumorigenesis. The efficacy of each fraction was correlated with rosmarinic acid (RA) and luteolin concentration. Topical application of perilla extract (PE) that contained 68% RA or an equivalent amount of commercially available RA showed nearly identical antiinflammatory activity 5 h after TPA treatment. Application of luteolin had less anti-inflammatory activity. Marked neutrophil infiltration was observed in TPA-challenged skin by histological examination using hematoxylin–eosin. This change was greatly reduced by pre-treatment with PE or RA. Myeloperoxidase activity, a marker of neutrophil recruitment, was also increased in TPA-challenged skin and was significantly decreased in the PE and RA treated groups. Intercellular adhesion molecule 1 and vascular cell adhesion molecule-1 mRNA expression levels were reduced by pre-treatment with PE or RA. TPA-induced increases in synthesis of the chemokines KC and macrophage inflammatory protein-2 were significantly decreased by pre-treatment with PE or RA. Prostaglandin E2 and leukotriene B4 levels were slightly increased 5 h after TPA treatment. These levels were only numerically decreased in the PE and RA treated groups. However, induction of cyclooxygenase-2 mRNA expression was obviously reduced by pre-treatment with PE or RA. Reactive oxygen radical production, detected as thiobarbituric acid reactive substance and lipid peroxide, by double treatment of TPA was reduced by pre-treatment with PE or RA. Production of 8-hydroxy-2′deoxyguanosine, which was detected immunohistochemically, was also induced by double treatment with TPA. This adduct was barely visible in PE or RA treated mice. Thus, we conclude that part of the anticarcinogenic effects of P.frutescens extract is due to RA via two independent mechanisms: inhibition of the inflammatory response and scavenging of reactive oxygen radicals.

Keywords: COX-2, cyclooxygenase-2; DMBA, 7,12-dimethyl benz[a]anthracene; ICAM-1, intercellular adhesion molecule 1; LPO, lipid peroxide; LTB4, leukotriene B4; MIP-2, macrophage inflammatory protein-2; MPO, myeloperoxidase; NFκB, nuclear factor κB; 8OH-dG, 8-hydroxy-2′deoxyguanosine; PE, perilla extract; PF, perilla fraction; PGE2, prostaglandin E2; PKC, protein kinase C; RA, rosmarinic acid; TBARS, thiobarbituric acid reactive substance; TFA, trifluoroacetic acid; TPA, 12-tetradecanoylphorbol 13-acetate; VCAM-1, vascular cell adhesion molecule-1

Journal Article.  5615 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

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