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Volume 224, Issue 2, Pages 193-202 (28 June 2005)


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Inhibition of tumour promotion in mouse skin by extracts of rooibos (Aspalathus linearis) and honeybush (Cyclopia intermedia), unique South African herbal teas

Jeanine MarnewickaCorresponding Author Informationemail address, Elizabeth Joubertb, Shamiel Josepha, Sonja Swanevelderc, Pieter Swartd, Wentzel Gelderbloma

Received 27 September 2004; received in revised form 30 October 2004; accepted 4 November 2004.

Abstract 

The modulating effect of ethanol/acetone (E/A) soluble fractions, prepared from methanolic extracts of processed and unprocessed rooibos (Aspalathus linearis) and honeybush (Cyclopia intermedia) as well as green (Camellia sinensis) teas was established in a two-stage mouse skin carcinogenesis assay. Topical application of the tea fractions prior to the tumour promoter, 12-O-tetradecanoylphorbol-13-acetate (TPA), on ICR mouse skin initiated with 7,12-dimethylbenz[a]anthracene (DMBA) suppressed skin tumorigenesis significantly (P<0.001) with the green tea E/A fraction exhibiting a 100% inhibition, unprocessed honeybush 90%, processed honeybush 84.2%, processed rooibos 75% and unprocessed rooibos 60%. The green tea fraction, with the highest flavanol/proanthocyanidin content, also exhibited the highest protective activity (99%) against hepatic microsomal lipid peroxidation, and completely inhibited skin tumour formation. Differences in the flavanol/proanthocyanidin and flavonol/flavone composition and/or non polyphenolic constituents are likely to be important determinants in the inhibition of tumour promotion by the herbal tea E/A fractions in mouse skin.

a PROMEC Unit, Medical Research Council, P.O. Box 19070, Tygerberg 7505, South Africa

b ARC Infruitec-Nietvoorbij, Private Bag X5026, Stellenbosch 7599, South Africa

c Biostatistic Unit, Medical Research Council, P.O. Box 19070, Tygerberg, 7505, South Africa

d Department of Biochemistry, Stellenbosch University, Private Bag X1, Stellenbosch 7602, South Africa

Corresponding Author InformationCorresponding author. Tel.: +27 21 938 0289; fax: +27 21 938 0260.

PII: S0304-3835(04)00868-7

doi:10.1016/j.canlet.2004.11.014


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