Journal
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE
Volume 12, Issue 2, Pages 133-139Publisher
MARY ANN LIEBERT, INC
DOI: 10.1089/acm.2006.12.133
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Funding
- NCCIH NIH HHS [F31 AT00804, F31 AT000804, F31 AT24232, P50 AT000155, F31 AT002423, P50 AT00155] Funding Source: Medline
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Objectives: To document the chemical and biologic profile of a clinical phase 11 red clover(Trifolium pratense L.) extract by identifying and measuring the major and minor components visible in the high-performance liquid chromatography-ultraviolet (HPLC-UV) chromatogram and evaluating each compound for estrogenic and antioxidant activity. Design: Individual compounds in the preformulated (i.e., no exciplents present) extract were identified by either chemical isolation followed by structure elucidation or matching to retention time and molecular mass of chemical standards via liquid chromatography-mass spectrometry (LC-MS) analysis. Quantitation of the amounts of compounds found in the prefomulated extract was done using HPLC-UV or LC-MS. Isolated compounds or standards were evaluated for their ability to: (1) induce alkaline phosphatase (AP) in an endometrial carcinoma cell line, (2) competitively bind to recombinant human estrogen receptors (ERs) alpha (alpha) and beta (beta), and (3) act as antioxidants by scavenging 2,2-di(4-tert-octylphenyl)-1-picrylliydi-azyl (DPPH) free radicals. Results: The preformulated red clover extract had 50% effective concentration (EC50) of 2.0 to 2.2 mu g/mL in the AP estrogenicity assay, and 50% inhibitory concentrations (IC(50)s) Of 18.4 to 32.6 mu g/mL and 1.9 to 3.4 Ag/mL in the ER alpha and ER beta binding assays, respectively. The prefomulated extract was composed of 35.54% isoflavones, 1.11% flavoiloids, 0.06% pterocarpans, <= 0.03% cournarins, and <= 0.03% tyramine. Daidzein, genistein, formononetin, biochanin A, coumestrol, and naringenin were estrogenic in the AP assay, and all of these, except formononetin, bound to one or both ERs. Conclusions: The major and minor chemical and active estrogenic components of a preformulated phase II red clover clinical extract were identified, quantitatively measured, and the final capsule doses were calculated. The extract is currently under evaluation in a year-long clinical study for the alleviation of menopausal hot flashes. This is the first report to thoroughly summarize the chemistry and biology of all major peaks observed in the HPLC-UV chromatogram of a clinical red clover dietary supplement.
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