Planta Med 2010; 76(14): 1550-1557
DOI: 10.1055/s-0029-1241016
Pharmacology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Phytochemical Characterization of Rhododendron ferrugineum and In Vitro Assessment of an Aqueous Extract on Cell Toxicity

Andrea Louis1 , Frank Petereit1 , Matthias Lechtenberg1 , Alexandra Deters1 , Andreas Hensel1
  • 1Institute of Pharmaceutical Biology and Phytochemistry, University of Münster, Münster, Germany
Weitere Informationen

Publikationsverlauf

received Dec. 21, 2009 revised February 19, 2010

accepted February 24, 2010

Publikationsdatum:
22. März 2010 (online)

Preview

Abstract

Within a systematic phytochemical investigation of the leaves of Rhododendron ferrugineum L. (Ericaceae), the volatile oil was isolated (0.7 %) and its constituents were characterized. Eleven flavonoids were isolated and characterized, with quercetin 3-O-[6′′-O-(2-methyl-1-oxobutyl)]-β-D-glucopyranoside and 2R,3R-dihydromyricetin 3-O-β-L-arabinopyranoside as new natural products. Beside monomeric flavan-3-ols (catechin, epicatechin, gallocatechin, epigallocatechin) from the tannin fraction (about 3.5 % calculated as pyrogallol), the dimeric procyanidins B1 to B7 were identified, as well as the trimeric compounds procyanidin C1, epicatechin-(4β → 8)-epicatechin-(4β → 8)-catechin and the trimeric A type-linked cinnamtannin B1. Additionally, phloroacetophenon 4-O-β-D-glucopyranoside and chlorogenic acid were isolated. Water-soluble carbohydrates comprised about 13.5 % of the dried leaves, including fructans (3 %), polysaccharides (1 %) (mainly type II arabinogalactans), glucose, fructose, sucrose, stachyose and raffinose. The in vitro effects on cellular vitality (MTT test), proliferation (BrdU incorporation) and necrosis (LDH release) of an aqueous extract were investigated. The extract did not exert any toxic effects, while the vitality and the proliferation rates of epithelial HaCaT keratinocytes were significantly increased at 100 µg/mL, indicating that the aqueous extract does not have negative effects against cellular activity.

References

Prof. Dr. Andreas Hensel

Institute of Pharmaceutical Biology and Phytochemistry
University of Münster

Hittorfstraße 56

48149 Münster

Germany

Telefon: + 49 25 18 33 33 80

Fax: + 49 25 18 33 83 41

eMail: ahensel@uni-muenster.de