Abstract

For more than four centuries, the intake of Narthecium ossifragum has been associated with poisoning in domesticated animals. Saponins occurring in flowering tops of the plant are considered to cause kidney damage in calves. At present, there are more than 30 papers on the saponins of N. ossifragum in the literature, although the structures of these compounds have hitherto not been determined. Here, we identify the saponins of N. ossifragum as sarsasapogenin, sarsasapogenin-3-O-β-galactopyranoside, sarsasapogenin-3-O-(2′-O-β-glucopyranosyl-β-galactopyranoside) and sarsasapogenin-3-O-(2′-O-β-glucopyranosyl-3′-O-α-arabinopyranosyl-β-galactopyranoside). Moreover, six aromatic natural products were isolated and characterized from the methanolic extract from flowers of N. ossifragum. Five of these aromatic compounds, chrysoeriol 6-C-β-arabinofuranoside-8-C-β-glucopyranoside, chrysoeriol 6-C-β-arabinopyranosyl-8-C-β-glucopyranoside, chrysoeriol 6-C-β-xylopyranosyl-8-C-β-galactopyranoside, chrysoeriol 6-C-β-galactopyranosyl-8-C-β-glucopyranoside and chrysoeriol 6-C-β-glucopyranosyl-8-C-β-galactopyranoside are undescribed. All compounds were tested for cytotoxicity in mammalian cell lines derived from the heart, kidney, and haematological tissues. The saponins exhibited cytotoxicity in the micromolar range, with proportionally increasing cytotoxicity with increasing number of glycosyl substituents. The most potent compound was the main saponin sarsasapogenin-3-O-(2′-O-β-glucopyranosyl-3′-O-α-arabinopyranosyl-β-galactopyranoside), which produced cell death at concentrations below 3–4 μM in all three cell lines tested. This indicates that the saponins are the toxicants mainly responsible for kidney damage observed in cattle after ingestion of N. ossifragum. Our findings also pave the way for analysis of individual compounds isolated during the biopsies of intoxicated animals.

Highlights

  • Narthecium ossifragum (L.) Huds. (Nartheciaceae) is a perennial flowering plant (Fig. 1), which natively grows on bogs in western and north-western Europe

  • The methanolic extracts of 1.7 kg of flowering tops of N. ossifragum were concentrated under reduced pressure and subjected to liquid/liquid separation with petroleum ether followed by ethyl acetate

  • The individual pure saponins were identified as sarsasapogenin (1), sarsasapogenin-3-O-β-galactopyranoside (2), sarsasapogenin3-O-(2′-O-β-glucopyranosyl-β-galactopyranoside) (3) and sarsasapogenin-3-O-(2′-O-β-glucopyranosyl-3′-O-α-arabinopyranosyl-β-galactopyranoside) (4) by 1D and 2D NMR spectroscopy

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Summary

Introduction

Narthecium ossifragum (L.) Huds. (Nartheciaceae) is a perennial flowering plant (Fig. 1), which natively grows on bogs in western and north-western Europe. The plant has in several instances been associated with toxic effects in grazing animals (Stabursvik, 1953; Flåøyen et al, 1995a; Wisløff et al, 2003) and is considered to cause the phototoxic disease alveld in lambs (Stabursvik, 1953). Saponins occurring in the flowering tops of the plant are presumed to cause kidney damage in calves (Flåøyen et al, 1997) These compounds have been suggested as playing a role in the development of hypothesized secondary phototoxicity this view has been challenged. Even though the connection between the intake of N. ossifragum and the occurrence of alveld in lambs seems to be well documented (Abdelkader et al, 1984; Ceh and Hauge, 1981) the original assumption about a potential connection between saponins of this plant species and the phototoxic disease is controversial and has been challenged (Flåøyen et al, 1991). As part of our on-going research concerning the characterization of aromatic compounds from N. ossifragum, several di-C-glycosylflavones, including several previously undescribed compounds, were isolated for the first time from this plant source

Results and discussion
Concluding remarks
Plant material
Extraction of compounds and partitions with organic solvents
Amberlite XAD-7 column chromatography
Sephadex LH-20 column chromatography
Preparative HPLC
Analytical HPLC
Isolation of pure saponins from crystallized mixture of saponins
Purification of saponins by Sephadex LH-20 column chromatography
Silica gel column chromatography
4.10. Analytical TLC
4.11. Spectroscopy
4.12. Brine shrimp lethality assay
4.13. Cytotoxicity towards mammalian cell lines

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