Planta Med 2017; 83(09): 790-796
DOI: 10.1055/s-0043-102494
Pharmacokinetic Investigations
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

In Vitro and In Vivo Study of the Gastrointestinal Absorption and Metabolisation of Hymenocardine, a Cyclopeptide Alkaloid

Emmy Tuenter
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
,
Sebastiaan Bijttebier
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
2   Flemish Institute for Technological Research (VITO), Business Unit Separation and Conversion Technology (SCT), Mol, Belgium
,
Kenn Foubert
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
,
Annelies Breynaert
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
,
Sandra Apers
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
,
Nina Hermans
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
,
Luc Pieters
1   Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium
› Institutsangaben
Weitere Informationen

Publikationsverlauf

received 23. November 2016
revised 09. Januar 2017

accepted 23. Januar 2017

Publikationsdatum:
02. Februar 2017 (online)

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Abstract

Hymenocardine is a cyclopeptide alkaloid present in the root bark of Hymenocardia acida. In traditional African medicine, the leaves and roots of this plant are used to treat malaria, and moderate in vitro antiplasmodial activity has been reported for hymenocardine. However, in view of its peptide-like nature, potential metabolisation after oral ingestion has to be taken into account when considering in vivo experiments. In this study, the stability and small intestinal absorption of hymenocardine was assessed using an in vitro gastrointestinal dialysis model. In addition, potential liver metabolisation was investigated in vitro by incubation with a human S9 fraction. Moreover, hymenocardine was administered to rats per os, and blood and urine samples were collected until 48 and 24 h after oral administration, respectively. All samples resulting from these three experiments were analyzed by LC-MS. Analysis of the dialysate and retentate, obtained from the gastrointestinal dialysis model, indicated that hymenocardine is absorbed unchanged from the gastrointestinal tract, at least in part. After S9 metabolisation, several metabolites of hymenocardine could be identified, the major ones being formed by the reduction and/or the loss of an N-methyl group. The in vivo study confirmed that hymenocardine is absorbed from the gastrointestinal tract unchanged, since it could be identified in both rat plasma and urine, together with hymenocardinol, its reduction product.

Supporting Information

An experimental overview (Fig. S1), the possible metabolisation reactions in hymenocardine, as predicted by Meteor and Metaprint2D-React Web Server (Fig. 2S), and an overview of the spectral and chromatographic data of hymenocardine and the metabolites formed during in vitro metabolisation with human S9 fraction (Table 1S) are available as Supporting Information. Furthermore, detailed descriptions of the methodology followed in the gastrointestinal dialysis experiment, the S9 experiment, and the analysis of plasma and urine samples are also available as Supporting Information.