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Dive into the research topics where Robert Anton is active.

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Featured researches published by Robert Anton.


Nutrition and Cancer | 2000

Suppression of Azoxymethane-Induced Preneoplastic Lesions and Inhibition of Cyclooxygenase-2 Activity in the Colonic Mucosa of Rats Drinking a Crude Green Tea Extract

Nadia Metz; Annelise Lobstein; Yann Schneider; Francine Gossé; R. Schleiffer; Robert Anton; Francis Raul

We determined the effects of a crude green tea extract given as drinking fluid on the promotion/progression phase of colon carcinogenesis in rats after induction of the neoplastic process by azoxymethane. Adult Wistar rats were given azoxymethane (15 mg/kg ip) once a week for two weeks. One week after the second injection, the rats were randomly divided into two groups. One group (n = 8) received daily prepared aqueous solutions of green tea extracts (GTE; 0.02%, wt/vol); the control group (n = 8) received tap water. After six weeks, rats receiving GTE showed a 60% reduction in the number of colonic preneoplastic lesions (aberrant crypts). The number of individual crypts per aberrant crypt focus (crypt multiplicity) was significantly reduced in the GTE group; the majority (80%) of the remaining aberrant foci contained only one or two preneoplastic crypts. A significant and selective decrease of cyclooxygenase (COX)-2 activity was observed in the colon of rats receiving GTE (23 ± 3 vs. 117 ± 30 mU/mg protein in controls), whereas COX-1 showed no alterations. Our data demonstrate that GTE reduces COX-2 and suppresses the formation of colonic preneoplastic lesions. They provide new insights into the mechanism of chemopreventive and anti-inflammatory properties of green tea.


Phytochemistry | 1992

Dimeric alkaloids fromPsychotria forsteriana

Yacoub Adjibade; Bernard Weniger; Jean C. Quirion; B. Kuballa; Pierre Cabalion; Robert Anton

Abstract Three alkaloids, (−)-calycanthine, iso -calycanthine and meso -chimonanthine, a dimeric indole isomeric with the former compounds have been isolated from Psychotria forsteriana and identified on the basis of their spectral data and by comparison with those of previously described compounds.


Phytochemistry | 1999

Chemotaxonomical investigation in the genus Viburnum

Annelise Lobstein; Gisèle Haan-Archipoff; Jürgen Englert; Jean-Georges Kuhry; Robert Anton

A chemical examination of the leaves and branchlets of Viburnum sp. (Adoxaceae) has been carried out in order to find chemical clues of possible taxonomic value. Precise quantitative data of the amentoflavone content were obtained for about sixty representative taxa of the genus. A great heterogeneity of distribution of this biflavone was observed between the sections. The highest average concentration (more than 0.5%) was found in the section Lantana.


Phytochemistry | 1986

Kaempferol coumaroyl glucorhamnoside from Ginkgo biloba

Chamel Nasr; Micheline Haag-Berrurier; Annelise Lobstein-Guth; Robert Anton

Abstract A new flavonoid glycoside was isolated from the leaves of Ginkgo biloba and its structure elucidated as kaempferol 3-O-α-(6‴-p-coumaroylglucosyl-β-1,4-rhamnoside).


Phytochemistry | 1991

Triterpenoid glycosides from the bark of Mimosa tenuiflora.

Yulin Jiang; Georges Massiot; Catherine Lavaud; Jean-Marie Teulon; Christophe Guéchot; Micheline Haag-Berrurier; Robert Anton

Two new saponins were isolated from Mimosa tenuiflora and their structures established as 3-O-[alpha-L-rhamnopyranosyl(1----2)-beta-D-glucopyranosyl-(1----3]-(alp ha-L- arabinopyranosyl-(1----4]-beta-D-xylopyranosyl-(1----2)]-[beta-D- xylopyranosyl-(1----4)]-beta-D-glucopyranosyl)-28-O-alpha-L-rhamnopyrano syl oleanolic acid and 3-O-[alpha-L-rhamnopyranosyl-(1----2)-beta-D-glucopyranosyl-(1----3]-(al pha- L-arabinopyranosyl-(1----4]beta-D-xylopyranosyl-(1----2)]-[beta-D- xylopyranosyl-(1----4)]-beta-D-glucopyranosyl) oleanolic acid.


Phytochemistry | 1987

Quercetin coumaroyl glucorhamnoside from Ginkgo biloba

Chamel Nasr; Annelise Lobstein-Guth; Micheline Haag-Berrurier; Robert Anton

Abstract A new flavonoid glycoside was isolated from the leaves of Ginkgo biloba (Ginkgoaceae) and its structure elucidated as quercetin-3-O-α-(6‴-p-coumaroylglucosyl-β-1,4-rhamnoside).


Molecular Membrane Biology | 1999

Interactions of the monomeric and dimeric flavones apigenin and amentoflavone with the plasma membrane of L929 cells; a fluorescence study.

Anne-Frederique Lenne-Gouverneur; Annelise Lobstein; Gisèle Haan-Archipoff; Guy Duportail; Robert Anton; Jean-Georges Kuhry

Flavonoids are ubiquitous polyphenolic compounds, found in vascular plants, which are endowed with a large variety of biological effects. Some of these effects have been assumed to result from interactions with the cell plasma membrane. In order to investigate the nature of these interactions a fluorescence study was performed with two flavonoids, currently used in one of the laboratories: apigenin and its homologous dimer amentoflavone. After preliminary assays with DPH in several types of phospholipid liposomes, the effects of these flavonoids on the membrane of mouse L929 fibroblasts were compared, using the non-permeant probe TMA-DPH. Amentoflavone, unlike apigenin, induced a static quenching effect, which denoted an important, but reversible, association of the molecule with the plasma membrane. In addition, amentoflavone treatment induced a dose-dependent increase in TMA-DPH fluorescence anisotropy, which could be interpreted as an increase in membrane lipidic order. For apigenin, the effect was much less important. Moreover, exploiting the capacity of TMA-DPH to label endocytic compartments, it was shown that, after association with the membrane, amentoflavone is not internalized into the cell. Possible correlations of these membrane effects with other biological properties are discussed.


Phytochemistry | 1980

La 5′-méthoxybilobétine, une biflavone extraite du Ginkgo biloba

Marc Joly; Micheline Haag-Berrurier; Robert Anton

Abstract A new biflavone, I-5′-methoxybilobetin has been isolated from Ginkgo biloba leaves. 1 H and 13 C NMR spectral data show that it is a II-4′, I-5, II-5, I-7, II-7-pentahydroxy-I-4′, I-5′-dimethoxy- [I-3′, II-8] biflavone.


Phytochemistry | 1996

Sulphated steroidal derivatives from Ruscus aculeatus

Ali Oulad-Ali; Dominique Guillaume; René Belle; Bruno David; Robert Anton

Abstract Two novel steroidal derivatives, (1β-hydroxyruscogenin 1-sulphate and 26-O-β- d -glucopyranosyl furost-5-en-1β,22ζ-triol 1-sulphate) were isolated from the rhizome of Ruscus aculeatus . The structures were established by spectroscopic methods.


Phytochemistry | 1993

Oxindole alkaloids from Neolaugeria resinosa

Bernard Weniger; Yulin Jiang; Robert Anton; Jaume Bastida; Teresa Varea; Jean-Charles Quirion

Abstract The new alkaloids neolaugerine, isoneolaugerine and 15-hydroxyneolaugerine, possessing an original oxindole skeleton, have been isolated from the root

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Bernard Weniger

Centre national de la recherche scientifique

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Dominique Guillaume

Centre national de la recherche scientifique

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Byung-Hun Um

Korea Institute of Science and Technology

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Jean-Charles Quirion

Centre national de la recherche scientifique

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Bruno David

Institut de Chimie des Substances Naturelles

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