Anti-Helicobacter pylori activities of natural isopentenyloxycinnamyl derivatives from Boronia pinnata.

Cécile Ribeiro da Silva (1) , Valérie Michel (1) , Salvatore Genovese (2) , Marie-Christine Prévost (3) , Francesco Epifano (2) , Eliette Touati (1)

1 Pathogenèse de Helicobacter
2 Dipartimento di Scienze del Farmaco
3 Microscopie Ultrastructurale (Plate-forme)

In this study we investigated the anti-Helicobacter pylori activity of four isopentenyloxycinnamyl derivatives from the Australian shrub Boronia pinnata Sm. (Rutaceae), structurally related to boropinic acid: (E)-3-(4-(3-methylbut-2-enyloxy)-3,5-dimethoxyphenyl)acrylaldehyde (1), boropinol C (2), boropinal (3) and boropinol A (4). In vitro growth of H. pylori strains 26695 and B128 was analyzed in liquid culture with increasing doses of these compounds. Bacterial morphology was visualized by scanning electron microscopy. The in vivo effects of the two most efficient molecules that reduced bacterial growth in vitro, compounds 3 and 4, were investigated on H. pylori gastric colonization in the mouse model. The presence of these compounds in the bacterial cultures led to alterations of bacterial surface and flagella. In vivo, both compounds 3 and 4 at 250 microM reduced significantly the ability of H pylori to colonize the gastric mucosa of mice, compared with untreated ones. These data indicate that these natural isopentenyloxycinnamyl derivatives related to boropinic acid can be considered as novel antibacterial agents with anti-H. pylori activity.

Mots clés: Anti-bacterial compounds; Plant secondary metabolites; Mouse model; Oxyprenylated derivatives; Helicobacter pylori infection

Domaines: Bactériologie; Pharmacologie

Cécile Ribeiro da Silva, Valérie Michel, Salvatore Genovese, Marie-Christine Prévost, Francesco Epifano, et al.. Anti-Helicobacter pylori activities of natural isopentenyloxycinnamyl derivatives from Boronia pinnata.. Natural Product Communications , 2012, 7 (10), pp.1347-50. ⟨10.1177/1934578X1200701024⟩. ⟨pasteur-01737658⟩