In vitroandin vivo antibacterial activities of rhizophora man-gle l. against helicobacter pylori. chemical compounds elucida-tion

Authors

  • Sánchez Perera Luz María National Center of Animal Health
  • Morales Espinosa María Rosario rsity Autonomous of Mexico
  • Delgado Lamas Guillermo University Autonomous of Mexico
  • de Mendonça Sergio Universidade Bandeirante de São Paulo
  • Cortes Diego Miguel Valencia University
  • Ramírez Miranda Rafael National Center of Animal Health

DOI:

https://doi.org/10.14419/ijpt.v5i1.6235

Published:

2017-03-03

Keywords:

Rhizophora Mangle L., In Vitro and in Vivo Anti- Helicobacter Effect, Chemical Compounds Elucidation.

Abstract

Rhizophora mangle L. is a vegetal species widely distributed in Cuba and other Caribbean countries with ethno- pharmacology relevance and preview reports as antiulcer and wound healing properties. The present work describes the in vitro and in vivo antibacterial activities of dried aqueous extract of bark and polyphenol fractions from R. mangle against Helicobacter pylori and the identification of new compounds in the active extracts. Minimum inhibitory concentration (MIC) and Minimum bactericide concentration (MBC) were evaluated against reference and clinical Helicobacter pylori strains with total extract, High Molecular Weight and Low Molecular Weight fractions isolated from total extract. Positive active fractions in vitro tests were evaluated in vivo using H. pylori C57BL/6 mice. Fractionation, isolation and structural elucidation of the compounds on High Molecular Weigh fraction and on Low Molecular Weight fraction were made using Chromatography methods and Mass and H+NMR spectrometry. Total aqueous extract from bark of R. mangle and some fraction shown promissory antibacterial activity on in vitro and in vivo models. It was isolated and identified proantocyanidin, catechin and epicatechin derivates, cyanidin and other compounds in this promissory extract. These results appoint to total extract with a promissory active principle in the development of phytodrug with antibacterial effect and as proton pump inhibitor by the treatment of gastroduodenal ulcer.

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