Introduction: Mart. (araticum) is a widely distributed tree in the cerrado. Its value is attributed principally to the consumption of its fruit which possesses a large nutritive potential. The objective was to identify the chemical profile and evaluate the antimicrobial and cytoprotective activity of the hydroethanol extract of Mart. (HEAC) leaves against the toxicity of mercury chloride.

Materials And Methods: The characterization of components was carried out using high-performance liquid chromatography (HPLC). The minimum inhibitory concentration (MIC) was determined by microdilution method in broth with strains of , , and . For evaluation of the modulatory and cytoprotective activity of aminoglycoside antibiotics (gentamicin and amikacin) and mercury chloride (HgCl), the substances were associated with the HEAC at subinhibitory concentrations (MIC/8).

Results And Discussion: The HPLC analysis revealed the presence of flavonoids such as Luteolin (1.84%) and Quercetin (1.19%) in elevated concentrations. The HEAC presented an MIC ≥512 μg/mL and significant antagonistic action in aminoglycosides modulation, and it also showed cytoprotective activity to (significance < 0.0001) and (significance < 0.05) bacteria against the mercury chloride heavy metal with significance, this action being attributed to the chelating properties of the flavonoids found in the chemical identification.

Conclusions: The results acquired in this study show that the HEAC presents cytoprotective activity over the tested strains and can also present antagonistic effect when associated with aminoglycosides, reinforcing the necessity of taking caution when combining natural and pharmaceutical products.

Summary: The hydroalcoholic extract of Mart. presents cytoprotective activity against the toxic effect of Hg. : HPLC-DAD: High-performance liquid chromatography with a diode array detector; MIC: Minimum inhibitory concentration; DMSO: Dimethyl sulfoxide.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004515PMC
http://dx.doi.org/10.4103/0974-8490.188882DOI Listing

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