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. 2015 Jun 15:9:3067-72.
doi: 10.2147/DDDT.S84676. eCollection 2015.

Antibiotic-modifying activity of riachin, a non-cyanogenic cyanoglycoside extracted from Bauhinia pentandra

Pablo Antonio Maia de Farias  1 , Fernando Gomes Figueredo  2 , Aline Maria Brito Lucas  3 , Rafael Barbosa de Moura  3 , Henrique Douglas Melo Coutinho  4 , Tania Maria Sarmento da Silva  5 , Ana Luiza de Aguiar Rocha Martin  2 , Marta Maria de França Fonteles  6
Affiliations

Antibiotic-modifying activity of riachin, a non-cyanogenic cyanoglycoside extracted from Bauhinia pentandra

Pablo Antonio Maia de Farias et al. Drug Des Devel Ther. .

Abstract

Background: The search for new active compounds from the Brazilian flora has intensified in recent years, especially for new drugs with antibiotic potential. Accordingly, the aim of this study was to determine whether riachin has antibiotic activity in itself or is able to modulate the activity of conventional antibiotics.

Methods: A non-cyanogenic cyanoglycoside known as riachin was isolated from Bauhinia pentandra, and was tested alone and in combination with three antibiotics (clindamycin, amikacin, and gentamicin) against multiresistant bacterial strains (Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus).

Results: Riachin did not show significant antibiotic activity when tested alone against any strain (P>0.05). However, when combined with conventional antibiotics, it showed drug-modifying activity against strains of S. aureus exposed to clindamycin (P<0.001) as well as against P. aeruginosa exposed to amikacin (P<0.001). Although riachin did not show direct antibiotic activity, it had synergistic activity when combined with amikacin or clindamycin. The mechanism of action of this synergism is under investigation.

Conclusion: The results of this work demonstrate that some substances of natural origin can enhance the effectiveness of certain antibiotics, which means a substantial reduction in the drug dose required and possibly in consequent adverse events for patients.

Keywords: Escherichia coli; Pseudomonas aeruginosa; Staphylococcus aureus; riachin.

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Figures

Figure 1
Figure 1
Chemical structure of riachin.
Figure 2
Figure 2
MIC of aminoglycosides and clindamycin in the presence and absence of riachin (C14H19NO8) at MIC/8 (128 μg/mL), against Pseudomonas aeruginosa and Staphylococcus aureus and MIC/8 (32 μg/mL) against Escherichia coli. Note: ***P<0.001. Abbreviations: MIC, minimal inhibitory concentration; MIC/8, eight-fold reduced minimal inhibitory concentration.
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