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leaves as source of anti- agents. | LitMetric

leaves as source of anti- agents.

Front Pharmacol

School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Trinity Biomedical Sciences Institute, Dublin, Ireland.

Published: October 2024

AI Article Synopsis

  • Infection is a global health concern linked to serious conditions like gastritis and gastric cancer, with challenges arising from antibiotic resistance and treatment compliance.
  • This study investigates the antimicrobial properties of sacha inchi leaves, identifying bioactive compounds like astragalin through various chemical analysis techniques.
  • The results demonstrate that the leaf extracts and isolated astragalin can inhibit the growth of certain resistant bacterial strains, suggesting potential therapeutic applications with further research.

Article Abstract

Introduction: infection is a major issue worldwide, with widespread prevalence, combined with its link to gastritis, peptic ulcers, gastric cancer, and mucosa-associated lymphoid tissue (MALT) lymphoma. Meanwhile, effectiveness of current treatment protocols is limited by increasing antibiotic resistance and patient compliance issues due to long regimens and side effects. , or sacha inchi, is a valuable source of bioactive molecules. However, studies on its antimicrobial activity, especially against , are lacking.

Methods: In this study, the anti- activity of leaves water extract was explored using and approaches. High-Performance Liquid Chromatography coupled to Electrospray Ionisation and Quadrupole Time-of-Flight Mass Spectrometry (HPLC-ESI- QTOF-MS-MS) analysis of the water extract from the leaves was used to characterise the chemical composition of the plant and allowed identification of some flavonoids, such as astragalin, and some phenolic compounds. Then, high-speed counter current chromatography (HSCCC) was used to fractionate the ethyl acetate partition obtained from the water extract from the leaves.

Results And Discussion: The presence of flavonoids derived from kaempferol was confirmed and astragalin was isolated for the first time in . The water infusion, ethyl acetate extract and the isolated astragalin exhibited anti-bacterial activity against J99 and two clinical isolates (e.g., minimum inhibitory concentrations of 0.53, 0.51 and 0.49 μg/mL, respectively, for clarithromycin-resistant clinical isolate SSR366). Then, using molecular docking for potential protein targets for , it was verified that astragalin could interact with these proteins by analysis.

Conclusion: These findings highlight that and astragalin produce a bacteriostatic activity against and may have potential to be used in treatment against , after further research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537943PMC
http://dx.doi.org/10.3389/fphar.2024.1461447DOI Listing

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