Boosting the Anti‐Helicobacter Efficacy of Azithromycin through Natural Compounds: Insights From In Vitro, In Vivo, Histopathological, and Molecular Docking Investigations

Author:

Bendary Mahmoud M.1ORCID,Elmanakhly Arwa R.2,Mosallam Farag M.3,Alblwi Noaf Abdullah N.4,Mosbah Rasha A.5,Alshareef Walaa A.6,Selim Heba M. R. M.7,Alhomrani Majid89,Alamri Abdulhakeem S.89,Safwat Nesreen A.2,Hamdan Ahmed M. E.10ORCID,Elshimy Rana11

Affiliation:

1. Department of Microbiology and Immunology, Faculty of Pharmacy Port Said University Port Said Egypt

2. Department of Microbiology and Immunology, Faculty of Pharmacy Modern University of Technology and Information Cairo Egypt

3. Drug Radiation Research Department, National Center for Radiation Research and Technology (NCRRT) Egyptian Atomic Energy Authority Cairo Egypt

4. Al Hadithah General Hospital Al‐Qurayyat Al Hadithah Saudi Arabia

5. Infection Control Unit Zagazig University Hospital Zagazig Egypt

6. Department of Microbiology and Immunology, Faculty of Pharmacy 6th October University Giza Egypt

7. Department of Pharmaceutical Science, College of Pharmacy AlMaarefa University Riyadh Saudi Arabia

8. Department of Clinical Laboratories Sciences, the Faculty of Applied Medical Science Taif University Taif Saudi Arabia

9. Centre of Biomedical Science Research (CBSR), Deanship of Scientific Research Taif University Taif Saudi Arabia

10. Department of Pharmacy Practice, Faculty of Pharmacy University of Tabuk Tabuk Saudi Arabia

11. Department of Microbiology and Immunology, Faculty of Pharmacy Alhram Canadian University Giza Egypt

Abstract

ABSTRACTBackgroundAntimicrobial‐resistant Helicobacter pylori (H. pylori) poses a significant public health concern, especially given the limited therapeutic options for azithromycin‐resistant strains. Hence, there is a necessity for new studies to reconsider the use of azithromycin, which has diminished in effectiveness against numerous strains. Thus, we aimed to augment azithromycin's anti‐Helicobacter properties by combining it with curcumin in different formulations, including curcumin in clove oil, curcumin nano‐gold emulsion, and curcumin nanoemulsion.MethodsThe antimicrobial activities of the investigated compounds, both individually and in combination with other anti‐Helicobacter drugs, were evaluated. Their antibiofilm and anti‐virulence properties were assessed using both phenotypic and genotypic methods, alongside molecular docking studies. Our findings were further validated through mouse protection assays and histopathological analysis.ResultsWe observed high anti‐Helicobacter activities of curcumin, especially curcumin nanoemulsion. A synergistic effect was detected between curcumin nanoemulsion and azithromycin with fraction inhibitory concentration index (FICI) values <0.5. The curcumin nanoemulsion was the most active anti‐biofilm and anti‐virulence compound among the examined substances. The biofilm‐correlated virulence genes (babA and hopQ) and ureA genes were downregulated (fold change <1) post‐treatment with curcumin nanoemulsion. On the protein level, the anti‐virulence activities of curcumin nanoemulsion were documented based on molecular docking studies. These findings aligned with histopathological scoring of challenge mice, affirming the superior efficacy of curcumin nanoemulsion/azithromycin combination.ConclusionThe anti‐Helicobacter activities of all curcumin physical forms pose significant challenges due to their higher  minimum inhibitory concentration (MIC) values exceeding the maximum permissible level. However, using curcumin nanoemulsion at sub‐MIC levels could enhance the anti‐Helicobacter activity of azithromycin and exhibit anti‐virulence properties, thereby improving patient outcomes and addressing resistant pathogens. Therefore, more extensive studies are necessary to assess the safety of incorporating curcumin nanoemulsion into H. pylori treatment.

Publisher

Wiley

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