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Review
. 2022 Sep 6:2022:9966750.
doi: 10.1155/2022/9966750. eCollection 2022.

Flavonols and Flavones as Potential anti-Inflammatory, Antioxidant, and Antibacterial Compounds

Affiliations
Review

Flavonols and Flavones as Potential anti-Inflammatory, Antioxidant, and Antibacterial Compounds

Maria do Socorro S Chagas et al. Oxid Med Cell Longev. .

Abstract

Plant preparations have been used to treat various diseases and discussed for centuries. Research has advanced to discover and identify the plant components with beneficial effects and reveal their underlying mechanisms. Flavonoids are phytoconstituents with anti-inflammatory, antimutagenic, anticarcinogenic, and antimicrobial properties. Herein, we listed and contextualized various aspects of the protective effects of the flavonols quercetin, isoquercetin, kaempferol, and myricetin and the flavones luteolin, apigenin, 3',4'-dihydroxyflavone, baicalein, scutellarein, lucenin-2, vicenin-2, diosmetin, nobiletin, tangeretin, and 5-O-methyl-scutellarein. We presented their structural characteristics and subclasses, importance, occurrence, and food sources. The bioactive compounds present in our diet, such as fruits and vegetables, may affect the health and disease state. Therefore, we discussed the role of these compounds in inflammation, oxidative mechanisms, and bacterial metabolism; moreover, we discussed their synergism with antibiotics for better disease outcomes. Indiscriminate use of antibiotics allows the emergence of multidrug-resistant bacterial strains; thus, bioactive compounds may be used for adjuvant treatment of infectious diseases caused by resistant and opportunistic bacteria via direct and indirect mechanisms. We also focused on the reported mechanisms and intracellular targets of flavonols and flavones, which support their therapeutic role in inflammatory and infectious diseases.

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Conflict of interest statement

The authors declare no conflicts of interest regarding the publication of this paper.

Figures

Figure 1
Figure 1
The basic skeleton of flavonoids (C6-C3-C6).
Figure 2
Figure 2
Chemical structures of some representative flavonoids and the basic skeleton of the flavonoids in the middle.
Figure 3
Figure 3
Chemical structures of quercetin, myricetin, and kaempferol.
Figure 4
Figure 4
Chemical structures of luteolin and apigenin.
Figure 5
Figure 5
Chemical structures of 3′,4′-dihydroxyflavone, baicalein, scutellarein, lucenin-2, vicenin-2, diosmetin, nobiletin, tangeretin, and 5-O-methyl-scutellarein.
Figure 6
Figure 6
Summary of the effects of flavonols and flavones. The figure presents a range of signaling pathways of the inflammatory process and the stages where the compounds block the signaling cascade. The number represents the pathways inhibited by different compounds. For example, pathway 1 is blocked by the following compounds: quercetin, luteolin, 3′,4′-dihydroxyflavone, baicalein, nobiletin, and tangeretin. Scutellarin, vicenin-2, apigenin, 5-O-methyl-scutellarin, and the substances are able to block pathway 1 and inhibit pathway 2. Only luteolin and lucenin-2 inhibit pathway 3. Furthermore, pathway 4 can only be inhibited by luteolin. Most of the compounds previously mentioned in this review block pathway 5, except nobiletin, tangeretin, vicenin-2, and lucenin-2. Furthermore, luteolin, scutellarin, vicenin-2, and lucenin-2 inhibited pathway 6. Only isoquercetin blocks pathway 7, and luteolin blocks pathway 8.

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References

    1. Yang S. C., Chen P. J., Chang S. H., et al. Luteolin attenuates neutrophilic oxidative stress and inflammatory arthritis by inhibiting Raf1 activity. Biochemical Pharmacology . 2018;1(154):384–396. doi: 10.1016/j.bcp.2018.06.003. - DOI - PubMed
    1. Ahmed S. I., Hayat M. Q., Tahir M., et al. Pharmacologically active flavonoids from the anticancer, antioxidant and antimicrobial extracts of Cassia angustifolia Vahl. BMC Complementary Medicine and Therapies . 2016;16(1):p. 460. doi: 10.1186/s12906-016-1443-z. - DOI - PMC - PubMed
    1. Carullo G., Cappello A. R., Frattaruolo L., Badolato M., Armentano B., Aiello F. Quercetin and derivatives: useful tools in inflammation and pain management. Future Medicinal Chemistry . 2017;9(1):79–93. - PubMed
    1. Park K. Y., Jung G. O., Lee K. T., et al. Antimutagenic activity of flavonoids from the heartwood of Rhus verniciflua. The Journal of Ethnopharmacology . 2004;90(1):73–79. doi: 10.1016/j.jep.2003.09.043. - DOI - PubMed
    1. Panche A. N., Diwan A. D., Chandra S. R. Flavonoids: an overview. Journal of Nutritional Science . 2016;5, article e47 doi: 10.1017/jns.2016.41. - DOI - PMC - PubMed

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