Cited by 175Phytochemicals and Antioxidant ActivitiesFree Radicals and AntioxidantsMetal complexes synthesis and properties

Antioxidant vs. Prooxidant Properties of the Flavonoid, Kaempferol, in the Presence of Cu(II) Ions: A ROS-Scavenging Activity, Fenton Reaction and DNA Damage Study

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Simunkova, Miriama, Barbierikova, Zuzana, Jomova, Klaudia, Hudecova, Lenka, Lauro, Peter, Alwasel, Saleh H., Alhazza, Ibrahim, Rhodes, Christopher J. +1 more·2021·International Journal of Molecular Sciences

Abstract

Kaempferol is a flavonoid that occurs in tea and in many vegetables and fruits, including broccoli, cabbage, beans, grapes, apples, and strawberries. The efficacy of Kaempferol has been demonstrated in the treatment of breast, esophageal, cervical, ovarian, and liver cancers and leukemia, which very likely arises from its prooxidant properties and the activation of pro-apoptotic pathways. Indeed, this matter has already been the focus of a number of published studies and reviews. The aim of the present study was to elucidate the antioxidant vs. prooxidant properties of flavonoids in the presence of the redox-active metal, copper (II) ion, by means of the Fenton reaction. The specific motivation of this work is that, since an increased level of Cu(II) ions is known to be associated with many disease states such as neurological conditions (Alzheimer’s disease) and cancer, any interaction between these ions and flavonoids might affect the outcome of therapeutic uses of the latter. The structure of the Cu-kaempferol complex in DMSO was investigated by means of low temperature EPR spectroscopy, which confirmed the existence of at least two distinct coordination environments around the copper (II) ion. UV vis-spectra of kaempferol and its Cu(II) complex in DMSO revealed an interaction between the 5-OH (A ring) group and the 4-CO (C ring) group of kaempferol with Cu(II) ions. An ABTS assay confirmed that kaempferol acted as an effective radical scavenger, and that this effect was further enhanced in the form of the Cu(II)-kaempferol complex. Quantitative EPR spin trapping experiments, using DMPO as the spin trap, confirmed suppression of the formation of a mixture of hydroxyl, superoxide, and methyl radicals, in a Fenton reaction system, upon coordination of kaempferol to the redox-active Cu(II) ions, by 80% with respect to the free Cu(II) ions. A viscometric study revealed a better DNA-intercalating ability of the Cu-kaempferol complex than for free kaempferol, essential for conferring anticancer activity of these substances. The results of the viscometric measurements were compared with those from a DNA damage study of Cu-kaempferol complexes in a Fenton reaction system, using gel electrophoresis. At low concentrations of kaempferol (Cu–kaempferol ratios of 1:1 and 1:2), a very weak protective effect on DNA was noted, whereas when kaempferol was present in excess, a significant DNA-protective effect was found. This can be explained if the weakly intercalated kaempferol molecules present at the surface of DNA provide protection against attack by ROS that originate from the Fenton reaction involving intercalated Cu(II)-kaempferol complexes. Following the application of ROS scavengers, L-histidine, DMSO, and SOD, gel electrophoresis confirmed the formation of singlet oxygen, hydroxyl radicals, and superoxide radical anions, respectively. We propose that the prooxidant properties of Cu-kaempferol complexes may provide anticancer activity of these substances. When present in excess, kaempferol displays antioxidant properties under Cu-Fenton conditions. This suggests that kaempferol might prove a suitable candidate for the prevention or treatment of oxidative stress related medical conditions that involve a disturbed metabolism of redox metals such as copper, for example, Menkes disease, and neurological disorders, including Alzheimer’s disease. For the potential use of kaempferol in clinical practice, it will be necessary to optimize the dose size and critical age of the patient so that this flavonoid may be beneficial as a preventive drug against cancer and neurological disorders.

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  • Antioxidant properties of flavonoids predominantly depend on the number and position of hydroxyl groups and their metal-chelating ability.

    “Antioxidant properties of flavonoids predominantly depend on the number and position of hydroxyl groups and their metal-chelating ability (Fig. 12) (Lomozova et al. 2022; Simunkova et al. 2021).”
  • Metal flavonoid chelates can intercalate into DNA of cancer cells, triggering cell death.

    “The metal chelating activity of flavonoids results either (i) in the formation of metal-chelates which have lower catalytic efficiency in Fenton reaction than pure flavonoids (decreased number of metal binding sites is usually associated with lower catalytic activity) or (ii) metal flavonoid chelates can intercalate into DNA of cancer cells, triggering cell death (Simunkova et al. 2021).”
  • Metal chelating activity of flavonoids results in formation of metal-chelates which have lower catalytic efficiency in Fenton reaction than pure flavonoids.

    “The metal chelating activity of flavonoids results either (i) in the formation of metal-chelates which have lower catalytic efficiency in Fenton reaction than pure flavonoids (decreased number of metal binding sites is usually associated with lower catalytic activity) or (ii) metal flavonoid chelates can intercalate into DNA of cancer cells, triggering cell death (Simunkova et al. 2021).”
  • There are many examples of efficient antioxidants under in vitro conditions that undergo a switch from antioxidant to prooxidant behavior, or partly or completely lose their antioxidant properties under in vivo conditions.

    “There are many examples of efficient antioxidants under in vitro conditions that undergo a switch from antioxidant to prooxidant behavior, or partly or completely lose their antioxidant properties under in vivo conditions (Simunkova et al. 2021).”

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References 70 · Cited by 175

Authors
Simunkova, M., Barbierikova, Z., Jomova, K., Hudecova, L., Lauro, P., Alwasel, S. H., Alhazza, I., Rhodes, C. J., & Valko, M.
Affiliations
  • Institute of Physical Chemistry and Chemical Physics, Faculty of Chemical and Food Technology, Slovak University of Technology, 812 37 Bratislava, Slovakia
  • Department of Chemistry, Faculty of Natural Sciences, Constantine the Philosopher University in Nitra, 949 74 Nitra, Slovakia
  • Constantine the Philosopher University in Nitra (SK)
  • King Saud University (SA)
  • Fresh-Lands Environmental Actions, Reading, Berkshire RG4 5BE, UK
Corresponding author
Rhodes, Christopher J.
Venue
International Journal of Molecular Sciences
Publisher
MDPI AG
Published
2021-02-05
Volume
22
Issue
4
Pages
1619
ISSN
1422-0067 (ISSN-L)
OpenAlex
W3127934055
Cited by
175
References
70
Citations by year
2026: 35 · 2025: 44 · 2024: 26 · 2023: 38 · 2022: 21 · 2021: 10
FWCI
12.93
Type
journal article
Language
en
Open access
Locations
  • International Journal of Molecular Sciences (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Scientific Grant Agency (VEGA Project 1/0482/20)
  • Research and Development Support Agency (APVV-15-0079 and APVV-19-0087)
  • Slovak University of Technology (Young Researcher Grant - FLAVMET)
  • Slovak University of Techology (Excellent Team of Young Researchers CUSPK)
  • King Saud University, Riyadh, Saudi Arabia (Researchers Supporting Project (RSP-2020/59))
Topics
  • Health Sciences › Medicine › Biochemistry › Phytochemicals and Antioxidant Activities
  • Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
  • Health Sciences › Medicine › Oncology › Metal complexes synthesis and properties
Keywords
kaempferol, flavonoids, copper(II) ions, pro-oxidant activity, antioxidant activity, Fenton reaction, reactive oxygen species scavenging, DNA intercalation, DNA damage, spin trapping, electron spin resonance, anticancer activity, hydroxyl radicals, superoxide, methyl radical
MeSH terms
Antineoplastic Agents, Antioxidants, Copper, Dimethyl Sulfoxide, DNA Damage, Humans, Organometallic Compounds, Molecular Structure, Reactive Oxygen Species, Oxidative Stress, Kaempferols

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