Skip to main content
Log in

Antioxidant, antiproliferative, anti-inflammatory, and enzyme inhibition potentials of Ficus carica wood bark and related bioactive phenolic metabolites

  • Original
  • Published:
Wood Science and Technology Aims and scope Submit manuscript

Abstract

Considering the bioactive composition and therapeutic interest of Ficus carica, much research has been conducted on its fruits and leaves. However, there has been relatively little investigation regarding the wood bark, despite its potential as a rich source of phytochemical compounds with diverse biological activities. The aim of this work is the determination of the phenolic composition of the wood bark extracts of F. carica from three cultivars (Aberkane, Aghanime, and Bakour) and the assessment of their potential cytotoxicity and bioactive capacities such as antioxidant, anticancer, and anti-inflammatory activities. The phytochemical compounds were identified and quantified using UPLC-ESI-MS. The results revealed that Aberkane wood bark cultivar had the highest content of total polyphenols and ascorbic acid, while Aghanime cultivar had the highest content of flavonoids. The wood bark of the Aberkane cultivar exhibited the highest DPPH and ABTS scavenging activities (48.55% and 71.81%, respectively). This extract exhibited strong cytotoxic effects against cancer cell lines MCF-7 (IC50 143.30 µg/mL) and carcinoma HepG2 (IC50 240.18 µg/mL), as well as potent anti-inflammatory activity demonstrated by the BSA assay and inhibition of NO production in RAW 264.7 cells. Aghanime wood bark extract exhibited the highest ORAC value (446.078 µmol TE/g). However, the Bakour wood bark cultivar was particularly noteworthy for its iron-chelating properties. The UPLC-ESI-MS analysis revealed the presence of various phenolic compounds, notably chlorogenic acid and rutin. These findings demonstrate that the wood bark extract of fig possesses a diverse range of beneficial biological activities, which are associated with its phytochemical composition.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

Data will be made available on request.

References

Download references

Acknowledgements

We gratefully acknowledge all the members of the team “Glyco et Nano-Vecteurs pour le Ciblage Thérapeutique” at the “Institut de Biomolécules Max Mousseron”, Montpellier, France, and the technical support of the Laboratory of Applied Biochemistry of the Faculty of Natural and Life Sciences, University of Bejaia, Algeria.

Funding

This investigation was supported by the General Directorate of Scientific Research and Technological Development (Algeria).

Author information

Authors and Affiliations

Authors

Contributions

S.Y. Methodology, Investigation, Data curation, Writing – original draft. D.E.K. Resources, M.C. Conceptualization, L.M.A.A: Investigation, K.C. Data curation, G.D. Software, Formal analysis. A.M. Data curation, C.M. Data curation, N.B. Supervision. M.B. Validation, Supervision.

Corresponding author

Correspondence to Mostapha Bachir-Bey.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yahiaoui, S., Kati, D.E., Chaalal, M. et al. Antioxidant, antiproliferative, anti-inflammatory, and enzyme inhibition potentials of Ficus carica wood bark and related bioactive phenolic metabolites. Wood Sci Technol (2024). https://doi.org/10.1007/s00226-024-01549-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00226-024-01549-y

Navigation