Investigation of the Proliferative Effects of Artichoke (Cynara scolymus) Leaf and Stem Extracts on Human Dermal Fibroblast Cells


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Aydın M., Korgun A. S., Erdoğan Orhan .

7th International Symposium on Medicinal and Aromatic Plants (SIPAM-7), Madaniyin, Tunus, 11 - 13 Nisan 2025, ss.183-184, (Özet Bildiri)

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Madaniyin
  • Basıldığı Ülke: Tunus
  • Sayfa Sayıları: ss.183-184
  • Lokman Hekim Üniversitesi Adresli: Evet

Özet

Wound healing is a complex biological process that involves cell proliferation and migration,

particularly of dermal fibroblasts. Natural products have gained increasing attention as potential

agents to support and heal this process. In this study, we investigated the proliferative and

wound-healing effects of the cultured sample of Cynara scolymus L. (artichoke, Asteraceae)

leaf and stem extracts on human dermal fibroblast cells. Artichoke leaf and stem extracts were

prepared and applied to cultured human dermal fibroblast cells at concentrations ranging from

0.015 to 1 mg/mL. Cell viability was assessed using the MTT assay at 24 and 48 hours. In order

to evaluate the wound-healing potential, an in vitro scratch assay was performed and wound

closure was monitored at 0, 24, and 48 hours. The leaf extract demonstrated a concentration-

dependent effect on fibroblast proliferation and migration. At 0.031 and 0.062 mg/mL, the leaf extract significantly increased cell viability and promoted wound closure, indicating enhanced

proliferative and migratory activity. However, at concentrations of 0.250 mg/mL and above, a

marked reduction in both cell viability and wound closure capacity was observed. The stem

extract also exhibited moderate proliferative and wound-healing effects at lower concentrations

(0.015–0.062 mg/mL). Notably, the stem extract at concentration of 0.125 mg/mL induced

cytotoxic effects, characterized by decreased viability and observable morphological alterations

in fibroblast cells, suggesting loss of structural integrity. In conclusion, both artichoke leaf and

stem extracts exerted concentration-dependent effects on dermal fibroblasts. While the leaf

extract demonstrated stronger proliferative and wound-healing activity at optimal

concentrations, the stem extract was revealed with limited efficacy and cytotoxicity at higher

doses. These findings suggest that artichoke-derived compounds, particularly from the leaf,

may have therapeutic potential in promoting skin regeneration, whose phytochemical analysis

is in progress in our laboratory.