PHYTOCHEMICAL CHARACTERIZATION AND BIOACTIVITY ASSESSMENT OF AETHIONEMA SCHISTOSUM WITH A FOCUS ON ENZYME INHIBITION AND ANTIOXIDANT POTENTIAL


PEKACAR S., Güverti Ö. F., Özüpek B., Negiz H., Tugay O., DELİORMAN ORHAN D.

Studia Universitatis Babes-Bolyai Chemia, cilt.2025, sa.2, ss.67-79, 2025 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 2025 Sayı: 2
  • Basım Tarihi: 2025
  • Doi Numarası: 10.24193/subbchem.2025.2.05
  • Dergi Adı: Studia Universitatis Babes-Bolyai Chemia
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, CAB Abstracts, Central & Eastern European Academic Source (CEEAS)
  • Sayfa Sayıları: ss.67-79
  • Anahtar Kelimeler: Aethionema schistosum, Antidiabetic, Antioxidant, Reverse phase-HPLC
  • Gazi Üniversitesi Adresli: Evet

Özet

The study examines the antioxidant, antidiabetic, antihyperlipidemic, and antiobesity properties of the 80% methanol extract prepared from the aerial parts of Aethionema schistosum, a plant widely distributed in certain regions. The extract was evaluated in vitro for its inhibitory effects on α-glucosidase (antidiabetic), α-amylase (antidiabetic), pancreatic lipase (antiobesity), and pancreatic cholesterol esterase (antihyperlipidemic) enzymes. It exhibited moderate α-glucosidase inhibition (99.15±0.04%) compared to acarbose (56.94±3.88%). The DPPH radical scavenging activity of the extract at a concentration of 2 mg/ml was measured at 80.50±1.23%. This value is considered close to the inhibitory effect of ascorbic acid, which was recorded at 90.60±0.29% at the same concentration. The extract's total phenol (74.73±4.76 mg GAE/g) and flavonoid (42.80±2.25 mg QE/g) contents were measured, and chlorogenic acid was identified as a major compound via HPLC. This is the first study to analyze the phytochemical composition and enzyme inhibitory effects of A. schistosum. Further research is needed to isolate its bioactive compounds and assess its therapeutic potential through diverse in vitro and in vivo models, highlighting its potential in drug discovery efforts.