Unravelling the antifungal and antiprotozoal activities and LC-MS/MS quantification of steroidal saponins isolated from Panicum turgidum

• Published in: RSC advances 2022-01, Vol.12 (5), p.2980-2991
• Main Authors: Zaki, Ahmed A, Kaddah, Mohamed M Y, Abulkhair, Hamada S, Ashour, Ahmed
• Format: Article
• Language: English
• Subjects: Chemistry; Elongation; Fungicides; Liquid chromatography; Mass spectrometry; Reductases; Residues; Saponins
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/d1ra08532h

Bioassay-guided investigation of extract resulted in the identification of seven steroidal saponins (Turgidosterones 1-7). They were evaluated for their antifungal, antileishmanial, and antitrypanosomal activities. Turgidosterone 6 was the most active antifungal against and (IC values of 2.84 and 1.08 μg mL , respectively). Turgidosterones 4-7 displayed antileishmanial activity against promastigotes with IC values ranging from 4.95 to 8.03 μg mL and against amastigote/THP with IC values range of 4.50-9.29 μg mL . Activity against was also observed for Turgidosterones 4-7 with an IC values range of 1.26-3.77 μg mL . Turgidosterones 1-3 did not display any activity against the tested pathogens. The study of structure-activity relationships of the isolated saponins indicated that the antifungal, antileishmanial, and antitrypanosomal activities are markedly affected by the presence of spirostane-type saponins and the elongation of the sugar residue at C-3. To quantitatively determine the most abundant active ingredient in extract, a single run, sensitive, and highly selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method has been applied under positive and negative modes. The obtained results showed that compound 5 was the most abundant (95.93 ± 1.10 mg per gram of dry ), followed by 6 (52.51 ± 1.05 mg gm ), 4 (32.71 ± 0.48 mg gm ), and 7 (13.19 ± 0.50 mg gm ). Docking of these saponins against the oxidoreductases and trypanothione reductase active sites revealed their potential to effectively bind with a number of key residues in both receptor targets.