4.7 Article

Volatile and phenolic profiling of a traditional medicinal plant, Hypericum empetrifolium with in vitro biological activities

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 272, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2021.113933

关键词

Hypericum empetrifolium Willd; LC-MS/MS; Cytotoxicity; Anticandidal; Traditional uses

资金

  1. Dicle University [D.U. BAP/14-EZF-69]
  2. TUBITAK 2219-International Postdoctoral Research Fellowship Program

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The study investigated the phytochemical profiles of Hypericum empetrifolium extracts from aerial parts and roots, revealing the presence of various compounds with antioxidant and antimicrobial activities. The aerial parts extract demonstrated significant antioxidant effects and antimicrobial activity, while the roots extract showed strong inhibitory effects on cholinesterase enzymes. Further research is needed to explore additional therapeutic properties of this plant.
Ethnopharmacological relevance: Hypericum empetrifolium Willd is a member of the Hypericaceae family, mainly known in southern Greece, and western Turkey. Being a centuries-old medicinal plant, the aerial parts of the plant have been used for the treatment of herpes, kidney stones, gastric ulcer, and also for their anti-helminthic, and diuretic purposes traditionally. Aim of the study: The current study aimed to investigate the phytochemical profiles of the essential oil, and two ethanol extracts prepared from the aerial parts (H. empetrifolium aerial parts extract HEA), and roots of the plant (H. empetrifolium roots extract HER), and to provide data on antioxidant, anticholinesterase, antityrosinase, antiurease, cytotoxic, and antimicrobial activities of the extracts. Materials and methods: In this study, volatile and phenolic compounds of the HEA and HER were analyzed by GC MS and LC-MS/MS, respectively. Antioxidant potential of the extracts was clarified by using DPPH radical scavenging assay, ABTS cation radical assay, and the CUPRAC assay. Acetylcholinesterase, butyrylcholinesterase, urease, and tyrosinase inhibitory activity assays were used to determine enzyme inhibition capacity of the extracts. Cytotoxic activity of the extracts was established by using XTT assay. The antimicrobial activity of the extracts was determined by the microbroth dilution technique. Results: The major compounds of the essential oil were revealed as alloaromodendrene (24.7%), alpha-pinene (14.7%), beta-pinene (10.7%), and alpha-terpineol (7.7%) by the GC-MS analysis. According to the LC-MS/MS analysis results, quinic acid was the most abundant constituent in both extracts with 20612.42 +/- 169.02 mu g/g extract in HEA extract, and with 2254.34 +/- 18.49 mu g/g extract in HER extract, respectively. The HEA extract was also found to be rich in terms of chlorogenic acid (5583.14 +/- 38.52 mu g/g extract), isoquercitrin (3076.77 +/- 40.92 mu g/g extract), and malic acid (2822.90 +/- 31.90 mu g/g extract). HEA extract exhibited a significant antioxidant effect with an IC50 value of 11.98 +/- 0.22 mu g/mL according to the DPPH radical scavenging assay. Similar results were obtained with the ABTS cation radical assay, and the CUPRAC assay. HER extract showed a strong butyrylcholinesterase inhibitory effect with 88.69 +/- 0.62% at 200 mu g/mL concentration. Both extracts were considered to have moderate anti-tyrosinase activity compared to the standard at 200 mu g/mL. The best antimicrobial activity was obtained for HEA against C. parapsilosis with an MIC value of 4.88 mu g/mL. HEA also exhibited antifungal activity against C. tropicalis with 19.53 mu g/mL. Only HER exhibited low cytotoxicity on A498 renal cell lines with 60.6% cell viability. Conclusion: Unquestionably, H. empetrifolium Willd has ethnopharmacological importance according to these results, and further investigations are required to evaluate other therapeutic properties of the plant.

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