LC‐MS/MS and GC‐MS profiling, antioxidant, enzyme inhibition, and antiproliferative activities of Thymus leucostomus Hausskn. & Velen. extracts

Author:

Fayez Shaimaa1,Fahmy Nouran M.1,Zengin Gokhan2ORCID,Yagi Sakina3,Uba Abdullahi Ibrahim4,Eldahshan Omayma A.15ORCID,Koyuncu Ismail6,Temiz Ebru7,Dall'Acqua Stefano8,Sut Stefania8,Selvi Selami9

Affiliation:

1. Department of Pharmacognosy, Faculty of Pharmacy Ain Shams University Cairo Abbassia Egypt

2. Physiology and Biochemistry Laboratory, Department of Biology, Science Faculty Selcuk University Konya Turkey

3. Department of Botany, Faculty of Science University of Khartoum Khartoum Sudan

4. Department of Molecular Biology and Genetics Istanbul AREL University Istanbul Turkey

5. Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, Centre of Drug Discovery Research and Development Ain Shams University Cairo Abbassia Egypt

6. Department of Medical Biochemistry, Faculty of Medicine Harran University Sanliurfa Turkey

7. Program of Medical Promotion and Marketing, Health Services Vocational School Harran University Sanliurfa Turkey

8. Department of Pharmaceutical and Pharmacological Sciences University of Padova Padova Italy

9. Department of Plant and Animal Production, Altınoluk Vocational School Balıkesir University Balıkesir Turkey

Abstract

AbstractThe chemical composition as well as antioxidant, antiproliferative, and enzyme inhibition activities of extracts from aerial parts of Thymus leucostomus H ausskn. & V elen. obtained with hexane, methanol, and water were evaluated. Results showed that the methanol extract had significantly (p < 0.05) the highest total phenolic content (TPC; 107.80 mg GAE/g) and total flavonoids content (TFC; 25.21 mg RE/g) followed by the aqueous extract (102.72 mg GAE/g and 20.88 mg RE/g, respectively). LC‐MS/MS‐guided profiling of the three extracts revealed that rosmarinic acid (34.8%), hesperetin (42.9%), and linoleic acid (18%) were the dominant compounds in the methanol, aqueous and hexane extracts, respectively. GC‐MS analysis of the hexane extract showed that ɣ‐sitosterol (29.9%) was the major constituent. The methanol extract displayed significantly (p < 0.05) the highest Cu++, Fe+++, and Mo(VI) ions scavenging and reducing properties while the aqueous extract exerted significantly (p < 0.05) the highest metal chelating power (42.51 mg EDTAE/g). Both the hexane and methanol extracts effectively inhibited the acetylcholinesterase enzyme (2.63 and 2.65 mg GALAE/g, respectively) while the former extract exerted significantly (p < 0.05) the highest butyrylcholinesterase (2.32 mg GALAE/g), tyrosinase (19.73 mg KAE/g), and amylase (1.16 mmol ACAE/g) inhibition capacity. The aqueous extract exhibited the best glucosidase inhibition property (0.49 mmol ACAE/g). The methanol and hexane extracts exerted a higher cytotoxic effect on HT‐29 (IC50: 8.12 µg/mL) and HeLa (IC50 = 8.08 µg/mL) cells, respectively. In conclusion, these results provide valuable insight into the potential use of T. leucostomus bioactive extracts in different pharmaceutical applications.

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

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