Affiliations 

  • 1 Institute of Pharmaceutical Sciences (IPS), University of Veterinary & Animal Sciences (UVAS), Lahore, Pakistan. Electronic address: [email protected]
  • 2 Bahawalpur College of Pharmacy, Bahawalpur Medical and Dental College, Bahawalpur, Pakistan
  • 3 College of Pharmacy, Al Ain University, Al Ain, United Arab Emirates
  • 4 Department of Pharmacy, The Islamia University of BahawalPur, Pakistan
  • 5 Department of Pharmacology & Toxicology, College of Pharmacy, University of Hail, Saudi Arabia
  • 6 Department of Clinical Laboratory Sciences, College of Applied Medical Science, Taif University, P. O. Box 11099, Taif, 21944, Saudi Arabia
  • 7 Department of Pharmacy, University 'G. D'Annunzio" of Chieti-Pescara, 66100, Chieti, Italy
  • 8 Department of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Mauritius
  • 9 Liquid Chromatography Mass Spectrometry (LCMS) Platform, Monash University, Jalan Lagoon Selatan, Bandar Sunway, 47500, Malaysia
  • 10 School of Pharmacy, Monash University, Jalan Lagoon Selatan, 47500, Bandar Sunway, Selangor Darul Ehsan, Malaysia
Food Chem Toxicol, 2021 Sep;155:112404.
PMID: 34246708 DOI: 10.1016/j.fct.2021.112404

Abstract

Capparis spinose L. also known as Caper is of great significance as a traditional medicinal food plant. The present work was targeted on the determination of chemical composition, pharmacological properties, and in-vitro toxicity of methanol and dichloromethane (DCM) extracts of different parts of C. spinosa. Chemical composition was established by determining total bioactive contents and via UHPLC-MS secondary metabolites profiling. For determination of biological activities, antioxidant capacity was determined through DPPH, ABTS, CUPRAC, FRAP, phosphomolybdenum, and metal chelating assays while enzyme inhibition against cholinesterase, tyrosinase, α-amylase and α-glucosidase were also tested. All the extracts were also tested for toxicity against two breast cell lines. The methanolic extracts were found to contain highest total phenolic and flavonoids which is correlated with their significant radical scavenging, cholinesterase, tyrosinase and glucosidase inhibition potential. Whereas DCM extracts showed significant activity for reducing power, phosphomolybdenum, metal chelation, tyrosinase, and α-amylase inhibition activities. The secondary metabolites profiling of both methanolic extracts exposed the presence of 21 different secondary metabolites belonging to glucosinolate, alkaloid, flavonoid, phenol, triterpene, and alkaloid derivatives. The present results tend to validate folklore uses of C. spinose and indicate this plant to be used as a potent source of designing novel bioactive compounds.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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