Evaluation of Antioxidant and Enzyme Inhibition Properties of Croton hirtus L'Hér. Extracts Obtained with Different Solvents

Molecules. 2021 Mar 28;26(7):1902. doi: 10.3390/molecules26071902.

Abstract

Croton hirtus L'Hér methanol extract was studied by NMR and two different LC-DAD-MSn using electrospray (ESI) and atmospheric pressure chemical ionization (APCI) sources to obtain a quali-quantitative fingerprint. Forty different phytochemicals were identified, and twenty of them were quantified, whereas the main constituents were dihydro α ionol-O-[arabinosil(1-6) glucoside] (133 mg/g), dihydro β ionol-O-[arabinosil(1-6) glucoside] (80 mg/g), β-sitosterol (49 mg/g), and isorhamnetin-3-O-rutinoside (26 mg/g). C. hirtus was extracted with different solvents-namely, water, methanol, dichloromethane, and ethyl acetate-and the extracts were assayed using different in vitro tests. The methanolic extracts presented the highest 1,1-diphenyl-2-picrylhydrazyl (DPPH), 2,2'-azino-bis(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS), and ferric reducing antioxidant power (FRAP) values. All the tested extracts exhibited inhibitory effects on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), with a higher activity observed for dichloromethane (AChE: 5.03 and BChE: 16.41 mgGALAE/g), while the methanolic extract showed highest impact against tyrosinase (49.83 mgKAE/g). Taken together, these findings suggest C. hirtus as a novel source of bioactive phytochemicals with potential for commercial development.

Keywords: Croton hirtus; bioactive agents; enzyme; flavonoid glycosides.

MeSH terms

  • Acetates / chemistry
  • Acetylcholinesterase / chemistry
  • Acetylcholinesterase / metabolism
  • Antioxidants / chemistry*
  • Antioxidants / classification
  • Antioxidants / isolation & purification
  • Benzothiazoles / antagonists & inhibitors
  • Benzothiazoles / chemistry
  • Biphenyl Compounds / antagonists & inhibitors
  • Biphenyl Compounds / chemistry
  • Butyrylcholinesterase / chemistry
  • Butyrylcholinesterase / metabolism
  • Cholinesterase Inhibitors / chemistry*
  • Cholinesterase Inhibitors / isolation & purification
  • Croton / chemistry*
  • Croton / metabolism
  • Glucosides / chemistry*
  • Glucosides / classification
  • Glucosides / isolation & purification
  • Humans
  • Methanol / chemistry
  • Methylene Chloride / chemistry
  • Phytochemicals / chemistry*
  • Phytochemicals / classification
  • Phytochemicals / isolation & purification
  • Phytosterols / chemistry*
  • Phytosterols / classification
  • Phytosterols / isolation & purification
  • Picrates / antagonists & inhibitors
  • Picrates / chemistry
  • Plant Extracts / chemistry
  • Solvents / chemistry
  • Structure-Activity Relationship
  • Sulfonic Acids / antagonists & inhibitors
  • Sulfonic Acids / chemistry
  • Terpenes / chemistry*
  • Terpenes / classification
  • Terpenes / isolation & purification
  • Water / chemistry

Substances

  • Acetates
  • Antioxidants
  • Benzothiazoles
  • Biphenyl Compounds
  • Cholinesterase Inhibitors
  • Glucosides
  • Phytochemicals
  • Phytosterols
  • Picrates
  • Plant Extracts
  • Solvents
  • Sulfonic Acids
  • Terpenes
  • Water
  • 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid
  • Methylene Chloride
  • ethyl acetate
  • 1,1-diphenyl-2-picrylhydrazyl
  • Acetylcholinesterase
  • Butyrylcholinesterase
  • Methanol