Chemical composition and biological activities of Helicteres vegae and Heliopsis sinaloensis

Pharm Biol. 2017 Dec;55(1):1473-1482. doi: 10.1080/13880209.2017.1306712.

Abstract

Context: Helicteres vegae Cristóbal (Sterculiaceae) (Hv) and Heliopsis sinaloensis B.L. Turner (Asteraceae) (Hs) are endangered and poorly studied plant species; related plants have been used against chronic-degenerative and infectious diseases. Therefore, Hv and Hs could be sources of bioactive compounds against these illnesses.

Objective: To determine the chemical composition and biological activities (antioxidant, antimutagenic and antimicrobial) of Hv and Hs leaves (L) and stems (S).

Materials and methods: Methanol extracts (ME) of each plant/tissue were evaluated for their phytochemicals; phenolics (HPLC-DAD-ESI-MS); antioxidant activity (AA) (0.125-4 mg/mL) (DPPH, ABTS, ORAC and β-carotene discoloration); antimutagenicity (0.5 and 1 mg/plate) (Ames assay, tester strain Salmonella enterica serovar Typhimurium YG1024, 1-nitropyrene as mutagen); activity against human pathogens (1 mg/mL); and toxicity (0.01-2 mg/mL) (Artemia salina assay).

Results: All ME showed flavonoids and triterpenes/steroids. The ME-SHv had the highest content of total phenolics (TP) (2245.82 ± 21.45 mg GAE/100 g d.w.) and condensed tannins (603.71 ± 1.115 mg CE/100 g d.w.). The compounds identified were flavonoids (kaempferol 7-O-coumaroylhexoside, and two kaempferol 7-O-rhamnosylhexosides) and phenolics [rosmarinic acid, and 3'-O-(8″-Z-caffeoyl) rosmarinic acid]. The ME-LHs showed the highest content of flavonoids (357.88 mg RE/g d.w.) and phenolic acids (238.58 mg CAE/g d.w.) by HPLC. The ME-SHv showed the highest AA. All ME were strong antimutagens (63.3-85.7%). Only the Hs extracts were toxic (ME-LHs, LC50 = 94.9 ± 1.7 μg/mL; ME-SHs, LC50 = 89.03 ± 4.42 μg/mL).

Discussion and conclusions: Both Hv and Hs are potential sources of preventive and therapeutic agents against chronic-degenerative diseases.

Keywords: Phenolics; antimicrobial; antimutagenic; antioxidant; electrospray ionization; flavonoids; liquid chromatography; mass spectrometry; toxicity.

MeSH terms

  • Animals
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / isolation & purification
  • Anti-Infective Agents / pharmacology*
  • Anti-Infective Agents / toxicity
  • Antimutagenic Agents / chemistry
  • Antimutagenic Agents / isolation & purification
  • Antimutagenic Agents / pharmacology*
  • Antimutagenic Agents / toxicity
  • Antioxidants / chemistry
  • Antioxidants / isolation & purification
  • Antioxidants / pharmacology*
  • Antioxidants / toxicity
  • Artemia / drug effects
  • Asteraceae / chemistry*
  • Bacteria / drug effects
  • Bacteria / growth & development
  • Benzothiazoles / chemistry
  • Biphenyl Compounds / chemistry
  • Chromatography, High Pressure Liquid
  • Giardia lamblia / drug effects
  • Giardia lamblia / growth & development
  • Malvaceae / chemistry*
  • Methanol / chemistry
  • Microbial Sensitivity Tests
  • Mutagenicity Tests
  • Oxygen Radical Absorbance Capacity
  • Parasitic Sensitivity Tests
  • Phytotherapy
  • Picrates / chemistry
  • Plant Extracts / chemistry
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Plant Extracts / toxicity
  • Plant Leaves / chemistry
  • Plant Stems / chemistry
  • Plants, Medicinal
  • Salmonella typhimurium / drug effects
  • Salmonella typhimurium / genetics
  • Solvents / chemistry
  • Spectrometry, Mass, Electrospray Ionization
  • Sulfonic Acids / chemistry
  • beta Carotene / chemistry

Substances

  • Anti-Infective Agents
  • Antimutagenic Agents
  • Antioxidants
  • Benzothiazoles
  • Biphenyl Compounds
  • Picrates
  • Plant Extracts
  • Solvents
  • Sulfonic Acids
  • beta Carotene
  • 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid
  • 1,1-diphenyl-2-picrylhydrazyl
  • Methanol

Grants and funding

This work was supported by the CONACYT [grant number CB201 0-156645-Z] Mexico and PROFAPI (Autonomous University of Sinaloa) [grant number PROFAPI2014-062].