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Food Chem Toxicol ; 145: 111703, 2020 Nov.
Article in English | MEDLINE | ID: mdl-32858133

ABSTRACT

Hippeastrum psittacinum, Amaryllidaceae, is used in traditional medicine as a purgative, aphrodisiac, and anticough remedy. The ethanol extract (EE) and alkaloid-rich fractions (ARF) from H. psittacinum bulbs were evaluated for their acetylcholinesterase (AChE) inhibition. The EE cytotoxic and anti-inflammatory effects in RAW 264.7 cells, and the neuroprotective and genotoxic activities in SH-SY5Y cells, were also estimated. Fifteen alkaloids were identified in the EE by gas chromatography-mass spectrometry. ARFs were less active for AChE inhibition than EE. The viability of both cell lines was higher than 70% with EE concentrations below 25 µg/mL. The EE decreased nitrite release in RAW cells stimulated with lipopolysaccharide, showing values of 83, 67, and 53% at 6.25, 12.5, and 25 µg/mL, respectively. Furthermore, the EE partially protected SH-SY5Y cells from hydrogen peroxide-mediated deleterious effects by approximately 50% at the same concentrations. The micronucleus assays showed that the extract caused chromosomal missegregation at concentrations above 12.5 µg/mL. The in silico analyses showed that some alkaloids presented properties of permeation of the blood-brain barrier and the intestine. Our findings present new evidence of the potential of H. psittacinum potential as an AChE inhibitor, as well as an anti-inflammatory and neuroprotective agent.


Subject(s)
Amaryllidaceae/chemistry , Anti-Inflammatory Agents/pharmacology , Cholinesterase Inhibitors/pharmacology , Neuroprotective Agents/pharmacology , Acetylcholinesterase/chemistry , Alkaloids/chemistry , Alkaloids/pharmacology , Amaryllidaceae Alkaloids/chemistry , Amaryllidaceae Alkaloids/pharmacology , Animals , Anti-Inflammatory Agents/chemistry , Cell Line, Tumor , Cholinesterase Inhibitors/chemistry , Computer Simulation , Flowers/chemistry , Gas Chromatography-Mass Spectrometry , Humans , Macrophages/drug effects , Macrophages/immunology , Mice , Molecular Docking Simulation , Neuroprotective Agents/chemistry , RAW 264.7 Cells
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