4.7 Article

Hippeastrum stapfianum (Kraenzl.) R.S.Oliveira & Dutilh (Amaryllidaceae) Ethanol Extract Activity on Acetylcholinesterase and PPAR-α/γ Receptors

Journal

PLANTS-BASEL
Volume 11, Issue 22, Pages -

Publisher

MDPI
DOI: 10.3390/plants11223179

Keywords

acetylcholinesterase; antioxidant activity; nuclear receptors; alkaloids; Cerrado

Categories

Funding

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior, Brasil (CAPES) [001]
  2. Fundacao de Apoio a Pesquisa do Distrito Federal (FAP-DF) [0193.000810/2015]
  3. CNPq
  4. FINEP

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The ethanol extract of Hippeastrum stapfianum leaves showed inhibitory effects on acetylcholinesterase enzyme, antioxidant activity, and selective activation of PPAR-alpha and PPAR-gamma. Major compounds identified were lycorine, 7-demethoxy-9-O-methylhostasine, and rutin, indicating its potential as a source of drugs for Alzheimer's disease.
Hippeastrum stapfianum (Kraenzl.) R.S.Oliveira & Dutilh (Amaryllidaceae) is an endemic plant species from the Brazilian savannah with biological and pharmacological potential. This study evaluated the effects of ethanol extract from H. stapfianum leaves on acetylcholinesterase enzyme activity and the action on nuclear receptors PPAR-alpha and PPAR-gamma. A gene reporter assay was performed to assess the PPAR agonist or antagonist activity with a non-toxic dose of H. stapfianum ethanol extract. The antioxidant capacity was investigated using DPPH center dot scavenging and fosfomolybdenium reduction assays. The identification of H. stapfianum's chemical composition was performed by gas chromatography-mass spectrometry (GC-MS) and HPLC. The ethanol extract of H. stapfianum activated PPAR-alpha and PPAR-gamma selectively, inhibited the acetylcholinesterase enzyme, and presented antioxidant activity in an in vitro assay. The major compounds identified were lycorine, 7-demethoxy-9-O-methylhostasine, and rutin. Therefore, H. stapfianum is a potential source of drugs for Alzheimer's disease due to its ability to activate PPAR receptors, acetylcholinesterase inhibition activity, and antioxidant attributes.

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