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HPLC-DAD fingerprinting analysis, antioxidant activities of Tithonia diversifolia (Hemsl.) A. Gray leaves and its inhibition of key enzymes linked to Alzheimer’s disease

[Display omitted] •Current study supports antioxidant activity of Tithonia diversifolia leaves.•Current study also supports anti cholinesterase activity of Tithonia diversifolia leaves.•Current investigation adequately characterized the phenolic compounds of Tithonia diversifolia leaves. Tithonia di...

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Published in:Toxicology reports 2018-01, Vol.5, p.585-592
Main Authors: Ojo, Oluwafemi Adeleke, Ojo, Adebola Busola, Ajiboye, Basiru Olaitan, Olaiya, Oluranti, Okesola, Mary Abiola, Boligon, Aline Augusti, de Campos, Marli Matiko Anraku, Oyinloye, Babatunji Emmanuel, Kappo, Abidemi Paul
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Language:English
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Summary:[Display omitted] •Current study supports antioxidant activity of Tithonia diversifolia leaves.•Current study also supports anti cholinesterase activity of Tithonia diversifolia leaves.•Current investigation adequately characterized the phenolic compounds of Tithonia diversifolia leaves. Tithonia diversifolia (Hemsl.) A. Gray leaves have long been used to manage neurodegenerative diseases without scientific basis. This study characterized the phenolic constituents, evaluated the antioxidant properties of phenolic extracts from T. diversifolia leaves used as traditional medicine in Africa and its inhibition of key enzymes linked to Alzheimer’s disease. The extract was rich in phenolic acids (gallic acid, chlorogenic acid, caffeic acid and p-coumaric acid) and flavonoids (apigenin) and had 1,1-diphenyl-2-picryl-hydrazil radical scavenging abilities (IC50 = 41.05 μg. mL−1), 2,2-Azino-bis3-ethylbenthiazoline-6sulphonic acid radical scavenging ability (IC50 = 33.51 μg. mL−1), iron chelation (IC50 = 38.50 μg. mL−1), reducing power (Fe3+- Fe2+) (7.34 AAEmg/100 g), inhibited acetylcholinesterase (IC50 = 39.27 μg mL−1) and butyrylcholinesterase (IC50 = 35.01 μg mL−1) activities. These results reveal the leaf as a rich source of phenolic compounds with antioxidant and cholinesterase inhibitory activity.
ISSN:2214-7500
2214-7500
DOI:10.1016/j.toxrep.2018.05.003