Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13967
Title: Neuritogenic and neuroprotective activities of fruit residues
Authors: Tadtong S.
Kanlayavattanakul M.
Lourith N.
Keywords: Achras sapota extract
flavonoid
hydrogen peroxide
Litchi chinensis extract
neuroprotective agent
phenol derivative
plant extract
Salacca edulis extract
Tamarindus indica extract
unclassified drug
animal cell
article
cell death
cell structure
cell survival
cholinergic nerve cell
concentration response
controlled study
drug activity
drug cytotoxicity
embryo
fruit
lychee
mouse
nerve fiber growth
neuritogenic activity
neuroprotection
nonhuman
oxidative stress
pericarp
phase contrast microscopy
Salacca edulis
sapodilla
seed husk
tamarind
Arecaceae
Caesalpinioideae
Litchi chinensis
Manilkara zapota
Salacca
Salacca edulis
Sapindaceae
Sapotaceae
Tamarindus indica
Animals
Arecaceae
Embryonal Carcinoma Stem Cells
Fruit
Litchi
Mice
Neurites
Neuroprotective Agents
Plant Extracts
Sapindaceae
Issue Date: 2013
Abstract: Neuritogenic and neuroprotective activities of litchi (Litchi chinensis Sonn., Sapindaceae) and salacca (Salacca edulis Reinw., Arecaceae) pericarp, and sapodilla (Achras sapota L., Sapotaceae) and tamarind Srichompu cultivar (Tamarindus indica L., Caesalpiniaceae) seed coat extracts were evaluated on cultured cholinergic P19-derived neurons. All the extracts, at a very low concentration (1 ng/mL of litchi and salacca pericarp extracts, 10 ng/mL of sapodilla and 100 ng/mL of tamarind seed coat extracts), enhanced the survival of cultured neurons (% viability more than 100%) by XTT reduction assay. The extracts were further evaluated for their neuritogenicity by observing cell morphology by phase-contrast microscopy and neuroprotective activity in serum deprivation and pre- and co-administration of hydrogen peroxide models. The phase-contrast micrographs displayed that all of the extracts possessed neurogenic activity by promoting the neurite outgrowth of the cultured neurons. Moreover, these extracts can protect neurons from oxidative stress-caused cell death in a serum deprivation model, and prevent and protect neuron cells from the toxicity of hydrogen peroxide. In this study we assured that the neuritogenic and neuroprotective activities of these extracts derived from the phenolic components and flavonoids contained in the extracts by acting as signaling molecules to enhance neuron survival and promote neurite outgrowth. These results suggest that all of the extracts are potentially sources of neuritogenic and neuroprotective components which might be used either as pharmaceutical products or dietary supplements for neurodegenerative disorder patients, for example, those suffering from Alzheimer's disease.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13967
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84887453077&doi=10.1177%2f1934578x1300801121&partnerID=40&md5=3b90a12da1262f28174c1836ac79ede4
ISSN: 1934578X
Appears in Collections:Scopus 1983-2021

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