Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells
The stem bark extracts of Knema laurina inhibited the hydrogen peroxide (H2O2)-and aggregated amyloid β-peptide 1-42 length (Aβ1-42)-induced cell death in differentiated SH-SY5Y cells. Exposure of 250 μMH2O2 or 20 μM Aβ1-42 to the cells for 24 h reduced 50% of cell viability. Pretreatment of cells w...
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2015
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2-s2.0-84938959981 Ismail N.; Akhtar M.N.; Ismail M.; Zareen S.; Shah S.A.A.; Lajis N.H.; Tajuddin S.N. Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells 2015 Natural Product Research 29 16 10.1080/14786419.2014.985676 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84938959981&doi=10.1080%2f14786419.2014.985676&partnerID=40&md5=5f6250603f37b1e99488f7cf1966a24e The stem bark extracts of Knema laurina inhibited the hydrogen peroxide (H2O2)-and aggregated amyloid β-peptide 1-42 length (Aβ1-42)-induced cell death in differentiated SH-SY5Y cells. Exposure of 250 μMH2O2 or 20 μM Aβ1-42 to the cells for 24 h reduced 50% of cell viability. Pretreatment of cells with ethyl acetate extract (EAE) or n-butanol extract (BE) at 300 μg/mL and then exposure to H2O2 protected the cells against the neurotoxic effects of H2O2. Besides, methanolic extract (ME) at 1 and 10 μg/mL exerted neuroprotective effect on Aβ1-42-induced toxicity to the cells. These results showed that EAE, BE and ME exhibited neuroprotective activities against H2O2-and Aβ1-42-induced cell death. Flavonoids (3-6) and β-sitosterol glucoside (8) were isolated from the EAE. Compound 1 was isolated from hexane extract, and compounds 2 and 7 were isolated from dichloromethane extract. All these observations provide the possible evidence for contribution in the neuroprotective effects. © 2014 Taylor and Francis. Taylor and Francis Ltd. 14786419 English Article |
author |
Ismail N.; Akhtar M.N.; Ismail M.; Zareen S.; Shah S.A.A.; Lajis N.H.; Tajuddin S.N. |
spellingShingle |
Ismail N.; Akhtar M.N.; Ismail M.; Zareen S.; Shah S.A.A.; Lajis N.H.; Tajuddin S.N. Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
author_facet |
Ismail N.; Akhtar M.N.; Ismail M.; Zareen S.; Shah S.A.A.; Lajis N.H.; Tajuddin S.N. |
author_sort |
Ismail N.; Akhtar M.N.; Ismail M.; Zareen S.; Shah S.A.A.; Lajis N.H.; Tajuddin S.N. |
title |
Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
title_short |
Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
title_full |
Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
title_fullStr |
Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
title_full_unstemmed |
Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
title_sort |
Neuroprotective effect from stem bark extracts of Knema laurina against H2O2-and Aβ1-42-induced cell death in human SH-SY5Y cells |
publishDate |
2015 |
container_title |
Natural Product Research |
container_volume |
29 |
container_issue |
16 |
doi_str_mv |
10.1080/14786419.2014.985676 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84938959981&doi=10.1080%2f14786419.2014.985676&partnerID=40&md5=5f6250603f37b1e99488f7cf1966a24e |
description |
The stem bark extracts of Knema laurina inhibited the hydrogen peroxide (H2O2)-and aggregated amyloid β-peptide 1-42 length (Aβ1-42)-induced cell death in differentiated SH-SY5Y cells. Exposure of 250 μMH2O2 or 20 μM Aβ1-42 to the cells for 24 h reduced 50% of cell viability. Pretreatment of cells with ethyl acetate extract (EAE) or n-butanol extract (BE) at 300 μg/mL and then exposure to H2O2 protected the cells against the neurotoxic effects of H2O2. Besides, methanolic extract (ME) at 1 and 10 μg/mL exerted neuroprotective effect on Aβ1-42-induced toxicity to the cells. These results showed that EAE, BE and ME exhibited neuroprotective activities against H2O2-and Aβ1-42-induced cell death. Flavonoids (3-6) and β-sitosterol glucoside (8) were isolated from the EAE. Compound 1 was isolated from hexane extract, and compounds 2 and 7 were isolated from dichloromethane extract. All these observations provide the possible evidence for contribution in the neuroprotective effects. © 2014 Taylor and Francis. |
publisher |
Taylor and Francis Ltd. |
issn |
14786419 |
language |
English |
format |
Article |
accesstype |
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record_format |
scopus |
collection |
Scopus |
_version_ |
1820775476476510208 |