Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia

Introduction: The potential immunoregulatory effects of tocotrienols, the less studied form of vitamin E, had not been determined for microglia until our last publication showcased primary evidence of palm tocotrienols limiting microglia activation, explicitly by inhibiting nitric oxide (NO) product...

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Main Authors: Tan, Shi Wei, Abdullah, Maha, Israf Ali, Daud Ahmad, Vidyadaran, Sharmili
Format: Article
Language:English
Published: Faculty of Medicine and Health Sciences, Universiti Putra Malaysia 2016
Online Access:http://psasir.upm.edu.my/id/eprint/50415/1/FKUSK1_MJMHS_V2_NO2_1.pdf
http://psasir.upm.edu.my/id/eprint/50415/
http://www.medic.upm.edu.my/dokumen/FKUSK1_MJMHS_V2_NO2_1.pdf
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Institution: Universiti Putra Malaysia
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spelling my.upm.eprints.504152017-02-28T07:27:20Z http://psasir.upm.edu.my/id/eprint/50415/ Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia Tan, Shi Wei Abdullah, Maha Israf Ali, Daud Ahmad Vidyadaran, Sharmili Introduction: The potential immunoregulatory effects of tocotrienols, the less studied form of vitamin E, had not been determined for microglia until our last publication showcased primary evidence of palm tocotrienols limiting microglia activation, explicitly by inhibiting nitric oxide (NO) production. Here we further explored the nitrite scavenging activity of the two most potent NO-reducing tocotrienol isoforms - δ-tocotrienol and Tocomin®50% (contains a spectrum of tocotrienols and α-tocopherol) based on their inhibitory effects on NO production and also their effects on CD40 (a microglial co-stimulator molecule) expression of BV2 microglia. Methods: BV2 cells were treated with two different doses of tocotrienols (δ-tocotrienol: 3.96 μg/mL and 19.80 μg/mL; Tocomin®50%:47.50 μg/mL and 237.50 μg/mL) followed by stimulation with 1μg/mL of lipopolysaccharide (LPS). A chemical scavenging assay was conducted to study the nitrite scavenging activity of δ-tocotrienol. Together with Tocomin®50%, we also determined their effects on CD40 expression of BV2 microglia via flow cytometry. Results: We demonstrate that the inhibitory effect of tocotrienols on NO production by microglia is not attributed to their nitrite scavenging activity. Additionally, tocotrienols also reduced the expression of the microglial co-stimulator molecule, CD40. Conclusions: Our data aids the further characterisation of the actions of tocotrienols on microglia, offering insight into the potential modulatory properties of palm tocotrienols on microglial inflammatory responses within the central nervous system (CNS). Faculty of Medicine and Health Sciences, Universiti Putra Malaysia 2016 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/50415/1/FKUSK1_MJMHS_V2_NO2_1.pdf Tan, Shi Wei and Abdullah, Maha and Israf Ali, Daud Ahmad and Vidyadaran, Sharmili (2016) Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia. Malaysian Journal of Medicine and Health Sciences, 12 (2). pp. 1-7. ISSN 1675-8544 http://www.medic.upm.edu.my/dokumen/FKUSK1_MJMHS_V2_NO2_1.pdf
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Introduction: The potential immunoregulatory effects of tocotrienols, the less studied form of vitamin E, had not been determined for microglia until our last publication showcased primary evidence of palm tocotrienols limiting microglia activation, explicitly by inhibiting nitric oxide (NO) production. Here we further explored the nitrite scavenging activity of the two most potent NO-reducing tocotrienol isoforms - δ-tocotrienol and Tocomin®50% (contains a spectrum of tocotrienols and α-tocopherol) based on their inhibitory effects on NO production and also their effects on CD40 (a microglial co-stimulator molecule) expression of BV2 microglia. Methods: BV2 cells were treated with two different doses of tocotrienols (δ-tocotrienol: 3.96 μg/mL and 19.80 μg/mL; Tocomin®50%:47.50 μg/mL and 237.50 μg/mL) followed by stimulation with 1μg/mL of lipopolysaccharide (LPS). A chemical scavenging assay was conducted to study the nitrite scavenging activity of δ-tocotrienol. Together with Tocomin®50%, we also determined their effects on CD40 expression of BV2 microglia via flow cytometry. Results: We demonstrate that the inhibitory effect of tocotrienols on NO production by microglia is not attributed to their nitrite scavenging activity. Additionally, tocotrienols also reduced the expression of the microglial co-stimulator molecule, CD40. Conclusions: Our data aids the further characterisation of the actions of tocotrienols on microglia, offering insight into the potential modulatory properties of palm tocotrienols on microglial inflammatory responses within the central nervous system (CNS).
format Article
author Tan, Shi Wei
Abdullah, Maha
Israf Ali, Daud Ahmad
Vidyadaran, Sharmili
spellingShingle Tan, Shi Wei
Abdullah, Maha
Israf Ali, Daud Ahmad
Vidyadaran, Sharmili
Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
author_facet Tan, Shi Wei
Abdullah, Maha
Israf Ali, Daud Ahmad
Vidyadaran, Sharmili
author_sort Tan, Shi Wei
title Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
title_short Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
title_full Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
title_fullStr Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
title_full_unstemmed Palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
title_sort palm tocotrienols reduce lipopolysaccharide-stimulated inflammatory responses of microglia
publisher Faculty of Medicine and Health Sciences, Universiti Putra Malaysia
publishDate 2016
url http://psasir.upm.edu.my/id/eprint/50415/1/FKUSK1_MJMHS_V2_NO2_1.pdf
http://psasir.upm.edu.my/id/eprint/50415/
http://www.medic.upm.edu.my/dokumen/FKUSK1_MJMHS_V2_NO2_1.pdf
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