Effects of oil palm tocotrienol rich fraction on the viability and morphology of astrocytes injured with glutamate
Tocotrienol-rich fraction (TRF) is an extract of palm oil that consists of 25% α-tocopherol and 75% tocotrienols. TRF was shown to possess antioxidant, anti-inflammatory, anticancer, neuroprotective and cholesterol-lowering activities. Glutamate is the major mediator of excitatory signals in the m...
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English English |
| Published: |
Elsevier BV
2017
|
| Subjects: | |
| Online Access: | http://irep.iium.edu.my/62822/ http://irep.iium.edu.my/62822/ http://irep.iium.edu.my/62822/ http://irep.iium.edu.my/62822/1/62822_Effects%20of%20oil%20palm%20tocotrienol%20rich%20fraction_complete.pdf http://irep.iium.edu.my/62822/2/62822_Effects%20of%20oil%20palm%20tocotrienol%20rich%20fraction_scopus.pdf |
| Summary: | Tocotrienol-rich fraction (TRF) is an extract of palm oil that consists of 25% α-tocopherol and 75% tocotrienols.
TRF was shown to possess antioxidant, anti-inflammatory, anticancer, neuroprotective and cholesterol-lowering
activities. Glutamate is the major mediator of excitatory signals in the mammalian central nervous system.
Extreme amounts of glutamate in the extracellular spaces can lead to numerous neurodegenerative diseases.
Hence, the efficacy of oil palm TRF and α-tocopherol in protecting astrocytes against glutamate-induced cell
death was studied. Specifically, the effectiveness of pre- or post-treatment of TRF and α-tocopherol upon glutamate
excitotoxicity was determined by evaluating cell viability and morphology of astrocytes. Cell viability
was measured using MTT assay while cell morphology was monitored under fluorescent microscope using the
acridine orange/propidium iodide (AO/PI) assay. Exposure to 230 mM glutamate significantly reduced cell
viability to 50% in both the pre- and post-treatment studies; however, pre- and post-treatment with TRF and α-
tocopherol attenuated the cytotoxic effect of glutamate. Compared to glutamate-injured astrocytes, pre-treatment
with 100, 200 and 300 ng/ml TRF significantly improved cell viability following glutamate injury to
86.6%, 86.7% and 93.9%, respectively (p < 0.05). On the contrary, high concentrations of α-tocopherol promote
cell death. This study shows that TRF not only provide a better protection against glutamate toxicity (pretreatment),
but was also able to reverse the lipid peroxidation resulting from glutamate insults (post-treatment).
The present results demonstrate that TRF, but not α-tocopherol, protected the astrocytes against glutamateinduced
cell death, indicating its neuro-protective potential. |
|---|