The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin
Endometriosis is a gynaecological disease in which endometrial tissues are found outside the uterus. Due to a lack of understanding of its pathophysiology, the global prevalence rate of endometriosis is unknown. Recent findings suggests that inflammation and oxidative stress are involved in this dis...
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2022
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Sheikh Abdul Kadir, Siti Hamimah |
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RG Gynecology and obstetrics Antibacterial agents Individual drugs and other agents Md Amin, Nur Amira The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin |
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Endometriosis is a gynaecological disease in which endometrial tissues are found outside the uterus. Due to a lack of understanding of its pathophysiology, the global prevalence rate of endometriosis is unknown. Recent findings suggests that inflammation and oxidative stress are involved in this disease pathophysiology and progression. Tocotrienols, a form of vitamin E derived from palm oil, have long been known for their potent antioxidant and anti-inflammatory properties in other inflammatory diseases; however, their effect on endometriosis is not well reported. Therefore, this study aimed to investigate the effect of tocotrienol-rich fraction (TRF) supplementation on pro-inflammatory and antioxidant markers of endometriosis. In here, human primary endometrial stromal fibroblast (eSF) cells isolated from the endometrium of patients with (PEC) and without endometriosis (NEC) were cultured and subjected for cell characterisation by immunocytochemistry staining (vimentin and platelet-derived growth factor receptor beta (PDGFRβ)). NEC and PEC cells were then divided into three groups: control, TRF in long-chain triglyceride (LCT) carrier (TRF) and new enhanced formulation of TRF (ETRF) in medium-chain triglyceride (MCT) (ETRF). After that the cells were subjected to cell viability assay, quantitative real-time polymerase chain reaction (RT-qPCR) for cyclooxygenase-2 (COX-2), macrophage migration inhibitory factor (MIF), interleukin-6 (IL-6), interleukin-8 (IL-8), glutathione peroxidase 1 (GPX1) superoxide dismutase 1 (SOD1), and superoxide dismutase 2 (SOD2) gene expression and Luminex assay for MIF, IL-6 and IL-8 protein expression. In treated NEC cells, a dose-dependent increase (more than 10%) in cell viability was observed in TRF and ETRF when compared to control. However, in PEC cells treated with more than 25μg/ml of TRF and ETRF, a significant decreased by 10% in cell viability were observed. Hence, for following study, PEC and NEC cells were treated for 24 hours with 25μg/ml of TRF and ETRF, and their anti-inflammatory and antioxidant properties were investigated and analysed (p < 0.05). The results showed that treatment with TRF and ETRF significantly downregulate pro-inflammatory markers gene expression in NEC cells; COX-2 (0.80 ± 0.11; 0.79 ± 0.04), MIF (0.82 ± 0.07; 0.86 ± 0.12), and IL-6 (0.80 ± 0.05; 0.87 ± 0.07) when compared to control. Whereas, in PEC cells, treatment with TRF and ETRF significantly downregulate pro-inflammatory markers gene expression of COX-2 (0.82 ± 0.05; 0.69 ± 0.07), MIF (0.42 ± 0.05; 0.49 ± 0.07), and IL-8 (0.78 ± 0.08; 0.69 ± 0.06). For antioxidant genes expression, TRF and ETRF treatment significantly upregulate the expression of GPX1 (1.77 ± 0.16; 1.69 ± 0.13) in NEC cells but significantly upregulate the expression of GPX1 (1.78 ± 0.11; 1.69 ± 0.08), SOD1 (1.45 ± 0.15; 1.50 ± 0.13) and SOD2 (2.15 ± 0.12; 1.77 ± 0.09) in PEC cells when compared to control. For IL-6, no significance differences were seen at protein level for treated NEC and PEC. However, significance increases in IL-8 protein level were observed for treated NEC and PEC. In accordance, TRF and ETRF treatment at a concentration of 25μg/ml had a significant favourable effect on endometriosis-related pro-inflammatory and antioxidant gene expression. In conclusion, our findings provided a new insight into the effects of TRF and ETRF treatment on human primary eSF cells isolated from NEC and PEC groups and demonstrates their potential as potent anti-inflammatory and antioxidant agent that can reduce endometriosis-associated inflammation and oxidative stress. |
| format |
Thesis |
| qualification_level |
Master's degree |
| author |
Md Amin, Nur Amira |
| author_facet |
Md Amin, Nur Amira |
| author_sort |
Md Amin, Nur Amira |
| title |
The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin |
| title_short |
The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin |
| title_full |
The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin |
| title_fullStr |
The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin |
| title_full_unstemmed |
The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin |
| title_sort |
effects of palm oil tocotrienol-rich fraction (trf) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / nur amira md amin |
| granting_institution |
Universiti Teknologi MARA (UiTM) |
| granting_department |
Faculty of Medicine |
| publishDate |
2022 |
| url |
https://ir.uitm.edu.my/id/eprint/77970/1/77970.pdf |
| _version_ |
1783736189804609536 |
| spelling |
my-uitm-ir.779702023-05-29T07:41:53Z The effects of palm oil tocotrienol-rich fraction (TRF) on endometriosis-related pro-inflammatory and oxidative stress markers of human endometrial stromal fibroblast cells / Nur Amira Md Amin 2022 Md Amin, Nur Amira RG Gynecology and obstetrics Antibacterial agents Individual drugs and other agents Endometriosis is a gynaecological disease in which endometrial tissues are found outside the uterus. Due to a lack of understanding of its pathophysiology, the global prevalence rate of endometriosis is unknown. Recent findings suggests that inflammation and oxidative stress are involved in this disease pathophysiology and progression. Tocotrienols, a form of vitamin E derived from palm oil, have long been known for their potent antioxidant and anti-inflammatory properties in other inflammatory diseases; however, their effect on endometriosis is not well reported. Therefore, this study aimed to investigate the effect of tocotrienol-rich fraction (TRF) supplementation on pro-inflammatory and antioxidant markers of endometriosis. In here, human primary endometrial stromal fibroblast (eSF) cells isolated from the endometrium of patients with (PEC) and without endometriosis (NEC) were cultured and subjected for cell characterisation by immunocytochemistry staining (vimentin and platelet-derived growth factor receptor beta (PDGFRβ)). NEC and PEC cells were then divided into three groups: control, TRF in long-chain triglyceride (LCT) carrier (TRF) and new enhanced formulation of TRF (ETRF) in medium-chain triglyceride (MCT) (ETRF). After that the cells were subjected to cell viability assay, quantitative real-time polymerase chain reaction (RT-qPCR) for cyclooxygenase-2 (COX-2), macrophage migration inhibitory factor (MIF), interleukin-6 (IL-6), interleukin-8 (IL-8), glutathione peroxidase 1 (GPX1) superoxide dismutase 1 (SOD1), and superoxide dismutase 2 (SOD2) gene expression and Luminex assay for MIF, IL-6 and IL-8 protein expression. In treated NEC cells, a dose-dependent increase (more than 10%) in cell viability was observed in TRF and ETRF when compared to control. However, in PEC cells treated with more than 25μg/ml of TRF and ETRF, a significant decreased by 10% in cell viability were observed. Hence, for following study, PEC and NEC cells were treated for 24 hours with 25μg/ml of TRF and ETRF, and their anti-inflammatory and antioxidant properties were investigated and analysed (p < 0.05). The results showed that treatment with TRF and ETRF significantly downregulate pro-inflammatory markers gene expression in NEC cells; COX-2 (0.80 ± 0.11; 0.79 ± 0.04), MIF (0.82 ± 0.07; 0.86 ± 0.12), and IL-6 (0.80 ± 0.05; 0.87 ± 0.07) when compared to control. Whereas, in PEC cells, treatment with TRF and ETRF significantly downregulate pro-inflammatory markers gene expression of COX-2 (0.82 ± 0.05; 0.69 ± 0.07), MIF (0.42 ± 0.05; 0.49 ± 0.07), and IL-8 (0.78 ± 0.08; 0.69 ± 0.06). For antioxidant genes expression, TRF and ETRF treatment significantly upregulate the expression of GPX1 (1.77 ± 0.16; 1.69 ± 0.13) in NEC cells but significantly upregulate the expression of GPX1 (1.78 ± 0.11; 1.69 ± 0.08), SOD1 (1.45 ± 0.15; 1.50 ± 0.13) and SOD2 (2.15 ± 0.12; 1.77 ± 0.09) in PEC cells when compared to control. For IL-6, no significance differences were seen at protein level for treated NEC and PEC. However, significance increases in IL-8 protein level were observed for treated NEC and PEC. In accordance, TRF and ETRF treatment at a concentration of 25μg/ml had a significant favourable effect on endometriosis-related pro-inflammatory and antioxidant gene expression. In conclusion, our findings provided a new insight into the effects of TRF and ETRF treatment on human primary eSF cells isolated from NEC and PEC groups and demonstrates their potential as potent anti-inflammatory and antioxidant agent that can reduce endometriosis-associated inflammation and oxidative stress. 2022 Thesis https://ir.uitm.edu.my/id/eprint/77970/ https://ir.uitm.edu.my/id/eprint/77970/1/77970.pdf text en public masters Universiti Teknologi MARA (UiTM) Faculty of Medicine Sheikh Abdul Kadir, Siti Hamimah |