Department of Biochemistry, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Sime Darby Foods & Beverages Marketing Sdn Bhd, Petaling Jaya, Selangor, Malaysia.
Clinics (Sao Paulo). 2019 Mar 7;74:e688. doi: 10.6061/clinics/2019/e688.
This study aims to compare the differential gene expression resulting from tocotrienol-rich fraction and α-tocopherol supplementation in healthy older adults.
A total of 71 eligible subjects aged 50 to 55 years from Gombak and Kuala Lumpur, Malaysia, were divided into three groups and supplemented with placebo (n=23), α-tocopherol (n=24) or tocotrienol-rich fraction (n=24). Blood samples were collected at baseline and at 3 and 6 months of supplementation for microarray analysis.
The number of genes altered by α-tocopherol was higher after 6 months (1,410) than after 3 months (273) of supplementation. α-Tocopherol altered the expression of more genes in males (952) than in females (731). Similarly, tocotrienol-rich fraction modulated the expression of more genes after 6 months (1,084) than after 3 months (596) and affected more genes in males (899) than in females (781). α-Tocopherol supplementation modulated pathways involving the response to stress and stimuli, the immune response, the response to hypoxia and bacteria, the metabolism of toxins and xenobiotics, mitosis, and synaptic transmission as well as activated the mitogen-activated protein kinase and complement pathways after 6 months. However, tocotrienol-rich fraction supplementation affected pathways such as the signal transduction, apoptosis, nuclear factor kappa B kinase, cascade extracellular signal-regulated kinase-1 and extracellular signal-regulated kinase-2, immune response, response to drug, cell adhesion, multicellular organismal development and G protein signaling pathways.
Supplementation with either α-tocopherol or tocotrienol-rich fraction affected the immune and drug response and the cell adhesion and signal transduction pathways but modulated other pathways differently after 6 months of supplementation, with sex-specific responses.
本研究旨在比较富含生育三烯酚和α-生育酚对健康老年人的差异基因表达。
从马来西亚瓜拉冷岳和吉隆坡招募了 71 名年龄在 50 至 55 岁的符合条件的受试者,将他们分为三组,分别补充安慰剂(n=23)、α-生育酚(n=24)或富含生育三烯酚的部分(n=24)。在补充的第 3 和 6 个月时收集血液样本进行微阵列分析。
在补充 6 个月后(1410 个),α-生育酚改变的基因数量高于 3 个月(273 个)。α-生育酚在男性(952 个)中改变的基因多于女性(731 个)。同样,富含生育三烯酚的部分在 6 个月后(1084 个)改变的基因多于 3 个月(596 个),并且在男性(899 个)中影响的基因多于女性(781 个)。α-生育酚补充剂在 6 个月后调节了涉及应激和刺激反应、免疫反应、缺氧和细菌反应、毒素和外源性化合物代谢、有丝分裂和突触传递的途径,并且激活了丝裂原激活蛋白激酶和补体途径。然而,富含生育三烯酚的部分补充剂影响了信号转导、细胞凋亡、核因子 kappa B 激酶、细胞外信号调节激酶-1 和细胞外信号调节激酶-2、免疫反应、药物反应、细胞黏附、多细胞生物发育和 G 蛋白信号转导途径等途径。
补充α-生育酚或富含生育三烯酚的部分均影响免疫和药物反应以及细胞黏附和信号转导途径,但在 6 个月的补充后,以性别特异性的方式调节了其他途径。