Effect of tocotrienol enriched mixed fraction on prevention and treatment of early and established atherosclerosis

• Main Author: Nurul Aishah Muhammad
• Format: Thesis Book
• Language: English
• Published: Sungai Buloh, Selangor Universiti Teknologi MARA. Faculty of Medicine 2015
• Subjects: Tocotrienols > pharmacokinetics; Tocotrienols > administration and dosage; Atherosclerosis > prevention and control; Atherosclerosis > epidemiology
• Online Access: Click Here to View Status and Holdings.

 Effects of palm tocotrienol-enriched mixed fraction (TEMF) supplementation in the prevention and treatment of early and established atherosclerotic lesion remain unclear. The objectives of this study is to determine the prevention and treatment effect of TEMF towards (i) atherosclerotic lesion (ii) lipids profile (iii) inflammation (iv) endothelial activation and. (v) vascular proliferation and plaque stability in early and established experimentally-induced atherosclerotic. Forty New Zealand white rabbits were randomized into two major groups of prevention and treatment groups which were further divided into two subgroups of early and established atherosclerosis. In the prevention group, rabbits were given normal diet (ND) for 8 weeks (8W) followed by high cholesterol diet (HCD) for either 2 weeks (2W) or 8W to induce early and established atherosclerosis respectively while in the treatment groups, rabbits were fed with HCD for either 2W or 8W followed by ND for another 8W. Supplementation of either (i) TEMF (15mg/kg) or (ii) placebo was given continuously in the prevention groups, while in the treatment groups, TEMF supplementation was given following HCD for 2W and 8W for early and established atherosclerosis respectively. Blood samples at various intervals were analyzed for fasting serum lipids (FSL) and soluble C- reactive protein (sCRP). At the end of the study, the aortas were evaluated for atherosclerotic lesions using Sudan IV and immunohistochemistry staining for the biomarkers of atherosclerosis. In the prevention of established atherosclerosis, TEMF significantly reduced both total cholesterol, TC (227%) and low density lipoprotein, LDL-c (89.6%) levels at 8W compared to placebo. At 16W, triglycerides, TG levels were increased and high density lipoprotein, HDL-c levels were reduced but TC and LDL-c levels remain unchanged in TEMF groups compared to placebo. TEMF reduced LDL-c levels in the treatment of early atherosclerosis by 55.3%, but TC, TG and HDL-c levels remain unchanged. In the prevention of early atherosclerosis groups, there were reduced atherosclerotic lesions (68.6%) and trend of reduction in tissue biomarkers. In the prevention of established atherosclerosis, TEMF reduced atherosclerosis lesions (71.2%), aortic tissue expression of interleukin-6, IL-6 (71.6%), CRP (88.7%), E-selectin (68.4%), smooth muscle actin, SMA (55.9%) and matrix metalloproteinase-12, MMP-12 (85.1%) compared to placebo. In the treatment groups, TEMF showed no reduction in atherosclerotic lesions in both early and established groups but significant reduction in aortic tissue expression of CRP (88.2%), SMA (75.9%) and MMP-12 (82%) in the early atherosclerosis group. In conclusion, TEMF is beneficial in reducing atherosclerotic lesion despite neutral effects on lipids and tissue biomarkers in prevention of early atherosclerotic. In the prevention of established atherosclerosis TEMF is beneficial as an anti-atherosclerotic agent in terms of reducing atherosclerotic lesions, inflammation, endothelial, activation, smooth muscle proliferation and migration as well as plaque stability despite non-beneficial effects on lipids. TEMF leads to LDL-lowering effects and high therapeutic potential as an anti-inflammatory and anti-smooth muscle proliferative and migration agent in the treatment of early atherosclerosis. Treatment of TEMF in established atherosclerosis is not beneficial in terms of lipids, atherosclerotic lesion and tissue biomarkers. Thus, TEMF is effective in the prevention of both early and established atherosclerosis and has therapeutic potential in the treatment of early atherosclerosis