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Assessing Whole-Body Lipid-Handling Capacity in Mice
Published on: November 24, 2020
Tocotrienols Attenuate White Adipose Tissue Accumulation and Improve Serum Cholesterol Concentration in High-Fat
Yugo Kato1, Yoshinori Aoki2, Chikako Kiyose3
1Molecular Cell Biology Laboratory, Department of Functional Control Systems, Graduate School of Engineering and Science, Shibaura Institute of Technology, Fukasaku 307, Minuma-ku, Saitama 337-8570, Japan.
Abstract:
Tocotrienols (T3s), which are vitamin E homologs, have not only antioxidant function but also inhibitory effects on body weight gain and hepatic lipid droplet accumulation. However, the mechanisms of the anti-obesity effects of T3s are not yet understood. In this study, C57BL/6 mice were fed a high-fat diet in the presence or absence of T3s. Treatment with T3s inhibited white adipose tissue accumulation and elevation of serum cholesterol concentrations. Additionally, to clarify the relationship between obesity-induced cognitive dysfunction and the neuroprotective effect of T3s, cognitive function, brain oxidation, and protein expression levels of brain-derived neurotrophic factor (BDNF), which is strongly involved in neuronal growth and differentiation, were measured. Although mice behaviors were improved by oral T3 intake, there were no significant differences in brain oxidation levels and BDNF expression. These results suggest that T3s attenuate obesity via inhibition of body fat and serum cholesterol increase.
Insights
Tocotrienols (T3s), a form of vitamin E, can help reduce body fat and lower cholesterol levels. This study suggests T3s may be a potential therapeutic for managing obesity by inhibiting fat accumulation.
Area of Science:
- Biochemistry
- Nutrition Science
- Metabolic Research
Background:
- Tocotrienols (T3s), vitamin E homologs, possess antioxidant properties and show potential in mitigating obesity.
- The precise mechanisms underlying the anti-obesity effects of T3s remain largely unexplored.
- Obesity is often associated with cognitive dysfunction, prompting investigation into T3s' neuroprotective roles.
Purpose of the Study:
- To investigate the anti-obesity mechanisms of Tocotrienols (T3s).
- To evaluate the impact of T3s on body weight, adipose tissue, and serum lipid profiles.
- To explore the potential neuroprotective effects of T3s in the context of obesity-induced cognitive changes.
Main Methods:
- C57BL/6 mice were administered a high-fat diet with or without T3 supplementation.
- Measurements included white adipose tissue accumulation, serum cholesterol levels, cognitive function tests, brain oxidation markers, and BDNF expression.
- Behavioral assessments were conducted to evaluate cognitive performance.
Main Results:
- T3 treatment significantly inhibited white adipose tissue accumulation in mice.
- Oral T3 intake led to reduced serum cholesterol concentrations.
- While behavioral improvements were observed, no significant differences in brain oxidation or BDNF expression were found.
Conclusions:
- Tocotrienols (T3s) demonstrate efficacy in attenuating obesity by reducing body fat accumulation.
- T3s effectively lower elevated serum cholesterol levels associated with high-fat diets.
- The study suggests T3s' anti-obesity effects are primarily mediated through metabolic pathways rather than direct neuroprotective actions on BDNF or oxidation.
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