Open Access. Powered by Scholars. Published by Universities.®
![Digital Commons Network](http://assets.bepress.com/20200205/img/dcn/DCsunburst.png)
Molecular, Genetic, and Biochemical Nutrition Commons™
Open Access. Powered by Scholars. Published by Universities.®
Articles 1 - 2 of 2
Full-Text Articles in Molecular, Genetic, and Biochemical Nutrition
Role Of Beta-Hydroxy-Beta-Methylbutyrate (Hmb) In Leucine Stimulation Of Mitochondrial Biogenesis And Fatty Acid Oxidation, Renee Ashley Stancliffe
Role Of Beta-Hydroxy-Beta-Methylbutyrate (Hmb) In Leucine Stimulation Of Mitochondrial Biogenesis And Fatty Acid Oxidation, Renee Ashley Stancliffe
Masters Theses
Mitochondrial dysfunction and the resulting oxidative stress is widely recognized as a contributing factor to the development of numerous pathophysiologies including obesity, diabetes, cardiovascular disease, sarcopenia, liver disease, dementia, amongst others. Mitochondrial dysfunction results in a reduced mitochondrial number and oxidative capacity, causing an increase in free radical production and consequently oxidative stress. As such, the characterization of compounds that can upregulate mitochondrial biogenesis and function could provide the foundation for the development of therapeutic nutraceuticals that promote mitochondrial health, and consequently reduce oxidative stress. Leucine is well recognized to stimulate muscle protein synthesis, and we have recently demonstrated that …
The Effects Of Leucine On Mitochondrial Biogenesis And Cell Cycle In A-375 Melanoma Cells, Tia Marie Filhiol
The Effects Of Leucine On Mitochondrial Biogenesis And Cell Cycle In A-375 Melanoma Cells, Tia Marie Filhiol
Masters Theses
Most cancer cells undergo the Warburg effect, a shift from oxidative to glycolytic metabolism accompanied by suppression of p53. We have demonstrated leucine stimulation of mitochondrial biogenesis, fatty acid oxidation, and p53 expression in both muscle and fat cells. Accordingly, we now sought to determine if leucine stimulates mitochondrial biogenesis and exit from cell cycle in A-375 melanoma cells. Because these cells use glucose as their primary substrate, cells were grown under both standard (11.1 mM) and reduced (5.5 mM) glucose conditions. Increasing glucose reduced mitochondrial mass 50-60%, and accelerated cell proliferation by ~20%. Leucine (0.25, 0.5, 0.75, and 1.0 …