Abstract
BackgroundMitochondria are both the cellular powerhouse and the major source of reactive oxygen species. Coenzyme Q10 plays a key role in mitochondrial energy production and is recognized as a powerful antioxidant. For these reasons it can be argued that higher mitochondrial ubiquinone levels may enhance the energy state and protect from oxidative stress. Despite the large number of clinical studies on the effect of CoQ10 supplementation, there are very few experimental data about the mitochondrial ubiquinone content and the cellular bioenergetic state after supplementation. Controversial clinical and in vitro results are mainly due to the high hydrophobicity of this compound, which reduces its bioavailability.Principal FindingsWe measured the cellular and mitochondrial ubiquinone content in two cell lines (T67 and H9c2) after supplementation with a hydrophilic CoQ10 formulation (Qter®) and native CoQ10. Our results show that the water soluble formulation is more efficient in increasing ubiquinone levels. We have evaluated the bioenergetics effect of ubiquinone treatment, demonstrating that intracellular CoQ10 content after Qter supplementation positively correlates with an improved mitochondrial functionality (increased oxygen consumption rate, transmembrane potential, ATP synthesis) and resistance to oxidative stress.ConclusionsThe improved cellular energy metabolism related to increased CoQ10 content represents a strong rationale for the clinical use of coenzyme Q10 and highlights the biological effects of Qter®, that make it the eligible CoQ10 formulation for the ubiquinone supplementation.
Highlights
Coenzyme Q10 (CoQ10), known as ubiquinone, is the predominant form of coenzyme Q in humans
The improved cellular energy metabolism related to increased CoQ10 content represents a strong rationale for the clinical use of coenzyme Q10 and highlights the biological effects of QterH, that make it the eligible CoQ10 formulation for the ubiquinone supplementation
We found that mitochondrial CoQ10 content in cells treated with 100 nM QterH was similar to that measured in cells treated with 10 mM native CoQ10 (Fig. 2C and 2D)
Summary
Coenzyme Q10 (CoQ10), known as ubiquinone, is the predominant form of coenzyme Q in humans It is a lipid-soluble molecule composed of a redox active quinone ring and a hydrophobic tail. Kidney, brain and liver tissues show the highest concentration of CoQ10, which is endogenously synthesized and in small part assimilated from the diet [5] Mitochondria are both the cellular powerhouse and the major source of reactive oxygen species. Coenzyme Q10 plays a key role in mitochondrial energy production and is recognized as a powerful antioxidant. For these reasons it can be argued that higher mitochondrial ubiquinone levels may enhance the energy state and protect from oxidative stress. Controversial clinical and in vitro results are mainly due to the high hydrophobicity of this compound, which reduces its bioavailability
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