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Faria-Pereira, A.

Publications and source records attributed to Faria-Pereira, A..

2 recordsLinked to original sources

Mitochondria at synapse utilize fatty acids as a bioenergetic fuel source

Mitochondria process glucose, glutamine, and fatty acids (FAs) to produce ATP, with fuel choice dependent on tissue-specific metabolism. The brain harbors two distinct mitochondrial populations--synaptic and non-synaptic. While glucose is the primary fuel for brain bioenergetics, the role of FAs remains elusive. A preliminary proteomic analysis revealed that synaptic mitochondria favor FA metabolism, corroborated by biochemical and respiratory assays showing their higher capacity for {beta}-oxidation and greater respiratory flexibility compared to non-synaptic mitochondria. Additionally, synaptic mitochondria showed higher capacity for FA uptake and less susceptibility to inhibition of the carnitine shuttle system. In neurons, oxygen consumption rate assays indicate that medium to long-chain FA fueling enhances neuronal respiratory flexibility and ATP content, while whole-cell patch-clamp recordings show that long-chain FA fueling sustains increased pre-synaptic activity. Our findings demonstrate that FAs can contribute effectively to synaptic metabolism under normal physiological conditions, where there is a constant demand for energy.

cell biology↗

Bioenergetic signature of Synaptic mitochondria

Synaptic transmission is the most energy-demanding processes in the brain and here we show that mitochondria have developed specific properties to efficiently support neurotransmission. It is a known fact that mitochondria at synapses need to be able to deal with a dynamic range of energetic needs overtime and to adapt between resting and high stimulation conditions. However, how mitochondria are adjusting to this requirement was not yet clear. Here, we show that synaptic mitochondria have a distinct bioenergetic profile presenting a stronger ability to respond to respiratory stimulus. These features are explained by a dichotomic Complex I activity pattern where synaptic mitochondria present a decreased enzymatic activity of individual Complex I, yet mitochondria at synapse present a dramatically enhanced Complex I+III combined activity. These bioenergetics features may endow synaptic mitochondria with the necessary mechanisms to adapt to the flexible bioenergetic environment present at synapses.

cell biology↗