Metabolic regulation of synaptic activity.

Rev Neurosci

Department of Pharmacology, University of Oxford, Oxford, UK.

Published: November 2018

AI Article Synopsis

  • Brain tissue is energy-intensive, making up about 2% of body weight but consuming 20% of calories, primarily for maintaining synaptic function.
  • Synapses are particularly vulnerable in neurological diseases, often showing damage before neurons die, as seen in conditions like ischemic stroke and hypoglycemia.
  • A ketogenic diet is suggested as a potential treatment to enhance synaptic function and may help in managing conditions such as epilepsy by shifting energy sources from carbohydrates to fats.

Article Abstract

Brain tissue is bioenergetically expensive. In humans, it composes approximately 2% of body weight and accounts for approximately 20% of calorie consumption. The brain consumes energy mostly for ion and neurotransmitter transport, a process that occurs primarily in synapses. Therefore, synapses are expensive for any living creature who has brain. In many brain diseases, synapses are damaged earlier than neurons start dying. Synapses may be considered as vulnerable sites on a neuron. Ischemic stroke, an acute disturbance of blood flow in the brain, is an example of a metabolic disease that affects synapses. The associated excessive glutamate release, called excitotoxicity, is involved in neuronal death in brain ischemia. Another example of a metabolic disease is hypoglycemia, a complication of diabetes mellitus, which leads to neuronal death and brain dysfunction. However, synapse function can be corrected with "bioenergetic medicine". In this review, a ketogenic diet is discussed as a curative option. In support of a ketogenic diet, whereby carbohydrates are replaced for fats in daily meals, epileptic seizures can be terminated. In this review, we discuss possible metabolic sensors in synapses. These may include molecules that perceive changes in composition of extracellular space, for instance, ketone body and lactate receptors, or molecules reacting to changes in cytosol, for instance, KATP channels or AMP kinase. Inhibition of endocytosis is believed to be a universal synaptic mechanism of adaptation to metabolic changes.

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Source
http://dx.doi.org/10.1515/revneuro-2017-0090DOI Listing

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