High Concentration of Ketone Body β-Hydroxybutyrate Modifies Synaptic Vesicle Cycle and Depolarizes Plasma Membrane of Rat Brain Synaptosomes

Ketoacidosis is a dangerous complication of diabetes mellitus in which plasma levels of ketone bodies can reach 20–25 mM. This condition is life-threatening. In contrast, a ketogenic diet, achieving plasma levels of ketone bodies of about 4–5 mM, can be used for treating different brain diseases. Ho...

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Veröffentlicht in:Journal of molecular neuroscience 2020, Vol.70 (1), p.112-119
Hauptverfasser: Voronina, Polina P., Adamovich, Ksenia V., Adamovich, Tatyana V., Dubouskaya, Tatsiana G., Hrynevich, Sviatlana V., Waseem, Tatsiana V., Fedorovich, Sergei V.
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container_end_page 119
container_issue 1
container_start_page 112
container_title Journal of molecular neuroscience
container_volume 70
creator Voronina, Polina P.
Adamovich, Ksenia V.
Adamovich, Tatyana V.
Dubouskaya, Tatsiana G.
Hrynevich, Sviatlana V.
Waseem, Tatsiana V.
Fedorovich, Sergei V.
description Ketoacidosis is a dangerous complication of diabetes mellitus in which plasma levels of ketone bodies can reach 20–25 mM. This condition is life-threatening. In contrast, a ketogenic diet, achieving plasma levels of ketone bodies of about 4–5 mM, can be used for treating different brain diseases. However, the factors leading to the conversion of the neuroprotective ketone bodies’ action to the neurotoxic action during ketoacidosis are still unknown. We investigated the influence of high concentration (25 mM) of the main ketone body, β-hydroxybutyrate (BHB), on intrasynaptosomal pH (pHi), synaptic vesicle cycle, plasma membrane, and mitochondrial potentials. Using the fluorescent dye BCECF-AM, it was shown that BHB at concentrations of 8 and 25 mM did not influence pHi in synaptosomes. By means of the fluorescent dye acridine orange, it was demonstrated that 25 mM of BHB had no effect on exocytosis but inhibited compensatory endocytosis by 5-fold. Increasing buffer capacity with 25 mM HEPES did not affect endocytosis. Glucose abolished BHB-induced endocytosis inhibition. Using the fluorescent dye DiSC3(5), it was shown that 25 mM of BHB induced a significant plasma membrane depolarization. This effect was not impacted by glucose. Using the fluorescent dye rhodamine-123, it was shown that BHB alone (25 mМ) did not alter the potential of intrasynaptosomal mitochondria. Importantly, the high concentration of BHB (25 mМ) causes the depolarization of the plasma membrane and stronger inhibition of endocytosis compared with the intermediate concentration (8 mM).
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This condition is life-threatening. In contrast, a ketogenic diet, achieving plasma levels of ketone bodies of about 4–5 mM, can be used for treating different brain diseases. However, the factors leading to the conversion of the neuroprotective ketone bodies’ action to the neurotoxic action during ketoacidosis are still unknown. We investigated the influence of high concentration (25 mM) of the main ketone body, β-hydroxybutyrate (BHB), on intrasynaptosomal pH (pHi), synaptic vesicle cycle, plasma membrane, and mitochondrial potentials. Using the fluorescent dye BCECF-AM, it was shown that BHB at concentrations of 8 and 25 mM did not influence pHi in synaptosomes. By means of the fluorescent dye acridine orange, it was demonstrated that 25 mM of BHB had no effect on exocytosis but inhibited compensatory endocytosis by 5-fold. Increasing buffer capacity with 25 mM HEPES did not affect endocytosis. Glucose abolished BHB-induced endocytosis inhibition. Using the fluorescent dye DiSC3(5), it was shown that 25 mM of BHB induced a significant plasma membrane depolarization. This effect was not impacted by glucose. Using the fluorescent dye rhodamine-123, it was shown that BHB alone (25 mМ) did not alter the potential of intrasynaptosomal mitochondria. 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Using the fluorescent dye DiSC3(5), it was shown that 25 mM of BHB induced a significant plasma membrane depolarization. This effect was not impacted by glucose. Using the fluorescent dye rhodamine-123, it was shown that BHB alone (25 mМ) did not alter the potential of intrasynaptosomal mitochondria. 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subjects 3-Hydroxybutyric Acid - pharmacology
Acridine orange
Animals
Biomedical and Life Sciences
Biomedicine
Brain
Brain - cytology
Brain - metabolism
Cell Biology
Depolarization
Diabetes mellitus
Diabetic ketoacidosis
Dyes
Endocytosis
Exocytosis
Fluorescent dyes
Fluorescent indicators
Glucose
High fat diet
Hydrogen-Ion Concentration
Ketoacidosis
Ketogenesis
Ketones
Ketosis - metabolism
Low carbohydrate diet
Male
Membrane potential
Membrane Potentials
Membranes
Mitochondria
Neurochemistry
Neurology
Neuroprotection
Neurosciences
Neurotoxicity
Plasma
Plasma levels
Proteomics
Rats
Rats, Wistar
Rhodamine
Synaptic Vesicles - drug effects
Synaptic Vesicles - metabolism
Synaptosomes
Synaptosomes - drug effects
Synaptosomes - metabolism
Synaptosomes - physiology
title High Concentration of Ketone Body β-Hydroxybutyrate Modifies Synaptic Vesicle Cycle and Depolarizes Plasma Membrane of Rat Brain Synaptosomes
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