2Bauman Moscow State Technical University, 105005 Moscow, Russia
3Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia
4Moscow Institute of Physics and Technology, 141701 Dolgoprudny, Russia
* To whom correspondence should be addressed.
# These authors contributed equally to the work.
Received: December 10, 2024; Revised: December 27, 2024; Accepted: January 16, 2025
Nicotinamide adenine dinucleotide and its derivatives – NAD+, NADP+, NADH, NADPH – play an important role in cell metabolism, act as substrates or cofactors for a large number of enzymes involved in the DNA regulation of replication and repair, maintenance of calcium homeostasis in cells, biosynthetic processes, and energy production mechanisms. Changes in the ratio of oxidized and reduced forms of pyridine nucleotides accompanies development of oxidative and reductive stress that significantly contribute to the cell damage and induction of adaptive responses. Currently, a huge number of protocols aimed at quantitative or qualitative assessment of the pyridine nucleotide pool are in use, but all of them have their limitations associated with sample preparation processes, difficulties in the metabolite spectrum assessment, and complexity of data interpretation. Measuring pyridine nucleotide levels is relevant in the studies of pathophysiological regulatory mechanisms of the cell functional activity and intercellular communication. This is of particular relevance when studying the mechanisms of plasticity of the central nervous system in health and disease, since significant changes in the pools of pyridine nucleotides in cells are evident in neurodevelopmental disorders, neurodegeneration, and aging. Simple and reliable non-invasive methods for measuring levels of NAD+ and NADH are necessary to assess the brain cells metabolism with diagnostic and research purposes. The goal of this review is to conduct comparative analysis of the main methods for measuring the levels of oxidized and reduced pyridine nucleotides in cells and to identify key principles of their application for correct interpretation of the obtained data, including those used for studying central nervous system.
KEY WORDS: pyridine nucleotides, brain, neuroplasticity, neurodegeneration, brain aging, metabolomics, chromatography, mass spectrometry, fluorometryDOI: 10.1134/S0006297924604477
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