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Improved cognition, mild anxiety-like behavior and decreased motor performance in pyridoxal phosphatase-deficient mice

Please always quote using this URN: urn:nbn:de:bvb:20-opus-323396
  • Pyridoxal 5′-phosphate (PLP) is an essential cofactor in the catalysis of ~140 different enzymatic reactions. A pharmacological elevation of cellular PLP concentrations is of interest in neuropsychiatric diseases, but whole-body consequences of higher intracellular PLP levels are unknown. To address this question, we have generated mice allowing a conditional ablation of the PLP phosphatase PDXP. Ubiquitous PDXP deletion increased PLP levels in brain, skeletal muscle and red blood cells up to 3-fold compared to control mice, demonstrating thatPyridoxal 5′-phosphate (PLP) is an essential cofactor in the catalysis of ~140 different enzymatic reactions. A pharmacological elevation of cellular PLP concentrations is of interest in neuropsychiatric diseases, but whole-body consequences of higher intracellular PLP levels are unknown. To address this question, we have generated mice allowing a conditional ablation of the PLP phosphatase PDXP. Ubiquitous PDXP deletion increased PLP levels in brain, skeletal muscle and red blood cells up to 3-fold compared to control mice, demonstrating that PDXP acts as a major regulator of cellular PLP concentrations in vivo. Neurotransmitter analysis revealed that the concentrations of dopamine, serotonin, epinephrine and glutamate were unchanged in the brains of PDXP knockout mice. However, the levels of γ-aminobutyric acid (GABA) increased by ~20%, demonstrating that elevated PLP levels can drive additional GABA production. Behavioral phenotyping of PDXP knockout mice revealed improved spatial learning and memory, and a mild anxiety-like behavior. Consistent with elevated GABA levels in the brain, PDXP loss in neural cells decreased performance in motor tests, whereas PDXP-deficiency in skeletal muscle increased grip strength. Our findings suggest that PDXP is involved in the fine-tuning of GABA biosynthesis. Pharmacological inhibition of PDXP might correct the excitatory/inhibitory imbalance in some neuropsychiatric diseases.show moreshow less

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Metadaten
Author: Elisabeth Jeanclos, Monique Albersen, Rúben J. J. Ramos, Annette Raab, Christian Wilhelm, Leif Hommers, Klaus-Peter Lesch, Nanda M. Verhoeven-Duif, Antje Gohla
URN:urn:nbn:de:bvb:20-opus-323396
Document Type:Journal article
Faculties:Medizinische Fakultät / Institut für Pharmakologie und Toxikologie
Medizinische Fakultät / Lehrstuhl für Molekulare Psychiatrie
Medizinische Fakultät / Deutsches Zentrum für Herzinsuffizienz (DZHI)
Language:English
Parent Title (English):BBA - Molecular Basis of Disease
Year of Completion:2019
Volume:1865
Pagenumber:193-205
Source:BBA - Molecular Basis of Disease (2019) 1865:193-2005. https://doi.org/10.1016/j.bbadis.2018.08.018
DOI:https://doi.org/10.1016/j.bbadis.2018.08.018
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:motor performance; neuropsychiatric diseases; neurotransmitter biosynthesis; pyridoxal phosphatase; vitamin B6; γ-Aminobutyric acid (GABA)
Release Date:2024/08/08
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International