Date published: 2025-9-19

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ALDH9A1 Activators

ALDH9A1, or Aldehyde Dehydrogenase 9 Family Member A1, is an enzyme encoded by the ALDH9A1 gene in humans. It belongs to the aldehyde dehydrogenase (ALDH) family, which is responsible for the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. ALDH enzymes are key players in various metabolic processes and are involved in the conversion of aldehydes to their corresponding carboxylic acids using NAD+ or NADP+ as cofactors.ALDH9A1 specifically is a mitochondrial and cytosolic enzyme that plays a significant role in the metabolism of gamma-aminobutyraldehyde to gamma-aminobutyric acid (GABA), an important neurotransmitter in the brain. This reaction is part of the polyamine metabolic pathway and is crucial for maintaining the balance of neural signaling substances in the central nervous system.

In addition to its role in neurotransmitter metabolism, ALDH9A1 also participates in the detoxification of aldehydes from amino acid and polyamine metabolism. This function is essential for preventing the accumulation of toxic aldehydes in cells, which can damage DNA, proteins, and lipids, leading to cell dysfunction and death.The activity of ALDH9A1 is also involved in the biosynthesis of the osmolyte betaine, which plays a role in the regulation of cell osmolarity and protection against osmotic stress, dehydration, and high salt concentrations.Dysregulation or mutations in the ALDH9A1 gene can lead to various metabolic disorders. Given its role in neurotransmitter and osmolyte metabolism, ALDH9A1 is a protein of interest in research on neurodegenerative diseases and conditions related to cellular stress responses.

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