Protein Metabolism Changes and Alterations in Behavior of Trace Amine-Associated Receptor 1 Knockout Mice Fed a High-Fructose Diet.
Sergey A ApryatinIlya S ZhukovEkaterina A ZolotoverkhayaSaveliy R KuvarzinTemirkan A KhunagovSanelya V UshmuginaVictor M KlimenkoPublished in: Neurology international (2023)
Trace amines and their receptors are a family of G protein-coupled receptors widely distributed in the central nervous system and periphery. The trace amine-associated receptor 1 (TAAR1) plays a significant role as a therapeutic target for schizophrenia, depression, diabetes, and obesity. In this study, TAAR1 knockout mice and WT groups were tested in conditions of a high-fructose diet. The consumption of a high-fructose diet may be due to the influence on the metabolism processes by dopamine in the brain, neuromotor function, and level of anxiety of TAAR1 knockout mice. During a comparative analysis of behavioral, biochemical, and morphological parameters, significant differences were found between liver and biochemical parameters, the regulation of protein metabolism (AST/ALT ratio, creatine kinase activity, urea), and alterations in behavior. An elevated plus maze analysis showed the influence of fructose and genetic factors on the level of anxiety. A new marker of the grooming microstructure (depression ratio) was tested, which showed high efficiency as a marker of depression-like behavioral changes and a possible association with dopamine-dependent regulation of protein metabolism. These results confirm a possible association of the TAAR1 gene knockout with an increase in catabolic reaction levels by AST/ALT-dependent and possible dopamine-mediated protein metabolism regulation and depression-like behavior.
Keyphrases
- sleep quality
- depressive symptoms
- weight loss
- physical activity
- binding protein
- high efficiency
- protein protein
- type diabetes
- uric acid
- white matter
- cardiovascular disease
- amino acid
- heavy metals
- insulin resistance
- metabolic syndrome
- small molecule
- bipolar disorder
- weight gain
- multiple sclerosis
- prefrontal cortex
- gene expression
- tyrosine kinase