In mice, anxiety-depressive disorder has been associated with impaired energy metabolism in the brain, found Russian neuroscientists. The obtained data provides a fresh look at the depression development mechanism and other psycho-emotional diseases formation. The results of the study supported by Russian Science Foundation are published in the BMC Neuroscience.
The World Health Organization claims that 5 out of 10 major causes of disability in most countries of the world are related to mental and behavioral disorders. Up to 95% of people with depression have a diagnosis of anxiety disorder. As recent research shows. such conditions might be associated with mitochondria defects. These "energy stations" of cells are responsible for the formation of ATP molecules, which are necessary for most reactions in living organisms. Defects of mitochondria appear due to congenital mutations or adverse external conditions, violating the work of mitochondrial genes with no mutations. As a result, the amount of proteins encoded by these genes changes.
‘Psycho-emotional disorders due to constant social conflicts cause severe mitochondrial dysfunction in the brain. The consequences of these disorders can be observed in many neurological and psychoemotional diseases, including depression, bipolar disorder and schizophrenia.’
Neurobiologists from the Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences conducted an experiment on depression modeled in mice to find out whether some mitochondria defects in different brain parts accompany psycho-emotional disorders in animals. In total, the study compared the work of 47 genes encoding numerous carrier proteins located on the inner membrane of the mitochondria.
A detailed study of the mechanisms of development of mitochondrial dysfunction may provide the key to new methods of treating these diseases," says Natalia Kudryavtseva, senior researcher at the Institute of Cytology and Genetics of the SB RAS.
Scientists conducted experiments on mice placed in terms of social conflict, triggering depression and anxiety. They compared how selected genes worked in this mice group with some control mice, who did not experience such a stress. It turned out that expression of most genes in the hypothalamus, the part of the brain that regulates stress reactions, has changed. Gene expression has also changed in the hippocampus, which plays a crucial role in memory formation, emotional reactions and new neurons formation. These data show that in chronic social conflicts that lead to the development of anxiety-depressive disorder in animals, the work of mitochondria is disrupted in several parts of the brain.