1) The ganglia of the sympathetic part of the ANS, in which the neurons of the efferent part of the arc of the unconditioned reflex are localized, are supplied with blood (oxygen and nutrients) on a common basis with other cells of the body. while the neurons of the afferent part of the arc, located in the nerve nodes of the spinal cord and the brain stem, are supplied with oxygen and nutrients in priority, like the neurons of the central nervous system.
2) Degeneration of the afferent part of the arc of the unconditioned reflex, which provides negative feedback between the periphery and the central structures of the ANS located in the parts of the brain stem, leads to irreversible activation of the work of the efferent part of the arc. Long-term non-stop work of neurons of the efferent part of the arc leads to their depletion and death.
However, even before the onset of depletion and subsequent death of neurons in the efferent part of the arc, such irreversible activation of neurons in the sympathetic part of the ANS leads to a number of pathological manifestations. Apparently, it is the long-term functioning of only the efferent part of the autonomic reflex arc, without feedback from the periphery that leads to hyperactivity of the sympathetic nervous system and to the initiation of the development of metabolic syndrome with an increased risk of developing type 2 diabetes, cardiovascular diseases and premature mortality [11].
An obvious additional mechanism for accelerating the pathogenesis of aging at this stage is the wasted oxygen consumption for the excessive and generally not required by the periphery of the activity of the sympathetic nervous system in the absence of a reverse inhibitory afferent connection with the periphery (autocatalytic process). This is one example of the aggravation of hypoxia at one of the stages of the pathogenesis of aging. The second mechanism for the aggravation of hypoxia, initiated by impaired afferent connections, is due to the cessation of the supply of inhibitory signals to the brain stem structures through the neural networks of the second afferent system.
Normally, the second afferent system transmits signals to the structures of the brain stem and, in particular, to the hypothalamus, inhibiting the activity of some of its nuclei. The cessation of this inhibitory activity due to the death of afferent endings, as a result, leads to a gradual release of inhibition and to the activation with age of some nuclei of the hypothalamus. A decrease with age in the intensity of inhibitory signals entering the hypothalamus through this system leads to activation of the endocrine system, designed to replace the regulatory function of the degenerated ANS.
Replacement of the nervous regulation of the periphery with the endocrine one is also realized in additional non-productive oxygen consumption, that is, in an increase in hypoxia. Degeneration of the afferent nerve processes of the sympathetic division of the ANS through the second afferent system activates the production of corticotropin releasing hormone (CRH) by the hypothalamus, which stimulates the synthesis and export of adrenocorticotropic hormone (ACTH) by the pituitary gland, followed by an increase in the synthesis and export of cortisol by the adrenal glands.
![Bo][ing Day истребить «колхозника»](/uploads/covers/fe/bo-ing-day-istrebit-kolhoznika.jpg)
