Abstract
Over the years, neurons undergo functional changes initially linked to the maturation of the brain and then are progressively linked to normal aging. The curious relationship between brain decay, aging, and neuronal diseases has aroused the interest of numerous studies to better understand and contrast the evolution of these pathologies. The objective of this research is to apply the non-equilibrium thermodynamic theory with the internal variables of the study of the rheological properties of the brain, focusing on the study of viscoelastic properties. After a thermodynamic introduction of the principal rheological phenomena, this paper discusses the results by the application of our mathematical technique, which revealed a prevalence of anelastic properties in the old central nervous system compared to the young one. Furthermore, the entropy production trend tested identifies a greater disorder in the young brain in respect to the old one. The results obtained highlight that a lower stiffness in the old central nervous system may be interpreted with dendritic regression associated with neuronal death, both being potential consequences of an increased production of free radicals due to reduced antioxidant defenses and/or an altered mitochondrial dysfunction in aging.