A model of traumatic brain injury in rats is influenced by neuroprotection of diurnal variation which improves motor behavior and histopathology in white matter myelin

Traumatic brain injury (TBI) represents a significant public health concern and has been asso-ciated with high rates of morbidity and mortality. TBI generates two types of brain damage: primary and secondary. Secondary damage originates a series of pathophysiological processes, which include metabolic crisis, excitotoxicity, and neuroinflammation, which have deleterious consequences for neuronal function. However, neuroprotective mechanisms are also activated. The balance among these tissue responses, and its variations throughout the day determines the fate of the damage tissue. We have demonstrated less behavioral and morphological damage when a rat model of TBI was induced during the light hours of the day.Moreover, here we show that rats subjected to TBI in the dark lost less body weight than those subjected to TBI in the light, despite no change in food intake. Besides, the rats subjected to TBI in the dark had better performance in the beam walking test and presented less histological damage in the corpus callosum and the cingulum bundle, as shown by the Kluver-Barrera staining.Our results suggest that the time of day when the injury occurs is important. Thus, this data should be used to evaluate the pathophysiological processes of TBI events and develop better therapies.

Automated summary

Traumatic brain injury (TBI) is a significant public health concern with high rates of morbidity and mortality. TBI causes primary and secondary brain damage, with secondary damage leading to metabolic crisis, excitotoxicity, and neuroinflammation that have detrimental effects on neuronal function. However, neuroprotective mechanisms are also activated. The timing of the injury plays a role in the severity of the damage, as shown by our study on a rat model of TBI induced during light hours, which resulted in less behavioral and morphological damage.