Abstract

Traumatic brain injury (TBI) induces two types of brain damage: primary and secondary. Damage initiates a series of pathophysiological processes, such as metabolic crisis, excitotoxicity with oxidative stress-induced damage, and neuroinflammation. The long-term perpetuation of these processes has deleterious consequences for neuronal function. However, it remains to be elucidated further whether physiological variation in the brain microenvironment, depending on diurnal variations, influences the damage, and consequently, exerts a neuroprotective effect. Here, we established an experimental rat model of TBI and evaluated the effects of TBI induced at two different time points of the light–dark cycle. Behavioral responses were assessed using a 21-point neurobehavioral scale and the cylinder test. Morphological damage was assessed in different regions of the central nervous system. We found that rats that experienced a TBI during the dark hours had better behavioral performance than those injured during the light hours. Differences in behavioral performance correlated with less morphological damage in the perilesional zone. Moreover, certain brain areas (CA1 and dentate gyrus subregions of the hippocampus) were less prone to damage in rats that experienced a TBI during the dark hours. Our results suggest that diurnal variation is a crucial determinant of TBI outcome, and the hour of the day at which an injury occurs should be considered for future research.

Highlights

  • Traumatic brain injury (TBI) is defined as the alteration of brain function, or other evidence of brain pathology, caused by an external force (Menon et al, 2010)

  • TBI causes two types of brain damage: primary damage is the result of tearing, shearing and rupture of nervous tissue and is considered irreversible; secondary damage is a cascade of pathophysiological processes that could exacerbate the damage of the primary lesion (Maas et al, 2008)

  • To test whether the general health parameters changed depending upon the time of TBI induction in rats, food intake and body weight were measured in both sham and TBI subgroups before and at 24, 48, and 72 h after TBI (Figure 1)

Read more

Summary

Introduction

Traumatic brain injury (TBI) is defined as the alteration of brain function, or other evidence of brain pathology, caused by an external force (Menon et al, 2010). TBI causes two types of brain damage: primary damage is the result of tearing, shearing and rupture of nervous tissue and is considered irreversible; secondary damage is a cascade of pathophysiological processes that could exacerbate the damage of the primary lesion (Maas et al, 2008). Some of these pathophysiological processes, namely excitotoxicity through N-methyl-D-aspartate (NMDA) receptor expression (Estrada-Rojo et al, 2018), oxidative stress (O’Neill and Feeney, 2014), and neuroinflammation (Griffin et al, 2019) are related to diurnal variation in the levels of hormones, neurotransmitters, and metabolic intermediates of cognitive pathways. Differences in immune response activation could be reflected in social behavioral tests

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call