scholarly journals Examining the Effects of Anabolic–Androgenic Steroids on Repetitive Mild Traumatic Brain Injury (RmTBI) Outcomes in Adolescent Rats

2020 ◽  
Vol 10 (5) ◽  
pp. 258
Author(s):  
Jason Tabor ◽  
David. K. Wright ◽  
Jennaya Christensen ◽  
Akram Zamani ◽  
Reid Collins ◽  
...  

Background: Repetitive mild traumatic brain injury (RmTBI) is increasingly common in adolescents. Anabolic–androgenic steroid (AAS) consumption among younger professional athletes is a significant risk factor for impaired neurodevelopment. Given the increased rates and overlapping symptomology of RmTBI and AAS use, we sought to investigate the behavioural and neuropathological outcomes associated with the AAS Metandienone (Met) and RmTBI on rats. Methods: Rats received either Met or placebo and were then administered RmTBIs or sham injuries, followed by a behavioural test battery. Post-mortem MRI was conducted to examine markers of brain integrity and qRT-PCR assessed mRNA expression of markers for neurodevelopment, neuroinflammation, stress responses, and repair processes. Results: Although AAS and RmTBI did not produce cumulative deficits, AAS use was associated with detrimental outcomes including changes to depression, aggression, and memory; prefrontal cortex (PFC) atrophy and amygdala (AMYG) enlargement; damaged white matter integrity in the corpus callosum; and altered mRNA expression in the PFC and AMYG. RmTBI affected general activity and contributed to PFC atrophy. Conclusions: Findings corroborate previous results indicating that RmTBI negatively impacts neurodevelopment but also demonstrates that AAS results in significant neuropathological insult to the developing brain.

2017 ◽  
Vol 4 (9) ◽  
pp. 640-654 ◽  
Author(s):  
David K. Wright ◽  
Terence J. O'Brien ◽  
Sandy R. Shultz ◽  
Richelle Mychasiuk

2018 ◽  
Vol 35 (16) ◽  
pp. 1895-1905 ◽  
Author(s):  
Sabrina Salberg ◽  
Jennaya Christensen ◽  
Glenn R. Yamakawa ◽  
Connor Lengkeek ◽  
Haris Malik ◽  
...  

2019 ◽  
Vol 376 ◽  
pp. 112225 ◽  
Author(s):  
Sabrina Salberg ◽  
Himanthri Weerwardhena ◽  
Reid Collins ◽  
Raylene A. Reimer ◽  
Richelle Mychasiuk

PLoS ONE ◽  
2017 ◽  
Vol 12 (11) ◽  
pp. e0187218 ◽  
Author(s):  
Glenn R. Yamakawa ◽  
Connor Lengkeek ◽  
Sabrina Salberg ◽  
Simon C. Spanswick ◽  
Richelle Mychasiuk

Author(s):  
Wenxing Cui ◽  
Xun Wu ◽  
Dayun Feng ◽  
Jianing Luo ◽  
Yingwu Shi ◽  
...  

AbstractTraumatic brain injury (TBI)-induced coagulopathy has increasingly been recognized as a significant risk factor for poor outcomes, but the pathogenesis remains poorly understood. In this study, we aimed to investigate the causal role of acrolein, a typical lipid peroxidation product, in TBI-induced coagulopathy, and further explore the underlying molecular mechanisms. We found that the level of plasma acrolein in TBI patients suffering from coagulopathy was higher than that in those without coagulopathy. Using a controlled cortical impact mouse model, we demonstrated that the acrolein scavenger phenelzine prevented TBI-induced coagulopathy and recombinant ADAMTS-13 prevented acrolein-induced coagulopathy by cleaving von Willebrand factor (VWF). Our results showed that acrolein may contribute to an early hypercoagulable state after TBI by regulating VWF secretion. mRNA sequencing (mRNA-seq) and transcriptome analysis indicated that acrolein over-activated autophagy, and subsequent experiments revealed that acrolein activated autophagy partly by regulating the Akt/mTOR pathway. In addition, we demonstrated that acrolein was produced in the perilesional cortex, affected endothelial cell integrity, and disrupted the blood-brain barrier. In conclusion, in this study we uncovered a novel pro-coagulant effect of acrolein that may contribute to TBI-induced coagulopathy and vascular leakage, providing an alternative therapeutic target.


2018 ◽  
Vol 5 (12) ◽  
pp. 1588-1598 ◽  
Author(s):  
Ryan C. Wortman ◽  
Alicia Meconi ◽  
Katie J. Neale ◽  
Rhys D. Brady ◽  
Stuart J. McDonald ◽  
...  

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