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Decoupling the mutual promotion of inflammation and oxidative stress mitigates cognitive decline and depression-like behavior in rmTBI mice by promoting myelin renewal and neuronal survival - 22/03/24

Doi : 10.1016/j.biopha.2024.116419 
Shenghua Lu a, b, QianQian Ge a, MengShi Yang a, b, Yuan Zhuang a, b, Xiaojian Xu b, Fei Niu b, Baiyun Liu a, b, c, d, , Runfa Tian a, b, c, d,
a Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China 
b Beijing Key Laboratory of Central Nervous System Injury, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China 
c Center for Nerve Injury and Repair, Beijing Institute of Brain Disorders, Beijing, China 
d China National Clinical Research Center for Neurological Diseases, Beijing, China 

Corresponding authors at: Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical UniversityBeijingChina

Abstract

Background

Repetitive mild traumatic brain injury (rmTBI) can lead to somatic, emotional, and cognitive symptoms that persist for years after the initial injury. Although the ability of various treatments to promote recovery after rmTBI has been explored, the optimal time window for early intervention after rmTBI is unclear. Previous research has shown that hydrogen-rich water (HRW) can diffuse through the blood-brain - barrier, attenuate local oxidative stress, and reduce neuronal apoptosis in patients with severe traumatic brain injury. However, research on the effect of HRW on rmTBI is scarce.

Aims

The objectives of this study were to explore the following changes after rmTBI and HRW treatment: (i) temporal changes in inflammasome activation and oxidative stress-related protein expression through immunoblotting, (ii) temporal changes in neuron/myelin-related metabolite concentrations in vivo through magnetic resonance spectroscopy, (iii) myelin structural changes in late-stage rmTBI via immunofluorescence, and (iv) postinjury anxiety/depression-like behaviors and spatial learning and memory impairment.

Results

NLRP-3 expression in the rmTBI group was elevated at 7 and 14 DPI, and inflammasome marker levels returned to normal at 30 DPI. Oxidative stress persisted throughout the first month postinjury. HRW replacement significantly decreased Nrf2 expression in the prefrontal cortex and hippocampal CA2 region at 14 and 30 DPI, respectively. Edema and local gliosis in the hippocampus and restricted diffusion in the thalamus were observed on MR-ADC images. The tCho/tCr ratio in the rmTBI group was elevated, and the tNAA/tCr ratio was decreased at 30 DPI. Compared with the mice in the other groups, the mice in the rmTBI group spent more time exploring the open arms in the elevated plus maze (P < 0.05) and were more active in the maze (longer total distance traveled). In the sucrose preference test, the rmTBI group exhibited anhedonia. In the Morris water maze test, the latency to find the hidden platform in the rmTBI group was longer than that in the sham and HRW groups (P < 0.05).

Conclusion

Early intervention with HRW can attenuate inflammasome assembly and reduce oxidative stress after rmTBI. These changes may restore local oligodendrocyte function, promote myelin repair, prevent axonal damage and neuronal apoptosis, and alleviate depression-like behavior and cognitive impairment.

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Graphical Abstract




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Highlights

We used "breakable platform" as modeling methods to avoid cranial bone crushing and to imitate the shear force injury in the real-world patients.
We provide multiple temporal features (1/3/7/14/30 day post injury) of the pathological change after rmTBI.
Using western blot, immunofluorescence, MRI/MRS scans, and behavioral tests, we explore rmTBI's effects on pathology, physiology, and behavior comprehensively.
The therapeutic potential of employing hydrogen-rich water as a dietary supplement to alleviate late-onset symptoms of rmTBI was initially elucidated in this study.

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Keywords : Mild traumatic brain injury, Hydrogen water, Inflammation, Oxidative stress, Cognitive dysfunction


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Vol 173

Article 116419- avril 2024 Retour au numéro
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