scholarly journals Overexpression of aquaporin-1 aggravates hippocampal damage in mouse traumatic brain injury models

2014 ◽  
Vol 9 (3) ◽  
pp. 916-922 ◽  
Author(s):  
BO QIU ◽  
XINGUO LI ◽  
XIYANG SUN ◽  
YONG WANG ◽  
ZHITAO JING ◽  
...  
2020 ◽  
Vol 37 (4) ◽  
pp. 665-674 ◽  
Author(s):  
Katrin Rauen ◽  
Viorela Pop ◽  
Raimund Trabold ◽  
Jerome Badaut ◽  
Nikolaus Plesnila

2020 ◽  
pp. 1-12
Author(s):  
Cindy Santiago-Castañeda ◽  
Marysol Segovia-Oropeza ◽  
Luis Concha ◽  
Sandra Adela Orozco-Suárez ◽  
Luisa Rocha

Background: Severe traumatic brain injury (TBI), an important risk factor for Alzheimer’s disease, induces long-term hippocampal damage and hyperexcitability. On the other hand, studies support that propylparaben (PPB) induces hippocampal neuroprotection in neurodegenerative diseases. Objective: Experiments were designed to evaluate the effects of subchronic treatment with PPB on TBI-induced changes in the hippocampus of rats. Methods: Severe TBI was induced using the lateral fluid percussion model. Subsequently, rats received subchronic administration with PPB (178 mg/kg, TBI+PPB) or vehicle (TBI+PEG) daily for 5 days. The following changes were examined during the experimental procedure: sensorimotor dysfunction, changes in hippocampal excitability, as well as neuronal damage and volume. Results: TBI+PEG group showed sensorimotor dysfunction (p <  0.001), hyperexcitability (64.2%, p <  0.001), and low neuronal preservation ipsi- and contralateral to the trauma. Magnetic resonance imaging (MRI) analysis revealed lower volume (17.2%; p <  0.01) and great damage to the ipsilateral hippocampus. TBI+PPB group showed sensorimotor dysfunction that was partially reversed 30 days after trauma. This group showed hippocampal excitability and neuronal preservation similar to the control group. However, MRI analysis revealed lower hippocampal volume (p <  0.05) when compared with the control group. Conclusion: The present study confirms that post-TBI subchronic administration with PPB reduces the long-term consequences of trauma in the hippocampus. Implications of PPB as a neuroprotective strategy to prevent the development of Alzheimer’s disease as consequence of TBI are discussed.


Inflammation ◽  
2018 ◽  
Vol 41 (4) ◽  
pp. 1182-1193 ◽  
Author(s):  
Wei Zhu ◽  
Yuexia Ding ◽  
Wei Kong ◽  
Tuo Li ◽  
Hongguang Chen

2004 ◽  
Vol 6 (4) ◽  
pp. 333-342 ◽  
Author(s):  
Kenneth I. Strauss ◽  
Raj K. Narayan ◽  
Ramesh Raghupathi

Neurosurgery ◽  
2014 ◽  
Vol 74 (4) ◽  
pp. 382-394 ◽  
Author(s):  
Ryan C. Turner ◽  
Reyna L. VanGilder ◽  
Zachary J. Naser ◽  
Brandon P. Lucke-Wold ◽  
Julian E. Bailes ◽  
...  

2012 ◽  
Vol 507 (1) ◽  
pp. 84-89 ◽  
Author(s):  
Durgul Ozdemir ◽  
Basak Baykara ◽  
Ilkay Aksu ◽  
Muge Kiray ◽  
Ali Riza Sisman ◽  
...  

2021 ◽  
Author(s):  
Riccardo De Feo ◽  
Elina Hamalainen ◽  
Eppu Manninen ◽  
Riikka Immonen ◽  
Juan Miguel Valverde ◽  
...  

Registration-based methods are commonly used in the anatomical segmentation of magnetic resonance (MR) brain images. However, they are sensitive to the presence of deforming brain pathologies that may interfere with the alignment of the atlas image with the target image. Our goal was to develop an algorithm for automated segmentation of the normal and injured rat hippocampus. We implemented automated segmentation using a U-Net-like Convolutional Neural Network (CNN). of sham-operated experimental controls and rats with lateral-fluid-percussion induced traumatic brain injury (TBI) on MR images and trained ensembles of CNNs. Their performance was compared to three registration-based methods: single-atlas, multi-atlas based on majority voting and Similarity and Truth Estimation for Propagated Segmentations (STEPS). Then, the automatic segmentations were quantitatively evaluated using six metrics: Dice score, Hausdorff distance, precision, recall, volume similarity and compactness using cross-validation. Our CNN and multi-atlas -based segmentations provided excellent results (Dice scores > 0.90) despite the presence of brain lesions, atrophy and ventricular enlargement. In contrast, the performance of singe-atlas registration was poor (Dice scores < 0.85). Unlike registration-based methods, which performed better in segmenting the contralateral than the ipsilateral hippocampus, our CNN-based method performed equally well bilaterally. Finally, we assessed the progression of hippocampal damage after TBI by applying our automated segmentation tool. Our data show that the presence of TBI, time after TBI, and whether the location of the hippocampus was ipsilateral or contralateral to the injury explained hippocampal volume (p=0.029, p< 0.001, and p< 0.001 respectively).


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