Literature DB >> 22964852

Blood-brain barrier permeability is positively correlated with cerebral microvascular perfusion in the early fluid percussion-injured brain of the rat.

Yong Lin1, Yaohua Pan, Mingliang Wang, Xianjian Huang, Yuhua Yin, Yu Wang, Feng Jia, Wenhao Xiong, Nu Zhang, Ji-yao Jiang.   

Abstract

The blood-brain barrier (BBB) opening following traumatic brain injury (TBI) provides a chance for therapeutic agents to cross the barrier, yet the reduction of the cerebral microvascular perfusion after TBI may limit the intervention. Meanwhile, optimizing the cerebral capillary perfusion by the strategies such as fluid administration may cause brain edema due to the BBB opening post trauma. To guide the TBI therapy, we characterized the relationship between the changes in the cerebral capillary perfusion and BBB permeability after TBI. First, we observed the changes of the cerebral capillary perfusion by the intracardiac perfusion of Evans Blue and the BBB disruption with magnetic resonance imaging (MRI) in the rat subjected to lateral fluid percussion (FP) brain injury. The correlation between two variables was next evaluated with the correlation analysis. Since related to BBB breakdown, matrix metalloproteinase-9 (MMP-9) activity was finally detected by gelatin zymography. We found that the ratios of the perfused microvessel numbers in the lesioned cortices were significantly reduced at 0 and 1 h post trauma compared with that in the normal cortex, which then dramatically recovered at 4 and 24 h after injury, and that the BBB permeability was greatly augmented in the ipsilateral parts at 4, 12, and 24 h, and in the contralateral area at 24 h after injury compared with that in the uninjured brain. The correlation analysis showed that the BBB permeability increase was related to the restoration of the cerebral capillary perfusion over a 24-h period post trauma. Moreover, the gelatin zymography analysis indicated that the MMP-9 activity in the injured brain increased at 4 h and significantly elevated at 12 and 24 h as compared to that at 0 or 1 h after TBI. Our findings demonstrate that the 4 h post trauma is a critical turning point during the development of TBI, and, importantly, the correlation analysis may guide us how to treat TBI.

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Year:  2012        PMID: 22964852     DOI: 10.1038/labinvest.2012.118

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  19 in total

1.  bFGF Protects Against Blood-Brain Barrier Damage Through Junction Protein Regulation via PI3K-Akt-Rac1 Pathway Following Traumatic Brain Injury.

Authors:  Zhou-Guang Wang; Yi Cheng; Xi-Chong Yu; Li-Bing Ye; Qing-Hai Xia; Noah R Johnson; Xiaojie Wei; Da-Qing Chen; Guodong Cao; Xiao-Bing Fu; Xiao-Kun Li; Hong-Yu Zhang; Jian Xiao
Journal:  Mol Neurobiol       Date:  2015-12-21       Impact factor: 5.590

2.  Genetic activation of mTORC1 signaling worsens neurocognitive outcome after traumatic brain injury.

Authors:  Natalia S Rozas; John B Redell; Julia L Hill; James McKenna; Anthony N Moore; Michael J Gambello; Pramod K Dash
Journal:  J Neurotrauma       Date:  2014-12-10       Impact factor: 5.269

3.  A flow cytometric approach to analyzing mature and progenitor endothelial cells following traumatic brain injury.

Authors:  Poincyane Assis-Nascimento; Oliver Umland; Maria L Cepero; Daniel J Liebl
Journal:  J Neurosci Methods       Date:  2016-02-06       Impact factor: 2.390

4.  Posttraumatic therapeutic hypothermia alters microglial and macrophage polarization toward a beneficial phenotype.

Authors:  Jessie S Truettner; Helen M Bramlett; W Dalton Dietrich
Journal:  J Cereb Blood Flow Metab       Date:  2016-01-01       Impact factor: 6.200

5.  Aconitine induces brain tissue damage by increasing the permeability of the cerebral blood-brain barrier and over-activating endoplasmic reticulum stress.

Authors:  Xiaojun Zhang; Xuheng Jiang; Anyong Yu; Haizhen Duan
Journal:  Am J Transl Res       Date:  2022-05-15       Impact factor: 3.940

6.  Changes in mouse cognition and hippocampal gene expression observed in a mild physical- and blast-traumatic brain injury.

Authors:  David Tweedie; Lital Rachmany; Vardit Rubovitch; Yongqing Zhang; Kevin G Becker; Evelyn Perez; Barry J Hoffer; Chaim G Pick; Nigel H Greig
Journal:  Neurobiol Dis       Date:  2013-02-27       Impact factor: 5.996

7.  Disruption of the blood-brain barrier in pigs naturally infected with Taenia solium, untreated and after anthelmintic treatment.

Authors:  Cristina Guerra-Giraldez; Miguel Marzal; Carla Cangalaya; Diana Balboa; Miguel Ángel Orrego; Adriana Paredes; Eloy Gonzales-Gustavson; Gianfranco Arroyo; Hector H García; Armando E González; Siddhartha Mahanty; Theodore E Nash
Journal:  Exp Parasitol       Date:  2013-05-15       Impact factor: 2.011

8.  Chronic global analysis of vascular permeability and cerebral blood flow after bone marrow stromal cell treatment of traumatic brain injury in the rat: A long-term MRI study.

Authors:  Lian Li; Michael Chopp; Guangliang Ding; Qingjiang Li; Asim Mahmood; Quan Jiang
Journal:  Brain Res       Date:  2017-09-09       Impact factor: 3.252

9.  Alterations in the Timing of Huperzine A Cerebral Pharmacodynamics in the Acute Traumatic Brain Injury Setting.

Authors:  Ugur Damar; Roman Gersner; Joshua T Johnstone; Kush Kapur; Stephen Collins; Steven Schachter; Alexander Rotenberg
Journal:  J Neurotrauma       Date:  2017-11-21       Impact factor: 5.269

10.  Blood-brainbarrier disruption dictates nanoparticle accumulation following experimental brain injury.

Authors:  Vimala N Bharadwaj; Rachel K Rowe; Jordan Harrison; Chen Wu; Trent R Anderson; Jonathan Lifshitz; P David Adelson; Vikram D Kodibagkar; Sarah E Stabenfeldt
Journal:  Nanomedicine       Date:  2018-06-19       Impact factor: 5.307

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