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      Cerebrospinal fluid high mobility group box 1 is associated with neuronal death in subarachnoid hemorrhage

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          Abstract

          We aim to determine the cerebrospinal fluid levels of high mobility group box 1 in subarachnoid hemorrhage patients and to investigate the involvement of the receptor for advanced glycation end products and high mobility group box 1 in the pathogenesis of post-subarachnoid hemorrhage neuronal death. The study included 40 patients (mean age, 59 ± 19 years) with Fisher's grade ≥ III aneurysmal subarachnoid hemorrhage. Cerebrospinal fluid was collected on the seventh day post-hemorrhage. Receptor for advanced glycation end products expression was examined in rat brain tissue following subarachnoid hemorrhage and in cultured neurons exposed to post-subarachnoid hemorrhage cerebrospinal fluid. Therapeutic effects of the recombinant soluble form of RAGE on subarachnoid hemorrhage models were also investigated. The results indicated that a higher level of cerebrospinal fluid high mobility group box 1 was independently associated with unfavorable outcome at three months post-subarachnoid hemorrhage (OR = 1.061, 95% CI: 1.005–1.121). Expression of RAGE increased in post-subarachnoid hemorrhage rat brain cells and in cultured neuron with stimulation of post-subarachnoid hemorrhage cerebrospinal fluid. Administration of recombinant soluble form of RAGE significantly reduced the number of positive TUNEL staining cells in subarachnoid hemorrhage rat and improved cell viability in post-subarachnoid hemorrhage cerebrospinal fluid-treated cultured neurons. Thus, the level of cerebrospinal fluid high mobility group box 1 can be a prognostic indicator for patients with Fisher's grade ≥ III aneurysmal subarachnoid hemorrhage and that treatment with soluble form of RAGE is a novel approach for subarachnoid hemorrhage.

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          Author and article information

          Journal
          J Cereb Blood Flow Metab
          J. Cereb. Blood Flow Metab
          JCB
          spjcb
          Journal of Cerebral Blood Flow & Metabolism
          SAGE Publications (Sage UK: London, England )
          0271-678X
          1559-7016
          28 January 2016
          February 2017
          : 37
          : 2
          : 435-443
          Affiliations
          [1 ]Division of Neurosurgery, Department of Surgery, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
          [2 ]Department of Neurology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
          [3 ]Department of Neurology, Taipei Medical University-Wan Fang Hospital, Taipei, Taiwan
          [4 ]Department and Graduate Institute of Forensic Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan
          [5 ]Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan
          [6 ]Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
          [7 ]Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University Taipei, Taiwan
          [8 ]Department of Physiology, Yong Loo Lin School Medicine, National University of Singapore, Singapore
          Author notes
          [*]Sung-Chun Tang, Stroke center and Department of Neurology, National Taiwan University Hospital, No. 7 Chun-Shang South Road, Taipei 100, Taiwan. Email: sctang@ 123456ntuh.gov.tw
          Article
          PMC5381442 PMC5381442 5381442 10.1177_0271678X16629484
          10.1177/0271678X16629484
          5381442
          26823474
          0cb5031b-022f-462b-83ac-df7cb5776f01
          © The Author(s) 2016
          History
          : 9 October 2015
          : 24 November 2015
          : 28 December 2015
          Categories
          Original Articles

          Cell death mechanisms,inflammation,receptors,subarachnoid hemorrhage,cerebrospinal fluid

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