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2001 Fiscal Year Final Research Report Summary

Elucidation of the mechanisms of cross-talk between the neurological, endocrine, and immune systems in the biological response to physical insults

Research Project

Project/Area Number 10557111
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field General surgery
Research InstitutionOsaka University

Principal Investigator

SUGIMOTO Hisashi  Graduate School of Medicine, Osaka University, Professor, 医学研究科, 教授 (90127241)

Co-Investigator(Kenkyū-buntansha) KUWAGATA Yasuyuki  Graduate School of Medicine, Osaka University, Research Assistant, 医学研究科, 助手 (50273678)
TANAKA Hiroshi  Graduate School of Medicine, Osaka University, Associate Professor, 医学研究科, 助教授 (90252676)
SHIMAZU Takeshi  Graduate School of Medicine, Osaka University, Associate Professor, 医学研究科, 助教授 (50196474)
SHIOZAKI Tadahiko  Graduate School of Medicine, Osaka University, Research Assistant, 医学研究科, 助手 (60278687)
OGURA Hiroshi  Graduate School of Medicine, Osaka University, Research Assistant, 医学研究科, 助手 (70301265)
Project Period (FY) 1998 – 2000
Keywordscentral nervous system / endocrine system / immune system / insult / neutrophil function / cytokine / NF-κB / ADH
Research Abstract

The central nervous system (CNS), endocrine system and immune system closely affect each other in the organismal response to insult and injury, however, the main role is known to be taken by the CNS. In this study, we focus on the following four areas : (1) the alteration in endogeneous cytokine balance and neutrophil function in response to insults ; (2) the balance between pro- and anti-inflammatory responses ; (3) the role of peripheral leucocytes on ectopic antidiuretic hormone (ADH) in brain-dead patients ; and (4) the effect of mildhypothermia in patients with severely brain injury.
(1) In patients with CNS injury, acute pathologies such as increased blood levels of pro-inflammatory cytokines, enhanced leukocyte function, and apoptosis suppression were observed, suggesting that inflammatory responses are predominant in living organisms in such events. In contrast, in patients without CNS injury, the increase in blood levels of anti-inflammatory cytokines and inflammatory cytokine … More inhibitors revealed an organismal response to physical insult that was shifted towards an anti-inflammatory state, suggesting reduced immunocompetence or increased susceptibility to infection at the time of CNS injury. However, for brain-dead patients, the organismal CNS regulation disappeared, indicating an activation of inflammatory response.
(2) In an acute pathological condition, the nuclear NF-κB level in neutrophils increased significantly, indicating a predominantly pro-inflammatory state in which the leucocytes were activated. In patients with trauma and sepsis, the heat shock protein (HSP) expression level was enhanced, suggesting a crucial role for HSPs in functional changes of leucocytes. In contrast, the increased susceptibility to infection at the time of CNS injury suggests a role for the reduction in HSP60 in functional alteration.
(3) We examined ADH secretion in the blood of patients after brain-death using PCR to measure gene expression in peripheral leucocytes and confirmed that ADH gene expression is induced within leucocytes. This result suggests that the leucocytes which govern the immune functions may also play a role in hormonal secretion disorders in organs.
(4) We induced mildhypothermia to the patients with severe head injury. The results demonstrate that mildhypothermia is effective for decreasing problematic elevated intracranial pressure. In contrast, in patients with severe head injury who did not have higher intracranial pressure (<25 mmHg), mildhypothermia increased the complication rates, without showing any favorable effect on prognosis. Less

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Shiozaki T: "Delayed hemispheric meuronal loss in severely head-injured patients"J Neurotrauma. 18. 665-674 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hashiguchi N: "Enhanced expression of heat shock proteins in leukocytes from trauma patients"J Trauma. 50. 102-107 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ogura H: "Activated platelets enhance microparticle formation and platelet-leukocyte interaction in severe trauma and sepsis"J Trauma. 50. 801-807 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hashiguchi N: "Enhanced expression of heat shock proteins in activated polymorphonuclear leukocytes in patients with sepsis"J Trauma. (in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tanaka H: "Granulocyte colony-stimulating factor (G-CSF) stiffens leukocytes but attenuates inflammatory response without lung injury in septic patients"J Trauma. (in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Aoki M: "Hypothermic treatment restores glucose regulated protein 78 (GRP 78) expession in ischemic brain"Mol. Brain Res.. (in press).

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shiozaki T: "Delayed hemispheric neuronal loss in severely head-injured patients"J Neurotrauma. 18. 665-674 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hashiguchi N: "Enhanced expression of heat shock proteins in leukocytes from trauma patients"J Trauma. 50. 102-107 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ogura H: "Activated platelets enhance microparticle formation and platelet-leukocyte interaction in severe trauma and sepsis"J Trauma. 50. 801-807 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hashiguchi N: "Enhanced expression of heat shock proteins in activated polymorphonuclear leukocytes in patients with sepsis"J Trauma. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tanaka H: "Granulocyte colony-stimulating factor (G-CSF) stiffens leukocytes but attenuates inflammatory response without lung injury in septic patients"J Trauma. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Aoki M: "Hypothermic treatment restores glucose regulated protein 78 (GRP 78) expression in ischemic brain"Mol Brain Res. (in press).

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2003-09-17  

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