Expression of Heme-oxygenase 1 in the neonatal rat brain with hypoxic-ischemic encephalopathy.

缺氧缺血性脑病新生大鼠脑中血红素加氧酶 1 的表达

基本信息

  • 批准号:
    08671317
  • 负责人:
  • 金额:
    $ 1.34万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1996
  • 资助国家:
    日本
  • 起止时间:
    1996 至 1997
  • 项目状态:
    已结题

项目摘要

Heme-oxygenase 1 (HO-1) is a stress protein and a rate-limiting enzyme in heme degradation, generating carbon monoxide and bile pigment. To study the role of HO-1 in neonatal hypoxia-iachemia (HI), 1 week old wats were subjected to left carotid ligation and exposure to 8% O2/92% N2 for 2 hours.1.Expression of HO-1 in the neonatal rat brain after HIImmuno-histochemical staining revealed that HO-1 positive cells were rich in the CA3 region of hippocampus at 6 hours after HI loading. Western blot analysis showed increased HO-1 staining in the ipsilateral region including hipocampus and striatum at 12 hours upto 24hours after HI.The HO-1levels peaked at 12 hours, and were localized perifocally.2. Effect of HI on the expression of HO-1 mRNA in the neonatal rat brain.We studied HO-1 expression in the neonatal rat brain after HI by using Northern blot analysis, and found increased levels in the ischemic region at 6 hours after HI.Though the bilirubin produced by HO-1 may act as an antioxidant in many tissues, it may also be toxic to the neonatal brain.
血红素加氧酶 1 (HO-1) 是一种应激蛋白,也是血红素降解过程中的限速酶,可产生一氧化碳和胆色素。为了研究HO-1在新生大鼠缺氧缺血(HI)中的作用,对1周龄大鼠进行左颈动脉结扎,并置于8%O2/92%N2环境中2小时。 1.HII后新生大鼠脑内HO-1的表达免疫组织化学染色显示,HI负荷后6小时,海马CA3区HO-1阳性细胞丰富。 Western blot分析显示HI后12小时至24小时,同侧海马和纹状体HO-1染色增加。HO-1水平在12小时达到峰值,并集中于灶周。2. HI对新生大鼠脑中HO-1 mRNA表达的影响。我们通过Northern印迹分析研究了HI后新生大鼠脑中HO-1的表达,发现HI后6小时缺血区的水平升高。虽然HO-1产生的胆红素可能在许多组织中充当抗氧化剂,但它也可能对新生大鼠脑有毒。

项目成果

期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
高田哲: "新生児の低酸素性虚血性脳症" Journal of Clinical Rehabilitation. 7. 81-88 (1998)
Satoshi Takada:“新生儿缺氧缺血性脑病”《临床康复杂志》7. 81-88 (1998)。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Wada, H.: "Severe neonatal nemaline myopathy with delayed maturation of muscle." Brain Dev.18. 135-138 (1996)
Wada, H.:“严重的新生儿线状肌病,伴有肌肉成熟延迟。”
  • DOI:
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  • 影响因子:
    0
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TAKADA Satoshi其他文献

TAKADA Satoshi的其他文献

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{{ truncateString('TAKADA Satoshi', 18)}}的其他基金

THE AVAILABILITY OF THE OLFACTORY ENSHEATHING CELLS TRANSPLANTATION TO INJURED PERIPHERAL NERVE.
嗅觉鞘细胞移植到受损周围神经的可用性。
  • 批准号:
    20592378
  • 财政年份:
    2008
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of the balance assessment method for preschool and school aged children and its application to the children with developmental disorders
学龄前和学龄儿童平衡评估方法的建立及其在发育障碍儿童中的应用
  • 批准号:
    19591206
  • 财政年份:
    2007
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Mechanisms of behavioral disorders following neonatal Hypoxic Ischemic-Encephalopathy and effect of treatment with Caspase inhibitor
新生儿缺氧缺血性脑病行为障碍机制及Caspase抑制剂治疗效果
  • 批准号:
    15591156
  • 财政年份:
    2003
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Behavioral alterations following a hypoxic-ischemic brain injury in neonatal rats and the effects of treatment with caspase inhibitor.
新生大鼠缺氧缺血性脑损伤后的行为改变以及半胱天冬酶抑制剂治疗的效果。
  • 批准号:
    13671136
  • 财政年份:
    2001
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Effects of Caspase Inhibitor Administration against Hypoxic-Ischemic Brain Damage in Neonatal Rats.
半胱天冬酶抑制剂给药对新生大鼠缺氧缺血性脑损伤的影响。
  • 批准号:
    11671069
  • 财政年份:
    1999
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Das Legalitatsprinzip in Osterreich-Eine vergleichende Untersuchung
东欧国家的合法原则
  • 批准号:
    06620020
  • 财政年份:
    1994
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Expression of Mn-SOD gene in the neonatal rat with hypoxic-ischemic brain damage.
Mn-SOD基因在缺氧缺血性脑损伤新生大鼠中的表达
  • 批准号:
    06671168
  • 财政年份:
    1994
  • 资助金额:
    $ 1.34万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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