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Systemic and molecular analysis on the pathology of newly-developed myopathic chronic pain models

Systemic and molecular analysis on the pathology of newly-developed myopathic chronic pain models
新开发的肌病性慢性疼痛模型病理学的系统和分子分析
批准号:
18613020
负责人:
KUMAZAWA Takao
金额:
$2.6万
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:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007

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中文摘要
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英文摘要
In this study, two types of chronic pain animal models (myo-nociceptive model, cast-immobilization model) we had developed were used. The characteristics of these models are: 1) direct nerve injuries are not given; 2) bilateral wide-spread long-lasting pain behaviors are developed. The purpose of this study is to clarify the chronic pain mechanisms of these models.1. In the chronic pain phase of these models, the contralateral hyperalgesia in the hind-paw was not affected by the ipsilateral sciatic nerve block. This result suggests the implication of central plasticity.2. In the L4 dorsal horn of the cast-immobilization model, the microglias at the early phase after cast-removal and the astrocytes at the chronic pain phase had activated. When the paw hyperalgesia tend to attenuate, the activation of both types of spinal glial cells reduced. In the coccygeal cord, the microglial activation appeared in retard of that in the L4. The implication of spinal glial cells is suggested in this model. As the preliminary examination, IL-6 and BDNF mRNA expressions in spinal cord and muscles were determined by PCR.3. In the cast-immobilization model, the autonomic parameters (blood pressure, heart rate) were telemetrically recorded, The sympathetic activity was augmented during cast-immobilization period and then decreased below the normal level while persisting pain behavior continued. In the chronic pain condition, the autonomic reactivities to cold-exposure were higher than in normal. Autonomic dysfunction in the chronic pain patients (e.g. CRPS type-I) is reported, so this model may be a partial explanation for those pathogenic conditions.4. In the myo-nociceptive model, the treatment to young-age was not produced chronic pain behaviors. It is suggested any factors as a trigger to chronic pain may be immature.5. Both of the minocycline injection and the treadmill exercise tended to decrease pain behaviors, though reexamination should be required.
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会议论文
The change of the pain concept, the treatments.(in Japanese)
疼痛观念的转变、治疗方法。(日语)
DOI: --
发表时间: 2006
期刊: Management of Pain : The Approaches for Chronic Pain, Cancer Pain.(ed. Kumazawa T) Shorinsha, Tokyo
影响因子: --
作者: [橋本 辰幸, ら, Kumzawa T]
通讯作者: Kumzawa T
慢性的な痛みを起こす下肢不動化では自律系にも異常きたす
下肢固定会导致慢性疼痛,也会导致自主神经系统异常。
DOI: --
发表时间: 2008
期刊:
影响因子: --
作者: [吉本 隆彦, ら]
通讯作者:
筋障害による慢性痛症モデル動物における検討II:若齢時の処置では慢性痛症を発症しなかった
肌病慢性疼痛模型动物研究二:年轻时治疗不会引起慢性疼痛。
DOI: --
发表时间: 2006
期刊:
影响因子: --
作者: [櫻井 博紀, ら]
通讯作者:
痛みのケア : 慢性通、がん性疼痛へのアプローチ
疼痛护理:治疗慢性疼痛和癌痛的方法
DOI: --
发表时间: 2006
期刊:
影响因子: --
作者: [橋本 辰幸, ら, 熊澤孝朗]
通讯作者: 熊澤孝朗
67
    Development of nonstationary point process model of swarm activity for monitoring of volcanic activity and aseismic slip
    Analysis of nociceptive system in pathologic conditions
    • 批准号:
      07044318
    • 项目类别:
      Grant-in-Aid for International Scientific Research.
    • 资助金额:
      $0.0万
    • 财政年份:
      1995
    • 负责人:
      KUMAZAWA Takao
    • 依托单位:
    Analysis of nociceptive system in pathologic conditions
    • 批准号:
      06044255
    • 项目类别:
      Grant-in-Aid for Overseas Scientific Survey.
    • 资助金额:
      $0.0万
    • 财政年份:
      1994
    • 负责人:
      KUMAZAWA Takao
    • 依托单位:
    Physiological and Morphological Studies on Characteristics of Nociceptive Primary Afferent Neurons (Polymodal Receptors).
    • 批准号:
      01480122
    • 项目类别:
      Grant-in-Aid for General Scientific Research (B)
    • 资助金额:
      $3.84万
    • 财政年份:
      1989
    • 负责人:
      KUMAZAWA Takao
    • 依托单位:
    海外基金