Neuroscientific Investigation of the Pathophysiology of Mood Disorder and Suicide Behavior

情绪障碍和自杀行为病理生理学的神经科学研究

基本信息

  • 批准号:
    11470200
  • 负责人:
  • 金额:
    $ 9.6万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 财政年份:
    1999
  • 资助国家:
    日本
  • 起止时间:
    1999 至 2001
  • 项目状态:
    已结题

项目摘要

We have investigated disorder-specific pathophysiology of mood disorder, including suicide behavior, by using ^<18>F-FDG-Positron Emission Tomography (PET) and combined endocrinological examination of dexamethasone (DEX) and corticotropin-releasing hormone (CRH). Drug-naive 24 patients with major depression and 10 patients who were investigated by brain imaging analysis and neuroendocrinological examination at pre-treatment and at post-treatment when they were well responded to antidepressant treatment, are included in this study. 75 % of 24 mood disorder patients were non-suppressor in DEX/CRH examination, who have had more frequently the past history of suicide attempt than suppressor. After recovery from depression, most of non-suppressors were changed to suppressors, but 20 % of mood disorders were still non-suppressor, suggesting that some parts of non-suppressor are trait marker of mood disorder or susceptive factor of mood disorder.On the other hand, ^<18>F-FDG-PET study has reveal that left pre-frontal cortex and right superior temporal gyrus of mood disorder patients are significantly decreased to take up ^<18>F-FDG than healthy controls, whereas para-hippocampal gyrus is increased in ^<18>F-FDG intake. These pathological alterations during depressive phase were normalized after recovery from depression, except right superior temporal gyrus. In addition, SPM analysis has clearly demonstrated that ^<18>F-FDG intake into right para-hippocampal gyrus was smaller in non-suppressor than in suppressor. Further studies are needed to clarify the histological alterations in left pre-frontal cortex, right superior temporal gyrus, and right para-hippocampal gyrus from postmortem brain of mood disorder.
我们通过使用^<18 b> f - fdg -正电子发射断层扫描(PET)和地塞米松(DEX)和促肾上腺皮质激素释放激素(CRH)的联合内分泌检查,研究了包括自杀行为在内的情绪障碍的疾病特异性病理生理学。本研究纳入24例未接受药物治疗的重度抑郁症患者和10例在治疗前和治疗后经脑成像分析和神经内分泌检查对抗抑郁药物治疗有良好反应的患者。24例情绪障碍患者中75%的DEX/CRH检查为非抑制性,既往有自杀企图史者多于抑制性者。抑郁症康复后,大部分非抑制性基因转化为抑制性基因,但20%的情绪障碍患者仍为非抑制性基因,提示部分非抑制性基因是情绪障碍的特质标志或情绪障碍的易感因素。另一方面,^<18 b> F-FDG- pet研究显示,情绪障碍患者左侧前额叶皮层和右侧颞上回摄取^<18>F-FDG的量明显低于健康对照组,而海马旁回摄取^<18>F-FDG的量明显增加。抑郁症恢复后,除右侧颞上回外,其余病理改变均恢复正常。此外,SPM分析清楚地表明,非抑制组的右侧海马旁回的F-FDG摄入量小于抑制组。心境障碍患者死后大脑左前额叶皮层、右颞上回和右海马旁回的组织学改变尚需进一步研究。

项目成果

期刊论文数量(36)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Ikemoto K, Nishimura A, Okado N, Mikuni M, Nishi K, Nagatsu I: "Human midbrain dopamine neurons express serotonin 2A receptor : an immunohistochemical demonstration"Brain Research. 853. 377-380 (2000)
Ikemoto K、Nishimura A、Okado N、Mikuni M、Nishi K、Nagatsu I:“人类中脑多巴胺神经元表达血清素 2A 受体:免疫组织化学演示”大脑研究。
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    0
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福田正人, 三國雅彦他: "近赤外線巣ペクトロスポピーによる脳機能イメージング"臨床精神医学. 30. 937-951 (2001)
Masato Fukuda、Masahiko Mikuni 等人:“使用近红外光谱进行脑功能成像”临床精神病学 30. 937-951 (2001)
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    0
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Inoue T, Shibasaki T, Oriuchi N, Aoyagi K, Tomiyoshi K, Amano S, Mikuni M, Ida I, Endo K: "18F-α-methyl tyrosine PET studies in patients with brain tumors"J Nuclear Medicine. 40. 399-405 (1999)
Inoue T、Shibasaki T、Oriuchi N、Aoyagi K、Tomiyoshi K、Amano S、Mikuni M、Ida I、Endo K:“脑肿瘤患者的 18F-α-甲基酪氨酸 PET 研究”J 核医学 40。 399-。 405 (1999)
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    0
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三國雅彦: "セロトニン選択的再取り込み阻害薬"心療内科. 3. 147-152 (1999)
Masahiko Mikuni:“血清素选择性再摄取抑制剂”心身医学。 3. 147-152 (1999)
  • DOI:
  • 发表时间:
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  • 影响因子:
    0
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三國雅彦: "「感情障害(躁うつ病)」生物学的アプローチによる精神科ケア"南光堂(印刷中). (1999)
Masahiko Mikuni:“使用生物学方法治疗‘情感障碍(躁狂抑郁症)’的精神科护理”Nankodo(正在出版)(1999 年)。
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    0
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MIKUNI Masahiko其他文献

MIKUNI Masahiko的其他文献

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{{ truncateString('MIKUNI Masahiko', 18)}}的其他基金

Neuropathological studies on the vulnerability to mood disorders and refractoriness to antidepressant treatment.
关于情绪障碍易感性和抗抑郁治疗无效的神经病理学研究。
  • 批准号:
    14570909
  • 财政年份:
    2002
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
What kind of neural circuit in the brain of prenatally stressed offspring may be responsible to the vulnerabill to chronic stress in adulthood
产前应激后代大脑中的哪种神经回路可能导致其成年后容易遭受慢性应激
  • 批准号:
    09670975
  • 财政年份:
    1997
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Strategies for the study of the disinhibition of Hypothalamic-Pituitary-Adrenal axis in affective disorders, using prenatal stress model.
使用产前应激模型研究情感障碍中下丘脑-垂体-肾上腺轴去抑制的策略。
  • 批准号:
    06670994
  • 财政年份:
    1994
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
Molecular Pharmacological Study on the Dysfunction of 5-HT-2 receptor-stimulated Transduction Signaling in Depression.
抑郁症中 5-HT-2 受体刺激转导信号功能障碍的分子药理学研究。
  • 批准号:
    03454295
  • 财政年份:
    1991
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Hyperresponsiveness of 5-HT-2 Receptor-Mediated Intracellular Camobilization in Platelets from the Depressed Patients and in C6 Glioma Cells Pretreated with Dexamethasone.
抑郁症患者血小板和地塞米松预处理的 C6 胶质瘤细胞中 5-HT-2 受体介导的细胞内固定化的高反应性。
  • 批准号:
    01570621
  • 财政年份:
    1989
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
Study on the function of monoamine receptors and transmembrane signal control in the affective disorders.
情感障碍中单胺受体功能和跨膜信号控制的研究。
  • 批准号:
    62570482
  • 财政年份:
    1987
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
Mechanism of Action of Various Psychotropic Agents on Monoaminergic Receptors and Transmembrane signal Control.
各种精神药物对单胺能受体的作用机制和跨膜信号控制。
  • 批准号:
    60570490
  • 财政年份:
    1985
  • 资助金额:
    $ 9.6万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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