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神经元再生:抑郁症治疗的新策略 被引量:18

Neurogenesis: A Novel Strategy for the Treatment of Depression
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摘要 成年哺乳动物一生中,海马等脑区神经元是可以再生的, 而海马脑区神经元再生的减少和增多分别是抑郁症发生和恢复的重要因素。如果神经元再生过程被抑制,在抑郁症的动物模型上抗抑郁剂将会失去其行为学效应。长期给予不同种类的抗抑郁剂可以显著地促进动物海马神经元再生。随着对神经元再生调节机制研究的不断深入,为进一步探讨抑郁症的发生机制,以及发展新型抗抑郁治疗药物提供了新的思路与视角。 It is now generally accepted that the birth of new neurons occurs in brain areas such as hippocampus throughout the lifespan. The waning and waxing of neurogenesis in hippocampus is proposed as a key factor in the decent into and recovery from depression. If hippocampal neurogenesis was blocked, antidepressant would lose its behavioral effects in behavioral models of depression. Long-term, but not short-term, treatment with different classes of antidepressant could stimulate neurogenesis in the hippocampus remarkably. As the regulation of adult neurogenesis continues to be identified, it will provide novel avenues of studying the mechanism and developing pharmacological agents for depressive disorder.
出处 《生理科学进展》 CAS CSCD 北大核心 2005年第2期109-112,共4页 Progress in Physiological Sciences
基金 国家自然科学基金资助课题(30300419) 北京市自然科学基金资助课题(7042052)
关键词 神经元再生 应激 抑郁症 海马 Neurogenesis Stress Depression Hippocampus
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参考文献19

  • 1Malberg JE, Eisch AJ , Nestler EJ, et al. Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus. J Neurosci. 2000,20:9104~9110.
  • 2Kempermann G. Regulation of adult hippocampal neurogenesis - implications for novel theories of major depression. Bipolar Disord, 2002,4:17~33.
  • 3Duman RS, Malberg JE, Nakagawa S, et al. Regulation of adult neurogenesis by psychotropic drugs and stress. J Pharmacol Exp Ther, 2001,299:401~407.
  • 4Benninghoff J, Schmitt A, Mossner R, et al. When cells become depressed: focus on neural stem cells in novel treatment strategies against depression. J Neural Transm, 2002,109:947~962.
  • 5Garcia R. Stress, metaplasticity, and antidepressants. Curr Mol Med, 2002,2:629~638.
  • 6Sapolsky RM. Glucocorticoids and hippocampal atrophy in neuropsychiatric disorders. Arch Gen Psychiatry, 2000,57:925~935.
  • 7Barinaga M. Newborn neurons search for meaning. Science, 2003,299:32~34.
  • 8Jacobs BL. Adult brain neurogenesis and depression. Brain Behav Immun, 2002,16:602~609.
  • 9Lee AL, Ogle WO, Sapolsky RM. Stress and depression: possible links to neuron death in the hippocampus. Bipolar Disord, 2002, 4:117~128.
  • 10李云峰 罗质璞.抑郁症发病机制及治疗药物[A].见:朱兴族罗质璞.神经药理学新论[C].北京:人民卫生出版社,2004.1-20.

二级参考文献10

  • 1[1]Garcia R. Stress, metaplasticity, and antidepressants. Curr Mol Med, 2002; 2(7):629~38
  • 2[2]Lee AL, Ogle WO, Sapolsky RM. Stress and depression:Possible links to neuron death in the hippocampus. Bipolar Disord, 2002;4(2):117~28
  • 3[3]Sapolsky RM. Glucocorticoids and hippocampal atrophy in neuropsychiatric disorders. Arch Gen Psychiatry, 2000;57(10):925~35
  • 4[4]McEwen BS, Magarinos AM. Stress and hippocampal plasticity:Implications for the pathophysiology of affective disorders. Hum Psychopharmacol, 2001;16(S1):S7~19
  • 5[5]Barinaga M. Newborn neurons search for meaning. Science, 2003;299(5603):32~4
  • 6[6]Jacobs BL. Adult brain neurogenesis and depression. Brain Behav Immun, 2002;16(5):602~9
  • 7[7]Kempermann G. Regulation of adult hippocampal neurogenesis-implications for novel theories of major depression. Bipolar Disord, 2002;4(1):17~33
  • 8[8]Gould E, Tanapat P. Stress and hippocampal neurogenesis. Biol Psychiatry, 1999;46(11):1472~9
  • 9[9]Li YF, Liu YQ, Huang WC, Luo ZP. Cytoprotective effect is one of the common action pathways for antidepressants. Acta Pharmacol Sin, 2003;24(10):996~1000
  • 10[10]Li YF, Luo ZP. Antistress effect of oligosaccharides extracted from Morinda officinalis in mice and rats. Acta Pharmacol Sin, 2001;22(12):1084~8

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