Medical Hypotheses
Volume 73, Issue 6 , Pages 994-995, December 2009

Anti-protein aggregation is a potential target for preventing delayed neuronal death after transient ischemia

  • Pengfei Ge

      Affiliations

    • Department of Neurosurgery, Xuanwu hospital, Capital Univeristy of Medical Science, 45 Changchun Street, Beijing 100053, PR China
    • Department of Neurosurgery, 1st Hospital of Jilin University, 71 Xinmin Street, Changchun 130021, PR China
    • Contributed equally to this work.
  • ,
  • Yinan Luo

      Affiliations

    • Department of Neurosurgery, 1st Hospital of Jilin University, 71 Xinmin Street, Changchun 130021, PR China
    • Contributed equally to this work.
  • ,
  • Haifeng Wang

      Affiliations

    • Department of Neurosurgery, 1st Hospital of Jilin University, 71 Xinmin Street, Changchun 130021, PR China
  • ,
  • Feng Ling

      Affiliations

    • Department of Neurosurgery, Xuanwu hospital, Capital Univeristy of Medical Science, 45 Changchun Street, Beijing 100053, PR China
    • Corresponding Author InformationCorresponding author. Tel.: +86 10 15001056267.

Received 11 October 2008; accepted 23 October 2008. published online 29 June 2009.

Summary 

Brain ischemia has been an important risk factor for human being health, there is no effective medicine can be used to protect delayed neuronal injury or death secondary to blood reperfusion following ischemia. Recent discovery shows protein aggregation is an important factor resulting in ischemia-induced neuron death. Therefore, we propose the hypothesis that inhibiting protein aggregation may be an effective way to prevent delayed neuronal death after transient ischemia. At present, in vitro studies show some chemicals such as 4PBA (sodium 4-phenylbutyrate) and trehalose have the features of antagonizing protein aggregation in vitro. Moreover, polyQ-binding peptide (QBP1), geldanamycin, amino acids and amino acid derivatives have been also used in vitro to decrease aggregation and to increase protein stability. Although in vivo and systematical study should be performed to evaluate their effects of anti-protein aggregation, this enlightening us on using them to protect ischemic-induced neuronal death, and find new potential chemicals or methods which could be effective in keeping protein stable and prevent forming aggregates.

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PII: S0306-9877(09)00383-1

doi:10.1016/j.mehy.2008.10.041

Medical Hypotheses
Volume 73, Issue 6 , Pages 994-995, December 2009