4.3 Article Proceedings Paper

The mitochondrial permeability transition as a target for neuroprotection

期刊

JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
卷 36, 期 4, 页码 309-312

出版社

KLUWER ACADEMIC/PLENUM PUBL
DOI: 10.1023/B:JOBB.0000041759.35731.70

关键词

mitochondria; permeability transition; neuroprotection; apoptosis; oxidants; zinc; aldehydes; Huntington's disease

资金

  1. NINDS NIH HHS [R01 NS038741] Funding Source: Medline

向作者/读者索取更多资源

Mitochondria serve as checkpoints and amplifiers on cell death pathways. In the central nervous system, mitochondrial involvement seems essential for normal expression of cell death phenotypes, and interference with these pathways thus seems a reasonable approach to neuroprotection. We have been involved in examining the potential involvement of the mitochondrial permeability transition (mPT) as one of several possible mechanisms by which mitochondria may be drawn into these death cascades. This possibility, though still controversial, is supported by evidence that factors that may stimulate mPT induction are associated with some forms of cell death (e.g., in stroke) and are modulated by diseases of the central nervous system (e.g., Huntington's). Evidence of neuroprotection seen with compounds such as N-Met-Val cyclosporine also support this possibility.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据