Neural actions of immunophilin ligands

被引:174
作者
Snyder, SH
Sabatini, DM
Lai, MM
Steiner, JP
Hamilton, GS
Suzdak, PD
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[2] Guilford Pharmaceut, Baltimore, MD 21224 USA
关键词
D O I
10.1016/S0165-6147(97)01146-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Immunophilins, protein receptors for immunosuppressant drugs such as cyclosporin A and FK506, are enriched far more in the brain than in the immune system. Drug-immunophilin complexes bind to calcineurin, inhibiting its phosphatase activity and leading to immunosuppressant effects. The immunophilin FKBP-12 (FK506 binding protein, 12 kDa) forms a complex with the ryanodine and inositol (1,4,5) trisphosphate (IP3) receptors to regulate their physiological release of intracellular Ca2+. Here, Solomon Snyder and colleagues describe how non-immunosuppressant as well as immunosuppressant immunophilin ligands are neurotrophic for numerous classes of damaged neurones, both in culture systems and intact animals. Their ability to stimulate functional regrowth of damaged sciatic, cortical cholinergic, dopamine and 5-HT neurones may have therapeutic relevance.
引用
收藏
页码:21 / 26
页数:6
相关论文
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