Therapeutic strategies for the inhibition of inducible nitric oxide synthase - Potential for a novel class of anti-inflammatory agents

被引:40
作者
Pfeilschifter, J
Eberhardt, W
Hummel, R
Kunz, D
Muhl, H
Nitsch, D
Pluss, C
Walker, G
机构
[1] Department of Pharmacology, Biozentrum, University of Basel, CH-4056 Basel
关键词
nitric oxide; nitric oxide synthases; glucocorticoids; cyclosporin; nuclear factor KB; tetrahydrobiopterin; L-arginine;
D O I
10.1006/cbir.1996.0008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In recent years, NO, a gas previously considered a potentially toxic chemical, has become established as a diffusible universal messenger mediating cell-cell communication throughout the body. In mammals, NO is a recognized mediator of blood vessel relaxation that helps to maintain blood pressure. In the central nervous system NO acts as a non-conventional neurotransmitter and participates in the establishment of long-term plasticity required for memory formation. In addition, NO is responsible for some parts of the host response to sepsis and inflammation and contributes to certain disease states. A number of strategies have emerged with regard to a pharmacological control of pathological NO overproductions. This review will discuss these novel therapeutic approaches that may provide new means for clinical medicine. (C) 1996 Academic Press Limited
引用
收藏
页码:51 / 58
页数:8
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