共 202 条
Drugs to interfere with orexins (hypocretins)
被引:6
作者:

Selbach, O
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机构:
Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany

Eriksson, KS
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Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany

Haas, HL
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机构:
Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany
机构:
[1] Univ Dusseldorf, Dept Neurophysiol, D-40001 Dusseldorf, Germany
关键词:
D O I:
10.1358/dnp.2003.16.10.829298
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Orexins (hypocretins) are bioactive peptides linking arousal, appetite and neuroendocrine-autonomic control. Dysfunction of the orexin system is associated with narcolepsy-cataplexy. Here, we review drugs interfering with orexins directly such as novel selective orexin receptor agonists and antagonists, as well as drugs interfering with orexins indirectly such as those used for the treatment of narcolepsy-cataplexy, and pharmacological targets within the complex network of endogenous neurohumoral signals integrated and relayed by the orexin system. These include amines, acetylcholine, purines, GABA and glutamate, as well as nutritional-metabolic, circadian-photic, immunological and neuroendocrine-peptidergic influences. Basic and clinical evaluation of drugs interfering with the orexin system will lead to a better understanding of the molecular prerequisites that control behavioral state, stress responses, energy homeostasis and survival, and yield therapeutic advances for the treatment of narcolepsy and other disorders of sleep, eating, mood and memory. (C) 2003 Prous Science. All rights reserved.
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页码:669 / 681
页数:13
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