Emerging therapies in narcolepsy-cataplexy

被引:68
作者
Mignot, E
Nishino, S
机构
[1] Stanford Univ, Ctr Narcolepsy, Sch Med, Palo Alto, CA 94304 USA
[2] Stanford Univ, Howard Hughes Med Res Inst, Sch Med, Palo Alto, CA 94304 USA
关键词
treatment; narcolepsy; cataplexy;
D O I
10.1093/sleep/28.6.754
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In the past, narcolepsy was primarily treated using amphetannine-like stimulants and tricyclic antidepressants. Newer and novel agents, such as the wake-promoting compound modafinil and more selective reuptake inhibitors targeting the adrenergic, dopaminergic, and/or serotoninergic reuptake sites (ie, venlafaxine, atomoxetine) are better-tolerated available alternatives. The development of these agents, together with sodium oxybate (a slow-wave sleep-enhancing agent that consolidates nocturnal sleep, reduces cataplexy, and improves sleepiness), has led to improved functioning and quality of life for many patients with the disorder. However, these treatments are all symptomatically based and do not target hypocretin, a major neurotransmitter involved in the pathophysiology of narcolepsy. In this review, we discuss emerging therapies in the area of narcolepsy. These include novel antidepressant or anticataplectic, wake-promoting, and hypnotic compounds. We also report on novel strategies designed to compensate for hypocretin deficiency and on the use of immunosupression at the time of narcolepsy onset.
引用
收藏
页码:754 / 763
页数:10
相关论文
共 111 条
[1]  
[Anonymous], J SLEEP RES
[2]   Transplantation of hypocretin neurons into the pontine reticular formation:: Preliminary results [J].
Arias-Carriòn, O ;
Murillo-Rodriguez, E ;
Xu, M ;
Blanco-Centurion, C ;
Drucker-Colin, R ;
Shiromani, PJ .
SLEEP, 2004, 27 (08) :1465-1470
[3]   CSF hypocretin-1 (orexin-A) levels in childhood narcolepsy and neurologic disorders [J].
Arii, J ;
Kanbayashi, T ;
Tanabe, Y ;
Sawaishi, Y ;
Kimura, S ;
Watanabe, A ;
Mishima, K ;
Hishikawa, Y ;
Shimizu, T ;
Nishino, S .
NEUROLOGY, 2004, 63 (12) :2440-2442
[4]  
Arnulf I, 2004, SLEEP, V27, P1242
[5]   Development of an orexin-2 receptor selective agonist, [Ala11, D-Leu15]orexin-B [J].
Asahi, S ;
Egashira, SI ;
Matsuda, M ;
Iwaasa, H ;
Kanatani, A ;
Ohkubo, M ;
Ihara, M ;
Morishima, H .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (01) :111-113
[6]   Acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist [J].
Barbier, AJ ;
Berridge, C ;
Dugovic, C ;
Laposky, AD ;
Wilson, SJ ;
Boggs, J ;
Aluisio, L ;
Lord, B ;
Mazur, C ;
Pudiak, CM ;
Langlois, X ;
Xiao, W ;
Apodaca, R ;
Carruthers, NI ;
Lovenberg, TW .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 143 (05) :649-661
[7]  
Becker PM, 2000, NEUROLOGY, V54, P1166
[8]   DOV 216,3039 a 'Triple" reuptake inhibitor: Safety, tolerability, and pharmacokinetic profile [J].
Beer, B ;
Stark, J ;
Krieter, P ;
Czobor, P ;
Beer, G ;
Lippa, A ;
Skolnick, P .
JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 44 (12) :1360-1367
[9]   NEUROBIOLOGY - BETTER CELLS FOR BRAIN REPAIR [J].
BJORKLUND, A .
NATURE, 1993, 362 (6419) :414-415
[10]   The abrupt cessation of therapeutically administered sodium oxybate (GHB) does not cause withdrawal symptoms [J].
Black, J ;
Emsellem, H ;
Feldman, N ;
Hagaman, M ;
Hayduk, R ;
Kathawalla, S ;
Lankford, D ;
Marmion, L ;
Mitler, M ;
Pascualy, R ;
Sahota, P ;
Scharf, M ;
Scrima, L ;
Swick, T ;
Ware, J .
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY, 2003, 41 (02) :131-135