LY248686, A NEW INHIBITOR OF SEROTONIN AND NOREPINEPHRINE UPTAKE

被引:199
作者
WONG, DT
BYMASTER, FP
MAYLE, DA
REID, LR
KRUSHINSKI, JH
ROBERTSON, DW
机构
[1] Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN
关键词
UPTAKE; INHIBITOR; SEROTONIN; NOREPINEPHRINE;
D O I
10.1038/npp.1993.4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
LY248686 is an inhibitor of serotonin (5-hydroxytryptamine; 5-HT) and norepinephrine (NE) uptake in synaptosomal preparations of hypothalamus and cerebral cortex, and 5-HT uptake in human blood platelets, with inhibitor constants near nanomolar concentrations. Upon administration to rats 1 hour before sacrifice, LY248686 caused dose-dependent and parallel decreases of 5-HT and NE uptake in hypothalamus homogenates ex vivo. LY248686 is a positive enantiomer and was slightly more potent than its negative isomer, LY248685, as an inhibitor of 5-HT uptake. Both isomers were only weak inhibitors of dopamine (DA) uptake in striatal synaptosomes. The inhibitory effects on 5-HT and NE uptake after a single administration of LY248686 followed similar time courses and simultaneously persisted for as long as 6 hours. LY248686 in vivo could effectively antagonize the p-chloroamphetamine-induced decreases of 5-HT uptake and levels of 5-HT and 5-hydroxyindoleacetic acid in cerebral cortex, and block the accumulation of C-14-NE in rat hearts. In food deprived rats, LY248686 suppressed food intake synergistically with 5-hydroxytryptophan, a precursor amino acid of 5-HT. Because of its lack of affinity for receptors of 5-HT, NE, DA, acetylcholine, histamine and naloxone, and its ability to inhibit 5-HT and NE uptake simultaneously, LY248686 has a favorable pharmacological profile as a potential antidepressant drug.
引用
收藏
页码:23 / 33
页数:11
相关论文
共 54 条
[1]   DEVELOPMENT OF BETA-ADRENERGIC-RECEPTOR SUBSENSITIVITY BY ANTIDEPRESSANTS [J].
BANERJEE, SP ;
KUNG, LS ;
RIGGI, SJ ;
CHANDA, SK .
NATURE, 1977, 268 (5619) :455-456
[2]  
BEASLEY CM, 1990, PSYCHOPHARMACOL BULL, V26, P18
[3]   FLUOXETINE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES, AND THERAPEUTIC EFFICACY IN DEPRESSIVE-ILLNESS [J].
BENFIELD, P ;
HEEL, RC ;
LEWIS, SP .
DRUGS, 1986, 32 (06) :481-508
[4]  
BERGSTROM DA, 1977, NATURE, V268, P455
[5]  
BLUNDELL JE, 1977, INT J OBESITY, V1, P15
[6]   DOWN-REGULATION OF BETA-ADRENERGIC RECEPTORS FOLLOWING REPEATED INJECTIONS OF DESMETHYLIMIPRAMINE - PERMISSIVE ROLE OF SEROTONERGIC AXONS [J].
BRUNELLO, N ;
BARBACCIA, ML ;
CHUANG, DM ;
COSTA, E .
NEUROPHARMACOLOGY, 1982, 21 (11) :1145-1149
[7]  
CHENG Y, 1973, BIOCHEM PHARMACOL, V22, P3099
[8]   AN EARLY PHASE-II CLINICAL-TRIAL OF TOMOXETINE (LY139603) IN THE TREATMENT OF NEWLY ADMITTED DEPRESSED-PATIENTS [J].
CHOUINARD, G ;
ANNABLE, L ;
BRADWEJN, J .
PSYCHOPHARMACOLOGY, 1984, 83 (01) :126-128
[9]   ASPECTS OF AMITRIPTYLINE AND NORTRIPTYLINE PLASMA-LEVELS MONITORING IN DEPRESSION [J].
CORONA, GL ;
CUCCHI, ML ;
FRATTINI, P ;
SANTAGOSTINO, G ;
SCHINELLI, S ;
ZERBI, F ;
SAVOLDI, F .
PSYCHOPHARMACOLOGY, 1990, 100 (03) :334-338
[10]   DIFFERENTIAL SELECTIVITIES OF RU-24969 AND 8-OH-DPAT FOR THE PURPORTED 5-HT1A AND 5-HT1B BINDING-SITES - CORRELATION BETWEEN 5-HT1A AFFINITY AND HYPOTENSIVE ACTIVITY [J].
DOODS, HN ;
KALKMAN, HO ;
DEJONGE, A ;
THOOLEN, MJMC ;
WILFFERT, B ;
TIMMERMANS, PBMWM ;
VANZWIETEN, PA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1985, 112 (03) :363-370