Potential involvement of serotonergic signaling in ketamine's antidepressant actions: A critical review

被引:43
作者
du Jardin, Kristian Gaarn [1 ]
Mueller, Heidi Kaastrup [1 ]
Elfving, Betina [1 ]
Dale, Elena [2 ]
Wegener, Gregers [1 ,3 ]
Sanchez, Connie [1 ,2 ]
机构
[1] Aarhus Univ, Dept Clin Med, Translat Neuropsychiat Unit, Skovagervej 2, DK-8240 Risskov, Denmark
[2] Lundbeck US LLC, 215 Coll Rd, Paramus, NJ 07652 USA
[3] North West Univ, Sch Pharm Pharmacol, 11 Hoffman St, ZA-2531 Potchefstroom, South Africa
关键词
Ketamine; Serotonin; Antidepressant; Glutamate; Pharmacology; METHYL-D-ASPARTATE; NMDA RECEPTOR BLOCKADE; NICOTINIC ACETYLCHOLINE-RECEPTORS; DEPRESSIVE-LIKE BEHAVIOR; RAT PREFRONTAL CORTEX; 5-HT3; RECEPTOR; PYRAMIDAL NEURONS; DOUBLE-BLIND; IN-VIVO; GABAERGIC TRANSMISSION;
D O I
10.1016/j.pnpbp.2016.05.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A single i.v. infusion of ketamine, classified as an N-methyl-D-aspartate (NMDA) receptor antagonist, may alleviate depressive symptoms within hours of administration in treatment resistant depressed patients, and the antidepressant effect may last for several weeks. These unique therapeutic properties have prompted researchers to explore the mechanisms mediating the antidepressant effects of ketamine, but despite many efforts, no consensus on its antidepressant mechanism of action has been reached. Recent preclinical reports have associated the neurotransmitter serotonin (5-hydroxytryptamine; 5-HT) with the antidepressant-like action of ketamine. Here, we review the current evidence for a serotonergic role in ketamine's antidepressant effects. The pharmacological profile of ketamine may include equipotent activity on several non-NMDA targets, and the current hypotheses for the mechanisms responsible for ketamine's antidepressant activity do not appear to preclude the possibility that non-glutamate neurotransmitters are involved in the antidepressant effects. At multiple levels, the serotonergic and glutamatergic systems interact, and such crosstalk could support the notion that changes in serotonergic neurotransmission may impact ketamine's antidepressant potential. In line with these prospects, ketamine may increase 5-HT levels in the prefrontal cortex of rats, plausibly via hippocampal NMDA receptor inhibition and activation of a-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors. In addition, a number of preclinical studies suggest that the antidepressant-like effects of ketamine may depend on endogenous activation of 5-HT receptors. Recent imaging and behavioral data predominantly support a role for 5-HT1A or 5-HT1B receptors, but the full range of 5-HT receptors has currently not been systematically investigated in this context. Furthermore, the nature of any 5-HT dependent mechanismin ketamine's antidepressant effect is currently not understood, and therefore, more studies arewarranted to confirm this hypothesis
引用
收藏
页码:27 / 38
页数:12
相关论文
共 141 条
[31]   Specificity and efficacy of noradrenaline, serotonin depletion in discrete brain areas of Swiss mice by neurotoxins [J].
Dailly, E ;
Chenu, F ;
Petit-Demoulière, B ;
Bourin, M .
JOURNAL OF NEUROSCIENCE METHODS, 2006, 150 (01) :111-115
[32]   Emerging mechanisms and treatments for depression beyond SSRIs and SNRIs [J].
Dale, Elena ;
Bang-Andersen, Benny ;
Sanchez, Connie .
BIOCHEMICAL PHARMACOLOGY, 2015, 95 (02) :81-97
[33]   Vortioxetine disinhibits pyramidal cell function and enhances synaptic plasticity in the rat hippocampus [J].
Dale, Elena ;
Zhang, Hong ;
Leiser, Steven C. ;
Xiao, Yixin ;
Lu, Dunguo ;
Yang, Charles R. ;
Plath, Niels ;
Sanchez, Connie .
JOURNAL OF PSYCHOPHARMACOLOGY, 2014, 28 (10) :891-902
[34]   The two faces of the pharmacological interaction of mGlu2 and 5-HT2A - Relevance of receptor heterocomplexes and interaction through functional brain pathways [J].
Delille, Hannah K. ;
Mezler, Mario ;
Marek, Gerard J. .
NEUROPHARMACOLOGY, 2013, 70 :296-305
[35]   Differentiated antidepressant-like profiles of ketamine, fluoxetine and vortioxetine in Flinders Sensitive Line (FSL) rats depleted of endogenous 5-HT [J].
Du Jardin, K. G. ;
Liebenberg, N. ;
Mueller, H. ;
Elfving, B. ;
Wegener, G. ;
Sanchez, C. .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2015, 25 :S431-S431
[36]   Differential interaction with the serotonin system by S-ketamine, vortioxetine, and fluoxetine in a genetic rat model of depression [J].
du Jardin, Kristian Gaarn ;
Liebenberg, Nico ;
Muller, Heidi Kaastrup ;
Elfving, Betina ;
Sanchez, Connie ;
Wegener, Gregers .
PSYCHOPHARMACOLOGY, 2016, 233 (14) :2813-2825
[37]   NEUROBIOLOGY OF STRESS, DEPRESSION, AND RAPID ACTING ANTIDEPRESSANTS: REMODELING SYNAPTIC CONNECTIONS [J].
Duman, Ronald S. .
DEPRESSION AND ANXIETY, 2014, 31 (04) :291-296
[38]  
Dwyer J.M., 2013, BIOL PSYCHIAT
[39]   Norketamine, the main metabolite of ketamine, is a non-competitive NMDA receptor antagonist in the rat cortex and spinal cord [J].
Ebert, B ;
Mikkelsen, S ;
Thorkildsen, C ;
Borgbjerg, FM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 333 (01) :99-104
[40]  
Eckert W.A., 2014, 2014 NEUR M PLANN