Serotonin Transporter and Plasma Membrane Monoamine Transporter Are Necessary for the Antidepressant-Like Effects of Ketamine in Mice.
Animals
Antidepressive Agents
/ pharmacology
CA3 Region, Hippocampal
/ drug effects
Equilibrative Nucleoside Transport Proteins
/ genetics
Ketamine
/ pharmacology
Male
Mice
Mice, Inbred C57BL
Nucleus Accumbens
/ drug effects
Serotonin
/ metabolism
Serotonin Plasma Membrane Transport Proteins
/ genetics
antidepressant-like activity
chronoamperometry
forced swim test
isoflurane
ketamine
plasma membrane monoamine transporter
serotonin clearance
serotonin transporter
tail suspension test
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
14 Oct 2020
14 Oct 2020
Historique:
received:
29
09
2020
revised:
09
10
2020
accepted:
12
10
2020
entrez:
17
10
2020
pubmed:
18
10
2020
medline:
26
2
2021
Statut:
epublish
Résumé
Major depressive disorder is typically treated with selective serotonin reuptake inhibitors (SSRIs), however, SSRIs take approximately six weeks to produce therapeutic effects, if any. Not surprisingly, there has been great interest in findings that low doses of ketamine, a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist, produce rapid and long-lasting antidepressant effects. Preclinical studies show that the antidepressant-like effects of ketamine are dependent upon availability of serotonin, and that ketamine increases extracellular serotonin, yet the mechanism by which this occurs is unknown. Here we examined the role of the high-affinity, low-capacity serotonin transporter (SERT), and the plasma membrane monoamine transporter (PMAT), a low-affinity, high-capacity transporter for serotonin, as mechanisms contributing to ketamine's ability to increase extracellular serotonin and produce antidepressant-like effects. Using high-speed chronoamperometry to measure real-time clearance of serotonin from CA3 region of hippocampus in vivo, we found ketamine robustly inhibited serotonin clearance in wild-type mice, an effect that was lost in mice constitutively lacking SERT or PMAT. As expected, in wild-type mice, ketamine produced antidepressant-like effects in the forced swim test. Mapping onto our neurochemical findings, the antidepressant-like effects of ketamine were lost in mice lacking SERT or PMAT. Future research is needed to understand how constitutive loss of either SERT or PMAT, and compensation that occurs in other systems, is sufficient to void ketamine of its ability to inhibit serotonin clearance and produce antidepressant-like effects. Taken together with existing literature, a critical role for serotonin, and its inhibition of uptake via SERT and PMAT, cannot be ruled out as important contributing factors to ketamine's antidepressant mechanism of action. Combined with what is already known about ketamine's action at NMDA receptors, these studies help lead the way to the development of drugs that lack ketamine's abuse potential but have superior efficacy in treating depression.
Identifiants
pubmed: 33066466
pii: ijms21207581
doi: 10.3390/ijms21207581
pmc: PMC7589995
pii:
doi:
Substances chimiques
Antidepressive Agents
0
Equilibrative Nucleoside Transport Proteins
0
Serotonin Plasma Membrane Transport Proteins
0
Slc6a4 protein, mouse
0
Serotonin
333DO1RDJY
Ketamine
690G0D6V8H
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NINDS NIH HHS
ID : T32 NS082145
Pays : United States
Organisme : NIH HHS
ID : R01MH093320
Pays : United States
Organisme : NIH HHS
ID : R01MH106978
Pays : United States
Références
Psychopharmacology (Berl). 2013 Jul;228(1):157-66
pubmed: 23455595
Front Neurosci. 2019 Feb 27;13:156
pubmed: 30872996
ACS Chem Neurosci. 2014 Oct 15;5(10):908-19
pubmed: 25089765
Nat Rev Drug Discov. 2005 Sep;4(9):775-90
pubmed: 16138108
Neuropsychopharmacology. 2018 Aug;43(9):1900-1907
pubmed: 29802366
Behav Pharmacol. 1997 Nov;8(6-7):523-32
pubmed: 9832966
Anesth Analg. 2007 Apr;104(4):836-9
pubmed: 17377090
Neuropharmacology. 2012 Jan;62(1):391-7
pubmed: 21867718
Biol Psychiatry. 2018 Jul 1;84(1):e3-e6
pubmed: 29174592
Eur J Neurosci. 2018 May 24;:
pubmed: 29797618
J Pharm Pract. 2011 Dec;24(6):520-33
pubmed: 22095575
Psychopharmacology (Berl). 2008 Jun;198(3):421-30
pubmed: 18458881
Brain Res. 1997 Jun 13;759(2):205-12
pubmed: 9221938
J Affect Disord. 2014 Mar;156:1-7
pubmed: 24314926
Naunyn Schmiedebergs Arch Pharmacol. 2015 Jan;388(1):43-9
pubmed: 25332055
Physiol Behav. 2013 Jun 13;118:227-39
pubmed: 23685235
Neuropharmacology. 1977 May;16(5):349-56
pubmed: 17078
Neuropsychopharmacology. 2016 Mar;41(4):1046-56
pubmed: 26245499
Neurosci Biobehav Rev. 2005;29(4-5):547-69
pubmed: 15893822
Neurochem Res. 1990 Oct;15(10):969-73
pubmed: 2150219
Int J Neuropsychopharmacol. 2006 Oct;9(5):565-73
pubmed: 16316487
Acta Psychiatr Scand. 2016 Jul;134(1):48-56
pubmed: 27028832
J Psychiatry Neurosci. 2004 Nov;29(6):417-26
pubmed: 15644983
CNS Drugs. 2012 Mar 1;26(3):189-204
pubmed: 22303887
Curr Protoc Neurosci. 2011 Apr;Chapter 8:Unit 8.10A
pubmed: 21462162
Biochem Pharmacol. 2007 Jan 1;73(1):147-54
pubmed: 17046718
Neuroscience. 2015 Apr 2;290:49-60
pubmed: 25595985
Int J Neuropsychopharmacol. 2019 Oct 1;22(10):665-674
pubmed: 31325908
Drugs. 2012 Jul 9;72(10):1313-33
pubmed: 22731961
J Biol Chem. 2013 Feb 1;288(5):3535-44
pubmed: 23255610
Brain Res Bull. 2006 Apr 14;69(3):338-45
pubmed: 16564431
Br J Anaesth. 1979 Dec;51(12):1167-73
pubmed: 526385
J Neurosci. 2010 Nov 10;30(45):15185-95
pubmed: 21068324
Psychopharmacology (Berl). 2001 May;155(3):315-22
pubmed: 11432695
Curr Opin Neurobiol. 2015 Feb;30:139-43
pubmed: 25562451
J Pharmacol Exp Ther. 2017 Apr;361(1):9-16
pubmed: 28115553
Proc Natl Acad Sci U S A. 2020 Feb 4;117(5):2656-2662
pubmed: 31941713
Pharmacol Ther. 2009 Jan;121(1):89-99
pubmed: 19022290
Int J Neuropsychopharmacol. 2018 Feb 1;21(2):145-153
pubmed: 29045739
J Neurochem. 2003 Jul;86(1):210-9
pubmed: 12807440
Biol Psychiatry. 1998 Aug 1;44(3):151-62
pubmed: 9693387
Biol Psychiatry. 2008 Jan 15;63(2):178-83
pubmed: 17568566
Neuron. 2020 Jun 3;106(5):715-726
pubmed: 32497508
J Neurosci. 2006 Jun 14;26(24):6431-8
pubmed: 16775130
Pharmacol Rev. 2018 Jul;70(3):621-660
pubmed: 29945898
Behav Brain Res. 2016 Oct 1;312:305-12
pubmed: 27343934
Nature. 2016 May 04;533(7604):481-6
pubmed: 27144355
Science. 2010 Aug 20;329(5994):959-64
pubmed: 20724638
Psychopharmacology (Berl). 1985;85(3):367-70
pubmed: 3923523
Behav Brain Res. 2019 Dec 30;376:112153
pubmed: 31419519
Anesth Analg. 2006 Jul;103(1):92-8, table of contents
pubmed: 16790633
Neuroscience. 2003;118(3):819-29
pubmed: 12710989
Neuropsychopharmacology. 2013 Dec;38(13):2666-74
pubmed: 23880871
Anesthesiology. 1998 Mar;88(3):768-74
pubmed: 9523822
Nature. 2011 Jun 15;475(7354):91-5
pubmed: 21677641
Psychopharmacology (Berl). 2016 Jul;233(14):2813-25
pubmed: 27236785
Neurosci Lett. 2015 Oct 8;606:129-34
pubmed: 26321152
Int J Neuropsychopharmacol. 2018 Mar 1;21(3):305-310
pubmed: 29370396
Neurosci Lett. 2003 May 29;343(1):9-12
pubmed: 12749985
ACS Chem Neurosci. 2019 Jul 17;10(7):3318-3326
pubmed: 31244055
Behav Brain Res. 2011 Oct 10;224(1):107-11
pubmed: 21669235
Biol Psychiatry. 2013 Nov 15;74(10):750-9
pubmed: 23790225
Neuropharmacology. 2013 Jul;70:27-34
pubmed: 23337256
Synapse. 1999 Jun 1;32(3):212-24
pubmed: 10340631
Psychopharmacology (Berl). 2014 Jun;231(11):2291-8
pubmed: 24402133
J Pharmacol Exp Ther. 2016 Oct;359(1):159-70
pubmed: 27469513
Neuropharmacology. 2017 Jan;112(Pt A):198-209
pubmed: 27211253
Anal Chem. 2005 Feb 1;77(3):818-26
pubmed: 15679349
PLoS Biol. 2007 Oct 16;5(10):e274
pubmed: 17941718
Biol Psychiatry. 2012 Jun 1;71(11):939-46
pubmed: 22297150
Proc Natl Acad Sci U S A. 2008 Dec 2;105(48):18976-81
pubmed: 19033200
J Neurosci. 2013 Jun 19;33(25):10534-43
pubmed: 23785165
Auton Neurosci. 2015 Dec;193:51-6
pubmed: 26213357
Neuropharmacology. 1982 Feb;21(2):113-8
pubmed: 6460944