The role of mGluR5 on the therapeutic effects of ketamine in Wistar rats.

Anxiety Behavioral despair CDPPB EPM FST Fear Ketamine MTEP OFT mGluR5

Journal

Psychopharmacology
ISSN: 1432-2072
Titre abrégé: Psychopharmacology (Berl)
Pays: Germany
ID NLM: 7608025

Informations de publication

Date de publication:
09 Mar 2024
Historique:
received: 27 11 2023
accepted: 04 03 2024
medline: 9 3 2024
pubmed: 9 3 2024
entrez: 9 3 2024
Statut: aheadofprint

Résumé

Ketamine produces dissociative, psychomimetic, anxiolytic, antidepressant, and anesthetic effects in a dose dependent manner. It has a complex mechanism of action that involve alterations in other glutamate receptors. The metabotropic glutamate receptor 5 (mGluR5) has been investigated in relation to the psychotic and anesthetic properties of ketamine, while its role in mediating the therapeutic effects of ketamine remains unknown. We investigated the role of mGluR5 on the antidepressant, anxiolytic and fear memory-related effects of ketamine in adult male Wistar rats. Two sets of experiments were conducted. We first utilized the positive allosteric modulator CDPPB to investigate how acute mGluR5 activation regulates the therapeutic effects of ketamine (10 mg/kg). We then tested the synergistic antidepressant effect of mGluR5 antagonism and ketamine by combining MTEP with a sub-effective dose of ketamine (1 mg/kg). Behavioral despair, locomotor activity, anxiety-like behavior, and fear memory were respectively assessed in the forced swim test (FST), open field test (OFT), elevated plus maze (EPM), and auditory fear conditioning. Enhancing mGluR5 activity via CDPPB occluded the antidepressant effect of ketamine without changing locomotor activity. Furthermore, concomitant administration of MTEP and ketamine exhibited a robust synergistic antidepressant effect. The MTEP + ketamine treatment, however, blocked the anxiolytic effect observed by sole administration of MTEP or the low dose ketamine. These findings suggest that suppressed mGluR5 activity is required for the antidepressant effects of ketamine. Consequently, the antagonism of mGluR5 enhances the antidepressant effectiveness of low dose ketamine, but eliminates its anxiolytic effects.

Identifiants

pubmed: 38459971
doi: 10.1007/s00213-024-06571-3
pii: 10.1007/s00213-024-06571-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Boğaziçi Üniversitesi
ID : 22B07P1

Informations de copyright

© 2024. The Author(s).

Références

Akan M, Skorodumov I, Meinhardt MW, Canbeyli R, Unal G (2023) A shea butter-based ketamine ointment: The antidepressant effects of transdermal ketamine in rats. Behav Brain Res 452:114594. https://doi.org/10.1016/j.bbr.2023.114594
doi: 10.1016/j.bbr.2023.114594 pubmed: 37487837
Alagarsamy S, Marino MJ, Rouse ST, Gereau RW, Heinemann SF, Conn PJ (1999) Activation of NMDA receptors reverses desensitization of mGluR5 in native and recombinant systems. Nat Neurosci 2(3):234–240. https://doi.org/10.1038/6338
doi: 10.1038/6338 pubmed: 10195215
Alagarsamy S, Rouse ST, Junge C, Hubert GW, Gutman D, Smith Y, Conn PJ (2002) NMDA-induced phosphorylation and regulation of mGluR5. Pharmacol Biochem Behav 73(2):299–306. https://doi.org/10.1016/S0091-3057(02)00826-2
doi: 10.1016/S0091-3057(02)00826-2 pubmed: 12117583
Alagarsamy S, Saugstad J, Warren L, Mansuy IM, Gereau RW, Conn PJ (2005) NMDA-induced potentiation of mGluR5 is mediated by activation of protein phosphatase 2B/calcineurin. Neuropharmacology 49:135–145. https://doi.org/10.1016/j.neuropharm.2005.05.005
doi: 10.1016/j.neuropharm.2005.05.005 pubmed: 16005030 pmcid: 3799794
Aleksandrova LR, Phillips AG, Wang YT (2017) Antidepressant effects of ketamine and the roles of AMPA glutamate receptors and other mechanisms beyond NMDA receptor antagonism. J Psychiatry Neurosci 42(4):222–229. https://doi.org/10.1503/jpn.160175
doi: 10.1503/jpn.160175 pubmed: 28234212 pmcid: 5487269
Amiri S, Haj-Mirzaian A, Rahimi-Balaei M, Razmi A, Kordjazy N, Shirzadian A, Ejtemaei Mehr S, Sianati H, Dehpour AR (2015) Co-occurrence of anxiety and depressive-like behaviors following adolescent social isolation in male mice; possible role of nitrergic system. Physiol Behav 145:38–44. https://doi.org/10.1016/j.physbeh.2015.03.032
doi: 10.1016/j.physbeh.2015.03.032 pubmed: 25817356
Anchan D, Clark S, Pollard K, Vasudevan N (2014) GPR30 activation decreases anxiety in the open field test but not in the elevated plus maze test in female mice. Brain and Behavior 4(1):51–59. https://doi.org/10.1002/brb3.197
doi: 10.1002/brb3.197 pubmed: 24653954
Arabzadeh S, Hakkikazazi E, Shahmansouri N, Tafakhori A, Ghajar A, Jafarinia M, Akhondzadeh S (2018) Does oral administration of ketamine accelerate response to treatment in major depressive disorder? Results of a double-blind controlled trial. J Affect Disord 235:236–241. https://doi.org/10.1016/j.jad.2018.02.056
doi: 10.1016/j.jad.2018.02.056 pubmed: 29660637
Awad H, Hubert GW, Smith Y, Levey AI, Conn PJ (2000) Activation of metabotropic glutamate receptor 5 has direct excitatory effects and potentiates NMDA receptor currents in neurons of the subthalamic nucleus. J Neurosci 20(21):7871–7879. https://doi.org/10.1523/JNEUROSCI.20-21-07871.2000
doi: 10.1523/JNEUROSCI.20-21-07871.2000 pubmed: 11050106 pmcid: 6772731
Belozertseva I, Kos T, Popik P, Danysz W, Bespalov A (2007) Antidepressant-like effects of mGluR1 and mGluR5 antagonists in the rat forced swim and the mouse tail suspension tests. Eur Neuropsychopharmacol 17(3):172–179. https://doi.org/10.1016/j.euroneuro.2006.03.002
doi: 10.1016/j.euroneuro.2006.03.002 pubmed: 16630709
Benquet P, Gee CE, Gerber U (2002) Two distinct signaling pathways upregulate NMDA receptor responses via two distinct metabotropic glutamate receptor subtypes. J Neurosci 22(22):9679–9686. https://doi.org/10.1523/JNEUROSCI.22-22-09679.2002
doi: 10.1523/JNEUROSCI.22-22-09679.2002 pubmed: 12427823 pmcid: 6757830
Bertaso F, Roussignol G, Worley P, Bockaert J, Fagni L, Ango F (2010) Homer1a-dependent crosstalk between NMDA and metabotropic glutamate receptors in mouse neurons. PLoS ONE 5(3):e9755. https://doi.org/10.1371/journal.pone.0009755
doi: 10.1371/journal.pone.0009755 pubmed: 20305784 pmcid: 2841198
Bockaert J, Perroy J, Ango F (2021) The complex formed by group I Metabotropic Glutamate Receptor (mGluR) and Homer1a plays a central role in metaplasticity and homeostatic synaptic scaling. J Neurosci 41(26):5567–5578. https://doi.org/10.1523/JNEUROSCI.0026-21.2021
doi: 10.1523/JNEUROSCI.0026-21.2021 pubmed: 34193623 pmcid: 8244974
Brodkin J, Bradbury M, Busse C, Warren N, Bristow LJ, Varney MA (2002) Reduced stress-induced hyperthermia in mGluR5 knockout mice. Eur J Neurosci 16(11):2241–2244. https://doi.org/10.1046/j.1460-9568.2002.02294.x
doi: 10.1046/j.1460-9568.2002.02294.x pubmed: 12473093
Burghardt NS, Sullivan GM, McEwen BS, Gorman JM, LeDoux JE (2004) The selective serotonin reuptake inhibitor citalopram increases fear after acute treatment but reduces fear with chronic treatment: a comparison with tianeptine. Biol Psychiat 55(12):1171–1178. https://doi.org/10.1016/j.biopsych.2004.02.029
doi: 10.1016/j.biopsych.2004.02.029 pubmed: 15184036
Carreno FR, Donegan JJ, Boley AM, Shah A, DeGuzman M, Frazer A, Lodge DJ (2016) Activation of a ventral hippocampus-medial prefrontal cortex pathway is both necessary and sufficient for an antidepressant response to ketamine. Mol Psychiatry 21(9):1298–1308. https://doi.org/10.1038/mp.2015.176
doi: 10.1038/mp.2015.176 pubmed: 26619811
Castro CA, Hogan JB, Benson KA, Shehata CW, Landauer MR (1995) Behavioral effects of vehicles: DMSO, ethanol, Tween-20, Tween-80, and emulphor-620. Pharmacol Biochem Behav 50(4):521–526. https://doi.org/10.1016/0091-3057(94)00331-9
doi: 10.1016/0091-3057(94)00331-9 pubmed: 7617697
Chaki S, Watanabe M (2023) Antidepressants in the post-ketamine era: Pharmacological approaches targeting the glutamatergic system. Neuropharmacology 223:109348. https://doi.org/10.1016/j.neuropharm.2022.109348
doi: 10.1016/j.neuropharm.2022.109348 pubmed: 36423706
Chaki S, Ago Y, Palucha-Paniewiera A, Matrisciano F, Pilc A (2013) mGlu2/3 and mGlu5 receptors: Potential targets for novel antidepressants. Neuropharmacology 66:40–52. https://doi.org/10.1016/j.neuropharm.2012.05.022
doi: 10.1016/j.neuropharm.2012.05.022 pubmed: 22640631
Chan M-H, Chiu P-H, Sou J-H, Chen H-H (2008) Attenuation of ketamine-evoked behavioral responses by mGluR5 positive modulators in mice. Psychopharmacology 198(1):141–148. https://doi.org/10.1007/s00213-008-1103-1
doi: 10.1007/s00213-008-1103-1 pubmed: 18311557
Chen H-H, Liao P-F, Chan M-H (2011) mGluR5 positive modulators both potentiate activation and restore inhibition in NMDA receptors by PKC dependent pathway. J Biomed Sci 18(1):19. https://doi.org/10.1186/1423-0127-18-19
doi: 10.1186/1423-0127-18-19 pubmed: 21342491 pmcid: 3050796
Choi M, Lee SH, Chang HL, Son H (2016) Hippocampal VEGF is necessary for antidepressant-like behaviors but not sufficient for antidepressant-like effects of ketamine in rats. Biochim Biophys Acta (BBA) - Mol Basis Dis 1862(7):1247–1254. https://doi.org/10.1016/j.bbadis.2016.04.001
doi: 10.1016/j.bbadis.2016.04.001
Choi KH, Berman RY, Zhang M, Spencer HF, Radford KD (2020) Effects of ketamine on rodent fear memory. Int J Mol Sci 21(19):7173. https://doi.org/10.3390/ijms21197173
doi: 10.3390/ijms21197173 pubmed: 32998470 pmcid: 7582895
Clifton NE, Trent S, Thomas KL, Hall J (2019) Regulation and function of activity-dependent homer in synaptic plasticity. Complex Psychiatry 5(3):147–161. https://doi.org/10.1159/000500267
doi: 10.1159/000500267
Cooper MD, Rosenblat JD, Cha DS, Lee Y, Kakar R, McIntyre RS (2017) Strategies to mitigate dissociative and psychotomimetic effects of ketamine in the treatment of major depressive episodes: a narrative review. World J Biol Psychiatry 18(6):410–423. https://doi.org/10.3109/15622975.2016.1139747
doi: 10.3109/15622975.2016.1139747 pubmed: 26752601
Cryan JF, Valentino RJ, Lucki I (2005) Assessing substrates underlying the behavioral effects of antidepressants using the modified rat forced swimming test. Neurosci Biobehav Rev 29(4–5):547–569. https://doi.org/10.1016/j.neubiorev.2005.03.008
doi: 10.1016/j.neubiorev.2005.03.008 pubmed: 15893822
de Bartolomeis A, Sarappa C, Buonaguro EF, Marmo F, Eramo A, Tomasetti C, Iasevoli F (2013) Different effects of the NMDA receptor antagonists ketamine, MK-801, and memantine on postsynaptic density transcripts and their topography: Role of Homer signaling, and implications for novel antipsychotic and pro-cognitive targets in psychosis. Prog Neuropsychopharmacol Biol Psychiatry 46:1–12. https://doi.org/10.1016/j.pnpbp.2013.06.010
doi: 10.1016/j.pnpbp.2013.06.010 pubmed: 23800465
DeLorenzo C, DellaGioia N, Bloch M, Sanacora G, Nabulsi N, Abdallah C, Yang J, Wen R, Mann JJ, Krystal JH, Parsey RV, Carson RE, Esterlis I (2015) In Vivo Ketamine-Induced Changes in [11 C]ABP688 Binding to Metabotropic Glutamate Receptor Subtype 5. Biol Psychiat 77(3):266–275. https://doi.org/10.1016/j.biopsych.2014.06.024
doi: 10.1016/j.biopsych.2014.06.024 pubmed: 25156701
Deyama S, Bang E, Wohleb ES, Li X-Y, Kato T, Gerhard DM, Dutheil S, Dwyer JM, Taylor SR, Picciotto MR, Duman RS (2019) Role of Neuronal VEGF Signaling in the Prefrontal Cortex in the Rapid Antidepressant Effects of Ketamine. Am J Psychiatry 176(5):388–400. https://doi.org/10.1176/appi.ajp.2018.17121368
doi: 10.1176/appi.ajp.2018.17121368 pubmed: 30606046 pmcid: 6494682
Domin H, Szewczyk B, Woźniak M, Wawrzak-Wleciał A, Śmiałowska M (2014) Antidepressant-like effect of the mGluR5 antagonist MTEP in an astroglial degeneration model of depression. Behav Brain Res 273:23–33. https://doi.org/10.1016/j.bbr.2014.07.019
doi: 10.1016/j.bbr.2014.07.019 pubmed: 25043733
Ecevitoglu A, Canbeyli R, Unal G (2019) Oral ketamine alleviates behavioral despair without cognitive impairment in Wistar rats. Behav Brain Res 372:112058. https://doi.org/10.1016/j.bbr.2019.112058
doi: 10.1016/j.bbr.2019.112058 pubmed: 31247234
Engin E, Treit D, Dickson CT (2009) Anxiolytic- and antidepressant-like properties of ketamine in behavioral and neurophysiological animal models. Neuroscience 161(2):359–369. https://doi.org/10.1016/j.neuroscience.2009.03.038
doi: 10.1016/j.neuroscience.2009.03.038 pubmed: 19321151
Esterlis I, DellaGioia N, Pietrzak RH, Matuskey D, Nabulsi N, Abdallah CG, Yang J, Pittenger C, Sanacora G, Krystal JH, Parsey RV, Carson RE, DeLorenzo C (2018) Ketamine-induced reduction in mGluR5 availability is associated with an antidepressant response: an [11C]ABP688 and PET imaging study in depression. Mol Psychiatry 23(4):824–832. https://doi.org/10.1038/mp.2017.58
doi: 10.1038/mp.2017.58 pubmed: 28397841
Fraser LM, Brown RE, Hussin A, Fontana M, Whittaker A, O’Leary TP, Lederle L, Holmes A, Ramos A (2010) Measuring anxiety- and locomotion-related behaviours in mice: a new way of using old tests. Psychopharmacology 211(1):99–112. https://doi.org/10.1007/s00213-010-1873-0
doi: 10.1007/s00213-010-1873-0 pubmed: 20454890
Fukumoto K, Iijima M, Chaki S (2016) The Antidepressant effects of an mGlu2/3 receptor antagonist and ketamine require AMPA receptor stimulation in the mPFC and subsequent activation of the 5-HT neurons in the DRN. Neuropsychopharmacology 41(4):1046–1056. https://doi.org/10.1038/npp.2015.233
doi: 10.1038/npp.2015.233 pubmed: 26245499
Garcia LSB, Comim CM, Valvassori SS, Réus GZ, Barbosa LM, Andreazza AC, Stertz L, Fries GR, Gavioli EC, Kapczinski F, Quevedo J (2008) Acute administration of ketamine induces antidepressant-like effects in the forced swimming test and increases BDNF levels in the rat hippocampus. Prog Neuropsychopharmacol Biol Psychiatry 32(1):140–144. https://doi.org/10.1016/j.pnpbp.2007.07.027
doi: 10.1016/j.pnpbp.2007.07.027 pubmed: 17884272
Gerhard DM, Pothula S, Liu RJ, Wu M, Li XY, Girgenti MJ, Taylor SR, Duman CH, Delpire E, Picciotto M, Wohleb ES, Duman RS (2020) GABA interneurons are the cellular trigger for ketamine’s rapid antidepressant actions. J Clin Investig 130(3):1336–1349. https://doi.org/10.1172/JCI130808
doi: 10.1172/JCI130808 pubmed: 31743111 pmcid: 7269589
Girgenti MJ, Ghosal S, LoPresto D, Taylor JR, Duman RS (2017) Ketamine accelerates fear extinction via mTORC1 signaling. Neurobiol Dis 100:1–8. https://doi.org/10.1016/j.nbd.2016.12.026
doi: 10.1016/j.nbd.2016.12.026 pubmed: 28043916
Gravius A, Barberi C, Schäfer D, Schmidt WJ, Danysz W (2006) The role of group I metabotropic glutamate receptors in acquisition and expression of contextual and auditory fear conditioning in rats – a comparison. Neuropharmacology 51(7–8):1146–1155. https://doi.org/10.1016/j.neuropharm.2006.07.008
doi: 10.1016/j.neuropharm.2006.07.008 pubmed: 16905160
Henry S (2002) The mGluR5 antagonist MPEP, but not the mGluR2/3 agonist LY314582, augments PCP effects on prepulse inhibition and locomotor activity. Neuropharmacology 43(8):1199–1209. https://doi.org/10.1016/S0028-3908(02)00332-5
doi: 10.1016/S0028-3908(02)00332-5 pubmed: 12527469
Hetzler BE, Swain Wautlet B (1985) Ketamine-induced locomotion in rats in an open-field. Pharmacol Biochem Behav 22(4):653–655. https://doi.org/10.1016/0091-3057(85)90291-6
doi: 10.1016/0091-3057(85)90291-6 pubmed: 3991775
Holz A, Mülsch F, Schwarz MK, Hollmann M, Döbrössy MD, Coenen VA, Bartos M, Normann C, Biber K, van Calker D, Serchov T (2019) Enhanced mGlu5 signaling in excitatory neurons promotes rapid antidepressant effects via AMPA receptor activation. Neuron 104(2):338-352.e7. https://doi.org/10.1016/j.neuron.2019.07.011
doi: 10.1016/j.neuron.2019.07.011 pubmed: 31420117
Horsley RR, Páleníček T, Kolin J, Valeš K (2018) Psilocin and ketamine microdosing: effects of subchronic intermittent microdoses in the elevated plus-maze in male Wistar rats. Behav Pharmacol 29(6):530–536. https://doi.org/10.1097/FBP.0000000000000394
doi: 10.1097/FBP.0000000000000394 pubmed: 29537989
Jesse CR, Bortolatto CF, Savegnago L, Rocha JB, Nogueira CW (2008) Involvement of L-arginine-nitric oxide-cyclic guanosine monophosphate pathway in the antidepressant-like effect of tramadol in the rat forced swimming test. Prog Neuropsychopharmacol Biol Psychiatry 32(8):1838–1843. https://doi.org/10.1016/j.pnpbp.2008.08.010
doi: 10.1016/j.pnpbp.2008.08.010 pubmed: 18773934
Jin D, Guo M, Xue B, Mao L, Wang JQ (2013) Differential regulation of CaMKIIα interactions with mGluR5 and NMDA receptors by Ca(2+) in neurons. J Neurochem 127(5):620–631. https://doi.org/10.1111/jnc.12434
doi: 10.1111/jnc.12434 pubmed: 24032403 pmcid: 3933469
Kim J-W, Suzuki K, Kavalali ET, Monteggia LM (2023) Bridging rapid and sustained antidepressant effects of ketamine. Trends Mol Med 29(5):364–375. https://doi.org/10.1016/j.molmed.2023.02.003
doi: 10.1016/j.molmed.2023.02.003 pubmed: 36907686
Kingir E, Sevinc C, Unal G (2023) Chronic oral ketamine prevents anhedonia and alters neuronal activation in the lateral habenula and nucleus accumbens in rats under chronic unpredictable mild stress. Neuropharmacology 228:109468. https://doi.org/10.1016/j.neuropharm.2023.109468
doi: 10.1016/j.neuropharm.2023.109468 pubmed: 36813161
Koike H, Chaki S (2014) Requirement of AMPA receptor stimulation for the sustained antidepressant activity of ketamine and LY341495 during the forced swim test in rats. Behav Brain Res 271:111–115. https://doi.org/10.1016/j.bbr.2014.05.065
doi: 10.1016/j.bbr.2014.05.065 pubmed: 24909673
Koike H, Iijima M, Chaki S (2011) Involvement of AMPA receptor in both the rapid and sustained antidepressant-like effects of ketamine in animal models of depression. Behav Brain Res 224(1):107–111. https://doi.org/10.1016/j.bbr.2011.05.035
doi: 10.1016/j.bbr.2011.05.035 pubmed: 21669235
Kokras N, Polissidis A, Antoniou K, Dalla C (2017) Head shaking in the forced swim test: A robust but unexplored sex difference. Pharmacol Biochem Behav 152:90–96. https://doi.org/10.1016/j.pbb.2016.05.007
doi: 10.1016/j.pbb.2016.05.007 pubmed: 27184928
Konieczny J, Ossowska K, Wolfarth S, Pilc A (1998) LY354740, a group II metabotropic glutamate receptor agonist with potential antiparkinsonian properties in rats. Naunyn Schmiedebergs Arch Pharmacol 358(4):500–502. https://doi.org/10.1007/pl00005284
doi: 10.1007/pl00005284 pubmed: 9826074
Krystal JH, Mathew SJ, D’Souza DC, Garakani A, Gunduz-Bruce H, Charney DS (2010) Potential psychiatric applications of metabotropic glutamate receptor agonists and antagonists. CNS Drugs 24(8):669–693. https://doi.org/10.2165/11533230-000000000-00000
doi: 10.2165/11533230-000000000-00000 pubmed: 20658799
Krystal JH, Karper LP, Seibyl JP, Freeman GK, Delaney R, Bremner JD, Heninger GR, Bowers MB Jr, Charney DS (1994) Subanesthetic effects of the noncompetitive NMDA antagonist, ketamine, in humans. Psychotomimetic, perceptual, cognitive, and neuroendocrine responses. Arch Gen Psychiatry 51(3):199–214. https://doi.org/10.1001/archpsyc.1994.03950030035004
Lapidus KAB, Levitch CF, Perez AM, Brallier JW, Parides MK, Soleimani L, Feder A, Iosifescu DV, Charney DS, Murrough JW (2014) A randomized controlled trial of intranasal ketamine in major depressive disorder. Biol Psychiat 76(12):970–976. https://doi.org/10.1016/j.biopsych.2014.03.026
doi: 10.1016/j.biopsych.2014.03.026 pubmed: 24821196
Lea PM, Faden AI (2006) Metabotropic glutamate receptor subtype 5 antagonists MPEP and MTEP. CNS Drug Rev 12(2):149–166. https://doi.org/10.1111/j.1527-3458.2006.00149.x
doi: 10.1111/j.1527-3458.2006.00149.x pubmed: 16958988 pmcid: 6494124
Lee K-W, Westin L, Kim J, Chang JC, Oh Y-S, Amreen B, Gresack J, Flajolet M, Kim D, Aperia A, Kim Y, Greengard P (2015) Alteration by p11 of mGluR5 localization regulates depression-like behaviors. Mol Psychiatry 20(12):1546–1556. https://doi.org/10.1038/mp.2015.132
doi: 10.1038/mp.2015.132 pubmed: 26370144 pmcid: 4907335
Li Y, Zhu ZR, Ou BC, Wang YQ, Tan ZB, Deng CM, Gao YY, Tang M, So JH, Mu YL, Zhang LQ (2015) Dopamine D2/D3 but not dopamine D1 receptors are involved in the rapid antidepressant-like effects of ketamine in the forced swim test. Behav Brain Res 279:100–105. https://doi.org/10.1016/j.bbr.2014.11.016
doi: 10.1016/j.bbr.2014.11.016 pubmed: 25449845
Li X, Du ZJ, Xu JN, Liang ZM, Lin S, Chen H, Li SJ, Li XW, Yang JM, Gao TM (2023) mGluR5 in hippocampal CA1 pyramidal neurons mediates stress-induced anxiety-like behavior. Neuropsychopharmacology 48(8):1164–1174. https://doi.org/10.1038/s41386-023-01548-w
doi: 10.1038/s41386-023-01548-w pubmed: 36797374
Lindemann L, Porter RH, Scharf SH, Kuennecke B, Bruns A, von Kienlin M, Harrison AC, Paehler A, Funk C, Gloge A, Schneider M, Parrott NJ, Polonchuk L, Niederhauser U, Morairty SR, Kilduff TS, Vieira E, Kolczewski S, Wichmann J, Hartung T, … Jaeschke G (2015) Pharmacology of Basimglurant (RO4917523, RG7090), a unique metabotropic glutamate receptor 5 negative allosteric modulator in clinical development for depression. J Pharmacol Exp Ther 353(1):213–233. https://doi.org/10.1124/jpet.114.222463
Liu R-J, Fuchikami M, Dwyer JM, Lepack AE, Duman RS, Aghajanian GK (2013) GSK-3 inhibition potentiates the synaptogenic and antidepressant-like effects of subthreshold doses of ketamine. Neuropsychopharmacology 38(11):2268–2277. https://doi.org/10.1038/npp.2013.128
doi: 10.1038/npp.2013.128 pubmed: 23680942 pmcid: 3773678
Maeng S, Zarate CA, Du J, Schloesser RJ, McCammon J, Chen G, Manji HK (2008) Cellular mechanisms underlying the antidepressant effects of ketamine: Role of α-Amino-3-Hydroxy-5-Methylisoxazole-4-Propionic acid receptors. Biol Psychiat 63(4):349–352. https://doi.org/10.1016/j.biopsych.2007.05.028
doi: 10.1016/j.biopsych.2007.05.028 pubmed: 17643398
Matta JA, Ashby MC, Sanz-Clemente A, Roche KW, Isaac JTR (2011) mGluR5 and NMDA receptors drive the experience- and activity-dependent NMDA receptor NR2B to NR2A subunit switch. Neuron 70(2):339–351. https://doi.org/10.1016/j.neuron.2011.02.045
doi: 10.1016/j.neuron.2011.02.045 pubmed: 21521618 pmcid: 3087383
Niswender CM, Conn PJ (2010) Metabotropic glutamate receptors: Physiology, pharmacology, and disease. Annu Rev Pharmacol Toxicol 50(1):295–322. https://doi.org/10.1146/annurev.pharmtox.011008.145533
doi: 10.1146/annurev.pharmtox.011008.145533 pubmed: 20055706 pmcid: 2904507
Pałucha A, Brański P, Szewczyk B, Wierońska JM, Kłak K, Pilc A (2005) Potential antidepressant-like effect of MTEP, a potent and highly selective mGluR5 antagonist. Pharmacol Biochem Behav 81(4):901–906. https://doi.org/10.1016/j.pbb.2005.06.015
doi: 10.1016/j.pbb.2005.06.015 pubmed: 16040106
Pałucha-Poniewiera A, Podkowa K, Pilc A (2019) Role of AMPA receptor stimulation and TrkB signaling in the antidepressant-like effect of ketamine co-administered with a group II mGlu receptor antagonist, LY341495, in the forced swim test in rats. Behav Pharmacol 30(6):471–477. https://doi.org/10.1097/FBP.0000000000000471
doi: 10.1097/FBP.0000000000000471 pubmed: 30724804
Pennington ZT, Dong Z, Feng Y, Vetere LM, Page-Harley L, Shuman T, Cai DJ (2019) ezTrack: An open-source video analysis pipeline for the investigation of animal behavior. Sci Rep 9(1):19979. https://doi.org/10.1038/s41598-019-56408-9
doi: 10.1038/s41598-019-56408-9 pubmed: 31882950 pmcid: 6934800
Pietraszek M, Gravius A, Schäfer D, Weil T, Trifanova D, Danysz W (2005a) mGluR5, but not mGluR1, antagonist modifies MK-801-induced locomotor activity and deficit of prepulse inhibition. Neuropharmacology 49(1):73–85. https://doi.org/10.1016/j.neuropharm.2005.01.027
doi: 10.1016/j.neuropharm.2005.01.027 pubmed: 15992582
Pietraszek M, Sukhanov I, Maciejak P, Szyndler J, Gravius A, Wisłowska A, Płaźnik A, Bespalov AY, Danysz W (2005b) Anxiolytic-like effects of mGlu1 and mGlu5 receptor antagonists in rats. Eur J Pharmacol 514(1):25–34. https://doi.org/10.1016/j.ejphar.2005.03.028
doi: 10.1016/j.ejphar.2005.03.028 pubmed: 15878321
Piva A, Caffino L, Padovani L, Pintori N, Mottarlini F, Sferrazza G, Paolone G, Fumagalli F, Chiamulera C (2020) The metaplastic effects of ketamine on sucrose renewal and contextual memory reconsolidation in rats. Behav Brain Res 379:112347. https://doi.org/10.1016/j.bbr.2019.112347
doi: 10.1016/j.bbr.2019.112347 pubmed: 31706797
Podkowa K, Pochwat B, Brański P, Pilc A, Pałucha-Poniewiera A (2016) Group II mGlu receptor antagonist LY341495 enhances the antidepressant-like effects of ketamine in the forced swim test in rats. Psychopharmacology 233(15–16):2901–2914. https://doi.org/10.1007/s00213-016-4325-7
doi: 10.1007/s00213-016-4325-7 pubmed: 27286960 pmcid: 4933730
Pomierny-Chamioło L, Poleszak E, Pilc A, Nowak G (2010) NMDA but not AMPA glutamatergic receptors are involved in the antidepressant-like activity of MTEP during the forced swim test in mice. Pharmacol Rep 62(6):1186–1190. https://doi.org/10.1016/S1734-1140(10)70381-9
doi: 10.1016/S1734-1140(10)70381-9 pubmed: 21273676
Porsolt RD, Le Pichon M, Jalfre M (1977) Depression: a new animal model sensitive to antidepressant treatments. Nature 266(5604):730–732. https://doi.org/10.1038/266730a0
doi: 10.1038/266730a0 pubmed: 559941
Prut L, Belzung C (2003) The open field as a paradigm to measure the effects of drugs on anxiety-like behaviors: a review. Eur J Pharmacol 463(1–3):3–33. https://doi.org/10.1016/s0014-2999(03)01272-x
doi: 10.1016/s0014-2999(03)01272-x pubmed: 12600700
Quiroz JA, Tamburri P, Deptula D, Banken L, Beyer U, Rabbia M, Parkar N, Fontoura P, Santarelli L (2016) Efficacy and safety of Basimglurant as adjunctive therapy for major depression: A randomized clinical trial. JAMA Psychiat 73(7):675–684. https://doi.org/10.1001/jamapsychiatry.2016.0838
doi: 10.1001/jamapsychiatry.2016.0838
Radford KD, Park TY, Jaiswal S, Pan H, Knutsen A, Zhang M, Driscoll M, Osborne-Smith LA, Dardzinski BJ, Choi KH (2018) Enhanced fear memories and brain glucose metabolism (18F-FDG-PET) following sub-anesthetic intravenous ketamine infusion in Sprague-Dawley rats. Transl Psychiatry 8(1):263. https://doi.org/10.1038/s41398-018-0310-8
doi: 10.1038/s41398-018-0310-8 pubmed: 30504810 pmcid: 6269482
Razoux F, Garcia R, Léna I (2007) Ketamine, at a Dose that disrupts motor behavior and latent inhibition, enhances prefrontal cortex synaptic efficacy and glutamate release in the nucleus accumbens. Neuropsychopharmacology 32(3):719–727. https://doi.org/10.1038/sj.npp.1301057
doi: 10.1038/sj.npp.1301057 pubmed: 16525415
Romano C, Sesma MA, McDonald CT, O’malley K, van den Pol AN, Olney JW (1995) Distribution of metabotropic glutamate receptor mGluR5 immunoreactivity in rat brain. J Comp Neurol 355(3):455–469. https://doi.org/10.1002/cne.903550310
doi: 10.1002/cne.903550310 pubmed: 7636025
Serchov T, Clement H-W, Schwarz MK, Iasevoli F, Tosh DK, Idzko M, Jacobson KA, de Bartolomeis A, Normann C, Biber K, van Calker D (2015) Increased signaling via adenosine A1 receptors, sleep deprivation, imipramine, and ketamine inhibit depressive-like behavior via induction of homer1a. Neuron 87(3):549–562. https://doi.org/10.1016/j.neuron.2015.07.010
doi: 10.1016/j.neuron.2015.07.010 pubmed: 26247862 pmcid: 4803038
Sethna F, Wang H (2014) Pharmacological enhancement of mGluR5 facilitates contextual fear memory extinction. Learn Mem 21(12):647–650. https://doi.org/10.1101/lm.035857.114
doi: 10.1101/lm.035857.114 pubmed: 25403451 pmcid: 4236415
Silote GP, de Oliveira SFS, Ribeiro DE, Machado MS, Andreatini R, Joca SRL, Beijamini V (2020) Ketamine effects on anxiety and fear-related behaviors: Current literature evidence and new findings. Prog Neuropsychopharmacol Biol Psychiatry 100:109878. https://doi.org/10.1016/j.pnpbp.2020.109878
doi: 10.1016/j.pnpbp.2020.109878 pubmed: 31982463
Sofia RD, Harakal JD (1975) Evaluation of ketamine HCl for anti-depressant activity. Arch Int Pharmacodyn Ther 214(1):68–74
pubmed: 1156026
Sou J-H, Chan M-H, Chen H-H (2006) Ketamine, but not propofol, anaesthesia is regulated by metabotropic glutamate 5 receptors. Br J Anaesth 96(5):597–601. https://doi.org/10.1093/bja/ael046
doi: 10.1093/bja/ael046 pubmed: 16531447
Sturman O, Germain P-L, Bohacek J (2018) Exploratory rearing: a context- and stress-sensitive behavior recorded in the open-field test. Stress 21(5):443–452. https://doi.org/10.1080/10253890.2018.1438405
doi: 10.1080/10253890.2018.1438405 pubmed: 29451062
Su LD, Wang N, Han J, Shen Y (2022) Group 1 Metabotropic glutamate receptors in neurological and psychiatric diseases: Mechanisms and prospective. Neuroscientist 28(5):453–468. https://doi.org/10.1177/10738584211021018
doi: 10.1177/10738584211021018 pubmed: 34088252
Tanyeri P, Buyukokuroglu ME, Mutlu O, Ulak G, Yıldız Akar F, Komsuoglu Celikyurt I, Erden BF (2013) Involvement of serotonin receptor subtypes in the antidepressant-like effect of beta receptor agonist Amibegron (SR 58611A): an experimental study. Pharmacol Biochem Behav 105:12–16. https://doi.org/10.1016/j.pbb.2013.01.010
doi: 10.1016/j.pbb.2013.01.010 pubmed: 23380524
Treit D, Engin E, McEown K (2010) Animal models of anxiety and anxiolytic drug action. Curr Top Behav Neurosci 2:121–160. https://doi.org/10.1007/7854_2009_17
doi: 10.1007/7854_2009_17 pubmed: 21309109
Truppman Lattie D, Nehoff H, Neehoff S, Gray A, Glue P (2021) Anxiolytic effects of acute and maintenance ketamine, as assessed by the fear questionnaire subscales and the Spielberger State anxiety rating scale. J Psychopharmacol 35(2):137–141. https://doi.org/10.1177/0269881120953991
doi: 10.1177/0269881120953991 pubmed: 32900266
Tu JC, Xiao B, Naisbitt S, Yuan JP, Petralia RS, Brakeman P, Doan A, Aakalu VK, Lanahan AA, Sheng M, Worley PF (1999) Coupling of mGluR/Homer and PSD-95 complexes by the shank family of postsynaptic density proteins. Neuron 23(3):583–592. https://doi.org/10.1016/S0896-6273(00)80810-7
doi: 10.1016/S0896-6273(00)80810-7 pubmed: 10433269
Unal G, Canbeyli R (2019) Psychomotor retardation in depression: A critical measure of the forced swim test. Behav Brain Res 372:112047. https://doi.org/10.1016/j.bbr.2019.112047
doi: 10.1016/j.bbr.2019.112047 pubmed: 31255672
Valle FP (1970) Effects of strain, sex, and illumination on open-field behavior of rats. Am J Psychol 83(1):103. https://doi.org/10.2307/1420860
doi: 10.2307/1420860 pubmed: 5465190
Walf AA, Frye CA (2007) The use of the elevated plus maze as an assay of anxiety-related behavior in rodents. Nat Protoc 2(2):322–328. https://doi.org/10.1038/nprot.2007.44
doi: 10.1038/nprot.2007.44 pubmed: 17406592 pmcid: 3623971
Wang Y, He W, Zhang H, Yao Z, Che F, Cao Y, Sun H (2020) mGluR5 mediates ketamine antidepressant response in susceptible rats exposed to prenatal stress. J Affect Disord 272:398–408. https://doi.org/10.1016/j.jad.2020.03.104
doi: 10.1016/j.jad.2020.03.104 pubmed: 32553383
Widman AJ, McMahon LL (2018) Disinhibition of CA1 pyramidal cells by low-dose ketamine and other antagonists with rapid antidepressant efficacy. Proc Natl Acad Sci 115(13). https://doi.org/10.1073/pnas.1718883115
Yankelevitch-Yahav R, Franko M, Huly A, Doron R (2015) The forced swim test as a model of depressive-like behavior. J Vis Exp 97:52587. https://doi.org/10.3791/52587
doi: 10.3791/52587
Yilmaz A, Schulz D, Aksoy A, Canbeyli R (2002) Prolonged effect of an anesthetic dose of ketamine on behavioral despair. Pharmacol Biochem Behav 71(1–2):341–344. https://doi.org/10.1016/S0091-3057(01)00693-1
doi: 10.1016/S0091-3057(01)00693-1 pubmed: 11812542
Youssef EA, Berry-Kravis E, Czech C, Hagerman RJ, Hessl D, Wong CY, Rabbia M, Deptula D, John A, Kinch R, Drewitt P, Lindemann L, Marcinowski M, Langland R, Horn C, Fontoura P, Santarelli L, Quiroz JA, FragXis Study Group (2018) Effect of the mGluR5-NAM Basimglurant on behavior in adolescents and adults with fragile X syndrome in a randomized, double-blind, placebo-controlled trial: FragXis phase 2 results. Neuropsychopharmacology 43(3):503–512. https://doi.org/10.1038/npp.2017.177
doi: 10.1038/npp.2017.177 pubmed: 28816242
Zanos P, Gould TD (2018) Mechanisms of ketamine action as an antidepressant. Mol Psychiatry 23(4):801–811. https://doi.org/10.1038/mp.2017.255
doi: 10.1038/mp.2017.255 pubmed: 29532791 pmcid: 5999402
Zanos P, Highland JN, Stewart BW, Georgiou P, Jenne CE, Lovett J, Morris PJ, Thomas CJ, Moaddel R, Zarate CA, Gould TD (2019) 2R,6R hydroxynorketamine exerts mGlu2/3 receptor-dependent antidepressant actions. Proc Natl Acad Sci 116(13):6441–6450. https://doi.org/10.1073/pnas.1819540116
doi: 10.1073/pnas.1819540116 pubmed: 30867285 pmcid: 6442605
Zanos P, Brown KA, Georgiou P, Yuan P, Zarate CA, Thompson SM, Gould TD (2023) NMDA receptor activation-dependent antidepressant-relevant behavioral and synaptic actions of ketamine. J Neurosci 43(6):1038–1050. https://doi.org/10.1523/JNEUROSCI.1316-22.2022
doi: 10.1523/JNEUROSCI.1316-22.2022 pubmed: 36596696 pmcid: 9908316
Zarate CA, Singh JB, Carlson PJ, Brutsche NE, Ameli R, Luckenbaugh DA, Charney DS, Manji HK (2006) A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression. Arch Gen Psychiatry 63(8):856. https://doi.org/10.1001/archpsyc.63.8.856
doi: 10.1001/archpsyc.63.8.856 pubmed: 16894061
Zhang LM, Zhou WW, Ji YJ, Li Y, Zhao N, Chen HX, Xue R, Mei XG, Zhang YZ, Wang HL, Li YF (2015) Anxiolytic effects of ketamine in animal models of posttraumatic stress disorder. Psychopharmacology 232(4):663–672. https://doi.org/10.1007/s00213-014-3697-9
doi: 10.1007/s00213-014-3697-9 pubmed: 25231918
Zhang K, Yamaki VN, Wei Z, Zheng Y, Cai X (2017) Differential regulation of GluA1 expression by ketamine and memantine. Behav Brain Res 316:152–159. https://doi.org/10.1016/j.bbr.2016.09.002
doi: 10.1016/j.bbr.2016.09.002 pubmed: 27599619
Zhang B, Yang X, Ye L, Liu R, Ye B, Du W, Shen F, Li Q, Guo F, Liu J, Guo F, Li Y, Xu Z, Liu Z (2021) Ketamine activated glutamatergic neurotransmission by GABAergic disinhibition in the medial prefrontal cortex. Neuropharmacology 194:108382. https://doi.org/10.1016/j.neuropharm.2020.108382
doi: 10.1016/j.neuropharm.2020.108382 pubmed: 33144117
Zhang K, Xu T, Yuan Z, Wei Z, Yamaki VN, Huang M, Huganir RL, Cai X (2016) Essential roles of AMPA receptor GluA1 phosphorylation and presynaptic HCN channels in fast-acting antidepressant responses of ketamine. Sci Signal 9(458). https://doi.org/10.1126/scisignal.aai7884
Zomkowski AD, Santos AR, Rodrigues AL (2005) Evidence for the involvement of the opioid system in the agmatine antidepressant-like effect in the forced swimming test. Neurosci Lett 381(3):279–283. https://doi.org/10.1016/j.neulet.2005.02.026
doi: 10.1016/j.neulet.2005.02.026 pubmed: 15896484

Auteurs

Dilan Gokalp (D)

Behavioral Neuroscience Laboratory, Department of Psychology, Boğaziçi University, 34342, Istanbul, Turkey.

Gunes Unal (G)

Behavioral Neuroscience Laboratory, Department of Psychology, Boğaziçi University, 34342, Istanbul, Turkey. gunes.unal@bogazici.edu.tr.

Classifications MeSH