Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-24T21:13:02.291Z Has data issue: false hasContentIssue false

Ketamine-induced antidepressant effects are associated with AMPA receptors-mediated upregulation of mTOR and BDNF in rat hippocampus and prefrontal cortex

Published online by Cambridge University Press:  15 April 2020

W. Zhou
Affiliation:
Department of Anesthesiology, School of Medicine, Jinling Hospital, Nanjing University, No. 305, East Zhongshan Road, Nanjing210002, China
N. Wang
Affiliation:
Department of Anesthesiology, School of Medicine, Jinling Hospital, Nanjing University, No. 305, East Zhongshan Road, Nanjing210002, China
C. Yang
Affiliation:
Department of Anesthesiology, School of Medicine, Jinling Hospital, Nanjing University, No. 305, East Zhongshan Road, Nanjing210002, China
X.-M. Li
Affiliation:
Department of Anesthesiology, School of Medicine, Jinling Hospital, Nanjing University, No. 305, East Zhongshan Road, Nanjing210002, China
Z.-Q. Zhou*
Affiliation:
Department of Anesthesiology, School of Medicine, Jinling Hospital, Nanjing University, No. 305, East Zhongshan Road, Nanjing210002, China
J.-J. Yang*
Affiliation:
Department of Anesthesiology, School of Medicine, Jinling Hospital, Nanjing University, No. 305, East Zhongshan Road, Nanjing210002, China
*
**Co-corresponding author. E-mail addresses: [email protected] (Z.-Q. Zhou), [email protected] (J.-J. Yang).
*Corresponding author. Tel.: +86 25 52323834; fax: +86 25 84806839.
Get access

Abstract

Ketamine exerts fast acting, robust, and lasting antidepressant effects in a sub-anesthetic dose, however, the underlying mechanisms are still not fully elucidated. Recent studies have suggested that ketamine's antidepressant effects are probably attributed to the activation of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. The present study aimed to observe the effects of AMPA receptor modulators on mammalian target of rapamycin (mTOR) and brain-derived neurotrophic factor (BDNF) expression during the procedure of ketamine exerting antidepressant effects. Therefore, we pretreated rats with NBQX, an AMPA receptor antagonist, or CX546, an AMPA receptor agonist, and subsequently observed the immobility time during the forced swimming test (FST) and the hippocampal and prefrontal cortical levels of mTOR and BDNF. The results showed ketamine decreased the immobility time of rats during the FST and increased the hippocampal and prefrontal cortical mTOR and BDNF. NBQX pretreatment significantly increased the immobility time and decreased the levels of mTOR and BDNF when compared with vehicle 1 (DMSO) pretreatment. CX546 pretreatment significantly decreased the immobility time and increased the levels of mTOR and BDNF when compared with vehicle 2 (DMSO + ethanol) pretreatment. Our results suggest ketamine-induced antidepressant effects are associated with AMPA receptors-mediated upregulation of mTOR and BDNF in rat hippocampus and prefrontal cortex.

Type
Original article
Copyright
Copyright © 2013 Elsevier Masson SAS

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

1

The two authors contributed equally to this work.

References

Acheson, A., Conover, J.C., Fandl, J.P., Dechiara, T.M., Russell, M., Thadant, A.et al.A BDNF autocrine loop in adult sensory neurons prevents cell death. Nature 1995;374(6521):450453.CrossRefGoogle ScholarPubMed
Akinfiresoye, L., Tizabi, Y.Antidepressant effects of AMPA and ketamine combination: role of hippocampal BDNF, synapsin, and mTOR. Psychopharmacology (Berl) 2013;4 [Epub ahead of print].Google Scholar
Autry, A.E., Adachi, M., Nosyreva, E., Na, E.S., Los, M.F., Cheng, P.F.et al.NMDA receptor blockade at rest triggers rapid behavioural antidepressant responses. Nature 2011;75(7354):9195.CrossRefGoogle Scholar
Beurel, E., Song, L., Jope, R.S.Inhibition of glycogen synthase kinase-3 is necessary for the rapid antidepressant effect of ketamine in mice. Mol Psychiatry 2011;16(11):10681070.CrossRefGoogle ScholarPubMed
Denk, M.C., Rewerts, C., Holsboer, F., Erhardt-Lehmann, A., Turck, C.W.Monitoring ketamine treatment response in a depressed patient via peripheral mammalian target of rapamycin activation. Am J Psychiatry 2011;168(7):751752.CrossRefGoogle Scholar
Detke, M.J., Rickels, M., Lucki, I.Active behaviors in the rat forced swimming test differentially produced by serotonergic and noradrenergic antidepressants. Psychopharmacology (Berl) 1995;121(1):6672.CrossRefGoogle ScholarPubMed
Diazgranados, N., Ibrahim, L., Brutsche, N.E., Newberg, A., Kronstein, P., Khalife, S.et al.A randomized add-on trial of an N-methyl-D-aspartate antagonist in treatment-resistant bipolar depression. Arch Gen Psychiatry 2010;67(8):793802.CrossRefGoogle ScholarPubMed
Duman, R.S., Li, N., Liu, R.J., Vanja, D., Aghajanian, G.Signaling pathways underlying the rapid antidepressant actions of ketamine. Neuropharmacology 2012;62(8):3541.CrossRefGoogle ScholarPubMed
Garcia, L.S., Comim, C.M., Valvassori, S.S., Réusa, G.Z., Barbosaa, L.M., Andreazzab, A.C.et al.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 2008;32(1):140144.CrossRefGoogle ScholarPubMed
Giacobbe, P., Mayberg, H.S., Lozano, A.M.Treatment resistant depression as a failure of brain homeostatic mechanisms: implications for deep brain stimulation. Exp Neurol 2009;219(1):4452.CrossRefGoogle ScholarPubMed
Huang, E.J., Reichardt, L.F., Neurotrophins:, roles in neuronal development and function. Annu Rev Neurosci 2001;24:677736.CrossRefGoogle ScholarPubMed
Kessler, R.C., Berglund, P., Demler, O., Jin, R., Merikangas, K.R., Walters, E.E.Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry 2005;62(6):593602.CrossRefGoogle ScholarPubMed
Koike, H., Iijima, M., Chaki, S.Involvement of AMPA receptor in both the rapid and sustained antidepressant-like effects of ketamine in animalmodels of depression. Behav Brain Res 2011;224(1):107111.CrossRefGoogle Scholar
Li, N., Lee, B., Liu, R.J., Banasr Mounira, , Dwyer, J.M., Iwata, M.et al.mTOR-dependent synapse formation underlies the rapid antidepressant effects of NMDA antagonists. Science 2010;329(5994):959964.CrossRefGoogle ScholarPubMed
Lindholm, J.S., Autio, H., Vesa, L., Antilaa, H., Lindemannc, L., Hoenerc, M.C.et al.The antidepressant-like effects of glutamatergic drugs ketamine and AMPA receptor potentiator LY 451646 are preserved in bdnf (+/-) heterozygous null mice. Neuropharmacology 2011;62(1):391397.CrossRefGoogle ScholarPubMed
Machado-Vieira, R., Salvadore, G., Diazgranados, N., Zarate, C.A. Jr.Ketamine and the next generation of antidepressants with a rapid onset of action. Pharmacol Ther 2009;123(2):143150.CrossRefGoogle ScholarPubMed
Machado-Vieira, R., Salvadore, G., Ibrahim, L.A., Diaz-Granados, N., Zarate, C.A. Jr.Targeting glutamatergic signaling for the development of novel therapeutics for mood disorders. Curr Pharm Des 2009;15(14):15951611.CrossRefGoogle ScholarPubMed
Maeng, S., Zarate, C.A. Jr., Du, J., Schloesser, R.J., McCammon, J., Chen, G.et al.Cellular mechanisms underlying the antidepressant effects of ketamine: role of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors. Biol Psychiatry 2008;63(4):349352.CrossRefGoogle ScholarPubMed
Mayberg, H.S.Targeted electrode-based modulation of neural circuits for depression. J Clin Invest 2009;119(4):717725.CrossRefGoogle ScholarPubMed
Messer, M., Haller, I.V., Larson, P., Pattison-Crisostomo, J., Gessert, C.E.The use of a series of ketamine infusions in two patients with treatment-resistant depression. J Neuropsychiatry Clin Neurosci 2010;22(4):442444.CrossRefGoogle ScholarPubMed
Nibuya, M., Morinobu, S., Duman, R.S.Regulation of BDNF and trkB mRNA in rat brain by chronic electroconvulsive seizure and antidepressant drug treatments. J Neurosci 1995;15(11):75397547.CrossRefGoogle ScholarPubMed
Nibuya, M., Nestler, E.J., Duman, R.S.Chronic antidepressant administration increases the expression of cAMP response element binding protein (CREB) in rat hippocampus. J Neurosci 1996;16(7):23652372.CrossRefGoogle Scholar
Pittenger, C., Sanacora, G., Krystal, J.H.The NMDA receptor as a therapeutic target in major depressive disorder. CNS Neurol Disord Drug Targets 2007;6(2):101115.CrossRefGoogle ScholarPubMed
Porsolt, R.D., Pichon, M.L., Jalfre, M.Depression: a new animal model sensitive to antidepressant treatments. Nature 1977;266(5604):730733.CrossRefGoogle ScholarPubMed
Savitz, J., Drevets, W.C.Bipolar and major depressive disorder: neuroimaging the developmental-degenerative divide. Neurosci Biobehav Rev 2009;33(5):699771.CrossRefGoogle ScholarPubMed
Tizabi, Y., Bhatti, B.H., Manaye, K.F., Das, J.R., Akinfiresoye, L.Antidepressant-like effects of low ketamine dose is associated with increased hippocampal AMPA/NMDA receptor density ratio in female Wistar-Kyoto rats. Neuroscience 2012;213:7280.CrossRefGoogle ScholarPubMed
Yang, C., Zhou, Z.Q., Gao, Z.Q., Shi, J.Y., Yang, J.J.Acute increases in plasma Mammalian target of rapamycin, glycogen synthase kinase-3β, and eukaryotic elongation factor 2 phosphorylation after ketamine treatment in three depressed patients. Biol Psychiatry 2013;73(12):e35e36.CrossRefGoogle ScholarPubMed
Yang, C., Hu, Y.M., Zhou, Z.Q., Zhang, G.F., Yang, J.J.Acute administration of ketamine in rats increases hippocampal BDNF and mTOR levels during forced swimming test. Ups J Med Sci 2013;118(1):38.CrossRefGoogle ScholarPubMed
Submit a response

Comments

No Comments have been published for this article.