Abstract
Optogenetics, the light-induced reversible control of specific neuronal ensembles, has revolutionized the circuit level analysis of depression, leading to the identification of relevant circuitries in several brain regions including—but not limited to—medial prefrontal cortex, ventral tegmental area, and nucleus accumbens in rodents. While it is still early to observe a direct translational utility, the continuous progress in optogenetic interrogation of specific neural populations has great potential for untangling the complex pathophysiology of depression.
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Notes
- 1.
https://www.who.int/news-room/fact-sheets/detail/depression retrieved in 03.04.2021
Abbreviations
- 5-HT:
-
5-Hydroxytryptamine
- AAVs:
-
Adeno-associated viruses
- ACC:
-
Anterior cingulate cortex
- AD:
-
Antidepressant
- AMY:
-
Amygdala
- avBNST:
-
Anteroventral bed nuclei of the stria terminalis
- BDNF:
-
Brain-derived neurotrophic factor
- BLA:
-
Basolateral amygdala
- BMA:
-
Basomedial amygdala
- BNST:
-
Bed nucleus of the stria terminalis
- CaMKIIa:
-
Ca2+/calmodulin-dependent protein kinase II
- CCK:
-
Cholecystokinin
- CCK-B:
-
Cholecystokinin-B receptor
- CeA:
-
Central amygdala
- ChR2:
-
Channelrhodopsin-2
- CMS:
-
Chronic mild stress
- CRF:
-
Corticotropin-releasing factor
- CSDS:
-
Chronic social defeat stress
- D1:
-
Dopamine 1
- D2:
-
Dopamine 2
- DA:
-
Dopamine
- DG:
-
Dentate gyrus
- Drd1:
-
Dopamine receptor 1
- Drd2:
-
Dopamine receptor 2
- DRN:
-
Dorsal raphe nucleus
- EPM:
-
Elevated plus maze
- FST:
-
Forced swim test
- GABA:
-
Gamma-aminobutyric acid
- GABA(A)Rs:
-
Gamma-aminobutyric acid A receptors
- GluClR:
-
Glutamate-gated chloride channel receptor
- HPA system:
-
Hypothalamus-pituitary-adrenal system
- IL-PFC:
-
Infralimbic prefrontal cortex
- ILT:
-
Intralaminar thalamus
- LHb:
-
Lateral habenula
- MDT:
-
Medial dorsal thalamus
- mHb:
-
Medial habenula
- mPFC:
-
Medial prefrontal cortex
- MSNs:
-
Medium spiny neurons
- NAc:
-
Nucleus accumbens
- NMDAR:
-
N-Methyl-D-aspartate receptor
- NSF:
-
Novelty-suppressed feeding test
- PIT:
-
Pavlovian-to-instrumental transfer
- PR:
-
Progressive ratio
- PrL:
-
Prelimbic area
- PVH:
-
Paraventricular hypothalamus
- RMTg:
-
Rostromedial tegmental nucleus
- RN:
-
Raphe nucleus
- SDS:
-
Social defeat stress
- SPT:
-
Sucrose preference test
- SSDS:
-
Subthreshold social defeat stress
- TST:
-
Tail suspension test
- vGlut:
-
Vesicular glutamate transporter 2
- vHipp:
-
Ventral hippocampus
- vlPAG:
-
Ventrolateral periaqueductal gray
- vmPFC:
-
Ventral medial prefrontal cortex
- VP:
-
Ventral pallidum
- vSTR:
-
Ventral striatum
- VTA:
-
Ventral tegmental area
- ΔFosB:
-
DeltaFosB
References
James SL, Abate D, Abate KH, Abay SM, Abbafati C, Abbasi N et al (2018) Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: a systematic analysis for the global burden of disease study 2017. Lancet 392:1789–1858
Vos T, Barber RM, Bell B, Bertozzi-Villa A, Biryukov S, Bolliger I et al (2015) Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: a systematic analysis for the global burden of disease study 2013. Lancet 386:743–800
Malhi GS, Mann JJ (2018) Depression. Lancet 392:2299–2312. https://doi.org/10.1016/S0140-6736(18)31948-2
Arslan A (2015) Genes, brains, and behavior: imaging genetics for neuropsychiatric disorders. J Neuropsychiatry Clin Neurosci 27:81–92
Arslan A (2018) Imaging genetics of schizophrenia in the post-GWAS era. Prog Neuro-Psychopharmacology Biol Psychiatry 80:155–165
Coplan JD, Andrews MW, Rosenblum LA, Owens MJ, Friedman S, Gorman JM et al (1996) Persistent elevations of cerebrospinal fluid concentrations of corticotropin-releasing factor in adult nonhuman primates exposed to early-life stressors: implications for the pathophysiology of mood and anxiety disorders. Proc Natl Acad Sci U S A 93:1619–1623
Murphy BEP, Wolkowitz OM (1993) The pathophysiologic significance of hyperadrenocorticism: antiglucocorticoid strategies. Psychiatr Ann 23:682–690
Saxe MD, Battaglia F, Wang JW, Malleret G, David DJ, Monckton JE et al (2006) Ablation of hippocampal neurogenesis impairs contextual fear conditioning and synaptic plasticity in the dentate gyrus. Proc Natl Acad Sci U S A 103:17501–17506. https://doi.org/10.1073/pnas.0607207103
Santarelli L, Saxe M, Gross C, Surget A, Battaglia F, Dulawa S et al (2003) Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science 301:805–809. https://doi.org/10.1126/science.1083328
Luscher B, Shen Q, Sahir N (2011) The GABAergic deficit hypothesis of major depressive disorder. Mol Psychiatry 16:383–406
Inserra A, Rogers GB, Licinio J, Wong M (2018) The microbiota-inflammasome hypothesis of major depression. Bioessays 40:1800027
Fava M, Davidson KG (1996) Definition and epidemiology of treatment-resistant depression. Psychiatr Clin North Am 19:179–200
Machado-Vieira R, Baumann J, Wheeler-Castillo C, Latov D, Henter ID, Salvadore G et al (2010) The timing of antidepressant effects: a comparison of diverse pharmacological and somatic treatments. Pharmaceuticals (Basel) 3:19–41
Aydin O, Aydin PU, Arslan A (2019) Development of neuroimaging-based biomarkers in psychiatry. Adv Exp Med Biol 1192:159–195
Arslan A (2018) Application of neuroimaging in the diagnosis and treatment of depression. In: Understanding depression. Springer, pp 69–81
Unal Aydin P, Aydin O, Arslan A (2021) Genetic architecture of depression: Where do we stand now? Adv Exp Med Biol 1305:203–230
Kim Y-K, Park S-C (2021) An alternative approach to future diagnostic standards for major depressive disorder. Prog Neuro-Psychopharmacol Biol Psychiatry 105:110133
Arslan A (2018) Mapping the schizophrenia genes by neuroimaging: the opportunities and the challenges. Int J Mol Sci 19:219
Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P et al (2002) Initial sequencing and comparative analysis of the mouse genome. Nature 420:520–562
Nestler EJ, Hyman SE (2010) Animal models of neuropsychiatric disorders. Nat Neurosci 13:1161–1169. https://doi.org/10.1038/nn.2647
Barkus C (2013) Genetic mouse models of depression. Curr Top Behav Neurosci 14:55–78
Alexander B, Warner-Schmidt J, Eriksson TM, Tamminga C, Arango-Lievano M, Ghose S et al (2010) Reversal of depressed behaviors in mice by p11 gene therapy in the nucleus accumbens. Sci Transl Med 2:54ra76
Chourbaji S, Gass P (2008) Glucocorticoid receptor transgenic mice as models for depression. Brain Res Rev 57:554–560
Wang YM, Xu F, Gainetdinov RR, Caron MG (1999) Genetic approaches to studying norepinephrine function: Knockout of the mouse norepinephrine transporter gene. Biol Psychiatry 46:1124–1130. https://doi.org/10.1016/s0006-3223(99)00245-0
Holmes A, Yang RJ, Murphy DL, Crawley JN (2002) Evaluation of antidepressant-related behavioral responses in mice lacking the serotonin transporter. Neuropsychopharmacology 27:914–923
Urani A, Chourbaji S, Gass P (2005) Mutant mouse models of depression: candidate genes and current mouse lines. Neurosci Biobehav Rev 29:805–828. https://doi.org/10.1016/j.neubiorev.2005.03.020
Perona MTG, Waters S, Hall FS, Sora I, Lesch KP, Murphy DL et al (2008) Animal models of depression in dopamine, serotonin, and norepinephrine transporter knockout mice: prominent effects of dopamine transporter deletions. Behav Pharmacol 19:566–574. https://doi.org/10.1097/FBP.0b013e32830cd80f
Gallagher JJ, Zhang X, Hall FS, Uhl GR, Bearer EL, Jacobs RE (2013) Altered reward circuitry in the norepinephrine transporter knockout mouse. PLoS One 8:e57597
Stuber GD, Stamatakis AM, Kantak PA (2015) Considerations when using cre-driver rodent lines for studying ventral tegmental area circuitry. Neuron 85:439–445. https://doi.org/10.1016/j.neuron.2014.12.034
Liu G, Wang Y, Zheng W, Cheng H, Zhou R (2019) P11 loss-of-function is associated with decreased cell proliferation and neurobehavioral disorders in mice. Int J Biol Sci 15:1383
Wulff P, Goetz T, Leppä E, Linden AM, Renzi M, Swinny JD et al (2007) From synapse to behavior: rapid modulation of defined neuronal types with engineered GABAA receptors. Nat Neurosci 10:923–929. https://doi.org/10.1038/nn1927
Sullivan PF, Neale MC, Kendler KS (2000) Genetic epidemiology of major depression: review and meta-analysis. Am J Psychiatry 157:1552–1562
Arslan A (2015) The complexity of mental disorders. Period Eng Nat Sci 3
Bosker FJ, Hartman CA, Nolte IM, Prins BP, Terpstra P, Posthuma D et al (2011) Poor replication of candidate genes for major depressive disorder using genome-wide association data. Mol Psychiatry 16:516–532
Wray NR, Pergadia ML, Blackwood DHR, Penninx B, Gordon SD, Nyholt DR et al (2012) Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. Mol Psychiatry 17:36–48
Sullivan P, Andreassen OA, Anney RJL, Asherson P, Ashley-Koch A, Blackwood D et al (2012) Don’t give up on GWAS. Mol Psychiatry 17:2–3. https://doi.org/10.1038/mp.2011.94
Cai N, Bigdeli TB, Kretzschmar W, Li Y, Liang J, Song L et al (2015) Sparse whole-genome sequencing identifies two loci for major depressive disorder. Nature 523:588–591
Vaquero A, Scher M, Erdjument-Bromage H, Tempst P, Serrano L, Reinberg D (2007) SIRT1 regulates the histone methyl-transferase SUV39H1 during heterochromatin formation. Nature 450:440–444
Yokoi F, Hiraishi H, Izuhara K (2003) Molecular cloning of a cDNA for the human phospholysine phosphohistidine inorganic pyrophosphate phosphatase. J Biochem 133:607–614
Okbay A, Baselmans BML, De Neve J-E, Turley P, Nivard MG, Fontana MA et al (2016) Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat Genet 48:624–633
Direk N, Williams S, Smith JA, Ripke S, Air T, Amare AT et al (2017) An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biol Psychiatry 82:322–329
Hyde CL, Nagle MW, Tian C, Chen X, Paciga SA, Wendland JR et al (2016) Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. Nat Genet 48:1031
Berman RM, Cappiello A, Anand A, Oren DA, Heninger GR, Charney DS et al (2000) Antidepressant effects of ketamine in depressed patients. Biol Psychiatry 47:351–354
Murrough JW, Iosifescu DV, Chang LC, Al Jurdi RK, Green CE, Perez AM et al (2013) Antidepressant efficacy of ketamine in treatment-resistant major depression: a two-site randomized controlled trial. Am J Psychiatry 170:1134–1142. https://doi.org/10.1176/appi.ajp.2013.13030392
Fava M, Freeman MP, Flynn M, Judge H, Hoeppner BB, Cusin C et al (2020) Double-blind, placebo-controlled, dose-ranging trial of intravenous ketamine as adjunctive therapy in treatment-resistant depression (TRD). Mol Psychiatry 25:1592–1603
Zarate CA, Singh JB, Carlson PJ, Brutsche NE, Ameli R, Luckenbaugh DA et al (2006) A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression. Arch Gen Psychiatry 63:856–864. https://doi.org/10.1001/archpsyc.63.8.856
Domino EF, Chodoff P, Corssen G (1965) Pharmacologic effects of CI-581, a new dissociative anesthetic, in man. Clin Pharmacol Ther 6:279–291
Na KS (2021) Kim YK, vol 104. Prog Neuro-Psychopharmacol Biol Psychiatry, Increased use of ketamine for the treatment of depression: benefits and concerns, p 110060
Hodgkin AL (1958) The Croonian lecture-ionic movements and electrical activity in giant nerve fibres. Proc R Soc London Ser B Biol Sci 148:1–37
Arslan A (2021) Extrasynaptic δ-subunit containing GABAA receptors. J Integr Neurosci 20:173–184
Goetz T, Arslan A, Wisden W, Wulff P (2007) GABAA receptors: structure and function in the basal ganglia. Prog Brain Res 160:21–41
Arslan A (2015) Clustering of gamma-aminobutyric acid type A receptors. Period Eng Nat Sci 3
Lynagh T, Lynch JW (2010) An improved ivermectin-activated chloride channel receptor for inhibiting electrical activity in defined neuronal populations. J Biol Chem 285:14890–14897
Islam R, Keramidas A, Xu L, Durisic N, Sah P, Lynch JW (2016) Ivermectin-activated, cation-permeable glycine receptors for the chemogenetic control of neuronal excitation. ACS Chem Neurosci 7:1647–1657
Molday RS, Molday LL (1998) Molecular properties of the cGMP-gated channel of rod photoreceptors. Vision Res 38:1315–1323. https://doi.org/10.1016/s0042-6989(97)00409-4
Terakita A (2005) The opsins. Genome Biol 6:213. https://doi.org/10.1186/gb-2005-6-3-213
Takahashi T, Yoshihara K, Watanabe M, Kubota M, Johnson R, Derguini F et al (1991) Photoisomerization of retinal at 13-ene is important for phototaxis of Chlamydomonas reinhardtii: simultaneous measurements of phototactic and photophobic responses. Biochem Biophys Res Commun 178:1273–1279
Hegemann P, Gärtner W, Uhl R (1991) All-trans retinal constitutes the functional chromophore in Chlamydomonas rhodopsin. Biophys J 60:1477–1489
Hegemann P, Oesterhelt D, Steiner M (1985) The photocycle of the chloride pump halorhodopsin. I: Azidecatalyzed deprotonation of the chromophore is a side reaction of photocycle intermediates inactivating the pump. EMBO J 4:2347–2350
Kalaidzidis IV, Kalaidzidis YL, Kaulen AD (1998) Flash-induced voltage changes in halorhodopsin from Natronobacterium pharaonis. FEBS Lett 427:59–63
Oesterhelt D, Stoeckenius W (1971) Rhodopsin-like protein from the purple membrane of Halobacterium halobium. Nat New Biol 233:149–152. https://doi.org/10.1038/newbio233149a0
Eisenbach M, Bakker EP, Korenstein R, Caplan SR (1976) Bacteriorhodopsin: biphasic kinetics of phototransients and of light-induced proton transfer by sub-bacterial Halobacterium halobium particles and by reconstituted liposomes. FEBS Lett 71:228–232
Matsuno-Yagi A, Mukohata Y (1977) Two possible roles of bacteriorhodopsin; a comparative study of strains of Halobacterium halobium differing in pigmentation. Biochem Biophys Res Commun 78:237–243. https://doi.org/10.1016/0006-291x(77)91245-1
Lanyi JK (1986) Halorhodopsin: a light-driven chloride ion pump. Annu Rev Biophys Biophys Chem 15:11–28
Naldini L, Blömer U, Gallay P, Ory D, Mulligan R, Gage FH et al (1996) In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 272:263–267. https://doi.org/10.1126/science.272.5259.263
Dull T, Zufferey R, Kelly M, Mandel RJ, Nguyen M, Trono D et al (1998) A third-generation lentivirus vector with a conditional packaging system. J Virol 72:8463–8471
Wang X, McManus M (2009) Lentivirus production. J Vis Exp 32:1499. https://doi.org/10.3791/1499
Watakabe A, Sadakane O, Hata K, Ohtsuka M, Takaji M, Yamamori T (2017) Application of viral vectors to the study of neural connectivities and neural circuits in the marmoset brain. Dev Neurobiol 77:354–372. https://doi.org/10.1002/dneu.22459
Kwon KY, Lee H-M, Ghovanloo M, Weber A, Li W (2015) Design, fabrication, and packaging of an integrated, wirelessly-powered optrode array for optogenetics application. Front Syst Neurosci 9:69
Wang HX, Li M, Lee CM, Chakraborty S, Kim HW, Bao G et al (2017) CRISPR/Cas9-based genome editing for disease modeling and therapy: challenges and opportunities for nonviral delivery. Chem Rev 117:9874–9906. https://doi.org/10.1021/acs.chemrev.6b00799
Jinek M, Chylinski K, Fonfara I, Hauer M, Doudna JA, Charpentier E (2012) A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science 337:816–821. https://doi.org/10.1126/science.1225829
Niu Y, Shen B, Cui Y, Chen Y, Wang J, Wang L et al (2014) Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos. Cell 156:836–843. https://doi.org/10.1016/j.cell.2014.01.027
Cox DBT, Platt RJ, Zhang F (2015) Therapeutic genome editing: prospects and challenges. Nat Med 21:121–131
Haas SA, Dettmer V, Cathomen T (2017) Therapeutic genome editing with engineered nucleases. Hamostaseologie 37:45–52
Nishimasu H, Ran FA, Hsu PD, Konermann S, Shehata SI, Dohmae N et al (2014) Crystal structure of Cas9 in complex with guide RNA and target DNA. Cell 156:935–949. https://doi.org/10.1016/j.cell.2014.02.001
Hsu PD, Lander ES, Zhang F (2014) Development and applications of CRISPR-Cas9 for genome engineering. Cell 157:1262–1278
Polstein LR, Gersbach CA (2015) A light-inducible CRISPR-Cas9 system for control of endogenous gene activation. Nat Chem Biol 11:198–200. https://doi.org/10.1038/nchembio.1753
Bubeck F, Hoffmann MD, Harteveld Z, Aschenbrenner S, Bietz A, Waldhauer MC et al (2018) Engineered anti-CRISPR proteins for optogenetic control of CRISPR–Cas9. Nat Methods 15:924–927
Hoffmann MD, Mathony J, Zu Belzen JU, Harteveld Z, Stengl C, Correia BE et al (2021) Optogenetic control of Neisseria meningitidis Cas9 genome editing using an engineered, light-switchable anti-CRISPR protein. Nucleic Acids Res 49(5):e29
Duman RS, Sanacora G, Krystal JH (2019) Altered connectivity in depression: GABA and glutamate neurotransmitter deficits and reversal by novel treatments. Neuron Elsevier 102:75–90
Xu P, Chen A, Li Y, Xing X, Lu H (2019) Medial prefrontal cortex in neurological diseases. Physiol Genomics 51:432–442
Fuchikami M, Thomas A, Liu R, Wohleb ES, Land BB, DiLeone RJ et al (2015) Optogenetic stimulation of infralimbic PFC reproduces ketamine’s rapid and sustained antidepressant actions. Proc Natl Acad Sci U S A 112:8106–8111
Covington HE, Lobo MK, Maze I, Vialou V, Hyman JM, Zaman S et al (2010) Antidepressant effect of optogenetic stimulation of the medial prefrontal cortex. J Neurosci 30:16082–16090
Kumar S, Black SJ, Hultman R, Szabo ST, Demaio KD, Du J et al (2013) Cortical control of affective networks. J Neurosci 33:1116–1129
Son H, Baek JH, Go BS, Jung D-H, Sontakke SB, Chung HJ et al (2018) Glutamine has antidepressive effects through increments of glutamate and glutamine levels and glutamatergic activity in the medial prefrontal cortex. Neuropharmacology 143:143–152
Warden MR, Selimbeyoglu A, Mirzabekov JJ, Lo M, Thompson KR, Kim SY et al (2012) A prefrontal cortex-brainstem neuronal projection that controls response to behavioural challenge. Nature 492:428–432
Hare BD, Duman RS (2020) Prefrontal cortex circuits in depression and anxiety: contribution of discrete neuronal populations and target regions. Mol Psychiatry 25:2742–2758
Hare BD, Shinohara R, Liu RJ, Pothula S, DiLeone RJ, Duman RS (2019) Optogenetic stimulation of medial prefrontal cortex Drd1 neurons produces rapid and long-lasting antidepressant effects. Nat Commun 10:1–12. https://doi.org/10.1038/s41467-018-08168-9
Felix-Ortiz AC, Burgos-Robles A, Bhagat ND, Leppla CA, Tye KM (2016) Bidirectional modulation of anxiety-related and social behaviors by amygdala projections to the medial prefrontal cortex. Neuroscience 321:197–209
Liu RJ, Ota KT, Dutheil S, Duman RS, Aghajanian GK (2015) Ketamine strengthens CRF-activated amygdala inputs to basal dendrites in mPFC layer v pyramidal cells in the prelimbic but not infralimbic subregion, a key suppressor of stress responses. Neuropsychopharmacology 40:2066–2075
Carreno FR, Donegan JJ, Boley AM, Shah A, DeGuzman M, Frazer A et al (2016) Activation of a ventral hippocampus-medial prefrontal cortex pathway is both necessary and sufficient for an antidepressant response to ketamine. Mol Psychiatry 21:1298–1308
Carlson D, David LK, Gallagher NM, Vu MAT, Shirley M, Hultman R et al (2017) Dynamically timed stimulation of corticolimbic circuitry activates a stress-compensatory pathway. Biol Psychiatry 82:904–913
Chaudhury D, Walsh JJ, Friedman AK, Juarez B, Ku SM, Koo JW et al (2013) Rapid regulation of depression-related behaviours by control of midbrain dopamine neurons. Nature 493:532–536
Venzala E, García-García AL, Elizalde N, Tordera RM (2013) Social vs. environmental stress models of depression from a behavioural and neurochemical approach. Eur Neuropsychopharmacol 23:697–708
Tanaka K, Furuyashiki T, Kitaoka S, Senzai Y, Imoto Y, Segi-Nishida E et al (2012) Prostaglandin E 2-mediated attenuation of mesocortical dopaminergic pathway is critical for susceptibility to repeated social defeat stress in mice. J Neurosci 32:4319–4329
Shinohara R, Taniguchi M, Ehrlich AT, Yokogawa K, Deguchi Y, Cherasse Y et al (2018) Dopamine D1 receptor subtype mediates acute stress-induced dendritic growth in excitatory neurons of the medial prefrontal cortex and contributes to suppression of stress susceptibility in mice. Mol Psychiatry 23:1717–1730
Tye KM, Mirzabekov JJ, Warden MR, Ferenczi EA, Tsai HC, Finkelstein J et al (2013) Dopamine neurons modulate neural encoding and expression of depression-related behaviour. Nature 493:537–541
Fakhoury M (2021) Optogenetics: a revolutionary approach for the study of depression. Prog Neuro Psychopharmacol Biol Psychiatry 106:110094
Friedman AK, Walsh JJ, Juarez B, Ku SM, Chaudhury D, Wang J et al (2014) Enhancing depression mechanisms in midbrain dopamine neurons achieves homeostatic resilience. Science 344:313–319. https://doi.org/10.1126/science.1249240
Francis TC, Chandra R, Friend DM, Finkel E, Dayrit G, Miranda J et al (2015) Nucleus accumbens medium spiny neuron subtypes mediate depression-related outcomes to social defeat stress. Biol Psychiatry 77:212–222
Christoffel DJ, Golden SA, Walsh JJ, Guise KG, Heshmati M, Friedman AK et al (2015) Excitatory transmission at thalamo-striatal synapses mediates susceptibility to social stress. Nat Neurosci 18:962–964
Soares-Cunha C, Coimbra B, David-Pereira A, Borges S, Pinto L, Costa P et al (2016) Activation of D2 dopamine receptor-expressing neurons in the nucleus accumbens increases motivation. Nat Commun 7:11829
Bagot RC, Parise EM, Peña CJ, Zhang HX, Maze I, Chaudhury D et al (2015) Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression. Nat Commun 6:7062
Walsh EC, Eisenlohr-Moul TA, Minkel J, Bizzell J, Petty C, Crowther A et al (2019) Pretreatment brain connectivity during positive emotion upregulation predicts decreased anhedonia following behavioral activation therapy for depression. J Affect Disord 243:188–192
Walsh JJ, Friedman AK, Sun H, Heller EA, Ku SM, Juarez B et al (2014) Stress and CRF gate neural activation of BDNF in the mesolimbic reward pathway. Nat Neurosci 17:27–29
Vialou V, Bagot RC, Cahill ME, Ferguson D, Robison AJ, Dietz DM et al (2014) Prefrontal cortical circuit for depression- and anxiety-related behaviors mediated by cholecystokinin: role of ΔFosB. J Neurosci 34:3878–3887
Zhang X, Abdellaoui A, Rucker J, de Jong S, Potash JB, Weissman MM et al (2019) Genome-wide burden of rare short deletions is enriched in major depressive disorder in four cohorts. Biol Psychiatry 85:1065–1073
Knowland D, Lilascharoen V, Pacia CP, Shin S, Wang EHJ, Lim BK (2017) Distinct ventral pallidal neural populations mediate separate symptoms of depression. Cell 170:284–297.e18
Wook Koo J, Labonté B, Engmann O, Calipari ES, Juarez B, Lorsch Z et al (2016) Essential role of mesolimbic brain-derived neurotrophic factor in chronic social stress–induced depressive behaviors. Biol Psychiatry 80:469–478
Ohmura Y, Tsutsui-Kimura I, Sasamori H, Nebuka M, Nishitani N, Tanaka KF et al (2020) Different roles of distinct serotonergic pathways in anxiety-like behavior, antidepressant-like, and anti-impulsive effects. Neuropharmacology 167:107703
Fakhoury M (2017) The habenula in psychiatric disorders: More than three decades of translational investigation. Neurosci Biobehav Rev 83:721–735
Matsumoto M, Hikosaka O (2009) Representation of negative motivational value in the primate lateral habenula. Nat Neurosci 12:77–84
Proulx CD, Aronson S, Milivojevic D, Molina C, Loi A, Monk B et al (2018) A neural pathway controlling motivation to exert effort. Proc Natl Acad Sci U S A 115:5792–5797. https://doi.org/10.1073/pnas.1801837115
Albert PR, Benkelfat C, Descarries L (2012) The neurobiology of depression-revisiting the serotonin hypothesis. I. Cellular and molecular mechanisms. Philos Trans R Soc Lond B Biol Sci 367:2378–2381
Adell A (2015) Revisiting the role of raphe and serotonin in neuropsychiatric disorders. J Gen Physiol 145:257–259
Fakhoury M (2016) Revisiting the serotonin hypothesis: implications for major depressive disorders. Mol Neurobiol 53:2778–2786
Challis C, Beck SG, Berton O (2014) Optogenetic modulation of descending prefrontocortical inputs to the dorsal raphe bidirectionally bias socioaffective choices after social defeat. Front Behav Neurosci 8:43. https://doi.org/10.3389/fnbeh.2014.00043
Zhang H, Li K, Chen HS, Gao SQ, Xia ZX, Zhang JT et al (2018) Dorsal raphe projection inhibits the excitatory inputs on lateral habenula and alleviates depressive behaviors in rats. Brain Struct Funct 223:2243–2258
Ramirez S, Liu X, MacDonald CJ, Moffa A, Zhou J, Redondo RL et al (2015) Activating positive memory engrams suppresses depression-like behaviour. Nature 522:335–339
Johnson SB, Emmons EB, Anderson RM, Glanz RM, Romig-Martin SA, Narayanan NS et al (2016) A basal forebrain site coordinates the modulation of endocrine and behavioral stress responses via divergent neural pathways. J Neurosci 36:8687–8699
Cai YQ, Wang W, Paulucci-Holthauzen A, Pan ZZ (2018) Brain circuits mediating opposing effects on emotion and pain. J Neurosci 38:6340–6349
Phelps EA, LeDoux JE (2005) Contributions of the amygdala to emotion processing: from animal models to human behavior. Neuron 48:175–187
Crestani C, Alves F, Gomes F, Resstel L, Correa F, Herman J (2013) Mechanisms in the bed nucleus of the Stria terminalis involved in control of autonomic and neuroendocrine functions: a review. Curr Neuropharmacol 11:141–159
Chapin JC, Monahan PH (2018) Gene Therapy for Hemophilia: Progress to Date
Jean, Bennett Jennifer, Wellman Kathleen A, Marshall Sarah, McCague Manzar, Ashtari Julie, DiStefano-Pappas Okan U, Elci Daniel C, Chung Junwei, Sun J Fraser, Wright Dominique R, Cross Puya, Aravand Laura L, Cyckowski Jeannette L, Bennicelli Federico, Mingozzi Alberto, Auricchio Eric A, Pierce Jason, Ruggiero Bart P, Leroy Francesca, Simonelli Katherine A, High Albert M, Maguire (2016) Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial. The Lancet 388(10045):661–672. https://doi.org/10.1016/S0140-6736(16)30371-3
Naso MF, Tomkowicz B, Perry WL, Strohl WR (2017) Adeno-Associated Virus (AAV) as a vector for gene therapy. BioDrugs 31(4):317–334. https://doi.org/10.1007/s40259-017-0234-5
Joshi J, Rubart M, Zhu W (2020) Optogenetics: background, methodological advances and potential applications for cardiovascular research and medicine. Front Bioeng Biotechnol 7:466
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Arslan, A., Unal-Aydin, P., Dogan, T., Aydin, O. (2022). Optogenetic Animal Models of Depression: From Mice to Men. In: Kim, YK., Amidfar, M. (eds) Translational Research Methods for Major Depressive Disorder. Neuromethods, vol 179. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2083-0_8
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