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Covariation of activity in habenula and dorsal raphe nuclei following tryptophan depletion
Open accessAbstract
Abnormal serotonergic function is implicated in the pathogenesis of affective disorders. We induced transient depressive relapses in volunteer patients by rapidly depleting plasma tryptophan, the precursor of serotonin (5-HT), and measured neural activity during different cognitive tasks using positron emission tomography (PET). Neural activity in several 5-HT-related brain areas, e.g., dorsal raphé, habenula, septal region, amygdala, and orbitofrontal cortex, covaried significantly with plasma levels of tryptophan and ratings of depressed mood. Task-specific responses in left amygdala and left anterior cingulate were attenuated by tryptophan depletion. We used these PET data to test the hypothesis that projections from the habenula modulate dorsal raphé activity and that this modulation is enhanced in patients experiencing a profound mood change following serotonergic challenge. A strong linear correlation (r(2) > 0.5) between habenula and raphé activity was observed in subjects with postdepletion ratings >/=10 on a modified Hamilton depression scale, whereas subjects experiencing milder changes in mood had weaker habenula-raphé coupling (r(2) < 0.5). These data support a model of the serotonergic system in which the habenula projection to the raphé represents a convergent feedback pathway that controls the release of 5-HT throughout the brain. In our experiment we were able to engage this system in patients who were sensitive to tryptophan depletion.
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Cites
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
Statistical parametric maps in functional imaging: A general linear approach
Friston, K. J., Holmes, A. P., Worsley, K. J., Poline, J. ‐., Frith, C. D., & Frackowiak, R. S. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020402 · Cited by 9,688
Self-citationCo-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726
Psychophysiological and Modulatory Interactions in Neuroimaging
Friston, K. J., Buechel, C., Fink, G. R., Morris, J., Rolls, E., & Dolan, R. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0291 · Cited by 3,097
Self-citation(1995) · Choice Reviews Online · doi:10.5860/choice.32-5931 · Cited by 2,337
Paxinos, G., & Jürgen, K. (2004) · Cited by 1,478
Jeurgen, K., Assheuer, J., & Paxinos, G. (1997) · Medical Entomology and Zoology · Cited by 1,403
A functional anatomical study of unipolar depression
Drevets, W., Videen, T., Price, J., Preskorn, S., Carmichael, S., & Raichle, M. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-09-03628.1992 · Cited by 1,266
The Biochemistry of Affective Disorders
Coppen, A. (1967) · British Journal of Psychiatry · doi:10.1192/bjp.113.504.1237 · Cited by 1,230
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Deakin, J. F. W. (2003) · Journal of Neural Transmission. Supplementa · doi:10.1007/978-3-7091-6020-6_5 · Cited by 65
A unified model of ketamine’s dissociative and psychedelic properties
Marguilho, M., Figueiredo, I., & Castro-Rodrigues, P. (2022) · Journal of Psychopharmacology · doi:10.1177/02698811221140011 · Cited by 71
Fusar‐Poli, P., Allen, P., McGuire, P. K., Placentino, A., Cortesi, M., & Pérez, J. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0493-1 · Cited by 70
Beyond depression: Toward a process‐based approach to research, diagnosis, and treatment.
Forgeard, M. J. C., Haigh, E. A. P., Beck, A. T., Davidson, R. J., Henn, F. A., Maier, S. F., Mayberg, H. S., & Seligman, M. E. P. (2011) · Clinical Psychology Science and Practice · doi:10.1111/j.1468-2850.2011.01259.x · Cited by 70
Borgonovo, J. E., Allende-Castro, C., Laliena, A., Guerrero, N., Hernán Silva, I., & Concha, M. L. (2016) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2016.11.009 · Cited by 64
Han, L., Zhang, L., Li, L., Sun, Y., Wang, Y., Chen, L., Guo, Y., Zhang, Y., Zhang, Q.-J., & Liu, J. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.01.024 · Cited by 63
Benarroch, E. E. (2015) · Neurology · doi:10.1212/wnl.0000000000001937 · Cited by 61
Nathan, F. M., Ogawa, S., & Parhar, I. S. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13105 · Cited by 59
Milak, M. S., Parsey, R. V., Lee, L., Oquendo, M. A., Olvet, D. M., Eipper, F., Malone, K. M., & Mann, J. J. (2009) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2008.09.004 · Cited by 58
Generalizability of Footwear Traction Performance across Flooring and Contaminant Conditions
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Conserved expression of the GPR151 receptor in habenular axonal projections of vertebrates
Jester-Broms, J., Antolin‐Fontes, B., Tingström, A., & Ibáñez-Tallon, I. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23664 · Cited by 54
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Hutchinson, A. N., Deng, J. V., Cohen, S., & West, A. E. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2156-12.2012 · Cited by 53
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Jeon, S. G., Yoo, A., Chun, D. W., Hong, S. B., Chung, H., Kim, J.-I., & Moon, M. (2020) · Aging and Disease · doi:10.14336/ad.2019.0718 · Cited by 57
Decreased anxiety-like behavior in beta3 nicotinic receptor subunit knockout mice
Booker, T. K., Butt, C. M., Wehner, J. M., Heinemann, S. F., & Collins, A. C. (2007) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2007.04.011 · Cited by 49
Volumetric MRI study of the habenula in first episode, recurrent and chronic major depression
Carceller‐Sindreu, M., de Diego-Adeliño, J., Serra-Blasco, M., Vives‐Gilabert, Y., n-Blanco, A. M., Puigdemont, D., Álvarez, E., Pérez, V., & Portella, M. J. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.08.009 · Cited by 49
Morphologic and immunohistochemical organization of the human habenular complex
Dı́az, E., Bravo, D., Rojas, X., & Concha, M. L. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22687 · Cited by 50
Sourani, D., Eitan, R., Gordon, N., & Goelman, G. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08200.x · Cited by 53
A Sex-Specific Role of Type VII Adenylyl Cyclase in Depression
Hines, L. M., Hoffman, P. L., Bhave, S. V., Saba, L. M., Kaiser, A., Snell, L. D., Goncharov, I., Legault, L., Dongier, M., Grant, B. F., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1040-06.2006 · Cited by 50
Li, N., Zhang, X., Dong, H., Hu, Y., & Qian, Y. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.01.006 · Cited by 47
White Matter Injury, Neural Connectivity and the Pathophysiology of Psychiatric Disorders
Kumar, A., & Cook, I. A. (2002) · Developmental Neuroscience · doi:10.1159/000066746 · Cited by 48
Predominant Striatal Input to the Lateral Habenula in Macaques Comes from Striosomes
Hong, S., Amemori, S., Chung, E., Gibson, D. J., Amemori, K., & Graybiel, A. M. (2018) · Current Biology · doi:10.1016/j.cub.2018.11.008 · Cited by 43
van der Veen, F. M., Evers, E. A. T., van Deursen, J. A., Deutz, N. E. P., Backes, W. H., & Schmitt, J. A. J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.014 · Cited by 45
Effect of acute tryptophan depletion on pre-frontal engagement
Allen, P., Cleare, A. J., Lee, F. L. F., Fusar‐Poli, P., Tunstall, N., Fu, C. H. Y., BRAMMER, M. J., & McGuire, P. K. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0444-x · Cited by 46
Chang, S.-Y., & Kim, U. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4891-03.2004 · Cited by 44
Luo, X., Zhang, B. L., Li, J. C., Yang, Y., Sun, Y., & Zhao, H. (2014) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2014.11.006 · Cited by 42
Rizvi, S. J., Donovan, M., Giacobbe, P., Placenza, F., Rotzinger, S., & Kennedy, S. H. (2011) · International Review of Psychiatry · doi:10.3109/09540261.2011.630993 · Cited by 42
Wang, T., Zhang, L., Zhang, Q.-J., Wang, Y., Du, C., Sun, Y., Zhang, J., Lv, S.-X., Chen, L., & Liu, J. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.01.015 · Cited by 43
Patterning and Compartment Formation in the Diencephalon
Chatterjee, M., & Li, J. Y. H. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00066 · Cited by 40
Mapping of the internal structure of human habenula with ex vivo MRI at 7T
Strotmann, B., Kögler, C., Bazin, P., Weiß, M., Villringer, A., & Turner, R. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00878 · Cited by 40
Lateral habenula perturbation reduces default-mode network connectivity in a rat model of depression
Clemm von Hohenberg, C., Weber-Fahr, W., Lebhardt, P., Ravi, N., Braun, U., Gass, N., Becker, R., Sack, M., Cosa Linan, A., Gerchen, M. F., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0121-y · Cited by 39
Response Flexibility: The Role of the Lateral Habenula
Hones, V. I., & Mizumori, S. J. Y. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.852235 · Cited by 41
Kim, Y., Morath, B. A., Hu, C., Byrne, L. K., Sutor, S. L., Frye, M. A., & Tye, S. J. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.02.039 · Cited by 38
Substance P receptor antagonist in lateral habenula improves rat depression-like behavior
Yang, L.-M., Yu, L., Jin, H., & Zhao, H. (2013) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.10.007 · Cited by 36
Information processing in the vertebrate habenula
Fore, S., Palumbo, F., Pelgrims, R., & Yaksi, E. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.019 · Cited by 37
Toward an understanding of the habenula's various roles in human depression
Aizawa, H., & Zhu, M. (2019) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12892 · Cited by 38
Connections of the laterodorsal tegmental nucleus with the habenular‐interpeduncular‐raphe system
Bueno, D., Lima, L. B., Souza, R., Gonçalves, L., Leite, F., Souza, S., Furigo, I. C., Donato, J., & Metzger, M. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24729 · Cited by 46
Molecular Profiling of the Lateral Habenula in a Rat Model of Depression
Christensen, T. T., Jensen, L., Bouzinova, E. V., & Wiborg, O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080666 · Cited by 38
Ongoing habenular activity is driven by forebrain networks and modulated by olfactory stimuli
Bartoszek, E. M., Ostenrath, A. M., Jetti, S. K., Serneels, B., Mutlu, A. K., Chau, K. T. P., & Yaksi, E. (2021) · Current Biology · doi:10.1016/j.cub.2021.08.021 · Cited by 31
Zheng, Z., Liu, Y., Mu, R., Guo, X., Feng, Y., Chen, G., Yang, L., Qiu, W., Zhang, Q., Yang, W., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.09.012 · Cited by 36
Neural circuit adaptations during drug withdrawal — Spotlight on the lateral habenula
Meye, F. J., Trusel, M., Soiza‐Reilly, M., & Mameli, M. (2017) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.08.007 · Cited by 38
Oscillatory serotonin function in depression
Salomon, R. M., & Cowan, R. L. (2013) · Synapse · doi:10.1002/syn.21675 · Cited by 36
Habenular connectivity may predict treatment response in depressed psychiatric inpatients
Gosnell, S. N., Curtis, K. N., Velasquez, K. M., Fowler, J. C., Madan, A., Goodman, W. K., & Salas, R. (2018) · Journal of Affective Disorders · doi:10.1016/j.jad.2018.08.026 · Cited by 33
Imaging the serotonergic system in depression
D’Haenen, H. (2001) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf03035133 · Cited by 33
Modulation of Locomotor Activation by the Rostromedial Tegmental Nucleus
Lavezzi, H. N., Parsley, K. P., & Zahm, D. S. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.223 · Cited by 35
Neuronal substrates underlying stress resilience and susceptibility in rats
Febbraro, F., Svenningsen, K., Tran, T. P., & Wiborg, O. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179434 · Cited by 35
A habenula-insular circuit encodes the willingness to act
Khalighinejad, N., Garrett, N., Priestley, L., Lockwood, P., & Rushworth, M. F. S. (2021) · Nature Communications · doi:10.1038/s41467-021-26569-1 · Cited by 32
Zepf, F. D., Gaber, T. J., Baurmann, D., Bubenzer, S., Konrad, K., Herpertz‐Dahlmann, B., Stadler, C., Poustka, F., & Wöckel, L. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s146114571000012x · Cited by 33
Hunter, A. M., Korb, A. S., Cook, I. A., & Leuchter, A. F. (2013) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.11110330 · Cited by 33
Lateral Habenula Gone Awry in Depression: Bridging Cellular Adaptations With Therapeutics
Nuno‐Perez, A., Tchenio, A., Mameli, M., & Lecca, S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00485 · Cited by 31
Luan, S., Zhang, L., Wang, R., Zhao, H., & Liu, C. (2019) · Brain and Behavior · doi:10.1002/brb3.1229 · Cited by 29
Medina, L. M., Abellán, A., Vicario, A., Castro‐Robles, B., & Desfilis, E. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00019-1 · Cited by 32
Sonkusare, S., Ding, Q., Zhang, Y., Wang, L., Gong, H., Mandali, A., Manssuer, L. R., Zhao, Y.-J., Pan, Y., Zhang, C., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01830-3 · Cited by 24
Mapping of the habenulo-interpeduncular pathway in living mice using manganese-enhanced 3D MRI
Watanabe, T., Radulović, J., Boretius, S., Frahm, J., & Michaelis, T. (2006) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2005.10.034 · Cited by 28
Shumake, J., Colorado, R. A., Barrett, D. W., & Gonzalez-Lima, F. (2010) · Brain Research · doi:10.1016/j.brainres.2010.05.015 · Cited by 27
Han, L. N., Zhang, L., Sun, Y., Du, C., Zhang, Y. M., Wang, T., Zhang, J., & Liu, J. (2016) · Brain Research · doi:10.1016/j.brainres.2016.05.016 · Cited by 27
Huang, Y., Sun, B., Debarros, J., Zhang, C., Zhan, S., Li, D., Zhang, C., Wang, T., Huang, P., Lai, Y., et al. (2021) · eLife · doi:10.7554/elife.65444 · Cited by 26
Activation of the septohippocampal system differentiates anxiety from fear in startle paradigms
Veening, J. G., Böcker, K. B. E., Verdouw, P. M., Olivier, B., de Jongh, R., & Groenink, L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.06.064 · Cited by 26
Wang, Z., Jiang, C. Q., Guan, L., Zhao, L., Fan, T., Wang, J., Cai, X., Zhang, Y., Chen, Y., Peng, B., et al. (2024) · Nature Mental Health · doi:10.1038/s44220-024-00286-2 · Cited by 26
Padilla‐Tolentino, E., Shumake, J., Barrett, D. W., Sheridan, E. C., & Gonzalez-Lima, F. (2011) · Brain Research · doi:10.1016/j.brainres.2011.02.080 · Cited by 24
Cortico‐limbic connectivity in MAOA‐L carriers is vulnerable to acute tryptophan depletion
Eisner, P. D., Klasen, M., Wolf, D., Zerres, K., Eggermann, T., Eisert, A., Zvyagintsev, M., Sarkheil, P., Mathiak, K. A., Zepf, F. D., et al. (2016) · Human Brain Mapping · doi:10.1002/hbm.23475 · Cited by 25
The rostromedial tegmental nucleus modulates the development of stress-induced helpless behavior
Elmer, G. I., Palacorolla, H., Mayo, C. L., Brown, P. L., Jhou, T. C., Brady, D. L., & Shepard, D. S. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.06.014 · Cited by 23
Zebrafish Tools for Deciphering Habenular Network-Linked Mental Disorders
Bühler, A., & Carl, M. (2021) · Biomolecules · doi:10.3390/biom11020324 · Cited by 23
Lyu, S., Guo, Y., Zhang, L., Tang, G., Li, R., Yang, J., Gao, S., Li, W., & Liu, J. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108691 · Cited by 23
Wang, M., Chen, X., Hu, Y., Zhou, Y., Wang, C., Zheng, W., Liu, W., Lan, X., Ning, Y., & Zhang, B. (2021) · Depression and Anxiety · doi:10.1002/da.23238 · Cited by 21
Time series fMRI measures detect changes in pontine raphé following acute tryptophan depletion
Salomon, R. M., Cowan, R. L., Rogers, B. P., Dietrich, M. S., Bauernfeind, A. L., KESSLER, R. M., & Gore, J. C. (2011) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2010.10.007 · Cited by 21
The mu opioid receptor and the orphan receptor GPR151 contribute to social reward in the habenula
Allain, F., Carter, M., Dumas, S., Darcq, E., & Kieffer, B. L. (2022) · Scientific Reports · doi:10.1038/s41598-022-24395-z · Cited by 20
The behavioral relevance of a modular organization in the lateral habenula
Michel, L., Molina, P., & Mameli, M. (2024) · Neuron · doi:10.1016/j.neuron.2024.04.026 · Cited by 24
Zhang, Z., Zhang, W., Fang, Y., Wang, N., Liu, G., Zou, N., Song, Z., Liu, H., Wang, L., Xiao, Q., et al. (2024) · Current Biology · doi:10.1016/j.cub.2024.05.075 · Cited by 21
Zhang, J., Wang, Y., Sun, Y., Li, L. B., Zhang, L., Guo, Y., Wang, T., Yao, L., Chen, L., & Liu, J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107687 · Cited by 20
Clerke, J. A., Congiu, M., & Mameli, M. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108617 · Cited by 21
Lecca, S., Trusel, M., & Mameli, M. (2016) · Synapse · doi:10.1002/syn.21948 · Cited by 20
Disconnectivity between Dorsal Raphe Nucleus and Posterior Cingulate Cortex in Later Life Depression
Ikuta, T., Matsuo, K., Harada, K., Nakashima, M., Hobara, T., Higuchi, N., Higuchi, F., Otsuki, K., Shibata, T., Watanuki, T., et al. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00236 · Cited by 23
Hartung, H., Tan, S. K. H., Temel, Y., & Sharp, T. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13397 · Cited by 20
Zhang, J., Lv, S.-X., Tang, G., Bian, G., Yang, Y., Li, R., Yang, J., & Liu, J. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113058 · Cited by 19
Amino acid challenge and depletion techniques in human functional neuroimaging studies: an overview
Biskup, C. S., Gaber, T. J., Helmbold, K., Bubenzer‐Busch, S., & Zepf, F. D. (2015) · Amino Acids · doi:10.1007/s00726-015-1919-z · Cited by 19
Lyu, S., Guo, Y., Zhang, L., Wang, Y., Tang, G., Li, R., Yang, J., Gao, S., Ma, B.-R., & Liu, J. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108369 · Cited by 18
Nakamura, T., Kurosaki, K., Kanemoto, M., Sasahara, M., & Ichijo, H. (2021) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.200226 · Cited by 19
Cui, Y., Yang, Y., Dong, Y., & Hu, H. (2018) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2018.83.036871 · Cited by 20
Post, R. J., Bulkin, D. A., Bulkin, D. A., Ebitz, R. B., Lee, V., Han, K., & Warden, M. R. (2022) · Current Biology · doi:10.1016/j.cub.2022.08.016 · Cited by 21
Nugent, A. C., Neumeister, A., Goldman, D. A., Herscovitch, P., Charney, D. S., & Drevets, W. C. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.07.040 · Cited by 17
Roddy, D. W., Roman, E., Rooney, S., Andrews, S., Farrell, C., Doolin, K., Levins, K. J., Tozzi, L., Tierney, P., Barry, D., et al. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00039 · Cited by 16
Silva, J. C. H., Pausic, N., Marroquín-Rivera, A., Labonté, B., & Proulx, C. D. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2082-23.2024 · Cited by 16
Kocabıçak, E., Jahanshahi, A., Schönfeld, L.-M., Hescham, S., Temel, Y., & Tan, S. K. H. (2014) · Turkish Neurosurgery · doi:10.5137/1019-5149.jtn.11230-14.0 · Cited by 15
Skandalakis, G. P., Koutsarnakis, C., Kalyvas, A., Skandalakis, P. N., Johnson, E. O., & Stranjalis, G. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.041 · Cited by 15
Laterality and Sex Differences of Human Lateral Habenula Afferent and Efferent Fiber Tracts
Hitti, F. L., Parker, D., Yang, A. I., Brem, S. S., & Verma, R. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.837624 · Cited by 14
Jakobs, M., Pitzer, C., Sartorius, A., Unterberg, A. W., & Kiening, K. L. (2019) · Brain Research · doi:10.1016/j.brainres.2019.06.002 · Cited by 16
Functional opposition between habenula metabolism and the brain reward system
Shumake, J., & Gonzalez-Lima, F. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00662 · Cited by 14
Wang, L., Feng, Z., Zheng, T., Dai, G., Wang, M., Zhou, L., Zheng, Y., & Chen, G. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110675 · Cited by 15
Habenular functional connections are associated with depression state and modulated by ketamine
Chen, C., Wang, M., Yu, T., Feng, W., Xu, Y., Ning, Y., & Zhang, B. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.10.136 · Cited by 13
Effects of acute tryptophan depletion on raphé functional connectivity in depression
Weinstein, J. J., Rogers, B. P., Taylor, W. D., Boyd, B. D., Cowan, R. L., Shelton, K. M., & Salomon, R. M. (2015) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2015.08.015 · Cited by 15
Deep Brain Stimulation for Depression
Filkowski, M. M., & Sheth, S. A. (2019) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2018.12.007 · Cited by 13
The habenula in mood disorders: A systematic review of human studies
Fortin, J., Lafleur, M., Parisien, C., & Hétu, S. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03105-x · Cited by 13
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Metadata
- Authors
- Morris, J. S., Smith, K. A., Cowen, P. J., Friston, K. J., & Dolan, R. J.
- Affiliations
- National Hospital for Neurology and Neurosurgery (GB)
- Warneford Hospital (GB)
- The Royal Free Hospital (GB)
- Corresponding author
- Dolan, R.J.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 1999-08
- Volume
- 10
- Issue
- 2
- Pages
- 163-172
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2030196595
- Cited by
- 288
- References
- 45
- Citations by year
- 2026: 5 · 2025: 6 · 2024: 18 · 2023: 9 · 2022: 14 · 2021: 15 · 2020: 8 · 2019: 16 · 2018: 18 · 2017: 17 · 2016: 16 · 2015: 16 · 2014: 17 · 2013: 21 · 2012: 14
- FWCI
- 1.57
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Max Planck Digital Library (submittedVersion, other-oa)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Keywords
- tryptophan depletion, serotonin, habenula, dorsal raphe nucleus, serotonergic system, depression, amygdala, anterior cingulate cortex, mood disorders, depressive mood
- MeSH terms
- Adult, Amygdala, Arousal, Attention, Brain Mapping, Major Depressive Disorder, Gyrus Cinguli, Humans, Image Processing, Computer-Assisted, Male, Middle Aged, Raphe Nuclei, Recurrence, Serotonin, Tomography, Emission-Computed, Tryptophan, Verbal Behavior, Habenula
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