The DOI matches its Crossref record; 74 of the 76 references it cites were found in a registry or an index.
Dendritic remodeling of D1 neurons by RhoA/Rho-kinase mediates depression-like behavior
Open accessAbstract
Depression alters the structure and function of brain reward circuitry. Preclinical evidence suggests that medium spiny neurons (MSNs) in the nucleus accumbens (NAc) undergo structural plasticity; however, the molecular mechanism and behavioral significance is poorly understood. Here we report that atrophy of D1, but not D2 receptor containing MSNs is strongly associated with social avoidance in mice subject to social defeat stress. D1-MSN atrophy is caused by cell-type specific upregulation of the GTPase RhoA and its effector Rho-kinase. Pharmacologic and genetic reduction of activated RhoA prevents depressive outcomes to stress by preventing loss of D1-MSN dendritic arbor. Pharmacologic and genetic promotion of activated RhoA enhances depressive outcomes by reducing D1-MSN dendritic arbor and is sufficient to promote depressive-like behaviors in the absence of stress. Chronic treatment with Rho-kinase inhibitor Y-27632 after chronic social defeat stress reverses depression-like behaviors by restoring D1-MSN dendritic complexity. Taken together, our data indicate functional roles for RhoA and Rho-kinase in mediating depression-like behaviors via dendritic remodeling of NAc D1-MSNs and may prove a useful target for new depression therapeutics.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Susceptibility to chronic social defeat stress is accompanied by atrophy of MSN dendrites, specifically in D1 MSNs and not D2 MSNs, and a corresponding loss of dendritic spines [226,234,235].”
From Plasticity of synapses and reward circuit function in the genesis and treatment of depression (2023) · cites this paper as [235]
In the citing paper
“Susceptibility to chronic social defeat stress is accompanied by atrophy of MSN dendrites, specifically in D1 MSNs and not D2 MSNs, and a corresponding loss of dendritic spines [226,234,235].”
From Plasticity of synapses and reward circuit function in the genesis and treatment of depression (2023) · cites this paper as [235]
In the citing paper
“The GTPase RhoA, which negatively regulates dendritic complexity, is increased specifically in D1-MSNs of susceptible mice [138].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“The GTPase RhoA, which negatively regulates dendritic complexity, is increased specifically in D1-MSNs of susceptible mice [138].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“After CSDS, inhibiting downstream effector Rho-kinase reverses social withdrawal and forced-swim immobility [138].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“Upregulation of RhoA in D1-MSNs either by Egr3 overexpression or RhoA over-expression promotes stress susceptibility [88, 138].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“RhoA is transcriptionally regulated by Egr3 [88] and in stress-naive mice, increased RhoA in D1-MSNs decreases sucrose preference in males, grooming behavior in females, and forced-swim immobility.”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“Reduced D1-MSN complexity is sufficient to drive CSDS-susceptibility [88, 138].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“The mechanism underlying structural plasticity of MSNs in CSDS is altered expression and activity of Rho GTPases [88, 89, 138, 141].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
In the citing paper
“In the NAc, dendritic complexity of D1-, but not D2-MSNs, is reduced in CSDS-susceptible mice.”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [138]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nestler, E. J., Barrot, M., DiLeone, R. J., Eisch, A. J., Gold, S. J., & Monteggia, L. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00653-0 · Cited by 3,217
Krishnan, V., Han, M.-H., Graham, D. L., Berton, O., Renthal, W., Russo, S. J., LaPlant, Q., Graham, A., Lutter, M., Lagace, D. C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.09.018 · Cited by 2,307
The brain reward circuitry in mood disorders
Russo, S. J., & Nestler, E. J. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3381 · Cited by 1,870
Modulation of Striatal Projection Systems by Dopamine
Gerfen, C. R., & Surmeier, D. J. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113641 · Cited by 1,700
A standardized protocol for repeated social defeat stress in mice
Golden, S. A., Covington, H. E., Berton, O., & Russo, S. J. (2011) · Nature Protocols · doi:10.1038/nprot.2011.361 · Cited by 1,581
The neostriatal mosaic: multiple levels of compartmental organization
Gerfen, C. R. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90355-c · Cited by 1,471
Pizzagalli, D. A., Holmes, A. J., Dillon, D. G., Goetz, E. L., Birk, J. L., Bogdan, R., Dougherty, D. D., Iosifescu, D. V., Rauch, S. L., & Fava, M. (2009) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.08081201 · Cited by 1,232
Rapid regulation of depression-related behaviours by control of midbrain dopamine neurons
Chaudhury, D., Walsh, J. J., Friedman, A. K., Juarez, B., Ku, S. M., Koo, J. W., Ferguson, D., Tsai, H.-C., Pomeranz, L., Christoffel, D. J., et al. (2013) · Nature · doi:10.1038/nature11713 · Cited by 1,156
Self-citationDrevets, W. C. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00203-8 · Cited by 1,146
The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia
Gerfen, C. R. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.001441 · Cited by 1,004
Cited by
Sorted by citations
Castro, D. C., & Bruchas, M. R. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.003 · Cited by 306
The molecular and cellular mechanisms of depression: a focus on reward circuitry
Fox, M. E., & Lobo, M. K. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0415-3 · Cited by 232
Self-citationMicroRNA mediators of early life stress vulnerability to depression and suicidal behavior
Allen, L., & Dwivedi, Y. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0597-8 · Cited by 152
Gebara, E., Zanoletti, O., Ghosal, S., Grosse, J., Schneider, B. L., Knott, G. W., Astori, S., & Sandi, C. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.12.003 · Cited by 152
Microglial deletion and inhibition alleviate behavior of post-traumatic stress disorder in mice
Li, S., Liao, Y., Dong, Y., Li, X., Li, J., Cheng, Y., Cheng, J., & Yuan, Z. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-020-02069-9 · Cited by 118
Golden, S. A., Jin, M., Heins, C., Vènniro, M., Michaelides, M., & Shaham, Y. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2409-18.2019 · Cited by 116
Synaptic Mechanisms Regulating Mood State Transitions in Depression
Parekh, P. K., Johnson, S. B., & Liston, C. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-040422 · Cited by 101
Warren, B. L., Mazei‐Robison, M. S., Robison, A. J., & Iñiguez, S. D. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.02.004 · Cited by 78
Depression and substance use disorders: Clinical comorbidity and shared neurobiology
Calarco, C. A., & Lobo, M. K. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.09.004 · Cited by 74
Self-citationHe, J., Zhou, H.-Y., Xue, S.-G., Lu, J.-J., Xu, J.-F., Zhou, B., Hu, Z., Wu, P., Long, L., Ni, L., et al. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.09.003 · Cited by 63
Francis, T. C., Gaynor, A., Chandra, R., Fox, M. E., & Lobo, M. K. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.007 · Cited by 61
Self-citationBayassi-Jakowicka, M., Lietzau, G., Czuba, E., Patrone, C., & Kowiański, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052618 · Cited by 55
Alipio, J. B., Haga, C. W., Fox, M. E., Arakawa, K., Balaji, R., Cramer, N., Lobo, M. K., & Keller, A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2470-20.2020 · Cited by 49
Self-citationReduced nucleus accumbens enkephalins underlie vulnerability to social defeat stress
Nam, H., Chandra, R., Francis, T. C., Dias, C., Cheer, J. F., & Lobo, M. K. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0422-8 · Cited by 51
Self-citationPorcu, A., Vaughan, M. E., Nilsson, A., Arimoto, N., Lamia, K. A., & Welsh, D. K. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2000258117 · Cited by 44
Bayassi-Jakowicka, M., Lietzau, G., Czuba, E., Steliga, A., Waśkow, M., & Kowiański, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22189806 · Cited by 43
Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
Fox, M. E., Figueiredo, A. M. P. D., Menken, M. S., & Lobo, M. K. (2020) · Scientific Reports · doi:10.1038/s41598-020-69339-7 · Cited by 47
Self-citationAllichon, M., Ortiz, V., Pousinha, P. A., Andrianarivelo, A., Petitbon, A., Heck, N., Trifilieff, P., Barik, J., & Vanhoutte, P. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.799274 · Cited by 43
Plasticity of synapses and reward circuit function in the genesis and treatment of depression
Thompson, S. M. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-022-01422-1 · Cited by 40
Fox, M. E., Wulff, A. B., Franco, D., Choi, E. Y., Calarco, C. A., Engeln, M., Turner, M. D., Chandra, R., Rhodes, V. M., Thompson, S. M., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.08.023 · Cited by 40
Self-citationMartín-Cámara, O., Cores, Á., López‐Alvarado, P., & Menéndez, J. C. (2021) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2021.113742 · Cited by 39
Zhang, Y. F., Wu, J., Wang, Y., Johnson, N. L., Bhattarai, J. P., Li, G., Wang, W., Guevara, C., Shoenhard, H., Fuccillo, M. V., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42662-z · Cited by 37
Mono-methylation of lysine 27 at histone 3 confers lifelong susceptibility to stress
Torres‐Berrío, A., Estill, M. S., Patel, V., Ramakrishnan, A., Kronman, H. G., Minier-Toribio, A. M., Issler, O., Browne, C. J., Parise, E. M., van der Zee, Y. Y., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.06.006 · Cited by 34
Persistent behavioral and neurobiological consequences of social isolation during adolescence
Li, D. C., Hinton, E. A., & Gourley, S. L. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.05.017 · Cited by 38
Epigenetics: A Missing Link Between Early Life Stress and Depression
Saavedra, K., & Salazar, L. A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-33-6044-0_8 · Cited by 35
Zhao, J., Li, Y., Liu, Y., Liu, N., Tu, G., Zhu, M., Wu, Y. H., Xiao, B., Ye, L., Li, J., et al. (2019) · Theranostics · doi:10.7150/thno.34655 · Cited by 35
Le Merrer, J., Detraux, B., Gandía, J., De Groote, A., Fonteneau, M., de Kerchove d’Exaerde, A., & Becker, J. A. J. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.05.008 · Cited by 35
Lasconi, C., Pahl, M. C., Cousminer, D. L., Doege, C. A., Chesi, A., Hodge, K. M., Leonard, M. E., Lu, S., Johnson, M. E., Su, C., et al. (2020) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2020.10.004 · Cited by 32
Mitofusin-2 in nucleus accumbens D2-MSNs regulates social dominance and neuronal function
Ghosal, S., Gebara, E., Ramos‐Fernández, E., Chioino, A., Grosse, J., de Suduiraut, I. G., Zanoletti, O., Schneider, B. L., Antonio Zorzano, A., Astori, S., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112776 · Cited by 33
Engeln, M., Mitra, S., Chandra, R., Gyawali, U., Fox, M. E., Dietz, D., & Lobo, M. K. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.10.019 · Cited by 32
Self-citationPagliusi, M., Franco, D., Cole, S. L., Morais‐Silva, G., Chandra, R., Fox, M. E., Iñiguez, S. D., Sartori, C. R., & Lobo, M. K. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.854494 · Cited by 32
Self-citationMolecular, Circuit, and Stress Response Characterization of Ventral Pallidum Npas1-Neurons
Morais‐Silva, G., Campbell, R. R., Nam, H., Basu, M., Pagliusi, M., Fox, M. E., Chan, C. S., Iñiguez, S. D., Ament, S. A., Cramer, N., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0971-22.2022 · Cited by 33
Self-citationIndividual differences in stereotypy and neuron subtype translatome with TrkB deletion
Engeln, M., Song, Y., Chandra, R., La, A. M., Fox, M. E., Evans, B., Turner, M. D., Thomas, S., Francis, T. C., Hertzano, R. P., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0746-0 · Cited by 24
Self-citationMao, Y., Fisher, D. W., Yang, S., Keszycki, R. M., & Dong, H. (2020) · PLOS ONE · doi:10.1371/journal.pone.0226021 · Cited by 28
Cocaine-induced neuron subtype mitochondrial dynamics through Egr3 transcriptional regulation
Cole, S. L., Chandra, R., Harris, M., Patel, I., Wang, T., Kim, H.-J., Jensen, L., Russo, S. J., Turecki, G., Gancarz, A. M., et al. (2021) · Molecular Brain · doi:10.1186/s13041-021-00800-y · Cited by 28
Self-citationNucleus Accumbens Tac1-Expressing Neurons Mediate Stress-Induced Anhedonia-like Behavior in Mice
He, Z., Yin, Y.-Y., Xi, K., Xing, Z., Cao, J., Liu, T., Liu, L., He, X., Yu, H., & Zhu, X. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108343 · Cited by 27
Shisa6 mediates cell-type specific regulation of depression in the nucleus accumbens
Kim, H.-D., Wei, J., Call, T., Quintus, N. T., Summers, A. J., Carotenuto, S., Johnson, R., Ma, X., Xu, C., Park, J. G., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01217-8 · Cited by 24
Chen, G., Zhang, Y., Li, R., Jin, L., Hao, K., Rong, J., Duan, H., Du, Y., Yao, L., Xiang, D., et al. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100624 · Cited by 23
E3 Ubiquitin-Protein Ligase SMURF1 in the Nucleus Accumbens Mediates Cocaine Seeking
Werner, C. T., Viswanathan, R., Martin, J. A., Gobira, P. H., Mitra, S., Thomas, S. A., Wang, Z.-J., Liu, J., Stewart, A. F., Neve, R. L., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.07.013 · Cited by 22
Franco, D., Wulff, A. B., Lobo, M. K., & Fox, M. E. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.821080 · Cited by 20
Self-citationEngeln, M., Fox, M. E., Chandra, R., Choi, E. Y., Nam, H., Qadir, H., Thomas, S., Rhodes, V. M., Turner, M. D., Herman, R. J., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01668-7 · Cited by 20
Self-citationHerzog, D. P., Perumal, N., Manicam, C., Treccani, G., Nadig, J., Rossmanith, M., Engelmann, J., Jene, T., Hasch, A., van der Kooij, M. A., et al. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100404 · Cited by 19
Pan, G., Zhao, B. T., Zhang, M., Guo, Y., Yu-hua, Y., Dai, D., Zhang, X., Yang, H., Ni, J. D., Huang, Z., et al. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01233-y · Cited by 19
Hada, K., Wulaer, B., Nagai, T., Itoh, N., Sawahata, M., Sobue, A., Mizoguchi, H., Mori, D., Kushima, I., Nabeshima, T., et al. (2021) · Molecular Brain · doi:10.1186/s13041-021-00735-4 · Cited by 17
Licinio, J., & Wong, M. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0798-1 · Cited by 19
Chen, S.-J., Gao, C., Lv, Q., Zhao, M.-Q., Qin, X., & Liao, H. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-021-00823-0 · Cited by 18
Zhang, X., Liang, Y., Huang, Y. S., Liu, S., Li, Q., Wang, S., Wu, G., Du, Z., Wang, Y., Wang, J., et al. (2024) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.65.3.12 · Cited by 19
Social experience in adolescence shapes prefrontal cortex structure and function in adulthood
Li, D. C., Hinton, E. A., Guo, J., Knight, K. A., Sequeira, M. K., Wynne, M. E., Dighe, N. M., & Gourley, S. L. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02540-6 · Cited by 18
Engeln, M., Fox, M. E., & Lobo, M. K. (2020) · Psychopharmacology · doi:10.1007/s00213-020-05657-y · Cited by 17
Self-citationKajitani, N., Okada‐Tsuchioka, M., Inoue, A., Miyano, K., Masuda, T., Boku, S., Iwamoto, K., Ohtsuki, S., Uezono, Y., Aoki, J., et al. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01727-9 · Cited by 16
Menken, M. S., Rivera, P. J. R., Isaiah, A., Ernst, T., Cloak, C. C., & Chang, L. (2023) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2023.101247 · Cited by 15
Self-citationMechanisms of nucleus accumbens deep brain stimulation in treating mental disorders
Ruan, H., Tong, G., Jin, M., Koch, K., & Wang, Z. (2024) · Fundamental Research · doi:10.1016/j.fmre.2024.06.009 · Cited by 14
Rodent models of stress and dendritic plasticity – Implications for psychopathology
Laine, M. A., & Shansky, R. M. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100438 · Cited by 14
Miceli, M. D., Martinat, M., Rossitto, M., Aubert, A., Alashmali, S. M., Bosch‐Bouju, C., Fioramonti, X., Joffre, C., Bazinet, R. P., & Layé, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126650 · Cited by 14
Siemsen, B. M., Franco, D., & Lobo, M. K. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.12.014 · Cited by 12
Self-citationEffects of RhoA on Depression-Like Behavior in Prenatally Stressed Offspring Rats
Zhou, J., Ma, Y., Chen, J., Yao, D., Feng, C., Dong, Y., Ren, Y., Ma, H., Wang, Z., Li, G., et al. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113973 · Cited by 12
Ding, X., Zhang, H., Qiu, H., Wen, X., & Zhang, L. (2022) · Child s Nervous System · doi:10.1007/s00381-022-05646-w · Cited by 11
Stress-induced vulnerability to develop cocaine addiction depends on cofilin modulation
Rigoni, D., Avalos, M. P., Boezio, M. J., Guzman, A. S., Calfa, G. D., Perassi, E. M., Pierotti, S. M., Bisbal, M., García‐Keller, C., Cancela, L. M., et al. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2021.100349 · Cited by 11
Yan, L., Wang, W., Cheng, T., Yang, D.-R., Wang, Y., Wang, Y., Yang, F., So, K., & Zhang, L. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01302-y · Cited by 9
An accumbal microcircuit for the transition from acute to chronic pain
Yu, Y., Xia, S.-H., Xu, Z., Zhao, W.-N., Song, L., Pan, X., Zhong, C., Wang, D., Gao, Y., Yang, J., et al. (2025) · Current Biology · doi:10.1016/j.cub.2025.02.055 · Cited by 9
Hwang, H.-G., Park, J.-W., Lee, H. J., Ko, M. Y., Ka, M., Lee, Y. K., Choi, J., In, S.-A., Lee, Y.-E., Lee, S., et al. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2508424 · Cited by 9
Liu, H., Chen, S., Hong, X., Xiao, J., Zhao, S., Zhang, X., Shu, Z., Zhang, J., Ouyang, J., Liu, Q., et al. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111256 · Cited by 8
Deng, Q., Zhang, S.-Q., Yang, P., Dong, W., Wang, F., Long, L., & Chen, J. (2023) · Acta Pharmacologica Sinica · doi:10.1038/s41401-023-01074-x · Cited by 7
Involvement of brain cell phenotypes in stress-vulnerability and resilience
Favoretto, C. A., Pagliusi, M., & Morais‐Silva, G. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1175514 · Cited by 10
Borland, J. M. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105809 · Cited by 8
Shi, Z., Wen, K., Sammudin, N. H., LoRocco, N. C., & Zhuang, X. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03013-0 · Cited by 7
Alcohol and lactation: Developmental deficits in a mouse model
Perez, R. F., Conner, K. E., Erickson, M. A., Nabatanzi, M., & Huffman, K. J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1147274 · Cited by 8
Chen, Y.-C., Tsai, F., & Chen, M. (2020) · Behavioural Neurology · doi:10.1155/2020/4163274 · Cited by 6
Merrer, J. L., Detraux, B., Gandía, J., Groote, A. D., Fonteneau, M., d’Exaerde, A. D. K., & Becker, J. A. J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.28.518147 · Cited by 6
Lv, R., Wang, Y., Chen, D., Bao, Z., & Lin, S. (2025) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c04473 · Cited by 5
Kamens, H. M., Anziano, E. K., Horton, W. J., & Cavigelli, S. A. (2024) · Genes · doi:10.3390/genes15070873 · Cited by 4
Snippe-Strauss, M., Zamir, A. T., Benhos, A., & Richter‐Levin, G. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101403 · Cited by 2
Wang, W., & Rui, M. (2024) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2024.06.010 · Cited by 2
Synaptic plasticity in fronto-insular circuits underlying stress susceptibility and resilience
Rocks, D., & Liston, C. M. (2024) · Neuroscience Research · doi:10.1016/j.neures.2024.12.006 · Cited by 2
Advances in research on stress and behavior: special issue, 2020
Licinio, J. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0741-5 · Cited by 2
Fox, M. E., Wulff, A. B., Franco, D., Choi, E. Y., Calarco, C. A., Engeln, M., Turner, M. D., Chandra, R., Rhodes, V. M., Thompson, S. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.15.491856 · Cited by 2
Self-citationG protein-biased LPAR1 agonism promotes prototypic antidepressant effectsPreprint
Kajitani, N., Okada‐Tsuchioka, M., Inoue, A., Miyano, K., Masuda, T., Boku, S., Iwamoto, K., Ohtsuki, S., Uezono, Y., Aoki, J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.02.514841 · Cited by 2
Nucleus accumbens neuron subtype translatome signatures in socially stressed females
Kumar, G., Franco, D., Basu, M., Olusakin, J., Campbell, R. R., Ament, S. A., Fox, M. E., & Lobo, M. K. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02414-1 · Cited by 1
Self-citationMeCP2 regulates cell-type-specific functions of depressive-like symptoms in the nucleus accumbens
Bae, J., Kim, S. H., Jung, S. Y., Frankiv, N., Jin, H., Hwang, E. M., Kim, Y., Lee, S.-J., & Im, H. (2026) · Experimental & Molecular Medicine · doi:10.1038/s12276-026-01721-3 · Cited by 2
Ifrah, S., Knoll, M. A., Jagsi, R., Weinstock, C., Pennebaker, J. W., Samuels, L., & Edelman, D. C. (2020) · Women s Health Reports · doi:10.1089/whr.2020.0033 · Cited by 1
Nato, A. Q., Mustafa, H. A. U., Sexton, H. G., Moore, S. D., Denvir, J., Primerano, D. A., & Risher, M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.02.365841 · Cited by 1
Olusakin, J., Dewan, M., Kashyap, A., Franco, D., Kumar, G., Luján, M. Á., Mark, K., Cheer, J. F., & Lobo, M. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.26.661775 · Cited by 1
Self-citationLicinio, J., & Wong, M. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0845-y
Anxiety and depression: A matter of stiffness?
Traverso, S. (2020) · Medical Hypotheses · doi:10.1016/j.mehy.2020.110344
Ghaffari‐Nasab, A., Javani, G., Mohaddes, G., & Alipour, M. R. (2023) · Research Square · doi:10.21203/rs.3.rs-2762123/v1
Ghaffari‐Nasab, A., Javani, G., Mohaddes, G., & Alipour, M. R. (2023) · Biogerontology · doi:10.1007/s10522-023-10056-9
Hada, K., Wulaer, B., Nagai, T., Itoh, N., Sawahata, M., Sobue, A., Mizoguchi, H., Mori, D., Kushima, I., Nabeshima, T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13633089
Cole, S. L., Chandra, R., Harris, M., Patel, I., Wang, T., Kim, H., Jensen, L., Russo, S. J., Turecki, G., Gancarz, A. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14880435
Self-citationCole, S. L., Chandra, R., Harris, M., Patel, I., Wang, T., Kim, H., Jensen, L., Russo, S. J., Turecki, G., Gancarz, A. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14880432
Self-citationCole, S. L., Chandra, R., Harris, M., Patel, I., Wang, T., Kim, H., Jensen, L., Russo, S. J., Turecki, G., Gancarz, A. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14880426
Self-citationHada, K., Wulaer, B., Nagai, T., Itoh, N., Sawahata, M., Sobue, A., Mizoguchi, H., Mori, D., Kushima, I., Nabeshima, T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13633086
Cole, S. L., Chandra, R., Harris, M., Patel, I., Wang, T., Kim, H., Jensen, L., Russo, S. J., Turecki, G., Gancarz, A. M., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14880429
Self-citationLi, Y. F., He, X., Deng, X., Zhou, J., Shi, M., Tian, Y., Li, Z., Yang, D., & Yang, X. (2025) · BMJ Open · doi:10.1136/bmjopen-2025-104287
Kayedi-Bakhtiari, N., & Vatanparast, J. (2026) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2026.01.004
Olusakin, J., Dewan, M., Kashyap, A., Franco, D., Kumar, G., Luján, M. Á., Mark, K., Cheer, J. F., & Lobo, M. K. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-04049-8 · Cited by 1
Self-citationNiu, Y., Li, K., Zhan, K., Pi, M., Xiong, Q., Wang, J., Wang, X. J., Shu, X., Xia, Y., & Huang, M. (2026) · Biomolecules · doi:10.3390/biom16050639
Tanaka, R., Zhu, W., Nagai, T., Nabeshima, T., Kaibuchi, K., Ozaki, N., Ikesue, H., Mizoguchi, H., & Yamada, K. (2026) · Neuropsychopharmacology Reports · doi:10.1002/npr2.70124
Ventral Tegmental Area Amylin Receptors Mediate Maladaptive Responses to Social StressPreprint
Fox, M., Ostman, A. E., Murdaugh, L., Sohail, H., Montemarano, A., & Briones, A. (2026) · Research Square · doi:10.21203/rs.3.rs-9889675/v1
Self-citationCSF1R-Mediated Microglial Engagement Is Required for Stress-Induced MMP-2/9 ActivityPreprint
Taborda-Bejarano, J. P., Tovar, J. P., Allen, M., Natarajan, J., Meyerink, M. E., & García‐Keller, C. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.08.730923
Mesolimbic and mesocortical pathways differentially support fentanyl-context associations
Montemarano, A., Sohail, H., Murdaugh, L. B., Derr, K., Alkhaleel, F. A., Fox, L. D., Pandey, S., & Fox, M. E. (2026) · Psychopharmacology · doi:10.1007/s00213-026-07151-3 · Cited by 1
Self-citation
Metadata
- Authors
- Fox, M. E., Chandra, R., Menken, M. S., Larkin, E. J., Nam, H., Engeln, M., Francis, T. C., & Lobo, M. K.
- Affiliations
- University of Maryland, Baltimore (US)
- Corresponding author
- Lobo, Mary Kay
- Venue
- Molecular Psychiatry
- Published
- 2018-08-17
- Volume
- 25
- Issue
- 5
- Pages
- 1022-1034
- ISSN
- 1359-4184 (ISSN-L)
- 1476-5578
- PMC
- PMC6378138
- OpenAlex
- W2885753453
- Cited by
- 100
- References
- 76
- Citations by year
- 2026: 9 · 2025: 7 · 2024: 12 · 2023: 10 · 2022: 16 · 2021: 19 · 2020: 18 · 2019: 8 · 2018: 1
- FWCI
- 7.42
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (R01MH106500, F32MH116574)
- One Mind/ Janssen Rising Star Translational Research Award
- Topics
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- depression, RhoA, Rho kinase, dopamine D1 receptor, medium spiny neurons, nucleus accumbens, dendritic remodeling, dendritic atrophy, social defeat stress, social avoidance, Y-27632, structural plasticity, reward systems
- MeSH terms
- Animals, Dendrites, Depression, Male, Mice, Inbred C57BL, Mice, Transgenic, Neuronal Plasticity, Nucleus Accumbens, Receptors, Dopamine D1, Receptors, Dopamine D2, rhoA GTP-Binding Protein, Mice, rho-Associated Kinases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review