The DOI matches its Crossref record; 208 of the 208 references it cites were found in a registry or an index.
Behavioural and neurochemical effects of post-weaning social isolation in rodents—Relevance to developmental neuropsychiatric disorders
Abstract
Exposing mammals to early-life adverse events, including maternal separation or social isolation, profoundly affects brain development and adult behaviour and may contribute to the occurrence of psychiatric disorders, such as depression and schizophrenia in genetically predisposed humans. The molecular mechanisms underlying these environmentally induced developmental adaptations are unclear and best evaluated in animal paradigms with translational salience. Rearing rat pups from weaning in isolation, to prevent social contact with conspecifics, produces reproducible, long-term changes including; neophobia, impaired sensorimotor gating, aggression, cognitive rigidity, reduced prefrontal cortical volume and decreased cortical and hippocampal synaptic plasticity. These alterations are associated with hyperfunction of mesolimbic dopaminergic systems, enhanced presynaptic dopamine (DA) and serotonergic (5-HT) function in the nucleus accumbens (NAcc), hypofunction of mesocortical DA and attenuated 5-HT function in the prefrontal cortex and hippocampus. These behavioural, morphological and neurochemical abnormalities, as reviewed herein, strongly resemble core features of schizophrenia. Therefore unravelling the mechanisms that trigger these sequelae will improve our knowledge of the aetiology of neurodevelopmental psychiatric disorders, enable identification of longitudinal biomarkers of dysfunction and permit predictive screening for novel compounds with potential antipsychotic efficacy.
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“Chronic social isolation, particularly in rodents, has been used as a developmental model of early life stress since many of the long-term maladaptive changes resemble features of human neuropsychiatric disease33.”
From Neural mechanisms of social homeostasis (2019) · cites this paper as [33]
Citations
Cites
Depression: a new animal model sensitive to antidepressant treatments
PORSOLT, R. D., LE PICHON, M., & JALFRE, M. (1977) · Nature · doi:10.1038/266730a0 · Cited by 4,451
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229
A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data
Ennaceur, A., & Delacour, J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90157-x · Cited by 3,223
Behavioural despair in rats: A new model sensitive to antidepressant treatments
Porsolt, R. D., Anton, G., Blavet, N., & Jalfre, M. (1978) · European Journal of Pharmacology · doi:10.1016/0014-2999(78)90118-8 · Cited by 3,138
Cannabis use and risk of psychotic or affective mental health outcomes: a systematic review.
Moore, T. H., Zammit, S., Lingford-Hughes, A., Barnes, T. R., Jones, P. B., Burke, M., & Lewis, G. (2007) · The Lancet · doi:10.1016/s0140-6736(07)61162-3 · Cited by 2,224
BRAFF, D. L., Geyer, M. A., & Swerdlow, N. R. (2001) · Psychopharmacology · doi:10.1007/s002130100810 · Cited by 1,701
Dissociation in prefrontal cortex of affective and attentional shifts
Dias, R., Robbins, T. W., & Roberts, A. C. (1996) · Nature · doi:10.1038/380069a0 · Cited by 1,527
Geyer, M. A., Krebs-Thomson, K., Braff, D. L., & Swerdlow, N. R. (2001) · Psychopharmacology · doi:10.1007/s002130100811 · Cited by 1,484
Medial Frontal Cortex Mediates Perceptual Attentional Set Shifting in the Rat
Birrell, J. M., & Brown, V. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04320.2000 · Cited by 1,421
Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates
Dalley, J. W., Cardinal, R. N., & Robbins, T. W. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.006 · Cited by 1,329
Research works printed but not linked: 4
- Harte, 2006, Deficits in parvalbumin and calbindin immunoreactivity in the hippocampus of isolation reared rats, Schizophr. Res., 81, 210
- King, 2007, The novel 5-HT6 receptor antagonist, PRX-07037, enhances memory and reduces food intake in a neurodevelopmental model of schizophrenia, J. Psychopharmacol., 21, A57
- Porkess, 2006, Aniracetam has no effect on isolation rearing induced hyperactivity, PPI deficits or passive avoidance impairment in rats, but does improve novel object recognition, J. Psychopharmacology, 20, A46
- Porkess, 2007, Isolation rearing of rats induces a reduction in prefrontal cortex volume measured by MR volumetry, J. Psychopharmacology, 21, A57
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Novick, A. M., Levandowski, M. L., Laumann, L. E., Philip, N. S., Price, L. H., & Tyrka, A. R. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.02.002 · Cited by 192
Vanderschuren, L. J. M. J., & Trezza, V. (2013) · Current Topics in Behavioral Neurosciences · doi:10.1007/978-3-662-45758-0_268 · Cited by 200
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Hermes, G., Li, N., Duman, C., & Duman, R. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2010.12.019 · Cited by 111
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Lammel, S., Tye, K. M., & Warden, M. R. (2014) · Genes, Brain and Behavior · doi:10.1111/gbb.12049 · Cited by 98
Brand, S., Moller, M., & Harvey, B. (2015) · Current Neuropharmacology · doi:10.2174/1570159x13666150307004545 · Cited by 95
Sciolino, N. R., Bortolato, M., Eisenstein, S. A., Fu, J., Oveisi, F., Hohmann, A. G., & Piomelli, D. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.007 · Cited by 89
Disrupted social development enhances the motivation for cocaine in rats
Baarendse, P. J. J., Limpens, J. H. W., & Vanderschuren, L. J. M. J. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3362-8 · Cited by 87
Isolation rearing effects on probabilistic learning and cognitive flexibility in rats
Amitai, N., Young, J. W., Higa, K., Sharp, R. F., Geyer, M. A., & Powell, S. B. (2014) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-013-0204-4 · Cited by 74
Play fighting and the development of the social brain: The rat’s tale
Pellis, S. M., Pellis, V. C., Ham, J. R., & Stark, R. A. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105037 · Cited by 76
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Schipper, L., Harvey, L., van der Beek, E. M., & van Dijk, G. (2018) · Obesity Reviews · doi:10.1111/obr.12663 · Cited by 67
Turner, K. M., & Burne, T. H. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093411 · Cited by 66
Ouchi, H., Ono, K., Murakami, Y., & Matsumoto, K. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.10.029 · Cited by 64
Willi, R., Weinmann, O., Winter, C., Klein, J., Sohr, R., Schnell, L., Yee, B. K., Feldon, J., & Schwab, M. E. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4393-09.2010 · Cited by 52
Haj-Mirzaian, A., Amiri, S., Kordjazy, N., Momeny, M., Razmi, A., Rahimi-Balaei, M., Amini-Khoei, H., Haj-Mirzaian, A., Marzban, H., Mehr, S. E., et al. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.12.024 · Cited by 46
Forster, G. L., Anderson, E. M., Scholl, J. L., Lukkes, J. L., & Watt, M. J. (2018) · Neurobiology of Stress · doi:10.1016/j.ynstr.2018.08.001 · Cited by 40
Robbins, T. (2016) · Journal of Psychopharmacology · doi:10.1177/0269881116664450 · Cited by 31
Stark, R., & Pellis, S. M. (2020) · International Journal of Play · doi:10.1080/21594937.2020.1720142 · Cited by 32
Ago, Y., Araki, R., Yano, K., Kawasaki, T., Chaki, S., Nakazato, A., Onoe, H., Hashimoto, H., Baba, A., Takuma, K., et al. (2012) · Journal of Pharmacological Sciences · doi:10.1254/jphs.11200sc · Cited by 29
Vedovelli, K., Silveira, E., Velho, E., Stertz, L., Kapczinski, F., Schröder, N., & Bromberg, E. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.012 · Cited by 26
de Bruin, N. M. W. J., van Loevezijn, A., Wicke, K. M., de Haan, M., Venhorst, J., Lange, J. H. M., de Groote, L., van der Neut, M. A. W., Prickaerts, J., Andriambeloson, E., et al. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.020 · Cited by 22
Kim, W. Y., Cho, B. R., Kwak, M. J., & Kim, J.-H. (2017) · Scientific Reports · doi:10.1038/s41598-017-06408-4 · Cited by 19
Colonnello, V., Iacobucci, P., Anderson, M. P., & Panksepp, J. (2011) · Developmental Psychobiology · doi:10.1002/dev.20520 · Cited by 13
Postweaning isolation affects responses to incentive contrast in adulthood
Cuenya, L., Mustaca, A., & Kamenetzky, G. (2015) · Developmental Psychobiology · doi:10.1002/dev.21273 · Cited by 9
Metadata
- Authors
- Fone, K. C. F., & Porkess, M. V.
- Affiliations
- University of Nottingham (GB)
- Corresponding author
- Fone, Kevin C.F.
- ORCID
- Fone, Kevin C.F.
- Venue
- Neuroscience & Biobehavioral Reviews
- Publisher
- Elsevier BV
- Published
- 2008-08
- Volume
- 32
- Issue
- 6
- Pages
- 1087-1102
- ISSN
- 0149-7634 (ISSN-L)
- OpenAlex
- W2019243277
- Cited by
- 864
- References
- 208
- Citations by year
- 2026: 28 · 2025: 34 · 2024: 37 · 2023: 46 · 2022: 41 · 2021: 64 · 2020: 51 · 2019: 47 · 2018: 41 · 2017: 62 · 2016: 50 · 2015: 71 · 2014: 55 · 2013: 57 · 2012: 54
- FWCI
- 5.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience & Biobehavioral Reviews (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- post-weaning social isolation, maternal separation, childhood adversity, schizophrenia, depression, neophobia, sensorimotor gating, aggression, synaptic plasticity, mesolimbic dopamine system, mesocortical dopamine, nucleus accumbens, serotonin, prefrontal cortex, hippocampus, brain development, biomarkers
- MeSH terms
- Animals, Animals, Newborn, Behavior, Animal, Brain Chemistry, Child, Developmental Disabilities, Disease Models, Animal, Humans, Rodentia, Social Isolation
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