The DOI matches its Crossref record; 96 of the 96 references it cites were found in a registry or an index.
Variations in Nucleus Accumbens Dopamine Associated with Individual Differences in Maternal Behavior in the Rat
Open accessAbstract
Lactating rats exhibit stable individual differences in pup licking/grooming. We used in vivo voltammetry to monitor changes in extracellular dopamine (DA) in the nucleus accumbens (n. Acc) shell of lactating rats interacting with pups and found that (1) the DA signal increased significantly with pup licking/grooming; (2) the onset of such increases preceded pup licking/grooming; and (3) the magnitude and duration of the increase in the DA signal were significantly correlated with the duration of the licking/grooming bout. In females characterized on the basis of behavioral observations as high-licking/grooming mothers, the magnitude of the increase in the DA signal associated with licking/grooming was significantly greater than in low-licking/grooming dams. Dopamine transporter binding in the n. Acc was increased in low-compared with high-licking/grooming mothers. Injection of the selective DA uptake inhibitor GBR 12909 [1-(2-(Bis-(4-fluorophenyl)methoxy)ethyl)-4-(3 phenypropyl)piperazine dihydrochloride] (5 mg/kg, s.c.) increased the DA signal in the n. Acc and pup licking/grooming in low-licking/grooming mothers to levels comparable with those observed in high-licking/grooming dams. Receptor autoradiographic studies showed elevated levels of D 1 and D 3 receptors in the n. Acc shell region in high-licking/grooming dams. These results suggest that high- and low-licking/grooming dams differ in mesolimbic dopaminergic activity associated with mother-pup interactions. Such differences may serve as neural substrates for individual differences in the motivational component of maternal behavior.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Studies on rodent models and neuroimaging studies have shown that activation of the attachment system underpinning both caregiving and partner preference is associated with the activation of two specific systems that have consistently been shown to play an important role in promoting and maintaining maternal behavior: (a) the dopaminergic reward processing system (Champagne et al., 2004; Strathe”
From A developmental, mentalization-based approach to the understanding and treatment of borderline personality disorder (2009) · cites this paper as Champagne et al., 2004
Experimental — accuracy not yet measuredIn the citing paper
“Non-human primate studies have shown that the firing rate of dopaminergic neurons is increased in response to “positive prediction errors”, meaning unexpected natural or conditioned rewards (56).”
From What’s in a smile? Maternal brain responses to infant facial cues (2008) · cites this paper as [56]
In the citing paper
“Although functional MRI only measures blood-oxygen level dependent changes in brain activity, together these studies suggest that positive sensory cues from infants, such as a smiling facial expression, may stimulate dopamine release in the striatum, and promote responsive maternal care.”
From What’s in a smile? Maternal brain responses to infant facial cues (2008) · cites this paper as [56]
In the citing paper
“Maternal rats exhibiting high levels of pup licking and grooming behavior tend to exhibit larger increases in dopaminergic activity in the nucleus accumbens as a result of grooming their pups relative to their low licking and grooming counterparts (Shahrokh et al., 2010, Champagne et al., 2004).”
From Oxytocin, motivation and the role of dopamine (2014) · cites this paper as Champagne et al., 2004
In the citing paper
“Dopamine is released within the nucleus accumbens when a mother rat grooms or licks her offspring or after being reunited with her offspring after forced separation (Champagne et al., 2004, Hansen et al., 1993).”
From Oxytocin, motivation and the role of dopamine (2014) · cites this paper as Champagne et al., 2004
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
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501
Liu, D., Diorio, J., Tannenbaum, B., Caldji, C., Francis, D., Freedman, A., Sharma, S., Pearson, D., Plotsky, P. M., & Meaney, M. J. (1997) · Science · doi:10.1126/science.277.5332.1659 · Cited by 3,170
Self-citationNongenomic Transmission Across Generations of Maternal Behavior and Stress Responses in the Rat
Francis, D., Diorio, J., Liu, D., & Meaney, M. J. (1999) · Science · doi:10.1126/science.286.5442.1155 · Cited by 1,965
Self-citationIkemoto, S., & Panksepp, J. (1999) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00023-5 · Cited by 1,450
Caldji, C., Tannenbaum, B., Sharma, S., Francis, D., Plotsky, P. M., & Meaney, M. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.9.5335 · Cited by 1,437
Self-citationMaternal care, hippocampal synaptogenesis and cognitive development in rats
Liu, D., Diorio, J., Day, J. C., Francis, D. D., & Meaney, M. J. (2000) · Nature Neuroscience · doi:10.1038/77702 · Cited by 1,195
Self-citationNeurobehavioural mechanisms of reward and motivation
Robbins, T. W., & Everitt, B. J. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80077-8 · Cited by 1,187
Champagne, F. A., Francis, D. D., Mar, A., & Meaney, M. J. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00149-5 · Cited by 1,021
Modulation of neurotransmitter release by presynaptic autoreceptors
Starke, K., Göthert, M., & Kilbinger, H. J. (1989) · Physiological Reviews · doi:10.1152/physrev.1989.69.3.864 · Cited by 927
Research works printed but not linked: 9
Cited by
Sorted by citations
Assessment of positive emotions in animals to improve their welfare
Boissy, A., Manteuffel, G., Jensen, M. B., Moe, R. O., Spruijt, B., Keeling, L. J., Winckler, C., Forkman, B., Dimitrov, I., Langbein, J., et al. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.02.003 · Cited by 1,486
Epigenetics and the biological definition of gene×environment interactions
Meaney, M. J. (2010) · Child Development · doi:10.1111/j.1467-8624.2009.01381.x · Cited by 1,239
Self-citationFonagy, P., & Luyten, P. (2009) · Development and Psychopathology · doi:10.1017/s0954579409990198 · Cited by 1,146
Dopamine: Functions, Signaling, and Association with Neurological Diseases
Klein, M. O., Battagello, D. S., Cardoso, A. R., Hauser, D. N., Bittencourt, J. C., & Correa, R. G. (2019) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0632-3 · Cited by 1,073
Gene-environment interplay and psychopathology: multiple varieties but real effects
Rutter, M., Moffitt, T. E., & Caspi, A. (2006) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2005.01557.x · Cited by 1,058
The oxytocin receptor: from intracellular signaling to behavior
Jurek, B., & Neumann, I. D. (2018) · Physiological Reviews · doi:10.1152/physrev.00031.2017 · Cited by 999
The habenula: from stress evasion to value-based decision-making
Hikosaka, O. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2866 · Cited by 955
Epigenetic mechanisms and the transgenerational effects of maternal care
Champagne, F. A. (2008) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2008.03.003 · Cited by 812
Self-citationOxytocin and social affiliation in humans
Feldman, R. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.01.008 · Cited by 767
Adult attachment predicts maternal brain and oxytocin response to infant cues.
Strathearn, L., Fonagy, P., Amico, J., & Montague, P. R. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.103 · Cited by 773
Taylor, S. E. (2012) · The Oxford Handbook of Health Psychology · doi:10.1093/oxfordhb/9780195342819.013.0009 · Cited by 993
Epigenetic mechanisms mediating the long-term effects of maternal care on development
Champagne, F. A., & Curley, J. P. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.10.009 · Cited by 520
Self-citationSwain, J. E., Lorberbaum, J. P., Kose, S., & Strathearn, L. (2007) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2007.01731.x · Cited by 499
Aragona, B. J., Liu, Y., Yu, Y. J., Curtis, J. T., Detwiler, J. M., Insel, T. R., & Wang, Z. (2006) · Nature Neuroscience · doi:10.1038/nn1613 · Cited by 473
Oxytocin and the development of parenting in humans
Gordon, I., Zagoory-Sharon, O., Leckman, J. F., & Feldman, R. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.02.005 · Cited by 469
What’s in a smile? Maternal brain responses to infant facial cues
Strathearn, L., Li, J., Fonagy, P., & Montague, P. R. (2008) · Pediatrics · doi:10.1542/peds.2007-1566 · Cited by 460
Pathophysiological mechanisms implicated in postpartum depression
Payne, J. L., & Maguire, J. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.12.001 · Cited by 459
Kim, P., Leckman, J. F., Mayes, L. C., Feldman, R., Wang, X., & Swain, J. E. (2010) · Behavioral Neuroscience · doi:10.1037/a0020884 · Cited by 440
Barrett, J., & Fleming, A. S. (2011) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2010.02306.x · Cited by 433
The parent–infant dyad and the construction of the subjective self
Fonagy, P., Gergely, G., & Target, M. (2007) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2007.01727.x · Cited by 555
Atzil, S., Hendler, T., & Feldman, R. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.172 · Cited by 399
Kaffman, A., & Meaney, M. J. (2007) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2007.01730.x · Cited by 391
Self-citationBaskerville, T. A., & Douglas, A. J. (2010) · CNS Neuroscience & Therapeutics · doi:10.1111/j.1755-5949.2010.00154.x · Cited by 377
Oxytocin, motivation and the role of dopamine
Love, T. M. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.06.011 · Cited by 369
Oxytocin–dopamine interactions mediate variations in maternal behavior in the rat
Shahrokh, D. K., Zhang, T.-Y., Diorio, J., Gratton, A., & Meaney, M. J. (2010) · Endocrinology · doi:10.1210/en.2009-1271 · Cited by 366
Self-citationThe origins of altruism in offspring care.
Preston, S. D. (2013) · Psychological Bulletin · doi:10.1037/a0031755 · Cited by 368
Numan, M., & Young, L. J. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.05.015 · Cited by 355
Numan, M., & Stolzenberg, D. S. (2008) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2008.10.002 · Cited by 361
The ventral pallidum: Subregion-specific functional anatomy and roles in motivated behaviors
Root, D. H., Meléndez, R. I., Záborszky, L., & Napier, T. C. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.03.005 · Cited by 359
Maternal programming of steroid receptor expression and phenotype through DNA methylation in the rat
Szyf, M., Weaver, I. C. G., Champagne, F. A., Diorio, J., & Meaney, M. J. (2005) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2005.10.002 · Cited by 348
Self-citationNeuroendocrine regulation of maternal behavior
Bridges, R. S. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.11.007 · Cited by 346
Cameron, N. M., Champagne, F. A., Parent, C., Fish, E. W., Ozaki-Kuroda, K., & Meaney, M. J. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.03.022 · Cited by 320
Self-citationOlazábal, D. E., & Young, L. J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.04.017 · Cited by 289
Mother–infant bonding and the evolution of mammalian social relationships
Broad, K. D., Curley, J. P., & Keverne, E. B. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1940 · Cited by 283
The maternal brain and its plasticity in humans
Kim, P., Strathearn, L., & Swain, J. E. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.08.001 · Cited by 278
Bridging the transmission gap: An end to an important mystery of attachment research?
Fonagy, P., & Target, M. (2005) · Attachment & Human Development · doi:10.1080/14616730500269278 · Cited by 298
Maternal neglect: oxytocin, dopamine and the neurobiology of attachment
Strathearn, L. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02228.x · Cited by 268
Maternal Care and DNA Methylation of a Glutamic Acid Decarboxylase 1 Promoter in Rat Hippocampus
Zhang, T., Hellstrom, I. C., Bagot, R. C., Wen, X., Diorio, J. C., & Meaney, M. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1039-10.2010 · Cited by 271
Self-citationHypothalamic Neural Circuits Regulating Maternal Responsiveness Toward Infants
Numan, M. (2006) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582306288790 · Cited by 258
Gene–environment interdependence
Rutter, M. L. (2006) · Developmental Science · doi:10.1111/j.1467-7687.2007.00557.x · Cited by 247
Olazábal, D. E., & Young, L. J. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.12.010 · Cited by 230
Aragona, B. J., Cleaveland, N. A., Stuber, G. D., Day, J. J., Carelli, R. M., & Wightman, R. M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2225-08.2008 · Cited by 234
Bornstein, M. H. (2015) · Wiley eBooks · doi:10.1002/9781118963418.childpsy403 · Cited by 229
A cry in the dark: depressed mothers show reduced neural activation to their own infant’s cry
Laurent, H. K., & Ablow, J. C. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq091 · Cited by 224
Ferris, C. F., Kulkarni, P. P., Sullivan, J. M., Harder, J. A., Messenger, T. L., & Febo, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3156-04.2005 · Cited by 222
Oxytocin and social motivation
Gordon, I., Martin, C., Feldman, R., & Leckman, J. F. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.07.007 · Cited by 211
Ellingsen, D., Leknes, S., Løseth, G. E., Wessberg, J., & Olausson, H. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01986 · Cited by 214
Numan, M., Numan, M. J., Pliakou, N., Stolzenberg, D. S., Mullins, O. J., Murphy, J. M., & Smith, C. D. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.6.1588 · Cited by 186
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission
Karayannis, T., Au, E., Patel, J. C., Kruglikov, I., Markx, S., Delorme, R., Héron, D., Salomon, D., Glessner, J., Restituito, S., et al. (2014) · Nature · doi:10.1038/nature13248 · Cited by 183
Responses and functions of dopamine in nucleus accumbens core during social behaviors
Dai, B., Sun, F., Tong, X., Ding, Y., Kuang, A., Osakada, T., Li, Y., & Lin, D. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111246 · Cited by 187
Hellstrom, I. C., Dhir, S. K., Diorio, J. C., & Meaney, M. J. (2012) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0223 · Cited by 171
Self-citationBorderline personality disorder, mentalization, and the neurobiology of attachment
Fonagy, P., Luyten, P., & Strathearn, L. (2011) · Infant Mental Health Journal · doi:10.1002/imhj.20283 · Cited by 202
Cameron, N. M., Shahrokh, D. K., Corpo, A. D., Dhir, S. K., Szyf, M., Champagne, F. A., & Meaney, M. J. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01725.x · Cited by 171
Self-citationRapid effects of ovarian hormones in dorsal striatum and nucleus accumbens
Yoest, K. E., Quigley, J. A., & Becker, J. B. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.04.002 · Cited by 171
Barth, C., Crestol, A., de Lange, A. G., & Galea, L. A. M. (2023) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(23)00224-3 · Cited by 162
Lonstein, J. S., Lévy, F., & Fleming, A. S. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.06.011 · Cited by 158
GABAA receptor-acting neurosteroids: a role in the development and regulation of the stress response
Gunn, B. G., Cunningham, L., Mitchell, S. G., Swinny, J. D., Lambert, J. J., & Belelli, D. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.06.001 · Cited by 149
Epigenetics and parental effects
Kappeler, L., & Meaney, M. J. (2010) · BioEssays · doi:10.1002/bies.201000015 · Cited by 159
Self-citationPereira, M., & Morrell, J. I. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02200.x · Cited by 146
Buisman‐Pijlman, F. T. A., Sumracki, N. M., Gordon, J. J., Hull, P. R., Carter, C. S., & Tops, M. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.09.005 · Cited by 147
Rutherford, H. J. V., Williams, S. K., Moy, S., Mayes, L. C., & Johns, J. M. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00037 · Cited by 140
The social brain: Neurobiological basis of affiliative behaviours and psychological well-being
Walker, S. C., & McGlone, F. P. (2013) · Neuropeptides · doi:10.1016/j.npep.2013.10.008 · Cited by 145
Numan, M., Numan, M. J., Schwarz, J. M., Neuner, C. M., Flood, T. F., & Smith, C. D. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.08.008 · Cited by 139
The paraventricular nucleus of the thalamus: an integrative node underlying homeostatic behavior
Penzo, M. A., & Gao, C. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.03.001 · Cited by 138
Stolzenberg, D. S., & Numan, M. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.003 · Cited by 137
Neural and behavioral responses to attractiveness in adult and infant faces
Hahn, A. C., & Perrett, D. I. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.08.015 · Cited by 167
Distinct preoptic‐BST nuclei dissociate paternal and infanticidal behavior in mice
Tsuneoka, Y., Tokita, K., Yoshihara, C., Amano, T., Esposito, G., Huang, A. J. Y., Yu, L. M. Y., Odaka, Y. S., Shinozuka, K., McHugh, T. J., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201591942 · Cited by 129
A Multilevel Perspective on the Development of Borderline Personality Disorder
Fonagy, P., & Luyten, P. (2016) · Wiley eBooks · doi:10.1002/9781119125556.devpsy317 · Cited by 136
Oxytocin, vasopressin, and the motivational forces that drive social behaviors
Caldwell, H. K., & Albers, H. E. (2015) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2015_390 · Cited by 129
In Search of Neural Endophenotypes of Postpartum Psychopathology and Disrupted Maternal Caregiving
Moses‐Kolko, E. L., Horner, M. S., Phillips, M. L., Hipwell, A. E., & Swain, J. E. (2014) · Journal of Neuroendocrinology · doi:10.1111/jne.12183 · Cited by 134
Lee, A. W., & Brown, R. E. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.05.008 · Cited by 128
The Neurobiology of Social Affiliation and Pair Bonding
Carter, C. S., & Keverne, E. B. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00004-8 · Cited by 130
Dopamine regulation of social choice in a monogamous rodent species
Aragona, B. J. (2009) · Frontiers in Behavioral Neuroscience · doi:10.3389/neuro.08.015.2009 · Cited by 119
Peña, C. J., Neugut, Y. D., Calarco, C. A., & Champagne, F. A. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12479 · Cited by 120
Self-citationOxytocin and postpartum depression: Delivering on what's known and what's not
Kim, S., Soeken, T. A., CROMER, S. J., Martinez, S. R., Hardy, L. R., & Strathearn, L. (2013) · Brain Research · doi:10.1016/j.brainres.2013.11.009 · Cited by 121
Stolzenberg, D. S., McKenna, J. B., Keough, S., Hancock, R., Numan, M. J., & Numan, M. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.5.907 · Cited by 117
Naef, L., Srivastava, L. K., Gratton, A. P., Hendrickson, H. P., Owens, S. M., & Walker, C. (2007) · Psychopharmacology · doi:10.1007/s00213-007-1008-4 · Cited by 119
Self-citationκ-Opioid Receptors within the Nucleus Accumbens Shell Mediate Pair Bond Maintenance
Resendez, S. L., Kuhnmuench, M., Krzywosinski, T., & Aragona, B. J. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5779-11.2012 · Cited by 110
Stolzenberg, D. S., & Champagne, F. A. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.07.005 · Cited by 115
Self-citationYoung, K. A., Gobrogge, K. L., & Wang, Z. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.06.004 · Cited by 118
Epigenetic epidemiology: Promises for public health research
Bakulski, K. M., & Fallin, M. D. (2014) · Environmental and Molecular Mutagenesis · doi:10.1002/em.21850 · Cited by 113
Oxytocin in schizophrenia: a review of evidence for its therapeutic effects
MacDonald, K. S., & Feifel, D. (2011) · Acta Neuropsychiatrica · doi:10.1111/j.1601-5215.2011.00634.x · Cited by 117
Afonso, V. M., King, S., Chatterjee, D., & Fleming, A. S. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.02.003 · Cited by 112
New theoretical and experimental approaches on maternal motivation in mammals
Olazábal, D. E., Pereira, M., Agrati, D., Ferreira, A., Fleming, A. S., González‐Mariscal, G., Lévy, F., Lucion, A. B., Morrell, J. I., Numan, M., et al. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.04.003 · Cited by 107
Neurobiology of social attachments
Coria‐Ávila, G. A., Manzo, J., García, L. I., Carrillo, P., Miquel, M., & Pfaus, J. G. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.04.004 · Cited by 108
Pereira, M., & Morrell, J. I. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.06.026 · Cited by 107
Liu, Y., Aragona, B. J., Young, K. A., Dietz, D. M., Kabbaj, M., Mazei-Robison, M., Nestler, E. J., & Wang, Z. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911998107 · Cited by 101
Miller, S. M., & Lonstein, J. S. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.1072 · Cited by 102
Rapid Habituation of Ventral Striatal Response to Reward Receipt in Postpartum Depression
Moses‐Kolko, E. L., Fraser, D., Wisner, K. L., James, J. A., Saul, A. T., Fiez, J. A., & Phillips, M. L. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.021 · Cited by 104
From Autism to Eating Disorders and More: The Role of Oxytocin in Neuropsychiatric Disorders
Romano, A., Tempesta, B., Bonaventura, M. V. M. D., & Gaetani, S. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00497 · Cited by 106
Gammie, S. C. (2005) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582305281086 · Cited by 110
Hoekzema, E. A., Tamnes, C. K., Berns, P., Barba‐Müller, E., Pozzobon, C., Picado, M., Lucco, F., Martínez‐Garcia, M., Desco, M., Ballesteros, A., et al. (2019) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2019.104507 · Cited by 112
Pereira, M., & Ferreira, A. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.08.013 · Cited by 91
Dopamine and opioid systems interact within the nucleus accumbens to maintain monogamous pair bonds
Resendez, S. L., Keyes, P. C., Day, J. J., Hambro, C., Austin, C. J., Maina, F. K., Eidson, L. N., Porter-Stransky, K. A., Nevárez, N., McLean, J. W., et al. (2016) · eLife · doi:10.7554/elife.15325 · Cited by 88
Mesolimbic Dopamine Transients in Motivated Behaviors: Focus on Maternal Behavior
Robinson, D. L., Zitzman, D. L., & Williams, S. K. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00023 · Cited by 89
Previous maternal experience affects accumbal dopaminergic responses to pup-stimuli
Afonso, V. M., Grella, S. L., Chatterjee, D., & Fleming, A. S. (2008) · Brain Research · doi:10.1016/j.brainres.2007.12.042 · Cited by 89
Numan, M., Stolzenberg, D. S., Dellevigne, A. A., Correnti, C. M., & Numan, M. J. (2009) · Behavioral Neuroscience · doi:10.1037/a0016204 · Cited by 86
Dwyer, C. M. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01657.x · Cited by 86
The maternal brain: Region‐specific patterns of brain aging are traceable decades after childbirth
de Lange, A. G., Barth, C., Kaufmann, T., Anatürk, M., Suri, S., Ebmeier, K. P., & Westlye, L. T. (2020) · Human Brain Mapping · doi:10.1002/hbm.25152 · Cited by 84
Modulation of singing‐related activity in the songbird ventral tegmental area by social context
Yanagihara, S., & Hessler, N. A. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05228.x · Cited by 96
Metadata
- Authors
- Champagne, F. A., Chretien, P., Stevenson, C. W., Zhang, T. Y., Gratton, A., & Meaney, M. J.
- Affiliations
- Douglas Mental Health University Institute (CA)
- Corresponding author
- Meaney, Michael J.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2004-04-28
- Volume
- 24
- Issue
- 17
- Pages
- 4113-4123
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6729285
- OpenAlex
- W2114537245
- Cited by
- 398
- References
- 95
- Citations by year
- 2026: 11 · 2025: 11 · 2024: 7 · 2023: 6 · 2022: 13 · 2021: 13 · 2020: 43 · 2019: 14 · 2018: 19 · 2017: 17 · 2016: 18 · 2015: 21 · 2014: 18 · 2013: 23 · 2012: 16
- FWCI
- 19.93
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DMU Open Research Archive (De Montfort University) (submittedVersion)
- Funders
- Canadian Institutes of Health Research
- National Institute of Mental Health (MH060381, R01MH060381)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- maternal behavior, nucleus accumbens shell, dopamine, lactating rats, individual differences, dopamine transporter binding, GBR 12909, dopamine D1 receptor, dopamine D3 receptor, mother-pup interaction
- MeSH terms
- Animals, Animals, Newborn, Behavior, Animal, Binding, Competitive, Dopamine, Electrochemistry, Electrodes, Implanted, Female, Grooming, Individuality, Lactation, Maternal Behavior, Membrane Glycoproteins, Nerve Tissue Proteins, Nucleus Accumbens, Receptors, Dopamine, Time Factors, Tongue, Dopamine Uptake Inhibitors, Rats, Long-Evans, Membrane Transport Proteins, Dopamine Plasma Membrane Transport Proteins, Rats
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