The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
The Functional Neuroanatomy of Maternal Love: Mother’s Response to Infant’s Attachment Behaviors
Abstract
Background Maternal love, which may be the core of maternal behavior, is essential for the mother-infant attachment relationship and is important for the infant's development and mental health. However, little has been known about these neural mechanisms in human mothers. We examined patterns of maternal brain activation in response to infant cues using video clips.Methods We performed functional magnetic resonance imaging (fMRI) measurements while 13 mothers viewed video clips, with no sound, of their own infant and other infants of approximately 16 months of age who demonstrated two different attachment behaviors (smiling at the infant's mother and crying for her).Results We found that a limited number of the mother's brain areas were specifically involved in recognition of the mother's own infant, namely orbitofrontal cortex (OFC), periaqueductal gray, anterior insula, and dorsal and ventrolateral parts of putamen. Additionally, we found the strong and specific mother's brain response for the mother's own infant's distress. The differential neural activation pattern was found in the dorsal region of OFC, caudate nucleus, right inferior frontal gyrus, dorsomedial prefrontal cortex (PFC), anterior cingulate, posterior cingulate, thalamus, substantia nigra, posterior superior temporal sulcus, and PFC.Conclusions Our results showed the highly elaborate neural mechanism mediating maternal love and diverse and complex maternal behaviors for vigilant protectiveness.
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“In several human fMRI studies, responses to own- versus other-baby stimuli of first-time mothers during this early postpartum period show increased brain activity in several regions, including the orbitofrontal cortex (OFC), midbrain, striatum, cingulate, amygdala and insula (4,5,8,9,19,20).”
From Neuroendocrinology of Parental Response to Baby‐Cry (2011) · cites this paper as [19]
In the citing paper
“Furthermore, orbitofrontal cortex responses to own-baby visual stimuli correlate with ratings of pleasant mood, excitement and love that mothers may experience when viewing the stimuli (19,58).”
From Neuroendocrinology of Parental Response to Baby‐Cry (2011) · cites this paper as [19]
In the citing paper
“Indeed, human mothers showed a greater activity of response in the midbrain, periaqueductal grey and striatum, OFC, medial prefrontal, anterior cingulate cortex, anterior insula and precuneus to their own- versus other-baby pictures (20,44) or videos (19,57).”
From Neuroendocrinology of Parental Response to Baby‐Cry (2011) · cites this paper as [19]
In the citing paper
“Activation of the medial and lateral PFC and ACC are consistently observed among new mothers in response to an infant’s cry (Laurent and Ablow, 2012; Lorberbaum et al., 2002), to videos of a distressed infant (Noriuchi et al., 2008), and to one’s own child greater than to familiar/unknown faces (Leibenluft et al., 2004) were observed among new mothers.”
From The maternal brain and its plasticity in humans (2016) · cites this paper as Noriuchi et al., 2008
In the citing paper
“Furthermore, they found strong and specific differential responses of mother’s brain to her own-infant’s distress in substantia nigra, caudate nucleus, thalamus, posterior and superior temporal sulcus, anterior cingulate, dorsal regions of OFC, right inferior frontal gyrus and dorsomedial prefrontal cortex.”
From The human parental brain: In vivo neuroimaging (2011) · cites this paper as Noriuchi et al., 2008
In the citing paper
“They also found correlations in OFC with own baby-response and happiness as well as to their own distressed baby response in the superior temporal regions.”
From The human parental brain: In vivo neuroimaging (2011) · cites this paper as Noriuchi et al., 2008
In the citing paper
“First, they confirmed the increased activity, associated with recognizing own baby pictures, in certain brain regions including cortical orbitofrontal, anterior insula and precuneus cortical areas as well as subcortical regions including the periaqueductal gray and putamen.”
From The human parental brain: In vivo neuroimaging (2011) · cites this paper as Noriuchi et al., 2008
In the citing paper
“Second, they found strong and specific differential responses of mother’s brain to her own-infant’s distress in substantia nigra, caudate nucleus, thalamus, posterior and superior temporal sulcus, anterior cingulate, dorsal regions of OFC, right inferior frontal gyrus and dorsomedial prefrontal cortex”
From Approaching the biology of human parental attachment: Brain imaging, oxytocin and coordinated assessments of mothers and fathers (2014) · cites this paper as Noriuchi et al., 2008
In the citing paper
“First, these authors confirmed increased activation associated with own baby pictures, in cortical orbitofrontal, anterior insula and precuneus areas, as well as subcortical regions including periaqueductal gray and putamen.”
From Approaching the biology of human parental attachment: Brain imaging, oxytocin and coordinated assessments of mothers and fathers (2014) · cites this paper as Noriuchi et al., 2008
In the citing paper
“They also found correlations in OFC with own baby-response and happiness as well as to their own distressed baby response in superior temporal regions.”
From Approaching the biology of human parental attachment: Brain imaging, oxytocin and coordinated assessments of mothers and fathers (2014) · cites this paper as Noriuchi et al., 2008
Citations
Cites
Functional neuroanatomy of emotion: A meta-analysis of emotion activation studies in PET and fMRI
Phan, K. L., Wager, T., Taylor, S. F., & Liberzon, I. (2002) · NeuroImage · doi:10.1006/nimg.2002.1087 · Cited by 3,502
Rethinking feelings: an fMRI study of the cognitive regulation of emotion
Ochsner, K. N., Bunge, S. A., Gross, J. J., & Gabrieli, J. D. E. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/089892902760807212 · Cited by 2,520
Social perception from visual cues: Role of the STS region
Allison, T., Puce, A., & McCarthy, G. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01501-1 · Cited by 2,461
Functional imaging of ‘theory of mind’
Gallagher, H. L., & Frith, C. D. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)00025-6 · Cited by 2,092
Abstract reward and punishment representations in the human orbitofrontal cortex
O'Doherty, J., Kringelbach, M. L., Rolls, E. T., Hornak, J., & Andrews, C. (2001) · Nature Neuroscience · doi:10.1038/82959 · Cited by 2,003
Neural systems for recognizing emotion
Adolphs, R. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00301-x · Cited by 1,933
The neural correlates of maternal and romantic love
Bartels, A., & Zeki, S. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.003 · Cited by 1,497 · cited 1×
“Additionally, it is suggested that maternal love and attachment are involved in the OFC activation while the mother views the photo of her own child (2,4).”
The primate basal ganglia: Parallel and integrative networks
Haber, S. N. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.10.003 · Cited by 1,479
Multiple reward signals in the brain
Schultz, W. (2000) · Nature Reviews Neuroscience · doi:10.1038/35044563 · Cited by 1,303
Unmyelinated tactile afferents signal touch and project to insular cortex
Olausson, H., Lamarre, Y., Backlund, H., Morin, C., Wallin, B. G., Starck, G., EKHOLM, S. E., Strigo, I. A., Worsley, K. J., Vallbo, Å. B., et al. (2002) · Nature Neuroscience · doi:10.1038/nn896 · Cited by 1,034
The triune brain in evolution: Role in paleocerebral functions
Legg, C. R. (1990) · Biological Psychology · doi:10.1016/0301-0511(90)90083-9 · Cited by 976
(1990) · Medical Entomology and Zoology · Cited by 919
The Anatomical Connections of the Macaque Monkey Orbitofrontal Cortex. A Review
Cavada, C. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.220 · Cited by 917
INFANT CRYING AND MATERNAL RESPONSIVENESS
Bell, S. M. V., & Ainsworth, M. D. S. (1972) · Child Development · doi:10.2307/1127506 · Cited by 899
Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning
Schoenbaum, G. M., Chiba, A. A., & Gallagher, M. (1998) · Nature Neuroscience · doi:10.1038/407 · Cited by 849
Hornak, J., Rolls, E. T., & Wade, D. (1996) · Neuropsychologia · doi:10.1016/0028-3932(95)00106-9 · Cited by 735
The retrosplenial cortex and emotion: new insights from functional neuroimaging of the human brain
Maddock, R. J. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01374-5 · Cited by 733
Neuroanatomical correlates of externally and internally generated human emotion
(1997) · American Journal of Psychiatry · doi:10.1176/ajp.154.7.918 · Cited by 711 · cited 1×
“own emotional state to make personally relevant decisions (42).”
O'Doherty, J., Critchley, H., Deichmann, R., & Dolan, R. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-21-07931.2003 · Cited by 611
Neural activation during selective attention to subjective emotional responses
Lane, R., Fink, G., Chau, P., & Dolan, R. (1997) · NeuroReport · doi:10.1097/00001756-199712220-00024 · Cited by 596
Representations of Pleasant and Painful Touch in the Human Orbitofrontal and Cingulate Cortices
Rolls, E. T. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.308 · Cited by 535
Areas of brain activation in males and females during viewing of erotic film excerpts
Karama, S., Lecours, A. R., Leroux, J., Bourgouin, P., Beaudoin, G., Joubert, S., & Beauregard, M. (2002) · Human Brain Mapping · doi:10.1002/hbm.10014 · Cited by 522
Elliott, R., Newman, J. L., Longe, O. A., & Deakin, J. F. W. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00303.2003 · Cited by 512
Mothers' neural activation in response to pictures of their children and other children
Leibenluft, E., Gobbini, M. I., Harrison, T., & Haxby, J. V. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.05.017 · Cited by 493
Anatomy of Motor Learning. II. Subcortical Structures and Learning by Trial and Error
Jueptner, M., Frith, C., Brooks, D. J., Frackowiak, R. S. J., & Passingham, R. E. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.3.1325 · Cited by 466
Francis, S., Rolls, E. T., Bowtell, R. W., McGlone, F. P., O’Doherty, J. P., Browning, A., Clare, S., & Smith, E. (1999) · Neuroreport · doi:10.1097/00001756-199902250-00003 · Cited by 421
Differential roles of monkey striatum in learning of sequential hand movement
Miyachi, S., Hikosaka, O., Miyashita, K., Kárádi, Z., & Rand, M. K. (1997) · Experimental Brain Research · doi:10.1007/pl00005669 · Cited by 374
Seifritz, E., Esposito, F., Neuhoff, J. G., Lüthi, A., Mustovic, H., Dammann, G., von Bardeleben, U., Radue, E. W., Cirillo, S., Tedeschi, G., et al. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00697-8 · Cited by 373
Orbitofrontal cortex tracks positive mood in mothers viewing pictures of their newborn infants
Nitschke, J. B., Nelson, E. E., Rusch, B. D., Fox, A. S., Oakes, T. R., & Davidson, R. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.10.005 · Cited by 371
A potential role for thalamocingulate circuitry in human maternal behavior
Lorberbaum, J. P., Newman, J. D., Horwitz, A. R., Dubno, J. R., Lydiard, R. B., Hamner, M. B., Bohning, D. E., & George, M. S. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01284-7 · Cited by 359
Brain Regions Involved in the Perception of Gaze: A PET Study
Wicker, B., Michel, F., Hénaff, M., & Jean Decety, A. (1998) · NeuroImage · doi:10.1006/nimg.1998.0357 · Cited by 274
Activation of the Right Inferior Frontal Cortex During Assessment of Facial Emotion
Nakamura, K., Kawashima, R., Ito, K., Sugiura, M., Kato, T., Nakamura, A., Hatano, K., Nagumo, S., Kubota, K., Fukuda, H., et al. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.3.1610 · Cited by 265
Functional Magnetic Resonance Imaging of Brain Reward Circuitry in the Human
BREITER, H. C., & Rosen, B. R. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09287.x · Cited by 233
Chemical anatomy of primate basal ganglia
Parent, A., Côté, P., & Lavoie, B. A. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(95)80010-6 · Cited by 186
Lonstein, J. S., & Stern, J. M. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00642-8 · Cited by 152
Disturbances of Maternal Behavior in the Rat Following Lesions of the Cingulate Cortex
Slotnick, B. M. (1967) · Behaviour · doi:10.1163/156853967x00127 · Cited by 147
Jaeger, D., Gilman, S., & Aldridge, J. W. (1995) · Brain Research · doi:10.1016/0006-8993(95)00780-t · Cited by 134
Vasopressin, oxytocin and neurophysins in the human brain and spinal cord
Jenkins, J. S., Ang, V. T. Y., Hawthorn, J., Rossor, M. N., & Iversen, L. L. (1984) · Brain Research · doi:10.1016/0006-8993(84)90656-5 · Cited by 126
A role for the periaqueductal grey in opioidergic inhibition of maternal behaviour
Miranda‐Paiva, C. M., Ribeiro-Barbosa, É. R., Canteras, N. S., & Felício, L. F. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02794.x · Cited by 62
Proprioceptive reflexes in patients with reflex sympathetic dystrophy
Schouten, A. C., de Beek, W. J. T. V., van Hilten, J. J., & van der Helm, F. C. T. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1420-x · Cited by 43
Unilateral striatal lesions in the cat disrupt well-learned motor plans in a GO/NO-GO reaching task
Aldridge, J. W., Thompson, J. F., & Gilman, S. (1997) · Experimental Brain Research · doi:10.1007/pl00005592 · Cited by 20
Worsley (1996) · doi:10.1002/(sici)1097-0193(1996)4:1
Flagged first, then by citations
Cited by
Sorted by citations
Compassion: an evolutionary analysis and empirical review
Goetz, J. L., Keltner, D., & Simon-Thomas, E. (2010) · Psychological Bulletin · doi:10.1037/a0018807 · Cited by 2,200
The Simulation of Smiles (SIMS) model: Embodied simulation and the meaning of facial expression
Niedenthal, P. M., Mermillod, M., Maringer, M., & Hess, U. (2010) · Behavioral and Brain Sciences · doi:10.1017/s0140525x10000865 · Cited by 618
The Peptide That Binds: A Systematic Review of Oxytocin and its Prosocial Effects in Humans
MacDonald, K., & MacDonald, T. M. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673220903523615 · Cited by 585
Emotion regulation in parenthood
Rutherford, H. J. V., Wallace, N. S., Laurent, H. K., & Mayes, L. C. (2015) · Developmental Review · doi:10.1016/j.dr.2014.12.008 · Cited by 485
“, reporting greater parental distress and/or less positive infant-directed feelings – have shown reduced midbrain volume and activation in the amygdala, striatum, and orbitofrontal cortex while viewing their infant’s emotional faces or videos of their own infant (Barrett et al., 2012; Kim et al., 2010; Noriuchi et al.…”
BackgroundKim, P., Leckman, J. F., Mayes, L. C., Feldman, R., Wang, X., & Swain, J. E. (2010) · Behavioral Neuroscience · doi:10.1037/a0020884 · Cited by 440
Metadata
- Authors
- Noriuchi, M., Kikuchi, Y., & Senoo, A.
- Affiliations
- Tokyo Metropolitan University (JP)
- Corresponding author
- Noriuchi, Madoka
- ORCID
- Senoo, Atsushi
- Venue
- Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2008-02
- Volume
- 63
- Issue
- 4
- Pages
- 415-423
- ISSN
- 0006-3223 (ISSN-L)
- OpenAlex
- W2051071356
- Semantic Scholar
- bc5ff3e851f5b3a2b8bda923e3ed29f1056105c0
- Cited by
- 334
- References
- 42
- Citations by year
- 2026: 5 · 2025: 17 · 2024: 10 · 2023: 16 · 2022: 14 · 2021: 14 · 2020: 14 · 2019: 21 · 2018: 19 · 2017: 24 · 2016: 24 · 2015: 29 · 2014: 19 · 2013: 17 · 2012: 26
- FWCI
- 19.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
- Social Sciences › Psychology › Social Psychology › Attachment and Relationship Dynamics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Infant Health and Development
- Keywords
- maternal love, maternal attachment, infant distress, orbitofrontal cortex, periaqueductal gray, anterior insula, putamen, caudate nucleus, dorsomedial prefrontal cortex, anterior cingulate cortex, thalamus, substantia nigra, superior temporal sulcus, maternal behavior
- MeSH terms
- Arousal, Brain, Female, Humans, Infant, Love, Magnetic Resonance Imaging, Maternal Behavior, Mother-Child Relations, Nerve Net, Object Attachment, Prefrontal Cortex, Infant Behavior
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