Cited by 55Memory and Neural MechanismsNeural and Behavioral Psychology StudiesFace Recognition and Perception

Facing the role of the amygdala in emotional information processing

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Baxter, Mark G., Croxson, Paula L.·2012·Proceedings of the National Academy of Sciences

Abstract

The neurobiology of social information processing provides a fascinating window into human nature and how primate brains evolved to deal with challenges of living in large social groups. Faces and facial expressions of emotion are critical for social identification and for modulation of appropriate responding in social situations. The decoding of emotional information, and the subsequent integration of this information into choices about behavior appropriate to particular contexts, is an integral part of everyday human behavior. Although, for most humans, these systems may be primarily taxed now by reading emotional cues to avoid embarrassing faux pas in social situations, evolutionary pressure to develop these systems likely emphasized rapid and reliable detection of threats. Hadj-Bouziane et al. (1), in PNAS, make remarkable strides in understanding these neural mechanisms, by using an unusual and powerful combination of methodologies in a study of rhesus monkeys.

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Crossref · 10.1073/pnas.1219167110

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  • The amygdala is involved in stimulus-value association, recognition of emotionally salient stimuli, and orchestration of an appropriate behavioral response.

    “On the other hand, the amygdala is involved in stimulus-value association, recognition of emotionally salient stimuli, and orchestration of an appropriate behavioral response (Phelps and LeDoux 2005; Paton et al. 2006; Baxter and Croxson 2012).”

    From Neuroanatomical correlates of peripersonal space: bridging the gap between perception, action, emotion and social cognition (2024) · cites this paper as Baxter and Croxson 2012

    The opening section (pp. 21180–21181) describes the amygdala's involvement in detecting threats, recognizing emotional facial expressions, and activating appropriate fear-related behavior. The section on amygdala damage also discusses attention to stimuli with uncertain consequences, but the paper does not establish the claimed role in forming stimulus–value associations. (LLM, conf=0.84)

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Research works printed but not linked: 11

  1. Pinsk MA, DeSimone K, Moore T, Gross CG, Kastner S (2005) Representations of faces and body parts in ma- caque temporal cortex: A functional MRI study. Proc Natl Acad Sci USA 102(19):6996-7001.
  2. Kanwisher N, McDermott J, Chun MM (1997) The fusiform face area: A module in human extrastriate cortex special- ized for face perception. J Neurosci 17(11):4302-4311.
  3. Adolphs R, et al. (1999) Recognition of facial emotion in nine individuals with bilateral amygdala damage. Neuropsychologia 37(10):1111-1117.
  4. Hadj-Bouziane F, Bell AH, Knusten TA, Ungerleider LG, Tootell RBH (2008) Perception of emotional expres- sions is independent of face selectivity in monkey in- ferior temporal cortex. Proc Natl Acad Sci USA 105(14): 5591-5596.
  5. Gallagher M, Holland PC (1994) The amygdala com- plex: Multiple roles in associative learning and atten- tion. Proc Natl Acad Sci USA 91(25):11771-11776.
  6. N'Diaye K, Sander D, Vuilleumier P (2009) Self-rele- vance processing in the human amygdala: gaze direc- tion, facial expression, and emotion intensity. Emotion 9(6):798-806.
  7. Adams RB, Jr., et al. (2012) Amygdala responses to averted vs direct gaze fear vary as a function of presen- tation speed. Soc Cogn Affect Neurosci 7(5):568-577.
  8. Sallet J, et al. (2011) Social network size affects neural circuits in macaques. Science 334(6056):697-700.
  9. Goense JBM, Whittingstall K, Logothetis NK (2010) Functional magnetic resonance imaging of awake be- having macaques. Methods 50(3):178-188.
  10. Mars RB, et al. (2012) Connectivity-based subdivisions of the human right "temporoparietal junction area": Evidence for different areas participating in different cortical networks. Cereb Cortex 22(8):1894-1903.
  11. Schmid MC, et al. (2010) Blindsight depends on the lateral geniculate nucleus. Nature 466(7304):373-377.

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Authors
Baxter, M. G., & Croxson, P. L.
Affiliations
Icahn School of Medicine at Mount Sinai (US)
Venue
Proceedings of the National Academy of Sciences
Published
2012-12-14
Volume
109
Issue
52
Pages
21180-21181
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2033725479
Cited by
55
References
4
Citations by year
2026: 4 · 2025: 4 · 2024: 12 · 2023: 12 · 2022: 13 · 2020: 1 · 2019: 3 · 2017: 2 · 2015: 3 · 2014: 1
FWCI
0.66
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
Keywords
amygdala, emotional processing, emotions, emotional memory, fear
MeSH terms
Amygdala, Animals, Evoked Potentials, Facial Expression, Macaca mulatta, Magnetic Resonance Imaging, Male, Temporal Lobe

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