Page 40 - AN-2-1

Advanced Neurology The anterior cingulate cortex in social empathy

56. Yesudas EH, Lee TM, 2015, The role of cingulate cortex in rodents as a model for empathy. Genes Brain Behav, 18: e12521.
vicarious pain. Biomed Res Int, 2015: 719615.
https://doi.org/10.1111/gbb.12521
https://doi.org/10.1155/2015/719615
68. Apps MA, Rushworth MF, Chang SW, 2016, The anterior
57. Urban-Ciecko J, Fanselow EE, Barth AL, 2015, Neocortical cingulate gyrus and social cognition: Tracking the
somatostatin neurons reversibly silence excitatory motivation of others. Neuron, 90: 692–707.
transmission via GABAb receptors. Curr Biol, 25: 722–731.
https://doi.org/10.1016/j.neuron.2016.04.018
https://doi.org/10.1016/j.cub.2015.01.035
69. Chang SW, Fagan NA, Toda K, et al., 2015, Neural
58. Scheggia D, Manago F, Maltese F, et al., 2020, Somatostatin mechanisms of social decision-making in the primate
interneurons in the prefrontal cortex control affective state amygdala. Proc Natl Acad Sci U S A, 112: 16012–16017.
discrimination in mice. Nat Neurosci, 23: 47–60.
https://doi.org/10.1073/pnas.1514761112
https://doi.org/10.1038/s41593–019–0551–8
70. Kim SW, Kim M, Baek J, et al., 2022, Hemispherically
59. Yizhar O, Fenno LE, Prigge M, et al., 2011, Neocortical lateralized rhythmic oscillations in the cingulate-amygdala
excitation/inhibition balance in information processing and circuit drive affective empathy in mice. Neuron, 111: 418-
social dysfunction. Nature, 477: 171–178. 429.
https://doi.org/10.1038/nature10360 https://doi.org/10.1016/j.neuron.2022.11.001
60. Ma Y, Hu H, Berrebi AS, et al., 2006, Distinct subtypes of 71. Chang SW, Dal Monte O, 2018, Shining light on social
somatostatin-containing neocortical interneurons revealed learning circuits. Trends Cogn Sci, 22: 673–675.
in transgenic mice. J Neurosci, 26: 5069–5082.
https://doi.org/10.1016/j.tics.2018.05.002
https://doi.org/10.1523/jneurosci.0661-06.2006
72. Kim SW, Kim M, Shin HS, 2021, Affective empathy and prosocial
61. Xu X, Callaway EM, 2009, Laminar specificity of functional behavior in rodents. Curr Opin Neurobiol, 68: 181–189.
input to distinct types of inhibitory cortical neurons. https://doi.org/10.1016/j.conb.2021.05.002
J Neurosci, 29: 70–85.
73. Ito W, Erisir A, Morozov A, 2015, Observation of distressed
https://doi.org/10.1523/jneurosci.4104-08.2009
conspecific as a model of emotional trauma generates
62. Lü YF, Yang Y, Li CL, et al., 2017, The locus coeruleus- silent synapses in the prefrontal-amygdala pathway and
norepinephrine system mediates empathy for pain through enhances fear learning, but ketamine abolishes those effects.
selective up-regulation of P2X3 receptor in dorsal root Neuropsychopharmacology, 40: 2536–2545.
ganglia in rats. Front Neural Circuits, 11: 66.
https://doi.org/10.1038/npp.2015.100
https://doi.org/10.3389/fncir.2017.00066
74. Ito W, Morozov A, 2019, Prefrontal-amygdala plasticity
63. Jodo E, Chiang C, Aston-Jones G, 1998, Potent excitatory enabled by observational fear. Neuropsychopharmacology,
influence of prefrontal cortex activity on noradrenergic 44: 1778–1787.
locus coeruleus neurons. Neuroscience, 83: 63–79.
https://doi.org/10.1038/s41386-019-0342-7
https://doi.org/10.1016/s0306-4522(97)00372-2
75. Rajasethupathy P, Sankaran S, Marshel JH, et al., 2015,
64. Arnsten AF, Goldman-Rakic PS, 1984, Selective prefrontal Projections from neocortex mediate top-down control of
cortical projections to the region of the locus coeruleus and memory retrieval. Nature, 526: 653–659.
raphe nuclei in the rhesus monkey. Brain Res, 306: 9–18.
https://doi.org/10.1038/nature15389
https://doi.org/10.1016/0006-8993(84)90351-2
76. Bruchey AK, Jones CE, Monfils MH, 2010, Fear conditioning
65. Luo WJ, Li CL, Geng KW, et al., 2020, The similar past by-proxy: Social transmission of fear during memory
pain experience evokes both observational contagious pain retrieval. Behav Brain Res, 214: 80–84.
and consolation in stranger rat observers. Neurosci Lett, https://doi.org/10.1016/j.bbr.2010.04.047
722: 134840.
77. Zheng C, Huang Y, Bo B, et al., 2020, Projection from the
https://doi.org/10.1016/j.neulet.2020.134840
anterior cingulate cortex to the lateral part of mediodorsal
66. Barroso AR, Araya EI, De Souza CP, et al., 2019, thalamus modulates vicarious freezing behavior. Neurosci
Characterization of rat ultrasonic vocalization in the Bull, 36: 217–229.
orofacial formalin test: Influence of the social context. Eur https://doi.org/10.1007/s12264-019-00427-z
Neuropsychopharmacol, 29: 1213–1226.
78. Nomura H, Teshirogi C, Nakayama D, et al., 2019, Prior
https://doi.org/10.1016/j.euroneuro.2019.08.298
observation of fear learning enhances subsequent self-
67. Kim A, Keum S, Shin HS, 2019, Observational fear behavior in experienced fear learning with an overlapping neuronal

Volume 2 Issue 1 (2023) 13 https://doi.org/10.36922/an.281