scholarly journals Faculty Opinions recommendation of Reset of hippocampal-prefrontal circuitry facilitates learning.

Author(s):  
Sajikumar Sreedharan ◽  
Mohammad Zaki Bin Ibrahim
Keyword(s):  
2019 ◽  
Vol 25 (1) ◽  
pp. 206-229 ◽  
Author(s):  
Ming Ren ◽  
Zhonghua Hu ◽  
Qiang Chen ◽  
Andrew Jaffe ◽  
Yingbo Li ◽  
...  

Author(s):  
Paul J. Whalen ◽  
Maital Neta ◽  
M. Justin Kim ◽  
Alison M. Mattek ◽  
F. C. Davis ◽  
...  

When it comes to being social, there is no other nonverbal environmental cue that is more important for humans than the facial expression of another person. Here we consider facial expressions as naturally conditioned stimuli that, when presented as images in an experimental paradigm, evoke neural and behavioral responses that serve to decipher the predictive meaning of the expression. We will cover data showing that the expressions of others alter our attention to the environment, our biases in interpreting these facial expressions, and our neural responses within an amygdala-prefrontal circuitry related to normal variations in reported anxiety.


2022 ◽  
Author(s):  
Peter Kirk ◽  
Avram J Holmes ◽  
Oliver Joe Robinson

A well documented amygdala-dorsomedial prefrontal circuit is theorized to promote attention to threat (‘threat vigilance’). Prior research has implicated a relationship between individual differences in trait anxiety/vigilance, engagement of this circuitry, and anxiogenic features of the environment (e.g. through threat-of-shock and movie-watching). In the present study, we predicted that—for those scoring high in self-reported anxiety and a behavioral measure of threat vigilance—this circuitry is chronically engaged, even in the absence of anxiogenic stimuli. Our analyses of resting-state fMRI data (N=639) did not, however, provide evidence for such a relationship. Nevertheless, in our planned exploratory analyses, we saw a relationship between threat vigilance behavior (but not self-reported anxiety) and intrinsic amygdala-periaqueductal gray connectivity. Here, we suggest this subcortical circuitry may be chronically engaged in hypervigilant individuals, but that the amygdala-prefrontal circuitry may only be engaged in response to anxiogenic stimuli.


2007 ◽  
Vol 13 (3) ◽  
pp. 313-324 ◽  
Author(s):  
J W Buckholtz ◽  
J H Callicott ◽  
B Kolachana ◽  
A R Hariri ◽  
T E Goldberg ◽  
...  

2013 ◽  
Vol 33 (10) ◽  
pp. 4584-4593 ◽  
Author(s):  
D. G. Gee ◽  
K. L. Humphreys ◽  
J. Flannery ◽  
B. Goff ◽  
E. H. Telzer ◽  
...  

2019 ◽  
Vol 30 (2) ◽  
pp. 550-562 ◽  
Author(s):  
K K Sharma ◽  
E A Kelly ◽  
C W Pfeifer ◽  
J L Fudge

Abstract Rodent fear-learning models posit that amygdala–infralimbic connections facilitate extinction while amygdala–prelimbic prefrontal connections mediate fear expression. Analogous amygdala–prefrontal circuitry between rodents and primates is not established. Using paired small volumes of neural tracers injected into the perigenual anterior cingulate cortex (pgACC; areas 24b and 32; a potential homologue to rodent prelimbic cortex) and subgenual anterior cingulate cortex (sgACC, areas 25 and 14c; a potential homologue to rodent infralimbic cortex) in a single hemisphere, we mapped amygdala projections to the pgACC and sgACC within single subjects. All injections resulted in dense retrograde labeling specifically within the intermediate division of the basal nucleus (Bi) and the magnocellular division of the accessory basal nucleus (ABmc). Areal analysis revealed a bias for connectivity with the sgACC, with the ABmc showing a greater bias than the Bi. Double fluorescence analysis revealed that sgACC and pgACC projections were intermingled within the Bi and ABmc, where a proportion were double labeled. We conclude that amygdala inputs to the ACC largely originate from the Bi and ABmc, preferentially connect to the sgACC, and that a subset collaterally project to both sgACC and pgACC. These findings advance our understanding of fear extinction and fear expression circuitry across species.


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