2022
DOI: 10.17219/acem/146756
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Neurobiological advances of learned fear in humans

Abstract: In the whole animal kingdom, fear learning is an essential process that allows living beings to survive. Therefore, revealing the neurophysiological processes that govern the expression of emotional fear memory and exploring its neurobiological underpinnings are the imperatives of affective neuroscience. Learned fear memories activate defensive behaviors in anticipation of harm, thus minimizing the impact of the threat. However, despite a century of research, the neural circuitry underlying fear learning in hu… Show more

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Cited by 55 publications
(40 citation statements)
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“…This interaction, however, may also be influenced by the pathophysiology of cognitive and behavioral brain functions because of the psychiatric disorders present. In this respect, we can refer to the contribution that prefrontal brain regions have in the assessment of rewarding, which underlies subsequent decision making and goal-directed behavior [ 6 , 46 ].…”
Section: Discussionmentioning
confidence: 99%
“…This interaction, however, may also be influenced by the pathophysiology of cognitive and behavioral brain functions because of the psychiatric disorders present. In this respect, we can refer to the contribution that prefrontal brain regions have in the assessment of rewarding, which underlies subsequent decision making and goal-directed behavior [ 6 , 46 ].…”
Section: Discussionmentioning
confidence: 99%
“…In AD, extracellular Aβ and tau deposits are found in the frontal cortex and the hippocampus [8]. The prefrontal cortex (PFC) has been determined to play a crucial role in learning and response to fear [75,76]. Alterations in the PFC determine cognitive changes in advanced aging, which are indicative of patterns of cognitive dysfunctions observed in patients with AD [77].…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, FDG-PET requires an injection of radiolabeled tracers, which is considered more invasive than other neuroimaging modalities. Nevertheless, FDG-PET can provide a more detailed diagnosis of brain cognitive metabolism and synaptic dysfunction by quantifying toxic Aβ and tau proteins in the brains of AD patients, which drive healthy neurons into the diseased state [ 60 , 61 , 62 ]. Moreover, hypometabolism is a result of neurodegeneration and therefore might not be suitable to detect the signs of AD in the earliest stages before neuronal loss occurs [ 63 ].…”
Section: Neuroimaging Modalities In Admentioning
confidence: 99%