No CrossRef data available.
Article contents
What BANE can offer GANE: Individual differences in function of hotspot mechanisms
Published online by Cambridge University Press: 05 January 2017
Abstract
In this commentary we focus on individual differences in proposed mechanisms underlying arousal-based enhancement of prioritized stimuli. We discuss the potential of genotyping studies for examining effects of noradrenergic processes on stimulus prioritization in humans and stress the importance of potential individual differences in the activity of specific receptor subtypes in hotspot processes proposed by the GANE model.
- Type
- Open Peer Commentary
- Information
- Copyright
- Copyright © Cambridge University Press 2016
References
Arnsten, A. F., Steere, J. C. & Hunt, R. D. (1996) The contribution of alpha 2-noradrenergic mechanisms of prefrontal cortical cognitive function: Potential significance for attention-deficit hyperactivity disorder. Archives of General Psychiatry
53:448–55.CrossRefGoogle ScholarPubMed
De Martino, B., Strange, B. A. & Dolan, R. J. (2008) Noradrenergic neuromodulation of human attention for emotional and neutral stimuli. Psychopharmacology (Berlin)
197:127–36.Google Scholar
de Quervain, D. J., Kolassa, I.-T., Ertl, V., Onyut, P. L., Neuner, F., Elbert, T. & Papassotiropoulos, A. (2007) A deletion variant of the α2b-adrenoceptor is related to emotional memory in Europeans and Africans. Nature Neuroscience
10(9):1137–39.Google Scholar
Ehlers, M. E., Palombo, D. J., Mueller, D., Levine, B., Anderson, A. K. & Todd, R. M. (2015) Grey matter differences are predicted by variation in the ADRA2b gene. Poster presented at the Annual Meeting of the Society for Neuroscience, Chicago, IL, USA.Google Scholar
Havranek, M. M., Hulka, L. M., Tasiudi, E., Eisenegger, C., Vonmoos, M., Preller, K. H., Mossner, R., Baumgartner, M. R., Seifritz, E., Grunblattt, E. & Quednow, B. B. (2015) α2A-adrenergic receptor polymorphisms and mRNA expression levels are associated with delay discounting in cocaine users. Addiction Biology. doi: 10.1111/adb.12324.Google Scholar
Hawrylycz, M. J., Lein, E. S., Guillozet-Bongaarts, A. L., Shen, E. H., Ng, L., Miller, J. A., van de Lagemaat, L. N., Smith, K. A., Ebbert, A., Riley, Z. L., Abajian, C., Beckmann, C. F., Bernard, A., Bertagnolli, D., Boe, A. F., Cartagena, P. M., Chakravarty, M. M., Chapin, M., Chong, J., Dalley, R. A., Daly, B. D., Dang, C., Datta, S., Dee, N., Dolbeare, T. A., Faber, V., Feng, D., Fowler, D. R., Goldy, J., Gregor, B. W., Haradon, Z., Haynor, D. R., Hohmann, J. G., Horvath, S., Howard, R. E., Jeromin, A., Jochim, J. M., Kinnunen, M., Lau, C., Lazarz, E. T., Lee, C., Lemon, T. A., Li, L., Li, Y., Morris, J. A., Overly, C. C., Parker, P. D., Parry, S. E., Reding, M., Royall, J. J., Schulkin, J., Sequeira, P. A., Slaughterbeck, C. R., Smith, S. C., Sodt, A. J., Sunkin, S. M., Swanson, B. E., Vawter, M. P., Williams, D., Wohnoutka, P., Zielke, H. R., Geschwind, D. H., Hof, P. R., Smith, S. M., Koch, C., Grant, S. G. & Jones, A. R. (2012) An anatomically comprehensive atlas of the adult human brain transcriptome. Nature
489:391–99.Google Scholar
Jasper, J. R., Lesnick, J. D., Chang, L. K., Yamanishi, S. S., Chang, T. K., Hsu, S. A., Daunt, D. A., Bonhaus, D. W. & Eglen, R. M. (1998) Ligand efficacy and potency at recombinant alpha2 adrenergic receptors: Agonist-mediated [35S]GTPgammaS binding. Biochemistry and Pharmacology
55:1035–43.Google Scholar
Markovic, J., Anderson, A. K. & Todd, R. M. (2014) Tuning to the significant: Neural and genetic processes underlying affective enhancement of visual perception and memory. Behavioural Brain Research
259:229–41.Google Scholar
Moriceau, S. & Sullivan, R. M. (2004) Unique neural circuitry for neonatal olfactory learning. The Journal of Neuroscience
24(5):1182–89. doi: 10.1523/jneurosci.4578-03.2004.Google Scholar
Ramos, B. P., Stark, D., Verduzco, L., van Dyck, C. H. & Arnsten, A. F. (2006) α2A-adrenoceptor stimulation improves prefrontal cortical regulation of behavior through inhibition of cAMP signaling in aging animals. Learning and Memory
13(6):770–76.Google Scholar
Rasch, B., Spalek, K., Buholzer, S., Luechinger, R., Boesiger, P., Papassotiropoulos, A. & Quervain, D. J. F. d. (2009) A genetic variation of the noradrenergic system is related to differential amygdala activation during encoding of emotional memories. Proceedings of the National Academy of Sciences of the United States of America
106(45):19191–96. doi: 10.2307/25593165.Google Scholar
Small, K. M., Brown, K. M., Forbes, S. L. & Liggett, S. B. (2001) Polymorphic deletion of three intracellular acidic residues of the alpha 2B-adrenergic receptor decreases G protein-coupled receptor kinase-mediated phosphorylation and desensitization. The Journal of Biological Chemistry
276:4917–22.Google Scholar
Strange, B. A., Hurlemann, R. & Dolan, R. J. (2003) An emotion-induced retrograde amnesia in humans is amygdala- and beta-adrenergic-dependent. Proceedings of the National Academy of Sciences of the United States of America
100(23):13626–31. Available at: http://www.ncbi.nlm.nih.gov/pubmed/14595032.Google Scholar
Todd, R. M., Cunningham, W. A., Anderson, A. K. & Thompson, E. (2012) Affect-biased attention as emotion regulation. Trends in Cognitive Sciences
16:365–72.Google Scholar
Todd, R. M., Ehlers, M. R., Muller, D. J., Robertson, A., Palombo, D. J., Freeman, N., Levine, B. & Anderson, A. K. (2015) Neurogenetic variations in norepinephrine availability enhance perceptual vividness. The Journal of Neuroscience
35:6506–16.Google Scholar
Todd, R. M., Müller, D. J., Lee, D. H., Robertson, A., Eaton, T., Freeman, N., Palombo, D. J., Levine, B. & Anderson, A. K. (2013) Genes for emotion-enhanced remembering are linked to enhanced perceiving. Psychological Science
24(11):2244–53. doi: 10.1177/0956797613492423.Google Scholar
Todd, R. M., Muller, D. J., Palombo, D. J., Robertson, A., Eaton, T., Freeman, N., Levine, B. & Anderson, A. K. (2014) Deletion variant in the ADRA2B gene increases coupling between emotional responses at encoding and later retrieval of emotional memories. Neurobiological Learning and Memory
112:222–29.Google Scholar
U'Prichard, D. C., Bechtel, W. D., Rouot, B. M. & Snyder, S. H. (1979) Multiple apparent alpha-noradrenergic receptor binding sites in rat brain: Effect of 6-hydroxydopamine. Molecular Pharmacology
16:47–60.Google ScholarPubMed
Target article
Norepinephrine ignites local hotspots of neuronal excitation: How arousal amplifies selectivity in perception and memory
Related commentaries (27)
Adaptive memory systems for remembering the salient and the seemingly mundane
Amplified selectivity in cognitive processing implements the neural gain model of norepinephrine function
Are there “local hotspots?” When concepts of cognitive psychology do not fit with physiological results
Arousal-biased preferences for sensory input: An agent-centered and multisource perspective
Bidirectional synaptic plasticity can explain bidirectional retrograde effects of emotion on memory
Bodily arousal differentially impacts stimulus processing and memory: Norepinephrine in interoception
Cognitive control, dynamic salience, and the imperative toward computational accounts of neuromodulatory function
Competition elicits arousal and affect
Contemplating the GANE model using an extreme case paradigm
Dentate gyrus and hilar region revisited
Does arousal enhance apical amplification and disamplification?
Effect of arousal on perception as studied through the lens of the motor correlates of sexual arousal
Emotional memory: From affective relevance to arousal
Emotionally arousing context modulates the ERP correlates of neutral picture processing: An ERP test of the GANE model
For better or worse, or for a change?
GANEing on emotion and emotion regulation
Glutamate and norepinephrine interaction: Relevance to higher cognitive operations and psychopathology
Importance of amygdala noradrenergic activity and large-scale neural networks in regulating emotional arousal effects on perception and memory1
Interactions of noradrenaline and cortisol and the induction of indelible memories
Locus coeruleus reports changes in environmental contingencies
Once more with feeling: On the explanatory limits of the GANE model and the missing role of subjective experience
The Fluency Amplification Model supports the GANE principle of arousal enhancement
The role of arousal in predictive coding
What BANE can offer GANE: Individual differences in function of hotspot mechanisms
What do we GANE with age?
Why we forget our dreams: Acetylcholine and norepinephrine in wakefulness and REM sleep
“What have we GANEd?” A theoretical construct to explain experimental evidence for noradrenergic regulation of sensory signal processing
Author response
GANEing traction: The broad applicability of NE hotspots to diverse cognitive and arousal phenomena