Glucocorticoids Enhance the Excitability of Principal Basolateral Amygdala Neurons
Open accessAbstract
A large body of pharmaco-behavioral data implicates the basolateral nucleus of the amygdala (BLA) in the facilitation of memory consolidation by emotions. Overall, this evidence suggests that stress hormones released during emotional arousal increase the activity of BLA neurons. In turn, this increased BLA activity would facilitate synaptic plasticity elsewhere in the brain, to which the BLA projects. However, the direct effects of glucocorticoids on BLA neurons are incompletely understood. In the present study, we examined the direct effects of corticosterone (CORT) on principal neurons of the rat BLA in vitro using whole-cell patch-clamp recordings. We found that application of a stress level of CORT for 20 min caused significant changes in the passive properties and responsiveness of BLA cells measured 1–2 h later. Indeed, CORT application produced a depolarization of the resting potential, an increase in input resistance, and a dramatic decrease in spike-frequency adaptation. In addition, GABA A IPSPs evoked by stimulation of the external capsule were significantly reduced by CORT application. This effect of CORT was not attributable to a reduction in the amount of GABA released because GABA B IPSPs were unchanged and the resistance drop associated with GABA A IPSPs was not altered. Rather, we found that this effect of CORT resulted from a positive shift of the GABA A reversal potential. Overall, these results suggest that, in agreement with previous behavioral findings, glucocorticoids enhance the excitability of principal BLA cells by increasing their intrinsic excitability and decreasing the impact of GABA A IPSPs.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The central amygdala nucleus (CEA) is rich in stress hormones and their receptors and contributes to processing of stress signals.
“The CEA is rich in stress hormones and their receptors,98, 99, 100, 101 and contributes to processing of stress signals.102, 103, 104”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [98]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Two receptor systems for corticosterone in rat brain: Microdistribution and differential occupation
REUL, J. M. H. M., & KLOET, E. R. D. (1985) · Endocrinology · doi:10.1210/endo-117-6-2505 · Cited by 2,580 · see citing works
THE AMYGDALA MODULATES THE CONSOLIDATION OF MEMORIES OF EMOTIONALLY AROUSING EXPERIENCES
McGaugh, J. L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144157 · Cited by 2,296 · see citing works
The Neuroendocrinology of Stress and Aging: The Glucocorticoid Cascade Hypothesis
Sapolsky, R. M., Krey, L. C., & McEwen, B. S. (1986) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2002.38.cp21 · Cited by 2,287 · see citing works
Vyas, A., Mitra, R., Shankaranarayana Rao, B. S., & Chattarji, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06810.2002 · Cited by 1,662 · see citing works
Stress and cognition: are corticosteroids good or bad guys?
de Kloet, E. R., Oitzl, M. S., & Joëls, M. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01438-1 · Cited by 1,258 · see citing works
Bormann, J., Hamill, O. P., & Sakmann, B. J. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016493 · Cited by 1,161 · see citing works
Role of adrenal stress hormones in forming lasting memories in the brain
McGaugh, J. L., & Roozendaal, B. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00306-9 · Cited by 818 · see citing works
Ionic basis of GABAA receptor channel function in the nervous system
Kaila, K. (1994) · Progress in Neurobiology · doi:10.1016/0301-0082(94)90049-3 · Cited by 670 · see citing works
Glucocorticoids and the regulation of memory consolidation
Roozendaal, B. (2000) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(99)00058-x · Cited by 665 · see citing works
Memory consolidation and the amygdala: a systems perspective
McGaugh, J. L. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02211-7 · Cited by 572 · see citing works
Amygdala modulation of hippocampal-dependent and caudate nucleus-dependent memory processes
Packard, M. G., Cahill, L., & McGaugh, J. L. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.18.8477 · Cited by 544 · see citing works
Morimoto, M., Morita, N., Ozawa, H., Yokoyama, K., & Kawata, M. (1996) · Neuroscience Research · doi:10.1016/s0168-0102(96)01105-4 · Cited by 475 · see citing works
Sandi, C., Loscertales, M., & Guaza, C. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01412.x · Cited by 447 · see citing works
Control of neuronal excitability by corticosteroid hormones
Joëls, M., & de Kloet, E. R. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90345-9 · Cited by 400 · see citing works
The Role of Chloride Transport in Postsynaptic Inhibition of Hippocampal Neurons
Misgeld, U., Deisz, R. A., Dodt, H. U., & Lux, H. D. (1986) · Science · doi:10.1126/science.2424084 · Cited by 398 · see citing works
Postsynaptic fall in intracellular pH induced by GABA-activated bicarbonate conductance
Kaila, K., & Voipio, J. (1987) · Nature · doi:10.1038/330163a0 · Cited by 365 · see citing works
Point mutation in the mouse glucocorticoid receptor preventing DNA binding impairs spatial memory
Oitzl, M. S., Reichardt, H. M., Joëls, M., & de Kloet, E. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.231313998 · Cited by 286 · see citing works
Roozendaal, B., & McGaugh, J. L. (1997) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1996.3765 · Cited by 282 · see citing works
Inhibitory transmission in the basolateral amygdala
Rainnie, D. G., Asprodini, E., & Shinnick‐Gallagher, P. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.3.999 · Cited by 280 · see citing works
Electrophysiological and morphological properties of rat basolateral amygdaloid neurons in vitro
Washburn, M., & Moises, H. C. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-10-04066.1992 · Cited by 270 · see citing works
Hatfield, T., & McGaugh, J. L. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3875 · Cited by 267 · see citing works
Manzanares, P. A. R., Isoardi, N. A., Carrer, H. F., & Molina, V. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2260-05.2005 · Cited by 262 · see citing works
Stress effects in the hippocampus: Synaptic plasticity and memory
Kim, J. J., Song, E. Y., Kim, J. J., Song, E. Y., & Kosten, T. A. (2006) · Stress · doi:10.1080/10253890600678004 · Cited by 255 · see citing works
Regulation of Intracellular Chloride by Cotransporters in Developing Lateral Superior Olive Neurons
Kakazu, Y., Akaike, N., Komiyama, S., & Nabekura, J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-08-02843.1999 · Cited by 253 · see citing works
Glucocorticoid and mineralocorticoid receptor mRNA expression in squirrel monkey brain
Patel, P. D., Lopez, J. F., Lyons, D. M., Burke, S., Wallace, M., & Schatzberg, A. F. (2000) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(00)00035-2 · Cited by 252 · see citing works
Physiological Role of Calcium-Activated Potassium Currents in the Rat Lateral Amygdala
Faber, E. S. L., & Sah, P. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01618.2002 · Cited by 234 · see citing works
Rohrbough, J. C., & Spitzer, N. C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00082.1996 · Cited by 229 · see citing works
Intracellular recordings from morphologically identified neurons of the basolateral amygdala
Rainnie, D. G., Asprodini, E., & Shinnick‐Gallagher, P. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.4.1350 · Cited by 185 · see citing works
de Kloet, E. R., Reul, J. M. H. M., & Sutanto, W. (1990) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(90)90489-8 · Cited by 175 · see citing works
Corticosteroid actions in hippocampus require DNA binding of glucocorticoid receptor homodimers
Karst, H., Karten, Y. J. G., Reichardt, H. M., de Kloet, E. R., Schütz, G., & Joëls, M. (2000) · Nature Neuroscience · doi:10.1038/79910 · Cited by 171 · see citing works
Faber, E., Callister, R., & Sah, P. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.2.714 · Cited by 170 · see citing works
McDonald, A. J. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90186-7 · Cited by 170 · see citing works
A Facilitative Role for Corticosterone in the Acquisition of a Spatial Task Under Moderate StressPreprint
Akirav, I., Kozenicky, M., Tal, D., Sandi, C., Venero, C., & Richter‐Levin, G. (2004) · Learning & Memory · doi:10.1101/lm.61704 · Cited by 170 · see citing works
Hui, G. K. (2003) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2003.09.002 · Cited by 168 · see citing works
Cell-Type-Specific GABA Responses and Chloride Homeostasis in the Cortex and Amygdala
Martina, M., Royer, S., & Paré, D. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.6.2887 · Cited by 151 · see citing works
Self-citationFerry, B., & McGaugh, J. L. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3904 · Cited by 149 · see citing works
Paré, D., Pape, H., & Dong, J. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.3.1179 · Cited by 147 · see citing works
Self-citationPelletier, J., Likhtik, E., Filali, M., & Paré, D. (2005) · Learning & memory (Cold Spring Harbor, N.Y.) · doi:10.1101/lm.88605 · Cited by 145 · see citing works
Self-citationKaila, K., Pasternack, M., Saarikoski, J., et al. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017755 · Cited by 144 · see citing works
Alfarez, D. N., Wiegert, O., Joëls, M., & Krugers, H. J. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00483-9 · Cited by 142 · see citing works
Glucocorticoid signalling—multiple variations of a common theme
Reichardt, H. M., & Schütz, G. (1998) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(98)00208-1 · Cited by 140 · see citing works
Karst, H., Nair, S., Velzing, E. H., Essen, L. R., Slagter, E., Shinnick‐Gallagher, P., & Joëls, M. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02172.x · Cited by 121 · see citing works
Vouimba, R., Yaniv, D., Diamond, D., & Richter‐Levin, G. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03294.x · Cited by 114 · see citing works
Effects of stress and corticosterone on activity and plasticity in the amygdala
Kavushansky, A., & Richter‐Levin, G. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.21058 · Cited by 106 · see citing works
Ionic Mechanisms of Intrinsic Oscillations in Neurons of the Basolateral Amygdaloid Complex
Pape, H., & Driesang, R. B. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.217 · Cited by 105 · see citing works
Verkuyl, J. M., Karst, H., & Joëls, M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03846.x · Cited by 97 · see citing works
Outward chloride/cation co-transport in mammalian cortical neurons
Thompson, S. M., Deisz, R. A., & Prince, D. A. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90479-x · Cited by 89 · see citing works
Inhibitory responses of rat basolateral amygdaloid neurons recorded in vitro
Washburn, M. S., & Moises, H. C. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90206-h · Cited by 72 · see citing works
Effect of corticosteroid hormones on electrical activity in rat hippocampus
Joëls, M., & de Kloet, E. R. (1991) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(91)90170-a · Cited by 57 · see citing works
Yamada, K., McEwen, B. S., & Pavlides, C. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1519-0 · Cited by 57 · see citing works
Danober, L., & Pape, H. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00092.x · Cited by 40 · see citing works
Bicuculline administered into the amygdala blocks benzodiazepine-induced amnesia
Dickinson-Anson, H., Mesches, M. H., Coleman, K., & McGaugh, J. L. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)90638-x · Cited by 36 · see citing works
Islet transplantation: an update.
Juang, J. (2004) · PubMed · Cited by 32 · see citing works
Faber, E. S. L., & Sah, P. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04357.x · Cited by 30 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- McDonald AJ (1992) Cell types and intrinsic connections of the amygdala. In: The amydala: neurobiological aspects of emotion, memory, and men- tal dysfunction (Aggleton JP, ed), pp 69 -76. New York: Wiley-Liss.
Cited by
Sorted by citations
Stress, memory and the amygdala
Roozendaal, B., McEwen, B. S., & Chattarji, S. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2651 · Cited by 1,760 · see citing works
Joëls, M., & Baram, T. Z. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2632 · Cited by 1,521 · see citing works
The neurobiology of depression: An integrated view
Dean, J., & Keshavan, M. (2017) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2017.01.025 · Cited by 765 · see citing works
Amygdala Microcircuits Controlling Learned Fear
Duvarci, S., & Pare, D. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.042 · Cited by 751 · see citing works
Self-citationThe neurobiology of depression and antidepressant action
Willner, P., Scheel-Krüger, J., & Belzung, C. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.12.007 · Cited by 519 · see citing works
Roozendaal, B., & McGaugh, J. L. (2011) · Behavioral Neuroscience · doi:10.1037/a0026187 · Cited by 445 · see citing works
Rapid non-genomic effects of corticosteroids and their role in the central stress response
Groeneweg, F. L., Karst, H., de Kloet, E. R., & Joëls, M. (2011) · Journal of Endocrinology · doi:10.1530/joe-10-0472 · Cited by 414 · see citing works
Acute corticosterone treatment is sufficient to induce anxiety and amygdaloid dendritic hypertrophy
Mitra, R., & Sapolsky, R. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705615105 · Cited by 409 · see citing works
Chronic stress: Implications for neuronal morphology, function and neurogenesis
Joëls, M., Karst, H., Krugers, H. J., & Lucassen, P. J. (2007) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2007.04.001 · Cited by 381 · see citing works
Myers, B., McKlveen, J. M., & Herman, J. P. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2013.12.003 · Cited by 318 · see citing works
Campolongo, P., Roozendaal, B., Trezza, V., Hauer, D., Schelling, G., McGaugh, J. L., & Cuomo, V. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900835106 · Cited by 294 · see citing works
The molecular and cellular mechanisms of depression: a focus on reward circuitry
Fox, M. E., & Lobo, M. K. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0415-3 · Cited by 232 · see citing works
Impact of early adversity on glucocorticoid regulation and later mental disorders
Strüber, N., Strüber, D., & Roth, G. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.10.015 · Cited by 173 · see citing works
Childhood trauma history differentiates amygdala response to sad faces within MDD
Grant, M. M., Cannistraci, C., Hollon, S. D., Gore, J., & Shelton, R. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.12.004 · Cited by 166 · see citing works
“Rodent and non-human primate models suggest heightened amygdala response is closely linked to glucocorticoid-mediated transformations in brain morphology, neuronal hyperexcitability (Duvarci and Pare, 2007; Vyas et al., 2003) and disinhibition via medial prefrontal cortex (mPFC) atrophy (Quirk et al.”
BackgroundResultInfluentialRemodeling of axo-spinous synapses in the pathophysiology and treatment of depression
Licznerski, P., & Duman, R. S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.057 · Cited by 157 · see citing works
Rao, R. P., Anilkumar, S., McEwen, B. S., & Chattarji, S. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.04.008 · Cited by 131 · see citing works
Neuner, F., Catani, C., Ruf, M., Schauer, E., Schauer, M., & Elbert, T. (2008) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2008.03.001 · Cited by 130 · see citing works
Hypothalamic-pituitary – adrenal axis-feedback control
Keller‐Wood, M. (2015) · Comprehensive Physiology · doi:10.1002/cphy.c140065 · Cited by 131 · see citing works
Maras, P. M., Molet, J., Chen, Y., Rice, C., Ji, S. G., Solodkin, A., & Baram, T. Z. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.12 · Cited by 118 · see citing works
Developmental emergence of fear learning corresponds with changes in amygdala synaptic plasticity
Thompson, J. V., Sullivan, R. M., & Wilson, D. A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.01.057 · Cited by 109 · see citing works
Krugers (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00024 · Cited by 102 · see citing works
Liu, Z.-P., Song, C., Wang, M., He, Y., Xu, X.-B., Pan, H.-Q., Chen, W.-B., Peng, W.-J., & Pan, B.-X. (2014) · Molecular Brain · doi:10.1186/1756-6606-7-32 · Cited by 99 · see citing works
Atsak, P., Roozendaal, B., & Campolongo, P. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.047 · Cited by 98 · see citing works
Endocannabinoids: The silent partner of glucocorticoids in the synapse
Hill, M. N., & McEwen, B. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901519106 · Cited by 98 · see citing works
Emerging pathways of non-genomic glucocorticoid (GC) signalling in T cells
Boldizsar, F., Talaber, G., Szabo, M., Bartis, D., Palinkas, L., Nemeth, P., & Berki, T. (2010) · Immunobiology · doi:10.1016/j.imbio.2009.10.003 · Cited by 76 · see citing works
Masneuf, S., Lowery-Gionta, E., Colacicco, G., Pleil, K. E., Li, C., Crowley, N., Flynn, S., Holmes, A., & Kash, T. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.04.015 · Cited by 69 · see citing works
Hetzel, A., & Rosenkranz, J. A. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.60 · Cited by 62 · see citing works
Acute stress potentiates brain response to milkshake as a function of body weight and chronic stress
Rudenga, K. J., Sinha, R., & Small, D. M. (2013) · International Journal of Obesity · doi:10.1038/ijo.2012.39 · Cited by 56 · see citing works
Logrip, M. L., Oleata, C., & Roberto, M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.11.021 · Cited by 56 · see citing works
“Corticosterone elevated resting membrane potential and input resistance in BLA neurons from male mice, shifting the population towards slower post-tetanus spike adaptation (Duvarci and Pare, 2007) and increased mEPSC frequency (Karst et al., 2010).”
- Authors
- Duvarci, S., & Paré, D.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2007-04-18
- Volume
- 27
- Issue
- 16
- Pages
- 4482-4491
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6672328
- OpenAlex
- W2062746952
- Cited by
- 249
- References
- 54
- Citations by year
- 2026: 4 · 2025: 9 · 2024: 7 · 2023: 8 · 2022: 4 · 2021: 11 · 2020: 10 · 2019: 8 · 2018: 7 · 2017: 10 · 2016: 16 · 2015: 13 · 2014: 25 · 2013: 18 · 2012: 20
- FWCI
- 7.40
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation (0208712)
- National Institute of Mental Health (R01MH073610, MH073610)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- glucocorticoids, corticosterone, basolateral amygdala, principal neurons, neuronal excitability, intrinsic excitability, spike frequency adaptation, input resistance, resting membrane potential, stress hormones, emotional memory consolidation
- MeSH terms
- Amygdala, Animals, Cell Membrane, Emotions, Glucocorticoids, Membrane Potentials, Memory, Neurons, Receptors, Glucocorticoid, Stress, Physiological, Rats, Sprague-Dawley, Patch-Clamp Techniques, Excitatory Postsynaptic Potentials, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review