Development of Inhibitory Timescales in Auditory Cortex — TEI-tagged view

Oswald, Reyes · 2011 · neuroscience · doi:10.1093/cercor/bhq214 · full text at the source · TEI xml · tagged edition · index · concepts · authors
Where this record's text came from. faceted 2026-08 by reading the locally held text (html); every evidence string verified as an exact substring of that text before merging. Replication status is 'contested' because the paper's own IPSP-amplitude result is explicitly set against two lines of prior work (other cortical areas showing increases with age; in vivo AI studies showing stable inhibitory strength), and the paper itself notes the excitatory/inhibitory tuning-lag literature is disputed ('but also see Sun et al. 2010'). The central timing claim is not itself reported as replicated or refuted. Claim type is 'mechanism' because the paper attributes the change in inhibitory timescale to specified maturing intrinsic and synaptic properties. One evidence quote for the fourth limitation contains curly quotation marks around FS, copied as they appear in the source. 2026-08-13, 2026-08-15 and 2026-08-25 schema-0.3 passes: every quote verified as an exact substring of the staged text and anchored at merge time; concept terms verified present; every edge endpoint an existing node.
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standard deviation 3 fields
Tags on this paper every tag the record carries, whether or not the words occur in the text below — a number is how many papers in the corpus carry that tag; a tag with no number is unique to this paper
FS3 PCs2 EPSP3 IPSP IPSC3 membrane time constant3 input resistance6 integration window2 short-term depression paired pulse ratio afterhyperpolarizations rheobase G42 biocytin L2/32 tonotopic map3 GABA A2 sag electrophysiology110

Our tag layer for this paper

Cross-disciplinary analysis
content-tags & facets: phenomenon · claim-type · cross-domain-transfer · mechanism · claim-relation · replication-status · limitation — grounded in the full text
phenomenonpostnatal development of inhibitory timing in auditory cortex layer 2/3— “We investigated the development of L2/3 inhibitory circuitry between fast-spiking (FS) interneurons and pyramidal cells (PCs) in auditory thalamocortical slices from mice between postnatal day 10 (P10) and P29.”
claim-typemechanism— “We found that the maturation of the intrinsic and synaptic properties of both FS cells and their connected PCs influence the timescales of inhibition.”
method — evidence— “Whole-cell current-clamp recordings were made from 116 FS cells that were synaptically connected to 134 PCs in L2/3 of AI.”
object of study — evidence— “The time course of inhibition plays an important role in cortical sensitivity, tuning, and temporal response properties. We investigated the development of L2/3 inhibitory circuitry between fast-spiking (FS) interneurons and pyramidal cells (PCs) in auditory thalamocortical slices from mice between postnatal day 10 (P10) and P29.”
research question — evidence— “In this study, we examine the development of L2/3 circuitry, which complements previous in vivo studies that focused on the thalamorecipient layers (L3–L5).”
contribution — evidence— “Finally, we show that during early development, the temporal properties that influence the recruitment of inhibition lag those of excitation.”
transferfrom transgenic mouse genetics: a GFP line used not as the object of study but as a check on an electrophysiological classification— “Since the majority of FS interneurons are PV+ ( Kawaguchi and Kondo 2002 ) and G42 mice express the EGFP transgene in (PV+) cells, we compared the properties of GFP+ interneurons recorded from G42 mice with FS cells recorded in SW mice of the same age. We found that the intrinsic membrane properties and AP properties ( Fig. 2 and…transfers[0]
transferfrom cable theory: the expectation that a synaptic potential's time course follows the membrane time constant of the cell receiving it— “At rest, the short duration EPSPs are consistent with predominantly AMPA receptor–mediated current and correlated with FS cell membrane time constants throughout development.”transfers[1]
mechanismShortening of the postsynaptic membrane time constant during development speeds the decay of synaptic potentials— “These age-dependent decreases in τ d may, in part, be attributed to changes in the membrane time constant of the FS cells since the mean τ d and τ m at each age were linearly correlated ( R : 0.88, P < 0.01, Fig. 3 H ).”mechanisms[0]
mechanismFalling input resistance of the postsynaptic pyramidal cell offsets a rising inhibitory current, so the measured IPSP amplitude declines with age— “One likely explanation for our results is that correlated decreases in PC input resistance during development counter increases in IPSC amplitude.”mechanisms[1]
mechanismLater IPSP peak times in young animals reduce excitation-inhibition overlap and thereby widen the synaptic integration window— “This would likely decrease overlap between EPSPs and IPSPs, broaden the integration window in young animals, and allow spike responses to nonoptimal or less precisely timed inputs.”mechanisms[2]
mechanismInhibitory decay constants longer than excitatory ones impose an upper frequency limit on responses to closely spaced inputs— “This suggests that inhibition sets an upper frequency bound for responses to inputs arriving at short intervals.”mechanisms[3]
mechanismDevelopmental expression of leak and repolarizing potassium channels in PV+ FS cells drives the change in intrinsic excitability— “These changes coincide with the early development (P7–P25) of potassium channels in PV+ FS cells that contribute to leak (Kcnk3 and Kcnk1) and spike repolarization (Kv3 and Kcnn2) ( Du et al. 1996 ; Rudy and McBain 2001 ; Tansey et al. 2002 ; Okaty et al. 2009 ).”mechanisms[4]
mechanismA switch from slow alpha-3 to faster alpha-1 GABA_A receptor subunits accelerates IPSP rise and decay— “However, the developmental transition from slow α 3 subunits in GABA A receptors to faster α 1 subunits may also contribute to changes in IPSP rise and decay times ( Gingrich et al. 1995 ; Xu et al. 2010 ).”mechanisms[5]
mechanismfaster firing in older cells follows from shorter membrane time constants, briefer afterhyperpolarisations and narrower spikes— “We found that the maturation of the intrinsic and synaptic properties of both FS cells and their connected PCs influence the timescales of inhibition. FS cell firing rates increased with age owing to decreased membrane time constants, shorter afterhyperpolarizations, and narrower action potentials.”mechanisms[6]
mechanismthe speed-up coincides with development of potassium channels handling leak and spike repolarisation— “These changes coincide with the early development (P7–P25) of potassium channels in PV+ FS cells that contribute to leak (Kcnk3 and Kcnk1) and spike repolarization (Kv3 and Kcnn2)”mechanisms[7]
mechanismexcitatory decay tracks the membrane time constant of the receiving cell, so a synaptic timescale is partly a membrane timescale— “At rest, the short duration EPSPs are consistent with predominantly AMPA receptor–mediated current and correlated with FS cell membrane time constants throughout development.”mechanisms[8]
mechanisminhibitory rise, peak and decay times shorten with age, attributed in part to the falling membrane time constant of the receiving pyramidal cell— “The rise, peak, and decay times of the IPSPs decreased with age, which may, in part, be attributed to correlated decreases in membrane time constant of the postsynaptic PCs.”mechanisms[9]
mechanismshorter inhibitory decays let older cells follow inputs at 20-40 Hz where younger ones summate and stop responding above 10 Hz— “We have shown that the decay constants of inhibitory synapses were significantly longer than excitation at all ages. This suggests that inhibition sets an upper frequency bound for responses to inputs arriving at short intervals. In young animals, IPSPs are approximately 60–200 ms long and can summate during repetitive ( Fig. 5 ) or…mechanisms[10]
extends Oswald and Reyes 2008 (development of L2/3 pyramidal cells in AI)— “As previously shown for PCs ( Oswald and Reyes 2008 ), both the intrinsic and the synaptic properties of FS cells undergo a transition between P10 and P18 and plateau between P19 and P29.”claim_relations[0]
builds-on Oswald and Reyes 2008 (companion study on PC–PC circuitry)— “In closing, the results of this and our companion study ( Oswald and Reyes 2008 ) suggest that the developmental changes in the intrinsic and synaptic properties of PC–FS circuitry lead to…claim_relations[1]
contradicts Doischer et al. 2008; Kobayashi et al. 2008 (age-related increase in IPSC amplitude in other cortical areas)claim_relations[2]
contradicts Dorrn et al. 2010; Sun et al. 2010 (in vivo reports that inhibitory strength is stable in early development)claim_relations[3]
contradicts reports from other cortical areas that inhibitory postsynaptic amplitudes increase with age
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claim_relations[4]
reconciles that disagreement, by proposing that falling input resistance converts a rising current into a falling voltage
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claim_relations[5]
extends their own companion study on pyramidal cell development in the same layer
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claim_relations[6]
supports the proposal that inhibitory tuning lags excitatory tuning, which the paper notes is itself disputed
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claim_relations[7]
builds-on in vivo work on thalamorecipient layers, by adding the supragranular circuit
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claim_relations[8]
senseFS is an ELECTROPHYSIOLOGICAL category whose defining features are absent in the youngest animals, which is exactly the age this paper is about
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senses[0]
sensethe transgenic label covers only a SUBSET - the PV cells that are also fast-spiking express EGFP - so GFP-positive is narrower than PV-positive
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senses[1]
senseIPSP and IPSC are not interchangeable measures of inhibitory strength: they differ by the postsynaptic input resistance, which itself falls with age
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senses[2]
sensereported PSP amplitudes are averaged over all trials INCLUDING failures, so they are a product of size and reliability rather than a size alone
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senses[3]
sensea successful PSP is defined by a three-part criterion on onset, amplitude and peak time, with anything else counted as a failure of amplitude zero
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senses[4]
controlthe location of AI verified in a subset of slices by stimulating the MG and recording field potential responses in layers 3 and 4 — held — rules out recording from the wrong cortical field - the functional check is independent of the stereotaxic estimate it verifies
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controls[0]
auditinput resistance —causes→ IPSP — Audit 2026-09-28: DOUBTFUL - read against its full span and kept, but 'one LIKELY explanation' is that decreasing input resistance counters rising IPSC amplitude; causes is hedged.
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concept_edges[1]
noteinput resistance —causes→ IPSP — the conversion factor between the measures is itself a developing variable, which is why a cross-paper comparison of inhibitory strength needs to know which was measured
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concept_edges[1]
auditmembrane time constant —causes→ IPSP — Audit 2026-09-28: DOUBTFUL - read against its full span and kept, but the IPSP time changes 'MAY, in part, be attributed to' the membrane time constant; causes is hedged.
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concept_edges[3]
notemembrane time constant —causes→ IPSP — same route on the inhibitory side, with a receptor subunit switch offered as an additional cause
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concept_edges[3]
weightmembrane time constant —causes→ IPSP — 0.8
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concept_edges[3]
auditGABA A —causes→ IPSP — Audit 2026-09-28: DOUBTFUL - read against its full span and kept, but the GABA A subunit transition 'MAY ALSO contribute' to IPSP kinetics; causes is hedged.
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concept_edges[4]
noteGABA A —causes→ IPSP — the alpha-3 to alpha-1 switch; an alternative not separated from the membrane route here
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concept_edges[4]
weightGABA A —causes→ IPSP — 0.7
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concept_edges[4]
noteFS —contrasted-with→ PCs — the mature separation rests on firing rate, spike width and afterhyperpolarisation - all of which are absent before P15
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concept_edges[6]
auditIPSP —causes→ integration window — Audit 2026-09-28: DOUBTFUL - read against its full span and kept, but later-peaking IPSPs 'WOULD LIKELY' broaden the integration window; causes is hedged.
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concept_edges[7]
noteIPSP —causes→ integration window — SIGN: later inhibitory peaks widen the window, so young cells accept less precisely timed inputs
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concept_edges[7]
edgeshort-term depression —operationalised-as→ paired pulse ratio
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concept_edges[8]
outcome (stated by the tagger, no quotation)control — heldcontrols[0]
for which uselimitation — every synaptic measurement in the paper: VOLTAGE CLAMP RECORDINGS WERE NOT PERFORMED BECAUSE THE STANDARD INTERNAL SOLUTIONS ... WOULD PROHIBIT THE CHARACTERIZATION OF INTRINSIC NEURAL P[roperties] - one measurement excludes the other
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limitations[0]
for which uselimitation — the extrapolation from paired recordings to the intact animal: IT REMAINS TO BE DETERMINED HOW CHANGES IN INHIBITORY STRENGTH BETWEEN PAIRS OF NEURONS ARE REFLECTED AT THE POPULATION LEVEL IN VIVO
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limitations[1]
for which uselimitation — any functional claim about auditory processing: FURTHER IN VIVO STUDIES ARE NECESSARY TO ELUCIDATE FUNCTIONAL IMPLICATIONS
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limitations[2]
for which uselimitation — the fast-spiking classification in the youngest animals: THE IDENTIFICATION OF FS CELLS BASED ON ELECTROPHYSIOLOGICAL PROPERTIES CAN BE DIFFICULT PARTICULARLY IN YOUNG ANIMALS (P10-P14) SINCE FS RESPONSES ARE LESS APPARENT
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limitations[3]
duplicate oflimitation — limitations[0]
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limitations[4]
for which uselimitation — the same scope as limitations[0] - the trade-off between clamp quality and intrinsic properties
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limitations[4]
for which uselimitation — every developmental comparison in the paper: THE TRANSITIONAL PERIOD WAS DIVIDED ARBITRARILY INTO AN EARLY PHASE (P10-P14) - the independent variable's boundaries are declared arbitrary
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limitations[5]
for which uselimitation — the fitted decay parameters: ONLY PSPS THAT WERE WELL FIT BY EQUATION 1 (CHI2 < 1.75) WERE CHOSEN - a goodness-of-fit threshold decides which data enter
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limitations[6]
for which uselimitation — the mechanistic attribution of the decay changes: OUR RESULTS DO NOT PRECLUDE THE POSSIBILITY THAT DEVELOPMENTAL CHANGES IN AMPA AND/OR NMDA RECEPTOR COMPOSITION also contribute
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limitations[7]
duplicate oflimitation — limitations[1]
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limitations[8]
for which uselimitation — the same scope as limitations[1] - paired cells versus population in vivo
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limitations[8]
replicationcontested
no type for thisEPSPs → FS cell membrane time constants — CORRELATED THROUGHOUT DEVELOPMENT, with no manipulation of either quantity. Recording it as 'causes' in either direction asserts more than the sentence does.
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unhoused_relations[0]
limitationVoltage clamp was deliberately not used, limiting the measurements to current-clamp postsynaptic potentials.
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limitations[0]
limitationWhether the paired-cell changes in inhibitory strength hold at the population level in vivo is unknown.
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limitations[1]
limitationThe functional consequences for auditory processing were not tested and require in vivo work.
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limitations[2]
limitationIdentifying fast-spiking cells electrophysiologically is unreliable in the youngest animals.
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limitations[3]
limitationvoltage clamp was deliberately not used, because the solutions needed for it would have prevented measuring intrinsic properties and bidirectional connections
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limitations[4]
limitationthe age bins were divided arbitrarily
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limitations[5]
limitationonly postsynaptic potentials that fitted the double-exponential model well were analysed
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limitations[6]
limitationreceptor composition changes are not excluded as an additional cause of the synaptic decay changes
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limitations[7]
limitationhow paired-cell inhibitory strength maps onto the population level in the intact animal is left open
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limitations[8]
Content tags
content-observations: finding · quantity · variable · definition · key-term — grounded in the full text
findingBetween P10 and P29 the firing rates of fast-spiking interneurons rose, driven by shorter membrane time constants, briefer afterhyperpolarizations and narrower action potentials.
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content_tags.findings[0]
findingIPSP latency, rise time and peak time, together with the decay constants of both EPSPs and IPSPs, all shortened between P10 and P29.
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content_tags.findings[1]
findingExcitatory PC-to-FS synapses in the youngest animals depressed most strongly (paired-pulse ratio 0.4) and this depression weakened with age (0.7 at P15-P18 and 0.8 at P19-P29).
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content_tags.findings[2]
findingBecause short-term depression at PC-to-FS synapses weakened with age, older synapses sustained their responses better during repetitive stimulation.
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content_tags.findings[3]
findingThe temporal properties that determine when inhibition is recruited mature later than the corresponding properties of excitation.
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content_tags.findings[4]
findingIPSP amplitude fell from 0.8 mV at P10-P14 to 0.5 mV at P19-P29.
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content_tags.findings[5]
findingThe EPSP decay time constant shortened from 37 ms at P10-P14 to 16 ms at P19-P29 while the rise time constant did not change with age.
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content_tags.findings[6]
findingFS-to-PC inhibitory responses to single pulses were entirely GABA_A-receptor mediated, being abolished by bicuculline.
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content_tags.findings[7]
findingAt resting potential, PC-to-FS excitatory responses were entirely AMPA-receptor mediated, being abolished by DNQX.
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content_tags.findings[8]
findingFS-cell intrinsic membrane and action-potential properties were indistinguishable between the GFP-expressing G42 line and Swiss Webster mice at every age tested.
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content_tags.findings[9]
findingExcept for latency, the rise, peak and decay of the IPSP were significantly longer than the corresponding excitatory timescales.
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content_tags.findings[10]
findingFast-spiking cells at P10-P14 were the least mature electrically, with the longest membrane time constants, highest input resistance and most depolarized resting potential.
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content_tags.findings[11]
findingspikes narrowed and afterhyperpolarisations shortened with age, raising firing rates
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content_tags.findings[13]
findingthe hyperpolarisation-activated sag was prominent at P10-P14
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content_tags.findings[14]
findingexcitatory amplitudes fell with age and correlated with input resistance across all ages
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content_tags.findings[15]
findingshort-term depression at excitatory synapses weakened with age, making repetitive responses more sustained
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content_tags.findings[16]
findinginhibitory rise, peak and decay times all shortened with age
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content_tags.findings[17]
findinginhibitory decays stayed longer than excitatory ones at every age, setting an upper frequency bound
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content_tags.findings[18]
findingproperties transitioned between P10 and P18 and plateaued from P19 to P29
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content_tags.findings[19]
findingexcitatory potentials were fully blocked by an AMPA receptor antagonist
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content_tags.findings[20]
findingCONTROL: GFP-labelled cells in the transgenic line and electrophysiologically identified cells did not differ at any age
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content_tags.findings[21]
findingUNEXPECTED RESULT: inhibitory potential amplitudes fell with age, where other cortical areas report the current rising
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content_tags.findings[22]
findingRESOLUTION OFFERED: falling input resistance would convert a rising inhibitory current into a falling inhibitory voltage
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content_tags.findings[23]
findingthe classification of fast-spiking cells is hardest exactly in the youngest animals, where the defining responses are less apparent
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content_tags.findings[24]
quantity116 FS cells / 134 PCs — number of fast-spiking interneurons recorded and pyramidal cells they were synaptically connected to
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[0]
quantity0.4 ± 0.1 vs 0.8 ± 0.2 — paired-pulse ratio at PC-to-FS synapses in the youngest versus oldest age group
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[1]
quantity1.4 ± 0.3 — spike-frequency adaptation ratio (last/first interspike interval) in P10-P14 FS cells, higher than in older animals
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[2]
quantity23 ± 11 ms; 294 ± 183 MΩ — membrane time constant and input resistance of FS cells at P10-P14, the highest values recorded
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[3]
quantityR : 0.88 — correlation between mean EPSP decay constant and mean FS-cell membrane time constant across ages
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[4]
quantityR : 0.77 — correlation between postsynaptic pyramidal-cell input resistance and mean IPSP amplitude
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[5]
quantityχ 2 < 1.75, n = 155 EPSPs, n = 167 IPSPs — goodness-of-fit cutoff and the number of postsynaptic potentials that passed it for kinetic analysis
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[6]
quantity60–200 ms — IPSP duration in young animals, long enough to summate and suppress responsiveness above 10 Hz
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[7]
quantity25–50 ms — IPSP duration in older animals, permitting responses to 20-40 Hz inputs
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[8]
quantity116 and 134 — fast-spiking cells and connected pyramidal cells recorded
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[9]
quantityP10 to P29 — age range, spanning hearing onset to the plateau
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[10]
quantity60-200 ms against 25-50 ms — inhibitory potential durations in young against older animals
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[11]
quantityabove 10 Hz against 20-40 Hz — input frequencies the young and older circuits can follow
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[12]
quantity0.4 against 0.8 — paired pulse ratio at 10 Hz in the youngest against the oldest group
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.quantities[13]
quantity72 — neurons filled with biocytin to confirm identity morphologically
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content_tags.quantities[14]
variablestep current (independent)
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content_tags.variables[1]
variableIPSP amplitude (dependent)
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.variables[3]
variabledecay of the EPSP (dependent)
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content_tags.variables[4]
variablereversal potential (control)
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content_tags.variables[5]
variablemembrane time constant
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content_tags.variables[6]
variablepaired pulse ratio
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.variables[7]
variableinput resistance
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content_tags.variables[8]
definitionspike frequency adaptation
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content_tags.definitions[0]
definitionfailure rate
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content_tags.definitions[1]
definitionpaired pulse ratio
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.definitions[2]
definitionEPSP latency
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content_tags.definitions[3]
definitionPSP latency
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content_tags.definitions[4]
definitionspike threshold
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content_tags.definitions[5]
definitionamplitude of the sag
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content_tags.definitions[6]
definitionpaired pulse ratio
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content_tags.definitions[7]
definitionintegration window
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content_tags.definitions[8]
definitionsag
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content_tags.definitions[9]
key-termsFS, PCs, EPSP, IPSP, IPSC, membrane time constant, input resistance, integration window, short-term depression, paired pulse ratio, G42, L2/3
Statistics — cross-field join keys
field-invariant statistical terms, used in their statistical sense (gated on a number / symbol / test). A p-value or a standard deviation means the SAME thing in physics, biology, psychology and sociology — so these are the strongest cross-field join keys. Grounded verbatim.
ANOVA F as written: univariate analysis of variance (ANOVA)
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content_tags.statistics[0]
Tukey's HSD post hoc test as written: Tukey's honestly significant difference post hoc test
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content_tags.statistics[1]
Levene's test for homogeneity of variance as written: Levene's test for homogeneity
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content_tags.statistics[2]
Mann-Whitney U test as written: nonparametric Mann–Whitney U test
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content_tags.statistics[3]
standard deviation SD as written: mean ± standard deviation (SD)
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content_tags.statistics[4]
least-squares curve fitting (chi-squared minimisation) χ 2 as written: Levenberg-Marquardt nonlinear, least-squares fitting algorithm
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content_tags.statistics[5]
correlation R as written: linearly correlated ( R : 0.88, P < 0.01
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content_tags.statistics[6]
F statistic F as written: F values and P values are for ANOVA comparisons
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content_tags.statistics[7]
evidence status noteF statistic — This quote ends with the stray word 'The', the first word of the next sentence. It is not trimmed, because the quote without it occurs more than once in the paper's text and could not be tied to one place. The claim is carried by the sentence before 'The'.content_tags.statistics[7]
Mann–Whitney U test
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.statistics[8]
ANOVA
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
content_tags.statistics[9]
Second readings
a facet read a second time, independently, from its own sentence — and whether the two readings agree
claim typemechanism — a second reading reaching the same value; recorded: mechanism
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
alternatives.claim_type
methodpaired whole-cell current-clamp recording from connected fast-spiking and pyramidal cells in auditory thalamocortical slices across three age bins — a second reading DIFFERING from the recorded value; recorded: electrophysiology
Quotation withheld — this paper is not ours to reproduce, and the page has already quoted as much of it as the rights layer allows. The tag, its field and its confidence stand; the sentence is at the publisher.
alternatives.method
phenomenonthe developmental narrowing of the synaptic integration window in auditory cortex — a second reading DIFFERING from the recorded value; recorded: postnatal development of inhibitory timing in auditory cortex layer 2/3
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alternatives.phenomenon

When we have changed our mind. Some entries in the table begin with a word in capitals and the reason for it. EVIDENCE CORRECTED — the finding still stands, but we had quoted the wrong sentence from the paper, and the quotation has been replaced with the right one. RETRACTED — the entry itself was wrong; it stays on the page, marked, with the reason, rather than being deleted. WITHDRAWN AND REPLACED — the entry was wrong, and a corrected version of it appears in the entries below. Each mark carries its own reason, in brackets, because the reasons differ from one entry to the next. An entry we have WITHDRAWN is removed from this page and kept in the record, with its reason. A line reading Audit and a date is a later re-reading of the entry against its whole sentence: DOUBTFUL means it was kept, and the reason says what is loose about it. Quotation marks inside the tagger's sentence. Where a tag is the tagger's own sentence, a phrase in quotation marks inside it is borrowed from the paper — the tagger's wording around it is not. The paper's own sentence is the evidence quote for that row; on this page it is withheld with the article, and the article is at its publisher. Nothing inside quotation marks anywhere on this page is ours: if it is quoted, it is the paper's. Whose words a concept carries. A concept entry records a term the paper itself uses, so the term, the sense given for it, and its evidence are the paper's own words, quoted where the paper fixes them. This is the opposite of a sense entry in the tag table, which is the tagger's sentence about how the paper uses a term. Where a concept entry could not be grounded in the paper's words, the entry says so on its own row.

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