The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index; none of the 25 sources its claims cite is checked for support yet.
Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo
Open accessAbstract
Elevation of intracellular Ca2+ in astrocytes can influence cerebral microcirculation and modulate synaptic transmission. Recently, in vivo imaging studies identified delayed, sensory-driven Ca2+ oscillations in cortical astrocytes; however, the long latencies of these Ca2+ signals raises questions in regards to their suitability for a role in short-latency modulation of cerebral microcirculation or rapid astrocyte-to-neuron communication. Here, using in vivo two-photon Ca2+ imaging, we demonstrate that approximately 5% of sulforhodamine 101-labeled astrocytes in the hindlimb area of the mouse primary somatosensory cortex exhibit short-latency (peak amplitude approximately 0.5 s after stimulus onset), contralateral hindlimb-selective sensory-evoked Ca2+ signals that operate on a time scale similar to neuronal activity and correlate with the onset of the hemodynamic response as measured by intrinsic signal imaging. The kinetics of astrocyte Ca2+ transients were similar in rise and decay times to postsynaptic neuronal transients, but decayed more slowly than neuropil Ca2+ transients that presumably reflect presynaptic transients. These in vivo findings suggest that astrocytes can respond to sensory activity in a selective manner and process information on a subsecond time scale, enabling them to potentially form an active partnership with neurons for rapid regulation of microvascular tone and neuron-astrocyte network properties.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
In urethane-anesthetized mice, a small subset (~5%) of SR101-labeled astrocytes in hindlimb somatosensory cortex showed contralateral hindlimb-selective sensory-evoked Ca²⁺ signals peaking ~0.5 s after stimulus onset. These rapid astrocyte signals matched neuronal timescales and correlated with the onset of the hemodynamic response, suggesting astrocytes can respond on subsecond timescales relevant to neurovascular coupling.
Key findings
- Of 355 astrocytes (7 mice), 18 (5.07%; 5.08 ± 1.28% per mouse) showed above-threshold Ca²⁺ elevation after contralateral hindlimb stimulation; no other limbs induced significant responses. Astrocyte peak amplitude was 19.1 ± 1.7% ΔF/F₀.
- Time-to-peak did not differ significantly among astrocytes (0.41 ± 0.11 s), neurons (0.56 ± 0.09 s), and neuropil (0.43 ± 0.09 s; F(2,18) = 0.67; p = 0.52). Decay tau was shorter in neuropil (0.55 ± 0.04 s) than astrocytes (1.07 ± 0.17 s; p = 0.011) and neurons (1.21 ± 0.18 s; p = 0.005).
- The IOS hemodynamic response began ~600–800 ms after stimulus onset, while astrocyte Ca²⁺ peaked ~0.5 s after onset. Endfoot transients occurred in 12.7% of endfeet (n = 102; 4 mice), with peak 18.8 ± 5.4%, time-to-peak 0.73 ± 0.19 s, and decay tau 0.93 ± 0.10 s.
- Astrocyte responses were unlikely to be neuropil contamination: mean absolute OGB-1 fluorescence increase was 44.4 ± 5.1 gray levels in astrocytes vs 13.3 ± 1.4 in neuropil ROIs (t test, p << 0.001).
Methods
- Urethane-anesthetized C57B6 mice (male and female, 2–4 months). Intrinsic optical signal imaging mapped hindlimb/forelimb cortex during mechanical limb stimulation; two-photon Ca²⁺ imaging used OGB-1 and SR101 in layers I–III of hindlimb somatosensory cortex.
- 355 astrocytes across 7 mice; stimuli were 0.5–1.0 s at 3, 10, or 100 Hz. Responses were thresholded as ΔF/F₀ >1 SD over baseline for ≥0.5 s; ANOVA with post hoc t tests and Bonferroni correction was used, and G/R ratio controlled for movement artifact in high-resolution endfoot imaging.
Limitations
- The paper does not present a formal limitations section; it notes significant intertrial variability in endfoot Ca²⁺ responses.
- Evident from the text: only a small subset of astrocytes responded (~5%; 18 responsive astrocytes), imaging was limited to anesthetized mice and layers I–III of hindlimb cortex, and the study reports correlations with hemodynamic onset rather than causal manipulation of astrocyte Ca²⁺ or blood flow.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
0 of 25 cited sources checked · 0 supported · 0 flagged
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Post hoc t tests using the Bonferroni correction revealed significantly shorter decay taus in neuropil ROIs (0.55 Ϯ 0.04 s) compared with astrocytes (1.07 Ϯ 0.17 s; p ϭ 0.011) and neurons (1.21 Ϯ 0.18 s; p ϭ 0.005).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIn the paper
“After the initial dip, increased blood flow (functional hyperemia) is associated with increased oxyhemoglobin concentration and blood volume, manifested in the IOS by increased light reflectance/decreased absorbance starting ϳ600 -800 ms after stimulus onset (Fig. 1 B) (Devor et al., 2003).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
What the sources say
- Not checked yetcites Devor et al., 2003
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“peak amplitude ϳ0.5 s after stimulus onset”
- Also stated in: § Results · plain
“Whereas time-to-peak (from stimulus onset) means did not differ significantly between astrocytes (0.41 Ϯ 0.11 s), neurons (0.56 Ϯ 0.09 s), and neuropil (0.43 Ϯ 0.09 s; F (2,18) ϭ 0.67; p ϭ 0.52)”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Abstract
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Also stated in: § Results · plain
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Eighteen astrocytes (5.07% of total astrocytes; an average of 5.08 Ϯ 1.28% per mouse) showed an above-threshold stimulus-driven Ca 2ϩ elevation after cHL stimulation.”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The mean increases in absolute OGB-1 fluorescence (peak Ϫ F o ) in astrocytes (44.4 Ϯ 5.1 gray levels) during the 1.5 s after stimulation was significantly greater than the mean increase in fluorescence in neuropil ROIs (13.3 Ϯ 1.4 gray levels) in the same images (t test, p Ͻ Ͻ 0.001).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesA result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“No other limbs induced a significant Ca 2ϩ response.”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Strength:plain· not yet calibratedn = 7Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesWhat the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Thresholds were set to identify cells where the change in Ca 2ϩ -induced fluorescence relative to baseline fluorescence was greater than one SD over baseline and remained above this criterion for at least 0.5 s (or three times the frame rate for frame rates Ͼ170 ms/frame).These criteria were found effective for separating responsive cells from noise.”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Two-photon image processing.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“Furthermore, different subpopulations of protoplasmic astrocytes possess varying glutamate-receptor complements, and the shortand long-latency responses may reflect the activation of different glutamate receptors (Matthias et al., 2003;Wallraff et al., 2004;Jabs et al., 2005)”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Discussion
What the sources say
- Not checked yetcites Matthias et al., 2003
- Not checked yetcites Wallraff et al., 2004
- Not checked yetcites Jabs et al., 2005
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“Astrocytes also form a close physical and functional partnership with brain arterioles, because elevation of intracellular Ca 2ϩ in astrocyte endfeet is sufficient to trigger rapid changes in vascular tone (Zonta et al., 2003;Mulligan and MacVicar, 2004;Takano et al., 2006).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Introduction
What the sources say
- Not checked yetcites Zonta et al., 2003
- Not checked yetcites Mulligan and MacVicar, 2004
- Not checked yetcites Takano et al., 2006
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesWhat the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“G/R ratios confirm that this transient is selective to the Ca 2ϩ indicator and cannot be explained by movement artifact, which would affect both OGB-1 and SR101 channels.”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes
- The quote only partly states this claim. 1
- It may state two separate claims as one. 4
- Probably not a substantial claim. 4
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The mean decay taus of astrocytes and neurons were not significantly different ( p ϭ 0.59).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe quote only partly states this claim.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Approximately 20 -30% of neurons and most neuropil ROIs in the same image planes showed Ca 2ϩ responses above threshold criteria.”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Results
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“and metabotropic glutamate receptors and glutamate uptake transporters on astrocytes have been implicated in the hemodynamic response to neuronal activity (Gurden et al., 2006;Takano et al., 2006).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Introduction
What the sources say
- Not checked yetcites Gurden et al., 2006
- Not checked yetcites Takano et al., 2006
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These in vivo findings suggest that astrocytes can respond to sensory activity in a selective manner and process information on a subsecond time scale”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“It has been suggested that neuron-to-astrocyte communication may be a key mediator of this functional hyperemia (Zonta et al., 2003;Takano et al., 2006)”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Introduction
What the sources say
- Not checked yetcites Zonta et al., 2003
- Not checked yetcites Takano et al., 2006
Tests✗ Asserted: fails✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. The authors may not put it forward as true.
None of the sources cited for this claim have been checked yet.
In the paper
“Previous evidence indicates that hyperemia begins ϳ600 ms after sensory stimulus onset and, thus, would require a rapid response from astrocytes (Kleinfeld et al., 1998;Devor et al., 2003).”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Discussion
What the sources say
- Not checked yetcites Kleinfeld et al., 1998
- Not checked yetcites Devor et al., 2003
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The presence of ionotropic glutamate receptors and rapid transporter-mediated currents suggest that astrocytes can communicate with neurons on a rapid subsecond time scale, and in vitro and in situ studies have shown that astrocyte Ca 2ϩ transients and synaptic-like currents can be triggered by neuronal activity (Dani et al., 1992;Murphy et al., 1993;Porter andMcCarthy, 1995a,b, 1996;Bergles and”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Introduction
What the sources say
- Not checked yetcites Dani et al., 1992
- Not checked yetcites Murphy et al., 1993
- Not checked yetcites Porter andMcCarthy, 1995a,b
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
In the paper
“although the authors note the large amplitude, long-lasting Ca 2ϩ oscillations that propagate throughout the glial network, careful examination of the data presented suggests that smaller, short-latency Ca 2ϩ transients were also triggered by electrical stimulation in some astrocytes.”
§ Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo > Discussion
What the sources say
- Not checked yetcites Gobel et al., 2007
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
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?
In the citing paper
“In vivo imaging studies of astrocytes have shown that astrocytes are sensitive to changes in neural activity and respond with increases in intracellular calcium levels (Wang et al., 2006; Winship et al., 2007).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Winship et al., 2007
Citations
Cites
Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains
Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578
Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation
Zonta, M., Angulo, M. C., Gobbo, S., Rosengarten, B., Hossmann, K.-A., Pozzan, T., & Carmignoto, G. (2002) · Nature Neuroscience · doi:10.1038/nn980 · Cited by 1,446
Astrocyte Control of Synaptic Transmission and Neurovascular Coupling
Haydon, P. G., & Carmignoto, G. (2006) · Physiological Reviews · doi:10.1152/physrev.00049.2005 · Cited by 1,371
In vivo two-photon calcium imaging of neuronal networks
Stosiek, C., Garaschuk, O., Holthoff, K., & Konnerth, A. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1232232100 · Cited by 1,341
Astrocyte-mediated control of cerebral blood flow
Takano, T., Tian, G.-F., Peng, W., Lou, N., Libionka, W., Han, X., & Nedergaard, M. (2005) · Nature Neuroscience · doi:10.1038/nn1623 · Cited by 1,137
Fellin, T., Pascual, O., Gobbo, S., Pozzan, T., Haydon, P. G., & Carmignoto, G. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.011 · Cited by 1,005
Frostig, R. D., Lieke, E. E., Ts’o, D. Y., & Grinvald, A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.16.6082 · Cited by 959
Calcium transients in astrocyte endfeet cause cerebrovascular constrictions
Mulligan, S. J., & MacVicar, B. A. (2004) · Nature · doi:10.1038/nature02827 · Cited by 872
Kleinfeld, D., Mitra, P. P., Helmchen, F., & Denk, W. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15741 · Cited by 832
Neuronal activity triggers calcium waves in hippocampal astrocyte networks
Dani, J. W., Chernjavsky, A., & Smith, S. J. (1992) · Neuron · doi:10.1016/0896-6273(92)90271-e · Cited by 823
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 218
Zhao, J. W., Wang, D., & Wang, J. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-12 · Cited by 44
Metabotropic glutamate receptor mGluR5 is not involved in the early hemodynamic response
Calcinaghi, N., Jolivet, R., Wyss, M. T., Ametamey, S. M., Gasparini, F., Buck, A., & Weber, B. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.96 · Cited by 44
Role of Astroglial Hemichannels and Pannexons in Memory and Neurodegenerative Diseases
Orellana, J. A., Retamal, M. A., Moraga‐Amaro, R., & Stehberg, J. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00026 · Cited by 44
Wan, J., Zhou, S., Mea, H. J., Guo, Y., Ku, H., & Urbina, B. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00480 · Cited by 45
Peripheral Nerve Injury Increases Glutamate-Evoked Calcium Mobilization in Adult Spinal Cord Neurons
Doolen, S., Blake, C. B., Smith, B. N., & Taylor, B. K. (2012) · Molecular Pain · doi:10.1186/1744-8069-8-56 · Cited by 41
Clasadonte, J., & Haydon, P. G. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02839.x · Cited by 40
Gibbons, M. B., Smeal, R. M., Takahashi, D. K., Vargas, J. R., & Wilcox, K. S. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.12.008 · Cited by 40
Intermediate‐conductance calcium‐activated potassium channels participate in neurovascular coupling
Longden, T. A., Dunn, K., Draheim, H. J., Nelson, M. T., Weston, A. H., & Edwards, G. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01447.x · Cited by 39
Purinergic Modulation of Spinal Neuroglial Maladaptive Plasticity Following Peripheral Nerve Injury
Cirillo, G., Colangelo, A. M., Berbenni, M., Ippolito, V. M., Luca, C. D., Verdesca, F., Savarese, L., Alberghina, L., Maggio, N., & Papa, M. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8943-y · Cited by 39
Acute two-photon imaging of the neurovascular unit in the cortex of active mice
Tran, C. H. T., & Gordon, G. R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00011 · Cited by 38
Robertson, J. M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19103033 · Cited by 38
Extracellular Calcium Influx Pathways in Astrocyte Calcium Microdomain Physiology
Ahmadpour, N., Kantroo, M., & Stobart, J. L. (2021) · Biomolecules · doi:10.3390/biom11101467 · Cited by 43
Therapeutic Potential of Astrocyte Transplantation
Hastings, N., Kuan, W., Osborne, A., & Kotter, M. (2022) · Cell Transplantation · doi:10.1177/09636897221105499 · Cited by 39
Honsek, S. D., Walz, C., Kafitz, K. W., & Rose, C. R. (2012) · Hippocampus · doi:10.1002/hipo.20843 · Cited by 42
Ca2+ Signaling in Astrocytes and its Role in Ischemic Stroke
Ding, S. (2014) · Advances in neurobiology · doi:10.1007/978-3-319-08894-5_10 · Cited by 40
Optical imaging of cortical networks via intracortical microstimulation
Brock, A. A., Friedman, R. M., Fan, R. H., & Roe, A. W. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00879.2012 · Cited by 37
TGF-β1 Regulation of Multidrug Resistance P-glycoprotein in the Developing Male Blood-Brain Barrier
Baello, S., Iqbal, M., Bloise, E., Javam, M., Gibb, W., & Matthews, S. G. (2013) · Endocrinology · doi:10.1210/en.2013-1472 · Cited by 37
A Slow or Modulatory Role of Astrocytes in Neurovascular Coupling
Rosenegger, D. G., & Gordon, G. R. (2015) · Microcirculation · doi:10.1111/micc.12184 · Cited by 37
Involvement of astrocytes in neurovascular communication
Nuriya, M., & Hirase, H. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.02.001 · Cited by 33
Stokum, J. A., Shim, B., Huang, W., Kane, M. A., Smith, J. A., Gerzanich, V., & Simard, J. M. (2021) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x211004182 · Cited by 33
Ryczko, D., Hanini‐Daoud, M., Condamine, S., Bréant, B. J. B., Fougère, M., Araya, R., & Kolta, A. (2020) · The Journal of Physiology · doi:10.1113/jp280501 · Cited by 32
MacDonald, C. L. (2008) · Frontiers in Neuroengineering · doi:10.3389/neuro.16.001.2008 · Cited by 34
Kjærby, C., Rasmussen, R. N., Andersen, M., & Nedergaard, M. (2017) · Neurochemical Research · doi:10.1007/s11064-017-2195-y · Cited by 34
Institóris, Á., Rosenegger, D. G., & Gordon, G. R. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.141 · Cited by 31
Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
Asada, A., Ujita, S., Nakayama, R., Oba, S., Ishii, S., Matsuki, N., & Ikegaya, Y. (2015) · Physiological Reports · doi:10.14814/phy2.12454 · Cited by 30
The computational power of the human brain
Gebicke‐Haerter, P. J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1220030 · Cited by 35
Feig, S., & Haberly, L. (2011) · The Journal of comparative neurology · doi:10.1002/cne.22615 · Cited by 23
The Barrel Cortex as a Model to Study Dynamic Neuroglial Interaction
Giaume, C., Maravall, M., Welker, E., & Bonvento, G. (2009) · The Neuroscientist · doi:10.1177/1073858409336092 · Cited by 31
Astrocyte and Microvascular Imaging in Awake Animals Using Two‐Photon Microscopy
Tran, C. H. T., & Gordon, G. R. (2015) · Microcirculation · doi:10.1111/micc.12188 · Cited by 27
New and emerging imaging techniques for mapping brain circuitry
Pan, H., Epstein, J., Silbersweig, D., & Stern, E. R. (2011) · Brain Research Reviews · doi:10.1016/j.brainresrev.2011.02.004 · Cited by 26
Somatotopic astrocytic activity in the somatosensory cortex
Ghosh, A., Wyss, M. T., & Weber, B. (2013) · Glia · doi:10.1002/glia.22458 · Cited by 26
Chronic multiscale imaging of neuronal activity in the awake common marmoset
Yamada, Y., Matsumoto, Y., Okahara, N., & Mikoshiba, K. (2016) · Scientific Reports · doi:10.1038/srep35722 · Cited by 26
Gebremedhin, D., Zhang, D. X., Carver, K. A., Rau, N., Rarick, K., Roman, R., & Harder, D. (2016) · Prostaglandins & other lipid mediators · doi:10.1016/j.prostaglandins.2016.04.003 · Cited by 27
Calcium Imaging of Living Astrocytes in the Mouse Spinal Cord following Sensory Stimulation
Cirillo, G., Luca, D. D., & Papa, M. (2012) · Journal of Neural Transplantation and Plasticity · doi:10.1155/2012/425818 · Cited by 24
Alles, S. R. A., Bandet, M. V., Eppler, K., Noh, M., Winship, I. R., Baker, G. B., Ballanyi, K., & Smith, P. A. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.11.011 · Cited by 26
Self-citationAstrocytic Endocannabinoids Mediate Hippocampal Transient Heterosynaptic Depression
Smith, N., Bekar, L. K., & Nedergaard, M. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02834-0 · Cited by 24
Chen, W., Park, K., Pan, Y., Koretsky, A. P., & Du, C. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116554 · Cited by 24
Astrocytic Calcium Dynamics Along the Pain Pathway
Cho, J., & Huh, Y. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.594216 · Cited by 22
Osswald, M., & Winkler, F. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1580-3 · Cited by 21
Jessen, S. B., Brazhe, A., Lind, B. L., Mathiesen, C., Thomsen, K., Jensen, K., & Lauritzen, M. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu058 · Cited by 21
Chapter 20 Regulated Exocytosis from Astrocytes
Calì, C., Marchaland, J., Spagnuolo, P., Gremion, J., & Bezzi, P. (2009) · International review of neurobiology · doi:10.1016/s0074-7742(09)85020-4 · Cited by 21
Graber, M. H., Helmchen, F., & Hahnloser, R. H. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081177 · Cited by 20
In Vivo Astrocytic Ca 2+ Signaling In Health and Brain Disorders
Ding, S. (2013) · Future Neurology · doi:10.2217/fnl.13.38 · Cited by 21
The Duality of Astrocyte Neuromodulation: Astrocytes Sense Neuromodulators and Are Neuromodulators
Lines, J., Corkrum, M., Aguilar, J., & Araque, A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70054 · Cited by 19
Clasadonte, J., & Haydon, P. G. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0046 · Cited by 19
Pittà, M. D. (2020) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_100691-1 · Cited by 21
Lim, D., Mapelli, L., Canonico, P. L., Moccia, F. D., & Genazzani, A. A. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102997 · Cited by 18
In Vivo Two-Photon Calcium Imaging in the Visual SystemPreprint
Ohki, K., & Reid, R. C. (2014) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot081455 · Cited by 18
Croft, W. D., Dobson, K. L., & Bellamy, T. C. (2015) · Neural Plasticity · doi:10.1155/2015/765792 · Cited by 20
Hadad, I., Veithen, A., Springael, J., Sotiropoulou, P. A., Costa, A. M. D., Miot, F., Naeije, R., Deken, X. D., & Entee, K. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0056007 · Cited by 17
Adenosine A1 Receptor mRNA Expression by Neurons and Glia in the Auditory Forebrain
Hackett, T. A. (2018) · The Anatomical Record · doi:10.1002/ar.23907 · Cited by 17
López-Hidalgo, M. A., Kellner, V., & Schummers, J. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00016 · Cited by 16
Devor, A., Boas, D. A., Einevoll, G. T., Buxton, R. B., & Dale, A. M. (2011) · Advances in neurobiology · doi:10.1007/978-1-4614-1788-0_15 · Cited by 16
Are astrocytes executive cells within the central nervous system?
Sica, R. E. P., Caccuri, R. L., Quarracino, C., & Capani, F. (2016) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20160101 · Cited by 18
Baranes, K., Hastings, N., Rahman, S. M. J., Poulin, N., Tavares, J. M., Kuan, W., Syed, N., Kunz, M., Blighe, K., Belgard, T. G., et al. (2023) · Glia · doi:10.1002/glia.24372 · Cited by 16
Sensory response in host and engrafted astrocytes of adult brain in Vivo
Zhang, K., & Chen, X. (2017) · Glia · doi:10.1002/glia.23181 · Cited by 14
Cortical astrocytes extend phasic norepinephrine signals and critically mediate learned behaviorPreprint
Drummond, G. T., Natesan, A., Celotto, M., Park, J., Shih, J., Ojha, P., Osako, Y., Fernandes, G., Jenks, K. R., Sipe, G. O., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.24.620009 · Cited by 15
Electrophysiological In Vitro Study of Long‐Range Signal Transmission by Astrocytic Networks
Hastings, N., Yu, Y., Huang, B., Middya, S., Inaoka, M., Erkamp, N. A., Mason, R. J., Carnicer‐Lombarte, A., Rahman, S. M. J., Knowles, T. P. J., et al. (2023) · Advanced Science · doi:10.1002/advs.202301756 · Cited by 13
Sigl‐Glöckner, J., & Seibt, J. (2018) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2018.09.011 · Cited by 13
The Causal Role of Astrocytes in Slow-Wave Rhythmogenesis: A Computational Modelling StudyPreprint
Kozachkov, L., & Michmizos, K. P. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1702.03993 · Cited by 14
Heterogeneity of Sensory-Induced Astrocytic Ca2+ Dynamics During Functional Hyperemia
Sharma, K., Gordon, G. R., & Tran, C. H. T. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.611884 · Cited by 12
Two-Photon Calcium Imaging in the Intact Brain
Maschio, M. D., Beltramo, R., Stasi, A. M. D., & Fellin, T. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-2888-2_4 · Cited by 13
Guerrero, A. A., & Turrigiano, G. G. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0807-25.2025 · Cited by 12
Neurovascular Coupling in Seizures
Teskey, G. C., & Tran, C. H. T. (2021) · Neuroglia · doi:10.3390/neuroglia2010005 · Cited by 10
Tran, C. H. T. (2022) · Neurophotonics · doi:10.1117/1.nph.9.2.021909 · Cited by 10
From nociception to pain perception, possible implications of astrocytes
Higinio-Rodríguez, F., Rivera-Villaseñor, A., Calero-Vargas, I., & López-Hidalgo, M. A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.972827 · Cited by 9
Linking brain activity across scales with simultaneous opto- and electrophysiology
Hoffmann, A., & Helmchen, F. (2023) · Neurophotonics · doi:10.1117/1.nph.11.3.033403 · Cited by 12
Gurden, H. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00021 · Cited by 9
The Mandala of the Present Moment
Gordon, W. V., Shonin, E., & García‐Campayo, J. (2017) · Mindfulness · doi:10.1007/s12671-017-0779-x · Cited by 10
Activity-dependent functions of non-electrical glial cells
Kato, D., Eto, K., Nabekura, J., & Wake, H. (2018) · The Journal of Biochemistry · doi:10.1093/jb/mvy023 · Cited by 10
Fedotova, A., Brazhe, A., & Semyanov, A. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.15.688660 · Cited by 8
Jackson, J. G., Krizman, E. N., Takano, H., Lee, M., Choi, G. H., Putt, M. E., & Robinson, M. B. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.831061 · Cited by 6
Mitterauer, B. (2010) · Advances in Bioscience and Biotechnology · doi:10.4236/abb.2010.15052 · Cited by 7
Smeal, R. M., & Economo, M. N. (2011) · Journal of Bioengineering and Biomedical Sciences · doi:10.4172/2155-9538.s5-002 · Cited by 5
Enhanced Primary Motor Cortex Astrocyte Calcium Signaling With Motor Learning
Padmashri, R., & Dunaevsky, A. (2025) · Neural Plasticity · doi:10.1155/np/5571169 · Cited by 4
The Astroglia Syncytial Theory of Consciousness
Robertson, J. M. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26125785 · Cited by 4
Bach, P., Schuster, R., Koopmann, A., Vollstädt‐Klein, S., Spanagel, R., & Kiefer, F. (2021) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-021-01240-4 · Cited by 3
Applications of Induced Pluripotent Stem Cell-Derived Glia in Brain Disease Research and Treatment
Yang, Z., Gong, M., Yang, C., Chen, C., & Zhang, K. (2023) · Handbook of experimental pharmacology · doi:10.1007/164_2023_697 · Cited by 3
Larriva-Sahd, J. A., Martı́nez-Cabrera, G., Lozano‐Flores, C., Concha, L., & Varela‐Echavarría, A. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25559 · Cited by 3
Tri, C., Manjaly, Z., Heinzle, J., Schöbi, D., Kasper, L., Pruessmann, K. P., Stephan, K. E., & Frässle, S. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14970 · Cited by 3
Yuan, J., Zhang, Y., Yang, H., Cao, S., Luo, Y., & Yu, T. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2205116 · Cited by 3
Optical imaging of visually guided reaching in macaque posterior parietal cortex
Heider, B., & Siegel, R. M. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0513-y · Cited by 3
Pittà, M. D. (2022) · Springer eBooks · doi:10.1007/978-1-0716-1006-0_100691 · Cited by 3
Lind, B. L., & Volterra, A. (2024) · Research Square · doi:10.1101/2024.06.28.601145 · Cited by 3
Central cytometabolic functional vascular coupling in health and disease
Sims, S. L., Lu, T., Weiss, B. E., Lin, R., Galopin, L. B., Wright, N. A., Norris, C. M., & Thibault, O. (2025) · npj Metabolic Health and Disease · doi:10.1038/s44324-025-00090-1 · Cited by 2
Two-Photon Microscopy to Measure Blood Flow and Concurrent Brain Cell Activity
Shih, A. Y., Driscoll, J. D., Pesavento, M. J., & Kleinfeld, D. (2013) · Neuromethods · doi:10.1007/978-1-62703-785-3_16 · Cited by 2
Hubbard, J. A., & Binder, D. K. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802401-0.00003-x · Cited by 2
Bandet, M. V., Dong, B., & Winship, I. R. (2021) · PLoS ONE · doi:10.1371/journal.pone.0236684 · Cited by 2
Self-citationDirect Deviations in Astrocyte Free Ca2+ Concentration Control Multiple Arteriole Tone States
Haidey, J. N., & Gordon, G. R. (2021) · Neuroglia · doi:10.3390/neuroglia2010006 · Cited by 2
Calì, C., Marchaland, J., Mirante, O., & Bezzi, P. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0793-6_12 · Cited by 2
Functional Imaging Using Two-Photon Microscopy in Living Tissue
Vanzetta, I., Deneux, T., Kaszás, A., Katona, G., & Rózsa, B. J. (2012) · Neuromethods · doi:10.1007/978-1-61779-897-9_7 · Cited by 1
Neuronal-Glial-Endothelial Interactions Regulate Central Nervous System Homeostasis
Gómez‐González, B., Cabañas-Morales, A. M., Hurtado‐Alvarado, G., & Velázquez‐Moctezuma, J. (2015) · CRC Press eBooks · doi:10.1201/b18028-4 · Cited by 1
The Neurovascular Unit and the Role of Astrocytes in the Regulation of Vascular Tone
Filosa, J. A. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00126ed1v01y201503ngl006 · Cited by 1
Glial Laminar Cortical Architecture Matches Metabolic Demand
Scott, N. A., & Murphy, T. H. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.205 · Cited by 1
Self-citationUltrasonic Modulation of Astrocytic and Neuronal Calcium Dynamics in Mouse CortexPreprint
Yong, Y., Jiang, H., Qiao, C., Liu, Z., Zhou, X., Zhou, Y., & Li, F. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.03.641164 · Cited by 1
Simulating calcium signaling in fine astrocytic processes
Denizot, A. (2019) · theses.fr (ABES) · doi:10.70675/970a38b3z8898z4ac0z896ez5ae9336af7f7 · Cited by 1
Diversity and specificity of glial cell responses in the thalamus (Commentary on Parri et al.)
Audinat, É. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07328.x
Role of Actin-mediated Motility of Peripheral Astrocytic Processes in Synaptic Function
Molotkov, D. (2014) · Työväentutkimus Vuosikirja
Mitterauer, B. (2010) · Journal of Biomedical Science and Engineering · doi:10.4236/jbise.2010.310127
ASTROCYTE-MEDIATED SHORT-TERM SYNAPTIC DEPRESSION
Andersson, M. (2009) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Metadata
- Authors
- Winship, I. R., Plaa, N., & Murphy, T. H.
- Affiliations
- University of British Columbia (CA)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2007-06-06
- Volume
- 27
- Issue
- 23
- Pages
- 6268-6272
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6672142
- OpenAlex
- W2054459050
- Semantic Scholar
- 9c442e4e61461e8b7b1b77e7f83d93c39f83a302
- Cited by
- 221
- References
- 32
- Citations by year
- 2025: 7 · 2024: 4 · 2023: 12 · 2022: 9 · 2021: 11 · 2020: 9 · 2019: 5 · 2018: 8 · 2017: 9 · 2016: 16 · 2015: 17 · 2014: 14 · 2013: 21 · 2012: 19
- FWCI
- 6.34
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Heart and Stroke Foundation of Canada
- Canadian Stroke Network
- Michael Smith Health Research BC
- Canadian Institutes of Health Research
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- calcium oscillations, sensory evoked potentials, primary somatosensory cortex, hemodynamic response, astrocyte-neuron communication, cerebral microcirculation, sulforhodamine 101, intrinsic signal imaging, microvascular tone, neuronal activity
- MeSH terms
- Action Potentials, Animals, Astrocytes, Female, Hindlimb, Male, Mice, Inbred C57BL, Microcirculation, Neurons, Somatosensory Cortex, Time Factors, Calcium Signaling, Mice
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.
A language model drew the claims from the paper on 2026-10-09, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-09 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
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