Skip to content
DraconiticResearch
Search Sources API
194,226 studies31 sourcesUpdated 33 min ago
PreprintCC BYbioRxiv

Brain state shapes the polarity of pulsed infrared neural stimulation responses in individual cortical neurons

  1. 1Zhejiang University

Abstract

Pulsed infrared neural stimulation (INS, 1875nm the peak of energy absorption by water) is a non-viral method developed to activate single submillimeter sites in the brain. When used in ultrahigh-field fMRI, it reveals functionally specific brain-wide columnar networks comprising synaptically activated nodes. INS is non-damaging and effective for use in the human cortex and is useful for neural and behavioral neuromodulation in primates. To investigate how physiological state influences its cellular effects, we performed in vivo two-photon calcium imaging with GCaMP6s in mice and tracked identified cortical neurons in awake vs anesthetized states. Across the tested radiant exposures, INS-evoked responses differed markedly between states: under anesthesia, stimulation produced predominantly positive-going calcium responses, whereas during wakefulness the same identified neurons exhibited negative-going responses. Pharmacological manipulation of this baseline level by GABAergic signaling shifted response polarity in opposite directions: picrotoxin under anesthesia produced awake-like negative responses, whereas muscimol during wakefulness produced anesthetized-like positive responses. Trial-by-trial analyses further showed that the relationship between pre-stimulus baseline level and INS-evoked response depended on physiological state. Because INS relies on transient tissue heating, we also developed an in situ EGFP-based calibration approach to estimate temperature-related fluorescence changes. These fluoro-thermal contributions were modest at lower radiant exposures and became increasingly important at higher exposures, particularly near the fiber pathway. The low-intensity results are consistent with, but do not establish, a state-dependent feed-forward inhibitory framework. Together, these findings show that the neuronal response to focal INS is shaped by ongoing brain state and provide a practical framework for separating state-dependent calcium responses from temperature-related fluorescence effects, making INS a potentially versatile tool for neuroscience and clinical applications.

Related

  1. Computational investigation of circuit mechanisms underlying short-latency responses to cortical stimulation
    K. Kumaravelu, G. J. Yu, A. S. Aberra +3
    bioRxivPreprintCC BY-NC-NDFull textNeurosciencebioRxiv
  2. Immediate cortical responses to transcranial magnetic stimulation of the human motor leg area
    M. M. Beck, M. Nuyts, L. Sakalauskaite +3
    bioRxivPreprintCC BY-NC-NDFull textNeurosciencebioRxiv
  3. Short-term cortical stimulation combined with targeted rehabilitation and Chondroitinase ABC improves upper limb function following a cervical contusion injury
    e. sinopoulou, E. R. Burnside, K. Bartus +1
    bioRxivPreprintAll rights reservedFull textNeurosciencebioRxiv
  4. Cortical diffusion restriction predicts individual cognitive ability and carries cellular information
    Demian Wassermann, Gabriela Gomez Jimenez, Reuben Dorent
    HALPreprintCC BY-NC-SA 4.0Full textNeuroscienceStatisticsHAL
  5. Human cortical slices reveal pulse-number-dependent synaptic plasticity during theta-burst magnetic stimulation
    C. Galanis, J. Straehle, Z. Turi +2
    bioRxivPreprintCC BYFull textNeurosciencebioRxiv
BibTeX
@misc{fu2026brain,
  title = {{Brain state shapes the polarity of pulsed infrared neural stimulation responses in individual cortical neurons}},
  author = {P. Fu and Y. Liu and L. Zhu and M. Wang and Y. Yu and H. Zhang and Y. Pei and S. Shoham and Y. Zeng and A. W. Roe and W. Xi},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.19.752571},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.19.752571v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Brain state shapes the polarity of pulsed infrared neural stimulation responses in individual cortical neurons
AU  - P. Fu
AU  - Y. Liu
AU  - L. Zhu
AU  - M. Wang
AU  - Y. Yu
AU  - H. Zhang
AU  - Y. Pei
AU  - S. Shoham
AU  - Y. Zeng
AU  - A. W. Roe
AU  - W. Xi
PY  - 2026
DA  - 2026/09/19
PB  - bioRxiv
DO  - 10.64898/2026.09.19.752571
UR  - https://www.biorxiv.org/content/10.64898/2026.09.19.752571v1
AB  - Pulsed infrared neural stimulation (INS, 1875nm the peak of energy absorption by water) is a non-viral method developed to activate single submillimeter sites in the brain. When used in ultrahigh-field fMRI, it reveals functionally specific brain-wide columnar networks comprising synaptically activated nodes. INS is non-damaging and effective for use in the human cortex and is useful for neural and behavioral neuromodulation in primates. To investigate how physiological state influences its cellular effects, we performed in vivo two-photon calcium imaging with GCaMP6s in mice and tracked identified cortical neurons in awake vs anesthetized states. Across the tested radiant exposures, INS-evoked responses differed markedly between states: under anesthesia, stimulation produced predominantly positive-going calcium responses, whereas during wakefulness the same identified neurons exhibited negative-going responses. Pharmacological manipulation of this baseline level by GABAergic signaling shifted response polarity in opposite directions: picrotoxin under anesthesia produced awake-like negative responses, whereas muscimol during wakefulness produced anesthetized-like positive responses. Trial-by-trial analyses further showed that the relationship between pre-stimulus baseline level and INS-evoked response depended on physiological state. Because INS relies on transient tissue heating, we also developed an in situ EGFP-based calibration approach to estimate temperature-related fluorescence changes. These fluoro-thermal contributions were modest at lower radiant exposures and became increasingly important at higher exposures, particularly near the fiber pathway. The low-intensity results are consistent with, but do not establish, a state-dependent feed-forward inhibitory framework. Together, these findings show that the neuronal response to focal INS is shaped by ongoing brain state and provide a practical framework for separating state-dependent calcium responses from temperature-related fluorescence effects, making INS a potentially versatile tool for neuroscience and clinical applications.
ER  -