Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.04.25.650615

Persistent Light-Induced Reduction of Neuronal Excitability: Implications for Non-Optogenetic control of Brain Actvity

Abstract

Visible light is widely used in neuroscience, yet its direct effects on neuronal activity in the absence of optogenetic manipulation remain incompletely understood. Here, we investigated whether light stimulation can induce sustained changes in neuronal excitability. Using ex vivo electrophysiological recordings, we show that repeated pulses of blue light (5 s, 430-495 nm, 19 mW) produce a robust and persistent reduction in evoked firing activity in cortical neurons from both male and female mice, with an average decrease of [~]60% relative to baseline. This inhibitory effect persisted for more than 20 minutes following stimulation and was associated with changes in both passive membrane properties and active ion channel conductance. In human cortical neurons, responses were more heterogeneous. While a subset of neurons exhibited similar inhibitory effects, others showed increased excitability, with this response occurring more frequently in neurons from female patients, suggesting a potential sex-dependent effect. In addition, a transient depolarizing response to light was observed in a minority of human neurons but not in mice. These findings indicate that visible light, independently of exogenous opsins, can induce long-lasting modulation of neuronal activity without evidence of acute cytotoxicity under the conditions tested. This raises the possibility that visible light may provide a previously underappreciated, opsin-independent mechanism for modulating neuronal activity, with potential relevance for disorders characterized by neuronal hyperexcitability. We outline a framework for future investigations, including validation in human systems, in vivo studies, optimization of stimulation parameters, and assessment of therapeutic potential in pathological models.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Lightning, A., Di Rocco, F., Guenot, M., Kuczewski, N.. 2025-04-29. Persistent Light-Induced Reduction of Neuronal Excitability: Implications for Non-Optogenetic control of Brain Actvity. https://doi.org/10.1101/2025.04.25.650615

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants

Autism spectrum disorder is a neurodevelopmental disorder with both genetic and environmental contributors. SCN2A, the gene which encodes the alpha subunit of the voltage-gated sodium channel Nav1.2, is a known monogenetic risk factor for autism spectrum disorder. The cerebellum is frequently implicated in autism spectrum disorder and other neurodevelopmental disorders but has largely been unexplored in relation to SCN2A variants, especially from a developmental perspective. Nav1.2 is highly expressed within the cerebellum, specifically within cerebellar granule neurons, where it helps to drive action potential generation and propagation. Cerebellar granule neuron activity and maturation is crucial for shaping the development and morphology of the rest of the cerebellar cortex. Here we investigated early-postnatal cerebellar development in two mouse models carrying patient-derived SCN2A premature termination codon variants, Scn2a-p.Y84X and -p.R1627X. Overall, both Scn2a premature termination codon variant mouse lines displayed largely normal physical development and unaffected non-cerebellar developmental milestones. Scn2aY84X/+ mice, but not Scn2aR1627X/+ mice, demonstrated alterations in cerebellar-driven motor behaviors, specifically faster performance in the surface righting reflex and cliff avoidance compared to wildtype littermates. Coinciding with the behavioral findings, Scn2a variants had divergent and age-dependent effects on cerebellar glutamatergic presynaptic marker expression, indicating that some, but not all, Scn2a premature termination codons impair glutamatergic synapse development. Both Scn2a variants exhibited changes to cerebellar cytoarchitecture, such as reductions in Purkinje cell density and soma size, which was more prominent in Scn2aY84X/+ mice, and faster migration of cerebellar granule neurons from the external granule layer to the internal, indicating a possible shift in the timing of cerebellar maturation. Our results situate the cerebellum as an early site for SCN2A pathophysiology and establish that cerebellar consequences of SCN2A premature termination codon variants may be position- and age-dependent, suggesting that influences beyond simple heterozygous loss of Nav1.2 drive phenotypes. Our characterization of how Scn2a premature termination codon variants differentially impair cerebellar development may help explain the heterogeneity of clinical presentations of SCN2A loss of function variants and potentially inform upon the timing of therapeutic intervention.

neuroscience↗

Association of object mnemonic discrimination deficit with age and AD biomarkers in older adults

Background Blood-based Alzheimers disease (AD) biomarkers provide scalable detection of AD pathology, yet their relationships with hippocampal-dependent mnemonic discrimination remain unclear. This study examined how object mnemonic discrimination relates to age, hippocampal structure, and plasma AD biomarkers in cognitively normal (CN) older adults and individuals with amnestic mild cognitive impairment (aMCI). Methods Forty-six CN and forty-one aMCI participants completed an object mnemonic similarity task (MST). Mnemonic discrimination was quantified using the overall lure discrimination index (LDI) and similarity-specific LDIs. Plasma pTau181, pTau217, pTau231, and GFAP were assayed, and hippocampal volumes were derived from 7T MR scanner. Multiple linear regression models assessed associations between LDI and biomarkers, controlling for age, sex, education, APOE4 status, and diagnosis. Repeated-measures ANCOVA and linear mixed-effects models evaluated similarity-dependent age effects. ROC analyses and stepwise logistic regression quantified diagnostic classification performance. Results LDI was significantly reduced in aMCI compared to CN. Total hippocampal volume and plasma pTau217 showed the strongest associations with LDI, exceeding those of pTau181, pTau231, and GFAP. LDI discriminated aMCI from CN with high accuracy (AUC = 0.836), comparable to hippocampal volume and plasma biomarkers. A combined model including LDI, pTau181, pTau217, and hippocampal volume achieved the highest diagnostic accuracy (AUC = 0.931). Age effects were similarity-dependent: discrimination declined with age only for low-similarity lures, independent of diagnosis. Sex differences emerged within aMCI, with females showing lower LDI than males. Conclusions Object mnemonic discrimination provides a sensitive behavioral marker linked to hippocampal volume and plasma pTau217, showing discriminative power comparable to established AD biomarkers in separating aMCI from CN participants. Similarity-dependent age effects highlight age-related deficits are not universal for lures with varying similarity levels.

neuroscience↗

A collicular somatostatinergic circuit gates sensory access to action

Animals are exposed to far more sensory information than can be converted into action and must prioritise behaviourally salient events. Although salience is commonly studied as modulation of sensory representations, stimulus prioritisation may also arise at premotor stages, through mechanisms that regulate the readiness of action-generating circuits to be recruited by sensory input. The superior colliculus links visual signals to spatially directed orienting and contains Pitx2-expressing spatial-motor modules that coordinate spatially targeted actions, providing a substrate for premotor regulation of sensory access to action. However, the circuit elements that regulate this access remain unknown. Here we identify an intersectionally targeted population of somatostatin-expressing inhibitory neurons in the mouse superior colliculus that is, at the population level, suppressed during orienting movements and visual stimulation. These neurons provide input to Pitx2-expressing spatial-motor modules, and their optogenetic silencing increased retinally evoked firing in Pitx2 neurons, showing that somatostatinergic inhibition constrains the visual recruitment of collicular motor output. Increasing somatostatinergic tone reduced interception of low- and intermediate-contrast visual targets while sparing responses to high-contrast targets, consistent with graded control of sensory access to action. Cholecystokinin-expressing inhibitory neurons and multiple cortical and subcortical regions provide anatomical input to the somatostatinergic population, identifying candidate routes for local and context-dependent regulation. Together, these findings establish somatostatinergic inhibition as a premotor control point that regulates the readiness of spatial-motor circuits for sensory recruitment and identify a circuit architecture through which the behavioural impact of salient sensory events could be regulated downstream of sensory encoding.

neuroscience↗