Biology subjects

Koenig, J. A.

Publications and source records attributed to Koenig, J. A..

3 recordsLinked to original sources

bioRxiv2025

Nicotinic Modulation of Fast-spiking Neurons in Rat Somatosensory Cortex Across Development

Signaling at nicotinic acetylcholine receptors (nAChRs) is vital for normal development of cerebral cortical circuits. These developing circuits are also shaped by fast-spiking (FS) inhibitory cortical neurons. While nicotinic dysfunction in FS neurons is implicated in a number of psychiatric and neurodevelopmental disorders, FS neurons are thought to not have nicotinic responses in adults. Here, we establish a timeline of FS neuron response to nicotine pre- and postsynaptically in primary somatosensory cortex in male and female rats. We found that nicotine increases the frequency of spontaneous synaptic inputs to FS neurons during the second postnatal week, and this effect persisted through development. In contrast, FS neurons in S1 had no postsynaptic responses to nicotine from as early as they can be reliably identified. This was not attributable to receptor desensitization, and we further revealed that FS neurons express abundant mRNA for several nAChR subunits, beginning early in development. To determine why FS neurons do not respond to nicotine, despite expressing these receptors, we probed for the expression of lynx1, a negative nicotinic modulator. Lynx1 mRNA was expressed in FS neurons from early development, with expression increasing dramatically during the second postnatal week. SIGNIFICANCE STATEMENTSignaling at nicotinic receptors is critical for development of cortical circuits. These circuits are also shaped by fast-spiking (FS) inhibitory neurons. We reveal how these developmental processes interact, by establishing a timeline of nicotinic effects on FS neurons in rats. We find that nicotine presynaptically regulates inputs to FS neurons from early development. However, FS neurons at all ages lack postsynaptic responses to nicotine, despite expressing nicotinic receptor mRNA. This might be due to the expression of lynx1, a negative nicotinic receptor modulator, which we identify in FS neurons as early as the first postnatal week. This work reveals novel aspects of development, relevant to both normal cortical development and the neuropsychiatric pathologies associated with abnormal FS neurons and nicotinic development.

neuroscience↗

bioRxiv2025

Lasting Increases in Neuronal Activity and Serotonergic Receptor Expression Following Gestational Chlorpyrifos Exposure

Perinatal exposure to the organophosphorus insecticide chlorpyrifos (CPF) is associated with an increased incidence of neurodevelopmental disorders, such as autism spectrum disorder. While these behavioral detriments have been modeled in rodents, the underlying functional alterations in the developing brain are largely unknown. Previous reports using a rat model have identified alterations to both inhibitory synaptic transmission and serotonergic (5-HT) receptor binding in the cortex following developmental CPF exposure. Here, we use a rat model of gestational CPF exposure to investigate whether this altered inhibitory activity is driven by increased spontaneous firing of inhibitory interneurons and altered 5-HT receptor expression. Using cell-attached ex vivo electrophysiology in young rats of both sexes, we identified a significant increase in the number of spontaneously firing neurons in the somatosensory cortex of CPF-exposed offspring. Analysis of action potential metrics identified a sub-set of these neurons as fast-spiking parvalbumin (PV) interneurons. Immunohistochemical labeling of c-Fos, a marker of neuronal activity, further revealed a pronounced increase in activity of neurons of the somatosensory cortex in both juvenile and adult rats that had been gestationally exposed to CPF. Finally, RNAscope in situ hybridization showed an increase in the expression of the inhibitory receptor 5-HT1B in PV neurons. The data here demonstrate that gestational exposure to CPF results in persistent hyper-excitation of the somatosensory cortex, potentially through increased expression of the receptor 5-HT1B and resulting disinhibition. These neurophysiological effects may contribute to the established behavioral outcomes resulting from gestational exposure to CPF and offer guidance for novel preventative interventions. SIGNIFICANCE STATEMENTWe report persistent increases in spontaneous neuronal firing in the somatosensory cortex following a brief gestational exposure to the organophosphorus insecticide CPF in rats. This occurred in conjunction with increased expression of the 5-HT1B receptor measured specifically in PV interneurons. The hyper-excitability of the somatosensory cortex described here agrees with the established hyper-sensitivity to sensory stimulation seen in neurodevelopmental disorders such as autism spectrum disorder. These results offer a possible mechanistic framework underlying the neurophysiological effects associated with early life exposures to the organophosphorus insecticide CPF.

neuroscience↗

bioRxiv2025

Gestational Chlorpyrifos Exposure Imparts Lasting Alterations to the Rat Somatosensory Cortex

Chlorpyrifos is an organophosphorus pesticide used extensively in agricultural and residential settings for nearly 60 years. Gestational, sub-acute exposure to chlorpyrifos is linked to increased prevalence of neurodevelopmental disorders. Animal studies have modeled these neurobehavioral detriments, however, the functional alterations in the brain induced by this exposure remain largely unknown. To address this, we used a rat model of gestational chlorpyrifos exposure to interrogate the alterations in the developing somatosensory (barrel) cortex. Rat dams were exposed to chlorpyrifos (5 mg/kg) or vehicle on gestational days 18-21 via subcutaneous injection, with no overt acute toxicity. Acetylcholinesterase was modestly inhibited but returned to baseline levels by postnatal day 12. We performed whole-cell patch clamp recordings on postnatal days 12-20 in both male and female progeny of the treated dams. A spike timing dependent plasticity protocol revealed changes to the normal development of use-dependent plasticity, including interference in long-term synaptic depression. Recording inhibitory synaptic activity revealed an increase in the frequency of spontaneous postsynaptic currents and in paired pulse ratios, in conjunction with a significant decrease in miniature postsynaptic currents. These findings suggest a presynaptic mechanism of inhibited GABA release, with potential disinhibition of inhibitory neurons. Evaluation of barrel cortex development displayed disruptions to normal barrel field patterning, with increases in both the septal area and total barrel field. We provide evidence for functional and structural alterations during brain development induced by in utero exposure to the organophosphorus pesticide chlorpyrifos that may account for the well-established behavioral outcomes. SIGNIFICANCE STATEMENTWe demonstrate persistent alterations to synaptic function and plasticity in the somatosensory cortex following a brief, sub-acute exposure to the organophosphorus pesticide chlorpyrifos in a gestational rat model. These occur in conjunction with structural changes to cellular patterning of this brain region. These previously unknown consequences are potential causal mechanisms to the well-established neurodevelopmental detriments associated with early life exposure to chlorpyrifos. Clarifying these mechanisms could aid in ameliorating or preventing their persistent effects.

neuroscience↗