Cocaine induced astrocytic activation was associated with its vasoconstricting effects independent of its neuronal effects in the prefrontal cortex

Astrocytes bridge neuronal and cerebrovascular systems, regulating neurotransmitter dynamics and modulating neurovascular coupling (NVC). Cocaine disrupts neuronal, astrocytic, and cerebrovascular system function, which in the prefrontal cortex (PFC), could interfere with executive function. Though astrocytes are known to influence neurotoxic and addictive effects of cocaine through their regulations of local neurotransmitter environments, their role in cocaine-induced vasoconstriction and dysregulated NVC remains unclear. To investigate astrocytic regulation of vascular response to cocaine, we expressed the genetically encoded calcium indicator GCaMP6f in either neurons or astrocytes alongside concurrent expression of astrocytic DREADD(Gq) in the mouse PFC. Hemodynamic changes and cellular Ca2+ responses to an acute cocaine challenge (1 mg/kg, i.v.) with and without DREADD(Gq) activation were recorded through a cranial window using a custom multi-wavelength imaging platform. We found that when naïve animals were exposed to acute cocaine, intracellular Ca2+ increased in both astrocytes (Ca2+A) and neurons (Ca2+N), cerebral blood vessels vasoconstricted, and oxygenated hemoglobin in tissue (HbO2) decreased. Activation of astrocytes by DREADD(Gq) exposure also caused long-lasting increases in Ca2+A and vasoconstriction. Consequently, when cocaine was administered after astrocytic activation, there was further Ca2+A elevation and vasoconstriction but limited in magnitude, suggesting a ceiling effect. Meanwhile, cocaine induced increases in Ca2+N were unaffected. Correlation analysis revealed a strong negative association between Ca2+A and cerebrovascular diameters, while Ca2+N was negatively correlated with HbO2 and this correlation remained unchanged by astrocytic activation. These findings support astrocytes’ involvement in regulating vascular tone including cocaine’s vasoconstricting effects and its disruption of neurovascular coupling. Astrocytes present a potential therapeutic target to alleviate cerebrovascular pathology triggered by cocaine that merits further investigation.

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2026-02-24
DOI
https://doi.org/10.1038/s41598-026-38521-8
Primary Topic
Neurotransmitter Receptor Influence on Behavior
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cocaine induced astrocytic activation was associated with its vasoconstricting effects independent of its neuronal effects in the prefrontal cortex

Yingtian Pan, Congwu Du, Yukta Jetalpuria, Kevin Clare et al.
Scientific Reports
Neurotransmitter Receptor Influence on Behavior
article

Cocaine induced astrocytic activation was associated with its vasoconstricting effects independent of its neuronal effects in the prefrontal cortex

Yingtian Pan, Congwu Du, Yukta Jetalpuria, Kevin Clare, Yanzuo Liu, Nora D. Volkow
article en

Abstract

Astrocytes bridge neuronal and cerebrovascular systems, regulating neurotransmitter dynamics and modulating neurovascular coupling (NVC). Cocaine disrupts neuronal, astrocytic, and cerebrovascular system function, which in the prefrontal cortex (PFC), could interfere with executive function. Though astrocytes are known to influence neurotoxic and addictive effects of cocaine through their regulations of local neurotransmitter environments, their role in cocaine-induced vasoconstriction and dysregulated NVC remains unclear. To investigate astrocytic regulation of vascular response to cocaine, we expressed the genetically encoded calcium indicator GCaMP6f in either neurons or astrocytes alongside concurrent expression of astrocytic DREADD(Gq) in the mouse PFC. Hemodynamic changes and cellular Ca2+ responses to an acute cocaine challenge (1 mg/kg, i.v.) with and without DREADD(Gq) activation were recorded through a cranial window using a custom multi-wavelength imaging platform. We found that when naïve animals were exposed to acute cocaine, intracellular Ca2+ increased in both astrocytes (Ca2+A) and neurons (Ca2+N), cerebral blood vessels vasoconstricted, and oxygenated hemoglobin in tissue (HbO2) decreased. Activation of astrocytes by DREADD(Gq) exposure also caused long-lasting increases in Ca2+A and vasoconstriction. Consequently, when cocaine was administered after astrocytic activation, there was further Ca2+A elevation and vasoconstriction but limited in magnitude, suggesting a ceiling effect. Meanwhile, cocaine induced increases in Ca2+N were unaffected. Correlation analysis revealed a strong negative association between Ca2+A and cerebrovascular diameters, while Ca2+N was negatively correlated with HbO2 and this correlation remained unchanged by astrocytic activation. These findings support astrocytes’ involvement in regulating vascular tone including cocaine’s vasoconstricting effects and its disruption of neurovascular coupling. Astrocytes present a potential therapeutic target to alleviate cerebrovascular pathology triggered by cocaine that merits further investigation.

Scientific ReportsVol. 16(1)
Stony Brook Medicine (US), National Institute on Alcohol Abuse and Alcoholism (US), Stony Brook University (US), Icahn School of Medicine at Mount Sinai (US)
Stony Brook University, National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, National Institute on Drug Abuse
Good health and well-being
Openalex Percentile: Top 46%
Neurotransmitter Receptor Influence on Behavior
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.