Evidence map›Paper›PMID 41013225›Full record

ArticleBMC anesthesiology2025

Neuronal activity in the cortex of mice under anesthesia depend on the type of anesthetic drug.

Renhao Xu, Rong Chen, Xiao Zhang, Xiangjian Zhang, Jin Zhang

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Article in BMC anesthesiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Renhao XuDepartment of Neurology, the Second Hospital of Hebei Medical University, 309 Zhongbei Dajie, Xinhua District, Shijiazhuang, Hebei, 050000, China.
Rong ChenDepartment of Neurology, the Second Hospital of Hebei Medical University, 309 Zhongbei Dajie, Xinhua District, Shijiazhuang, Hebei, 050000, China.
Xiao ZhangDepartment of Neurology, the Second Hospital of Hebei Medical University, 309 Zhongbei Dajie, Xinhua District, Shijiazhuang, Hebei, 050000, China.
Xiangjian ZhangDepartment of Neurology, the Second Hospital of Hebei Medical University, 309 Zhongbei Dajie, Xinhua District, Shijiazhuang, Hebei, 050000, China. zhang6xj@hebmu.edu.cn.
Jin ZhangDepartment of Anesthesiology, The First Hospital of Hebei Medical University, 89 Donggang Road, Shijiazhuang, Hebei, 050000, China. zhangjinydy@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile different anesthetic drugs induce distinct electrical characteristics in the anesthetized brain, the effects of different anesthetics on the activity of single neurons in the central nervous system remain unclear.

methodIn this study, mice were anesthetized with different agents (Remimazolam [REM], dexmedetomidine [DEX], and propofol [PRO]), and cortical electroencephalogram (EEG) and neuronal calcium signals were recorded before, during, and after anesthesia, followed by analysis of the changes in the power spectra of the EEG signals and the intensities of the neuronal calcium signals.

resultCompared with awake mice, mice under PRO-induced anesthesia primarily exhibited changes in low-frequency range brain electrical activity, whereas mice under REM-induced anesthesia exhibited significant increases in the power density in the low- and mid-frequency ranges (δ, θ, and α) postanesthesia, with minimal impact on the high-frequency (β) range. DEX not only suppressed brain cortical activity in the low-frequency range but also affected the mid-frequency range, indicating a broader effect. Reduced rates of transient calcium frequencies per minute were observed, as were reductions in the peak amplitudes of calcium activity (ΔF/F) and total signal intensity of calcium activity (ΔF/F) in anesthetized mice, with PRO showing more pronounced inhibition of neuronal calcium activity than REM and DEX did. These results demonstrate that propofol (PRO) exerts the strongest inhibitory effect on neuronal calcium activity during anesthesia, significantly suppressing transient calcium frequencies, peak amplitudes (ΔF/F), and total signal intensity (ΔF/F) compared to REM and DEX.

conclusionPRO primarily enhanced low-frequency δ oscillations in EEG during anesthesia, while REM increased low- to mid-frequency (δ, θ, α) power, and DEX broadly suppressed both low- and mid-frequency bands (δ, θ, α, β). These findings highlight PRO as the most potent suppressor of neuronal excitability during the maintenance phase of anesthesia.

Indexed as

AnestheticsCerebral CortexNeuronsAnimalsDexmedetomidineElectroencephalographyMaleMiceMice, Inbred C57BLPropofolAnestheticsDexmedetomidinePropofolAnesthesiaCalcium activity4Electroencephalogram2Electromyogram3

Identifiers

PMID41013225
PMCPMC12465817

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.