Evidence map›Paper›PMID 40494854›Full record

ArticleMicrosystems & nanoengineering2025

High-precision neural information detection of multiple brain regions in mice under different concentrations of isoflurane anesthesia based on microelectrode arrays.

Yiming Duan, Qianli Jia, Jinping Luo, Yu Wang, Qi Li, Shiya Lv, Luyi Jing, Wei Xu, Xiaoying Zhang, Yulong Ma and 2 more

Abstract read
In one paragraph

Article in Microsystems & nanoengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yiming DuanState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China.
Qianli JiaState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China.
Jinping LuoState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China. jpluo@mail.ie.ac.cn.ORCID http://orcid.org/0000-0003-4213-9185
Yu WangState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China.
Qi LiDepartment of Anesthesiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Shiya LvState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China.
Luyi JingState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China.
Wei XuState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China.
Xiaoying ZhangDepartment of Anesthesiology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Yulong MaDepartment of Anesthesiology, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Weidong MiDepartment of Anesthesiology, The First Medical Center of Chinese PLA General Hospital, Beijing, China. wwdd1962@163.com.
Xinxia CaiState Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, China. xxcai@mail.ie.ac.cn.ORCID http://orcid.org/0000-0001-5997-7252

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The precise neural mechanisms by which general anesthetics induce unconsciousness remain undetermined, with ongoing debate over whether they primarily affect the cortex directly or act predominantly on the sleep-wake brain regions. There is an urgent need for high-precision methodologies to detect and analyze neural information across cortical and subcortical regions. In this study, we designed and fabricated the microelectrode arrays to detect electrophysiological signals from nine brain regions, ranging from the secondary motor cortex to the preoptic area in mice under different concentrations of isoflurane anesthesia. The results demonstrate that isoflurane induces a synchronous inhibitory effect on neural activity in both cortical and subcortical regions of mice during the maintenance phase of anesthesia, which intensifies with increasing anesthesia concentration. Moreover, cortical neurons exhibit a more pronounced inhibitory response to isoflurane, as reflected by significant reductions in local field potential power and spike firing rates compared to subcortical neurons during the suppression phase. These findings suggest that isoflurane during the maintenance phase of anesthesia is more likely to align with the "top-down" paradigm by directly inhibiting cortical regions to maintain unconsciousness. In summary, these discoveries could further refine the study of the neural mechanisms of isoflurane-induced unconsciousness.

Identifiers

PMID40494854
PMCPMC12152167

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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.