Evidence map›Paper›PMID 38051019›Full record

ArticleHistology and histopathology2024

Region-specific response of central microglial cells to sciatic nerve demyelination through sensory and motor pathways.

Shuang Wu, Yuxin Su, Yuqing Wang, Jia Wang, Dongsheng Xu, Yihan Liu, Kunwu Yang, Junhong Gao, Jingjing Cui, Wanzhu Bai

Abstract read
PubMed Publisher
In one paragraph

Article in Histology and histopathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 38% of its field
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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 1 institution in 1 country.

Shuang Wu *Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Yuxin Su *Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Yuqing WangInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Jia WangInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Dongsheng XuInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Yihan LiuInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Kunwu YangInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Junhong GaoInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China.
Jingjing CuiInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China. cuijing101@163.com.
Wanzhu BaiInstitute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, PR China. wanzhubaisy@hotmail.com.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

CACMS Innovation Fund CI2021A03407Fundamental Research Funds for the Central Public Welfare Research Institutes of China ZZ13-YQ-068Fundamental Research Funds for the Central Public Welfare Research Institutes of China ZZ14-YQ-032Fundamental Research Funds for the Central Public Welfare Research Institutes of China ZZ14-YQ-034National Natural Science Foundation of China 81774432
6 · The paper itself

Abstract

Peripheral nerve injury can cause changes in microglial cells on the spinal dorsal and ventral horns. This region-specific response implies that central microglial cells could be activated through both sensory and motor pathways. In order to further determine how peripheral nerve injury activates central microglial cells through neural pathways, the sciatic nerve was selected as the target for neural tract tracing and demyelination. Firstly, we used cholera toxin subunit B (CTB) to map the central sensory and motor territories of the sciatic nerve. Secondly, we applied lysophosphatidylcholine to establish the model of sciatic nerve demyelination and examined the distribution of activated microglial cells via immunofluorescence with ionized calcium-binding adapter molecule 1. It was shown that CTB labeling included the transganglionically labeled sensory afferents and retrogradely labeled somata of motor neurons along the sensory and motor pathways of the sciatic nerve ipsilateral to the injection, in which sensory afferents terminated on the gracile nucleus, Clarke's nucleus, and spinal dorsal horn, while motor neurons located on the spinal ventral horn. Consistently, after sciatic nerve demyelination, the activated microglial cells were observed in the same territories as CTB-labeling, showing shortened processes and enlarged cell bodies. These results support the idea that central microglia might be activated by signals from the demyelinated sciatic nerve through both sensory and motor pathways.

Indexed as

Demyelinating DiseasesMicrogliaSciatic NerveAnimalsCholera ToxinDisease Models, AnimalEfferent PathwaysMaleMotor NeuronsRatsRats, Sprague-DawleySciatic NeuropathyCholera Toxin

Identifiers

PMID38051019
OpenAlexW4389397228

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.