Evidence map›Paper›PMID 41276799›Full record

ArticleChinese medicine2025

Spinal dorsal horn IGF1 mediates the preventive effect of electroacupuncture on cisplatin-induced peripheral neuropathy via neuronal IGF1R in mice.

Chieh-Ru Fu, Xiao-Chen Li, Ya-Chen Yang, Hui Chen, Ruo-Fan Zhang, Yu-Xia Chu, Yan-Qing Wang, Qi-Liang Mao-Ying

Abstract read
In one paragraph

Article in Chinese medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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

8 authors.

Chieh-Ru FuDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Xiao-Chen LiDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Ya-Chen YangDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Hui ChenDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Ruo-Fan ZhangDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Yu-Xia ChuDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Yan-Qing WangDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China.
Qi-Liang Mao-YingDepartment of Integrative Medicine and Neurobiology, School of Basic Medical Science, Institute of Acupuncture Research, Institutes of Integrative Medicine, Shanghai Medical College, Shanghai Key Laboratory of Acupuncture Mechanism and Acupoint Function, Fudan University, Shanghai, 200032, People's Republic of China. maoyql@fudan.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur previous study demonstrated that neuronal G protein-coupled receptor kinase (GRK2) upregulation alleviated chemotherapy-induced peripheral neuropathy (CIPN) in mice, which was characterized by numbness and pain in distal hind limbs. The neuronal GRK2 was identified as a mediator of electroacupuncture (EA) effects on CIPN. Given that spinal insulin-like growth factor 1 (IGF1), a known inducer of GRK2 in the peripheral neurons, decreases after oxaliplatin treatment in mice, this study is designed to investigate whether spinal IGF1 contributes to EA-mediated prevention of cisplatin-induced peripheral neuropathy via neuronal IGF1 receptor (IGF1R).

methodsA total of 133 male C57BL/6 J mice were included in this study and randomly assigned to different experimental groups. The level of Igf1 mRNA was detected by Real-time PCR, the p-IGF1R protein level by Western blot, after EA treatment in cisplatin-treated mice. The cellular distribution of p-IGF1R in the spinal dorsal horn was observed by immunofluorescent staining. To study the role of neuronal IGF1R in EA preventing cisplatin-induced mechanical allodynia, sensory deficit, and microglia activation and neuroinflammation in the spinal cord of mice, the neuronal IGF1R was downregulated by intraspinal injection of an AAV vector delivering IGF1R shRNA with hSyn promotor (AAV-shIGF1R). Finally, the regulatory effect of EA on spinal GRK2 was assessed by Western blot in AAV-shIGF1R mice.

resultsCisplatin treatment induced mechanical allodynia, sensory deficit, and a decrease of p-IGF1R in the spinal dorsal horn of mice. Immunofluorescence showed that p-IGF1R was localized within neurons (~ 82%), a small mount of microglia (~ 12%) and astrocytes (~ 4%). Cisplatin decreased NeuN

conclusionSpinal dorsal horn IGF1 contributes to the preventive effect of EA treatment against cisplatin-induced peripheral neuropathy through neuronal IGF1R signaling in mice. The enhanced neuronal IGF1/IGF1R signaling in the spinal cord presents a potential strategy for CIPN prevention.

Indexed as

CIPN (Chemotherapy-induced peripheral neuropathy)ElectroacupunctureIGF1 (Insulin-like growth factor 1)Microglia activationNeuroinflammationNeuron

Identifiers

PMID41276799
PMCPMC12642377

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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.