Evidence map›Paper›PMID 35401920›Full record

ArticleOxidative medicine and cellular longevity2022

Painful Diabetic Neuropathy Is Associated with Compromised Microglial IGF-1 Signaling Which Can Be Rescued by Green Tea Polyphenol EGCG in Mice.

Xin Chen, Yue Le, Si-Qi Tang, Wan-You He, Jian He, Yun-Hua Wang, Han-Bing Wang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Role of microglia in diabetic neuropathic pain.Frontiers in cell and developmental biology · 2024
    Review
  12. Review
  13. Article
  14. Review
  15. IGF/IGF-1R signal pathway in pain: a promising therapeutic target.International journal of biological sciences · 2023
    Review
  16. 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

7 authors at 2 institutions in 1 country.

Xin ChenDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.
Yue LeDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.
Si-Qi TangDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.
Wan-You HeDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.
Jian HeDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.
Yun-Hua WangDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.
Han-Bing WangDepartment of Anesthesiology, The First People's Hospital of Foshan, 81# North of Ling Nan Road, Foshan, 528000 Guangdong, China.ORCID https://orcid.org/0000-0003-0145-0081
First People's Hospital of Foshan · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Painful diabetic neuropathy (PDN) is a frequent and troublesome complication of diabetes, with little effective treatment. PDN is characterized by specific spinal microglia-mediated neuroinflammation. Insulin-like growth factor 1 (IGF-1) primarily derives from microglia in the brain and serves a vital role in averting the microglial transition into the proinflammatory M1 phenotype. Given that epigallocatechin-3-gallate (EGCG) is a potent anti-inflammatory agent that can regulate IGF-1 signaling, we speculated that EGCG administration might reduce spinal microglia-related neuroinflammation and combat the development of PDN through IGF-1/IGF1R signaling. Methods: Type 1 diabetes mellitus (T1DM) was established by a single intraperitoneal (i.p.) injection of streptozotocin (STZ) in mice. The protein expression level of IGF-1, its receptor IGF1R, interleukin 1 Results: The spinal IGF-1 expression markedly decreased along with the presence of pain-like behaviors, the spinal genesis of neuroinflammation (increased IL-1 Conclusions: Our data highlighted the importance of maintaining spinal IGF-1 signaling in treating microglia-related neuroinflammation in PDN. This study also provides novel insights into the neuroprotective mechanisms of EGCG against neuropathic pain and neuroinflammation through IGF-1 signaling, indicating that this agent may be a promising treatment for PDN in the clinical setting.

Indexed as

CatechinDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetic NeuropathiesAnimalsInsulin-Like Growth Factor IMiceMicrogliaPainPolyphenolsTeaTumor Necrosis Factor-alphaCatechinepigallocatechin gallateInsulin-Like Growth Factor IPolyphenolsTeaTumor Necrosis Factor-alpha

Identifiers

PMID35401920
PMCPMC8984065
OpenAlexW4226277689

What OpenQuestion holds

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Registered trials

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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.