Evidence map›Paper›PMID 36430617›Full record

ArticleInternational journal of molecular sciences2022

Silencing P2X7R Alleviates Diabetic Neuropathic Pain Involving TRPV1 via PKCε/P38MAPK/NF-κB Signaling Pathway in Rats.

Lisha Chen, Hongji Wang, Juping Xing, Xiangchao Shi, Huan Huang, Jiabao Huang, Changshui Xu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 36 citations in OpenAlex.

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  8. Activation of µ-δ Opioid Receptor Heteromer Attenuates Chemotherapy-Induced Neuropathic Pain in Mice.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Article
  9. Review
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  11. Electroacupuncture regulates the P2XPurinergic signalling · 2025
    Article
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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.

Lisha ChenDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Hongji WangDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Juping XingDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Xiangchao ShiDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Huan HuangDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Jiabao HuangDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Changshui XuDepartment of Physiology, Basic Medical College of Nanchang University, Nanchang 330006, China.
Nanchang University · CNFirst Affiliated Hospital of Jiangxi Medical College · CN

Funding

high-level and high-skilled leading talents training project of Jiangxi Province in 2021 2022233071National Natural Science Foundation of China 81660199National Natural Science Foundation of China 82060247Natural Science Foundation of Jiangxi Province 20202BAB206027
6 · The paper itself

Abstract

Transient receptor potential vanillic acid 1 (TRPV1) is an ion channel activated by heat and inflammatory factors involved in the development of various types of pain. The P2X7 receptor is in the P2X family and is associated with pain mediated by satellite glial cells. There might be some connection between the P2X7 receptor and TRPV1 in neuropathic pain in diabetic rats. A type 2 diabetic neuropathic pain rat model was induced using high glucose and high-fat diet for 4 weeks and low-dose streptozocin (35 mg/kg) intraperitoneal injection to destroy islet B cells. Male Sprague Dawley rats were administrated by intrathecal injection of P2X7 shRNA and p38 inhibitor, and we recorded abnormal mechanical and thermal pain and nociceptive hyperalgesia. One week later, the dorsal root ganglia from the L4-L6 segment of the spinal cord were harvested for subsequent experiments. We measured pro-inflammatory cytokines, examined the relationship between TRPV1 on neurons and P2X7 receptor on satellite glial cells by measuring protein and transcription levels of P2X7 receptor and TRPV1, and measured protein expression in the PKCε/P38 MAPK/NF-κB signaling pathway after intrathecal injection. P2X7 shRNA and p38 inhibitor relieved hyperalgesia in diabetic neuropathic pain rats and modulated inflammatory factors in vivo. P2X7 shRNA and P38 inhibitors significantly reduced TRPV1 expression by downregulating the PKCε/P38 MAPK/NF-κB signaling pathway and inflammatory factors in dorsal root ganglia. Intrathecal injection of P2X7 shRNA alleviates nociceptive reactions in rats with diabetic neuropathic pain involving TRPV1 via PKCε/P38 MAPK/NF-κB signaling pathway.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic NeuropathiesNeuralgiaReceptors, Purinergic P2X7AnimalsHyperalgesiaMaleNF-kappa Bp38 Mitogen-Activated Protein KinasesProtein Kinase C-epsilonRatsRats, Sprague-DawleyRNA, Small InterferingSignal TransductionTRPV Cation ChannelsNF-kappa Bp38 Mitogen-Activated Protein KinasesPrkce protein, ratProtein Kinase C-epsilonReceptors, Purinergic P2X7RNA, Small InterferingTrpv1 protein, ratTRPV Cation ChannelsDNPneuronP2X7 receptorsatellite glial cellTRPV1

Identifiers

PMID36430617
PMCPMC9696864
OpenAlexW4309269504

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.