Evidence map›Paper›PMID 37464341›Full record

ArticleMolecular medicine (Cambridge, Mass.)2023

Compound Qiying Granules alleviates diabetic peripheral neuropathy by inhibiting endoplasmic reticulum stress and apoptosis.

Yan Hu, Chen Chen, Zhengting Liang, Tao Liu, Xiaoling Hu, Guanying Wang, Jinxia Hu, Xiaolin Xie, Zhiyan Liu

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 2 institutions in 1 country.

Yan Hu *Xinjiang Medical University, Urumqi, 830011, Xinjiang, China.
Chen Chen *Xinjiang Medical University, Urumqi, 830011, Xinjiang, China.
Zhengting LiangXinjiang Medical University, Urumqi, 830011, Xinjiang, China.
Tao LiuXinjiang Medical University, Urumqi, 830011, Xinjiang, China. ltdoctor2001@126.com.ORCID 0000-0001-5756-6097
Xiaoling HuTraditional Chinese Medicine Hospital Affiliated With Xinjiang Medical University, Urumqi, 830000, Xinjiang, China.
Guanying WangGuizhou University of Traditional Chinese Medicine, Guiyang, 550025, Guizhou, China.
Jinxia HuTraditional Chinese Medicine Hospital Affiliated With Xinjiang Medical University, Urumqi, 830000, Xinjiang, China. hujinxia202210@126.com.
Xiaolin XieXinjiang Medical University, Urumqi, 830011, Xinjiang, China.
Zhiyan LiuXinjiang Medical University, Urumqi, 830011, Xinjiang, China.
Xinjiang Medical University · CNGuizhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic peripheral neuropathy (DPN) is a major complication of diabetes. This study aimed to investigate the therapeutic effects and molecular mechanisms of Compound Qiying Granules (CQYG) for DPN.

methodsRats and RSC96 cells of DPN models were established to evaluate the therapeutic effects of CQYG. Then the morphology and apoptotic changes of sciatic nerves were detected. Further, tandem mass tag based quantitative proteomics technology was used to identify differentially expressed proteins (DEPs) and the underlying molecular mechanisms. Protein expression of key signaling pathways was also detected.

resultsCQYG treatment significantly improved blood glucose and oxidative stress levels, and further reduced nerve fiber myelination lesions, denervation, and apoptosis in DPN rats. Further, 2176 DEPs were found in CQYG treated DPN rats. Enrichment analysis showed that protein processing in the endoplasmic reticulum (ER), and apoptosis were all inhibited after CQYG treatment. Next, CQYG treatment reduced inflammatory factor expression, mitochondrial damage, and apoptosis in RSC96 cells which induced by high glucose. Transmission electron microscopy results found that CQYG treatment improved the morphology of nerve myelin, mitochondria, and ER. CQYG treatment decreased ER stress and apoptosis pathway proteins that were highly expressed in DPN models. In addition, we also predicted the potential targets of CQYG in DEPs.

conclusionsCQYG exerts neuroprotective effects in experimental diabetic neuropathy through anti-ER stress and anti-apoptosis.

Indexed as

Diabetes MellitusDiabetic NeuropathiesAnimalsEndoplasmic Reticulum StressMyelin SheathRatsRats, Sprague-DawleySciatic NerveSignal TransductionApoptosisCQYGDiabetic peripheral neuropathyDifferentially expressed proteinsER stress

Identifiers

PMID37464341
PMCPMC10354983
OpenAlexW4384664188

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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.