Evidence map›Paper›PMID 39267098›Full record

ArticleChinese medicine2024

DMDD, isolated from Averrhoa carambola L., ameliorates diabetic nephropathy by regulating endoplasmic reticulum stress-autophagy crosstalk.

Jianmei Shi, Yuxiang Wang, Tao Liang, Xixi Wang, Jingxiao Xie, Renbin Huang, Xiaohui Xu, Xiaojie Wei

Abstract read
In one paragraph

Article in Chinese medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
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.

Jianmei Shi *Department of Physiology, College of Basic Medicine, Guangxi University of Chinese Medicine, Nanning, 530021, Guangxi, China.
Yuxiang Wang *Pharmaceutical College, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Tao Liang *Key Laboratory of Research and Application of Stomatological Equipment (College of Stomatology, Hospital of Stomatology, Education Department of Guangxi Zhuang Autonomous Region, Guangxi Medical University), Nanning, 530021, Guangxi, China.
Xixi WangDepartment of Physiology, College of Basic Medicine, Guangxi University of Chinese Medicine, Nanning, 530021, Guangxi, China.
Jingxiao XiePharmaceutical College, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Renbin HuangPharmaceutical College, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Xiaohui XuDepartment of Pharmacy, Guangxi Medical University Cancer Hospital, Nanning, 530021, Guangxi, China. 1056112307@qq.com.
Xiaojie WeiDepartment of Physiology, College of Basic Medicine, Guangxi University of Chinese Medicine, Nanning, 530021, Guangxi, China. 116190888@qq.com.

Funding

Guangxi University of Chinese Medicine Doctoral Research Start-up Fund 2018BS010National Natural Science Foundation of China 82260881Natural Science Foundation of Guangxi Province 2023GXNSFBA026155
6 · The paper itself

Abstract

backgroundStudies have shown that Averrhoa carambola L. possesses therapeutic potential for diabetes and related complications. However, the specific beneficial effects and molecular mechanisms of 2-dodecyl-6-meth-oxycyclohexa-2,5-diene-1,4-dione (DMDD) isolated from Averrhoa carambola L. on diabetic nephropathy (DN) require further investigation.

methods80 C57BL/6 J male mice were subjected to a 1-week adaptive feeding, followed by a high-fat diet and intraperitoneal injection of 100 mg/kg streptozotocin (STZ) to construct an in vivo DN model. Additionally, human renal proximal tubular epithelial cells (HK-2) induced by high glucose (HG) were used as an in vitro DN model. The expression levels of epithelial-mesenchymal transition (EMT), endoplasmic reticulum stress (ERS), and autophagy-related proteins in renal tubular cells were detected by Western Blot, flow cytometry, immunofluorescence, and enzyme-linked immunosorbent assay (ELISA) staining. Transcriptome analysis revealed was conducted to elucidate the specific mechanism of by which DMDD mitigates DN by inhibiting ERS and autophagy. HK-2 cells were transfected with IRE1α overexpression lentivirus to reveal the role of IRE1α overexpression in HG-induced HK-2.

resultsThe experimental data showed that DMDD significantly reduced blood glucose levels and improved renal pathological alterations in DN mice. Additionally, DMDD inhibited the calcium (Ca

conclusionDMDD effectively inhibits excessive ERS and autophagy, thereby reducing renal cell apoptosis through the IRE1α pathway and Ca

Indexed as

2-Dodecyl-6-Meth-Oxycyclohexa-2,5-Diene-1,4-DioneAutophagyDiabetic nephropathyEndoplasmic reticulum stress

Identifiers

PMID39267098
PMCPMC11391757

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.