Evidence map›Paper›PMID 30373106›Full record

ArticleInternational journal of molecular sciences2018

Protective Effects of Kaempferitrin on Advanced Glycation End Products Induce Mesangial Cell Apoptosis and Oxidative Stress.

Wenxian Jiang, Rongshen Wang, Di Liu, Min Zuo, Chunzhen Zhao, Tianliang Zhang, Wanzhong Li

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
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  8. Article
  9. Article
  10. Article
  11. Terpenoids from the Seeds ofMolecules (Basel, Switzerland) · 2022
    Article
  12. Review
  13. Review
  14. Effects ofExperimental and therapeutic medicine · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Pharmaceutical biology · 2019
    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

7 authors at 1 institution in 1 country.

Wenxian JiangSchool of Pharmacy, Weifang Medical University, Weifang 261053, China. jiangwenxian123@163.com.
Rongshen WangSchool of Pharmacy, Weifang Medical University, Weifang 261053, China. wangrs199012@126.com.ORCID 0000-0003-4504-531X
Di LiuSchool of Pharmacy, Weifang Medical University, Weifang 261053, China. ld0928928@163.com.
Min ZuoSchool of Pharmacy, Weifang Medical University, Weifang 261053, China. ZuoMin1026@163.com.
Chunzhen ZhaoSchool of Pharmacy, Weifang Medical University, Weifang 261053, China. zhaochunzhen@wfmc.edu.cn.
Tianliang ZhangExperimental Center for Medical Research, Weifang Medical University, Weifang 261053, China. zhangtl@wfmc.edu.cn.
Wanzhong LiSchool of Pharmacy, Weifang Medical University, Weifang 261053, China. liwz@wfmc.edu.cn.
Weifang Medical University · CN

Funding

National Nature Science Foundation of China 81274049Natural Science Foundation of Shandong Province ZR2018MH040Staring Foundation for Doctorate Research of Weifang medical university 2017BSQD50
6 · The paper itself

Abstract

Advanced glycation end products (AGEs) and the receptor for AGEs (RAGE) both play important roles in diabetic nephropathy (DN). Previous studies have identified glomerular mesangial cells (GMCs) injury as a key early risk factor in the development of DN. Kaempferitrin (KM) is a potent antioxidant with hypoglycemic action. Although KM is known to protect against AGE-induced damage in GMCs, the effects and the mechanisms by which they occur are poorly understood. In this study, cultured rat GMCs were exposed to AGE-induced oxidative stress (OS) to model DN in vitro. Reactive oxygen species (ROS) was analyzed by 2',7'-dichlorofluorescin diacetate (DCFH-DA). Superoxide dismutase (SOD) and malondialdehyde (MDA) were studied using commercial kits. Mitochondrial membrane potential (Δψm) was measured by rhodamine 123. Hoechst 33258 and annexin V and propidium iodide (PI) double staining were performed to observe the apoptosis states in GMCs, whereas apoptosis and protective mechanism in AGE-induced GMCs were investigated by Western blot. The data revealed that KM effectively increased SOD activity, decreased MDA levels, suppressed ROS generation, and protected against OS in AGE-induced GMCs. Treatment with KM also inhibited the expression of collagen IV and transforming growth factor-β1 (TGF-β1), improved mitochondrial membrane potential recovery, and suppressed the mitochondrial/cytochrome c-mediated apoptosis pathway through the expression of anti-apoptotic factors in GMCs in vitro. These findings suggest that KM may be a new potential agent in the treatment of DN in future.

Indexed as

AnimalsAntioxidantsApoptosisCell LineDiabetic NephropathiesGlycation End Products, AdvancedKaempferolsMalondialdehydeMesangial CellsOxidative StressRatsSignal TransductionSuperoxide DismutaseAntioxidantsGlycation End Products, AdvancedKaempferolslespenefrilMalondialdehydeSuperoxide Dismutaseadvanced glycation end productsapoptosiskaempferitrinmesangial cellsoxidative stresssignal pathway

Identifiers

PMID30373106
PMCPMC6274833
OpenAlexW2898553891

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.