Evidence map›Paper›PMID 29904053›Full record

ArticleScientific reports2018

NaoXinTong Capsules inhibit the development of diabetic nephropathy in db/db mice.

Shu Yang, Mengyang Liu, Yuanli Chen, Chuanrui Ma, Lipei Liu, Buchang Zhao, Yong Wang, Xiaoju Li, Yan Zhu, Xiumei Gao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

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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

14 authors at 4 institutions in 1 country.

Shu YangCollege of Biomedical Engineering, Hefei University of Technology, Hefei, China.
Mengyang LiuTianjin University of Traditional Chinese Medicine, Tianjin, China.
Yuanli ChenCollege of Biomedical Engineering, Hefei University of Technology, Hefei, China.
Chuanrui MaTianjin University of Traditional Chinese Medicine, Tianjin, China.
Lipei LiuCollege of Life Sciences and Key Lab of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, China.
Buchang ZhaoBuchang Pharmaceutical Co. Ltd., Xi'an, China.
Yong WangBuchang Pharmaceutical Co. Ltd., Xi'an, China.
Xiaoju LiCollege of Life Sciences and Key Lab of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, China.
Yan ZhuTianjin University of Traditional Chinese Medicine, Tianjin, China.
Xiumei GaoTianjin University of Traditional Chinese Medicine, Tianjin, China.
Deling KongCollege of Life Sciences and Key Lab of Bioactive Materials of Ministry of Education, Nankai University, Tianjin, China.
Yajun DuanCollege of Biomedical Engineering, Hefei University of Technology, Hefei, China.
Jihong HanCollege of Biomedical Engineering, Hefei University of Technology, Hefei, China. jihonghan2008@nankai.edu.cn.
Xiaoxiao YangCollege of Biomedical Engineering, Hefei University of Technology, Hefei, China. yangxiaoxiao@hfut.edu.cn.
Nankai University · CNTianjin University of Traditional Chinese Medicine · CNBuchang Pharma (China) · CNHefei University of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NaoXinTong Capsule (NXT), a Chinese medicine, is currently used to treat patients with cardiovascular and cerebrovascular diseases. Clinical observations indicate its anti-diabetic functions with unclear mechanisms. Herein, we report the effect of NXT on diabetic nephropathy (DN). Type 2 diabetic db/db mice were treated with NXT for 14 weeks. In the course of treatment, NXT reduced diabetes-increased glucose levels and improved renal functions. At the end of treatment, we found that NXT ameliorated serum lipid profiles and other biochemical parameters. In the kidney, NXT inhibited mesangial matrix expansion, expression of vascular endothelial growth factor A, fibronectin, advanced glycation end product and its receptor. Meanwhile, it reduced the diabetes-induced podocyte injury by increasing WT1 and nephrin expression. In addition, NXT inhibited accumulation of extracellular matrix proteins by increasing MMP2/9 expression through inactivation of TGFβ/Smad pathway and CTGF expression. Mechanically, NXT activated insulin signaling pathway by increasing expression of INSR, IRS and FGF21, phosphorylation of Akt and AMPKα in the liver, INSR phosphorylation in the kidney, and FGF21 and GLUT4 expression in adipose tissue and skeletal muscle. Taken together, our study demonstrates that NXT inhibits DN by ameliorating glucose/lipid metabolism, maintaining tissue structure integrity, and correcting diabetes-induced renal dysfunctions.

Indexed as

AnimalsBlood GlucoseDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diabetic NephropathiesDrugs, Chinese HerbalGene Expression RegulationKidneyMiceBlood GlucoseDrugs, Chinese Herbalnaoxintong

Identifiers

PMID29904053
PMCPMC6002396
OpenAlexW2805086921

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.