Evidence map›Paper›PMID 30344697›Full record

ArticleExperimental and therapeutic medicine2018

Tanshinone IIA improves diabetes mellitus via the NF-κB-induced AMPK signal pathway.

Feng-Yi Yuan, Min Zhang, Ping Xu, Dan Xu, Ping Chen, Min Ren, Qin Sun, Jing-Yan Chen, Juan Du, Xia-Lian Tang

Open access · diamondAbstract read
In one paragraph

Article in Experimental and therapeutic medicine, 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
2.9field-weighted citation impact, top 10% 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, 16 citations in OpenAlex.

  1. Review
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  10. The Effects ofEvidence-based complementary and alternative medicine : eCAM · 2021
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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

10 authors at 2 institutions in 1 country.

Feng-Yi YuanDepartment of Endocrinology and Metabolism, Second Affiliated Hospital of Jinan University, Shenzhen, Guangdong 518020, P.R. China.
Min ZhangGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Ping XuDepartment of Endocrinology and Metabolism, Second Affiliated Hospital of Jinan University, Shenzhen, Guangdong 518020, P.R. China.
Dan XuDepartment of Endocrinology and Metabolism, Second Affiliated Hospital of Jinan University, Shenzhen, Guangdong 518020, P.R. China.
Ping ChenGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Min RenGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Qin SunGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Jing-Yan ChenGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Juan DuGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Xia-Lian TangGeriatric Department of Endocrinology, Sichuan Province People's Hospital and Sichuan Academy of Medical Sciences, Chengdu, Sichuan 610072, P.R. China.
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes mellitus (DM) is a systemic metabolic disease. Tanshinone IIA (Tan-IIA) presents potential benefits for DM. The purpose of this study was to investigate the efficacy of Tan-IIA in type 2 DM rats and explore its potential mechanism in renal cells. A type 2 DM rat model was established and administered with Tan-IIA or PBS. It was demonstrated that Tan-IIA treatment significantly reduced levels of total cholesterol, non-esterified fatty acids, total triglyceride and low-density lipoprotein cholesterol in experimental DM rats compared with the control group. The results indicated that Tan-IIA treatment significantly decreased levels of interleukin (IL)-8, tumor necrosis factor-α, C-reactive protein and IL-6. It was identified that Tan-IIA treatment significantly decreased nuclear factor-κB levels and significantly elevated 5' adenosine monophosphate-activated protein kinase levels. Western blot analysis indicated that Tan-IIA elevated immunocyte precipitation in renal cells. Furthermore, Tan-IIA treatment improved lipid metabolism, glucose metabolism, insulin resistance and body weight of type 2 DM rats. In conclusion, Tan-IIA administration may inhibit inflammatory cytokines and alleviate type 2 DM symptoms in experimental rats.

Indexed as

5′ adenosine monophosphate-activated protein kinaseinflammationnuclear factor-κBTanshinone IIAtype 2 diabetes mellitus

Identifiers

PMID30344697
PMCPMC6176167
OpenAlexW2888780556

What OpenQuestion holds

Textmetadata
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.