Evidence map›Paper›PMID 35540763›Full record

ArticleRSC advances2018

Thymoquinone protects against cardiac damage from doxorubicin-induced heart failure in Sprague-Dawley rats.

Zuowei Pei, Jiahui Hu, Qianru Bai, Baiting Liu, Dong Cheng, Hainiang Liu, Rongmei Na, Qin Yu

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 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

8 authors at 2 institutions in 1 country.

Zuowei PeiDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.ORCID https://orcid.org/0000-0002-1009-0025
Jiahui HuDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.
Qianru BaiDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.
Baiting LiuInternational Medical Department, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian China.
Dong ChengDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.
Hainiang LiuDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.
Rongmei NaDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.
Qin YuDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University No. 6 Jiefang Street Dalian 116001 China yuqin@dlu.edu.cn +86-0411-62893517 +86-0411-62893517.
Affiliated Zhongshan Hospital of Dalian University · CNDalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure is a complex end stage result of various cardiovascular diseases, and has a poor prognosis. The mechanisms for the development and progression of heart failure have always been an important topic in cardiovascular research, and previous studies have shown that thymoquinone (TQ) protects against cardiotoxicity and cardiac damage. The aim of this study was to investigate the possible protective effects of thymoquinone against cardiac damage in doxorubicin (DOX)-induced heart failure in Sprague-Dawley Rats (SDR). Forty-five male SDR were randomly divided into three groups and administered different treatment regimens for 8 weeks. Left ventricular fractional shortening (LVFS) and ejection fraction (LVEF) were higher in the DOX + TQ group than those in the DOX group. Significant pathophysiology changes (HE and Masson staining) were observed in rats of the DOX group compared to those of the DOX + TQ group. The addition of Thymoquinone inhibited DOX-induced cardiac fibrosis (TGF-β, Smad3, collagen I, collagen III, and α-SMA) and apoptosis (P53, bcl-2, caspase-3, caspase-9, and BAX) in SDR, indicating that thymoquinone may be a potential therapeutic target for cardiac damage caused by DOX-induced heart failure.

Identifiers

PMID35540763
PMCPMC9081863
OpenAlexW2800919076

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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.