Evidence map›Paper›PMID 30343389›Full record

ArticleInflammation2019

Role of Thymoquinone in Cardiac Damage Caused by Sepsis from BALB/c Mice.

Hongyang Liu, Yan Sun, Ying Zhang, Guang Yang, Lipeng Guo, Yue Zhao, Zuowei Pei

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  15. Recent Progress on Chemical Constituents and Pharmacological Effects of the GenusEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  16. Article
  17. Article
  18. Role of TXNIP/NLRP3 in sepsis-induced myocardial dysfunction.International journal of molecular medicine · 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 3 institutions in 1 country.

Hongyang LiuDepartment of Heart Intensive Care Unit, The First Affiliated Hospital of Dalian Medical University, No.193 Lianhe Road, Dalian, China.
Yan SunDepartment of Cardiology, Zhejiang Rongjun Hospital, No.309 Shuangyuan Road, Jiaxing, Zhejiang, China.
Ying ZhangDepartment of Cardiology, The First Affiliated Hospital of Dalian Medical University, 193# Lianhe Road, Dalian, China.
Guang YangDepartment of Heart Intensive Care Unit, The First Affiliated Hospital of Dalian Medical University, No.193 Lianhe Road, Dalian, China.
Lipeng GuoDepartment of Cardiology, Dalian Third People's Hospital Affiliated to Dalian Medical University, No.40 Qianshan Road, Dalian, China.
Yue ZhaoGraduate school of Dalian Medical University, No.9 Lvshun South Road, Dalian, China.
Zuowei PeiDepartment of Cardiology, Affiliated Zhongshan Hospital of Dalian University, No. 6 Jiefang Street, Dalian, 116001, China. pzw_dl@163.com.
Dalian Medical University · CNAffiliated Zhongshan Hospital of Dalian University · CNFirst Affiliated Hospital of Dalian Medical University · CN

Funding

Posterdoctor Foundation of Liaoning Province (CN) No. 194008
6 · The paper itself

Abstract

Sepsis is a major health complication causing patient mortality and increased healthcare costs. Cardiac dysfunction, an important consequence of sepsis, affects mortality. We previously reported that thymoquinone (TQ) protected against hyperlipidemia and doxorubicin-induced cardiac damage. This study investigated the possible protective effects of TQ against cardiac damage in septic BALB/c mice. Eight-week-old male BALB/c mice were divided into four groups: control, TQ, cecal ligation and puncture (CLP), and TQ + CLP. CLP was performed after 2-week TQ gavage. After 48 h, we measured the histopathological alterations of the cardiac tissue and the plasma levels of troponin-T (cTnT) and ATP. We evaluated autophagy (p62 and beclin 1), pyroptosis (NLRP3, caspase-1, interleukin [IL]-1β, and IL-18) at the gene and protein levels and IL-6 and tumor necrosis factor-α (TNF-α) at the gene level. Our results demonstrated that TQ administration significantly reduced intestinal histological alterations. TQ inhibited plasma cTnT levels; improved ATP; significantly inhibited p62, NLRP3, caspase-1, IL-1β, IL-18, IL-6, TNF-α, and MCP-1expressions; and increased beclin 1 and IL-10 level. The phosphatidylinositide 3-kinase level was significantly decreased in the TQ + CLP group versus the CLP group. These results suggest that TQ effectively modulates autophagy, pyroptosis, and pro-inflammatory, making it important in the treatment of sepsis-induced cardiac damage.

Indexed as

AnimalsAutophagyBenzoquinonesCytokinesHeart DiseasesInflammationMaleMiceMice, Inbred BALB CPhosphatidylinositol 3-KinasesProtective AgentsPyroptosisSepsisTroponin TBenzoquinonesCytokinesPhosphatidylinositol 3-KinasesProtective AgentsthymoquinoneTroponin TBALB/c micecardiac damagepyroptosissepsisthymoquinone

Identifiers

PMID30343389
OpenAlexW2897572516

What Socratic 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 Socratic graph.