Evidence map›Paper›PMID 26617721›Full record

ArticleInternational journal of clinical and experimental pathology2015

Baicalin ameliorates isoproterenol-induced acute myocardial infarction through iNOS, inflammation and oxidative stress in rat.

Huaguo Chen, Yongfu Xu, Jianzhong Wang, Wei Zhao, Huihui Ruan

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In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 65 citations in OpenAlex.

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  18. Therapeutic Application of Betalains: A Review.Plants (Basel, Switzerland) · 2020
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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

5 authors at 2 institutions in 1 country.

Huaguo ChenDepartment of Emergency, Shanghai Tenth People's Hospital, Tongji University School of Medicine 301 Yanchang Road, Shanghai 200072, China.
Yongfu XuDepartment of Emergency, Shanghai Tenth People's Hospital, Tongji University School of Medicine 301 Yanchang Road, Shanghai 200072, China.
Jianzhong WangDepartment of Emergency, Shanghai Tenth People's Hospital, Tongji University School of Medicine 301 Yanchang Road, Shanghai 200072, China.
Wei ZhaoDepartment of Emergency, Shanghai Tenth People's Hospital, Tongji University School of Medicine 301 Yanchang Road, Shanghai 200072, China.
Huihui RuanDepartment of Emergency, Shanghai Tenth People's Hospital, Tongji University School of Medicine 301 Yanchang Road, Shanghai 200072, China.
Shanghai Tenth People's Hospital · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Baicalin belongs to glucuronic acid glycosides and after hydrolysis baicalein and glucuronic acid come into being. It has such effects as clearing heat and removing toxicity, anti-inflammation, choleresis, bringing high blood pressure down, diuresis, anti-allergic reaction and so on. In this study, we investigated whether baicalin ameliorates isoproterenol-induced acute myocardial infarction and its mechanism. Rat model of acute myocardial infarction was induced by isoproterenol. Casein kinase (CK), the MB isoenzyme of creatine kinase (CK-MB), lactate dehydrogenase (LDH), cardiac troponin T (cTnT) and infarct size measurement were used to measure the protective effect of baicalin on isoproterenol-induced acute myocardial infarction. iNOS protein expression in rat was analyzed using western blot analysis. Tumor necrosis factor-alpha (TNF-α), interleukin 6 (IL-6), malondialdehyde (MDA) and superoxide dismutase (SOD) and caspase-3 activation levels were explored using commercial ELISA kits. In the acute myocardial infarction experiment, baicalin effectively ameliorates the level of CK, CK-MB, LDH and cTnT, reduced infarct size in acute myocardial infarction rat model. Meanwhile, treatment with baicalin effectively decreased the iNOS protein expression, inflammatory factors and oxidative stresses in a rat model of acute myocardial infarction. However, baicalin emerged that anti-apoptosis activity and suppressed the activation of caspase-3 in a rat model of acute myocardial infarction. The data suggest that the protective effect of baicalin ameliorates isoproterenol-induced acute myocardial infarction through iNOS, inflammation and oxidative stress in rat.

Indexed as

AnimalsApoptosisCasein KinasesCaspase 3Creatine Kinase, MB FormEnzyme InhibitorsFlavonoidsInflammationInterleukin-6IsoproterenolL-Lactate DehydrogenaseMaleMalondialdehydeMyocardial InfarctionNitric Oxide Synthase Type IIOxidative StressbaicalinCasein KinasesCaspase 3Creatine Kinase, MB FormEnzyme InhibitorsFlavonoidsInterleukin-6IsoproterenolL-Lactate DehydrogenaseMalondialdehydeNitric Oxide Synthase Type IISuperoxide DismutaseTroponin TTumor Necrosis Factor-alphaacute myocardial infarctionBaicalininflammationINOSisoproterenoloxidative stress

Identifiers

PMID26617721
PMCPMC4637536
OpenAlexW2211693855

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.