Evidence map›Paper›PMID 26489513›Full record

ArticleCardiovascular diabetology2015

SIRT1 protects against myocardial ischemia-reperfusion injury via activating eNOS in diabetic rats.

Mingge Ding, Jingyi Lei, Hongcheng Han, Weibo Li, Yinxian Qu, Enqing Fu, Feng Fu, Xiaoming Wang

Open access · goldAbstract read
In one paragraph

Article in Cardiovascular diabetology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 3% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 133 citations in OpenAlex.

  1. Pooled it
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  16. The cardioprotective role of sirtuins is mediated in part by regulating KAmerican journal of physiology. Cell physiology · 2023
    Article
  17. Review
  18. The sirtuin family in health and disease.Signal transduction and targeted therapy · 2022
    Review
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  20. Review

8 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Mingge DingDepartment of Geriatrics, Xi'an Central Hospital, Xi'an, 710000, China. minggeding@163.com.
Jingyi LeiDepartment of Cardiology, Xi'an Central Hospital, Xi'an, 710000, China. 362304743@qq.com.
Hongcheng HanDepartment of Geriatrics, Xi'an Central Hospital, Xi'an, 710000, China. 435411499@qq.com.
Weibo LiDepartment of Geriatrics, Xi'an Central Hospital, Xi'an, 710000, China. 906144831@qq.com.
Yinxian QuDepartment of Geriatrics, Xi'an Central Hospital, Xi'an, 710000, China. 18991246091@126.com.
Enqing FuDepartment of Respiratory Medicine, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710032, China. fmmufuenqing@126.com.
Feng FuDepartment of Physiology, Fourth Military Medical University, 169 Changlexi Road, Xi'an, 710032, China. fufeng048@126.com.
Xiaoming WangDepartment of Geriatrics, Xijing Hospital, Fourth Military Medical University, 15 Changlexi Road, Xi'an, 710032, China. xmwang@fmmu.edu.cn.
First Hospital of Xi'an · CNXijing Hospital · CNAir Force Medical University · CNTang Du Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic patients are more sensitive to myocardial ischemic injury than non-diabetic patients. Silent information regulator 1 (SIRT1) is a nicotinamide adenine dinucleotide-dependent histone deacetylase making the heart more resistant to ischemic injury. As SIRT1 expression is considered to be reduced in diabetic heart, we therefore hypothesized that up-regulation of SIRT1 in the diabetic heart may overcome its increased susceptibility to ischemic injury.

methodsMale Sprague-Dawley rats were fed with high-fat diet and injected with streptozotocin once to induce diabetes. Diabetic rats received injections of adenoviral vectors encoding SIRT1 (Ad-SIRT1) at five myocardial sites. Four days after adenoviral injection, the rats were subjected to myocardial ischemia and reperfusion (MI/R). Outcome measures included left ventricular function, infarct size, cellular death and oxidative stress.

resultsDelivery of Ad-SIRT1 into the hearts of diabetic rats markedly increased SIRT1 expression. Up-regulation of SIRT1 in diabetic hearts improved cardiac function and reduced infarct size to the extent as in non-diabetic animals following MI/R, which was associated with reduced serum creatine kinase-MB, lactate dehydrogenase activities and cardiomyocyte apoptosis. Moreover, Ad-SIRT1 reduced the increase in the superoxide generation and malonaldialdehyde content and simultaneously increased the antioxidant capability. Furthermore, Ad-SIRT1 increased eNOS phosphorylation and reduced eNOS acetylation in diabetic hearts. NOS inhibitor L-NAME inhibited SIRT1-enhanced eNOS phosphorylation, and blunted SIRT1-mediated anti-apoptotic and anti-oxidative effects and cardioprotection.

conclusionsOverexpression of SIRT1 reduces diabetes-exacerbated MI/R injury and oxidative stress via activating eNOS in diabetic rats. The findings suggest SIRT1 may be a promising novel therapeutic target for diabetic cardiac complications.

Indexed as

AcetylationAnimalsApoptosisBlotting, WesternCreatine Kinase, MB FormDiabetes Mellitus, ExperimentalDiet, High-FatEnzyme InhibitorsGenetic VectorsL-Lactate DehydrogenaseMaleMalondialdehydeMyocardial InfarctionMyocardial Reperfusion InjuryMyocytes, CardiacNG-Nitroarginine Methyl EsterCreatine Kinase, MB FormEnzyme InhibitorsL-Lactate DehydrogenaseMalondialdehydeNG-Nitroarginine Methyl EsterNitric Oxide Synthase Type IIINos3 protein, ratSirt1 protein, ratSirtuin 1Superoxide DismutaseSuperoxides

Identifiers

PMID26489513
PMCPMC4618275
OpenAlexW1883271426

What OpenQuestion holds

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LicenceCC BY
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.