Evidence map›Paper›PMID 23658016›Full record

ArticleThe Journal of biological chemistry2013

High density lipoprotein protects against polymicrobe-induced sepsis in mice.

Ling Guo, Junting Ai, Zhong Zheng, Deborah A Howatt, Alan Daugherty, Bin Huang, Xiang-An Li

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
5.4field-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

71 citing papers in PubMed, 139 citations in OpenAlex.

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  12. SDMA as a marker and mediator in cerebrovascular disease.Clinical science (London, England : 1979) · 2024
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11 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

7 authors at 3 institutions in 2 countries.

Ling GuoDepartment of Pediatrics, University of Kentucky College of Medicine, Lexington, Kentucky 40536, USA.
Junting Ai
Zhong Zheng
Deborah A Howatt
Alan Daugherty
Bin Huang
Xiang-An Li
Pediatrics and Genetics · USCardiovascular Research Center · BRUniversity of Kentucky · US

Funding

Role of SR-BI in LPS detoxificationR01GM085231 · NIGMS · UNIVERSITY OF KENTUCKY · PI LI, XIANG-AN · 2008 to 2012
$1.5M
NIGMS NIH HHS R01 GM085231NIGMS NIH HHS R01 GM085231-2S1NIGMS NIH HHS R01 GM085231-5S1
6 · The paper itself

Abstract

HDL has been considered to be a protective factor in sepsis; however, most contributing studies were conducted using the endotoxic animal model, and evidence from clinically relevant septic animal models remains limited and controversial. Furthermore, little is known about the roles of HDL in sepsis other than LPS neutralization. In this study, we employed cecal ligation and puncture (CLP), a clinically relevant septic animal model, and utilized apoA-I knock-out (KO) and transgenic mice to elucidate the roles of HDL in sepsis. ApoA-I-KO mice were more susceptible to CLP-induced septic death as shown by the 47.1% survival of apoA-I-KO mice versus the 76.7% survival of C57BL/6J (B6) mice (p = 0.038). ApoA-I-KO mice had exacerbated inflammatory cytokine production during sepsis compared with B6 mice. Further study indicated that serum from apoA-I-KO mice displayed less capacity for LPS neutralization compared with serum from B6 mice. In addition, apoA-I-KO mice had less LPS clearance, reduced corticosterone generation, and impaired leukocyte recruitment in sepsis. In contrast to apoA-I-KO mice, apoA-I transgenic mice were moderately resistant to CLP-induced septic death compared with B6 mice. In conclusion, our findings reveal multiple protective roles of HDL in CLP-induced sepsis. In addition to its well established role in neutralization of LPS, HDL exerts its protection against sepsis through promoting LPS clearance and modulating corticosterone production and leukocyte recruitment. Our study supports efforts to raise HDL levels as a therapeutic approach for sepsis.

Indexed as

AnimalsApolipoprotein A-IBacterial InfectionsCecumCorticosteroneInterleukin-6LigationLipopolysaccharidesLipoproteinsLipoproteins, HDLMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNeutrophil InfiltrationPeritoneumApolipoprotein A-ICorticosteroneInterleukin-6LipopolysaccharidesLipoproteinsLipoproteins, HDLTumor Necrosis Factor-alphaApolipoprotein A-ICecal Ligation and PunctureDyslipidemiaHigh Density Lipoprotein (HDL)ImmunologyLipopolysaccharide (LPS)SCARB1Scavenger Receptor BISepsis

Identifiers

PMID23658016
PMCPMC3689940
OpenAlexW2050066090

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.