Evidence map›Paper›PMID 30002491›Full record

ArticleActa pharmacologica Sinica2019

Perivascular adipose tissue dysfunction aggravates adventitial remodeling in obese mini pigs via NLRP3 inflammasome/IL-1 signaling pathway.

Xiao Zhu, Hong-Wen Zhang, Hai-Nan Chen, Xiao-Jun Deng, Yi-Xuan Tu, Ampadu O Jackson, Ji-Na Qing, Ai-Ping Wang, Vaibhav Patel, Kai Yin

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

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  15. Extracellular vesicles in vascular remodeling.Acta pharmacologica Sinica · 2022
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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

10 authors at 2 institutions in 2 countries.

Xiao ZhuResearch Lab of Translational Medicine, Medical School, University of South China, Hengyang, 421001, China.
Hong-Wen ZhangDepartment of Interventional Medicine, The Affiliated Hospital of University of South China, Hengyang, 421001, China.
Hai-Nan ChenResearch Lab of Translational Medicine, Medical School, University of South China, Hengyang, 421001, China.
Xiao-Jun DengDepartment of Interventional Medicine, The Affiliated Hospital of University of South China, Hengyang, 421001, China.
Yi-Xuan TuResearch Lab of Translational Medicine, Medical School, University of South China, Hengyang, 421001, China.
Ampadu O JacksonResearch Lab of Translational Medicine, Medical School, University of South China, Hengyang, 421001, China.
Ji-Na QingResearch Lab of Translational Medicine, Medical School, University of South China, Hengyang, 421001, China.
Ai-Ping WangDepartment of Anatomy, Medical School, University of South China, Hengyang, 421001, China.
Vaibhav PatelDepartment of Physiology & Pharmacology, Cumming School of Medicine, Libin Cardiovascular Institute of Alberta, University of Calgary, Calgary, AB, T2N1N4, Canada.
Kai YinResearch Lab of Translational Medicine, Medical School, University of South China, Hengyang, 421001, China. kaiyinby@qq.com.
University of South China · CNUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perivascular adipose tissue (PVAT), a special type of adipose tissue, closely surrounds vascular adventitia and produces numerous bioactive substances to maintain vascular homeostasis. PVAT dysfunction has a crucial role in regulating vascular remodeling, but the exact mechanisms remain unclear. In this study, we investigated whether and how obesity-induced PVAT dysfunction affected adventitia remodeling in early vascular injury stages. Mini pigs were fed a high sugar and fat diet for 6 months to induce metabolic syndrome and obesity. In the mini pigs, left carotid vascular injury was then generated using balloon dilation. Compared with normal mini pigs, obese mini pigs displayed significantly enhanced vascular injury-induced adventitial responses, evidenced by adventitia fibroblast (AF) proliferation and differentiation, and adventitia fibrosis, as well as exacerbated PVAT dysfunction characterized by increased accumulation of resident macrophages, particularly the M1 pro-inflammatory phenotype, increased expression of leptin and decreased expression of adiponectin, and production of pro-inflammatory cytokines interleukin (IL)-1β and IL-18. Primary AFs cultured in PVAT-conditioned medium from obese mini pigs also showed significantly increased proliferation and differentiation. We further revealed that activated nod-like receptor protein 3 (NLRP3) inflammasome and its downstream products, i.e., IL-1 family members such as IL-1β and IL-18 were upregulated in the PVAT of obese mini pigs; PVAT dysfunction was also demonstrated in preadipocytes treated with palmitic acid. Finally, we showed that pretreatment with IL-1 receptor (IL-1R) antagonist or IL-1R knockdown blocked AF proliferation and differentiation in AFs cultured in PVAT-conditioned medium. These results demonstrate that obesity-induced PVAT dysfunction aggravates adventitial remodeling after early vascular injury with elevated AF proliferation and differentiation via activating the NLRP3/IL-1 signaling pathway.

Indexed as

Adipose TissueAdventitiaAnimalsBlood VesselsCell DifferentiationCell ProliferationFibroblastsInflammasomesInterleukin-1NLR Family, Pyrin Domain-Containing 3 ProteinObesitySignal TransductionSwineSwine, MiniatureVascular RemodelingInflammasomesInterleukin-1NLR Family, Pyrin Domain-Containing 3 Proteinadventitia fibroblastsIL-1NLRP3 inflammasomeobese mini pigsobesityperivascular adipose tissuepreadipocytesPVAT dysfunction

Identifiers

PMID30002491
PMCPMC6318288
OpenAlexW2839977856

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.