Evidence map›Paper›PMID 33654384›Full record

ArticleDrug design, development and therapy2021

Convallatoxin Promotes M2 Macrophage Polarization to Attenuate Atherosclerosis Through PPARγ-Integrin α

Yi Zhang, Xiujin Shi, Jialun Han, Wenxing Peng, Zhenwei Fang, Yang Zhou, Xiaoyu Xu, Jie Lin, Fucheng Xiao, Limin Zhao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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  19. Roles of Macrophages in Atherogenesis.Frontiers in pharmacology · 2021
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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

11 authors at 3 institutions in 1 country.

Yi ZhangDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Xiujin ShiDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Jialun HanDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Wenxing PengDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Zhenwei FangDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Yang ZhouDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Xiaoyu XuDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Jie LinDepartment of Endocrinology and Metabolism, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Fucheng XiaoDepartment of Cardiovascular Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Limin ZhaoDepartment of Atherosclerosis, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, 100029, People's Republic of China.
Yang LinDepartment of Pharmacy, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, People's Republic of China.
Beijing Anzhen Hospital · CNCapital Medical University · CNBeijing Institute of Water · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAs the primary immune cells, macrophages play a key role in atherosclerotic progression. M2 macrophage polarization has been reported to promote tissue repair and attenuate plaque formation upon the expression of anti-inflammatory factors. Convallatoxin (CNT) is a natural cardiac glycoside with anti-inflammatory pharmacological properties. However, whether CNT protects against atherosclerosis (AS) and underlying mechanisms is unknown. This work was designed to explore the potential effects of CNT on atherosclerosis.

methodsIn this study, Apolipoprotein E deficiency (ApoE

resultsOur results showed that the atherosclerotic lesions were reduced by CNT, as demonstrated by the downregulation of serum lipid level and aortic plaque area in AS mice. Furthermore, we found that CNT treatment promoted the expression of M2 macrophage markers (Arg1, Mrc1, Retnla and Chi3l3), and decreased the levels of pro-inflammatory cytokines (IL-6 and TNF-α), accompanied by the increase of anti-inflammatory factor (IL-10) in aortic vessels of AS mice. In ox-LDL-induced RAW264.7 cells, CNT administration also facilitated macrophages polarizing towards M2 subtype and inhibited inflammatory responses. Furthermore, both the in vivo and in vitro experiments showed CNT could increase the expression of PPARγ, Integrin α

conclusionTaken together, these data suggest that CNT may promote M2 macrophage polarization to exert an anti-atherosclerotic effect, partially through activating PPARγ-Integrin α

Indexed as

AnimalsApolipoproteins EAtherosclerosisDose-Response Relationship, DrugMacrophage ActivationMacrophagesMiceMice, Inbred C57BLMice, KnockoutMolecular ConformationPPAR gammaRAW 264.7 CellsReceptors, VitronectinSignal TransductionStrophanthinsStructure-Activity RelationshipApolipoproteins Econvallatoxinintegrin alphaVbeta5PPAR gammaReceptors, VitronectinStrophanthinsatherosclerosisconvallatoxinmacrophage polarizationox-LDLPPARγ-Integrin αvβ5 signaling pathway

Identifiers

PMID33654384
PMCPMC7914072
OpenAlexW3133466577

What OpenQuestion holds

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Registered trials

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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.