Evidence map›Paper›PMID 42151142›Full record

ArticleNature communications2026

Advanced nanoformulations of NUAK1 regulate NLRP3 inflammasome for preeclampsia management in mice.

Peiyue Jiang, Xue Ying, Zhi Li, Weidong Fei, Yao Yao, Jia Xu, Hetong Li, Lujiao Chen, Qiong Luo

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Peiyue JiangDepartment of Obstetrics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xue YingDepartment of Obstetrics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zhi LiDepartment of Obstetrics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Weidong FeiDepartment of Pharmacy, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yao YaoDepartment of Pharmacy, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-4560-6861
Jia XuDepartment of Obstetrics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Hetong LiSchool of Medicine, Zhejiang University, Hangzhou, China.
Lujiao ChenSchool of Medicine, Zhejiang University, Hangzhou, China.
Qiong LuoDepartment of Obstetrics, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, China. luoq@zju.edu.cn.ORCID http://orcid.org/0000-0002-0782-4462

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preeclampsia (PE) is a severe pregnancy complication driven by placental dysfunction and oxidative stress, which currently lacks effective targeted therapies. Here, we evaluated the therapeutic potential of folic acid-modified lipid nanoparticles (NPs) co-loaded with polydopamine and NUAK Family Kinase 1 (NUAK1), termed FLN@(PDA + NUAK1) NPs, for mitigating PE. In vitro, these NPs effectively reduced reactive oxygen species levels and suppressed activation of the NLR Family Pyrin Domain Containing 3 (NLRP3) inflammasome, while promoting autophagic activity and inhibiting apoptosis under oxidative stress. In vivo analysis using an L-NAME-induced PE mouse model further confirmed that FLN@(PDA + NUAK1) NPs improved placental structure and fetal growth parameters. This study highlights the dual functionality of NPs in activating protective autophagy and suppressing inflammasome overactivation, offering a promising strategy for the treatment of PE.

Indexed as

InflammasomesNanoparticlesNLR Family, Pyrin Domain-Containing 3 ProteinPre-EclampsiaAnimalsApoptosisAutophagyDisease Models, AnimalFemaleHumansMiceMice, Inbred C57BLNG-Nitroarginine Methyl EsterOxidative StressPlacentaPregnancyInflammasomesNG-Nitroarginine Methyl EsterNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseReactive Oxygen Species

Identifiers

PMID42151142
PMCPMC13381823

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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.