Evidence map›Paper›PMID 38065945›Full record

ArticleNature communications2023

Chiral metal-organic frameworks incorporating nanozymes as neuroinflammation inhibitors for managing Parkinson's disease.

Wei Jiang, Qing Li, Ruofei Zhang, Jianru Li, Qianyu Lin, Jingyun Li, Xinyao Zhou, Xiyun Yan, Kelong Fan

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
12.7field-weighted citation impact, top 1% 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

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

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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

9 authors at 4 institutions in 2 countries.

Wei Jiang *Application Center for Precision Medicine, the Second Affiliated Hospital of Zhengzhou University, Henan, 450052, China.ORCID 0000-0002-5306-1398
Qing Li *Application Center for Precision Medicine, the Second Affiliated Hospital of Zhengzhou University, Henan, 450052, China. lq1515012032@163.com.ORCID 0000-0002-5290-1172
Ruofei ZhangCAS Engineering Laboratory for Nanozyme, Key Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Beijing, 100101, China.
Jianru LiCAS Engineering Laboratory for Nanozyme, Key Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, 15 Datun Road, Beijing, 100101, China.
Qianyu LinApplication Center for Precision Medicine, the Second Affiliated Hospital of Zhengzhou University, Henan, 450052, China.
Jingyun LiNanozyme Medical Center, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Xinyao ZhouSchool of Engineering and Applied Science, University of Pennsylvania, Philadelphia, 19104, USA.
Xiyun YanNanozyme Medical Center, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, 450001, China. yanxy@ibp.ac.cn.ORCID 0000-0002-7290-352X
Kelong FanNanozyme Medical Center, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, 450001, China. fankelong@ibp.ac.cn.ORCID 0000-0001-6285-1933
Chinese Academy of Sciences · CNSecond Affiliated Hospital of Zhengzhou University · CNZhengzhou University · CNUniversity of Pennsylvania · US

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82122037Youth Innovation Promotion Association of the Chinese Academy of Sciences (Youth Innovation Promotion Association CAS) 2019093
6 · The paper itself

Abstract

Nanomedicine-based anti-neuroinflammation strategy has become a promising dawn of Parkinson's disease (PD) treatment. However, there are significant gaps in our understanding of the therapeutic mechanisms of antioxidant nanomedicines concerning the pathways traversing the blood-brain barrier (BBB) and subsequent inflammation mitigation. Here, we report nanozyme-integrated metal-organic frameworks with excellent antioxidant activity and chiral-dependent BBB transendocytosis as anti-neuroinflammatory agents for the treatment of PD. These chiral nanozymes are synthesized by embedding ultra-small platinum nanozymes (Ptzymes) into L-chiral and D-chiral imidazolate zeolite frameworks (Ptzyme@L-ZIF and Ptzyme@D-ZIF). Compared to Ptzyme@L-ZIF, Ptzyme@D-ZIF shows higher accumulation in the brains of male PD mouse models due to longer plasma residence time and more pathways to traverse BBB, including clathrin-mediated and caveolae-mediated endocytosis. These factors contribute to the superior therapeutic efficacy of Ptzyme@D-ZIF in reducing behavioral disorders and pathological changes. Bioinformatics and biochemical analyses suggest that Ptzyme@D-ZIF inhibits neuroinflammation-induced apoptosis and ferroptosis in damaged neurons. The research uncovers the biodistribution, metabolic variances, and therapeutic outcomes of nanozymes-integrated chiral ZIF platforms, providing possibilities for devising anti-PD drugs.

Indexed as

Metal-Organic FrameworksParkinson DiseaseAnimalsAntioxidantsMaleMiceNeuroinflammatory DiseasesTissue DistributionAntioxidantsMetal-Organic Frameworks

Identifiers

PMID38065945
PMCPMC10709450
OpenAlexW4389485169

What OpenQuestion holds

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LicenceCC BY
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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.