Evidence map›Paper›PMID 39556713›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Discovery of Balasubramide Derivative with Tissue-Specific Anti-Inflammatory Activity Against Acute Lung Injury by Targeting VDAC1.

Jin-Qian Song, Li-Juan Shen, Hao-Jie Wang, Qi-Bing Liu, Lian-Bao Ye, Kui Liu, Lei Shi, Bin Cai, Han-Sen Lin, Tao Pang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
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.

Jin-Qian SongState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, Key Laboratory of Drug Quality Control and Pharmacovigilance (Ministry of Education), China Pharmaceutical University, Nanjing, 210009, P. R. China.
Li-Juan ShenIntensive Care Unit, Department of Anorectal Surgery, Wuxi Hospital Affiliated to Nanjing University of Chinese Medicine, Wuxi, 214071, P. R. China.
Hao-Jie WangState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, Key Laboratory of Drug Quality Control and Pharmacovigilance (Ministry of Education), China Pharmaceutical University, Nanjing, 210009, P. R. China.
Qi-Bing LiuDepartment of Pharmacy, the First Affiliated Hospital of Hainan Medical University & Engineering Research Center of Tropical Medicine Innovation and Transformation, Ministry of Education, Hainan Medical University, Haikou, 571199, P.R. China.
Lian-Bao YeCollege of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, P. R. China.
Kui LiuState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, Key Laboratory of Drug Quality Control and Pharmacovigilance (Ministry of Education), China Pharmaceutical University, Nanjing, 210009, P. R. China.
Lei ShiCollege of Basic Medical Sciences, Dalian Medical University, No. 9 West Section, South Lv shun Road, Dalian, 116044, P. R. China.
Bin CaiIntensive Care Unit, Department of Anorectal Surgery, Wuxi Hospital Affiliated to Nanjing University of Chinese Medicine, Wuxi, 214071, P. R. China.
Han-Sen LinCollege of Pharmacy, Guangdong Pharmaceutical University, Guangzhou, 510006, P. R. China.
Tao PangState Key Laboratory of Natural Medicines, New Drug Screening and Pharmacodynamics Evaluation Center, Key Laboratory of Drug Quality Control and Pharmacovigilance (Ministry of Education), China Pharmaceutical University, Nanjing, 210009, P. R. China.ORCID 0000-0001-5420-2060

Funding

2024 Guangdong Pharmaceutical University's "Discipline Training Excellence, Innovation and Quality Improvement" Engineering Team Project No.2024ZZ05Department of Science and Technology of Guangdong Province 2015A020211031Department of Science and Technology of Guangdong Province 2016A020217022Double First-Class Project of China Pharmaceutical University CPUQNJC22_02National Natural Science Foundation of China 81973512National Natural Science Foundation of China 82174010National Natural Science Foundation of China 82205110Natural Medicines of China Pharmaceutical University SKLNMKF202405Open Project of Engineering Research Center of Tropical Medicine Innovation and Transformation of Ministry of Education of Hainan Medical University Grant No. TMIT2024Z03Top Talent Support Program for Young and Middle-aged People of Wuxi Health Committee No. BJ2023066
6 · The paper itself

Abstract

Macrophage-mediated inflammatory responses including pyroptosis are involved in the pathogenesis of sepsis and acute lung injury (ALI), for which there are currently no effective therapeutic treatments. The natural product (+)-Balasubramide is an eight-membered lactam compound extracted from the leaves of the Sri Lanka plant Clausena Indica and has shown anti-inflammatory activities, but its poor pharmacokinetic properties limit its further application for ALI. In this study, a compound (+)3C-20 is discovered with improved both pharmacokinetic properties and anti-inflammatory activity from a series of (+)-Balasubramide derivatives. The compound (+)3C-20 exhibits a markedly enhanced inhibitory effect against LPS-induced expressions of pro-inflammatory factors in mouse macrophages and human PBMCs from ALI patients and shows a preferable lung tissue distribution in mice. (+)3C-20 remarkably attenuates LPS-induced ALI through lung tissue-specific anti-inflammatory actions. Mechanistically, a chemical proteomics study shows that (+)3C-20 directly binds to mitochondrial VDAC1 and inhibits VDAC1 oligomerization to block mtDNA release, further preventing NLRP3 inflammasome activation. These findings identify (+)3C-20 as a novel VDAC1 inhibitor with promising therapeutic potential for ALI associated with inflammation.

Indexed as

Acute Lung InjuryAnti-Inflammatory AgentsDisease Models, AnimalVoltage-Dependent Anion Channel 1AnimalsHumansMaleMiceMice, Inbred C57BLAnti-Inflammatory AgentsVDAC1 protein, humanVoltage-Dependent Anion Channel 1acute lung injurybalasubramide derivativemacrophageNLRP3 inflammasomeVDAC1

Identifiers

PMID39556713
PMCPMC11672292

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.