Evidence map›Paper›PMID 37763673›Full record

ArticleMedicina (Kaunas, Lithuania)2023

Cheng-Han Lin, Yi-Ju Chen, Meng-Wei Lin, Ho-Ju Chang, Xin-Rui Yang, Chih-Sheng Lin

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Inhibitory Efficacy of Main Components ofInternational journal of molecular sciences · 2024
    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

6 authors at 1 institution in 1 country.

Cheng-Han LinDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Yi-Ju ChenDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Meng-Wei LinDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Ho-Ju ChangDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Xin-Rui YangDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Chih-Sheng LinDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
National Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 is a highly transmittable respiratory illness caused by SARS-CoV-2, and acute lung injury (ALI) is the major complication of COVID-19. The challenge in studying SARS-CoV-2 pathogenicity is the limited availability of animal models. Therefore, it is necessary to establish animal models that can reproduce multiple characteristics of ALI to study therapeutic applications. The present study established a mouse model that has features of ALI that are similar to COVID-19 syndrome to investigate the role of ACE2 and the administration of the Chinese herbal prescription NRICM101 in ALI. Mice with genetic modifications, including overexpression of human ACE2 (K18-hACE2 TG) and absence of ACE2 (mACE2 KO), were intratracheally instillated with hydrochloric acid. The acid intratracheal instillation induced severe immune cell infiltration, cytokine storms, and pulmonary disease in mice. Compared with K18-hACE2 TG mice, mACE2 KO mice exhibited dramatically increased levels of multiple inflammatory cytokines (IL-6 and TNF-α) in bronchoalveolar lavage fluid, histological evidence of lung injury, and dysregulation of MAPK and MMP activation. In mACE2 KO mice, NRICM101 could ameliorate the disease progression of acid-induced ALI. In conclusion, the established mouse model provided an effective platform for researchers to investigate pathological mechanisms and develop therapeutic strategies for ALI, including COVID-19-related ALI.

Indexed as

Acute Lung InjuryAngiotensin-Converting Enzyme 2Drugs, Chinese HerbalAnimalsCOVID-19COVID-19 Drug TreatmentCytokinesDisease Models, AnimalHumansInflammationMaleMedicine, Chinese TraditionalMiceMice, Inbred C57BLMice, KnockoutSARS-CoV-2ACE2 protein, humanAce2 protein, mouseAngiotensin-Converting Enzyme 2CytokinesDrugs, Chinese Herbalacute lung injury (ALI)angiotensin-converting enzyme type II (ACE2)animal modeltraditional Chinese medicine

Identifiers

PMID37763673
PMCPMC10533189
OpenAlexW4386224284

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.